glutamic acid and Genetic Predisposition

glutamic acid has been researched along with Genetic Predisposition in 211 studies

Research

Studies (211)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (0.95)	18.2507
2000's	111 (52.61)	29.6817
2010's	93 (44.08)	24.3611
2020's	5 (2.37)	2.80

Authors

Authors	Studies
Abdullah, U; Ali, Z; Asif, M; Baig, SM; Farooq, M; Fatima, A; Mang, Y; Mehrjouy, MM; Tommerup, N	1
Mi, YY; Song, NH; Wang, ZJ; Yuan, W; Zhang, LF; Zhang, W; Zhu, LJ; Zuo, L	1
Daly, E; Gudbrandsen, M; Hathway, P; Howes, O; Jauhar, S; McCutcheon, RA; Rogdaki, M	1
Cooney, KA; Helfand, BT; Hulick, PJ; Isaacs, WB; Na, R; Resurreccion, WK; Shi, Z; Wang, CH; Wei, J; Xu, J; Zheng, SL	1
Castillo-Maldonado, I; Delgadillo-Guzmán, D; Pedroza-Escobar, D; Quintanar-Escorza, MA; Sharara-Núñez, AI	1
Bararpour, N; Darrous, L; Froguel, P; Gasser, M; Gilardi, F; Kutalik, Z; Marques-Vidal, P; Porcu, E; Thomas, A; Waeber, G; Yengo, L	1
Chen, Y; Lu, SY; Wang, B; Wang, QW; Wang, YH; Yao, J	1
Alasmari, F; Althobaiti, YS; Hammad, AM; Sari, Y	1
Antonucci, LA; Attrotto, M; Bertolino, A; Blasi, G; Di Carlo, P; Fanelli, G; Maddalena, G; Masellis, R; Miccolis, G; Pergola, G; Pignataro, P; Rampino, A; Romano, R; Taurisano, P; Torretta, S; Ursini, G	1
Bonvicini, C; Gardella, R; Gennarelli, M; Giacopuzzi, E; Magri, C; Minelli, A; Sacchetti, E; Traversa, M; Valsecchi, P; Vita, A	1
Arnesano, C; Herring, BE; Katritch, V; Sadybekov, A; Tian, C	1
Arnsten, AFT; Datta, D	1
Fernandez, TV; Leckman, JF; Pittenger, C	1
Culmsee, C; Michels, S; Schwarting, RK; Wöhr, M	1
Anhøj, SJ; Broberg, BV; Brouwer, R; Fagerlund, B; Glenthøj, BY; Hilker, R; Jensen, MH; Legind, CS; Mandl, RCW; McGuire, P; Pol, HH; Rostrup, E	1
Lv, J; You, T; Zhou, L	1
Bean, JC; Chen, YJ; Lin, TW; Liu, X; Lu, YS; Mei, L; Sathyamurthy, A; Shen, C; Smith, CA; Xiong, WC; Yin, DM	1
Liu, HL; Liu, LZ; Wu, EP	1
Asano, H; Cho, MC; Hirashiki, A; Hirayama, H; Ichihara, G; Ichihara, S; Inagaki, H; Inoue, I; Iwase, M; Izawa, H; Jang, Y; Kim, HS; Kimura, A; Kitajima, H; Lee, JY; Matsubara, T; Minatoguchi, S; Murohara, T; Nakatochi, M; Nishigaki, K; Park, JE; Shimokawa, H; Sone, T; Sukegawa, M; Sunagawa, K; Tada-Oikawa, S; Takatsu, F; Umeda, H; Yamamoto, K; Yokota, M	1
Adolfsson, R; Alttoa, A; Freitag, CM; Freudenberg, F; Gessner, A; Grußendorf, H; Hempel, S; Herterich, S; Heupel, J; Jacob, CP; Kent, L; Kittel-Schneider, S; Klamer, D; Kopf, J; Kramer, A; Lesch, KP; Moltó, MD; Post, A; Reif, A; Rivero, O; Sanjuán, J; Schmidt, B; Scholz, CJ; Volkert, J; Weber, H	1
Furukawa, M; Hashida, S; Higasa, K; Ichimura, K; Kiura, K; Matsuda, F; Matsuo, K; Miyoshi, S; Sakaguchi, M; Shien, K; Soh, J; Takigawa, N; Toyooka, S; Tsukuda, K; Yamamoto, H	1
Anderson, CD; Rosand, J	1
Cohen, BM; Duncan, LE; Holmans, PA; Kirby, AW; Lee, PH; O'Dushlaine, CT; Öngür, D; Smoller, JW	1
Jeon, BS; Kim, YE	1
Ishikawa, H; Kiyokawa, T; Matsushita, K; Nomura, F; Shozu, M; Utsuno, E	1
Betz, BL; Brown, NA; Elenitoba-Johnson, KS; Furtado, LV; Kiel, MJ; Lim, MS; Weigelin, HC	1
Chen, W; He, Q; Lin, X; Ren, Z; Wang, F; Xing, X; Xu, J	1
Chen, Y; Cui, L; Cui, Z; Li, M; Shang, R; Sun, Y; Xu, F	1
Atwal, JK; Behrens, TW; Bhangale, TR; Cruchaga, C; Farrer, LA; Foreman, O; Goate, A; Graham, RR; Haines, J; Hansen, DV; Hunkapiller, J; Maloney, JA; Mayeux, R; Ortmann, W; Pericak-Vance, M; Rathore, N; Sa, SM; Schellenberg, GD; Srinivasan, K; Tessier-Lavigne, M; Watts, RJ; Wetzel-Smith, MK; Yaylaoglu, MB	1
Abecasis, GR; Absher, D; Adair, LS; Albrecht, E; Amin, N; Amouyel, P; Anderson, D; Ärnlöv, J; Arscott, GM; Arveiler, D; Asselbergs, FW; Assimes, TL; Attwood, AP; Bakker, SJL; Bandinelli, S; Barrett, A; Barroso, I; Bas, IN; Beckmann, JS; Beekman, M; Beilby, J; Bellis, C; Bennett, AJ; Bergman, RN; Berndt, SI; Berne, C; Blagieva, R; Blangero, J; Blüher, M; Bochud, M; Boehm, BO; Boehnke, M; Boerwinkle, E; Böhringer, S; Bolton, JL; Bonnycastle, LL; Borecki, IB; Bornstein, SR; Böttcher, Y; Bottinger, EP; Bouchard, C; Bovet, P; Boyd, HA; Bragg-Gresham, JL; Brennan, EP; Bruinenberg, M; Buchkovich, ML; Buyske, S; Campbell, H; Caspersen, IH; Cauchi, S; Caulfield, MJ; Cesana, G; Chakravarti, A; Chambers, JC; Chanock, SJ; Chasman, DI; Chen, J; Chen, YI; Chines, PS; Choi, M; Clarke, R; Collins, FS; Cooper, RS; Crawford, DC; Croteau-Chonka, DC; Cupples, LA; Cusi, D; Danesh, J; Dastani, Z; Daw, EW; Day, FR; de Bakker, PIW; de Craen, AJM; de Faire, U; Dedoussis, G; Delgado, G; Deloukas, P; Demirkan, A; den Ruijter, HM; Deng, G; Dimitriou, M; Dominiczak, AF; Doney, ASF; Dorajoo, R; Drong, AW; Ehret, GB; Eklund, N; Erbel, R; Erdmann, J; Eriksson, JG; Eriksson, P; Esko, T; Estrada, K; Eury, E; Fall, T; Farrall, M; Faul, JD; Feenstra, B; Fehrmann, R; Feitosa, MF; Felix, SB; Ferrannini, E; Ferreira, T; Ferrières, J; Ferrucci, L; Fischer, K; Folkersen, L; Ford, I; Forouhi, NG; Forrester, T; Fox, CS; Franco, OH; Franco-Cereceda, A; Franke, L; Franks, PW; Fraser, RM; Frayling, TM; Froguel, P; Gådin, JR; Gansevoort, RT; Garcia, ME; Gejman, PV; Geller, F; Gharavi, AG; Giedraitis, V; Gieger, C; Gigante, B; Go, AS; Goddard, ME; Goel, A; Golay, A; Gong, J; Goodall, AH; Gordon, SD; Gorski, M; Gottesman, O; Grabe, HJ; Grallert, H; Grammer, TB; Gräßler, J; Grönberg, H; Groop, LC; Groves, CJ; Gudnason, V; Gustafsson, S; Gusto, G; Gyllensten, U; Haessler, J; Haiman, CA; Hall, AS; Hall, P; Haller, T; Hallmans, G; Hamsten, A; Handsaker, RE; Harris, TB; Hartman, CA; Hassinen, M; Hattersley, AT; Hayward, C; Heard-Costa, NL; Heath, AC; Hedman, ÅK; Heid, IM; Helmer, Q; Hengstenberg, C; Hicks, AA; Hindorff, LA; Hingorani, AD; Hirschhorn, JN; Hofman, A; Holmen, O; Homuth, G; Hottenga, JJ; Hovingh, GK; Huang, J; Hui, J; Humphries, SE; Hunt, SC; Hunter, DJ; Hveem, K; Hyppönen, E; Illig, T; Ingelsson, E; Isaacs, A; Jackson, AU; Jacobs, KB; James, AL; Jarvelin, MR; Jeff, JM; Jöckel, KH; Johansen, B; Johansson, Å; Jolley, J; Jousilahti, P; Jukema, JW; Jula, AM; Juliusdottir, T; Justice, AE; Kahali, B; Kanoni, S; Kaplan, RC; Kaprio, J; Karjalainen, J; Karpe, F; Kastelein, JJP; Kathiresan, S; Keildson, S; Keinanen-Kiukaanniemi, SM; Kiemeney, LA; Kinnunen, L; Kiryluk, K; Kivimaki, M; Kleber, ME; Knekt, P; Koenig, W; Kooner, JS; Kooperberg, C; Koskenvuo, M; Kovacs, P; Kraja, AT; Kratzer, W; Kristiansson, K; Kubo, M; Kuh, D; Kumari, M; Kutalik, Z; Kuusisto, J; Laakso, M; Laitinen, J; Lakka, TA; Lamina, C; Langenberg, C; Leach, IM; Leander, K; Lee, JY; Lee, NR; Lehtimäki, T; Liang, L; Lichtner, P; Lifton, RP; Lim, U; Lind, L; Lindgren, CM; Lindström, J; Liu, Y; Lo, KS; Lobbens, S; Locke, AE; Loos, RJF; Lorbeer, R; Lotay, V; Lu, Y; Luan, J; Lyssenko, V; Ma, B; Mach, F; Madden, PAF; Mägi, R; Magnusson, PKE; Mahajan, A; Mangino, M; Männistö, S; Marchand, LL; Marette, A; Martin, NG; März, W; Matise, TC; McArdle, WL; McCarroll, SA; McCarthy, MI; McKenzie, CA; McKnight, AJ; McKnight, B; McLachlan, S; Medina-Gomez, C; Medland, SE; Melbye, M; Menni, C; Merger, S; Metspalu, A; Mihailov, E; Milani, L; Min, JL; Moayyeri, A; Moebus, S; Moffatt, MF; Mohlke, KL; Moll, FL; Monda, KL; Montgomery, GW; Morken, MA; Morris, AD; Morris, AP; Mulas, A; Müller, G; Müller-Nurasyid, M; Munroe, PB; Murabito, JM; Murray, JC; Musk, AW; Nagaraja, R; Nalls, MA; Nelis, M; Nicholson, G; Njølstad, I; Nolte, IM; North, KE; Nöthen, MM; Nyholt, DR; O'Connell, JR; Ohlsson, C; Okada, Y; Oldehinkel, AJ; Ong, KK; Oostra, BA; Palmer, CD; Palmer, CNA; Pasko, D; Pasterkamp, G; Pechlivanis, S; Peden, JF; Pedersen, NL; Perola, M; Perry, JRB; Pers, TH; Pérusse, L; Peters, A; Peters, MJ; Peters, U; Pilz, S; Postma, DS; Powell, C; Power, C; Pramstaller, PP; Price, JF; Prokopenko, I; Qi, L; Quertermous, T; Raitakari, OT; Randall, JC; Rankinen, T; Rao, DC; Rauramaa, R; Rayner, NW; Reinmaa, E; Renstrom, F; Rettig, R; Rice, TK; Ridker, PM; Ried, JS; Rioux, JD; Ripke, S; Ritchie, MD; Rivadeneira, F; Robertson, NR; Rose, LM; Rudan, I; Saaristo, TE; Saleheen, D; Salem, RM; Salomaa, V; Samani, NJ; Sandholm, N; Sanna, S; Saramies, J; Sarzynski, MA; Sattar, N; Schadt, EE; Scharnagl, H; Scherag, A; Schlessinger, D; Schmidt, EM; Scholtens, S; Schumacher, FR; Schunkert, H; Schwarz, PEH; Scott, RA; Scott, WR; Seufferlein, T; Sever, P; Shi, J; Shuldiner, AR; Shungin, D; Sinisalo, J; Slagboom, PE; Smith, AV; Smith, JA; Smolonska, J; Snieder, H; Spector, TD; Speliotes, EK; Stančáková, A; Stanton, AV; Stefansson, K; Steinthorsdottir, V; Stirrups, K; Stolk, L; Stolk, RP; Strachan, DP; Strauch, K; Strawbridge, RJ; Stringham, HM; Stumvoll, M; Sundström, J; Sung, YJ; Swertz, MA; Swift, AJ; Syvänen, AC; Takahashi, A; Tan, ST; Tanaka, T; Tayo, BO; Teumer, A; Thorand, B; Thorleifsson, G; Thorsteinsdottir, U; Tönjes, A; Trégouët, DA; Tremblay, A; Tremoli, E; Trompet, S; Tuomilehto, J; Tyrer, JP; Uh, HW; Uitterlinden, AG; Uusitupa, M; van 't Hooft, FM; van der Harst, P; van der Laan, SW; van Duijn, CM; van Setten, J; Van Vliet-Ostaptchouk, JV; Vandenput, L; Vedantam, S; Verhulst, FC; Vermeulen, SH; Verweij, N; Vinkhuyzen, AAE; Virtamo, J; Visscher, PM; Vohl, MC; Völker, U; Vonk, JM; Waeber, G; Waite, LL; Walker, M; Wallaschofski, H; Wang, Z; Wareham, NJ; Warren, HR; Waterworth, D; Watkins, H; Weedon, MN; Weir, DR; Westra, HJ; Wichmann, HE; Wilkens, LR; Willemsen, G; Willenborg, C; Willer, CJ; Wilsgaard, T; Wilson, JF; Winkler, TW; Witteman, JC; Wojczynski, MK; Wong, A; Wood, AR; Workalemahu, T; Wright, AF; Yang, J; Yengo, L; Zanen, P; Zhang, Q; Zhang, W; Zhao, JH; Zhao, W; Zheng, W; Zillikens, MC; Zondervan, KT	1
de Leeuw, C; Goudriaan, A; Mathews, CA; Posthuma, D; Scharf, JM; Smit, AB; Verheijen, MH; Yu, D	1
Deng, J; Fang, W; Lu, J; Qiu, F; Yang, L; Zhang, H; Zhang, L; Zhou, Y	1
Bacares, R; Figueiredo, J; Melo, S; Ruggeri, J; Seruca, R; Shah, MA; Simões-Correia, J; Somar, J; Xiao, A; Zhang, L	1
Bullmore, ET; Dean, AM; Goodby, E; Grainger, D; Griffin, JL; Jones, PB; Lennox, BR; Murray, GK; Nathan, PJ; Salek, RM; Scoriels, L; Suckling, J; West, JA	1
Hou, C; Huang, J; Li, N; Liu, Z; Pu, J; Shan, H	1
Chiu, SL; Huganir, RL; Sharma, K; Volk, L	1
Aguilar-Sosa, E; Alvarado-Moreno, A; Esparza-García, JC; Guadalupe Valades-Mejía, M; Hernández-Juárez, J; Isordia-Salas, I; Leaños-Miranda, A; Majluf-Cruz, A; Santiago-Germán, D	1
Alirol, S; Andres, CR; Barthélémy, C; Bazaud, S; Blanc, R; Bonnet-Brilhault, F; Gomot, M; Laumonnier, F; Lemonnier, É; Marouillat, S; Raynaud, M; Thépault, RA; Toutain, A	1
Cama, E; del Castillo, I; Santarelli, R; Scimemi, P; Starr, A	1
Bellivier, F; Besnard, A; Bolte, S; Caboche, J; Crettol, S; Daumas, S; Eap, CB; El Mestikawy, S; Giros, B; Gratton, A; Gutiérrez-Cuesta, J; Heck, N; Henrion, A; Herzog, E; Jamain, S; Lecca, S; Maldonado, R; Mameli, M; Marti, F; Martín-García, E; Moquin, L; Morel, LJ; Prado, MA; Prado, VF; Sakae, DY; Vanhoutte, P; Vorspan, F	1
de la Fuente-Sandoval, C; Favila, R; Graff-Guerrero, A; León-Ortiz, P; Mao, X; Reyes-Madrigal, F; Rodríguez-Mayoral, O; Shungu, DC; Solís-Vivanco, R	1
Howells, FM; Russell, VA; Sterley, TL	1
Ding, C; Hu, F; Jin, G; Liu, J; Wei, H; Yin, H	1
Xing, M; Zhang, T	1
Heese, K; Kutzner, A	1
Bernardo, M; Bioque, M; Cabrera, B; Corripio, I; Gassó, P; Gonzàlez-Pinto, A; Lafuente, A; Llerena, A; Lobo, A; Mas, S; Olmeda, MS; Saiz-Ruiz, J	1
Egerton, A; Kempton, MJ; McGuire, PK; Merritt, K; Taylor, MJ	1
Boer, VO; Cahn, W; Kahn, RS; Klomp, DW; Neggers, SF; Rösler, L; Thakkar, KN; Wijnen, JP	1
Alexander, SP; Fone, KC; Gaskin, PL; Toledo-Rodriguez, M	1
Breen, ME; de Klerk, K; DeLuca, AP; Gaynor, SC; Monson, ET; Parsons, M; Potash, JB; Scheetz, TE; Willour, VL; Zandi, PP	1
Christiansen, SH; Elbrønd-Bek, H; Lavebratt, C; Liu, JJ; Mathé, AA; Melas, PA; Villaescusa, JC; Wegener, G; Wei, YB; Woldbye, DP; Xu, N	1
Glazer, S; Rubin, K	1
Duncan, GE; Farrington, JS; Inada, K; Koller, BH	1
Bauer, L; Bertaso, F; Betz, H; Bockaert, J; Eulenburg, V; Fagni, L; Herin, GA; Lerner-Natoli, M; Scheschonka, A; Zhang, CS	1
Meador-Woodruff, J; Sodhi, M; Wood, KH	1
Inoue, N; Kasahara, M; Miyaishi, A; Osawa, K; Osawa, Y; Shimada, E; Tabuchi, Y; Takahashi, J; Tanaka, K; Tsutou, A; Yamamoto, M; Yoshida, K	1
Fukushima, M; Higashiyama, T; Hirokawa, M; Inoue, H; Ito, Y; Kihara, M; Kobayashi, K; Maruo, R; Matsuzuka, F; Miya, A; Miyauchi, A; Morita, S; Takamura, Y; Takano, T; Tomoda, C; Uruno, T; Yabuta, T; Yoshida, H	1
Osredkar, J; Petrovic, D; Petrovic, MG; Saraga-Babić, M	1
Jia, J; Jiang, H	1
Bordoni, A; Bresolin, N; Comi, GP; Corti, S; Crugnola, V; Del Bo, R; Donadoni, C; Fortunato, F; Lucchini, V; Moggio, M; Papadimitriou, D; Ronchi, D; Salani, S; Santoro, D	1
Arakaki, RF; Florez, JC; Goldstein, BJ; Hanson, RL; Jablonski, KA; Kahn, SE; Kitabchi, AE; Knowler, WC; Mason, CC; McAteer, JB; Moore, AF	1
Barbieri, M; Belluzzi, O; Binaschi, A; Buzzi, A; Cifelli, P; Coffin, JD; Marzola, A; Paradiso, B; Rodi, D; Simonato, M; Zucchini, S	1
Bougnères, P; Valleron, AJ	1
Benzel, I; de Belleroche, J; Hirsch, S; Kelly, F; Kew, JN; Maycox, PR; Sanderson, TH; Viknaraja, R	1
Bakker, SL; Baloh, RW; Boon, EM; de Vries, B; Ferrari, MD; Frants, RR; Haan, J; Howard, BD; Jen, JC; Mamsa, H; Stam, AH; Terwindt, GM; van den Maagdenberg, AM; Vanmolkot, KR; Wan, J	1
de Graan, PN; Hakvoort, TB; Lamers, WH; van der Hel, WS; van Gassen, KL	1
Harwood, CA; McDermott, CJ; Shaw, PJ	1
Clarke, NF; Domazetovska, A; Kornberg, A; McLean, C; North, KN; Waddell, L	1
Geyer, MA; Powell, SB; Zhou, X	1
Blendy, JA; Brodkin, ES; Christian, EP; Dow, HC; Ehrlichman, RS; Gur, RC; Gur, TL; Halene, TB; Jonak, GJ; Liang, Y; Schneider, F; Siegel, SJ	1
Budka, H; Ghetti, B; Haraszti, L; Horvath, S; Kovacs, GG; Majtenyi, K; Molnar, MJ; Murrell, JR; Spina, S	1
Chen, JF; Duan, W; Gui, L; Li, C; Tian, H; Zheng, J; Zhu, J	1
Kalela, A; Kortelainen, ML; Kunnas, T; Lahtio, R; Nikkari, ST	1
Li, J; Mo, K; Scherer, SS; Yum, SW; Zhang, J	1
Chen, PL; Cheng, YW; Koeh, H; Lee, H; Liu, YL; Tsai, YY; Yeh, KT	1
Brajusković, G; Cadez, I; Dimitrijević, R; Dobricić, V; Keckarević, D; Keckarević-Marković, M; Kecmanović, M; Romac, S; Savić-Pavićević, D	1
Biacabe, AG; Budka, H; Höftberger, R; Kapás, I; Kovacs, GG; László, L; Majtenyi, K; Meyronet, D; Perret-Liaudet, A; Quadrio, I; Sciot, R; Seguin, J; Streichenberger, N; Ströbel, T; Vandenberghe, R	1
Baggiani, A; Basolo, F; Berti, P; Elisei, R; Giannini, R; Lupi, C; Miccoli, M; Miccoli, P; Sensi, E; Torregrossa, L; Vitti, P	1
Jia, P; Meltzer, HY; Wang, L; Zhao, Z	1
Bizzi, A; Bugiani, O; Capobianco, R; Carella, F; Cupidi, C; Di Fede, G; Giaccone, G; Giovagnoli, A; Magoni, M; Mangieri, M; Marcon, G; Mazzoleni, G; Morbin, M; Padovani, A; Patruno, GM; Puoti, G; Romorini, A; Rossi, G; Salmaggi, A; Tagliavini, F	1
Buono, RJ; Eaton, MJ; Ferraro, TN; Inyushin, M; Kucheryavykh, LY; Kucheryavykh, YV; Nichols, CG; Skatchkov, SN	1
Abate, N; Adams-Huet, B; Bell, J; Chandalia, M; Grundy, SM; Szuszkiewicz, M; Vazquez, M	1
Bartsch, D; Brors, B; Dahmen, N; Deussing, J; Eils, R; Ende, G; Gallinat, J; Gebicke-Haerter, P; Heinz, A; Jäger, W; Kiefer, F; Mann, K; Matthäus, F; Nöthen, M; Rietschel, M; Sartorius, A; Schütz, G; Sommer, WH; Spanagel, R; Sprengel, R; Walter, H; Wichmann, E; Wienker, T; Wurst, W; Zimmer, A	1
Bredt, DS; Gill, MB	1
Ataei, F; Bakhtiyari, S; Gerayesh-Nejad, S; Gulkho, S; Hanachi, P; Larijani, B; Meshkani, R; Mohammadi, M; Mohammadtaghvaei, N; Parvaneh, L; Saberi, H; Zargari, M	1
Adamczyk, A; Gause, CD; Rothstein, JD; Sattler, R; Singer, H; Vidensky, S; Wang, T	1
Amin, N; Aulchenko, YS; Boomsma, DI; Breteler, M; de Geus, EJ; de Moor, MH; de Vries, B; Ferrari, MD; Gudnason, V; Hofman, A; Hottenga, JJ; Ikram, MA; Janssens, AC; Kattenberg, VM; Koelewijn, SC; Launer, LJ; Ligthart, L; Montgomery, GW; Nyholt, DR; Oostra, BA; Penninx, BW; Smit, JH; Smith, AV; Terwindt, GM; Uitterlinden, AG; van den Maagdenberg, AM; van Duijn, CM; Willemsen, G; Zitman, FG	1
Fu, L; Liu, N; Ma, Y; Qiao, J; Tu, B; Yan, L; Zhang, Q; Zhang, X	1
Cichon, S; Deufel, T; Kiehntopf, M; Koch, K; Mühleisen, TW; Nenadic, I; Nöthen, MM; Reichenbach, JR; Rietschel, M; Roebel, M; Sauer, H; Schachtzabel, C; Schlösser, RG; Schultz, CC; Wagner, G	1
Chen, YG; Hao, PP; Wang, JL; Wang, XL; Zhang, Y	1
Atchison, WD; Chitrakar, A; Hajela, RK; Johnson, FO; Parsell, DM; Yuan, Y	1
Hwang, TS; Jang, YM; Kim, DL; Kim, SK; Lee, EJ; Song, KH	1
