Page last updated: 2024-10-20

thymine and Genetic Predisposition

thymine has been researched along with Genetic Predisposition in 121 studies

Research Excerpts

ExcerptRelevanceReference
"This review assesses the associations of interleukin-8 gene (IL-8) -251A/T (rs4073) and -845T/C (rs2227532) polymorphisms with susceptibility to periodontitis."8.91Quantitative assessment of the associations between interleukin-8 polymorphisms and periodontitis susceptibility. ( Chen, X; Ding, C; Huang, J; Zhong, L, 2015)
"Certain mutations in ANKH, which encodes a multiple-pass transmembrane protein that regulates inorganic pyrophosphate (PPi) transport, are linked to autosomal-dominant familial chondrocalcinosis."7.73Association of sporadic chondrocalcinosis with a -4-basepair G-to-A transition in the 5'-untranslated region of ANKH that promotes enhanced expression of ANKH protein and excess generation of extracellular inorganic pyrophosphate. ( Brown, MA; Carr, AJ; Johnson, K; Russell, RG; Terkeltaub, RA; Wordsworth, BP; Zhang, Y, 2005)
"This review assesses the associations of interleukin-8 gene (IL-8) -251A/T (rs4073) and -845T/C (rs2227532) polymorphisms with susceptibility to periodontitis."4.91Quantitative assessment of the associations between interleukin-8 polymorphisms and periodontitis susceptibility. ( Chen, X; Ding, C; Huang, J; Zhong, L, 2015)
" Given two factors associated with high mutation rates, we tested how many previously known genes match with (i) proximity to telomeres or (ii) high adenine and thymine content in cardiovascular diseases (CVDs) related to vascular stiffening."4.02Factors Associated with Mutations: Their Matching Rates to Cardiovascular and Neurological Diseases. ( Hart, C; Hijazi, A; Kim, DG; Lee, C; Lee, PHU; Li, W; Lucas, HB; McKnight, I; Raines, R; Shim, JW, 2021)
"Certain mutations in ANKH, which encodes a multiple-pass transmembrane protein that regulates inorganic pyrophosphate (PPi) transport, are linked to autosomal-dominant familial chondrocalcinosis."3.73Association of sporadic chondrocalcinosis with a -4-basepair G-to-A transition in the 5'-untranslated region of ANKH that promotes enhanced expression of ANKH protein and excess generation of extracellular inorganic pyrophosphate. ( Brown, MA; Carr, AJ; Johnson, K; Russell, RG; Terkeltaub, RA; Wordsworth, BP; Zhang, Y, 2005)
"Plasma homocysteine concentrations, smoking status, and MTFHR 677 genotypes were determined in 275 white women who had pregnancies affected by CHDs and 118 white women who had a normal pregnancy."3.73Congenital heart defects, maternal homocysteine, smoking, and the 677 C>T polymorphism in the methylenetetrahydrofolate reductase gene: evaluating gene-environment interactions. ( Cleves, MA; Hobbs, CA; James, SJ; Jernigan, S; Lu, Y; Malik, S; Melnyk, S, 2006)
"Studies on dental caries suggest that in severe cases it may induce a systemic immune response."2.73Host and microbiological factors related to dental caries development. ( De Soet, JJ; Laine, ML; Morré, SA; van Amerongen, WE; van Gemert-Schriks, MC; van Winkelhoff, AJ, 2008)
"The overall OR (95% CI) of type 2 diabetes was 0."2.44Association between the T-381C polymorphism of the brain natriuretic peptide gene and risk of type 2 diabetes in human populations. ( Amouyel, P; Arveiler, D; Cottel, D; de Groote, P; Ferrières, J; Groves, CJ; Hattersley, AT; Hitman, GA; McCarthy, MI; Meirhaeghe, A; Sandhu, MS; Walker, M; Wareham, NJ, 2007)
"Twenty-nine chronic periodontitis patients and 31 healthy controls of North Indian origin from Chhattisgarh were recruited for the study."1.42Interleukin 1β (+3954, -511 and -31) polymorphism in chronic periodontitis patients from North India. ( Amirisetty, R; Das, S; Jyothy, A; Munshi, A; Patel, RP; Saraf, J, 2015)
"Meanwhile, we found COPD patients with CC genotype had significantly higher risk for PH (OR = 1."1.42A single nucleotide polymorphism in 3' untranslated region of epithelial growth factor receptor confers risk for pulmonary hypertension in chronic obstructive pulmonary disease. ( Fei, L; Li, M; Wang, R; Xu, X; Zeng, D; Zhang, Y; Zhou, S; Zhu, Q, 2015)
"Although chronic periodontitis (CP) is a multifactorial condition, few studies have investigated the potential association of gene variants with the outcome of periodontal therapy."1.40Clinical outcomes of periodontal therapy are not influenced by the ATC/TTC haplotype in the IL8 gene. ( Anovazzi, G; Cirelli, JA; Corbi, SC; Finoti, LS; Gerlach, RF; Kim, YJ; Marcaccini, AM; Orrico, SR; Scarel-Caminaga, RM; Secolin, R; Tanaka, MH, 2014)
"Sjogren's syndrome is characterized by T-cell infiltration of exocrine glands leading to parenchymal destruction and impaired glandular function."1.40Th1 and Th2 polymorphisms in Sjögren's syndrome and rheumatoid arthritis. ( de Albuquerque Tavares Carvalho, A; de Souza, TR; Duarte, ÂP; Gueiros, LA; Leão, JC; Porter, SR, 2014)
"A case-control study of 206 breast cancer patients and 262 controls was conducted in Iranian women."1.39Polymorphic CT dinucleotide repeat in the GATA3 gene and risk of breast cancer in Iranian women. ( Forousan, S; Manoochehr, T; Simin, H; Zakieh, A, 2013)
"Ameloblastoma is a common benign odontogenic tumour with inherently aggressive behaviour."1.39XRCC1 gene polymorphisms and risk of ameloblastoma. ( Boonsuwan, T; Kitkumthorn, N; Mutirangura, A; Yanatatsaneejit, P, 2013)
"It has been proposed that individual genetic predisposition may contribute to a persistent apical periodontitis condition."1.38Genetic susceptibility to periapical disease: conditional contribution of MMP2 and MMP3 genes to the development of periapical lesions and healing response. ( Deeley, K; Khaliq, S; Letra, A; Menezes-Silva, R; Vieira, AR, 2012)
"One-hundred and fourteen patients with chronic periodontitis and 77 periodontally healthy subjects were genotyped using TaqMan® allelic discrimination assays."1.37Single nucleotide polymorphisms of pattern recognition receptors and chronic periodontitis. ( De Nardin, E; Genco, RJ; Gunsolley, J; Sahingur, SE; Schenkein, HA; Xia, XJ, 2011)
"Tobacco-related oral squamous cell carcinoma (OSCC) is one of the most common cancers involving Indian males."1.37Functional variants of IL4 and IL6 genes and risk of tobacco-related oral carcinoma in high-risk Asian Indians. ( Das, S; Gaur, P; Mittal, M; Mohanti, B, 2011)
"203 head and neck cancer patients and 201 healthy controls were genotyped for functional polymorphisms of CYP2A13 and UGT1A7 genes using polymerase chain reaction-restriction fragment length polymorphism, denaturing high-performance liquid chromatography and sequencing."1.36Polymorphisms in CYP2A13 and UGT1A7 genes and head and neck cancer susceptibility in North Indians. ( Ahuja, M; Khullar, M; Panda, N; Sharma, R, 2010)
"Periodontitis is a multifactorial disease in which environmental and genetic determinant factors contribute to individual subjects susceptibility."1.35E-selectin and L-selectin polymorphisms in patients with periodontitis. ( Gholami, L; Hajilooi, M; Houshmand, B; Mani-Kashani, K; Rafiei, A, 2009)
"Little is known about the influence of genetic susceptibility on implant loss."1.35Analysis of the association of IL1B (C+3954T) and IL1RN (intron 2) polymorphisms with dental implant loss in a Brazilian population. ( Alvim-Pereira, F; de Castilhos, BB; Montes, CC; Olandoski, M; Sakurai, ML; Trevilatto, PC, 2009)
"Two families with frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17) resulting from the microtubule associated protein tau (MAPT) gene IVS10+16C>T splice site mutation are reported, members of which showed variable clinical phenotypes at presentation."1.35Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation. ( Larner, AJ, 2009)
"The discrimination of nonalcoholic steatohepatitis (NASH) from another NAFLD was made by NAFLD activity score (NAS), and a NAS>or=5 was considered NASH."1.34Methylenetetrahydrofolate reductase C677T mutation and nonalcoholic fatty liver disease. ( Ataç, FB; Bilezikçi, B; Güçlü, M; Kayaselçuk, F; Ozer, B; Serin, E; Verdi, H; Yilmaz, U, 2007)
"The etiology of preeclampsia (PE) is unknown, but endothelial cell injury plays a pivotal role."1.33Association of apolipoprotein J gene 866C-->T polymorphism with preeclampsia and essential hypertension. ( Chen, M; Shan, K; Yuan, Z, 2005)
"Metabolic syndrome was diagnosed on modified National Cholesterol Education Program Adult Treatment Panel III guidelines, using body mass index (BMI) instead of waist circumference."1.33Association of mitochondrial deoxyribonucleic acid 16189 variant (T->C transition) with metabolic syndrome in Chinese adults. ( Chen, IY; Chen, JF; Chen, MH; Chen, SD; Eng, HL; Lee, CF; Lin, TK; Liou, CW; Liu, RT; Wang, PW; Wei, YH; Weng, SW, 2005)
"Comparing women with uterine leiomyomas and controls, no statistically significant differences with respect to allele frequency and genotype distribution were ascertained for ESR1 IVS 1-397 T/C (PvuII) (P=0."1.33Genotype distribution of estrogen receptor-alpha, catechol-O-methyltransferase, and cytochrome P450 17 gene polymorphisms in Caucasian women with uterine leiomyomas. ( Bentz, EK; Denschlag, D; Hefler, L; Pietrowski, D; Tempfer, C; Tong, D; Zeillinger, R, 2006)
"Relative risks (RRs) of cancer and 95% confidence intervals (CIs) were calculated by Cox proportional hazards regression analysis."1.32Integrin beta3 Leu33Pro homozygosity and risk of cancer. ( Bojesen, SE; Nordestgaard, BG; Tybjaerg-Hansen, A, 2003)

Research

Studies (121)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (1.65)18.2507
2000's75 (61.98)29.6817
2010's43 (35.54)24.3611
2020's1 (0.83)2.80

Authors

AuthorsStudies
Lucas, HB1
McKnight, I1
Raines, R1
Hijazi, A1
Hart, C1
Lee, C1
Kim, DG1
Li, W1
Lee, PHU1
Shim, JW1
Zakieh, A1
Simin, H1
Forousan, S1
Manoochehr, T1
Alkhateeb, A1
Karasneh, J1
Abbadi, H1
Hassan, A1
Thornhill, M1
Corbi, SC1
Finoti, LS2
Anovazzi, G1
Tanaka, MH1
Kim, YJ1
Secolin, R2
Marcaccini, AM1
Gerlach, RF1
Orrico, SR1
Cirelli, JA1
Scarel-Caminaga, RM5
de Souza, TR1
de Albuquerque Tavares Carvalho, A1
Duarte, ÂP1
Porter, SR1
Leão, JC1
Gueiros, LA1
Niu, Y1
Yuan, H2
Shen, M1
Li, H2
Hu, Y2
Chen, N1
Han, Y1
Zhou, L1
Ma, L1
Li, D1
Xu, M1
Ma, J1
Zhang, W1
Jiang, H1
Wu, Y1
Wang, L1
Pan, Y2
Alves-Ferreira, M1
Pinho, T1
Sousa, A1
Sequeiros, J1
Lemos, C1
Alonso, I1
Chen, D1
Zhang, TL1
Wang, LM1
Mi, N1
Hao, Y1
Jiao, X2
Zheng, X2
Song, T2
Shi, J2
Dong, C1
Yan, Y1
Weng, H1
Shen, ZH1
Wu, L1
Zeng, XT2
Wang, Y1
Lin, L1
Xu, H1
Li, T1
Zhou, Y1
Dan, H1
Jiang, L1
Liao, G1
Zhou, M1
Li, L1
Zeng, X1
Li, J1
Chen, Q1
Amirisetty, R1
Patel, RP1
Das, S2
Saraf, J1
Jyothy, A1
Munshi, A1
Chen, X1
Huang, J1
Zhong, L1
Ding, C1
Antunes, LS1
Tannure, PN1
Antunes, LA1
Reis, MF1
Costa, MC1
Gouvêa, CV1
Olej, B1
Granjeiro, JM1
Küchler, EC1
Gao, P1
Zhao, H1
You, J1
Jing, F1
Su, S1
Chien, M1
Lin, C1
Chen, M2
Yang, S1
Liu, DY1
Kwong, JS1
Leng, WD1
Xia, LY1
Mao, M1
Søvik, JB1
Vieira, AR2
Tveit, AB1
Mulic, A1
Zhou, S1
Li, M1
Zeng, D1
Xu, X2
Fei, L1
Zhu, Q1
Zhang, Y2
Wang, R1
Yalcınkaya, M1
Erbek, SS1
Babakurban, ST1
Kupeli, E1
Bozbas, S1
Terzi, YK1
Sahin, FI1
Liu, FT1
Zhu, PQ1
Ou, YX1
Liu, WW1
Xia, GF1
Luo, HL1
Reichert, S1
Machulla, HK1
Klapproth, J1
Zimmermann, U1
Reichert, Y1
Gläser, C1
Schaller, HG1
Schulz, S1
De Soet, JJ1
van Gemert-Schriks, MC1
Laine, ML2
van Amerongen, WE1
Morré, SA2
van Winkelhoff, AJ2
Holla, LI2
Fassmann, A2
Augustin, P1
Halabala, T1
Znojil, V1
Vanek, J2
Houshmand, B2
Rafiei, A2
Hajilooi, M2
Mani-Kashani, K1
Gholami, L1
Montes, CC2
Alvim-Pereira, F4
de Castilhos, BB1
Sakurai, ML1
Olandoski, M1
Trevilatto, PC6
Yan, L1
Yanan, D1
Donglan, S1
Na, W1
Rongmiao, Z1
Zhifeng, C1
Maney, P1
Walters, JD1
Larner, AJ1
López, NJ1
Valenzuela, CY1
Jara, L1
Kobayashi, T1
Nagata, T1
Murakami, S1
Takashiba, S1
Kurihara, H1
Izumi, Y1
Numabe, Y1
Watanabe, H1
Kataoka, M1
Nagai, A1
Hayashi, J1
Ohyama, H1
Okamatsu, Y1
Inagaki, Y1
Tai, H1
Yoshie, H1
Jianyan, L1
Zeqiang, G1
Yongjuan, C1
Kaihong, D1
Bing, D1
Rongsheng, L1
Huang, SH1
Chang, PY1
Liu, CJ1
Lin, MW1
Hsia, KT1
Sharma, R1
Ahuja, M1
Panda, N1
Khullar, M2
Nikopensius, T1
Birnbaum, S1
Ludwig, KU1
Jagomägi, T1
Saag, M1
Herms, S1
Knapp, M1
Hoffmann, P1
Nöthen, MM2
Metspalu, A1
Mangold, E1
Wu, YM1
Chuang, HL1
Ho, YP1
Ho, KY1
Tsai, CC1
Mostowska, A1
Hozyasz, KK1
Biedziak, B1
Misiak, J1
Jagodzinski, PP1
Zhang, B1
Qin, C1
Cao, F1
Jang, JY1
Park, EK1
Ryoo, HM1
Shin, HI1
Kim, TH1
Jang, JS1
Park, HS1
Choi, JY1
Kwon, TG1
Yao, T1
Yang, L1
Li, PQ1
Wu, H1
Xie, HB1
Shen, X1
Xie, XD1
de Souza Pardo, AP1
de Brito, RB1
Alvim-Pereira, CC2
Probst, CM1
Garlet, GP1
Sallum, AW1
Line, SR3
Sahingur, SE1
Xia, XJ1
Gunsolley, J1
Schenkein, HA1
Genco, RJ1
De Nardin, E1
Deng, H1
Liu, F1
Jin, X1
Wang, H2
Cao, J1
Duan, W1
Xu, J1
Nie, C1
Yang, Z1
Wang, W1
Lu, D2
Gaur, P1
Mittal, M1
Mohanti, B1
Liu, CM1
Yeh, CJ1
Yu, CC1
Chou, MY1
Lin, CH1
Wei, LH1
Lin, CW1
Yang, SF1
Chien, MH1
Chen, LL1
Zhang, PP1
Wang, SM1
Costa-Junior, FR1
de Souza, AP1
Santos, MC1
Pigossi, SC1
Menezes-Silva, R1
Khaliq, S1
Deeley, K1
Letra, A1
e Silva, MR1
Moreira, PR2
da Costa, GC1
Saraiva, AM1
de Souza, PE1
Amormino, SA1
da Costa, JE1
Gollob, KJ1
Dutra, WO2
Yanatatsaneejit, P1
Boonsuwan, T1
Mutirangura, A1
Kitkumthorn, N1
Steinfath, M1
Seranski, P1
Singh, S1
Fiege, M1
Wappler, F1
Schulte Am Esch, J1
Scholz, J1
Kaneda, H1
Ohno, M1
Taguchi, J1
Togo, M1
Hashimoto, H1
Ogasawara, K1
Aizawa, T1
Ishizaka, N1
Nagai, R1
Hsieh, YY1
Chang, CC1
Tsai, FJ1
Tsai, HD1
Yeh, LS1
Lin, CC1
Tsai, CH1
Fukasawa, M1
Matsushita, K1
Kamiyama, M1
Mikami, Y1
Araki, I1
Yamagata, Z1
Takeda, M1
Souza, AP2
Brito, RB2
Benes, P1
Jurajda, M1
Zaloudík, J1
Izakovicová-Hollá, L1
Vácha, J1
Ingegni, T1
Nocentini, G1
Mariani, E1
Spazzafumo, L1
Polidori, MC1
Cherubini, A1
Catani, M1
Cadini, D1
Senin, U1
Mecocci, P1
Bojesen, SE1
Tybjaerg-Hansen, A1
Nordestgaard, BG1
Johansson, C1
Willeit, M1
Aron, L1
Smedh, C1
Ekholm, J1
Paunio, T1
Kieseppä, T1
Lichtermann, D1
Praschak-Rieder, N1
Neumeister, A1
Kasper, S1
Peltonen, L1
Adolfsson, R1
Partonen, T1
Schalling, M1
Gazouli, M1
Zacharatos, P1
Gorgoulis, V1
Mantzaris, G1
Papalambros, E1
Ikonomopoulos, J1
Huang, G1
Niu, T1
Peng, S1
Ling, D1
Liu, J1
Zhang, X1
Lin, SC1
Yen, JH1
Tsai, JJ1
Tsai, WC1
Ou, TT1
Liu, HW1
Chen, CJ1
Kikuchi, M1
Yamada, K1
Toyota, T1
Yoshikawa, T1
Camargo, LE1
Jiang, S1
Gitlin, J1
Deng, FM1
Liang, FX1
Lee, A1
Atala, A1
Bauer, SB1
Ehrlich, GD1
Feather, SA1
Goldberg, JD1
Goodship, JA1
Goodship, TH1
Hermanns, M1
Hu, FZ1
Jones, KE1
Malcolm, S1
Mendelsohn, C1
Preston, RA1
Retik, AB1
Schneck, FX1
Wright, V1
Ye, XY1
Woolf, AS1
Wu, XR1
Ostrer, H1
Shapiro, E1
Yu, J1
Sun, TT1
Sposito, AC1
Gonbert, S1
Turpin, G1
Chapman, MJ1
Thillet, J1
Zhang, L2
Rao, F1
Wessel, J1
Kennedy, BP1
Rana, BK1
Taupenot, L1
Lillie, EO1
Cockburn, M1
Schork, NJ1
Ziegler, MG1
O'Connor, DT1
Parodi, MB1
Di Crecchio, L1
Iacoviello, L1
Di Castelnuovo, A1
Gattone, M1
Pezzini, A1
Assanelli, D1
Lorenzet, R1
Del Zotto, E1
Colombo, M1
Napoleone, E1
Amore, C1
D'Orazio, A1
Padovani, A1
de Gaetano, G1
Giannuzzi, P1
Donati, MB1
Hong, CJ1
Liu, HC1
Liu, TY1
Liao, DL1
Tsai, SJ1
Johnson, K1
Russell, RG1
Wordsworth, BP1
Carr, AJ1
Terkeltaub, RA1
Brown, MA1
Tahara, M1
Aiba, A1
Yamazaki, M1
Ikeda, Y1
Goto, S1
Moriya, H1
Okawa, A1
Zhang, H1
Sun, K1
Song, Y1
Hui, R1
Huang, X1
Yuan, Z1
Shan, K1
Khalil, MS1
El Nahas, AM1
Blakemore, AI1
Weng, SW1
Liou, CW1
Lin, TK1
Wei, YH1
Lee, CF1
Eng, HL1
Chen, SD1
Liu, RT1
Chen, JF1
Chen, IY1
Chen, MH1
Wang, PW1
Mokone, GG1
Gajjar, M1
September, AV1
Schwellnus, MP1
Greenberg, J1
Noakes, TD1
Collins, M1
Nguyen, TV1
Esteban, LM1
White, CP1
Grant, SF1
Center, JR1
Gardiner, EM1
Eisman, JA1
Murillo, LS1
Peña, AS1
Hobbs, CA1
James, SJ1
Jernigan, S1
Melnyk, S1
Lu, Y1
Malik, S1
Cleves, MA1
Gottenberg, JE1
Sellam, J1
Ittah, M1
Lavie, F1
Proust, A1
Zouali, H1
Sordet, C1
Sibilia, J1
Kimberly, RP1
Mariette, X1
Miceli-Richard, C1
Denschlag, D1
Bentz, EK1
Hefler, L1
Pietrowski, D1
Zeillinger, R1
Tempfer, C1
Tong, D1
Mossbock, G1
Weger, M1
Faschinger, C1
Steinbrugger, I1
Temmel, W1
Schmut, O1
Renner, W1
Hufnagel, C1
Stanger, O1
Wong, CW1
Christen, T1
Pfenniger, A1
James, RW1
Kwak, BR1
Martinelli, N1
Trabetti, E2
Bassi, A1
Girelli, D1
Friso, S1
Pizzolo, F1
Sandri, M1
Malerba, G1
Pignatti, PF2
Corrocher, R1
Olivieri, O1
Gerhardt, A1
Scharf, RE1
Mikat-Drozdzynski, B1
Krüssel, JS1
Bender, HG1
Zotz, RB1
Lee, EJ1
Yoo, KJ1
Kim, SJ1
Lee, SH2
Cha, KY1
Baek, KH1
Yamada, Y1
Kato, K1
Hibino, T1
Yokoi, K1
Matsuo, H1
Segawa, T1
Watanabe, S1
Ichihara, S1
Yoshida, H1
Satoh, K1
Nozawa, Y1
Park, KS1
Nam, JH1
Choi, J1
Semmler, A1
Stein, RW1
Caplan, L1
Danilov, SM1
Klockgether, T1
Linnebank, M1
Noack, B1
Görgens, H1
Hoffmann, T1
Schackert, HK1
Bostanci, N1
Ilgenli, T1
Pirhan, DC1
Clarke, FM1
Marcenes, W1
Atilla, G1
Hughes, FJ1
McKay, IJ1
Listì, F1
Candore, G1
Balistreri, CR1
Caruso, M1
Incalcaterra, E1
Hoffmann, E1
Lio, D1
Caruso, C1
Genro, JP1
Zeni, C1
Polanczyk, GV1
Roman, T1
Rohde, LA1
Hutz, MH1
Bernardo, E1
Angiolillo, DJ1
Ramírez, C1
Cavallari, U1
Sabaté, M1
Hernández, R1
Moreno, R1
Escaned, J1
Alfonso, F1
Bañuelos, C1
Costa, MA1
Bass, TA1
Macaya, C1
Fernandez-Ortiz, A1
Muzík, J1
Vasku, A1
Vidarsdottir, L1
Bodvarsdottir, SK1
Hilmarsdottir, H1
Tryggvadottir, L1
Eyfjord, JE1
Schäfer, N1
Blaumeiser, B1
Becker, T1
Freudenberg-Hua, Y1
Hanneken, S1
Eigelshoven, S1
Schmael, C1
Lambert, J1
De Weert, J1
Kruse, R1
Betz, RC1
Lutz, UC1
Batra, A1
Kolb, W1
Machicao, F1
Maurer, S1
Köhnke, MD1
Sookoian, S1
Gianotti, TF1
González, CD1
Pirola, CJ1
Wang, CY1
Shen, YC1
Lo, FY1
Su, CH1
Lin, KH1
Tsai, HY1
Kuo, NW1
Fan, SS1
Vormittag, R1
Bencur, P1
Ay, C1
Tengler, T1
Vukovich, T1
Quehenberger, P1
Mannhalter, C1
Pabinger, I1
Markan, S1
Sachdeva, M1
Sehrawat, BS1
Kumari, S1
Jain, S1
Hoefle, G1
Muendlein, A1
Saely, CH1
Risch, L1
Rein, P1
Koch, L1
Schmid, F1
Aczel, S1
Marte, T1
Langer, P1
Drexel, H1
Serin, E1
Güçlü, M1
Ataç, FB1
Verdi, H1
Kayaselçuk, F1
Ozer, B1
Bilezikçi, B1
Yilmaz, U1
Boettiger, C1
Koch, W1
Mehilli, J1
Schoemig, A1
Kastrati, A1
Meirhaeghe, A1
Sandhu, MS1
McCarthy, MI1
de Groote, P1
Cottel, D1
Arveiler, D1
Ferrières, J1
Groves, CJ1
Hattersley, AT1
Hitman, GA1
Walker, M1
Wareham, NJ1
Amouyel, P1
de Sá, AR1
Xavier, GM1
Sampaio, I1
Kalapothakis, E1
Gomez, RS1
Richeti, F1
Noronha, RM1
Waetge, RT1
de Vasconcellos, JP1
de Souza, OF1
Kneipp, B1
Assis, N1
Rocha, MN1
Calliari, LE1
Longui, CA1
Monte, O1
de Melo, MB1
Nishijima, T1
Nakayama, M1
Yoshimura, M1
Abe, K1
Yamamuro, M1
Suzuki, S1
Shono, M1
Sugiyama, S1
Saito, Y1
Miyamoto, Y1
Nakao, K1
Yasue, H1
Ogawa, H1
Laing, ME1
Dicker, P1
Moloney, FJ1
Ho, WL1
Murphy, GM1
Conlon, P1
Whitehead, AS1
Shields, DC1
Qian, X1
Lu, Z1
Tan, M1
Liu, H1
Funke, S1
Morava, E1
Czakó, M1
Vida, G1
Ertl, T1
Kosztolányi, G1
Skibola, CF1
Nieters, A1
Bracci, PM1
Curry, JD1
Agana, L1
Skibola, DR1
Hubbard, A1
Becker, N1
Smith, MT1
Holly, EA1
Liu, L1
Dilworth, D1
Gao, L1
Monzon, J1
Summers, A1
Lassam, N1
Hogg, D1
Uemichi, T1
Uitti, RJ1
Koeppen, AH1
Donat, JR1
Benson, MD1
Harland, M1
Holland, EA1
Ghiorzo, P1
Mantelli, M1
Bianchi-Scarrà, G1
Goldstein, AM1
Tucker, MA1
Ponder, BA1
Mann, GJ1
Bishop, DT1
Newton Bishop, J1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Physiological and Psychological Effects of Testosterone During Severe Energy Deficit and Recovery: a Randomized, Placebo Controlled Trial[NCT02734238]Phase 453 participants (Actual)Interventional2016-04-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Body Composition at the End of Each Study Phase

Height was measured using a stadiometer. Weight was measured using a calibrated digital scale. Body composition was determined using dual-energy X-ray absorptiometry. These data were used to calculate fat-free body mass, fat mass, and total body tissue mass. (NCT02734238)
Timeframe: end of each study phase: Day 11 for Phase 1, Day 39 for Phase 2, up to Day 85 for Phase 3

,
Interventionkilograms (Least Squares Mean)
Total Body Mass at end of Phase 1Total Body Mass at end of Phase 2Total Body Mass at end of Phase 3Fat-free Mass at end of Phase 1Fat-free Mass at end of Phase 2Fat-free Mass at end of Phase 3Fat Mass at end of Phase 1Fat Mass at end of Phase 2Fat Mass at end of Phase 3
Energy Deficit78.373.376.558.358.060.516.812.212.8
Energy Deficit + Testosterone78.075.879.357.960.463.116.812.012.8

Reviews

10 reviews available for thymine and Genetic Predisposition

ArticleYear
Association between interleukin-4 gene -590 c/t, -33 c/t, and 70-base-pair polymorphisms and periodontitis susceptibility: a meta-analysis.
    Journal of periodontology, 2014, Volume: 85, Issue:11

    Topics: Alleles; Base Pairing; Cytosine; Genetic Predisposition to Disease; Genetic Variation; Genotype; Hum

2014
Quantitative assessment of the associations between interleukin-8 polymorphisms and periodontitis susceptibility.
    Journal of periodontology, 2015, Volume: 86, Issue:2

    Topics: Adenine; Asian People; Brazil; Cytosine; Ethnicity; Genetic Predisposition to Disease; Humans; Inter

2015
Association between interleukin-8 -251A/T polymorphism and risk of lung cancer: a meta-analysis.
    Cancer investigation, 2014, Volume: 32, Issue:10

    Topics: Adenine; Asian People; Computational Biology; Databases, Bibliographic; Genetic Association Studies;

2014
Meta-Analysis of Association Between Interleukin-1β C-511T Polymorphism and Chronic Periodontitis Susceptibility.
    Journal of periodontology, 2015, Volume: 86, Issue:6

    Topics: Alleles; Chronic Periodontitis; Cytosine; Gene Frequency; Genes, Dominant; Genes, Recessive; Genetic

2015
Positive association between IL-16 rs1131445 polymorphism and cancer risk: a meta-analysis.
    Minerva medica, 2016, Volume: 107, Issue:2

    Topics: Alleles; Asian People; Biomarkers, Tumor; Cytosine; Databases, Factual; Evidence-Based Medicine; Gen

2016
BsmI, TaqI, ApaI, and FokI polymorphisms in the vitamin D receptor gene and periodontitis: a meta-analysis of 15 studies including 1338 cases and 1302 controls.
    Journal of clinical periodontology, 2011, Volume: 38, Issue:3

    Topics: Adenine; Aggressive Periodontitis; Alleles; Chronic Periodontitis; Deoxyribonucleases, Type II Site-

2011
Association between vitamin D receptor polymorphisms and periodontitis: a meta-analysis.
    Journal of periodontology, 2012, Volume: 83, Issue:9

    Topics: Aggressive Periodontitis; Alleles; Asian People; Case-Control Studies; Chromosome Mapping; Chronic P

2012
Association of the C-344T aldosterone synthase gene variant with essential hypertension: a meta-analysis.
    Journal of hypertension, 2007, Volume: 25, Issue:1

    Topics: Aldosterone; Blood Pressure; Case-Control Studies; Cohort Studies; Cross-Sectional Studies; Cytochro

2007
Association between the T-381C polymorphism of the brain natriuretic peptide gene and risk of type 2 diabetes in human populations.
    Human molecular genetics, 2007, Jun-01, Volume: 16, Issue:11

    Topics: Adult; Aged; Animals; Case-Control Studies; Chlorocebus aethiops; COS Cells; Cytosine; Diabetes Mell

2007
A meta-analysis of association between C677T polymorphism in the methylenetetrahydrofolate reductase gene and hypertension.
    European journal of human genetics : EJHG, 2007, Volume: 15, Issue:12

    Topics: Asian People; Bias; Cytosine; Genetic Predisposition to Disease; Heterozygote; Humans; Hypertension;

2007

Trials

2 trials available for thymine and Genetic Predisposition

ArticleYear
Host and microbiological factors related to dental caries development.
    Caries research, 2008, Volume: 42, Issue:5

    Topics: C-Reactive Protein; Child; Cytosine; Dental Caries; Dental Caries Susceptibility; Dental Fistula; De

2008
MTHFR 677 CT/MTHFR 1298 CC genotypes are associated with increased risk of hypertension in Indians.
    Molecular and cellular biochemistry, 2007, Volume: 302, Issue:1-2

    Topics: Asian People; Case-Control Studies; Cytosine; Female; Folic Acid; Gene Frequency; Genetic Predisposi

2007

Other Studies

109 other studies available for thymine and Genetic Predisposition

ArticleYear
Factors Associated with Mutations: Their Matching Rates to Cardiovascular and Neurological Diseases.
    International journal of molecular sciences, 2021, May-11, Volume: 22, Issue:10

    Topics: Adenine; Cardiovascular Diseases; Genetic Predisposition to Disease; Humans; Mutation; Nervous Syste

2021
Polymorphic CT dinucleotide repeat in the GATA3 gene and risk of breast cancer in Iranian women.
    Medical oncology (Northwood, London, England), 2013, Volume: 30, Issue:2

    Topics: Adult; Aged; Aged, 80 and over; Biomarkers, Tumor; Breast Neoplasms; Case-Control Studies; Cytosine;

2013
Association of cell adhesion molecule gene polymorphisms with recurrent aphthous stomatitis.
    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:10

    Topics: Adenine; Adult; Alleles; Cell Adhesion Molecules; Cohort Studies; Cytosine; E-Selectin; Female; Gene

2013
Clinical outcomes of periodontal therapy are not influenced by the ATC/TTC haplotype in the IL8 gene.
    Journal of periodontal research, 2014, Volume: 49, Issue:4

    Topics: Adenine; Adult; Chronic Periodontitis; Cytosine; Dental Plaque Index; Female; Follow-Up Studies; Gen

2014
Th1 and Th2 polymorphisms in Sjögren's syndrome and rheumatoid arthritis.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2014, Volume: 43, Issue:6

    Topics: Adenine; Adult; Aged; Antibodies, Antinuclear; Arthritis, Rheumatoid; Autoantigens; Case-Control Stu

2014
Association between cyclooxygenase-2 gene polymorphisms and head and neck squamous cell carcinoma risk.
    The Journal of craniofacial surgery, 2014, Volume: 25, Issue:2

    Topics: 3' Untranslated Regions; Adenine; Adult; Aged; Alcohol Drinking; Carcinoma, Squamous Cell; Case-Cont

2014
The axis inhibition protein 2 polymorphisms and non-syndromic orofacial clefts susceptibility in a Chinese Han population.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2014, Volume: 43, Issue:7

    Topics: Adenine; Axin Protein; Case-Control Studies; China; Chromosome Mapping; Cleft Lip; Cleft Palate; Eth

2014
Identification of genetic risk factors for maxillary lateral incisor agenesis.
    Journal of dental research, 2014, Volume: 93, Issue:5

    Topics: Adenine; Anodontia; Axin Protein; Case-Control Studies; Cytosine; Ectodysplasins; Female; Fibroblast

2014
The association of CSF-1 gene polymorphism with chronic periodontitis in the Han Chinese population.
    Journal of periodontology, 2014, Volume: 85, Issue:8

    Topics: Adult; Aged; Alveolar Bone Loss; Case-Control Studies; China; Chronic Periodontitis; Cytosine; Ethni

2014
Association study of single nucleotide polymorphisms of MAFB with non-syndromic cleft lip with or without cleft palate in a population in Heilongjiang Province, northern China.
    The British journal of oral & maxillofacial surgery, 2014, Volume: 52, Issue:8

    Topics: Adenine; Case-Control Studies; Child; Child, Preschool; China; Cleft Lip; Cleft Palate; Cytosine; Et

2014
Genetic variants in AKT1 gene were associated with risk and survival of OSCC in Chinese Han Population.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2015, Volume: 44, Issue:1

    Topics: Aged; Alleles; Carcinoma, Squamous Cell; China; Cohort Studies; Cytosine; Disease Progression; Ethni

2015
Interleukin 1β (+3954, -511 and -31) polymorphism in chronic periodontitis patients from North India.
    Acta odontologica Scandinavica, 2015, Volume: 73, Issue:5

    Topics: Adult; Case-Control Studies; Chronic Periodontitis; Cytosine; Female; Gene Frequency; Genetic Predis

2015
Genetic association for caries susceptibility among cleft lip and/or palate individuals.
    The journal of contemporary dental practice, 2014, May-01, Volume: 15, Issue:3

    Topics: Adolescent; Bone Morphogenetic Protein 4; Child; Child, Preschool; Cleft Lip; Cleft Palate; Cohort S

2014
RAGE gene polymorphism and environmental factor in the risk of oral cancer.
    Journal of dental research, 2015, Volume: 94, Issue:3

    Topics: Adenine; Areca; Base Pairing; Base Sequence; Carcinogenesis; Case-Control Studies; Cytosine; Female;

2015
Enamel formation genes associated with dental erosive wear.
    Caries research, 2015, Volume: 49, Issue:3

    Topics: Adolescent; Amelogenesis; Amelogenin; Cytosine; Dental Enamel Proteins; Extracellular Matrix Protein

2015
A single nucleotide polymorphism in 3' untranslated region of epithelial growth factor receptor confers risk for pulmonary hypertension in chronic obstructive pulmonary disease.
    Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 2015, Volume: 36, Issue:1

    Topics: 3' Untranslated Regions; Aged; Aged, 80 and over; Cells, Cultured; Cytosine; ErbB Receptors; Female;

2015
Lack of association of matrix metalloproteinase-9 promoter gene polymorphism in obstructive sleep apnea syndrome.
    Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery, 2015, Volume: 43, Issue:7

    Topics: Adult; Body Mass Index; Cross-Sectional Studies; Cytosine; Female; Gene Frequency; Genetic Predispos

2015
Interferon-gamma and interleukin-12 gene polymorphisms and their relation to aggressive and chronic periodontitis and key periodontal pathogens.
    Journal of periodontology, 2008, Volume: 79, Issue:8

    Topics: Adenine; Adult; Age Factors; Aggregatibacter actinomycetemcomitans; Alleles; Bacteria; Cytosine; Fem

2008
The association of interleukin-4 haplotypes with chronic periodontitis in a Czech population.
    Journal of periodontology, 2008, Volume: 79, Issue:10

    Topics: 5' Flanking Region; Adult; Alleles; Base Pairing; Case-Control Studies; Chronic Periodontitis; Cytos

2008
E-selectin and L-selectin polymorphisms in patients with periodontitis.
    Journal of periodontal research, 2009, Volume: 44, Issue:1

    Topics: Adenine; Adolescent; Adult; Aggressive Periodontitis; Alleles; Arginine; Chronic Periodontitis; Cyto

2009
Analysis of the association of IL1B (C+3954T) and IL1RN (intron 2) polymorphisms with dental implant loss in a Brazilian population.
    Clinical oral implants research, 2009, Volume: 20, Issue:2

    Topics: Adult; Aged; Aged, 80 and over; Brazil; Case-Control Studies; Cytosine; Dental Implants; Dental Rest

2009
Polymorphisms of XRCC1 gene and risk of gastric cardiac adenocarcinoma.
    Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus, 2009, Volume: 22, Issue:5

    Topics: Adenine; Adenocarcinoma; Adult; Aged; Arginine; Cardia; Case-Control Studies; Codon; Cytosine; DNA R

2009
Formylpeptide receptor single nucleotide polymorphism 348T>C and its relationship to polymorphonuclear leukocyte chemotaxis in aggressive periodontitis.
    Journal of periodontology, 2009, Volume: 80, Issue:9

    Topics: 5' Flanking Region; Adolescent; Adult; Aggressive Periodontitis; Black or African American; Chemotax

2009
Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation.
    Journal of the neurological sciences, 2009, Dec-15, Volume: 287, Issue:1-2

    Topics: Atrophy; Base Sequence; Brain; Brain Chemistry; Cytosine; Disease Progression; DNA; DNA Mutational A

2009
Interleukin-1 gene cluster polymorphisms associated with periodontal disease in type 2 diabetes.
    Journal of periodontology, 2009, Volume: 80, Issue:10

    Topics: Adult; Age Factors; Aged; Alleles; Case-Control Studies; Chronic Periodontitis; Cytosine; Dental Pla

2009
Genetic risk factors for periodontitis in a Japanese population.
    Journal of dental research, 2009, Volume: 88, Issue:12

    Topics: Adult; Age Factors; Aggressive Periodontitis; Alveolar Bone Loss; Case-Control Studies; Chronic Peri

2009
Analysis of interactions between genetic variants of BMP4 and environmental factors with nonsyndromic cleft lip with or without cleft palate susceptibility.
    International journal of oral and maxillofacial surgery, 2010, Volume: 39, Issue:1

    Topics: Adolescent; Adult; Alcohol Drinking; Biomarkers; Bone Morphogenetic Protein 4; Case-Control Studies;

2010
O6-methylguanine-DNA methyltransferase gene coding region polymorphisms and oral cancer risk.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2010, Volume: 39, Issue:8

    Topics: Age Factors; Carcinoma, Squamous Cell; Case-Control Studies; Codon; Cytosine; Disease-Free Survival;

2010
Polymorphisms in CYP2A13 and UGT1A7 genes and head and neck cancer susceptibility in North Indians.
    Oral diseases, 2010, Volume: 16, Issue:8

    Topics: Alcohol Drinking; Aryl Hydrocarbon Hydroxylases; Carcinogens; Chromatography, High Pressure Liquid;

2010
Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients.
    European journal of oral sciences, 2010, Volume: 118, Issue:3

    Topics: Adenine; Case-Control Studies; Chromosome Mapping; Chromosomes, Human, Pair 10; Cleft Lip; Cleft Pal

2010
Investigation of interleukin-13 gene polymorphisms in individuals with chronic and generalized aggressive periodontitis in a Taiwanese (Chinese) population.
    Journal of periodontal research, 2010, Volume: 45, Issue:5

    Topics: Adult; Aggressive Periodontitis; Case-Control Studies; Chi-Square Distribution; China; Chronic Perio

2010
Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts.
    European journal of oral sciences, 2010, Volume: 118, Issue:4

    Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Alleles; Betaine-Homocysteine S-Methyltra

2010
CRISPLD2 polymorphisms are associated with non-syndromic cleft lip with or without cleft palate in a northern Chinese population.
    European journal of oral sciences, 2010, Volume: 118, Issue:4

    Topics: Adolescent; Adult; Case-Control Studies; Cell Adhesion Molecules; Child; Child, Preschool; China; Cl

2010
Polymorphisms in the Matrilin-1 gene and risk of mandibular prognathism in Koreans.
    Journal of dental research, 2010, Volume: 89, Issue:11

    Topics: Adenine; Adult; Cartilage Oligomeric Matrix Protein; Case-Control Studies; Cytosine; Exons; Extracel

2010
Association of Wnt3A gene variants with non-syndromic cleft lip with or without cleft palate in Chinese population.
    Archives of oral biology, 2011, Volume: 56, Issue:1

    Topics: Adenine; Alleles; Case-Control Studies; China; Cleft Lip; Cleft Palate; Female; Gene Frequency; Gene

2011
Association of IL1 gene polymorphisms with chronic periodontitis in Brazilians.
    Archives of oral biology, 2011, Volume: 56, Issue:1

    Topics: Adult; Asian People; Black People; Brazil; Chronic Periodontitis; Cytosine; Ethnicity; Female; Gene

2011
Single nucleotide polymorphisms of pattern recognition receptors and chronic periodontitis.
    Journal of periodontal research, 2011, Volume: 46, Issue:2

    Topics: Adenine; Chronic Periodontitis; Cytosine; Dental Plaque Index; Female; Gene Frequency; Genetic Predi

2011
Functionally significant nicotine acetylcholine receptor subunit α5 promoter haplotypes are associated with susceptibility to lung cancer in Chinese.
    Cancer, 2011, Oct-15, Volume: 117, Issue:20

    Topics: Adult; Aged; Asian People; Case-Control Studies; China; Cytosine; Female; Gene Deletion; Gene Freque

2011
Functional variants of IL4 and IL6 genes and risk of tobacco-related oral carcinoma in high-risk Asian Indians.
    Oral diseases, 2011, Volume: 17, Issue:7

    Topics: Adult; Aged; Aged, 80 and over; Asian People; Carcinoma, Squamous Cell; Case-Control Studies; Cytosi

2011
Impact of interleukin-8 gene polymorphisms and environmental factors on oral cancer susceptibility in Taiwan.
    Oral diseases, 2012, Volume: 18, Issue:3

    Topics: 3' Untranslated Regions; Adenine; Areca; Carcinogens; Carcinoma, Squamous Cell; Case-Control Studies

2012
Influence of MMP-8 promoter polymorphism in early osseointegrated implant failure.
    Clinical oral investigations, 2013, Volume: 17, Issue:1

    Topics: Alleles; Base Pairing; Cytosine; Dental Implants; Dental Restoration Failure; Gene Frequency; Geneti

2013
Genetic association study between Interleukin 10 gene and dental implant loss.
    Archives of oral biology, 2012, Volume: 57, Issue:9

    Topics: Adenine; Alleles; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non-Steroidal; Cardiovascular

2012
Influence of cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphisms in periodontitis.
    Archives of oral biology, 2012, Volume: 57, Issue:9

    Topics: Adenine; Adolescent; Adult; Aged; Aggressive Periodontitis; Alleles; Chronic Periodontitis; CTLA-4 A

2012
Genetic susceptibility to periapical disease: conditional contribution of MMP2 and MMP3 genes to the development of periapical lesions and healing response.
    Journal of endodontics, 2012, Volume: 38, Issue:5

    Topics: Adenine; Dental Caries; Dental Pulp Necrosis; Dentin; Female; Gene Frequency; Genetic Predisposition

2012
Association of CD28 and CTLA-4 gene polymorphisms with aggressive periodontitis in Brazilians.
    Oral diseases, 2013, Volume: 19, Issue:6

    Topics: Adenine; Adolescent; Adult; Aged; Aggressive Periodontitis; Brazil; CD28 Antigens; Chronic Periodont

2013
XRCC1 gene polymorphisms and risk of ameloblastoma.
    Archives of oral biology, 2013, Volume: 58, Issue:6

    Topics: Adenine; Adult; Ameloblastoma; Arginine; Codon; DNA Repair; DNA-Binding Proteins; Female; Gene Frequ

2013
Evidence for a spontaneous C1840-T mutation in the RYR1 gene after DNA fingerprinting in a malignant hyperthermia susceptible family.
    Naunyn-Schmiedeberg's archives of pharmacology, 2002, Volume: 366, Issue:4

    Topics: Adolescent; Adult; Aged; Child; Cytosine; DNA Fingerprinting; Female; Genetic Predisposition to Dise

2002
Heme oxygenase-1 gene promoter polymorphism is associated with coronary artery disease in Japanese patients with coronary risk factors.
    Arteriosclerosis, thrombosis, and vascular biology, 2002, Oct-01, Volume: 22, Issue:10

    Topics: Alleles; Coronary Angiography; Coronary Artery Disease; Dinucleotide Repeats; Female; Gene Expressio

2002
Estrogen receptor thymine-adenine dinucleotide repeat polymorphism is associated with susceptibility to leiomyoma.
    Fertility and sterility, 2003, Volume: 79, Issue:1

    Topics: Adenine; Dinucleotide Repeats; Female; Genetic Predisposition to Disease; Genotype; Humans; Leiomyom

2003
The methylentetrahydrofolate reductase C677T point mutation is a risk factor for vascular access thrombosis in hemodialysis patients.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2003, Volume: 41, Issue:3

    Topics: Arteriovenous Shunt, Surgical; Cross-Sectional Studies; Cytosine; Female; Genetic Predisposition to

2003
Investigation of IL4 gene polymorphism in individuals with different levels of chronic periodontitis in a Brazilian population.
    Journal of clinical periodontology, 2003, Volume: 30, Issue:4

    Topics: Adult; Alleles; Black People; Brazil; Chi-Square Distribution; Chronic Disease; Cytosine; Ethnicity;

2003
C766T low-density lipoprotein receptor-related protein 1 (LRP1) gene polymorphism and susceptibility to breast cancer.
    Breast cancer research : BCR, 2003, Volume: 5, Issue:3

    Topics: Adult; Aged; Aged, 80 and over; Alleles; Biomarkers, Tumor; Breast Neoplasms; Cytosine; Female; Gene

2003
Cathepsin D polymorphism in Italian elderly subjects with sporadic late-onset Alzheimer's disease.
    Dementia and geriatric cognitive disorders, 2003, Volume: 16, Issue:3

    Topics: Age of Onset; Aged; Alleles; Alzheimer Disease; Apolipoproteins E; Case-Control Studies; Cathepsin D

2003
Integrin beta3 Leu33Pro homozygosity and risk of cancer.
    Journal of the National Cancer Institute, 2003, Aug-06, Volume: 95, Issue:15

    Topics: Adult; Aged; Aged, 80 and over; Alleles; Animals; Cytosine; Denmark; Disease Progression; Female; Ge

2003
Seasonal affective disorder and the G-protein beta-3-subunit C825T polymorphism.
    Biological psychiatry, 2004, Feb-01, Volume: 55, Issue:3

    Topics: Alleles; Case-Control Studies; Cytosine; Female; Genetic Predisposition to Disease; Genotype; Hetero

2004
The C3435T MDR1 gene polymorphism is not associated with susceptibility for ulcerative colitis in Greek population.
    Gastroenterology, 2004, Volume: 126, Issue:1

    Topics: Colitis, Ulcerative; Cytosine; Genes, MDR; Genetic Predisposition to Disease; Greece; Humans; Polymo

2004
Association between the interleukin-1beta C(-511)T polymorphism and blood pressure in a Chinese hypertensive population.
    Immunology letters, 2004, Feb-15, Volume: 91, Issue:2-3

    Topics: Asian People; Blood Pressure; Cytosine; Female; Genetic Predisposition to Disease; Humans; Hypertens

2004
Association of a programmed death 1 gene polymorphism with the development of rheumatoid arthritis, but not systemic lupus erythematosus.
    Arthritis and rheumatism, 2004, Volume: 50, Issue:3

    Topics: Alleles; Antigens, CD; Antigens, Surface; Apoptosis Regulatory Proteins; Arthritis, Rheumatoid; Cyto

2004
C18orf1 located on chromosome 18p11.2 may confer susceptibility to schizophrenia.
    Journal of medical and dental sciences, 2003, Volume: 50, Issue:3

    Topics: Adult; Alleles; Case-Control Studies; Centromere; Chromosomes, Human, Pair 18; Cytosine; Exons; Fema

2003
Interleukin 10 gene promoter polymorphisms are associated with chronic periodontitis.
    Journal of clinical periodontology, 2004, Volume: 31, Issue:6

    Topics: Adenine; Adult; Chronic Disease; Cytosine; Female; Gene Frequency; Genetic Predisposition to Disease

2004
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity.
    Kidney international, 2004, Volume: 66, Issue:1

    Topics: Alanine; Amino Acid Substitution; Animals; Base Sequence; Case-Control Studies; Chromosome Mapping;

2004
Common promoter C516T polymorphism in the ApoB gene is an independent predictor of carotid atherosclerotic disease in subjects presenting a broad range of plasma cholesterol levels.
    Arteriosclerosis, thrombosis, and vascular biology, 2004, Volume: 24, Issue:11

    Topics: Apolipoproteins; Apolipoproteins B; Carotid Artery Diseases; Cholesterol; Cytosine; Female; Genetic

2004
Functional allelic heterogeneity and pleiotropy of a repeat polymorphism in tyrosine hydroxylase: prediction of catecholamines and response to stress in twins.
    Physiological genomics, 2004, Nov-17, Volume: 19, Issue:3

    Topics: Adenine; Adolescent; Adult; Age Factors; Aged; Aged, 80 and over; Alleles; Autonomic Nervous System;

2004
Hyperhomocysteinemia in central retinal vein occlusion in young adults.
    Seminars in ophthalmology, 2003, Volume: 18, Issue:3

    Topics: Adult; Case-Control Studies; Cytosine; Female; Genetic Predisposition to Disease; Homozygote; Humans

2003
Polymorphisms of the interleukin-1beta gene affect the risk of myocardial infarction and ischemic stroke at young age and the response of mononuclear cells to stimulation in vitro.
    Arteriosclerosis, thrombosis, and vascular biology, 2005, Volume: 25, Issue:1

    Topics: Adolescent; Adult; Child; Child, Preschool; Cytosine; Female; Genetic Predisposition to Disease; Hum

2005
Association studies of the adenosine A2a receptor (1976T > C) genetic polymorphism in Parkinson's disease and schizophrenia.
    Journal of neural transmission (Vienna, Austria : 1996), 2005, Volume: 112, Issue:11

    Topics: Age Distribution; Age of Onset; Aged; Asian People; Base Sequence; Brain; Brain Chemistry; Cytosine;

2005
Association of sporadic chondrocalcinosis with a -4-basepair G-to-A transition in the 5'-untranslated region of ANKH that promotes enhanced expression of ANKH protein and excess generation of extracellular inorganic pyrophosphate.
    Arthritis and rheumatism, 2005, Volume: 52, Issue:4

    Topics: 5' Untranslated Regions; Cell Line, Transformed; Chondrocalcinosis; Chondrocytes; Diphosphates; DNA

2005
The extent of ossification of posterior longitudinal ligament of the spine associated with nucleotide pyrophosphatase gene and leptin receptor gene polymorphisms.
    Spine, 2005, Apr-15, Volume: 30, Issue:8

    Topics: Adenine; Case-Control Studies; Female; Gene Deletion; Genetic Predisposition to Disease; Genetic Var

2005
The 825C/T polymorphism of G-protein beta3 subunit gene and risk of ischaemic stroke.
    Journal of human hypertension, 2005, Volume: 19, Issue:9

    Topics: Aged; Asian People; Brain Ischemia; Case-Control Studies; Cytosine; Female; Gene Frequency; Genetic

2005
Association of apolipoprotein J gene 866C-->T polymorphism with preeclampsia and essential hypertension.
    Gynecologic and obstetric investigation, 2005, Volume: 60, Issue:3

    Topics: Adult; Amino Acid Sequence; Case-Control Studies; China; Clusterin; Cytosine; DNA Mutational Analysi

2005
Transforming growth factor-beta1 SNPs: genetic and phenotypic correlations in progressive kidney insufficiency.
    Nephron. Experimental nephrology, 2005, Volume: 101, Issue:2

    Topics: Adult; Aged; Aged, 80 and over; Arginine; Case-Control Studies; Cytosine; Disease Progression; Femal

2005
Association of mitochondrial deoxyribonucleic acid 16189 variant (T->C transition) with metabolic syndrome in Chinese adults.
    The Journal of clinical endocrinology and metabolism, 2005, Volume: 90, Issue:9

    Topics: Aged; Asian People; Blood Glucose; Case-Control Studies; Cytosine; Diabetes Mellitus, Type 2; DNA, M

2005
The guanine-thymine dinucleotide repeat polymorphism within the tenascin-C gene is associated with achilles tendon injuries.
    The American journal of sports medicine, 2005, Volume: 33, Issue:7

    Topics: Achilles Tendon; Adult; Biomarkers; Case-Control Studies; Dinucleotide Repeats; Gene Frequency; Gene

2005
Contribution of the collagen I alpha1 and vitamin D receptor genes to the risk of hip fracture in elderly women.
    The Journal of clinical endocrinology and metabolism, 2005, Volume: 90, Issue:12

    Topics: Aged; Aged, 80 and over; Aging; Bone Density; Cohort Studies; Collagen Type I; Collagen Type I, alph

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 Su

2005
Congenital heart defects, maternal homocysteine, smoking, and the 677 C>T polymorphism in the methylenetetrahydrofolate reductase gene: evaluating gene-environment interactions.
    American journal of obstetrics and gynecology, 2006, Volume: 194, Issue:1

    Topics: Adult; Case-Control Studies; Cytosine; Female; Genetic Predisposition to Disease; Genotype; Heart De

2006
No evidence for an association between the -871 T/C promoter polymorphism in the B-cell-activating factor gene and primary Sjögren's syndrome.
    Arthritis research & therapy, 2006, Volume: 8, Issue:1

    Topics: Aged; B-Cell Activating Factor; Case-Control Studies; Cytosine; Female; Gene Frequency; Genetic Pred

2006
Genotype distribution of estrogen receptor-alpha, catechol-O-methyltransferase, and cytochrome P450 17 gene polymorphisms in Caucasian women with uterine leiomyomas.
    Fertility and sterility, 2006, Volume: 85, Issue:2

    Topics: Adenine; Adult; Case-Control Studies; Catechol O-Methyltransferase; Cytosine; Estrogen Receptor alph

2006
Methylenetetrahydrofolatereductase (MTHFR) 677C>T polymorphism and open angle glaucoma.
    Molecular vision, 2006, Apr-17, Volume: 12

    Topics: Aged; Aged, 80 and over; Case-Control Studies; Cytosine; Exfoliation Syndrome; Female; Gene Frequenc

2006
Do allelic variants of the connexin37 1019 gene polymorphism differentially predict for coronary artery disease and myocardial infarction?
    Atherosclerosis, 2007, Volume: 191, Issue:2

    Topics: Aged; Alleles; Connexins; Coronary Angiography; Coronary Artery Disease; Cytosine; Female; Gap Junct

2007
The -1131 T>C and S19W APOA5 gene polymorphisms are associated with high levels of triglycerides and apolipoprotein C-III, but not with coronary artery disease: an angiographic study.
    Atherosclerosis, 2007, Volume: 191, Issue:2

    Topics: Adult; Aged; Apolipoprotein A-V; Apolipoprotein C-III; Apolipoproteins A; Coronary Angiography; Coro

2007
Maternal IVS1-401 T allele of the estrogen receptor alpha is an independent predictor of late fetal loss.
    Fertility and sterility, 2006, Volume: 86, Issue:2

    Topics: Abortion, Spontaneous; Adenine; Alleles; Case-Control Studies; Cytosine; Estrogen Receptor alpha; Fa

2006
Single nucleotide polymorphism in exon 17 of the insulin receptor gene is not associated with polycystic ovary syndrome in a Korean population.
    Fertility and sterility, 2006, Volume: 86, Issue:2

    Topics: Adult; Asian People; Case-Control Studies; Cytosine; Exons; Female; Gene Frequency; Genetic Predispo

2006
Prediction of genetic risk for metabolic syndrome.
    Atherosclerosis, 2007, Volume: 191, Issue:2

    Topics: Aged; Apolipoprotein A-V; Apolipoproteins A; Asian People; Cholesterol, HDL; Cytosine; Female; Genet

2007
The short vitamin D receptor is associated with increased risk for generalized aggressive periodontitis.
    Journal of clinical periodontology, 2006, Volume: 33, Issue:8

    Topics: Adenine; Adult; Alveolar Bone Loss; Codon; Cytosine; Exons; Female; Gene Frequency; Genetic Predispo

2006
Hereditary hyper-ACE-emia due to the Pro1199Leu mutation of somatic ACE as a potential pitfall in diagnosis: a first family outside Europe.
    Clinical chemistry and laboratory medicine, 2006, Volume: 44, Issue:9

    Topics: Cytosine; Europe; Female; Genetic Predisposition to Disease; Granuloma; Humans; Leucine; Male; Pepti

2006
CARD15 gene variants in aggressive periodontitis.
    Journal of clinical periodontology, 2006, Volume: 33, Issue:11

    Topics: Adult; Arginine; Base Sequence; Case-Control Studies; Cytosine; Disease Susceptibility; DNA Transpos

2006
Relationship between IL-1A polymorphisms and gingival overgrowth in renal transplant recipients receiving Cyclosporin A.
    Journal of clinical periodontology, 2006, Volume: 33, Issue:11

    Topics: Adult; Age Factors; Alleles; Cyclosporine; Cytosine; Female; Genetic Predisposition to Disease; Geno

2006
Connexin37 1019 gene polymorphism in myocardial infarction patients and centenarians.
    Atherosclerosis, 2007, Volume: 191, Issue:2

    Topics: Aged, 80 and over; Alleles; Connexins; Cytosine; Gap Junction alpha-4 Protein; Gene Frequency; Genet

2007
A promoter polymorphism (-839 C > T) at the dopamine transporter gene is associated with attention deficit/hyperactivity disorder in Brazilian children.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2007, Mar-05, Volume: 144B, Issue:2

    Topics: Attention Deficit Disorder with Hyperactivity; Brazil; Child; Cytosine; Dopamine Plasma Membrane Tra

2007
Influence of the CD14 C260T promoter polymorphism on C-reactive protein levels in patients with coronary artery disease.
    The American journal of cardiology, 2006, Nov-01, Volume: 98, Issue:9

    Topics: Adult; Aged; Alleles; Analysis of Variance; Biomarkers; C-Reactive Protein; Coronary Artery Disease;

2006
Functional polymorphisms in the matrix metalloproteinase-9 gene in relation to severity of chronic periodontitis.
    Journal of periodontology, 2006, Volume: 77, Issue:11

    Topics: Adult; Alleles; Case-Control Studies; Chronic Disease; Cytosine; Czech Republic; Female; Gene Freque

2006
Breast cancer risk associated with AURKA 91T -->A polymorphism in relation to BRCA mutations.
    Cancer letters, 2007, Jun-08, Volume: 250, Issue:2

    Topics: Adenine; Alleles; Aurora Kinase A; Aurora Kinases; Case-Control Studies; Female; Genes, BRCA1; Genes

2007
Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata.
    International journal of immunogenetics, 2006, Volume: 33, Issue:6

    Topics: Adolescent; Adult; Aged; Alopecia Areata; Case-Control Studies; Child; Cytosine; Female; Genetic Pre

2006
Methylenetetrahydrofolate reductase C677T-polymorphism and its association with alcohol withdrawal seizure.
    Alcoholism, clinical and experimental research, 2006, Volume: 30, Issue:12

    Topics: Adult; Aged; Alcohol Drinking; Alcohol Withdrawal Seizures; Alcoholism; Case-Control Studies; Cytosi

2006
Polymorphism in the IL-1alpha (-889) locus associated with elevated risk of primary open angle glaucoma.
    Molecular vision, 2006, Nov-15, Volume: 12

    Topics: Adult; Aged; Aged, 80 and over; Alleles; Asian People; Cytosine; Female; Genetic Predisposition to D

2006
Low-density lipoprotein receptor-related protein 1 polymorphism 663 C > T affects clotting factor VIII activity and increases the risk of venous thromboembolism.
    Journal of thrombosis and haemostasis : JTH, 2007, Volume: 5, Issue:3

    Topics: Case-Control Studies; Cytosine; Factor VIII; Female; Gene Frequency; Genetic Predisposition to Disea

2007
The -11377 C>G promoter variant of the adiponectin gene, prevalence of coronary atherosclerosis, and incidence of vascular events in men.
    Thrombosis and haemostasis, 2007, Volume: 97, Issue:3

    Topics: Adiponectin; Cardiovascular Diseases; Cohort Studies; Coronary Angiography; Coronary Artery Disease;

2007
Methylenetetrahydrofolate reductase C677T mutation and nonalcoholic fatty liver disease.
    Digestive diseases and sciences, 2007, Volume: 52, Issue:5

    Topics: Adult; Case-Control Studies; Cytosine; Disease Progression; Fatty Liver; Female; Gene Frequency; Gen

2007
Glycoprotein VI polymorphisms and outcome after percutaneous coronary interventions.
    Thrombosis and haemostasis, 2007, Volume: 97, Issue:4

    Topics: Angioplasty, Balloon, Coronary; CD36 Antigens; