Compounds > threonine

threonine and Genetic Predisposition

threonine has been researched along with Genetic Predisposition in 119 studies

Research

Studies (119)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (0.84)18.2507
2000's70 (58.82)29.6817
2010's46 (38.66)24.3611
2020's2 (1.68)2.80

Authors

AuthorsStudies
Bai, Y; Cao, L; Chen, W; Fan, W; Ge, H; Hu, X; Li, B; Li, Y; Li, Z; Liu, H; Luo, S; Mao, Y; Qin, Q; Sun, L; Wang, D; Wang, Y; Yong, L; Yu, Y; Zhang, C; Zhang, R; Zhen, Q1
Mi, YY; Song, NH; Wang, ZJ; Yuan, W; Zhang, LF; Zhang, W; Zhu, LJ; Zuo, L1
Chen, Y; Ge, X; Huang, X; Jiang, M; Li, M; Liu, L; Liu, Y; Lu, M; Song, M; Wang, F; Wang, Y; Yang, D; Yin, J; Zhang, J; Zhang, R1
Bilgiç, B; Bonifati, V; Breedveld, GJ; Diler, Y; Doğan, T; Doğu, O; Elibol, B; Emre, M; Graafland, J; Gultekin, M; Hanagasi, HA; Kaleagasi, H; Kuipers, D; Olgiati, S; Quadri, M; Saka, E; Sünter, G; Sürmeli, R; Tufekcioglu, Z; Yalçın, AD1
Gagnon, F; Kassam, I; Medina-Rivera, A; Morange, PE; Trégouët, DA; Wilson, MD; Zwingerman, N1
Massoud, A; Mohammadzadeh, M; Najafi, S; Rezaei, N; Zare Bidoki, A1
Aida, I; Aouichat-Bouguerra, S; Belhocine, K; Boussafsaf, MA; Bousseloub, A; Chaib, S; Debzi, N; Gamar, L; Kadiri, H; Kecili, L; Meddour, Y; Smara, M1
An, SSA; Bagyinszky, E; Jeong, JH; Kim, S; Koh, SB; Lee, HM; Van Giau, V1
Kumar, P; Rai, V1
Dashti, S; Ghafouri-Fard, S; Keshtkar, A; Taherian-Esfahani, Z1
Baum, L; Chan, AY; Hui, KF; Kuo, SH; Kwan, JY; Lau, CY; Mizuno, Y; Mok, VC; Ng, PW; Tang, NL1
Cao, Y; Du, J; Fu, L; Huang, X; Wang, L; Xu, J; Zhang, A; Zhang, Z; Zheng, Q1
Hua-Lei, L; Jing, C; Li, Z; Qian-Wei, X; Weng-Guang, L; You, W; Yu-Ping, Z1
Gu, L; Liang, B; Qin, L; Su, L; Tan, J; Wei, H; Wu, G; Yan, Y1
Frolov, SA; Karpukhin, AV; Kashnikov, VN; Liubchenko, LN; Muzaffarova, TA; Pospekhova, NI; Shelygin, IuA; Shubin, VP; Tsukanov, AC1
Huang, S; Mao, S1
Díaz, CA; Monroy, VS; Peralta, JM; Soto, SM; Trenado, LM1
Alcais, A; Beldjord, C; Bouazza, N; Carel, JC; Chabadel, O; Chaussain, C; Courson, F; Davit-Béal, T; Droz, D; Gasse, B; Hennequin, M; Laboux, O; Laffont, AG; Moulis, E; Opsahl Vital, S; Sire, JY; Tassery, H; Treluyer, JM; Vaysse, F1
Cao, D; Liu, Z; Ma, F; Ouyang, S; Wu, J1
Asano, H; Furukawa, M; Hagiwara, K; Hashida, S; Miyoshi, S; Shien, K; Soh, J; Tanaka, T; Toyooka, S; Tsukuda, K; Yamamoto, H1
Bosi, P; Corrent, E; Gherpelli, Y; Mazzoni, M; Messori, S; Priori, D; Simongiovanni, A; Trevisi, P1
Hu, AM; Liu, HL; Sun, QQ; Wang, Q; Yin, YW1
Han, H; Liu, C; Liu, Z; Wang, X; Xu, Y; Yang, X; Zhang, J1
Lu, W; Wu, G; Zhang, B1
Gastecki, ML; Jurrissen, TJ; Padilla, J; Rector, RS; Sheldon, RD; Vieira-Potter, VJ; Woodford, ML; Zidon, TM1
Oner, DA; Tastan, H1
Chakravarty, K; Kathuria, P; Kumar, A; Kumar, P; Misra, S; Pandit, AK; Prasad, K; Sagar, R; Yadav, AK1
Jin, AL; Xie, XR; Yang, YM1
Agúndez, JA; Alonso-Navarro, H; Benito-León, J; García-Martín, E; Jiménez-Jiménez, FJ; Ledesma, MC; López-Alburquerque, T; Martínez, C; Puertas, I; Rubio, L1
Aulchenko, YS; Claes, S; Hofman, A; Janssens, AC; López-León, S; Oostra, BA; Snijders, PJ; Tiemeier, H; van Duijn, CM1
Alcina, A; Arnal, C; Delgado, C; Fedetz, M; Fernández, O; Guerrero, M; Leyva, L; Matesanz, F; Ndagire, D1
Chen, GS; Chen, ML; Lim, HQ; Lin, CH; Tan, EK; Tan, LC; Wu, RM1
Auff, E; Balzar, J; Brücke, T; Daniel, G; Edris, S; El Tawil, S; Foki, T; Gasser, T; Haubenberger, D; Katzenschlager, R; Lichtner, P; Pirker, W; Reinthaler, E; Schulte, C; Zimprich, A1
Ozturk, A; Vieira, AR1
Becker-Rose, P; Clausmeyer, S; Clemens, PC; Engelbach, M; Hesse, V; Kreuzer, M; Raue, F; Schulze, E; Spital, H1
Al-Mesfer, S; Aldahmesh, MA; Alkuraya, FS; Ghadhfan, FE; Khan, AO1
Abelli, M; Cardini, A; Cassano, GB; Costa, B; Gabelloni, P; Galderisi, S; Gesi, C; Landi, S; Lari, L; Lucacchini, A; Martini, C; Mucci, A; Muti, M; Pini, S1
Babenko, A; Bogdanova, M; Grineva, E; Kostareva, A; Larionova, V; Popcova, D; Vahrameeva, N1
Boeing, H; Döring, F; Fisher, E; Grallert, H; Illig, T; Klapper, M; Pfäfflin, A; Schrezenmeir, J1
Farrer, MJ; Keeling, BH; Rajput, A; Ross, OA; Soto-Ortolaza, AI; Uitti, RJ; Vilariño-Güell, C; Wszolek, ZK1
Christopoulos, TK; Iliadi, A; Ioannou, PC; Kanavakis, E; Makrythanasis, P; Rapti, A; Traeger-Synodinos, J; Tsipi, M; Tzetis, M1
España-Serrano, L; Hoenicka, J; Huertas, E; Jiménez-Arriero, MA; Koeneke, MA; Palomo, T; Poch, C; Ponce, G1
Bobińska, K; Florkowski, A; Gałecki, P; Pietras, T; Smigielski, J; Szemraj, J1
Banerjee, S; Das, JK; Ghosh, P; Giri, AK; Kundu, M; Mitra, S; Sau, TJ; States, JC1
Ballesteros, M; Conde, R; Cordero, M; de Luis, DA; Gonzalez Sagrado, M; Iglesias, P; Izaola, O; Lopez Guzman, A; Maldonado, A; Muñoz, C; Penacho, MA; Puigdevall, V; Romero, E; Ruiz, E; San Martin, L1
Abramzon, Y; Arepalli, S; Borghero, G; Brunetti, M; Calvo, A; Cannas, A; Chiò, A; Chong, S; Cossu, P; Floris, G; Hernandez, DG; Johnson, JO; Marrosu, MG; Moglia, C; Murru, MR; Mutani, R; Nalls, MA; Ossola, I; Parish, LD; Pugliatti, M; Restagno, G; Ticca, A; Traynor, BJ1
Bertelsen, S; Chiang, HH; Cruchaga, C; Goate, A; Graff, C; Hinrichs, AL; Mayo, K; Morris, JC; Norton, JB; Spiegel, N; Wang, J1
Alessi, MC; Amouyel, P; Antoni, G; Bertrand, M; Cohen, W; Dupuy, AM; Emmerich, J; Germain, M; Lambert, JC; Lathrop, M; Letenneur, L; Lopez, LM; Morange, PE; Oudot-Mellakh, T; Saut, N; Trégouët, DA1
Cao, A; Carta, D; Coiana, A; Faa', V; Puddu, R; Rosatelli, MC1
Asproudis, I; Bagli, E; Georgiou, I; Giannopoulos, S; Kostoulas, C; Kyritsis, AP; Markoula, S; Nikas, A1
Bonifati, V; Cossu, G; Melis, M; Murgia, D; Oostra, BA; Quadri, M; Saddi, V; Simons, EJ; Ticca, A1
Bwala, G; Hagenah, J; Hung, AY; Klein, C; Krainc, D; Mazzulli, J; Palada, V; Peterlin, B; Terzić, J1
Bayraktar, R; Cengiz, B; Cetin, GY; Demiryurek, AT; Donmez, S; Gogebakan, B; Kisacik, B; Koca, SS; Onat, AM; Ozgen, M; Oztuzcu, S; Pehlivan, Y; Sayarlioglu, M1
Bhowmik, AD; Chaudhuri, K; Mukherjee, S; Mukhopadhyay, K; Ray, JG; Roychoudhury, P1
Alavantić, D; Dinčić, E; Djurić, T; Stančić, O; Stanković, A; Stojković, L; Veljković, N; Zivković, M1
Haataja, R; Hallman, M; Huusko, JM; Karjalainen, MK; Luukkonen, A; Tuohimaa, A1
Berciano, J; Infante, J; Pelayo-Negro, AL; Rodríguez-Oroz, MC; Sánchez-Quintana, C; Tola-Arribas, MA; Volpini, V; Zeviani, M1
Cavalli, IJ; de Oliveira, BV; de Souza Fonseca Ribeiro, EM; de Syllos Cólus, IM; Dos Reis, MB; Losi-Guembarovski, R; Mizuno, LT; Morita, MC; Ramos, GH; Rogatto, SR1
Alp, E; Arli, B; Irkec, C; Menevse, S; Yilmaz, A1
Abicht, A; Bindoff, LA; Chinnery, PF; Czermin, B; de Coo, IF; De Vries, M; Dimauro, S; Gorman, GG; Hirano, M; Holinski-Feder, E; Horvath, R; Hudson, G; Jardel, C; Keiling, BC; Klopstock, T; Lochmüller, H; Lombès, A; Neeve, VC; Saft, C; Samuels, DC; Smeets, H; Smeitink, J; Smits, BW; Taylor, RW; Turnbull, DM; van den Bosch, B; Van Goethem, G1
Artigao, M; Carrión, L; Divisón, JA; Escribano, J; Fernández, JA; Martínez, E; Massó, J; Puras, A; Sanchis, C1
Gaertner, I; Koehnke, AM; Koehnke, MD; Kolb, W; Lutz, U; Schick, S; Willecke, M1
Akahoshi, M; Harada, M; Inoue, Y; Miyake, K; Nakashima, H; Okada, K; Otsuka, T; Shimizu, S; Tanaka, Y1
Boyle, P; English, DR; Giles, GG; Hopper, JL; McCredie, MR; Morris, H; Neufing, P; Severi, G; Southey, MC; Tesoriero, A; Tilley, W1
Abyholm, FE; Drevon, CA; Jugessur, A; Lie, RT; Murray, JC; Taylor, JA; Ulvik, A; Vindenes, HA; Wilcox, AJ1
Cyganek, K; Klupa, T; Malecki, MT; Sieradzki, J1
Klupa, T; Malecki, MT; Moczulski, DK; Rogus, JJ1
Ergül, E; Güzelhan, Y; Kara, I; Kaya, G; Sazci, A1
Adler, D; Fick, G; Hughes, RM; Kanji, N; Trpkov, K1
Gilliland, DG1
Dart, A; Davies, SL; Hickson, ID; Lakin, ND; North, PS1
Macgregor, GA; Swift, PA1
Buckland, P; Chowdari, KV; Kirov, G; McCreadie, RG; Nimgaonkar, V; Norton, N; O'Donovan, MC; Owen, MJ; Preece, A; Sharkey, V; Spurlock, G; Williams, HJ; Williams, NM; Zammit, S1
Abou-Sleiman, PM; Ahmadi, KR; Barone, P; Barrone, P; Berciano, J; Bhatia, K; Burk, K; Goldstein, DB; Healy, DG; Kamm, C; Lees, AJ; Moller, JC; Ozawa, T; Quinn, N; Tolosa, E; Wood, NW; Wullner, U1
Cheng, Z; Ding, J; Jiang, X; Lin, R; Lu, X; Turdi, J; Wang, S; Wang, X; Wen, H; Wu, G1
Leino-Arjas, P; Luoma, K; Raininko, R; Riihimäki, H; Saarela, J; Solovieva, S1
Cha, JH; Choi, MJ; Ham, BJ; Han, CS; Lee, HJ; Lee, MS; Lee, SH; Ryu, SH1
Deng, G; He, F; Li, S; Li, X; Li, Y; Qiang, B; Shen, Y; Wang, Y; Yao, Z; Zhai, Y; Zhang, R; Zhou, G1
Cooper, TG; Gromoll, J; Kostova, E; Luetjens, CM; Nieschlag, E; Tschanter, P1
Abe, H; Asaoka, R; Fujimaki, T; Fukuchi, T; Funayama, T; Hotta, Y; Ideta, H; Ishikawa, K; Iwata, T; Kanamoto, T; Kimura, I; Kudoh, J; Kurosaka, D; Mashima, Y; Mishima, H; Murakami, A; Nakamoto, K; Ohtake, Y; Shimada, N; Shimizu, N; Suzuki, K; Tanihara, H; Tanino, T; Yasuda, N1
Liu, P; Loh, M; Mondry, A; Nagel, M; Zhu, AL1
Beck, SR; Bowden, DW; Burdon, KP; Freedman, BI; Langefeld, CD; Liu, Y; Rich, SS; Wagenknecht, LE1
Kondo, H; Shimomura, I1
Hirose, H; Ishii, T1
Kaji, R; Kawakami, H; Kuno, S; Nishimura, M1
Abrahamsson, PA; Ahlgren, G; Gadaleanu, V; Giwercman, A; Giwercman, YL1
Honda, H; Honda, Z; Kono, H; Kyogoku, C; Suzuki, T; Tokunaga, K; Tsuchiya, N; Yamamoto, K1
Elikowski, W; Kwaśnikowski, P; Lewandowski, K; Rzeźniczak, M; Swierczyńska, A1
Cremonini, F; Saito, YA; Talley, NJ1
Laine, ML; Morré, SA; Murillo, LS; Peña, AS; van Winkelhoff, AJ1
Bell, DW; Brannigan, BW; Godin-Heymann, N; Gore, I; Haber, DA; Mohapatra, G; Mulloy, R; Okimoto, RA; Settleman, J; Sharma, SV; Sordella, R1
Dávid, M; Habon, T; Keszthelyi, Z; Kovács, N; Losonczy, H; Nagy, A; Tóth, O1
Alpert, B; Beckers, S; Eskan, MA; Kinane, DF; Knudsen, TB; Lappin, DF; Shiba, H; Singh, A; Stathopoulou, PG; Waigel, S; Zhao, H1
Buyan, N; Gönen, S; Hasanoğlu, E; Kalman, S; Misirlioğlu, M; Ozkaya, O; Söylemezoğlu, O; Tuncer, S1
Rodacker, V; Toustrup-Jensen, M; Vilsen, B1
Beutler, B; Dahiyat, BI; Du, X; Hoebe, K; Mann, N; Rutschmann, S; Steed, P; Zalevsky, J1
Jia, W; Li, M; Liu, L; Lu, H; Xiang, K; Zheng, T1
Lee, P; Medina, L; Ringman, JM1
Eberly, SW; Goldenberg, I; McNitt, S; Moss, AJ; Ryan, D; Zareba, W1
Backer, V; Baynam, G; Britton, J; Creegan, R; de Klerk, N; Di Prisco, MC; Goldblatt, J; Hagel, I; Hall, I; Khoo, SK; Le Souëf, PN; Lynch, N; Musk, AW; Nepper-Christensen, S; Porsbjerg, C; Rossi, GA; Zhang, G1
Akagawa, H; Hori, T; Inoue, I; Kasuya, H; Krischek, B; Narita, A; Tajima, A1
Carvalho, MA; Edelman, L; Friedman, E; Kaufman, B; Laitman, Y; Menachem, TD; Monteiro, AN; Zidan, J1
Boyle, P; Brown, HN; Guss, C; Han, X; Hoffman, A; Leaderer, D; Qin, Q; Stevens, RG; Zhang, Y; Zheng, T; Zhu, Y1
Houlston, RS; Hubner, RA1
Darwish Murad, S; de Bruijne, EL; de Maat, MP; Haagsma, EB; Janssen, HL; Leebeek, FW; Rosendaal, FR; Tanck, MW; van Hoek, B1
Bugert, P; Pabinger, I; Panzer, S; Skeate, RC; Stamer, K; Vormittag, R; Wahi, MM1
Bullard, JE; Nogee, LM1
Awomoyi, AA; Blanco, JC; Boukhvalova, MS; Hemming, VG; Lorenz, E; Pollin, TI; Rallabhandi, P; Sztein, MB; Vogel, SN1
Altshuler, D; Bell, DW; Daly, MB; Freedman, ML; Garber, JE; Godwin, AK; Haber, DA; Haiman, CA; Harris, PL; Haserlat, SM; Henderson, BE; Kim, SH; Le Marchand, L; Niendorf, KB; Olopade, OI; Schiripo, TA; Sgroi, DC; Smith, MR; Wahrer, DC1
Jiang, G; Song, S; Wang, L; Xu, L; Zhu, C1
Algar, U; Blokhuis, MM; Goldberg, PA; Govender, D; Pietersen, GE; Ramesar, RS; Vorster, AA1
Benndorf, K; Figulla, HR; Hensellek, S; Prochnau, D; Surber, R; Werner, GS; Zimmer, T1
Bermejo, JL; Gurzau, E; Hemminki, K; Koppova, K; Kumar, R; Rudnai, P; Scherer, D1
Acheampong, J; Adeyemo, A; Agyenim-Boateng, K; Akafo, S; Akinsola, FB; Amoah, A; Chen, G; Chen, Y; Doumatey, A; Eghan, BA; Ezepue, F; Fasanmade, O; Huang, H; Johnson, T; Lashley, K; Okafor, G; Oli, J; Rotimi, CN; Zhou, J1
Bras, J; Calado, A; Dias, M; Guerreiro, R; Hardy, J; Januario, C; Morgadinho, A; Oliveira, C; Ribeiro, M; Semedo, C; Singleton, A1
Franz, P; Frey, UH; Grehl, S; Jahnke, K; Lang, S; Lehnerdt, GF; Schmid, KW; Schmitz, KJ; Siffert, W; Zaqoul, A1
Cuajungco, MP; Samie, MA1
Albu, J; Allison, DB; Burn, P; Chin, W; Deng, N; Duprat, L; Fisher, SL; Franco, LS; Gu, W; Heymsfield, S; Kissebah, A; Kleyn, PW; Lee, J; Maruti, S; Nathan, J; Pi-Sunyer, FX; Tu, Z; Yagaloff, KA1
Amemiya, S; Aya, M; Ishihara, T; Kasuga, A; Kato, K; Kobayashi, K; Mochizuki, M; Nakazawa, S1

Reviews

18 review(s) available for threonine and Genetic Predisposition

ArticleYear
Sex-specific effect of CPB2 Ala147Thr but not Thr325Ile variants on the risk of venous thrombosis: A comprehensive meta-analysis.
    PloS one, 2017, Volume: 12, Issue:5

    Topics: Alanine; Carboxypeptidase B2; Female; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Risk Factors; Sex Factors; Threonine; Venous Thrombosis

2017
Methylenetetrahydrofolate reductase C677T polymorphism and susceptibility to epilepsy.
    Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2018, Volume: 39, Issue:12

    Topics: Cysteine; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Male; Methylenetetrahydrofolate Reductase (NADPH2); Odds Ratio; Polymorphism, Single Nucleotide; Risk Factors; Threonine

2018
Associations between XRCC3 Thr241Met polymorphisms and breast cancer risk: systematic-review and meta-analysis of 55 case-control studies.
    BMC medical genetics, 2019, 05-10, Volume: 20, Issue:1

    Topics: Breast Neoplasms; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Homologous Recombination; Humans; Methionine; Polymorphism, Single Nucleotide; Threonine

2019
MTHFR C677T and A1298C polymorphisms were associated with bladder cancer risk and disease progression: a meta-analysis.
    DNA and cell biology, 2013, Volume: 32, Issue:5

    Topics: Alanine; Amino Acid Substitution; Carcinoma; Case-Control Studies; Cysteine; Disease Progression; Genetic Predisposition to Disease; Humans; Methylenetetrahydrofolate Reductase (NADPH2); Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Urinary Bladder Neoplasms

2013
AGT M235T polymorphisms and ischemic stroke risk: a meta-analysis.
    Journal of the neurological sciences, 2013, Aug-15, Volume: 331, Issue:1-2

    Topics: Angiotensinogen; Asian People; Databases, Factual; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Ischemia; Methionine; Stroke; Threonine; White People

2013
Association of angiotensinogen gene M235T polymorphism with the risk of IgA nephropathy: a meta-analysis.
    Renal failure, 2014, Volume: 36, Issue:3

    Topics: Alleles; Angiotensinogen; Asian People; Genetic Association Studies; Genetic Predisposition to Disease; Glomerulonephritis, IGA; Humans; Methionine; Polymorphism, Genetic; Risk Factors; Threonine; White People

2014
Association of the ADIPOQ T45G polymorphism with insulin resistance and blood glucose: a meta-analysis.
    Endocrine journal, 2014, Volume: 61, Issue:5

    Topics: Adiponectin; Amino Acid Substitution; Blood Glucose; Case-Control Studies; Cross-Sectional Studies; Diabetes Mellitus, Type 2; Genetic Association Studies; Genetic Predisposition to Disease; Glycine; Humans; Insulin Resistance; Polymorphism, Single Nucleotide; Threonine

2014
Toll-like receptor 4 gene Asp299Gly and Thr399Ile polymorphisms in type 2 diabetes mellitus: a meta-analysis of 15,059 subjects.
    Diabetes research and clinical practice, 2015, Volume: 107, Issue:3

    Topics: Amino Acid Substitution; Aspartic Acid; Case-Control Studies; Diabetes Mellitus, Type 2; Genetic Predisposition to Disease; Glycine; Humans; Isoleucine; Models, Genetic; Observational Studies as Topic; Polymorphism, Single Nucleotide; Threonine; Toll-Like Receptor 4

2015
Association Between X-Ray Cross-complementing Group 3 (XRCC3) Thr241Met Polymorphism and Risk of Thyroid Cancer: A Meta-Analysis.
    Medical science monitor : international medical journal of experimental and clinical research, 2015, Dec-21, Volume: 21

    Topics: Amplified Fragment Length Polymorphism Analysis; DNA-Binding Proteins; Genetic Predisposition to Disease; Humans; Methionine; Threonine; Thyroid Neoplasms

2015
TLR4 as a risk factor for periodontal disease: a reappraisal.
    Journal of clinical periodontology, 2009, Volume: 36, Issue:4

    Topics: Aggressive Periodontitis; Alleles; Aspartic Acid; Chronic Periodontitis; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Glycine; Humans; Isoleucine; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Toll-Like Receptor 4

2009
ELAC2/HPC2 polymorphisms, prostate-specific antigen levels, and prostate cancer.
    Journal of the National Cancer Institute, 2003, Jun-04, Volume: 95, Issue:11

    Topics: Aged; Alanine; Case-Control Studies; Genetic Predisposition to Disease; Heterozygote; Homozygote; Humans; Leucine; Linear Models; Logistic Models; Male; Middle Aged; Neoplasm Proteins; Odds Ratio; Polymorphism, Genetic; Prostate-Specific Antigen; Prostatic Neoplasms; Research Design; Risk Assessment; Risk Factors; Serine; Threonine

2003
Genetic variation in the epithelial sodium channel: a risk factor for hypertension in people of African origin.
    Advances in renal replacement therapy, 2004, Volume: 11, Issue:1

    Topics: Amiloride; Black People; Diuretics; Epithelial Sodium Channels; Genetic Predisposition to Disease; Humans; Hypertension; London; Methionine; Polymorphism, Genetic; Risk Factors; Sodium Channels; Threonine

2004
Polymorphisms of the insertion / deletion ACE and M235T AGT genes and hypertension: surprising new findings and meta-analysis of data.
    BMC nephrology, 2005, Jan-11, Volume: 6

    Topics: Adult; Aged; Angiotensinogen; Cross-Sectional Studies; DNA Transposable Elements; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Hypertension; Male; Methionine; Middle Aged; Peptidyl-Dipeptidase A; Polymorphism, Genetic; Severity of Illness Index; Threonine

2005
[I164T polymorphism of adiponectin gene in diabetes].
    Nihon rinsho. Japanese journal of clinical medicine, 2005, Volume: 63 Suppl 2

    Topics: Adiponectin; Amino Acid Substitution; Animals; Diabetes Mellitus; Genetic Predisposition to Disease; Humans; Insulin Resistance; Intercellular Signaling Peptides and Proteins; Isoleucine; Mutation, Missense; Threonine

2005
[Fatty acid binding protein-2 (FABP2) gene polymorphism in diabetes].
    Nihon rinsho. Japanese journal of clinical medicine, 2005, Volume: 63 Suppl 2

    Topics: Adipocytes; Alanine; Amino Acid Substitution; Carrier Proteins; Diabetes Mellitus; Fatty Acid-Binding Proteins; Fatty Acids, Nonesterified; Genetic Predisposition to Disease; Glucose Intolerance; Humans; Insulin Resistance; Lipid Peroxidation; Polymorphism, Genetic; Racial Groups; Threonine

2005
[Type I antithrombin deficiency as a cause of arterial and venous thrombosis in a family with severe thrombophilia].
    Orvosi hetilap, 2005, Oct-09, Volume: 146, Issue:41

    Topics: Adult; C-Reactive Protein; Cholesterol; Cysteine; Female; Fibrin; Genetic Predisposition to Disease; Homocysteine; Humans; Male; Pedigree; Plasminogen Activator Inhibitor 1; Polymorphism, Genetic; Risk Factors; Threonine; Thrombophilia; Thrombosis; Venous Thrombosis; von Willebrand Factor

2005
MTHFR C677T and colorectal cancer risk: A meta-analysis of 25 populations.
    International journal of cancer, 2007, Mar-01, Volume: 120, Issue:5

    Topics: Adult; Aged; Aged, 80 and over; Colorectal Neoplasms; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Incidence; Male; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Polymorphism, Genetic; Risk; Threonine

2007
The varitint-waddler mouse phenotypes and the TRPML3 ion channel mutation: cause and consequence.
    Pflugers Archiv : European journal of physiology, 2008, Volume: 457, Issue:2

    Topics: Alanine; Animals; Calcium; Genetic Predisposition to Disease; Genotype; Hair Color; Hearing; Hearing Disorders; Isoleucine; Membrane Potentials; Mice; Mice, Mutant Strains; Models, Molecular; Mutation; Phenotype; Proline; Protein Conformation; Protein Structure, Tertiary; Skin Pigmentation; Threonine; Transient Receptor Potential Channels; TRPM Cation Channels

2008

Other Studies

101 other study(ies) available for threonine and Genetic Predisposition

ArticleYear
Imputation of the major histocompatibility complex region identifies major independent variants associated with bullous pemphigoid and dermatomyositis in Han Chinese.
    The Journal of dermatology, 2022, Volume: 49, Issue:10

    Topics: Alleles; Amino Acids; Asian People; China; Dermatomyositis; DNA Copy Number Variations; Genetic Predisposition to Disease; HLA-B Antigens; Humans; Major Histocompatibility Complex; Pemphigoid, Bullous; Polymorphism, Single Nucleotide; Threonine

2022
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
Identification of Ala2Thr mutation in insulin gene from a Chinese MODY10 family.
    Molecular and cellular biochemistry, 2020, Volume: 470, Issue:1-2

    Topics: Adult; Alanine; Cell Line; China; Diabetes Mellitus, Type 2; Endoplasmic Reticulum Stress; Family Health; Female; Genetic Predisposition to Disease; Glucose; Humans; Hyperglycemia; Insulin; Male; Middle Aged; Mutation; Mutation, Missense; Pedigree; Protein Structure, Secondary; Structure-Activity Relationship; Threonine; Young Adult

2020
The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN.
    Parkinsonism & related disorders, 2017, Volume: 39

    Topics: Adolescent; Adult; Child; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Methionine; Mitochondrial Proteins; Mutation; Neurodegenerative Diseases; Threonine; Turkey; Young Adult

2017
Autosomal dominant deficiency of the interleukin-17F in recurrent aphthous stomatitis: Possible novel mutation in a new entity.
    Gene, 2018, May-15, Volume: 654

    Topics: Algorithms; Case-Control Studies; Female; Gene Frequency; Genes, Dominant; Genetic Predisposition to Disease; Genotype; Heterozygote; Humans; Inflammation; Interleukin-17; Iran; Male; Mutation, Missense; Polymerase Chain Reaction; Probability; Proline; Sequence Analysis, DNA; Software; Stomatitis, Aphthous; Threonine

2018
T300A variant of AT16L1 gene in a cohort of Algerian Crohn disease patients.
    Current research in translational medicine, 2018, Volume: 66, Issue:1

    Topics: Adolescent; Adult; Age of Onset; Alanine; Algeria; Amino Acid Substitution; Autophagy-Related Proteins; Case-Control Studies; Cohort Studies; Crohn Disease; Female; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mutation, Missense; Polymorphism, Single Nucleotide; Severity of Illness Index; Threonine; Young Adult

2018
    International journal of molecular sciences, 2018, Sep-02, Volume: 19, Issue:9

    Topics: Adult; Age of Onset; Alzheimer Disease; Amino Acid Substitution; Female; Genetic Predisposition to Disease; Humans; Hydrogen Bonding; Isoleucine; Male; Middle Aged; Models, Molecular; Pedigree; Presenilin-1; Protein Structure, Secondary; Republic of Korea; Sequence Analysis, DNA; Structural Homology, Protein; Threonine

2018
The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson's disease.
    Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2013, Volume: 20, Issue:5

    Topics: Age of Onset; Alanine; Asian People; Genetic Predisposition to Disease; Hong Kong; Humans; Middle Aged; Parkinson Disease; Proton-Translocating ATPases; Risk Factors; Threonine

2013
Association study between FSHR Ala307Thr and Ser680Asn variants and polycystic ovary syndrome (PCOS) in Northern Chinese Han women.
    Journal of assisted reproduction and genetics, 2013, Volume: 30, Issue:5

    Topics: Adult; Alanine; Amino Acid Substitution; Asian People; Asparagine; Case-Control Studies; China; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Geography; Humans; Mutation, Missense; Polycystic Ovary Syndrome; Polymorphism, Single Nucleotide; Receptors, FSH; Serine; Threonine

2013
[Molecular genetics study of hereditary predisposition to diffuse gastric cancer in Russian patients].
    Voprosy onkologii, 2013, Volume: 59, Issue:5

    Topics: Adult; Antigens, CD; Cadherins; Carcinoma, Signet Ring Cell; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Molecular Biology; Pedigree; Polymorphism, Single Nucleotide; Russia; Sequence Deletion; Stomach Neoplasms; Threonine

2013
Thr130Ile polymorphism of HNF4A gene is associated with gestational diabetes mellitus in Mexican population.
    Journal of investigative medicine : the official publication of the American Federation for Clinical Research, 2014, Volume: 62, Issue:3

    Topics: Adult; Diabetes, Gestational; Female; Genetic Predisposition to Disease; Hepatocyte Nuclear Factor 4; Humans; Infant, Newborn; Isoleucine; Mexico; Polymorphism, Genetic; Population Surveillance; Postpartum Period; Pregnancy; Threonine; Young Adult

2014
Dental caries and enamelin haplotype.
    Journal of dental research, 2014, Volume: 93, Issue:4

    Topics: Amino Acid Substitution; Arginine; Child; Dental Caries; Dental Caries Susceptibility; DMF Index; Exons; Extracellular Matrix Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Glutamine; Haplotypes; Humans; Introns; Isoleucine; Linkage Disequilibrium; Male; Mutation, Missense; Polymorphism, Single Nucleotide; Proteins; Threonine; Young Adult

2014
Presence of the minor EGFR T790M mutation is associated with drug-sensitive EGFR mutations in lung adenocarcinoma patients.
    Oncology reports, 2014, Volume: 32, Issue:1

    Topics: Adenocarcinoma; Adenocarcinoma of Lung; Adult; Aged; Aged, 80 and over; Cell Line, Tumor; Drug Resistance, Neoplasm; ErbB Receptors; Exons; Female; Genetic Predisposition to Disease; Humans; Lung Neoplasms; Male; Methionine; Middle Aged; Mutation; Sequence Deletion; Threonine

2014
Effect of added dietary threonine on growth performance, health, immunity and gastrointestinal function of weaning pigs with differing genetic susceptibility to Escherichia coli infection and challenged with E. coli K88ac.
    Journal of animal physiology and animal nutrition, 2015, Volume: 99, Issue:3

    Topics: Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Antibodies, Bacterial; Diet; Escherichia coli Infections; Gene Expression Regulation; Genetic Markers; Genetic Predisposition to Disease; Immunoglobulin A; Immunoglobulin M; Mucin-4; Swine; Swine Diseases; Threonine

2015
Association of histamine N-methyltransferase Thr105Ile polymorphism with Parkinson's disease and schizophrenia in Han Chinese: a case-control study.
    PloS one, 2015, Volume: 10, Issue:3

    Topics: Adult; Alleles; Asian People; Case-Control Studies; China; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Histamine; Histamine N-Methyltransferase; Humans; Isoleucine; Male; Parkinson Disease; Polymorphism, Genetic; Schizophrenia; Threonine

2015
Ablation of eNOS does not promote adipose tissue inflammation.
    American journal of physiology. Regulatory, integrative and comparative physiology, 2016, Apr-15, Volume: 310, Issue:8

    Topics: Adipose Tissue, Brown; Adiposity; Animals; Diet, High-Fat; Disease Models, Animal; Genetic Predisposition to Disease; Inflammation Mediators; Insulin Resistance; Intra-Abdominal Fat; Macrophages; Male; Mice, Inbred C57BL; Mice, Knockout; Mitochondrial Proteins; Nitric Oxide; Nitric Oxide Synthase Type III; Obesity; Panniculitis; Phenotype; Phosphorylation; Serine; Signal Transduction; Threonine

2016
Identification of Novel Variants in the PVRL1 Gene in Patients With Nonsyndromic Cleft Lip With or Without Cleft Palate.
    Genetic testing and molecular biomarkers, 2016, Volume: 20, Issue:5

    Topics: Amino Acid Substitution; Case-Control Studies; Cell Adhesion Molecules; Child; Child, Preschool; Cleft Lip; Cleft Palate; DNA Mutational Analysis; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Nectins; Polymorphism, Single Nucleotide; Serine; Threonine; Turkey

2016
Association between Endothelial nitric oxide synthase G894T gene polymorphism and risk of ischemic stroke in North Indian population: a case-control study.
    Neurological research, 2016, Volume: 38, Issue:7

    Topics: Adult; Aged; Brain Ischemia; Case-Control Studies; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Glycine; Humans; India; Magnetic Resonance Imaging; Male; Middle Aged; Nitric Oxide Synthase Type III; Polymorphism, Single Nucleotide; Retrospective Studies; Severity of Illness Index; Stroke; Threonine; Tomography, X-Ray Computed

2016
Genetic polymorphisms in extracellular superoxide dismutase Leu53Leu, Arg213Gly, and Ala40Thr and susceptibility to type 2 diabetes mellitus.
    Genetics and molecular research : GMR, 2016, Dec-02, Volume: 15, Issue:4

    Topics: Adult; Alanine; Arginine; Asian People; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leucine; Male; Middle Aged; Polymorphism, Single Nucleotide; Regression Analysis; Superoxide Dismutase; Threonine

2016
The nonsynonymous Thr105Ile polymorphism of the histamine N-methyltransferase is associated to the risk of developing essential tremor.
    Neuromolecular medicine, 2008, Volume: 10, Issue:4

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Brain Chemistry; Child; Child, Preschool; DNA Mutational Analysis; Essential Tremor; Female; Genetic Predisposition to Disease; Genetic Testing; Histamine N-Methyltransferase; Humans; Isoleucine; Male; Middle Aged; Polymorphism, Genetic; Threonine; Young Adult

2008
Angiotensinogen M235T polymorphism and symptoms of depression in a population-based study and a family-based study.
    Psychiatric genetics, 2008, Volume: 18, Issue:4

    Topics: Aged; Aging; Amino Acid Substitution; Angiotensinogen; Antihypertensive Agents; Depression; Family; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Threonine

2008
The T244I variant of the interleukin-7 receptor-alpha gene and multiple sclerosis.
    Tissue antigens, 2008, Volume: 72, Issue:2

    Topics: Case-Control Studies; Gene Frequency; Genetic Predisposition to Disease; Humans; Interleukin-7 Receptor alpha Subunit; Isoleucine; Multiple Sclerosis; Polymorphism, Single Nucleotide; Spain; Threonine; White People

2008
Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore.
    Neurology, 2008, Nov-18, Volume: 71, Issue:21

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alanine; Asian People; DNA Mutational Analysis; Exons; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Models, Molecular; Mutation; Parkinson Disease; Positron-Emission Tomography; Proton-Translocating ATPases; Singapore; Taiwan; Threonine; Young Adult

2008
PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease.
    Parkinsonism & related disorders, 2009, Volume: 15, Issue:7

    Topics: Aged; Asparagine; Austria; Carrier Proteins; DNA Mutational Analysis; Egypt; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Germany; Humans; Male; Middle Aged; Parkinson Disease; Polymorphism, Single Nucleotide; Serine; Threonine; White People

2009
Mutational analysis of the PHEX gene: novel point mutations and detection of large deletions by MLPA in patients with X-linked hypophosphatemic rickets.
    Calcified tissue international, 2009, Volume: 85, Issue:3

    Topics: Amino Acid Sequence; Child, Preschool; DNA Mutational Analysis; Exons; Familial Hypophosphatemic Rickets; Female; Gene Deletion; Gene Frequency; Genetic Diseases, X-Linked; Genetic Markers; Genetic Predisposition to Disease; Genotype; Humans; Infant; Male; Molecular Biology; PHEX Phosphate Regulating Neutral Endopeptidase; Point Mutation; Polymorphism, Genetic; Threonine

2009
Founder heterozygous P23T CRYGD mutation associated with cerulean (and coralliform) cataract in 2 Saudi families.
    Molecular vision, 2009, Jul-24, Volume: 15

    Topics: Amino Acid Substitution; Asian People; Base Sequence; Cataract; Child; Child, Preschool; Family; Female; Founder Effect; gamma-Crystallins; Genetic Predisposition to Disease; Haplotypes; Heterozygote; Humans; Male; Molecular Sequence Data; Mutation; Pedigree; Proline; Saudi Arabia; Threonine

2009
Ala147Thr substitution in translocator protein is associated with adult separation anxiety in patients with depression.
    Psychiatric genetics, 2009, Volume: 19, Issue:2

    Topics: Adult; Alanine; Amino Acid Substitution; Anxiety, Separation; Depression; Female; Genetic Predisposition to Disease; Humans; Male; Polymorphism, Single Nucleotide; Receptors, GABA; Threonine

2009
Type 2 deiodinase Thr92Ala polymorphism impact on clinical course and myocardial remodeling in patients with Graves' disease.
    Cell cycle (Georgetown, Tex.), 2009, Aug-15, Volume: 8, Issue:16

    Topics: Adult; Alanine; Echocardiography; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Graves Disease; Humans; Male; Polymorphism, Genetic; Threonine; Ventricular Remodeling; Young Adult

2009
Evidence for the Thr79Met polymorphism of the ileal fatty acid binding protein (FABP6) to be associated with type 2 diabetes in obese individuals.
    Molecular genetics and metabolism, 2009, Volume: 98, Issue:4

    Topics: Amino Acid Substitution; Diabetes Mellitus, Type 2; Fatty Acid-Binding Proteins; Female; Gastrointestinal Hormones; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Methionine; Middle Aged; Molecular Weight; Obesity; Polymorphism, Single Nucleotide; Protein Isoforms; Threonine

2009
Histamine N-methyltransferase Thr105Ile is not associated with Parkinson's disease or essential tremor.
    Parkinsonism & related disorders, 2010, Volume: 16, Issue:2

    Topics: Adult; Aged; Aged, 80 and over; Essential Tremor; Female; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Histamine N-Methyltransferase; Humans; Isoleucine; Male; Middle Aged; Parkinson Disease; Polymorphism, Genetic; Psychiatric Status Rating Scales; Threonine

2010
Association of TLR4 single-nucleotide polymorphisms and sarcoidosis in Greek patients.
    Genetic testing and molecular biomarkers, 2009, Volume: 13, Issue:6

    Topics: Adult; Aged; Amino Acid Substitution; Aspartic Acid; Female; Genetic Predisposition to Disease; Greece; Humans; Luminescent Measurements; Male; Middle Aged; Polymorphism, Single Nucleotide; Sarcoidosis; Threonine; Toll-Like Receptor 4

2009
The D2 dopamine receptor gene variant C957T affects human fear conditioning and aversive priming.
    Genes, brain, and behavior, 2010, Volume: 9, Issue:1

    Topics: Adult; Attention; Conditioning, Psychological; Cysteine; Electroshock; Extinction, Psychological; Face; Fear; Female; Galvanic Skin Response; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Learning; Male; Mental Disorders; Pattern Recognition, Visual; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases; Receptors, Dopamine D2; Threonine; Young Adult

2010
Analysis of two polymorphisms of the manganese superoxide dismutase gene (Ile-58Thr and Ala-9Val) in patients with recurrent depressive disorder.
    Psychiatry research, 2010, Aug-30, Volume: 179, Issue:1

    Topics: Alanine; Amino Acids; Case-Control Studies; Depression; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Isoleucine; Male; Middle Aged; Polymorphism, Genetic; Sex Factors; Superoxide Dismutase; Threonine; Valine

2010
Precancerous and non-cancer disease endpoints of chronic arsenic exposure: the level of chromosomal damage and XRCC3 T241M polymorphism.
    Mutation research, 2011, Jan-10, Volume: 706, Issue:1-2

    Topics: Adult; Alleles; Amino Acid Substitution; Arsenic; Carcinogens; Case-Control Studies; Chromosome Aberrations; Conjunctivitis; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; India; Male; Methionine; Mutagens; Odds Ratio; Peripheral Nervous System Diseases; Polymorphism, Genetic; Precancerous Conditions; Skin Diseases; Threonine; Water Pollutants, Chemical

2011
Polymorphism Ala54Thr of fatty acid-binding protein 2: Allelic frequencies and influence on cardiovascular risk factors in a multicenter study of Castilla y Leon.
    Annals of nutrition & metabolism, 2010, Volume: 57, Issue:3-4

    Topics: Adult; Alanine; Anthropometry; Body Mass Index; C-Reactive Protein; Cardiovascular Diseases; Cross-Sectional Studies; Fatty Acid-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Insulin Resistance; Male; Mutation; Obesity; Phenotype; Polymorphism, Genetic; Risk Factors; Spain; Threonine

2010
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene.
    Archives of neurology, 2011, Volume: 68, Issue:5

    Topics: Aged; Alanine; Amino Acid Substitution; Amyotrophic Lateral Sclerosis; Case-Control Studies; DNA Mutational Analysis; DNA-Binding Proteins; Female; Founder Effect; Genetic Predisposition to Disease; Genotype; Humans; Italy; Male; Middle Aged; Mutation, Missense; Phenotype; Prospective Studies; RNA-Binding Protein FUS; Superoxide Dismutase; Superoxide Dismutase-1; Threonine

2011
Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels.
    Archives of neurology, 2011, Volume: 68, Issue:5

    Topics: Age of Onset; Aged; Alzheimer Disease; Amino Acid Substitution; Female; Frontotemporal Lobar Degeneration; Gene Expression; Genetic Predisposition to Disease; Heterozygote; Humans; Intercellular Signaling Peptides and Proteins; Kaplan-Meier Estimate; Linkage Disequilibrium; Male; Membrane Proteins; Middle Aged; Mutation; Nerve Tissue Proteins; Polymorphism, Single Nucleotide; Progranulins; Proportional Hazards Models; Risk Assessment; Risk Factors; Serine; Threonine; Time Factors

2011
KNG1 Ile581Thr and susceptibility to venous thrombosis.
    Blood, 2011, Mar-31, Volume: 117, Issue:13

    Topics: Alleles; Amino Acid Substitution; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Isoleucine; Kininogens; Male; Polymorphism, Single Nucleotide; Threonine; Venous Thrombosis

2011
Preconceptional identification of cystic fibrosis carriers in the Sardinian population: A pilot screening program.
    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2011, Volume: 10, Issue:3

    Topics: Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Gene Deletion; Gene Frequency; Genetic Carrier Screening; Genetic Predisposition to Disease; Genetic Testing; Homozygote; Humans; Isoleucine; Italy; Male; Mutation; Phenylalanine; Pilot Projects; Threonine

2011
Renin-angiotensin-aldosterone system genes and nonarteritic anterior ischemic optic neuropathy.
    Molecular vision, 2011, Volume: 17

    Topics: Age Factors; Aged; Aged, 80 and over; Alanine; Alleles; Angiotensinogen; Confidence Intervals; Cysteine; DNA Transposable Elements; Female; Gene Deletion; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Odds Ratio; Optic Neuropathy, Ischemic; Peptidyl-Dipeptidase A; Polymorphism, Genetic; Receptor, Angiotensin, Type 1; Renin-Angiotensin System; Sex Factors; Threonine

2011
Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia.
    Neurogenetics, 2011, Volume: 12, Issue:3

    Topics: Aged; Alanine; Amino Acid Substitution; Case-Control Studies; Cohort Studies; DNA Mutational Analysis; DNA-Binding Proteins; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Italy; Male; Middle Aged; Mutation, Missense; Nerve Degeneration; Parkinson Disease; Threonine

2011
Histamine N-methyltransferase Thr105Ile polymorphism is associated with Parkinson's disease.
    Neurobiology of aging, 2012, Volume: 33, Issue:4

    Topics: Asian People; Case-Control Studies; Chi-Square Distribution; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Histamine N-Methyltransferase; Humans; Isoleucine; Male; Meta-Analysis as Topic; Parkinson Disease; Polymorphism, Single Nucleotide; Threonine; White People

2012
Association between Thr21Met and Ser89Asn polymorphisms of the urotensin II gene and systemic sclerosis.
    The Journal of rheumatology, 2012, Volume: 39, Issue:1

    Topics: Adult; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Scleroderma, Systemic; Serine; Threonine; Turkey; Urotensins

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
The association of V249I and T280M fractalkine receptor haplotypes with disease course of multiple sclerosis.
    Journal of neuroimmunology, 2012, Volume: 245, Issue:1-2

    Topics: Adult; CX3C Chemokine Receptor 1; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Isoleucine; Male; Methionine; Middle Aged; Multiple Sclerosis, Chronic Progressive; Multiple Sclerosis, Relapsing-Remitting; Polymorphism, Genetic; Receptors, Chemokine; Threonine; Valine

2012
A study of collectin genes in spontaneous preterm birth reveals an association with a common surfactant protein D gene polymorphism.
    Pediatric research, 2012, Volume: 71, Issue:1

    Topics: Adolescent; Adult; Collectins; Female; Genetic Predisposition to Disease; Gestational Age; Haplotypes; Humans; Infant, Newborn; Infant, Premature; Infant, Premature, Diseases; Linkage Disequilibrium; Mannose-Binding Lectin; Methionine; Middle Aged; Polymorphism, Genetic; Pregnancy; Premature Birth; Pulmonary Surfactant-Associated Protein A; Pulmonary Surfactant-Associated Protein D; Threonine; Young Adult

2012
Screening for POLG W748S and A467T mutations in ataxia patients from Spain.
    Movement disorders : official journal of the Movement Disorder Society, 2012, Sep-01, Volume: 27, Issue:10

    Topics: Adult; Age of Onset; Aged; Alanine; Ataxia; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Middle Aged; Mutation; Polymorphism, Single Nucleotide; Serine; Spain; Threonine; Tryptophan; Young Adult

2012
Allelic variants of XRCC1 and XRCC3 repair genes and susceptibility of oral cancer in Brazilian patients.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2013, Volume: 42, Issue:2

    Topics: Adult; Aged; Aged, 80 and over; Alleles; Arginine; Carcinoma, Squamous Cell; Case-Control Studies; Codon; DNA Repair; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutamine; Humans; Lymphatic Metastasis; Male; Methionine; Middle Aged; Mouth Neoplasms; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Risk Factors; Threonine; Tryptophan; X-ray Repair Cross Complementing Protein 1; Young Adult

2013
Fractalkine gene receptor polymorphism in patients with multiple sclerosis.
    The International journal of neuroscience, 2013, Volume: 123, Issue:1

    Topics: Adolescent; Adult; Age of Onset; Analysis of Variance; Chemokine CX3CL1; Disability Evaluation; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genotype; Humans; Isoleucine; Male; Methionine; Middle Aged; Multiple Sclerosis; Polymorphism, Single Nucleotide; Statistics, Nonparametric; Threonine; Valine; Young Adult

2013
What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?
    Brain : a journal of neurology, 2012, Volume: 135, Issue:Pt 12

    Topics: Adolescent; Adult; Age of Onset; Alanine; Child; Cohort Studies; Diffuse Cerebral Sclerosis of Schilder; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Europe; Family Health; Female; Genetic Predisposition to Disease; Homozygote; Humans; Male; Middle Aged; Mitochondrial Diseases; Muscle, Skeletal; Mutation; Ophthalmoplegia, Chronic Progressive External; Statistics as Topic; Statistics, Nonparametric; Threonine; Young Adult

2012
Threonines at position 174 and 235 of the angiotensinogen polypeptide chain are related to familial history of hypertension in a Spanish-Mediterranean population.
    British journal of biomedical science, 2002, Volume: 59, Issue:2

    Topics: Adult; Aged; Angiotensinogen; Cross-Sectional Studies; Female; Genetic Predisposition to Disease; Humans; Hypertension; Male; Middle Aged; Polymorphism, Genetic; Threonine

2002
Severity of alcohol withdrawal symptoms and the T1128C polymorphism of the neuropeptide Y gene.
    Journal of neural transmission (Vienna, Austria : 1996), 2002, Volume: 109, Issue:11

    Topics: Adult; Alcohol Withdrawal Delirium; Alcoholism; Alleles; Case-Control Studies; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Neuropeptide Y; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Severity of Illness Index; Substance Withdrawal Syndrome; Threonine

2002
Influence of interleukin-12 receptor beta1 polymorphisms on tuberculosis.
    Human genetics, 2003, Volume: 112, Issue:3

    Topics: Adult; Aged; Alanine; Asian People; Blotting, Western; Case-Control Studies; Cysteine; Female; Genetic Predisposition to Disease; Genotype; Glycine; Haplotypes; Humans; Interferon-gamma; Japan; Killer Cells, Natural; Male; Middle Aged; Mutation, Missense; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Receptors, Interleukin; Receptors, Interleukin-12; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA; Threonine; Tuberculosis

2003
Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian case-parent triads.
    American journal of epidemiology, 2003, Jun-15, Volume: 157, Issue:12

    Topics: Adolescent; Adult; Alanine; Case-Control Studies; Cleft Lip; Cleft Palate; Cysteine; Female; Folic Acid; Genetic Predisposition to Disease; Genetic Variation; Haplotypes; Humans; Male; Methylenetetrahydrofolate Reductase (NADPH2); Norway; Oxidoreductases Acting on CH-NH Group Donors; Polymerase Chain Reaction; Registries; Risk Factors; Threonine

2003
The Ala45Thr polymorphism of BETA2/NeuroD1 gene and susceptibility to type 2 diabetes mellitus in a Polish population.
    Acta diabetologica, 2003, Volume: 40, Issue:2

    Topics: Adult; Alanine; Amino Acid Substitution; Basic Helix-Loop-Helix Transcription Factors; Case-Control Studies; Diabetes Mellitus, Type 2; DNA-Binding Proteins; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Islets of Langerhans; Mutation, Missense; Poland; Polymorphism, Genetic; Threonine; Trans-Activators

2003
The Ala45Thr polymorphism of BETA2/NeuroD1 gene and susceptibility to type 1 diabetes mellitus in caucasians.
    Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association, 2003, Volume: 111, Issue:5

    Topics: Adult; Age of Onset; Alanine; Amino Acid Substitution; Base Sequence; Basic Helix-Loop-Helix Transcription Factors; Case-Control Studies; Diabetes Mellitus, Type 1; DNA Primers; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Polymorphism, Genetic; Reference Values; Threonine; Trans-Activators; White People

2003
Methylenetetrahydrofolate reductase gene polymorphisms in patients with schizophrenia.
    Brain research. Molecular brain research, 2003, Sep-10, Volume: 117, Issue:1

    Topics: Alanine; Alleles; Chi-Square Distribution; Cysteine; DNA Mutational Analysis; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Lymphocytes; Methylenetetrahydrofolate Reductase (NADPH2); Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Schizophrenia; Threonine

2003
HPC2/ELAC2 gene variants associated with incident prostate cancer.
    Journal of human genetics, 2003, Volume: 48, Issue:12

    Topics: Age Factors; Alleles; Genetic Predisposition to Disease; Genetic Variation; Genotype; Heterozygote; Homozygote; Humans; Leucine; Logistic Models; Male; Neoplasm Proteins; Prostate; Prostatic Neoplasms; Risk; Serine; Threonine

2003
Proteolytic processing in development and leukemogenesis.
    Cell, 2003, Oct-31, Volume: 115, Issue:3

    Topics: Animals; DNA-Binding Proteins; Endopeptidases; Gene Expression Regulation; Genetic Predisposition to Disease; Histone-Lysine N-Methyltransferase; Homeodomain Proteins; Humans; Leukemia, Promyelocytic, Acute; Leukocyte Elastase; Mice; Myeloid-Lymphoid Leukemia Protein; Neoplasm Proteins; Oncogene Proteins, Fusion; Protein Processing, Post-Translational; Proto-Oncogenes; Threonine; Transcription Factors

2003
Phosphorylation of the Bloom's syndrome helicase and its role in recovery from S-phase arrest.
    Molecular and cellular biology, 2004, Volume: 24, Issue:3

    Topics: Adenosine Triphosphatases; Antineoplastic Agents; Ataxia Telangiectasia Mutated Proteins; Bloom Syndrome; Cell Cycle Proteins; DNA Helicases; Fibroblasts; Genetic Predisposition to Disease; Humans; Hydroxyurea; Phosphorylation; Phosphotransferases; Protein Serine-Threonine Kinases; RecQ Helicases; S Phase; Threonine

2004
Support for RGS4 as a susceptibility gene for schizophrenia.
    Biological psychiatry, 2004, Jan-15, Volume: 55, Issue:2

    Topics: Adult; Alanine; Alleles; Case-Control Studies; Chi-Square Distribution; Diagnostic and Statistical Manual of Mental Disorders; Female; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Linkage Disequilibrium; Male; Middle Aged; Polymorphism, Single Nucleotide; Reverse Transcriptase Polymerase Chain Reaction; RGS Proteins; RNA, Messenger; Schizophrenia; Threonine

2004
A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's disease.
    Annals of neurology, 2004, Volume: 55, Issue:3

    Topics: Animals; Case-Control Studies; Chi-Square Distribution; Cohort Studies; Dopamine beta-Hydroxylase; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Linkage Disequilibrium; Male; Middle Aged; Multiple System Atrophy; Odds Ratio; Pan troglodytes; Parkinson Disease; Polymorphism, Genetic; Threonine

2004
GNB3 gene C825T and ACE gene I/D polymorphisms in essential hypertension in a Kazakh genetic isolate.
    Journal of human hypertension, 2004, Volume: 18, Issue:9

    Topics: Adult; Blood Pressure; Case-Control Studies; China; Cysteine; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genetics, Population; Genotype; Heterotrimeric GTP-Binding Proteins; Humans; Hypertension; Kazakhstan; Logistic Models; Male; Middle Aged; Peptidyl-Dipeptidase A; Polymerase Chain Reaction; Polymorphism, Genetic; Threonine

2004
Possible association of interleukin 1 gene locus polymorphisms with low back pain.
    Pain, 2004, Volume: 109, Issue:1-2

    Topics: Adult; Alanine; Alleles; Cohort Studies; Cysteine; Finland; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Interleukin-1; Intervertebral Disc Displacement; Low Back Pain; Lumbar Vertebrae; Magnetic Resonance Imaging; Male; Middle Aged; Pain Measurement; Polymerase Chain Reaction; Polymorphism, Genetic; Receptors, Interleukin; Regression Analysis; Risk; RNA; Surveys and Questionnaires; Threonine

2004
Association between norepinephrine transporter gene polymorphism and major depression.
    Neuropsychobiology, 2004, Volume: 49, Issue:4

    Topics: Adult; Cysteine; Depressive Disorder, Major; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Norepinephrine Plasma Membrane Transport Proteins; Polymorphism, Genetic; Psychiatric Status Rating Scales; Random Allocation; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Symporters; Threonine

2004
Association of estrogen receptor alpha polymorphisms with susceptibility to chronic hepatitis B virus infection.
    Hepatology (Baltimore, Md.), 2004, Volume: 40, Issue:2

    Topics: Adult; Alanine; Alleles; Asian People; Chromosome Mapping; Cysteine; Estrogen Receptor alpha; Female; Genetic Predisposition to Disease; Haplotypes; Hepatitis B, Chronic; Heterozygote; Humans; Linkage Disequilibrium; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Estrogen; Threonine

2004
No association of the A260G and A386G DAZL single nucleotide polymorphisms with male infertility in a Caucasian population.
    Human reproduction (Oxford, England), 2004, Volume: 19, Issue:12

    Topics: Alanine; Amino Acid Sequence; Base Sequence; Case-Control Studies; Gene Frequency; Genetic Predisposition to Disease; Genetics, Population; Germany; Humans; Infertility, Male; Male; Molecular Sequence Data; Oligospermia; Polymorphism, Single Nucleotide; RNA-Binding Proteins; Spermatozoa; Threonine; White People

2004
Variants in optineurin gene and their association with tumor necrosis factor-alpha polymorphisms in Japanese patients with glaucoma.
    Investigative ophthalmology & visual science, 2004, Volume: 45, Issue:12

    Topics: Adult; Aging; Alleles; Asian People; Aspartic Acid; Cell Cycle Proteins; Chromatography, High Pressure Liquid; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glaucoma, Open-Angle; Heterozygote; Histidine; Humans; Intraocular Pressure; Male; Membrane Transport Proteins; Middle Aged; Mutation; Polymorphism, Genetic; Threonine; Transcription Factor TFIIIA; Tumor Necrosis Factor-alpha; Visual Fields

2004
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
Brain-derived neurotrophic factor gene polymorphisms in Japanese patients with sporadic Alzheimer's disease, Parkinson's disease, and multiple system atrophy.
    Movement disorders : official journal of the Movement Disorder Society, 2005, Volume: 20, Issue:8

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Brain-Derived Neurotrophic Factor; Cysteine; Female; Genetic Predisposition to Disease; Humans; Japan; Male; Methionine; Middle Aged; Multiple System Atrophy; Parkinson Disease; Polymorphism, Genetic; Threonine; Valine

2005
The 5alpha-reductase type II A49T and V89L high-activity allelic variants are more common in men with prostate cancer compared with the general population.
    European urology, 2005, Volume: 48, Issue:4

    Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Aged; Alanine; Alleles; Arginine; Biomarkers, Tumor; Case-Control Studies; Dihydrotestosterone; Disease Progression; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Leucine; Luteinizing Hormone; Male; Middle Aged; Point Mutation; Polymorphism, Genetic; Prostatic Hyperplasia; Prostatic Neoplasms; Receptors, Androgen; Risk Factors; Sex Hormone-Binding Globulin; Sweden; Terminal Repeat Sequences; Testosterone; Threonine; Valine

2005
FcgammaRIIB Ile232Thr transmembrane polymorphism associated with human systemic lupus erythematosus decreases affinity to lipid rafts and attenuates inhibitory effects on B cell receptor signaling.
    Human molecular genetics, 2005, Oct-01, Volume: 14, Issue:19

    Topics: Amino Acid Sequence; Amino Acid Substitution; Antigens, CD; B-Lymphocytes; Calcium Signaling; Cells, Cultured; Genetic Predisposition to Disease; Humans; Isoleucine; Lupus Erythematosus, Systemic; Membrane Microdomains; Molecular Sequence Data; Phosphatidylinositol Phosphates; Polymorphism, Genetic; Receptors, Antigen, B-Cell; Receptors, IgG; Signal Transduction; Threonine

2005
The prevalence of C807T mutation of glycoprotein Ia gene among young male survivors of myocardial infarction: a relation with coronary angiography results.
    Kardiologia polska, 2005, Volume: 63, Issue:2

    Topics: Adult; Alanine; Case-Control Studies; Coronary Angiography; Cysteine; Gene Expression; Gene Frequency; Genetic Predisposition to Disease; Humans; Integrin alpha2; Male; Middle Aged; Mutation; Myocardial Infarction; Polymorphism, Genetic; Threonine

2005
Association of the 1438G/A and 102T/C polymorphism of the 5-HT2A receptor gene with irritable bowel syndrome 5-HT2A gene polymorphism in irritable bowel syndrome.
    Journal of clinical gastroenterology, 2005, Volume: 39, Issue:9

    Topics: Alanine; Case-Control Studies; Cysteine; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glycine; Humans; Irritable Bowel Syndrome; Polymorphism, Genetic; Receptor, Serotonin, 5-HT2A; Threonine

2005
CD14 and TLR4 gene polymorphisms in adult periodontitis.
    Journal of dental research, 2005, Volume: 84, Issue:11

    Topics: Adult; Age Factors; Aged; Aggregatibacter actinomycetemcomitans; Aspartic Acid; Cytosine; Disease Susceptibility; Female; Genetic Predisposition to Disease; Glycine; Humans; Isoleucine; Lipopolysaccharide Receptors; Male; Middle Aged; Periodontitis; Polymorphism, Genetic; Porphyromonas gingivalis; Sex Factors; Smoking; Threonine; Thymine; Toll-Like Receptor 4

2005
Inherited susceptibility to lung cancer may be associated with the T790M drug resistance mutation in EGFR.
    Nature genetics, 2005, Volume: 37, Issue:12

    Topics: Antineoplastic Agents; Carcinoma, Non-Small-Cell Lung; Drug Resistance, Neoplasm; ErbB Receptors; Female; Genetic Predisposition to Disease; Germ-Line Mutation; Humans; Lung Neoplasms; Male; Methionine; Middle Aged; Pedigree; Protein Kinase Inhibitors; Protein-Tyrosine Kinases; Threonine

2005
Gingival epithelial cells heterozygous for Toll-like receptor 4 polymorphisms Asp299Gly and Thr399ile are hypo-responsive to Porphyromonas gingivalis.
    Genes and immunity, 2006, Volume: 7, Issue:3

    Topics: Amino Acid Substitution; Aspartic Acid; Cells, Cultured; Gene Expression Profiling; Genetic Predisposition to Disease; Gingiva; Glycine; Heterozygote; Humans; Isoleucine; Polymorphism, Genetic; Porphyromonas gingivalis; Threonine; Toll-Like Receptor 4; Toll-Like Receptors

2006
Renin-angiotensin system gene polymorphisms: association with susceptibility to Henoch-Schonlein purpura and renal involvement.
    Clinical rheumatology, 2006, Volume: 25, Issue:6

    Topics: Adolescent; Alanine; Angiotensinogen; Child; Child, Preschool; Cysteine; DNA Transposable Elements; Female; Gene Deletion; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; IgA Vasculitis; Kidney Diseases; Male; Methionine; Nephrotic Syndrome; Peptidyl-Dipeptidase A; Polymorphism, Genetic; Proteinuria; Receptor, Angiotensin, Type 1; Renin-Angiotensin System; Severity of Illness Index; Threonine

2006
Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms.
    The Journal of biological chemistry, 2006, Jul-07, Volume: 281, Issue:27

    Topics: Animals; Chlorocebus aethiops; COS Cells; Dystonia; Genetic Predisposition to Disease; Humans; Models, Molecular; Mutation; Parkinsonian Disorders; Phenylalanine; Protein Conformation; Rats; Sodium; Sodium-Potassium-Exchanging ATPase; Threonine

2006
PanR1, a dominant negative missense allele of the gene encoding TNF-alpha (Tnf), does not impair lymphoid development.
    Journal of immunology (Baltimore, Md. : 1950), 2006, Jun-15, Volume: 176, Issue:12

    Topics: Alleles; Amino Acid Substitution; Animals; Ethylnitrosourea; Female; Genes, Dominant; Genetic Predisposition to Disease; Germ-Line Mutation; Listeriosis; Male; Membrane Proteins; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Knockout; Mutation, Missense; Peyer's Patches; Proline; Protein Binding; Receptors, Tumor Necrosis Factor; Receptors, Tumor Necrosis Factor, Type I; Solubility; Spleen; Threonine; Tumor Necrosis Factor Decoy Receptors; Tumor Necrosis Factor-alpha

2006
Ala45Thr variation in neuroD1 gene is associated with early-onset type 2 diabetes with or without diabetic pedigree in Chinese.
    Molecular and cellular biochemistry, 2006, Volume: 290, Issue:1-2

    Topics: Adult; Aged; Alanine; Amino Acid Substitution; Basic Helix-Loop-Helix Transcription Factors; Case-Control Studies; China; Diabetes Mellitus, Type 2; Gene Frequency; Genetic Predisposition to Disease; Humans; Middle Aged; Pedigree; Polymorphism, Genetic; Threonine

2006
The Thr354Ile substitution in PSEN1:: disease-causing mutation or polymorphism?
    Neurology, 2006, Jun-27, Volume: 66, Issue:12

    Topics: Alzheimer Disease; Genetic Predisposition to Disease; Heterozygote; Humans; Male; Membrane Proteins; Middle Aged; Mutation; Polymorphism, Genetic; Presenilin-1; Threonine

2006
Polymorphism in the angiotensinogen gene, hypertension, and ethnic differences in the risk of recurrent coronary events.
    Hypertension (Dallas, Tex. : 1979), 2006, Volume: 48, Issue:4

    Topics: Aged; Angiotensin-Converting Enzyme Inhibitors; Angiotensinogen; Black People; Cardiovascular Diseases; Cohort Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Homozygote; Humans; Hypertension; Male; Methionine; Middle Aged; Myocardial Infarction; Polymorphism, Genetic; Prospective Studies; Recurrence; Threonine; White People

2006
Associations of a novel IL4RA polymorphism, Ala57Thr, in Greenlander Inuit.
    The Journal of allergy and clinical immunology, 2006, Volume: 118, Issue:3

    Topics: Adult; Alanine; Alleles; Amino Acid Substitution; Denmark; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Greenland; Haplotypes; Humans; Hypersensitivity, Immediate; Interleukin-4 Receptor alpha Subunit; Inuit; Male; Polymorphism, Single Nucleotide; Receptors, Interleukin-4; Rhinitis, Allergic, Seasonal; Threonine

2006
The alanine/threonine polymorphism of the alpha-1-antichymotrypsin (SERPINA3) gene and ruptured intracranial aneurysms in the Japanese population.
    Cerebrovascular diseases (Basel, Switzerland), 2007, Volume: 23, Issue:1

    Topics: Alanine; Aneurysm, Ruptured; Asian People; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Intracranial Aneurysm; Japan; Male; Middle Aged; Polymorphism, Single Nucleotide; Risk Factors; Serpins; Subarachnoid Hemorrhage; Threonine

2007
The P1812A and P25T BRCA1 and the 5164del4 BRCA2 mutations: occurrence in high-risk non-Ashkenazi Jews.
    Genetic testing, 2006,Fall, Volume: 10, Issue:3

    Topics: Adult; Aged; Alanine; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; BRCA1 Protein; BRCA2 Protein; Female; Genetic Predisposition to Disease; Humans; Jews; Male; Middle Aged; Molecular Sequence Data; Pedigree; Proline; Sequence Deletion; Threonine

2006
Ala394Thr polymorphism in the clock gene NPAS2: a circadian modifier for the risk of non-Hodgkin's lymphoma.
    International journal of cancer, 2007, Jan-15, Volume: 120, Issue:2

    Topics: Aged; Alanine; Amino Acid Substitution; Basic Helix-Loop-Helix Transcription Factors; Circadian Rhythm; CLOCK Proteins; Connecticut; Female; Genetic Predisposition to Disease; Genetic Testing; Humans; Lymphoma, B-Cell; Lymphoma, Non-Hodgkin; Middle Aged; Molecular Epidemiology; Nerve Tissue Proteins; Polymorphism, Genetic; Population; Risk; Threonine; Trans-Activators

2007
Genetic variation in thrombin-activatable fibrinolysis inhibitor (TAFI) is associated with the risk of splanchnic vein thrombosis.
    Thrombosis and haemostasis, 2007, Volume: 97, Issue:2

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alanine; Budd-Chiari Syndrome; Carboxypeptidase B2; Case-Control Studies; Female; Genetic Predisposition to Disease; Genetic Variation; Haplotypes; Humans; Male; Middle Aged; Netherlands; Odds Ratio; Polymorphism, Single Nucleotide; Portal Vein; Risk Factors; Threonine; Venous Thrombosis

2007
The risk for thromboembolic disease in lupus anticoagulant patients due to pathways involving P-selectin and CD154.
    Thrombosis and haemostasis, 2007, Volume: 97, Issue:4

    Topics: Adult; CD40 Ligand; Cohort Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Lupus Coagulation Inhibitor; Male; Membrane Glycoproteins; Middle Aged; Odds Ratio; P-Selectin; Polymorphism, Single Nucleotide; Predictive Value of Tests; Proline; Risk Assessment; Risk Factors; Threonine; Thromboembolism; Thrombosis; Venous Thrombosis

2007
Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation.
    Pediatric research, 2007, Volume: 62, Issue:2

    Topics: Amino Acid Substitution; ATP-Binding Cassette Transporters; Child, Preschool; Codon; DNA Mutational Analysis; Female; Fetal Diseases; Genetic Predisposition to Disease; Gestational Age; Heterozygote; Humans; Infant; Isoleucine; Lung Diseases, Interstitial; Male; Mutation; Pedigree; Phenotype; Pulmonary Surfactant-Associated Protein C; Severity of Illness Index; Threonine

2007
Association of TLR4 polymorphisms with symptomatic respiratory syncytial virus infection in high-risk infants and young children.
    Journal of immunology (Baltimore, Md. : 1950), 2007, Sep-01, Volume: 179, Issue:5

    Topics: Amino Acid Substitution; Aspartic Acid; Child; Child, Preschool; Female; Genetic Predisposition to Disease; Heterozygote; Humans; Infant; Male; Polymorphism, Single Nucleotide; Respiratory Syncytial Virus Infections; Respiratory Syncytial Viruses; Threonine; Toll-Like Receptor 4

2007
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.
    International journal of cancer, 2007, Dec-15, Volume: 121, Issue:12

    Topics: Adult; Age of Onset; Aged; Asian People; Black or African American; Breast Neoplasms; Case-Control Studies; Checkpoint Kinase 2; DNA Mutational Analysis; DNA, Complementary; Female; Gene Frequency; Genetic Predisposition to Disease; Germ-Line Mutation; Hawaii; Hispanic or Latino; Histidine; Humans; Isoleucine; Leucine; Male; Middle Aged; Mutation; Mutation, Missense; Predictive Value of Tests; Proline; Prostatic Neoplasms; Protein Serine-Threonine Kinases; Risk Assessment; Risk Factors; Threonine; Tyrosine; United States; White People

2007
Association study of human MTH1 Ile45Thr polymorphism with sporadic Parkinson's disease.
    European neurology, 2008, Volume: 59, Issue:1-2

    Topics: Aged; Aged, 80 and over; Chi-Square Distribution; China; DNA Repair Enzymes; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Middle Aged; Parkinson Disease; Phosphoric Monoester Hydrolases; Polymorphism, Genetic; Reverse Transcriptase Polymerase Chain Reaction; Sex Factors; Threonine

2008
The extracolonic cancer spectrum in females with the common 'South African' hMLH1 c.C1528T mutation.
    Familial cancer, 2008, Volume: 7, Issue:3

    Topics: Adaptor Proteins, Signal Transducing; Adult; Alleles; Case-Control Studies; Cohort Studies; Colorectal Neoplasms, Hereditary Nonpolyposis; Cysteine; Female; Genetic Predisposition to Disease; Humans; Incidence; Microsatellite Instability; Middle Aged; Mutation; MutL Protein Homolog 1; Neoplasms; Neoplasms, Multiple Primary; Nuclear Proteins; Phenotype; Population Surveillance; Risk Factors; Sex Factors; Siblings; South Africa; Threonine

2008
Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel.
    Cardiovascular research, 2008, Mar-01, Volume: 77, Issue:4

    Topics: Action Potentials; Adolescent; Adult; Ajmaline; Animals; Anti-Arrhythmia Agents; Bundle-Branch Block; Cell Line; Child; Death, Sudden, Cardiac; DNA Mutational Analysis; Electrocardiography; Female; Gene Transfer Techniques; Genetic Predisposition to Disease; Humans; Kinetics; Lidocaine; Long QT Syndrome; Lysine; Male; Muscle Proteins; Mutation; Myocardium; NAV1.5 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Pedigree; Sodium; Sodium Channels; Syncope; Threonine; Xenopus laevis

2008
MC1R variants associated susceptibility to basal cell carcinoma of skin: interaction with host factors and XRCC3 polymorphism.
    International journal of cancer, 2008, Apr-15, Volume: 122, Issue:8

    Topics: Adult; Aged; Arginine; Carcinoma, Basal Cell; Case-Control Studies; DNA-Binding Proteins; Female; Genetic Predisposition to Disease; Genotype; Glutamine; Humans; Hungary; Male; Methionine; Middle Aged; Polymorphism, Genetic; Receptor, Melanocortin, Type 1; Risk Factors; Romania; Sequence Analysis, DNA; Skin Neoplasms; Slovakia; Threonine

2008
Polymorphism of the endothelial nitric oxide synthase gene is associated with diabetic retinopathy in a cohort of West Africans.
    Molecular vision, 2007, Nov-26, Volume: 13

    Topics: Adult; Aged; Alleles; Black People; Cohort Studies; Diabetes Mellitus, Type 2; Diabetic Retinopathy; Female; Gene Deletion; Genetic Predisposition to Disease; Genotype; Ghana; Glycine; Humans; Male; Middle Aged; Mutagenesis, Insertional; Nigeria; Nitric Oxide Synthase Type III; Polymorphism, Genetic; Threonine

2007
Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2.
    BMC neurology, 2008, Jan-22, Volume: 8

    Topics: Aged; alpha-Synuclein; DNA Mutational Analysis; Exons; Family Health; Female; Genetic Predisposition to Disease; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Methionine; Middle Aged; Mutation; Parkinson Disease; Portugal; Protein Kinases; Protein Serine-Threonine Kinases; Threonine; Ubiquitin-Protein Ligases

2008
Overall and relapse-free survival in oropharyngeal and hypopharyngeal squamous cell carcinoma are associated with genotypes of T393C polymorphism of the GNAS1 gene.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2008, Mar-15, Volume: 14, Issue:6

    Topics: Adult; Aged; Amino Acid Substitution; Biomarkers, Tumor; Carcinoma, Squamous Cell; Chromogranins; Cysteine; Disease-Free Survival; Female; Genetic Predisposition to Disease; Genotype; GTP-Binding Protein alpha Subunits, Gs; Humans; Hypopharyngeal Neoplasms; Male; Middle Aged; Oropharyngeal Neoplasms; Polymorphism, Single Nucleotide; Prognosis; Recurrence; Survival Analysis; Threonine

2008
Identification and functional analysis of novel human melanocortin-4 receptor variants.
    Diabetes, 1999, Volume: 48, Issue:3

    Topics: Adolescent; Adult; Amino Acid Substitution; Animals; Body Mass Index; Cloning, Molecular; Diabetes Mellitus; Diabetes Mellitus, Type 2; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Isoleucine; Male; Methionine; Mice; Middle Aged; Obesity; Pedigree; Polymorphism, Single-Stranded Conformational; Receptor, Melanocortin, Type 4; Receptors, Peptide; Recombinant Proteins; Threonine; Valine

1999
The association of Ala45Thr polymorphism in NeuroD with child-onset Type 1a diabetes in Japanese.
    Diabetes research and clinical practice, 2002, Volume: 55, Issue:1

    Topics: Adolescent; Age of Onset; Alanine; Alleles; Asian People; Basic Helix-Loop-Helix Transcription Factors; Child; Diabetes Mellitus, Type 1; Genetic Carrier Screening; Genetic Predisposition to Disease; Genetic Variation; Helix-Loop-Helix Motifs; HLA-DR Antigens; HLA-DRB1 Chains; Homozygote; Humans; Japan; Nerve Tissue Proteins; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Reference Values; Threonine; Time Factors

2002