Al-Mohanna, F; Al-Saif, A; Bohlega, S	1
Binder, EB; Czamara, D; Czisch, M; Heck, A; Hennings, J; Holsboer, F; Kloiber, S; Kohli, MA; Lucae, S; Menke, A; Müller-Myhsok, B; Sämann, P	1
Ambrosio, E; Botreau, F; Coria, SM; Del Olmo, N; Higuera-Matas, A; Miguéns, M; Olías, O	1
Berghoff, AS; Birner, P; Capper, D; Habel, A; Hackl, M; Ilhan, A; Magerle, M; Meyer, J; Petzelbauer, P; Pichler, J; Preusser, M; Pusch, S; von Deimling, A; Wöhrer, A	1
Bhowmik, AD; Chaudhuri, K; Mukherjee, S; Mukhopadhyay, K; Ray, JG; Roychoudhury, P	1
Egerton, A; Fusar-Poli, P; Stone, JM	1
Bergseng, E; Bodd, M; Lundin, KE; Sollid, LM; Tollefsen, S	1
Chen, YJ; Mei, L; Sathyamurthy, A; Xiong, WC; Yin, DM	1
Rezaei, Z; Saadat, I; Saadat, M	1
Bramon, E; Chaddock, CA; Collier, DA; Ehlert, N; Fu, CH; Georgiades, A; Kalidindi, S; Kane, F; Kravariti, E; McDonald, C; McGuire, P; Mechelli, A; Murray, R; Pauli, A; Picchioni, M; Prata, DP; Toulopoulou, T; Walshe, M	1
Biagini, A; Ciofini, E; Colombo, MG; Manfrini, O; Paradossi, U; Pizzi, C; Xhyheri, B	1
Anderson, LR; Arnold, PD; Hanna, GL; Himle, JA; Jones, ST; Kennedy, JL; Richter, MA; Ruggiero, AM; Veenstra-VanderWeele, J; Xu, T	1
Adachi, Y; Aleksic, B; Banno, M; Hashimoto, R; Iidaka, T; Ikeda, M; Inada, T; Iwata, N; Kawano, N; Kikuchi, T; Kohmura, K; Koide, T; Kushima, I; Nakamura, Y; Ohi, K; Okada, T; Ozaki, N; Suzuki, M; Takeda, M; Ujike, H; Yamashita, S; Yasuda, Y	1
Acosta-Baena, N; Aguirre-Acevedo, DC; Arcos-Burgos, M; Chandrasekharappa, SC; Correa, JC; Garcia, G; Harper, U; Henao, E; Jaramillo-Elorza, MC; Jones, M; Kosik, KS; Lopera, F; Lopera-Gómez, CM; Lopez, L; Martinez, AF; Rivera, D; Schork, NJ; Solomon, BD; Swanson, JM; Vélez, JI	1
Chen, Z; Ding, Q; Dong, P; Gao, X; He, D; Jiang, H; Jiao, Y; Lin, X; Liu, F; Lu, D; Mo, Z; Na, R; Ou-Yang, J; Qi, J; Qu, L; Ren, S; Shao, Q; Shi, R; Sun, J; Sun, Y; Tao, S; Turner, AR; Wang, G; Wang, M; Wang, X; Wang, Z; Wu, D; Wu, Q; Xu, C; Xu, J; Xu, Y; Yang, J; Ye, D; Yin, C; Yuan, J; Zhang, Z; Zheng, SL; Zheng, Y; Zhou, F; Zhu, Y	1
Fujita, Y; Harai, T; Hashimoto, K; Hongou, K; Horio, M; Inoue, R; Miyawaki, T; Mori, H; Tanaka, A	1
Gururajan, A; Klug, M; Manning, EE; van den Buuse, M	1
Cacheiro, P; Carreño, O; Cormand, B; Fernández-Morales, J; Macaya, A; Narberhaus, B; Pozo-Rosich, P; Sintas, C; Sobrido, MJ	1
Baraban, SC; Choi, M; Coppola, G; Fu, YH; Geschwind, DH; Gibson, G; Hahn, AF; Howard, MA; Huang, A; Kirk, A; Klein, E; Kornberg, Z; Lee, HY; Lifton, RP; Merriman, B; Mirsattari, SM; Nelson-Williams, C; Ptáček, LJ; Russell, JF; Steckley, JL	1
Czerwinski, M; Duk, M; Grodecka, M; Jaskiewicz, E; Kaczmarek, R; Laskowska, A; Lisowska, E; Lukasiewicz, J; Majorczyk, E; Smolarek, D; Suchanowska, A; Wasniowska, K	1
Lee, KC; Li, C; Schneider, EB; Zeiger, MA	1
Agate, L; Basolo, F; Biagini, A; Elisei, R; Giannini, R; Lupi, C; Materazzi, G; Miccoli, P; Molinaro, E; Piaggi, P; Pinchera, A; Romei, C; Torregrossa, L; Ugolini, C; Valerio, L; Viola, D; Vitti, P	1
Drummond, JB; Haroutunian, V; Meador-Woodruff, JH; Simmons, M	1
Boomsma, DI; Byrne, EM; Haddad, S; Heath, AC; Jung, JY; Lee, PH; Madden, PA; Martin, NG; Mayerfeld, CE; Penninx, BW; Pergadia, ML; Perlis, RH; Purcell, SM; Rueckert, E; Siburian, R; Sklar, P; Smoller, JW; Wray, NR	1
Arnold, PD; Easter, P; Hanna, GL; Kennedy, JL; Rosenberg, DR; Wu, K	1
Boot, E; van Amelsvoort, TA	1
Castro-Fornieles, J; Gassó, P; Lafuente, A; Lazaro, L; Martinez, E; Mas, S; Milà, M; Moreno, E; Plana, MT	1
Anisman, H; McIntyre, DC; Merali, Z; Shin, RS	1
Lantner, F; Schori, H; Schwartz, M; Shachar, I	1
Doi, T; Mitsuyama, Y; Tokumaru, J; Tsuru, N; Ueda, Y	1
Massotti, M; Pulvirenti, L	1
Colagiuri, S; Duarte, NL; Palu, T; Wang, XL; Wilcken, DE	1
Schauwecker, PE	1
Rossi, GP; Seccia, TM	1
Häkli, T; Heinonen, S; Helisalmi, S; Hiltunen, M; Punnonen, K; Romppanen, EL	1
Calabuig, J; Macho-Azcarate, T; Marti, A; Martinez, JA	1
Bantubungi, K; Blum, D; Brouillet, E; Cuvelier, L; Galas, MC; Gall, D; Galluzzo, M; Ledent, C; Muller, CE; Pintor, A; Popoli, P; Rolland, AS; Schiffmann, SN	1
Corbalán, MS; Forga, L; Marti, A; Martínez, JA; Martínez-González, MA; Sánchez-Villegas, A	1
Faingold, CL; Feng, HJ; Raisinghani, M	1
Vanacore, N	1
Bajocchi, G; Boiardi, L; Casali, B; Catanoso, MG; Chen, Q; Farnetti, E; Macchioni, P; Nicoli, D; Salvarani, C	1
Collier, DA; Li, T	1
Du Bois, R; Fontenot, AP; Lympany, P; Maier, LA; McGrath, DS; Newman, LS; Sato, H; Sawyer, RT; Silveira, L; Welsh, K; Wilcox, E	1
Goldman, D; Heinz, A; Higley, JD; Krystal, JH; Schäfer, M	1
Belknap, JK; Buck, KJ; Crabbe, JC; Fehr, C; Kosobud, AE; Metten, P; Shirley, RL	1
Gulcher, JR; Stefansson, H; Stefansson, K; Steinthorsdottir, V; Thorgeirsson, TE	1
Hamajima, N; Ito, H; Kang, D; Lee, KM; Matsuo, K; Mitsudomi, T; Saito, T; Sato, S; Sugiura, T; Tajima, K; Ueda, R; Yasue, T; Yoo, KY	1
Bespalova, IN; Buxbaum, JD; Davis, KL; Ramoz, N; Reichert, JG; Silverman, JM; Smith, CJ	1
Cortes De Oliveira, JA; Galvis-Alonso, OY; Garcia-Cairasco, N	1
Hirooka, Y; Ito, K; Kimura, Y; Kishi, T; Shimokawa, H; Takeshita, A	1
Chapman, RW; Cullen, SN; Jewell, DP; Li, JH; Yang, X	1
O'Donovan, MC; Owen, MJ; Williams, NM	1
Allen, P; Hanstock, C; Tibbo, P; Valiakalayil, A	1
Higuchi, S; Kamakura, K; Masaki, T; Matsushita, S; Mochizuki, H; Yokoyama, A	1
Amore, M; Canaider, S; Carinci, P; Casadei, R; D'Addabbo, P; Ferrari, G; Frabetti, F; Laterza, C; Lenzi, L; Strippoli, P; Tagariello, P; Torroni, A; Vitale, L; Zannotti, M	1
Chian, D; Hornig, M; Lipkin, WI	1
Aznar, J; Carrell, RW; Corral, J; Gonzalez-Conejero, R; Huntington, JA; Miñano, A; Vayá, A; Vicente, V; Villa, P	1
Holcomb, HH; Tamminga, CA	1
Hashimoto, R; Ishimoto, T; Iwata, N; Kamijima, K; Kunugi, H; Numakawa, T; Okada, T; Ozaki, N; Straub, RE; Suzuki, T; Taguchi, T; Tatsumi, M; Weinberger, DR; Yagasaki, Y	1
Joyner, PW; McMillen, BA; Parmar, CA; Tyer, WE; Williams, HL	1
Granados, J; Hernández-Pacheco, G; Murguía, LE; Pérez-Hernández, N; Reyes, PA; Soto, ME; Vargas-Alarcón, G	1
Aschauer, HN; Schosser, A	1
Beck, SR; Bowden, DW; Burdon, KP; Freedman, BI; Langefeld, CD; Liu, Y; Rich, SS; Wagenknecht, LE	1
Aguiar, JF; Garcia-Cairasco, N; Mesquita, F; Oliveira, JA; Varanda, WA	1
Baloh, RW; Howard, BD; Jen, JC; Palos, TP; Wan, J	1
Halliwell, B; Hyun, DH; Jenner, P; Lee, M	1
Akahoshi, M; Cheng, L; Enomoto, K; Enomoto, T; Hirota, T; Hopkin, JM; Mao, XQ; Matsuda, A; Shimizu, M; Shirakawa, T; Takahashi, N; Tamari, M; Yamasaki, A	1
Gao, J; Hu, Z; Jin, G; Liu, J; Qing, J; Shen, H; Wang, S; Wang, X; Zhai, X	1
Añez, Y; Coutin-Churchman, P; Moreno, R; Vergara, F	1
Blanco, M; Castellanos, M; Castillo, J; Dávalos, A; Hurtado, O; Lizasoain, I; Mallolas, J; Moro, MA; Serena, J; Sobrino, T; Vivancos, J	1
Abu-Amero, KK; Al-Boudari, OM; Dzimiri, N; Mohamed, GH	1
Kalivas, PW; Szumlinski, KK; Worley, PF	1
Benjamini, Y; Elmer, GI; Frank, BC; Kafkafi, N; Lee, NH; Letwin, NE; Luu, T; Mayo, C	1
Galán, JJ; González-Mancha, R; González-Martín, A; Moreno-Nogueira, JA; Real, LM; Royo, JL; Ruiz, A	1
Atilla, G; Berdeli, A; Emingil, G; Gürkan, A; Köse, T	1
Del-Favero, J; Van Broeckhoven, C; Van Den Bogaert, A	1
Bertini, E; Boldrini, R; D'Amico, A; Feng, JJ; Graziano, C; Jacques, A; Laing, N; Limongelli, G; Marston, SB; Nowak, KJ; Pacileo, G; Petrini, S; Porfirio, B; Santorelli, FM; Sewry, CA	1
Förster, H; Huemer, M; Idriceanu, C; Kamper, A; Mayr, JA; Moslemi, AR; Muss, W; Oldfors, A; Sperl, W	1
Doggen, CJ; Eikenboom, JC; Nossent, AY; Rosendaal, FR; Tanis, BC	1
Avramopoulos, D; Cheslack-Postava, K; Connors, SL; Eberhart, CG; Fallin, MD; Newschaffer, CJ; Zimmerman, AW	1
Boks, MP; de Koning, TJ; Kahn, RS; Rietkerk, T; Sommer, IE; van de Beek, MH	1
Böcker, U; Haas, SL; Ruether, A; Schreiber, S; Singer, MV	1
Kanazawa, I; Kobayashi, S; Murayama, S; Sakurai, M; Takuma, H	1
Aasly, JO; Farrer, MJ; Haugarvoll, K; Ross, OA; Toft, M; White, LR	1
Albalushi, T; Arinami, T; Horiuchi, Y; Inada, T; Ishiguro, H; Iwata, N; Koga, M; Muratake, T; Ozaki, N; Someya, T; Ujike, H	1
Ee, HL; Goh, CL; Liu, L; McGrath, JA	1
Eberly, SW; Glazko, G; Goldenberg, I; Mathew, J; McNitt, S; Morray, B; Moss, AJ; Ryan, D; Zareba, W	1
Becker, AJ; Flor, PJ; Gueler, N; Pitsch, J; Schoch, S; van der Putten, H	1
Barbato, D; Di Angelantonio, E; Evangelista, A; Marchitti, S; Pirisi, A; Quarta, G; Rubattu, S; Stanzione, R; Volpe, M; Zanda, B	1
de Klerk, JB; Duran, M; Huijmans, JG; Poll-The, BT; van Maldegem, BT; Williams, M	1
Bennett, MR	1
Stahl, SM	1
Campbell, IL; Getts, DR; Getts, MT; King, NJ; Matsumoto, I; Müller, M; Radford, J; Shrestha, B	1
Catone, C; Chazalviel, L; Chuquet, J; Lecrux, C; MacKenzie, ET; Nicole, O; Touzani, O	1
du Bois, RM; Maier, LA; Newman, LS; Sato, H; Silveira, L; Spagnolo, P; Welsh, KI	1
Cheng, KC; Connor, JR; Goodman, SI; Housman, C; Jacobs, RE; LaNoue, K; Lazovic, J; O'Callaghan, JP; Simpson, I; Woontner, M; Zinnanti, WJ	1
Arnold, S; Brown, MA; Buchanan, D; Chenevix-Trench, G; Couch, FJ; Farrugia, DJ; Goldgar, DE; Healey, S; Henderson, BR; Lakhani, SR; Lovelock, PK; Mok, MT; Spurdle, AB; Tavtigian, SV	1
de Vries, RR; Feitsma, AL; Huizinga, TW; Plant, D; Thomson, W; Toes, RE; Ursum, J; van der Helm-van Mil, AH; van der Horst-Bruinsma, IE; van Rood, JJ; van Schaardenburg, D; Worthington, J	1
Li, S; Ma, X; Tan, S; Wang, B; Wang, J; Xie, YC; Yang, Z; Zheng, C; Zhou, S	1
Bai, C; Fukao, T; Kaneko, H; Kasahara, K; Kato, Z; Kimata, K; Kondo, N; Matsui, E; Ohnishi, H	1
Hanstock, CC; Purdon, SE; Seres, P; Tibbo, P; Valiakalayil, A	1
Gilliland, FD; Guo, YL; Lee, YC; Lee, YL; Wang, JY	1
Kloos, A; Weller, EB; Weller, RA	1
Maier, LA; Marrone, BL; Newman, LS; Petrovic, M; Tatum, OL; Wang, Z; White, PS	1
Baima, J; Baldwin, CT; Bresnahan, M; Burzstyn, M; DeStefano, AL; Farrer, L; Gavras, H; Gavras, I; Handy, DE; Joost, O; Manolis, A; Martel, T; Nicolaou, M; Schwartz, F	1
Bartell, SM; Faustman, EM; Omenn, GS; Ponce, RA; Takaro, TK; Zerbe, RO	1
Haas, OA; Muhr, D; Niederle, B; Scheuba, C; Schlegl, R; Vierhapper, H; Wagner, T; Weinhaeusel, A	1
du Bois, RM; Fiorillo, MT; Germain, C; Jones-Williams, W; Lechler, R; Lombardi, G; Saltini, C; Sorrentino, R; Uren, J	1
D'Hooge, R; De Deyn, PP; Engelborghs, S	1
Fei, J; Guo, LH; Hu, JH; Ma, Y; Mei, ZT; Yu, Y; Zhao, WJ; Zhou, XG	1
Amicosante, M; Arroyo, J; Berretta, F; Colizzi, V; Lechler, R; Lombardi, G; Saltini, C; Sanarico, N	1
Hauben, E; Kipnis, J; Schori, H; Schwartz, M; Shaked, I; Yoles, E	1
Albizzati, MG; Begni, B; Brighina, L; Crosti, F; Dalprà, L; Ferrarese, C; Frattola, L; Piolti, R; Ricci, G; Rigoldi, M; Sala, G; Tremolizzo, L	1
Fisher, J; Haggiag, S; Levkovitch-Verbin, H; Mizrahi, T; Revel, M; Schori, H; Schwartz, M; Yoles, E	1
Benjafield, AV; Ericsson, JO; Morris, BJ	1
Apter, A; Barkai, G; Carel, C; Danziger, Y; Fennig, S; Frisch, A; Gak, E; Goldman, B; Koronyo-Hamaoui, M; Laufer, N; Leor, S; Minoumi, M; Stein, D; Weizman, A	1
duBois, R; Lympany, P; Maier, L; Martyny, J; McGrath, D; Mroz, M; Murphy, J; Newman, LS; Zhang, L	1
Brown, ML; Eastwood, AL; Kumar, R; Laurie, GW	1

Reviews

33 review(s) available for glutamic acid and Genetic Predisposition

Article	Year
Unique Molecular Regulation of Higher-Order Prefrontal Cortical Circuits: Insights into the Neurobiology of Schizophrenia. ACS chemical neuroscience, 2018, 09-19, Volume: 9, Issue:9 Topics: Acetylcholine; Animals; Calcium Signaling; Cognitive Dysfunction; Cyclic AMP; GABAergic Neurons; Gene-Environment Interaction; Genetic Predisposition to Disease; Glutamic Acid; Haplorhini; Humans; Interneurons; Memory, Short-Term; Neural Pathways; Prefrontal Cortex; Pyramidal Cells; Schizophrenia; Schizophrenic Psychology; Stress, Psychological	2018
Genetic susceptibility in obsessive-compulsive disorder. Handbook of clinical neurology, 2018, Volume: 148 Topics: Animals; Disease Models, Animal; DNA Copy Number Variations; Genetic Predisposition to Disease; Glutamic Acid; Humans; Mice; Obsessive-Compulsive Disorder; Signal Transduction	2018
PON1 Q192R and L55M polymorphisms and organophosphate toxicity risk: a meta-analysis. DNA and cell biology, 2013, Volume: 32, Issue:5 Topics: Amino Acid Substitution; Arginine; Aryldialkylphosphatase; Case-Control Studies; Genetic Predisposition to Disease; Glutamic Acid; Humans; Leucine; Methionine; Organophosphate Poisoning; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; White People	2013
The genetic contribution of the NO system at the glutamatergic post-synapse to schizophrenia: further evidence and meta-analysis. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2014, Volume: 24, Issue:1 Topics: Adaptor Proteins, Signal Transducing; Animals; Computational Biology; Genetic Predisposition to Disease; Glutamic Acid; Humans; Nitric Oxide; Nitric Oxide Synthase Type I; Polymorphism, Single Nucleotide; Prefrontal Cortex; Promoter Regions, Genetic; Schizophrenia; Signal Transduction; Synapses	2014
Genetic susceptibility of impulse control and related behavior in Parkinson's disease. Journal of Parkinson's disease, 2014, Volume: 4, Issue:2 Topics: Disruptive, Impulse Control, and Conduct Disorders; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Parkinson Disease; Receptors, Dopamine; Receptors, Serotonin; Serotonin	2014
The Glu504Lys polymorphism of aldehyde dehydrogenase 2 contributes to development of coronary artery disease. The Tohoku journal of experimental medicine, 2014, Volume: 234, Issue:2 Topics: Aldehyde Dehydrogenase; Aldehyde Dehydrogenase, Mitochondrial; Alleles; Asian People; Cardiovascular Diseases; Coronary Artery Disease; Genetic Predisposition to Disease; Glutamic Acid; Humans; Inflammation; Lysine; Nitric Oxide Synthase Type III; Oxidative Stress; Polymorphism, Genetic; Risk Factors	2014
Genetic studies of body mass index yield new insights for obesity biology. Nature, 2015, Feb-12, Volume: 518, Issue:7538 Topics: Adipogenesis; Adiposity; Age Factors; Body Mass Index; Energy Metabolism; Europe; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Glutamic Acid; Humans; Insulin; Insulin Secretion; Male; Obesity; Polymorphism, Single Nucleotide; Quantitative Trait Loci; Racial Groups; Synapses	2015
The functional polymorphism of NBS1 p.Glu185Gln is associated with an increased risk of lung cancer in Chinese populations: case-control and a meta-analysis. Mutation research, 2014, Volume: 770 Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Case-Control Studies; Cell Cycle Proteins; China; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Lung Neoplasms; Male; Middle Aged; Nuclear Proteins; Polymorphism, Single Nucleotide; Risk Factors	2014
Glutamate synapses in human cognitive disorders. Annual review of neuroscience, 2015, Jul-08, Volume: 38 Topics: Animals; Autism Spectrum Disorder; Cognition Disorders; Genetic Predisposition to Disease; Glutamic Acid; Humans; Intellectual Disability; Models, Neurological; Schizophrenia; Synapses	2015
Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations. Hearing research, 2015, Volume: 330, Issue:Pt B Topics: Acoustic Stimulation; Animals; Audiometry, Evoked Response; Auditory Pathways; Auditory Threshold; Cochlea; Cochlear Implantation; Cochlear Microphonic Potentials; Cochlear Nerve; Cues; Genetic Predisposition to Disease; Glutamic Acid; Hearing; Hearing Loss; Humans; Loudness Perception; Membrane Proteins; Mutation; Persons With Hearing Impairments; Phenotype; Reaction Time; Speech Intelligibility; Speech Perception; Synaptic Transmission; Time Factors	2015
The pertussis hypothesis: Bordetella pertussis colonization in the pathogenesis of Alzheimer's disease. Immunobiology, 2017, Volume: 222, Issue:2 Topics: Alzheimer Disease; Amyloid beta-Peptides; Biomarkers; Bordetella pertussis; Genetic Predisposition to Disease; Glutamic Acid; Humans; Incidence; Nasopharynx; Neurons; Oxidative Stress; Pertussis Toxin; Pertussis Vaccine; Whooping Cough; Wnt Signaling Pathway	2017
Role of glutamate in schizophrenia: integrating excitatory avenues of research. Expert review of neurotherapeutics, 2008, Volume: 8, Issue:9 Topics: Antipsychotic Agents; Brain; Genetic Predisposition to Disease; Glutamic Acid; Humans; Receptors, Metabotropic Glutamate; Schizophrenia	2008
Physical activity as an exogenous risk factor in motor neuron disease (MND): a review of the evidence. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases, 2009, Volume: 10, Issue:4 Topics: Age of Onset; Animals; Genetic Predisposition to Disease; Glutamic Acid; Humans; Motor Activity; Motor Neuron Disease; Nerve Growth Factors; Oxidative Stress; Reproducibility of Results; Risk Factors; Sports	2009
An integrated genome research network for studying the genetics of alcohol addiction. Addiction biology, 2010, Volume: 15, Issue:4 Topics: Alcoholism; Animals; Brain; Cause of Death; Cooperative Behavior; Cross-Sectional Studies; Genetic Predisposition to Disease; Genetic Research; Genome-Wide Association Study; Genotype; Glutamic Acid; Humans; Interdisciplinary Communication; Polymorphism, Single Nucleotide; Quantitative Trait Loci; Rats; Recurrence; Risk; Survival Analysis	2010
Meta-analysis of genome-wide association for migraine in six population-based European cohorts. European journal of human genetics : EJHG, 2011, Volume: 19, Issue:8 Topics: Cell Adhesion Molecules; Genetic Predisposition to Disease; Genome-Wide Association Study; Glutamic Acid; Iceland; Membrane Proteins; Migraine Disorders; Nerve Tissue Proteins; Netherlands; Polymorphism, Single Nucleotide; Receptors, Nerve Growth Factor; RNA-Binding Proteins	2011
Meta-analysis of aldehyde dehydrogenase 2 gene polymorphism and Alzheimer's disease in East Asians. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 2011, Volume: 38, Issue:3 Topics: Aged; Aged, 80 and over; Aldehyde Dehydrogenase; Aldehyde Dehydrogenase, Mitochondrial; Alzheimer Disease; Apolipoprotein E4; Asia, Eastern; Confidence Intervals; Databases, Bibliographic; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Lysine; Male; Odds Ratio; Polymorphism, Single Nucleotide	2011
Glutamate and psychosis risk. Current pharmaceutical design, 2012, Volume: 18, Issue:4 Topics: Animals; Disease Models, Animal; Genetic Predisposition to Disease; Glutamic Acid; Humans; Psychotic Disorders; Risk Factors	2012
Synaptic dysfunction in schizophrenia. Advances in experimental medicine and biology, 2012, Volume: 970 Topics: Acetylcholine; Animals; Brain; Dopamine; gamma-Aminobutyric Acid; Gene Expression Regulation, Developmental; Genetic Predisposition to Disease; Glutamic Acid; Humans; Mice; Mutation; Nerve Tissue Proteins; Neuronal Plasticity; Receptors, Cholinergic; Receptors, Dopamine; Receptors, GABA; Receptors, Glutamate; Schizophrenia; Synapses; Synaptic Transmission	2012
Drugs of abuse and increased risk of psychosis development. The Australian and New Zealand journal of psychiatry, 2012, Volume: 46, Issue:12 Topics: Age of Onset; Animals; Behavioral Symptoms; Brain; Cannabis; Dopamine; Dopamine Uptake Inhibitors; Functional Neuroimaging; Genetic Predisposition to Disease; Glutamic Acid; Humans; Illicit Drugs; Methamphetamine; Models, Animal; Psychoses, Substance-Induced; Risk Factors; Schizophrenia; Substance-Related Disorders	2012
BRAF V600E mutation and its association with clinicopathological features of papillary thyroid cancer: a meta-analysis. The Journal of clinical endocrinology and metabolism, 2012, Volume: 97, Issue:12 Topics: Age Factors; Amino Acid Substitution; Carcinoma; Carcinoma, Papillary; Female; Genetic Association Studies; Genetic Predisposition to Disease; Glutamic Acid; Humans; Lymphatic Metastasis; Male; Mutation, Missense; Proto-Oncogene Proteins B-raf; Sex Characteristics; Thyroid Cancer, Papillary; Thyroid Neoplasms; Tumor Burden; Valine	2012
Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder. Translational psychiatry, 2012, Nov-13, Volume: 2 Topics: Depressive Disorder, Major; Genetic Predisposition to Disease; Genome-Wide Association Study; Glutamic Acid; Humans; Synaptic Transmission	2012
Neuroimaging correlates of 22q11.2 deletion syndrome: implications for schizophrenia research. Current topics in medicinal chemistry, 2012, Volume: 12, Issue:21 Topics: Brain; Catechol O-Methyltransferase; Diffusion Tensor Imaging; DiGeorge Syndrome; Genetic Predisposition to Disease; Glutamic Acid; Humans; Longitudinal Studies; Magnetic Resonance Imaging; Molecular Imaging; Neuroimaging; Proline Oxidase; Schizophrenia	2012
The genetics of schizophrenia: glutamate not dopamine? European journal of pharmacology, 2003, Nov-07, Volume: 480, Issue:1-3 Topics: Animals; Dopamine; Genetic Linkage; Genetic Predisposition to Disease; Glutamic Acid; Humans; Schizophrenia	2003
Neurobiological correlates of the disposition and maintenance of alcoholism. Pharmacopsychiatry, 2003, Volume: 36 Suppl 3 Topics: Acute Disease; Alcoholism; Brain; Chronic Disease; Dopamine; Drug Tolerance; Ethanol; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Recurrence; Reward; Risk Factors; Serotonin; Substance Withdrawal Syndrome; Synaptic Transmission	2003
Neuregulin 1 and schizophrenia. Annals of medicine, 2004, Volume: 36, Issue:1 Topics: Animals; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Glutamic Acid; Humans; Mice; Mice, Knockout; Molecular Sequence Data; Neuregulin-1; Paracrine Communication; Receptors, N-Methyl-D-Aspartate; Schizophrenia	2004
Phenotype of schizophrenia: a review and formulation. Molecular psychiatry, 2005, Volume: 10, Issue:1 Topics: Behavioral Symptoms; Biogenic Monoamines; Brain; Brain Chemistry; Genetic Predisposition to Disease; Glutamic Acid; Gyrus Cinguli; Hippocampus; Humans; Limbic System; Models, Neurological; Phenotype; Schizophrenia; Schizophrenic Psychology	2005
[In search of susceptibility genes for schizophrenia]. Wiener klinische Wochenschrift, 2004, Dec-30, Volume: 116, Issue:24 Topics: Abnormalities, Multiple; Adult; Animals; Brain; Catechol O-Methyltransferase; Chromosome Aberrations; Chromosomes, Human, Pair 22; Face; Gene Expression; Genetic Linkage; Genetic Predisposition to Disease; Glutamic Acid; Heart Defects, Congenital; Humans; Meta-Analysis as Topic; Mice; Mice, Knockout; Neuregulin-1; Palate, Soft; Proline Oxidase; RGS Proteins; Risk Factors; Schizophrenia; Syndrome	2004
Homer proteins: implications for neuropsychiatric disorders. Current opinion in neurobiology, 2006, Volume: 16, Issue:3 Topics: Animals; Brain; Carrier Proteins; Genetic Predisposition to Disease; Glutamic Acid; Homer Scaffolding Proteins; Humans; Mental Disorders; Neural Pathways; Polymorphism, Genetic; Protein Isoforms; Synaptic Transmission	2006
Major affective disorders and schizophrenia: a common molecular signature? Human mutation, 2006, Volume: 27, Issue:9 Topics: Dopamine; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Humans; Mood Disorders; Neurons; Risk Factors; Schizophrenia; Serotonin; Signal Transduction	2006
Reviewing the role of the genes G72 and DAAO in glutamate neurotransmission in schizophrenia. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2007, Volume: 17, Issue:9 Topics: Carrier Proteins; D-Amino-Acid Oxidase; Genetic Predisposition to Disease; Glutamic Acid; Humans; Intracellular Signaling Peptides and Proteins; Models, Biological; Schizophrenia; Synaptic Transmission	2007
Clinical and molecular dilemmas in the diagnosis of familial epidermolysis bullosa pruriginosa. Journal of the American Academy of Dermatology, 2007, Volume: 56, Issue:5 Suppl Topics: Adolescent; Adult; Amino Acid Substitution; Asian People; Child; Collagen Type VII; Diagnosis, Differential; Epidermolysis Bullosa Dystrophica; Female; Genes, Dominant; Genetic Predisposition to Disease; Glutamic Acid; Glycine; Heterozygote; Humans; Male; Middle Aged; Mutation; Pedigree	2007
Biologic basis of bipolar disorder in children and adolescents. Current psychiatry reports, 2008, Volume: 10, Issue:2 Topics: Adolescent; Antimanic Agents; Aspartic Acid; Bipolar Disorder; Brain; Brain-Derived Neurotrophic Factor; Child; Energy Metabolism; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Lithium Compounds; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Neuropsychological Tests	2008
Pathophysiology of epilepsy. Acta neurologica Belgica, 2000, Volume: 100, Issue:4 Topics: Adult; Animals; Anticonvulsants; Autoimmune Diseases; Calcium; Catecholamines; Cell Movement; Child; Child, Preschool; Electroencephalography; Encephalitis; Epilepsies, Partial; Epilepsy; Epilepsy, Temporal Lobe; gamma-Aminobutyric Acid; Genes, Dominant; Genetic Predisposition to Disease; Glutamic Acid; Hamartoma; Humans; Infant; Infant, Newborn; Ion Channels; Kindling, Neurologic; Membrane Potentials; Neurons; Potassium; Rats; Receptors, AMPA; Receptors, GABA; Receptors, Glutamate; Sodium; Spasms, Infantile; Syndrome; Thalamic Diseases	2000

Trials

3 trial(s) available for glutamic acid and Genetic Predisposition

Article	Year
The association of ENPP1 K121Q with diabetes incidence is abolished by lifestyle modification in the diabetes prevention program. The Journal of clinical endocrinology and metabolism, 2009, Volume: 94, Issue:2 Topics: Chromans; Combined Modality Therapy; Diabetes Mellitus, Type 2; Exercise Therapy; Female; Gene Frequency; Genetic Linkage; Genetic Predisposition to Disease; Glutamic Acid; Humans; Hypoglycemic Agents; Incidence; Lysine; Male; Metformin; Middle Aged; Phosphoric Diester Hydrolases; Polymorphism, Single Nucleotide; Pyrophosphatases; Risk Reduction Behavior; Thiazolidinediones; Troglitazone	2009
The BRAF(V600E) mutation is associated with malignant ultrasonographic features in thyroid nodules. Clinical endocrinology, 2011, Volume: 75, Issue:6 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Biopsy, Fine-Needle; Carcinoma; Carcinoma, Papillary; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Middle Aged; Mutation; Proto-Oncogene Proteins B-raf; Sensitivity and Specificity; Thyroid Cancer, Papillary; Thyroid Neoplasms; Thyroid Nodule; Ultrasonography; Valine; Young Adult	2011
A novel germline mutation in HOXB13 is associated with prostate cancer risk in Chinese men. The Prostate, 2013, Volume: 73, Issue:2 Topics: Aged; Aged, 80 and over; Amino Acid Substitution; Asian People; China; Genetic Predisposition to Disease; Germ-Line Mutation; Glutamic Acid; Glycine; Homeodomain Proteins; Humans; Male; Middle Aged; Prostatic Neoplasms	2013

Other Studies

175 other study(ies) available for glutamic acid and Genetic Predisposition

Article	Year
Rare Pathogenic Variants in Genes Implicated in Glutamatergic Neurotransmission Pathway Segregate with Schizophrenia in Pakistani Families. Genes, 2021, 11-26, Volume: 12, Issue:12 Topics: Adult; Exome; Female; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Glutamic Acid; Humans; Male; Middle Aged; Pakistan; Pedigree; Penetrance; Schizophrenia; Signal Transduction; Synaptic Transmission	2021
MMP-8 C-799 T, Lys460Thr, and Lys87Glu variants are not related to risk of cancer. BMC medical genetics, 2019, 10-21, Volume: 20, Issue:1 Topics: Genetic Predisposition to Disease; Glutamic Acid; Humans; Lysine; Matrix Metalloproteinase 8; Neoplasms; Polymorphism, Single Nucleotide; Threonine	2019
Glutamatergic function in a genetic high-risk group for psychosis: A proton magnetic resonance spectroscopy study in individuals with 22q11.2 deletion. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2019, Volume: 29, Issue:12 Topics: Adolescent; Adult; Corpus Striatum; Cross-Sectional Studies; DiGeorge Syndrome; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Gyrus Cinguli; Humans; Magnetic Resonance Spectroscopy; Male; Psychotic Disorders; Risk Factors; Thalamus; Young Adult	2019
Germline HOXB13 G84E mutation carriers and risk to twenty common types of cancer: results from the UK Biobank. British journal of cancer, 2020, Volume: 123, Issue:9 Topics: Adult; Aged; Amino Acid Substitution; Biological Specimen Banks; Case-Control Studies; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Germ-Line Mutation; Glutamic Acid; Glycine; Homeodomain Proteins; Humans; Male; Middle Aged; Mutation, Missense; Neoplasms; Risk Factors; United Kingdom	2020
Leptin G-2548A and Leptin Receptor Q223R Gene Polymorphisms are Differently Associated with Oxidative Process in Mexican Mestizo and Indigenous with Obesity. Endocrine, metabolic & immune disorders drug targets, 2021, Volume: 21, Issue:8 Topics: Adolescent; Adult; Amino Acid Substitution; Arginine; Case-Control Studies; Cross-Sectional Studies; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Glutamic Acid; Humans; Indigenous Peoples; Leptin; Lipid Peroxidation; Male; Mexico; Middle Aged; Obesity; Overweight; Oxidative Stress; Polymorphism, Single Nucleotide; Receptors, Leptin; Young Adult	2021
Triangulating evidence from longitudinal and Mendelian randomization studies of metabolomic biomarkers for type 2 diabetes. Scientific reports, 2021, 03-18, Volume: 11, Issue:1 Topics: Adult; Aged; Betaine; Biomarkers; Carnitine; Case-Control Studies; Diabetes Mellitus, Type 2; Early Diagnosis; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Leucine; Lysine; Male; Mannose; Mendelian Randomization Analysis; Metabolome; Middle Aged; Valine	2021
Synaptotagmin-7-mediated activation of spontaneous NMDAR currents is disrupted in bipolar disorder susceptibility variants. PLoS biology, 2021, Volume: 19, Issue:7 Topics: Animals; Bipolar Disorder; Calcium; Clustered Regularly Interspaced Short Palindromic Repeats; Disease Models, Animal; Genetic Predisposition to Disease; Glutamic Acid; HEK293 Cells; Hippocampus; Humans; Mice; Mice, Knockout; Neurons; Receptors, N-Methyl-D-Aspartate; Synaptotagmins	2021
Modulatory effects of Ampicillin/Sulbactam on glial glutamate transporters and metabotropic glutamate receptor 1 as well as reinstatement to cocaine-seeking behavior. Behavioural brain research, 2017, 08-14, Volume: 332 Topics: Amino Acid Transport Systems, Acidic; Ampicillin; Animals; Cocaine; Cocaine-Related Disorders; Dopamine Uptake Inhibitors; Drug-Seeking Behavior; Excitatory Amino Acid Agents; Excitatory Amino Acid Transporter 1; Excitatory Amino Acid Transporter 2; Genetic Predisposition to Disease; Glutamic Acid; Male; Motor Activity; Neuroglia; Nucleus Accumbens; Prefrontal Cortex; Rats; Receptors, Metabotropic Glutamate; Self Administration; Sulbactam	2017
A Polygenic Risk Score of glutamatergic SNPs associated with schizophrenia predicts attentional behavior and related brain activity in healthy humans. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2017, Volume: 27, Issue:9 Topics: Adult; Attention; Brain; Brain Mapping; Factor Analysis, Statistical; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Magnetic Resonance Imaging; Male; Memory, Short-Term; Multifactorial Inheritance; Neuropsychological Tests; Polymorphism, Single Nucleotide; Schizophrenia; Schizophrenic Psychology; Thinking; White People	2017
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways. PloS one, 2017, Volume: 12, Issue:8 Topics: Adolescent; Adult; Aged; DNA Mutational Analysis; Exome; Female; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Homozygote; Humans; Inbreeding; Male; Middle Aged; Mutation; Schizophrenia; Young Adult	2017
An autism spectrum disorder-related de novo mutation hotspot discovered in the GEF1 domain of Trio. Nature communications, 2017, 09-19, Volume: 8, Issue:1 Topics: Animals; Autism Spectrum Disorder; Female; Genetic Predisposition to Disease; Glutamic Acid; Guanine Nucleotide Exchange Factors; Humans; In Vitro Techniques; Male; Mutation; Nerve Tissue Proteins; Neurons; Patch-Clamp Techniques; Protein Serine-Threonine Kinases; Rats; Rats, Sprague-Dawley; Receptors, AMPA; Synapses	2017
Psychiatric risk gene Cacna1c determines mitochondrial resilience against oxidative stress in neurons. Cell death & disease, 2018, 05-29, Volume: 9, Issue:6 Topics: Animals; Calcium Channels, L-Type; Genetic Predisposition to Disease; Glutamic Acid; Mental Disorders; Mitochondria; Neurons; Oxidative Stress; Risk Factors	2018
Heritability of cerebral glutamate levels and their association with schizophrenia spectrum disorders: a Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2019, Volume: 44, Issue:3 Topics: Adult; Denmark; Female; Genetic Predisposition to Disease; Glutamic Acid; Gyrus Cinguli; Humans; Male; Middle Aged; Proton Magnetic Resonance Spectroscopy; Registries; Schizophrenia; Thalamus	2019
Reversal of behavioral deficits and synaptic dysfunction in mice overexpressing neuregulin 1. Neuron, 2013, May-22, Volume: 78, Issue:4 Topics: Age Factors; Animals; Disease Models, Animal; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Mice; Mice, Inbred C57BL; Mice, Neurologic Mutants; Mice, Transgenic; Neuregulin-1; Neurons; Prosencephalon; Schizophrenia; Synaptic Transmission; Tissue Distribution	2013
Relation between K469E gene polymorphism of ICAM-1 and recurrence of ACS and cardiovascular mortality. Asian Pacific journal of tropical medicine, 2013, Volume: 6, Issue:11 Topics: Acute Coronary Syndrome; Aged; Alleles; Asian People; Blood Glucose; Blood Pressure; China; Cholesterol, HDL; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Intercellular Adhesion Molecule-1; Leucine; Lipids; Logistic Models; Male; Middle Aged; Polymorphism, Single Nucleotide; Prospective Studies; Risk Factors; Risk Reduction Behavior; Secondary Prevention	2013
Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysis. Circulation. Cardiovascular genetics, 2013, Volume: 6, Issue:6 Topics: Age of Onset; Asian People; Cell Cycle Proteins; Cell Line; Chromosome Mapping; Chromosomes, Human, Pair 2; Coronary Artery Disease; Family Health; Gene Frequency; Genetic Linkage; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Glutamic Acid; Humans; Japan; Myocardial Infarction; Odds Ratio; Polymorphism, Single Nucleotide; Proteins; Repetitive Sequences, Amino Acid; Republic of Korea; Risk Factors	2013
Novel germline mutation in the transmembrane domain of HER2 in familial lung adenocarcinomas. Journal of the National Cancer Institute, 2014, Volume: 106, Issue:1 Topics: Adenocarcinoma; Adenocarcinoma of Lung; Adult; Asian People; Aspartic Acid; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Glutamic Acid; Glycine; Humans; Japan; Lung Neoplasms; Male; Middle Aged; Pedigree; Receptor, ErbB-2; Valine	2014
Genome-wide linkage approach yields novel early onset myocardial infarction locus in East Asians. Circulation. Cardiovascular genetics, 2013, Volume: 6, Issue:6 Topics: Cell Cycle Proteins; Genetic Predisposition to Disease; Glutamic Acid; Humans; Myocardial Infarction; Polymorphism, Single Nucleotide; Proteins; Repetitive Sequences, Amino Acid	2013
Pathway analyses implicate glial cells in schizophrenia. PloS one, 2014, Volume: 9, Issue:2 Topics: Bipolar Disorder; Case-Control Studies; Genetic Predisposition to Disease; Genome-Wide Association Study; Glutamic Acid; Humans; Mitochondria; Neuroglia; Polymorphism, Single Nucleotide; Schizophrenia; Signal Transduction	2014
Serous tubal intraepithelial carcinoma in a Japanese woman with a deleterious BRCA1 mutation. Japanese journal of clinical oncology, 2014, Volume: 44, Issue:6 Topics: Asian People; BRCA1 Protein; Cystadenocarcinoma, Serous; Fallopian Tube Neoplasms; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Glutamic Acid; Humans; Middle Aged; Pedigree	2014
High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative Langerhans cell histiocytosis. Blood, 2014, Sep-04, Volume: 124, Issue:10 Topics: Amino Acid Substitution; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamic Acid; Histiocytosis, Langerhans-Cell; Humans; Male; MAP Kinase Kinase 1; Mutation, Missense; Prevalence; Proto-Oncogene Proteins B-raf; Retrospective Studies; Valine	2014
Biological insights from 108 schizophrenia-associated genetic loci. Nature, 2014, Jul-24, Volume: 511, Issue:7510 Topics: Alleles; Brain; Enhancer Elements, Genetic; Genetic Loci; Genetic Predisposition to Disease; Genome-Wide Association Study; Glutamic Acid; Humans; Immunity; Multifactorial Inheritance; Mutation; Odds Ratio; Polymorphism, Single Nucleotide; Schizophrenia; Synaptic Transmission	2014
Associations of a polymorphism in the intercellular adhesion molecule-1 (ICAM1) gene and ICAM1 serum levels with migraine in a Chinese Han population. Journal of the neurological sciences, 2014, Oct-15, Volume: 345, Issue:1-2 Topics: Adolescent; Adult; Asian People; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Intercellular Adhesion Molecule-1; Logistic Models; Lysine; Male; Middle Aged; Migraine Disorders; Polymorphism, Single Nucleotide; Risk Factors; RNA, Messenger; Young Adult	2014
A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death. Nature medicine, 2014, Volume: 20, Issue:12 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Amyloid beta-Peptides; Animals; CA3 Region, Hippocampal; Cell Death; Female; Genetic Predisposition to Disease; Glutamic Acid; HEK293 Cells; Humans; Male; Mice; Netrin Receptors; Neurons; Rats; Receptors, Cell Surface; Receptors, Nerve Growth Factor; Staurosporine	2014
Involvement of astrocyte metabolic coupling in Tourette syndrome pathogenesis. European journal of human genetics : EJHG, 2015, Volume: 23, Issue:11 Topics: Astrocytes; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Glutamic Acid; Humans; Microglia; Neurons; Oligodendroglia; Tourette Syndrome	2015
The germline CDH1 c.48 G>C substitution contributes to cancer predisposition through generation of a pro-invasive mutation. Mutation research, 2014, Volume: 770 Topics: Amino Acid Substitution; Animals; Antigens, CD; Cadherins; CHO Cells; Cricetinae; Cricetulus; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Glutamic Acid; Histidine; Humans; Neoplasm Invasiveness; Pedigree; Stomach Neoplasms; Young Adult	2014
Behavioural and molecular endophenotypes in psychotic disorders reveal heritable abnormalities in glutamatergic neurotransmission. Translational psychiatry, 2015, Mar-31, Volume: 5 Topics: Adult; Analysis of Variance; Chromatography, Liquid; Endophenotypes; Excitatory Amino Acids; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Magnetic Resonance Spectroscopy; Male; Mass Spectrometry; Metabolomics; Neuropsychological Tests; Principal Component Analysis; Psychotic Disorders; Reaction Time; Receptors, N-Methyl-D-Aspartate; Synaptic Transmission; Young Adult	2015
A novel lamin A/C gene missense mutation (445 V > E) in immunoglobulin-like fold associated with left ventricular non-compaction. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 2016, Volume: 18, Issue:4 Topics: Adolescent; Death, Sudden, Cardiac; DNA Mutational Analysis; Echocardiography; Electrocardiography; Genetic Predisposition to Disease; Glutamic Acid; HEK293 Cells; Heterozygote; Humans; Isolated Noncompaction of the Ventricular Myocardium; Lamin Type A; Male; Membrane Potentials; Microscopy, Fluorescence; Models, Molecular; Mutagenesis, Site-Directed; Mutation, Missense; Phenotype; Protein Aggregates; Protein Conformation, beta-Strand; Protein Folding; Structure-Activity Relationship; Tachycardia, Ventricular; Transfection; Valine; Ventricular Fibrillation; Young Adult	2016
GLU298ASP and 4G/5G Polymorphisms and the Risk of Ischemic Stroke in Young Individuals. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 2015, Volume: 42, Issue:5 Topics: Adult; Aspartic Acid; Brain Ischemia; Case-Control Studies; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Male; Mexico; Nitric Oxide Synthase Type III; Plasminogen Activator Inhibitor 1; Polymorphism, Genetic; Stroke	2015
GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability. Molecular psychiatry, 2016, Volume: 21, Issue:3 Topics: Acoustic Stimulation; Autistic Disorder; Cell Adhesion Molecules, Neuronal; Child, Preschool; Electroencephalography; Evoked Potentials, Auditory; Family Health; Female; Follow-Up Studies; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Genomics; Glutamic Acid; Humans; Intellectual Disability; Male; Severity of Illness Index; Signal Transduction	2016
The absence of VGLUT3 predisposes to cocaine abuse by increasing dopamine and glutamate signaling in the nucleus accumbens. Molecular psychiatry, 2015, Volume: 20, Issue:11 Topics: Action Potentials; Adult; Animals; Cocaine; Cocaine-Related Disorders; Conditioning, Operant; Dopamine; Dopamine Uptake Inhibitors; Genetic Predisposition to Disease; Glutamic Acid; Humans; Mice; Mice, Transgenic; Middle Aged; Neurons; Nucleus Accumbens; Opioid-Related Disorders; Self Administration; Signal Transduction; Synaptic Potentials; Vesicular Glutamate Transport Proteins	2015
Cortico-Striatal GABAergic and Glutamatergic Dysregulations in Subjects at Ultra-High Risk for Psychosis Investigated with Proton Magnetic Resonance Spectroscopy. The international journal of neuropsychopharmacology, 2015, Sep-12, Volume: 19, Issue:3 Topics: Corpus Striatum; Female; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Humans; Interview, Psychological; Linear Models; Male; Prefrontal Cortex; Prodromal Symptoms; Proton Magnetic Resonance Spectroscopy; Psychotic Disorders; Risk; Schizophrenia; Young Adult	2015
Genetically determined differences in noradrenergic function: The spontaneously hypertensive rat model. Brain research, 2016, Jun-15, Volume: 1641, Issue:Pt B Topics: Animals; Bicuculline; Disease Models, Animal; Dizocilpine Maleate; Excitatory Amino Acid Antagonists; Female; GABA-A Receptor Antagonists; Genetic Predisposition to Disease; Glutamic Acid; Hippocampus; Male; Maternal Deprivation; Norepinephrine; Potassium; Random Allocation; Rats, Inbred SHR; Rats, Inbred WKY; Receptors, GABA-A; Receptors, N-Methyl-D-Aspartate; Species Specificity; Stress, Psychological	2016
Abnormal glutamate release in aged BTBR mouse model of autism. International journal of clinical and experimental pathology, 2015, Volume: 8, Issue:9 Topics: Animals; Autistic Disorder; Behavior, Animal; Cerebral Cortex; Dendritic Spines; Excitatory Postsynaptic Potentials; Genetic Predisposition to Disease; Glutamic Acid; Mice, Inbred C57BL; Microfilament Proteins; Nerve Tissue Proteins; Phenotype; Social Behavior; Synaptic Transmission	2015
HABP2 G534E Mutation in Familial Nonmedullary Thyroid Cancer. Journal of the National Cancer Institute, 2016, Volume: 108, Issue:6 Topics: Adult; Aged; Carcinoma; Carcinoma, Papillary; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Glutamic Acid; Glycine; Humans; Male; Middle Aged; Prevalence; Serine Endopeptidases; Thyroid Cancer, Papillary; Thyroid Neoplasms	2016
Glutamate E15 and E171 are Hotspots in p60TRP-Related Cancer. Cancer investigation, 2016, Volume: 34, Issue:2 Topics: Basic Helix-Loop-Helix Transcription Factors; Biomarkers, Tumor; Computational Biology; Databases, Genetic; DNA Mutational Analysis; Genetic Predisposition to Disease; Glutamic Acid; Humans; Mutation; Neoplasms; Phenotype; Protein Interaction Maps; Signal Transduction	2016
Pharmacogenetic study of antipsychotic induced acute extrapyramidal symptoms in a first episode psychosis cohort: role of dopamine, serotonin and glutamate candidate genes. The pharmacogenomics journal, 2016, Volume: 16, Issue:5 Topics: Adolescent; Adult; Antipsychotic Agents; Basal Ganglia Diseases; Case-Control Studies; Child; Dopamine; Female; Follow-Up Studies; Genetic Association Studies; Genetic Predisposition to Disease; GluK3 Kainate Receptor; Glutamic Acid; Haplotypes; Humans; Longitudinal Studies; Male; Pharmacogenetics; Pharmacogenomic Variants; Phenotype; Polymorphism, Single Nucleotide; Prospective Studies; Psychotic Disorders; Receptor, Serotonin, 5-HT2A; Receptors, Dopamine D2; Receptors, Kainic Acid; Risk Assessment; Risk Factors; Serotonin; Spain; Treatment Outcome; Vesicular Monoamine Transport Proteins; Young Adult	2016
Nature of Glutamate Alterations in Schizophrenia: A Meta-analysis of Proton Magnetic Resonance Spectroscopy Studies. JAMA psychiatry, 2016, 07-01, Volume: 73, Issue:7 Topics: Brain; Brain Mapping; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Proton Magnetic Resonance Spectroscopy; Reference Values; Risk Factors; Schizophrenia; Synaptic Transmission	2016
7T Proton Magnetic Resonance Spectroscopy of Gamma-Aminobutyric Acid, Glutamate, and Glutamine Reveals Altered Concentrations in Patients With Schizophrenia and Healthy Siblings. Biological psychiatry, 2017, 03-15, Volume: 81, Issue:6 Topics: Adult; Brain; Female; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Male; Proton Magnetic Resonance Spectroscopy; Schizophrenia; Siblings	2017
Down-Regulation of Hippocampal Genes Regulating Dopaminergic, GABAergic, and Glutamatergic Function Following Combined Neonatal Phencyclidine and Post-Weaning Social Isolation of Rats as a Neurodevelopmental Model for Schizophrenia. The international journal of neuropsychopharmacology, 2016, Volume: 19, Issue:11 Topics: Animals; Animals, Newborn; Behavior, Animal; Disease Models, Animal; Dopaminergic Neurons; GABAergic Neurons; Gene Expression Profiling; Gene Expression Regulation; Genetic Predisposition to Disease; Glutamic Acid; Hippocampus; Lamotrigine; Locomotion; Male; Oligonucleotide Array Sequence Analysis; Phencyclidine; Phenotype; Prepulse Inhibition; Rats, Inbred Strains; Recognition, Psychology; Reflex, Startle; Schizophrenia; Schizophrenic Psychology; Social Isolation; Sodium Channel Blockers; Synaptic Transmission; Time Factors; Triazines; Weaning	2016
A targeted sequencing study of glutamatergic candidate genes in suicide attempters with bipolar disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2016, Volume: 171, Issue:8 Topics: Adult; Aged; Aged, 80 and over; Bipolar Disorder; Calcium-Binding Proteins; Cell Adhesion Molecules, Neuronal; Excitatory Amino Acids; Female; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Glutamic Acid; High-Throughput Nucleotide Sequencing; Humans; Male; Middle Aged; Nerve Tissue Proteins; Neural Cell Adhesion Molecules; Polymorphism, Single Nucleotide; Receptors, N-Methyl-D-Aspartate; Suicidal Ideation; Suicide; Suicide, Attempted	2016
MicroRNA 101b Is Downregulated in the Prefrontal Cortex of a Genetic Model of Depression and Targets the Glutamate Transporter SLC1A1 (EAAT3) in Vitro. The international journal of neuropsychopharmacology, 2016, Volume: 19, Issue:12 Topics: Animals; Behavior, Animal; Depressive Disorder, Major; Disease Models, Animal; Down-Regulation; Excitatory Amino Acid Transporter 3; Gene Expression Profiling; Gene Regulatory Networks; Genetic Predisposition to Disease; Glutamic Acid; Male; MicroRNAs; Oligonucleotide Array Sequence Analysis; Phenotype; Prefrontal Cortex; Rats, Inbred Strains; RNA, Messenger; Signal Transduction	2016
Seizure responses and induction of Fos by the NMDA agonist (tetrazol-5-yl)glycine in a genetic model of NMDA receptor hypofunction. Brain research, 2008, Jul-24, Volume: 1221 Topics: Animals; Brain; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Resistance; Excitatory Amino Acid Agonists; Female; Genetic Predisposition to Disease; Glutamic Acid; Glycine; Hypothalamus; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Proto-Oncogene Proteins c-fos; Receptors, N-Methyl-D-Aspartate; Seizures; Septal Nuclei; Solitary Nucleus; Synaptic Transmission; Tetrazoles	2008
Knock-in mice lacking the PDZ-ligand motif of mGluR7a show impaired PKC-dependent autoinhibition of glutamate release, spatial working memory deficits, and increased susceptibility to pentylenetetrazol. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2008, Aug-20, Volume: 28, Issue:34 Topics: Amino Acid Motifs; Animals; Behavior, Animal; Brain; Carrier Proteins; Cell Cycle Proteins; Cells, Cultured; Cerebellum; Convulsants; Excitatory Amino Acid Antagonists; Genetic Predisposition to Disease; Glutamic Acid; Ligands; Memory Disorders; Mice; Mice, Transgenic; Mutation; Neural Inhibition; Nuclear Proteins; Oocytes; Pentylenetetrazole; Presynaptic Terminals; Protein Isoforms; Protein Kinase C; Receptors, Metabotropic Glutamate; Seizures; Signal Transduction; Space Perception; Synapses; Xenopus laevis	2008
Association of MUTYH Gln324His and APEX1 Asp148Glu with colorectal cancer and smoking in a Japanese population. Journal of experimental & clinical cancer research : CR, 2008, Sep-30, Volume: 27 Topics: Aged; Asian People; Aspartic Acid; Case-Control Studies; Colorectal Neoplasms; DNA Glycosylases; DNA-(Apurinic or Apyrimidinic Site) Lyase; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Histidine; Humans; Male; Middle Aged; Polymorphism, Genetic; Smoking	2008
BRAF mutation in papillary thyroid carcinoma in a Japanese population: its lack of correlation with high-risk clinicopathological features and disease-free survival of patients. Endocrine journal, 2009, Volume: 56, Issue:1 Topics: Adult; Amino Acid Substitution; Carcinoma, Papillary; Disease-Free Survival; Female; Genetic Linkage; Genetic Predisposition to Disease; Genetics, Population; Glutamic Acid; Humans; Japan; Male; Middle Aged; Neoplasm Staging; Point Mutation; Prognosis; Proto-Oncogene Proteins B-raf; Risk Factors; Thyroid Neoplasms; Valine	2009
K469E polymorphism of the intracellular adhesion molecule 1 gene is associated with proliferative diabetic retinopathy in Caucasians with type 2 diabetes. Clinical & experimental ophthalmology, 2008, Volume: 36, Issue:5 Topics: Aged; Alanine; Case-Control Studies; Cross-Sectional Studies; Diabetes Mellitus, Type 2; Diabetic Retinopathy; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glycine; Humans; Intercellular Adhesion Molecule-1; Lysine; Male; Middle Aged; Polymorphism, Genetic; Slovenia; White People	2008
Association between NR2B subunit gene (GRIN2B) promoter polymorphisms and sporadic Alzheimer's disease in the North Chinese population. Neuroscience letters, 2009, Feb-06, Volume: 450, Issue:3 Topics: Aged; Alzheimer Disease; Apolipoproteins E; Asian People; Brain; Brain Chemistry; DNA Mutational Analysis; Female; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glutamic Acid; HeLa Cells; Humans; Male; Middle Aged; Polymorphism, Genetic; Promoter Regions, Genetic; Receptors, N-Methyl-D-Aspartate	2009
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction. Journal of the neurological sciences, 2009, Jan-15, Volume: 276, Issue:1-2 Topics: Adult; Amyotrophic Lateral Sclerosis; Arginine; Cytochromes c; DNA Mutational Analysis; Family Health; Genetic Linkage; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Mitochondria, Muscle; Mitochondrial Diseases; Mutation; Superoxide Dismutase; Superoxide Dismutase-1	2009
Fgf-2 overexpression increases excitability and seizure susceptibility but decreases seizure-induced cell loss. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2008, Dec-03, Volume: 28, Issue:49 Topics: Animals; Cell Death; Convulsants; Disease Models, Animal; Epilepsy; Female; Fibroblast Growth Factor 2; Genetic Predisposition to Disease; Glutamic Acid; Growth Cones; Hippocampus; Humans; Male; Membrane Potentials; Mice; Mice, Transgenic; Nerve Degeneration; Neuronal Plasticity; Organ Culture Techniques; Patch-Clamp Techniques; Presynaptic Terminals; Pyramidal Cells; Synaptic Vesicles	2008
Causes of early-onset type 1 diabetes: toward data-driven environmental approaches. The Journal of experimental medicine, 2008, Dec-22, Volume: 205, Issue:13 Topics: Autoantibodies; Diabetes Mellitus, Type 1; Environment; Genetic Predisposition to Disease; Glutamic Acid; Humans; Insulin-Secreting Cells; Metabolomics	2008
Investigation of G72 (DAOA) expression in the human brain. BMC psychiatry, 2008, Dec-11, Volume: 8 Topics: Bipolar Disorder; Brain; Carrier Proteins; Cell Line; Chromosome Mapping; Chromosomes, Human, Pair 13; D-Amino-Acid Oxidase; Enzyme Activation; Genetic Predisposition to Disease; Glutamic Acid; Humans; Intracellular Signaling Peptides and Proteins; Molecular Probe Techniques; Polymorphism, Genetic; Promoter Regions, Genetic; Protein Interaction Domains and Motifs; RNA, Messenger; Schizophrenia	2008
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake. Archives of neurology, 2009, Volume: 66, Issue:1 Topics: Adult; Brain Chemistry; Cerebellum; DNA Mutational Analysis; Excitatory Amino Acid Transporter 1; Female; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glutamic Acid; Hemiplegia; Humans; Inheritance Patterns; Male; Middle Aged; Migraine Disorders; Mutation; Pedigree; Phenotype; Seizures; Spinocerebellar Degenerations	2009
Haploinsufficiency of glutamine synthetase increases susceptibility to experimental febrile seizures. Genes, brain, and behavior, 2009, Volume: 8, Issue:3 Topics: Animals; Biomarkers; Brain; Brain Chemistry; Disease Models, Animal; Down-Regulation; Excitatory Amino Acid Transporter 2; Genetic Predisposition to Disease; Glial Fibrillary Acidic Protein; Glutamate-Ammonia Ligase; Glutamic Acid; Haplotypes; Mice; Mice, Knockout; Reaction Time; Seizures, Febrile; Vesicular Glutamate Transport Protein 1; Vimentin	2009
Cap disease due to mutation of the beta-tropomyosin gene (TPM2). Neuromuscular disorders : NMD, 2009, Volume: 19, Issue:5 Topics: Adolescent; Amino Acid Sequence; Base Sequence; Cardiomyopathies; DNA Mutational Analysis; Female; Genetic Markers; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Muscle Fibers, Skeletal; Muscle Weakness; Muscle, Skeletal; Muscular Diseases; Myocardium; Sarcomeres; Sequence Deletion; Tropomyosin	2009
Prepulse inhibition and genetic mouse models of schizophrenia. Behavioural brain research, 2009, Dec-07, Volume: 204, Issue:2 Topics: Animals; Brain; Disease Models, Animal; Environment; Genetic Predisposition to Disease; Glutamic Acid; Glycine; Mice; Mice, Transgenic; Nerve Net; Phenotype; Schizophrenia; Sensory Gating	2009
Assessment of NMDA receptor NR1 subunit hypofunction in mice as a model for schizophrenia. Genes, brain, and behavior, 2009, Volume: 8, Issue:7 Topics: Animals; Anxiety; Auditory Diseases, Central; Behavior, Animal; Brain; Brain Chemistry; Disease Models, Animal; Evoked Potentials; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Mutation; Neural Inhibition; Perceptual Disorders; Phenotype; Receptors, N-Methyl-D-Aspartate; Schizophrenia; Social Behavior; Visual Pathways	2009
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. Movement disorders : official journal of the Movement Disorder Society, 2009, Sep-15, Volume: 24, Issue:12 Topics: Chorea; DNA Mutational Analysis; DNA-Binding Proteins; Family Health; Female; Frontotemporal Dementia; Genetic Predisposition to Disease; Glutamic Acid; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Neuropsychological Tests; Supranuclear Palsy, Progressive; Tomography Scanners, X-Ray Computed	2009
Adenosine A 2A receptor deficiency reduces striatal glutamate outflow and attenuates brain injury induced by transient focal cerebral ischemia in mice. Brain research, 2009, Nov-10, Volume: 1297 Topics: Adenosine; Animals; Brain Chemistry; Brain Infarction; Brain Ischemia; Corpus Striatum; Disease Models, Animal; Down-Regulation; Extracellular Fluid; Gene Expression Regulation; Genetic Predisposition to Disease; Glutamic Acid; Mice; Mice, Inbred C57BL; Mice, Knockout; Microdialysis; Receptor, Adenosine A2A; Up-Regulation	2009
Gln27Glu variant of Beta2-adrenoceptor gene affects male type fat accumulation in women. Lipids in health and disease, 2009, Oct-15, Volume: 8 Topics: Adolescent; Adult; Body Mass Index; Coronary Artery Disease; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Humans; Intra-Abdominal Fat; Male; Middle Aged; Polymorphism, Genetic; Receptors, Adrenergic, beta-2; Young Adult	2009
A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy. Annals of neurology, 2009, Volume: 66, Issue:6 Topics: Adolescent; Age of Onset; Animals; Axons; Child; Child, Preschool; Disease Models, Animal; Disease Progression; DNA Mutational Analysis; Family Health; Female; Follow-Up Studies; Genetic Predisposition to Disease; Glutamic Acid; Humans; Infant; Male; Mice; Mice, Knockout; Microscopy, Electron, Transmission; Mutagenesis, Site-Directed; Mutation; Neural Conduction; Neurofilament Proteins; Peripheral Nervous System Diseases; Severity of Illness Index; Sural Nerve; Young Adult	2009
XRCC1, but not APE1 and hOGG1 gene polymorphisms is a risk factor for pterygium. Molecular vision, 2010, Jun-04, Volume: 16 Topics: Aged; Aged, 80 and over; Alleles; Arginine; DNA Glycosylases; DNA-(Apurinic or Apyrimidinic Site) Lyase; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Pterygium; X-ray Repair Cross Complementing Protein 1	2010
Polymorphisms of the prion protein gene (PRNP) in a Serbian population. The International journal of neuroscience, 2010, Volume: 120, Issue:7 Topics: Amino Acid Substitution; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamic Acid; Humans; Lysine; Male; Mutagenesis, Insertional; Oligopeptides; Polymorphism, Genetic; Prion Diseases; Prion Proteins; Prions; Repetitive Sequences, Amino Acid; Sequence Deletion; Serbia	2010
Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy. Acta neuropathologica, 2011, Volume: 121, Issue:1 Topics: Amino Acid Substitution; Creutzfeldt-Jakob Syndrome; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Lysine; Male; Middle Aged; Prion Proteins; Prions	2011
Correlation between the BRAF V600E mutation and tumor invasiveness in papillary thyroid carcinomas smaller than 20 millimeters: analysis of 1060 cases. The Journal of clinical endocrinology and metabolism, 2010, Volume: 95, Issue:9 Topics: Adult; Amino Acid Substitution; Carcinoma, Papillary; Cohort Studies; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Middle Aged; Neoplasm Invasiveness; Point Mutation; Proto-Oncogene Proteins B-raf; Retrospective Studies; Thyroid Neoplasms; Tumor Burden; Valine	2010
Common variants conferring risk of schizophrenia: a pathway analysis of GWAS data. Schizophrenia research, 2010, Volume: 122, Issue:1-3 Topics: Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Glutamic Acid; Humans; Schizophrenia; Signal Transduction	2010
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP. Archives of neurology, 2010, Volume: 67, Issue:8 Topics: Aged; Amyloid beta-Peptides; Amyloid beta-Protein Precursor; Amyloidosis, Familial; Apolipoprotein E4; Cerebral Hemorrhage; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Glutamic Acid; Humans; Italy; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Peptide Fragments	2010
Potassium channel activity and glutamate uptake are impaired in astrocytes of seizure-susceptible DBA/2 mice. Epilepsia, 2010, Volume: 51, Issue:9 Topics: Amino Acid Substitution; Animals; Astrocytes; Barium; Channelopathies; Genetic Predisposition to Disease; Glutamic Acid; Hippocampus; Humans; Membrane Potentials; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Neuroglia; Patch-Clamp Techniques; Polymorphism, Single Nucleotide; Potassium; Potassium Channels; Potassium Channels, Inwardly Rectifying; Seizures	2010
ENPP1/PC-1 K121Q and other predictors of posttransplant diabetes. Metabolic syndrome and related disorders, 2011, Volume: 9, Issue:1 Topics: Adult; Age Factors; Amino Acid Substitution; Biomarkers; Diabetes Mellitus; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Lysine; Male; Middle Aged; Phosphoric Diester Hydrolases; Polymorphism, Single Nucleotide; Prognosis; Pyrophosphatases; Racial Groups; Transplantation	2011
An emerging role for TARPs in neuropsychiatric disorders. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Volume: 36, Issue:1 Topics: Animals; Brain Chemistry; Calcium Channels; Gene Expression Regulation; Genetic Predisposition to Disease; Glutamic Acid; Humans; Mice; Neurocognitive Disorders; Protein Subunits; Receptors, AMPA	2011
The ENPP1 K121Q polymorphism is not associated with type 2 diabetes and related metabolic traits in an Iranian population. Molecular and cellular biochemistry, 2011, Volume: 350, Issue:1-2 Topics: Adult; Aged; Amino Acid Substitution; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Genetics, Population; Genotype; Glutamic Acid; Humans; Insulin Resistance; Iran; Lysine; Male; Metabolic Diseases; Middle Aged; Phosphoric Diester Hydrolases; Polymorphism, Single Nucleotide; Pyrophosphatases; Young Adult	2011
Genetic and functional studies of a missense variant in a glutamate transporter, SLC1A3, in Tourette syndrome. Psychiatric genetics, 2011, Volume: 21, Issue:2 Topics: Alleles; Base Sequence; Behavior; Child; Child, Preschool; Conserved Sequence; DNA Mutational Analysis; Electrophoresis, Capillary; Excitatory Amino Acid Transporter 1; Gene Frequency; Genetic Predisposition to Disease; Glutamic Acid; HEK293 Cells; Humans; Infant; Molecular Sequence Data; Mutation, Missense; Polymorphism, Single-Stranded Conformational; Subcellular Fractions; Tourette Syndrome	2011
Association of TRB3 Q84R polymorphism with polycystic ovary syndrome in Chinese women. Reproductive biology and endocrinology : RB&E, 2011, Apr-14, Volume: 9 Topics: Adolescent; Adult; Amino Acid Substitution; Arginine; Asian People; Blood Glucose; Case-Control Studies; Cell Cycle Proteins; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Glutamic Acid; Humans; Obesity; Polycystic Ovary Syndrome; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases; Repressor Proteins; Young Adult	2011
Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2011, Volume: 36, Issue:8 Topics: Adult; Arginine; Carrier Proteins; Cerebral Cortex; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Glutamic Acid; Humans; Intracellular Signaling Peptides and Proteins; Lysine; Male; Polymorphism, Genetic; Schizophrenia; Young Adult	2011
Exposure to an environmental neurotoxicant hastens the onset of amyotrophic lateral sclerosis-like phenotype in human Cu2+/Zn2+ superoxide dismutase 1 G93A mice: glutamate-mediated excitotoxicity. The Journal of pharmacology and experimental therapeutics, 2011, Volume: 338, Issue:2 Topics: Amyotrophic Lateral Sclerosis; Animals; Excitatory Amino Acid Agonists; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Methylmercury Compounds; Mice; Mice, Transgenic; Phenotype; Superoxide Dismutase	2011
A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis. Annals of neurology, 2011, Volume: 70, Issue:6 Topics: Amyotrophic Lateral Sclerosis; Animals; Apoptosis; Cell Line; Child; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 9; Cloning, Molecular; Enzyme Inhibitors; Family Health; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; In Situ Nick-End Labeling; Infant; Male; Mice; Motor Neurons; Mutagenesis, Site-Directed; Phenotype; Polymorphism, Single Nucleotide; Receptors, sigma; Saudi Arabia; Sigma-1 Receptor; Thapsigargin; Transfection	2011
Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. Psychoneuroendocrinology, 2012, Volume: 37, Issue:4 Topics: Adolescent; Adult; Aged; Case-Control Studies; Corticotropin-Releasing Hormone; Depression; Depressive Disorder; Dexamethasone; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Hippocampus; Humans; Magnetic Resonance Spectroscopy; Male; Middle Aged; Phenotype; Pituitary-Adrenal Function Tests; Polymorphism, Single Nucleotide; Receptors, Metabotropic Glutamate	2012
Genetic differences in the modulation of accumbal glutamate and γ-amino butyric acid levels after cocaine-induced reinstatement. Addiction biology, 2013, Volume: 18, Issue:4 Topics: Analysis of Variance; Animals; Cocaine; Cocaine-Related Disorders; Disease Models, Animal; Dopamine Uptake Inhibitors; Drug-Seeking Behavior; Electrophoresis, Capillary; Extinction, Psychological; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Microdialysis; Nucleus Accumbens; Rats; Rats, Inbred F344; Rats, Inbred Lew; Recurrence; Self Administration; Sodium Chloride; Species Specificity	2013
Immunohistochemical testing of BRAF V600E status in 1,120 tumor tissue samples of patients with brain metastases. Acta neuropathologica, 2012, Volume: 123, Issue:2 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Brain Neoplasms; Female; Genetic Predisposition to Disease; Glutamic Acid; HEK293 Cells; Humans; Immunohistochemistry; Male; Middle Aged; Point Mutation; Proto-Oncogene Proteins B-raf; Valine; Young Adult	2012
Association of XRCC1, XRCC3, and NAT2 polymorphisms with the risk of oral submucous fibrosis among eastern Indian population. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2012, Volume: 41, Issue:4 Topics: Adult; Areca; Arginine; Arylamine N-Acetyltransferase; Case-Control Studies; Codon; DNA Repair; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Glycine; Heterozygote; Homozygote; Humans; India; Lysine; Male; Methionine; Multifactor Dimensionality Reduction; Oral Submucous Fibrosis; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Tobacco, Smokeless; Tryptophan; X-ray Repair Cross Complementing Protein 1	2012
Evidence that HLA-DQ9 confers risk to celiac disease by presence of DQ9-restricted gluten-specific T cells. Human immunology, 2012, Volume: 73, Issue:4 Topics: Amino Acid Sequence; Antigen Presentation; Celiac Disease; Epitopes, T-Lymphocyte; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Glutens; HLA-DQ Antigens; Humans; Molecular Sequence Data; Peptides; Protein Binding; Risk; T-Lymphocytes	2012
Association between three genetic polymorphisms of glutathione S-transferase Z1 (GSTZ1) and susceptibility to bipolar disorder. Psychiatry research, 2012, Jun-30, Volume: 198, Issue:1 Topics: Adolescent; Adult; Age Factors; Bipolar Disorder; Chi-Square Distribution; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutathione Transferase; Humans; Linkage Disequilibrium; Logistic Models; Lysine; Male; Middle Aged; Polymorphism, Single Nucleotide; Young Adult	2012
Interaction between effects of genes coding for dopamine and glutamate transmission on striatal and parahippocampal function. Human brain mapping, 2013, Volume: 34, Issue:9 Topics: Adult; Brain; Brain Mapping; Carrier Proteins; Dopamine; Dopamine Plasma Membrane Transport Proteins; Epistasis, Genetic; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Healthy Volunteers; Humans; Image Processing, Computer-Assisted; Intracellular Signaling Peptides and Proteins; Magnetic Resonance Imaging; Male; Polymorphism, Single Nucleotide; Psychotic Disorders; Reverse Transcriptase Polymerase Chain Reaction; Schizophrenia; Synaptic Transmission; Verbal Learning	2013
Weight is an independent predictor of vascular injury in healthy volunteers with aspartate allele. Journal of cardiovascular medicine (Hagerstown, Md.), 2012, Volume: 13, Issue:5 Topics: Adult; Aspartic Acid; Atherosclerosis; Body Weight; Brachial Artery; Carotid Artery Diseases; Carotid Intima-Media Thickness; Chi-Square Distribution; Endothelium, Vascular; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamic Acid; Homozygote; Humans; Italy; Linear Models; Male; Multivariate Analysis; Nitric Oxide Synthase Type III; Obesity; Phenotype; Polymorphism, Genetic; Risk Assessment; Risk Factors; Vasodilation	2012
Functional studies and rare variant screening of SLC1A1/EAAC1 in males with obsessive-compulsive disorder. Psychiatric genetics, 2012, Volume: 22, Issue:5 Topics: Adolescent; Adult; Child; Excitatory Amino Acid Transporter 3; Genetic Predisposition to Disease; Genetic Testing; Glutamic Acid; Humans; Kinetics; Male; Middle Aged; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Sequence Analysis, DNA; Young Adult	2012
Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients. PloS one, 2012, Volume: 7, Issue:5 Topics: Adaptor Proteins, Signal Transducing; Carrier Proteins; Case-Control Studies; Cognition Disorders; Genetic Association Studies; Genetic Predisposition to Disease; Glutamic Acid; Guanylate Kinases; Humans; Japan; Neuropsychological Tests; Polymorphism, Single Nucleotide; Schizophrenia	2012
Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease. Molecular psychiatry, 2013, Volume: 18, Issue:5 Topics: Age of Onset; Alanine; Alzheimer Disease; Cohort Studies; Databases, Factual; Female; Founder Effect; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Glutamic Acid; Humans; Male; Mutation; Polymorphism, Single Nucleotide; Presenilin-1; Quantitative Trait Loci	2013
Decreased susceptibility to seizures induced by pentylenetetrazole in serine racemase knockout mice. Epilepsy research, 2012, Volume: 102, Issue:3 Topics: Amino Acids; Analysis of Variance; Animals; Brain; Chromatography, High Pressure Liquid; Convulsants; Disease Models, Animal; Disease Susceptibility; Dose-Response Relationship, Drug; Genetic Predisposition to Disease; Glutamic Acid; Mice; Mice, Inbred C57BL; Mice, Knockout; Microdialysis; Microscopy, Confocal; Pentylenetetrazole; Proto-Oncogene Proteins c-fos; Racemases and Epimerases; Seizures; Statistics, Nonparametric; Time Factors	2012
A replication study of a GWAS finding in migraine does not identify association in a Spanish case-control sample. Cephalalgia : an international journal of headache, 2012, Volume: 32, Issue:14 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Case-Control Studies; Cell Adhesion Molecules; Child; Child, Preschool; Chromosomes, Human, Pair 8; Female; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Glutamic Acid; Humans; Male; Membrane Proteins; Middle Aged; Migraine with Aura; Migraine without Aura; Polymorphism, Single Nucleotide; Reproducibility of Results; Risk; RNA-Binding Proteins; Spain; Young Adult	2012
Familial cortical myoclonus with a mutation in NOL3. Annals of neurology, 2012, Volume: 72, Issue:2 Topics: Adolescent; Adult; Age of Onset; Animals; Apoptosis Regulatory Proteins; Canada; Cell Line, Transformed; Chromosome Mapping; Chromosomes, Human, Pair 16; Electroencephalography; Family Health; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Mice; Middle Aged; Muscle Proteins; Mutation; Myoclonus; Phenotype; Proline; Transfection	2012
A single point mutation in the gene encoding Gb3/CD77 synthase causes a rare inherited polyagglutination syndrome. The Journal of biological chemistry, 2012, Nov-02, Volume: 287, Issue:45 Topics: Amino Acid Substitution; Carbohydrate Sequence; Cell Line, Tumor; Embryonal Carcinoma Stem Cells; Flow Cytometry; Galactosyltransferases; Genetic Predisposition to Disease; Genotype; Globosides; Glutamic Acid; Glutamine; Hemagglutination; Humans; Molecular Sequence Data; Phenotype; Point Mutation; Polymorphism, Single Nucleotide; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Syndrome	2012
The BRAF(V600E) mutation is an independent, poor prognostic factor for the outcome of patients with low-risk intrathyroid papillary thyroid carcinoma: single-institution results from a large cohort study. The Journal of clinical endocrinology and metabolism, 2012, Volume: 97, Issue:12 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Carcinoma; Carcinoma, Papillary; Cohort Studies; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Middle Aged; Mutation, Missense; Prognosis; Proto-Oncogene Proteins B-raf; Risk Factors; Sample Size; Thyroid Cancer, Papillary; Thyroid Gland; Thyroid Neoplasms; Valine; Young Adult	2012
Upregulation of cornichon transcripts in the dorsolateral prefrontal cortex in schizophrenia. Neuroreport, 2012, Dec-05, Volume: 23, Issue:17 Topics: Aged; Aged, 80 and over; Animals; Antipsychotic Agents; Egg Proteins; Female; Frontal Lobe; Gene Expression Regulation; Genetic Markers; Genetic Predisposition to Disease; Glutamic Acid; Haloperidol; Humans; Male; Membrane Proteins; Middle Aged; Nerve Tissue Proteins; Prefrontal Cortex; Protein Isoforms; Rats; Rats, Sprague-Dawley; Receptors, AMPA; RNA, Messenger; Schizophrenia; Synaptic Transmission; Up-Regulation	2012
Glutamate system genes and brain volume alterations in pediatric obsessive-compulsive disorder: a preliminary study. Psychiatry research, 2013, Mar-30, Volume: 211, Issue:3 Topics: Adolescent; Brain; Child; Female; Genetic Association Studies; Genetic Predisposition to Disease; Glutamic Acid; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Nerve Tissue Proteins; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide	2013
Common genetic background in anorexia nervosa and obsessive compulsive disorder: preliminary results from an association study. Journal of psychiatric research, 2013, Volume: 47, Issue:6 Topics: Adolescent; Anorexia Nervosa; Child; Cohort Studies; Female; Genetic Association Studies; Genetic Markers; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Obsessive-Compulsive Disorder; Pilot Projects; Polymorphism, Single Nucleotide; Serotonin	2013
Changes in extracellular levels of amygdala amino acids in genetically fast and slow kindling rat strains. Brain research, 2002, Aug-09, Volume: 946, Issue:1 Topics: Amino Acids; Amygdala; Animals; Differential Threshold; Electrophysiology; Extracellular Space; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Hippocampus; Kindling, Neurologic; Male; Rats; Rats, Inbred Strains; Seizures; Time Factors	2002
Severe immunodeficiency has opposite effects on neuronal survival in glutamate-susceptible and -resistant mice: adverse effect of B cells. Journal of immunology (Baltimore, Md. : 1950), 2002, Sep-15, Volume: 169, Issue:6 Topics: Animals; B-Lymphocyte Subsets; Cell Survival; Genetic Predisposition to Disease; Glutamic Acid; Immunity, Innate; Injections; Lymphopenia; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, SCID; Mice, Transgenic; Neurons; Retinal Ganglion Cells; Severe Combined Immunodeficiency; Species Specificity; Vitreous Body	2002
Expression of glutamate transporters and ionotropic glutamate receptors in GLAST knockout mice. Brain research. Molecular brain research, 2002, Aug-15, Volume: 104, Issue:2 Topics: Amino Acid Transport System X-AG; Animals; Down-Regulation; Epilepsy; Excitatory Amino Acid Transporter 1; Excitatory Amino Acid Transporter 2; Female; Frontal Lobe; Genetic Predisposition to Disease; Glutamate Plasma Membrane Transport Proteins; Glutamic Acid; Hippocampus; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Receptors, AMPA; Receptors, Glutamate; Receptors, Kainic Acid; Receptors, N-Methyl-D-Aspartate; Symporters; Synaptic Transmission	2002
The neuroscience of drug addiction: Rome built in a day. Trends in pharmacological sciences, 2002, Volume: 23, Issue:12 Topics: Animals; Brain; Genetic Predisposition to Disease; Glutamic Acid; Humans; Neuronal Plasticity; Substance-Related Disorders	2002
Obesity, Type II diabetes and the beta 2 adrenoceptor gene Gln27Glu polymorphism in the Tongan population. Clinical science (London, England : 1979), 2003, Volume: 104, Issue:3 Topics: Adult; Blood Glucose; Body Constitution; Body Mass Index; Diabetes Mellitus, Type 2; Female; Gene Frequency; Genetic Predisposition to Disease; Genetics, Population; Genotype; Glutamic Acid; Glutamine; Humans; Male; Middle Aged; Obesity; Polymorphism, Genetic; Receptors, Adrenergic, beta-2; Tonga	2003
Differences in ionotropic glutamate receptor subunit expression are not responsible for strain-dependent susceptibility to excitotoxin-induced injury. Brain research. Molecular brain research, 2003, Apr-10, Volume: 112, Issue:1-2 Topics: Animals; Cell Death; Disease Models, Animal; Drug Resistance; Epilepsy; Genetic Predisposition to Disease; Glutamic Acid; Immunohistochemistry; Kainic Acid; Male; Mice; Mice, Inbred C57BL; Nerve Degeneration; Neurotoxins; Protein Subunits; Receptors, AMPA; Receptors, Glutamate; Receptors, Kainic Acid; Receptors, N-Methyl-D-Aspartate; Species Specificity; Synaptic Transmission	2003
Endothelial nitric oxide synthase gene polymorphisms and renal survival. Hypertension (Dallas, Tex. : 1979), 2003, Volume: 41, Issue:6 Topics: Amino Acid Substitution; Aspartic Acid; Genetic Predisposition to Disease; Glutamic Acid; Humans; Kidney Failure, Chronic; Nitric Oxide; Nitric Oxide Synthase; Nitric Oxide Synthase Type III; Polymorphism, Genetic	2003
Endothelial nitric oxide synthase polymorphism in preeclampsia. Journal of the Society for Gynecologic Investigation, 2003, Volume: 10, Issue:3 Topics: Adult; Aspartic Acid; Female; Finland; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Nitric Oxide Synthase; Nitric Oxide Synthase Type III; Polymorphism, Genetic; Pre-Eclampsia; Pregnancy; Retrospective Studies	2003
Basal fat oxidation and after a peak oxygen consumption test in obese women with a beta2 adrenoceptor gene polymorphism. The Journal of nutritional biochemistry, 2003, Volume: 14, Issue:5 Topics: Adipose Tissue; Adult; Alleles; Calorimetry, Indirect; Exercise; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Glycerol; Humans; Lipolysis; Obesity; Oxidation-Reduction; Oxygen Consumption; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Receptors, Adrenergic, beta-2; Triglycerides	2003
A dual role of adenosine A2A receptors in 3-nitropropionic acid-induced striatal lesions: implications for the neuroprotective potential of A2A antagonists. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003, Jun-15, Volume: 23, Issue:12 Topics: Adenosine; Animals; Body Weight; Cell Death; Corpus Striatum; Disease Models, Animal; Drug Administration Schedule; Encephalitis; Genetic Predisposition to Disease; Glutamic Acid; Huntington Disease; Male; Mice; Mice, Knockout; Neuroprotective Agents; Nitro Compounds; Phenethylamines; Propionates; Rats; Rats, Inbred Lew; Rats, Wistar; Receptor, Adenosine A2A; Receptors, Purinergic P1; RNA, Messenger; Signal Transduction; Survival Rate; Synapses; Xanthines	2003
Obesity risk is associated with carbohydrate intake in women carrying the Gln27Glu beta2-adrenoceptor polymorphism. The Journal of nutrition, 2003, Volume: 133, Issue:8 Topics: Adult; Case-Control Studies; Dietary Carbohydrates; Dose-Response Relationship, Drug; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Insulin; Male; Middle Aged; Obesity; Polymorphism, Genetic; Receptors, Adrenergic, beta-2; Sex Characteristics	2003
Glutamatergic activation of the amygdala differentially mimics the effects of audiogenic seizure kindling in two substrains of genetically epilepsy-prone rats. Experimental neurology, 2003, Volume: 183, Issue:2 Topics: Acoustic Stimulation; Amygdala; Animals; Behavior, Animal; Disease Models, Animal; Dose-Response Relationship, Drug; Epilepsy, Reflex; Female; Genetic Predisposition to Disease; Glutamic Acid; Kindling, Neurologic; Male; Microinjections; N-Methylaspartate; Rats; Rats, Inbred Strains; Rats, Sprague-Dawley; Seizures	2003
Premorbid weight, body mass, and varsity athletics in ALS. Neurology, 2003, Oct-14, Volume: 61, Issue:7 Topics: 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide); Amino Acids, Branched-Chain; Amyotrophic Lateral Sclerosis; Astrocytes; Body Weight; Case-Control Studies; Dietary Supplements; Genetic Predisposition to Disease; Glutamic Acid; Humans; Italy; Middle Aged; Mitochondria; Pyramidal Cells; Sports; Transaminases	2003
Endothelial nitric oxide synthase gene polymorphisms in giant cell arteritis. Arthritis and rheumatism, 2003, Volume: 48, Issue:11 Topics: Aged; Aspartic Acid; DNA; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Giant Cell Arteritis; Glutamic Acid; Heterozygote; Humans; Male; Middle Aged; Nitric Oxide Synthase; Nitric Oxide Synthase Type III; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic	2003
Influence of MHC class II in susceptibility to beryllium sensitization and chronic beryllium disease. Journal of immunology (Baltimore, Md. : 1950), 2003, Dec-15, Volume: 171, Issue:12 Topics: Adult; Aged; Berylliosis; Beryllium; Case-Control Studies; Chronic Disease; Epitopes; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Histocompatibility Antigens Class II; HLA Antigens; HLA-DP Antigens; HLA-DP beta-Chains; HLA-DQ Antigens; HLA-DQ beta-Chains; HLA-DR Antigens; HLA-DRB1 Chains; HLA-DRB3 Chains; HLA-DRB4 Chains; HLA-DRB5 Chains; Humans; Immunization; Male; Middle Aged; Polymorphism, Genetic; Severity of Illness Index	2003
Potential pleiotropic effects of Mpdz on vulnerability to seizures. Genes, brain, and behavior, 2004, Volume: 3, Issue:1 Topics: Amino Acid Motifs; Animals; Carrier Proteins; Chromosome Mapping; Convulsants; Ethanol; Female; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Male; Membrane Proteins; Mice; Mice, Inbred Strains; Pentobarbital; Phenotype; Quantitative Trait, Heritable; Seizures; Species Specificity; Substance Withdrawal Syndrome	2004
Gene-environment interactions between the smoking habit and polymorphisms in the DNA repair genes, APE1 Asp148Glu and XRCC1 Arg399Gln, in Japanese lung cancer risk. Carcinogenesis, 2004, Volume: 25, Issue:8 Topics: Adult; Aged; Alleles; Arginine; Aspartic Acid; Codon; DNA Repair; DNA-(Apurinic or Apyrimidinic Site) Lyase; DNA-Binding Proteins; Environment; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Humans; Japan; Lung Neoplasms; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Risk; Risk Factors; Smoking; X-ray Repair Cross Complementing Protein 1	2004
Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism. The American journal of psychiatry, 2004, Volume: 161, Issue:4 Topics: Aspartic Acid; Autistic Disorder; Chromosome Mapping; Chromosomes, Human, Pair 2; DNA Mutational Analysis; DNA, Mitochondrial; Genetic Linkage; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Haplotypes; Humans; Membrane Transport Proteins; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Point Mutation; Polymorphism, Genetic	2004
Limbic epileptogenicity, cell loss and axonal reorganization induced by audiogenic and amygdala kindling in wistar audiogenic rats (WAR strain). Neuroscience, 2004, Volume: 125, Issue:3 Topics: Acoustic Stimulation; Amygdala; Animals; Cell Count; Disease Models, Animal; Disease Progression; Epilepsy, Reflex; Epilepsy, Tonic-Clonic; Female; Genetic Predisposition to Disease; Glutamic Acid; Hippocampus; Kindling, Neurologic; Limbic System; Mossy Fibers, Hippocampal; Nerve Degeneration; Neuronal Plasticity; Presynaptic Terminals; Rats; Rats, Mutant Strains; Rats, Wistar	2004
Increased reactive oxygen species in rostral ventrolateral medulla contribute to neural mechanisms of hypertension in stroke-prone spontaneously hypertensive rats. Circulation, 2004, May-18, Volume: 109, Issue:19 Topics: 1,2-Dihydroxybenzene-3,5-Disulfonic Acid Disodium Salt; Animals; Blood Pressure; Brain Chemistry; Catalase; Cyclic N-Oxides; Deferoxamine; Genetic Predisposition to Disease; Genetic Therapy; Glutamic Acid; Hydrogen Peroxide; Hydroxyl Radical; Hypertension; Lipid Peroxidation; Male; Medulla Oblongata; Norepinephrine; Oxidative Stress; Rats; Rats, Inbred SHR; Rats, Inbred WKY; Reactive Oxygen Species; Recombinant Fusion Proteins; Spin Labels; Stroke; Superoxide Dismutase; Superoxides; Sympathetic Nervous System; Thiobarbituric Acid Reactive Substances; Transduction, Genetic; Vasomotor System	2004
Susceptibility to primary sclerosing cholangitis is associated with polymorphisms of intercellular adhesion molecule-1. Journal of hepatology, 2004, Volume: 40, Issue:3 Topics: Alleles; Arginine; Case-Control Studies; Cholangitis, Sclerosing; Cohort Studies; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glycine; Haplotypes; HLA Antigens; Homozygote; Humans; Intercellular Adhesion Molecule-1; Lysine; Polymorphism, Genetic; Primed In Situ Labeling	2004
Dysbindin-1 and schizophrenia: from genetics to neuropathology. The Journal of clinical investigation, 2004, Volume: 113, Issue:9 Topics: Brain; Carrier Proteins; Dysbindin; Dystrophin-Associated Proteins; Genetic Predisposition to Disease; Glutamic Acid; Hippocampus; Humans; Membrane Transport Proteins; Models, Biological; Neurons; Presynaptic Terminals; Schizophrenia; Tissue Distribution; Vesicular Glutamate Transport Protein 1; Vesicular Transport Proteins	2004
3-T proton MRS investigation of glutamate and glutamine in adolescents at high genetic risk for schizophrenia. The American journal of psychiatry, 2004, Volume: 161, Issue:6 Topics: Adolescent; Child of Impaired Parents; Cohort Studies; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamic Acid; Glutamine; Humans; Magnetic Resonance Spectroscopy; Male; Prefrontal Cortex; Psychiatric Status Rating Scales; Schizophrenia; Social Class	2004
Association of aldehyde dehydrogenase-2 polymorphism with alcoholic polyneuropathy in humans. Neuroscience letters, 2004, Jun-17, Volume: 363, Issue:3 Topics: Action Potentials; Alcoholic Neuropathy; Aldehyde Dehydrogenase; Aldehyde Dehydrogenase, Mitochondrial; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Lysine; Male; Middle Aged; Neural Conduction; Peripheral Nerves; Polymorphism, Genetic; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger	2004
Sequence analysis of ADARB1 gene in patients with familial bipolar disorder. Journal of affective disorders, 2004, Volume: 81, Issue:1 Topics: Adenosine Deaminase; Adolescent; Adult; Anticonvulsants; Bipolar Disorder; Chromosomes, Human, Pair 21; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Middle Aged; Molecular Sequence Data; Polymorphism, Genetic; Receptors, Glutamate; RNA Precursors; RNA-Binding Proteins; Sequence Analysis, DNA; Synaptic Transmission	2004
Neurotoxic effects of postnatal thimerosal are mouse strain dependent. Molecular psychiatry, 2004, Volume: 9, Issue:9 Topics: Animals; Autistic Disorder; Autoimmune Diseases; Behavior, Animal; Exploratory Behavior; Female; Genetic Predisposition to Disease; Glutamic Acid; Growth Disorders; Hippocampus; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Inbred Strains; Neurons; Neurotoxins; Preservatives, Pharmaceutical; Sex Factors; Species Specificity; Statistics, Nonparametric; Thimerosal; Vaccines	2004
Homozygous deficiency of heparin cofactor II: relevance of P17 glutamate residue in serpins, relationship with conformational diseases, and role in thrombosis. Circulation, 2004, Sep-07, Volume: 110, Issue:10 Topics: Adult; alpha 1-Antitrypsin; alpha 1-Antitrypsin Deficiency; Antithrombin III; Antithrombin III Deficiency; Codon, Nonsense; Codon, Terminator; Female; Genetic Predisposition to Disease; Glutamic Acid; Heparin Cofactor II; Homozygote; Humans; Liver; Models, Molecular; Point Mutation; Protein Conformation; Pulmonary Emphysema; Recurrence; Serpins; Thrombophilia; Venous Thrombosis	2004
Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia. Human molecular genetics, 2004, Nov-01, Volume: 13, Issue:21 Topics: Adult; Alleles; Animals; Carrier Proteins; Cells, Cultured; Cerebral Cortex; Chromones; Chromosomes, Human, Pair 6; Dysbindin; Dystrophin-Associated Proteins; Enzyme Inhibitors; Female; Gene Frequency; Genetic Linkage; Genetic Markers; Genetic Predisposition to Disease; Glutamic Acid; Haplotypes; Humans; Linkage Disequilibrium; Male; Membrane Proteins; Morpholines; Nerve Tissue Proteins; Neurons; Phosphatidylinositol 3-Kinases; Phosphorylation; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-akt; Rats; Rats, Inbred Strains; RNA, Small Interfering; Schizophrenia; Synapsins; Synaptosomal-Associated Protein 25	2004
Effects of NMDA glutamate receptor antagonist drugs on the volitional consumption of ethanol by a genetic drinking rat. Brain research bulletin, 2004, Sep-30, Volume: 64, Issue:3 Topics: Alcohol Drinking; Alcohol-Induced Disorders, Nervous System; Alcoholism; Amino Acids, Cyclic; Animals; Brain; Disease Models, Animal; Dizocilpine Maleate; Dose-Response Relationship, Drug; Ethanol; Excitatory Amino Acid Antagonists; Female; Genetic Predisposition to Disease; Glutamic Acid; Isoquinolines; Male; Motor Activity; Pyrrolidinones; Rats; Rats, Inbred Strains; Rats, Sprague-Dawley; Receptors, Glycine; Receptors, N-Methyl-D-Aspartate; Synaptic Transmission; Volition	2004
Comparative study of the residues 63 and 67 on the HLA-B molecule in patients with Takayasu's Arteritis. Immunology letters, 2005, Jan-31, Volume: 96, Issue:2 Topics: Alleles; Amino Acid Substitution; Female; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Glutamic Acid; HLA-B Antigens; Humans; Male; Mexico; Serine; Takayasu Arteritis	2005
T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study. Journal of the American Society of Nephrology : JASN, 2005, Volume: 16, Issue:4 Topics: Aged; Albuminuria; Aspartic Acid; Creatinine; Cysteine; Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2; Exons; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Homozygote; Humans; Linkage Disequilibrium; Male; Middle Aged; Nitric Oxide Synthase; Nitric Oxide Synthase Type III; Odds Ratio; Polymorphism, Genetic; Promoter Regions, Genetic; Threonine	2005
Electrophysiological properties of cultured hippocampal neurons from Wistar Audiogenic Rats. Brain research bulletin, 2005, Mar-15, Volume: 65, Issue:2 Topics: Action Potentials; Animals; Animals, Newborn; Cell Membrane; Cells, Cultured; Disease Models, Animal; Electric Impedance; Epilepsy, Reflex; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Hippocampus; Neural Inhibition; Neurons; Patch-Clamp Techniques; Potassium Channels; Rats; Rats, Wistar; Receptors, GABA; Synaptic Transmission	2005
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures. Neurology, 2005, Aug-23, Volume: 65, Issue:4 Topics: Animals; Ataxia; Brain; Brain Chemistry; Brain Edema; Child; Chlorocebus aethiops; COS Cells; DNA Mutational Analysis; Excitatory Amino Acid Transporter 1; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamic Acid; Hemiplegia; Heterozygote; Humans; Magnetic Resonance Imaging; Male; Mutation; Pedigree; Seizures	2005
Effect of overexpression of wild-type or mutant parkin on the cellular response induced by toxic insults. Journal of neuroscience research, 2005, Oct-15, Volume: 82, Issue:2 Topics: 1-Methyl-4-phenylpyridinium; Acetylcysteine; Aldehydes; Apoptosis; Cell Death; Cell Line, Tumor; Drug Resistance; Enzyme Inhibitors; Genetic Predisposition to Disease; Glutamic Acid; Guanine; Humans; Hydrogen Peroxide; Mutation; Nerve Degeneration; Neurons; Neurotoxins; Oxidative Stress; Parkinsonian Disorders; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Substantia Nigra; Tyrosine; Ubiquitin-Protein Ligases	2005
Lack of association between the IL13 variant Arg110Gln and susceptibility to cedar pollinosis in a Japanese population. International archives of allergy and immunology, 2006, Volume: 139, Issue:1 Topics: Arginine; Cryptomeria; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutamic Acid; Humans; Interleukin-13; Japan; Pollen; Rhinitis, Allergic, Seasonal	2006
Polymorphisms of ADPRT Val762Ala and XRCC1 Arg399Glu and risk of breast cancer in Chinese women: a case control analysis. Oncology reports, 2006, Volume: 15, Issue:1 Topics: Adult; Alanine; Amino Acid Substitution; Arginine; Asian People; Breast Neoplasms; Case-Control Studies; China; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Middle Aged; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerases; Polymorphism, Genetic; Risk; Valine; X-ray Repair Cross Complementing Protein 1	2006
Clinical correlates of quantitative EEG alterations in alcoholic patients. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2006, Volume: 117, Issue:4 Topics: Adult; Age Factors; Aged; Alcohol Withdrawal Seizures; Alcohol-Induced Disorders, Nervous System; Alcoholism; Atrophy; Benzodiazepines; Brain Damage, Chronic; Central Nervous System Depressants; Cerebral Cortex; Drug Interactions; Electroencephalography; Ethanol; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glutamic Acid; Hallucinations; Humans; Male; Middle Aged; Models, Neurological; Nerve Degeneration; Neurotoxins	2006
A polymorphism in the EAAT2 promoter is associated with higher glutamate concentrations and higher frequency of progressing stroke. The Journal of experimental medicine, 2006, Mar-20, Volume: 203, Issue:3 Topics: Aged; Aged, 80 and over; Animals; Astrocytes; Biological Transport; Brain Chemistry; Cells, Cultured; Disease Progression; Excitatory Amino Acid Transporter 2; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Glutamate Plasma Membrane Transport Proteins; Glutamic Acid; Humans; Male; Middle Aged; Point Mutation; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Rats; RNA-Binding Proteins; Stroke; Transcription Factor AP-2; Transfection	2006
The Glu27 genotypes of the beta2-adrenergic receptor are predictors for severe coronary artery disease. BMC medical genetics, 2006, Mar-30, Volume: 7 Topics: Arabs; Coronary Artery Disease; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Adrenergic, beta-2; Saudi Arabia	2006
Combined application of behavior genetics and microarray analysis to identify regional expression themes and gene-behavior associations. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006, May-17, Volume: 26, Issue:20 Topics: Alcoholism; Animals; Anxiety Disorders; Behavior, Animal; Brain; Brain Chemistry; Brain Mapping; Chromosome Mapping; Gene Expression Profiling; Gene Expression Regulation; Genetic Predisposition to Disease; Genetics, Behavioral; Genomics; Glutamic Acid; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Inbred DBA; Oligonucleotide Array Sequence Analysis; Phenotype; Signal Transduction; Species Specificity	2006
Lack of association between NOS3 Glu298Asp and breast cancer risk: a case-control study. Breast cancer research and treatment, 2006, Volume: 100, Issue:3 Topics: Aspartic Acid; Breast Neoplasms; Case-Control Studies; Female; Gene Expression Regulation, Neoplastic; Gene Frequency; Genetic Predisposition to Disease; Glutamic Acid; Humans; Nitric Oxide Synthase Type III; Odds Ratio; Polymorphism, Genetic; Risk Assessment; Risk Factors; Spain	2006
Endothelial nitric oxide synthase Glu298Asp gene polymorphism in periodontal diseases. Journal of periodontology, 2006, Volume: 77, Issue:8 Topics: Acute Disease; Adolescent; Adult; Amino Acid Substitution; Aspartic Acid; Chi-Square Distribution; Chronic Disease; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Logistic Models; Male; Middle Aged; Mutation, Missense; Nitric Oxide Synthase Type III; Periodontal Index; Periodontitis; Polymorphism, Single Nucleotide; Severity of Illness Index; Statistics, Nonparametric; Turkey	2006
Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation. Neuromuscular disorders : NMD, 2006, Volume: 16, Issue:9-10 Topics: Actinin; Actins; Amino Acid Substitution; Cardiomyopathy, Hypertrophic, Familial; Child, Preschool; DNA Mutational Analysis; Fatal Outcome; Genetic Predisposition to Disease; Genetic Testing; Glutamic Acid; Humans; Lysine; Male; Muscle Contraction; Muscle Fibers, Skeletal; Muscle, Skeletal; Mutation, Missense; Myocardium; Myopathies, Nemaline	2006
A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intolerance. Neuromuscular disorders : NMD, 2006, Volume: 16, Issue:12 Topics: Brain; Child; DNA Mutational Analysis; Exercise Tolerance; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Mitochondrial Diseases; Mitochondrial Myopathies; Muscle Fibers, Skeletal; Muscle Weakness; Muscle, Skeletal; Mutation; RNA; RNA, Mitochondrial; RNA, Transfer	2006
Haplotypes encoding the factor VIII 1241Glu variation and the risk of myocardial infarction. Journal of thrombosis and haemostasis : JTH, 2007, Volume: 5, Issue:3 Topics: Adult; Aged; Arterial Occlusive Diseases; Case-Control Studies; Factor VIII; Female; Gene Frequency; Genetic Predisposition to Disease; Glutamic Acid; Haplotypes; Humans; Male; Middle Aged; Myocardial Infarction; Odds Ratio; Polymorphism, Single Nucleotide; Population Surveillance; Risk Assessment; Risk Factors; Thrombosis	2007
beta2-Adrenergic receptor gene variants and risk for autism in the AGRE cohort. Molecular psychiatry, 2007, Volume: 12, Issue:3 Topics: Autistic Disorder; Child; Cohort Studies; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Linkage Disequilibrium; Male; Odds Ratio; Polymorphism, Genetic; Pregnancy; Receptors, Adrenergic, beta-2; Risk	2007
Functional P2X7 receptor polymorphisms (His155Tyr, Arg307Gln, Glu496Ala) in patients with Crohn's disease. Scandinavian journal of immunology, 2007, Volume: 65, Issue:2 Topics: Alanine; Amino Acid Substitution; Arginine; Case-Control Studies; Crohn Disease; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Histidine; Humans; Male; Polymorphism, Single Nucleotide; Receptors, Purinergic P2; Receptors, Purinergic P2X7; Tyrosine	2007
A Japanese family with early-onset ataxia with motor and sensory neuropathy. Journal of the neurological sciences, 2007, Mar-15, Volume: 254, Issue:1-2 Topics: Adult; Age of Onset; Cerebellum; Disease Progression; Female; Genes, Recessive; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glutamic Acid; Hereditary Sensory and Motor Neuropathy; Humans; Japan; Magnetic Resonance Imaging; Male; Middle Aged; Nerve Fibers, Myelinated; Pedigree; Peripheral Nerves; Spinocerebellar Degenerations; Up-Regulation	2007
Variants in the LRRK1 gene and susceptibility to Parkinson's disease in Norway. Neuroscience letters, 2007, Apr-18, Volume: 416, Issue:3 Topics: Adult; Aged; Aged, 80 and over; Case-Control Studies; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Lysine; Male; Middle Aged; Norway; Parkinson Disease; Polymorphism, Genetic; Protein Serine-Threonine Kinases	2007
Failure to confirm the association between the FEZ1 gene and schizophrenia in a Japanese population. Neuroscience letters, 2007, May-07, Volume: 417, Issue:3 Topics: Adaptor Proteins, Signal Transducing; Adult; Amino Acid Substitution; Asian People; Aspartic Acid; Brain; Brain Chemistry; DNA Mutational Analysis; DNA-Binding Proteins; Female; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Glutamic Acid; Humans; Japan; Male; Middle Aged; Mutation; Mutation, Missense; Nerve Tissue Proteins; Polymorphism, Genetic; Schizophrenia; Tumor Suppressor Proteins	2007
Polymorphisms in the paraoxonase and endothelial nitric oxide synthase genes and the risk of early-onset myocardial infarction. The American journal of cardiology, 2007, Apr-15, Volume: 99, Issue:8 Topics: Adult; Age of Onset; Aged; Aged, 80 and over; Arginine; Aryldialkylphosphatase; Aspartic Acid; Cohort Studies; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Humans; Male; Middle Aged; Myocardial Infarction; Nitric Oxide Synthase Type III; Polymorphism, Single Nucleotide; Prospective Studies; Risk Factors	2007
Functional role of mGluR1 and mGluR4 in pilocarpine-induced temporal lobe epilepsy. Neurobiology of disease, 2007, Volume: 26, Issue:3 Topics: Animals; Convulsants; Disease Models, Animal; Down-Regulation; Epilepsy; Epilepsy, Temporal Lobe; Gene Expression Regulation; Genetic Predisposition to Disease; Glutamic Acid; Green Fluorescent Proteins; Hippocampus; Mice; Mice, Knockout; Mice, Transgenic; Nerve Degeneration; Neurons; Pilocarpine; Receptors, Metabotropic Glutamate; Recombinant Fusion Proteins; Up-Regulation	2007
Beta2-adrenergic receptor gene polymorphisms and risk of ischemic stroke. American journal of hypertension, 2007, Volume: 20, Issue:6 Topics: Aged; Aged, 80 and over; Alleles; Case-Control Studies; DNA; Female; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Humans; Italy; Male; Middle Aged; Odds Ratio; Polymorphism, Genetic; Receptors, Adrenergic, beta-2; Risk Factors; Stroke	2007
[Lactic acidosis and accumulation of glutamate in the blood of neonates following treatment with calcium levulinate for hypocalcaemia]. Nederlands tijdschrift voor geneeskunde, 2007, May-26, Volume: 151, Issue:21 Topics: Acidosis, Lactic; Chromosome Deletion; Chromosomes, Human, Pair 22; Enzyme Inhibitors; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Hypocalcemia; Infant, Newborn; Lactates; Levulinic Acids; Male	2007
Synaptic P2X7 receptor regenerative-loop hypothesis for depression. The Australian and New Zealand journal of psychiatry, 2007, Volume: 41, Issue:7 Topics: Adenosine Triphosphate; Astrocytes; Bipolar Disorder; Brain; Cerebral Cortex; Depressive Disorder, Major; Genetic Predisposition to Disease; Glutamic Acid; Hippocampus; Humans; Infections; Interleukin-1beta; Microglia; Nerve Net; Nerve Regeneration; Polymorphism, Genetic; Receptors, AMPA; Receptors, Purinergic P2; Receptors, Purinergic P2X7; Synapses; Synaptic Transmission; Toll-Like Receptors; Tumor Necrosis Factor-alpha	2007
The genetics of schizophrenia converge upon the NMDA glutamate receptor. CNS spectrums, 2007, Volume: 12, Issue:8 Topics: Brain; Genetic Predisposition to Disease; Glutamic Acid; Humans; Long-Term Potentiation; Receptors, AMPA; Receptors, N-Methyl-D-Aspartate; Schizophrenia; Synapses	2007
Role of IFN-gamma in an experimental murine model of West Nile virus-induced seizures. Journal of neurochemistry, 2007, Volume: 103, Issue:3 Topics: Animals; Brain; Chlorocebus aethiops; Convulsants; Disease Models, Animal; Excitatory Amino Acid Antagonists; Female; Genetic Predisposition to Disease; Glutamic Acid; Interferon-gamma; Interleukin-6; Limbic Encephalitis; Mice; Mice, Inbred C57BL; Mice, Knockout; Neural Pathways; Receptors, N-Methyl-D-Aspartate; Seizures; Synaptic Transmission; Tumor Necrosis Factor-alpha; Vero Cells; West Nile Fever	2007
Spontaneously hypertensive rats are highly vulnerable to AMPA-induced brain lesions. Stroke, 2007, Volume: 38, Issue:11 Topics: alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid; Animals; Blood Pressure; Brain Damage, Chronic; Brain Ischemia; Calcium-Calmodulin-Dependent Protein Kinase Type 2; Cell Death; Genetic Predisposition to Disease; Glutamic Acid; Hypertension; Ion Channel Gating; Male; Membrane Potentials; Nerve Degeneration; Neurotoxins; Phosphorylation; Rats; Rats, Inbred SHR; Rats, Inbred WKY; Receptors, AMPA; Regional Blood Flow; Vascular Resistance	2007
BTNL2 allele associations with chronic beryllium disease in HLA-DPB1Glu69-negative individuals. Tissue antigens, 2007, Volume: 70, Issue:6* Topics: Alleles; Berylliosis; Butyrophilins; Female; Genetic Predisposition to Disease; Glutamic Acid; HLA-DP Antigens; HLA-DP beta-Chains; Homozygote; Humans; Male; Membrane Glycoproteins; Middle Aged; Polymorphism, Genetic; White People	2007
Mechanism of age-dependent susceptibility and novel treatment strategy in glutaric acidemia type I. The Journal of clinical investigation, 2007, Volume: 117, Issue:11 Topics: Aging; Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Child; Diet; Disease Models, Animal; gamma-Aminobutyric Acid; Genetic Predisposition to Disease; Glucose; Glutamic Acid; Glutarates; Glutaryl-CoA Dehydrogenase; Homoarginine; Humans; Lysine; Mice; Mice, Knockout; Mitochondria; Neurons; Nuclear Magnetic Resonance, Biomolecular; Tryptophan	2007
Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants? Breast cancer research : BCR, 2007, Volume: 9, Issue:6 Topics: Alanine; Arginine; Biomarkers, Tumor; Breast Neoplasms; Centrosome; DNA, Complementary; Factor Analysis, Statistical; Female; Genes, BRCA1; Genetic Predisposition to Disease; Glutamic Acid; Glutamine; Glycine; Humans; Immunohistochemistry; Keratins; Mutation, Missense; Nucleic Acid Amplification Techniques; Plasmids; Polymorphism, Single Nucleotide; Predictive Value of Tests; Receptors, Estrogen; Risk Assessment; Risk Factors; Sequence Analysis, DNA; Valine	2007
Protective effect of noninherited maternal HLA-DR antigens on rheumatoid arthritis development. Proceedings of the National Academy of Sciences of the United States of America, 2007, Dec-11, Volume: 104, Issue:50 Topics: Alanine; Alleles; Arginine; Arthritis, Rheumatoid; Aspartic Acid; Child; Cohort Studies; Epitopes; Fathers; Female; Genetic Predisposition to Disease; Glutamic Acid; HLA-DR Antigens; HLA-DRB1 Chains; Humans; Male; Mothers; Pregnancy; Prospective Studies	2007
Association between Alzheimer's disease and the NOS3 gene Glu298Asp polymorphism in Chinese. Journal of molecular neuroscience : MN, 2008, Volume: 34, Issue:2 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Apolipoprotein E4; Asian People; Aspartic Acid; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Nitric Oxide Synthase Type III; Polymorphism, Genetic	2008
A novel polymorphism, E254K, in the 5-lipoxygenase gene associated with bronchial asthma. International journal of molecular medicine, 2008, Volume: 21, Issue:2 Topics: Arachidonate 5-Lipoxygenase; Asthma; Base Sequence; Child; DNA Mutational Analysis; Female; Gene Expression Regulation, Enzymologic; Gene Frequency; Genetic Predisposition to Disease; Glutamic Acid; Humans; Ionomycin; Leukotriene B4; Leukotriene E4; Lysine; Male; Models, Molecular; Molecular Sequence Data; Neutrophils; Polymorphism, Genetic; RNA, Messenger; Structural Homology, Protein	2008
Elevated 3T proton MRS glutamate levels associated with poor Continuous Performance Test (CPT-0X) scores and genetic risk for schizophrenia. Schizophrenia research, 2008, Volume: 99, Issue:1-3 Topics: Adult; Attention; Cognition Disorders; Creatine; Discrimination, Psychological; Female; Frontal Lobe; Genetic Predisposition to Disease; Glutamic Acid; Humans; Inhibition, Psychological; Magnetic Resonance Spectroscopy; Male; Middle Aged; Neuropsychological Tests; Pattern Recognition, Visual; Psychomotor Performance; Reaction Time; Risk; Schizophrenia; Schizophrenic Psychology; Schizotypal Personality Disorder; Siblings	2008
Associations of FcepsilonRIbeta E237G polymorphism with wheezing in Taiwanese schoolchildren. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, 2008, Volume: 38, Issue:3 Topics: Air Pollution; Alleles; Case-Control Studies; Child; Environmental Exposure; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glycine; Humans; Male; Ozone; Polymorphism, Genetic; Receptors, IgE; Respiratory Sounds; Risk Assessment; Schools; Taiwan	2008
Differential susceptibilities to chronic beryllium disease contributed by different Glu69 HLA-DPB1 and -DPA1 alleles. Journal of immunology (Baltimore, Md. : 1950), 1999, Aug-01, Volume: 163, Issue:3 Topics: Alleles; Berylliosis; Chronic Disease; Dimerization; Gene Frequency; Genetic Carrier Screening; Genetic Predisposition to Disease; Glutamic Acid; HLA-DP alpha-Chains; HLA-DP Antigens; HLA-DP beta-Chains; Homozygote; Humans	1999
Identification of a polymorphic glutamic acid stretch in the alpha2B-adrenergic receptor and lack of linkage with essential hypertension. American journal of hypertension, 1999, Volume: 12, Issue:9 Pt 1 Topics: Alleles; Blood Pressure; DNA; DNA Primers; Gene Frequency; Genetic Linkage; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Hypertension; Mutation; Polymorphism, Genetic; Receptors, Adrenergic, alpha-2; Sympathetic Nervous System	1999
Risk estimation and value-of-information analysis for three proposed genetic screening programs for chronic beryllium disease prevention. Risk analysis : an official publication of the Society for Risk Analysis, 2000, Volume: 20, Issue:1 Topics: Berylliosis; Chronic Disease; Cohort Studies; Cost of Illness; Environmental Exposure; Ethics, Medical; Forecasting; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Glutamic Acid; Health Expenditures; HLA-DP Antigens; Humans; Jurisprudence; Lysine; Occupational Exposure; Polymorphism, Genetic; Prevalence; Probability; Risk Assessment; Risk Management; Sensitivity and Specificity; Social Values	2000
A novel mutation E179K of the MEN1 gene predisposes for multiple endocrine neoplasia-type 1 (MEN1). Human mutation, 2000, Volume: 16, Issue:6 Topics: Adenoma; Adolescent; Adult; Amino Acid Substitution; Diabetes Mellitus, Type 2; Genetic Predisposition to Disease; Glutamic Acid; Humans; Hyperinsulinism; Hyperparathyroidism; Insulinoma; Lysine; Male; Multiple Endocrine Neoplasia Type 1; Mutation, Missense; Nuclear Family; Pancreatic Neoplasms	2000
HLA-DP allele-specific T cell responses to beryllium account for DP-associated susceptibility to chronic beryllium disease. Journal of immunology (Baltimore, Md. : 1950), 2001, Mar-01, Volume: 166, Issue:5 Topics: Alleles; Amino Acid Substitution; Animals; Berylliosis; Beryllium; Cell Culture Techniques; Cell Line, Transformed; Chronic Disease; Clone Cells; Cytokines; Epitopes, T-Lymphocyte; Gene Rearrangement, alpha-Chain T-Cell Antigen Receptor; Gene Rearrangement, beta-Chain T-Cell Antigen Receptor; Genetic Predisposition to Disease; Glutamic Acid; HLA-DP Antigens; Humans; Male; Mice; T-Lymphocyte Subsets; Th1 Cells; Transfection	2001
Overexpression of gamma-aminobutyric acid transporter subtype I leads to susceptibility to kainic acid-induced seizure in transgenic mice. Cell research, 2001, Volume: 11, Issue:1 Topics: Action Potentials; Amino Acid Transport System X-AG; Animals; ATP-Binding Cassette Transporters; Brain; Carrier Proteins; Electroencephalography; Excitatory Amino Acid Agonists; GABA Plasma Membrane Transport Proteins; gamma-Aminobutyric Acid; Gene Expression Regulation; Genetic Predisposition to Disease; Glutamic Acid; Kainic Acid; Membrane Proteins; Membrane Transport Proteins; Mice; Mice, Transgenic; Neural Inhibition; Neurons; Organic Anion Transporters; Receptors, GABA-A; Seizures; Synaptosomes; Up-Regulation	2001
Beryllium binding to HLA-DP molecule carrying the marker of susceptibility to berylliosis glutamate beta 69. Human immunology, 2001, Volume: 62, Issue:7 Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Berylliosis; Beryllium; Biomarkers; Cell Line; Drosophila melanogaster; Genetic Predisposition to Disease; Genetic Vectors; Glutamic Acid; HLA-DP Antigens; Humans; Lysine; Molecular Sequence Data; Mutagenesis, Site-Directed; Protein Binding; Solubility	2001
Neuronal survival after CNS insult is determined by a genetically encoded autoimmune response. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2001, Jul-01, Volume: 21, Issue:13 Topics: Animals; Autoimmunity; Cell Count; Cell Survival; Central Nervous System; Disease Models, Animal; Drug Administration Routes; Encephalomyelitis, Autoimmune, Experimental; Female; Genetic Predisposition to Disease; Glutamic Acid; Immunity, Cellular; Injections; Male; Mice; Mice, Inbred Strains; Mice, Nude; Nerve Crush; Neurons; Optic Nerve Injuries; Rats; Rats, Inbred F344; Rats, Inbred Lew; Rats, Sprague-Dawley; Retinal Ganglion Cells; Species Specificity; Spinal Cord Injuries; T-Lymphocytes; Wounds, Nonpenetrating	2001
Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2001, Volume: 22, Issue:1 Topics: alpha-Synuclein; Apolipoproteins E; Blood Platelets; Brain; Cell Death; Energy Metabolism; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Humans; Mitochondria; Nerve Tissue Proteins; Oxidative Stress; Parkinson Disease; Polymorphism, Genetic; Risk Factors; Synucleins	2001
Increased post-traumatic survival of neurons in IL-6-knockout mice on a background of EAE susceptibility. Journal of neuroimmunology, 2001, Sep-03, Volume: 119, Issue:1 Topics: Animals; Cell Survival; Drug Resistance; Encephalomyelitis, Autoimmune, Experimental; Female; Genetic Predisposition to Disease; Glutamic Acid; Interleukin-6; Macrophages; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Nerve Crush; Nerve Degeneration; Neurons; Optic Nerve Injuries; Retinal Ganglion Cells	2001
Association of beta2-adrenoceptor Gln27Glu variant with body weight but not hypertension. American journal of hypertension, 2001, Volume: 14, Issue:12 Topics: Body Weight; Case-Control Studies; Chromosomes, Human, Pair 5; Cohort Studies; Genetic Markers; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Glutamine; Humans; Hypertension; Obesity; Receptors, Adrenergic, beta-2; Risk Factors	2001
Association between anorexia nervosa and the hsKCa3 gene: a family-based and case control study. Molecular psychiatry, 2002, Volume: 7, Issue:1 Topics: Adolescent; Alleles; Anorexia Nervosa; Case-Control Studies; Europe; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Haplotypes; Humans; Israel; Jews; Male; Nerve Tissue Proteins; Neurotransmitter Agents; Potassium Channels; Potassium Channels, Calcium-Activated; Risk; Signal Transduction; Small-Conductance Calcium-Activated Potassium Channels; Synaptic Transmission; Trinucleotide Repeats	2002
Genetic and environmental risk factors in beryllium sensitization and chronic beryllium disease. Chest, 2002, Volume: 121, Issue:3 Suppl Topics: Berylliosis; Beryllium; Case-Control Studies; Chronic Disease; Genetic Markers; Genetic Predisposition to Disease; Glutamic Acid; HLA-DP Antigens; HLA-DP beta-Chains; Humans; Logistic Models; Occupational Exposure; Respiratory Hypersensitivity; Risk Factors; Smoking	2002
Human genome search in celiac disease: mutated gliadin T-cell-like epitope in two human proteins promotes T-cell activation. Journal of molecular biology, 2002, Jun-07, Volume: 319, Issue:3 Topics: Amino Acid Sequence; Celiac Disease; Computational Biology; Databases as Topic; Epitopes, T-Lymphocyte; Genetic Predisposition to Disease; Genome, Human; Gliadin; Glutamic Acid; HLA-DQ Antigens; Humans; Lymphocyte Activation; Models, Molecular; Molecular Sequence Data; Mutation; Peptide Fragments; Phenylalanine; Protein Conformation; Sequence Homology; T-Lymphocytes; Transcription Factor TFIIA; Transcription Factors	2002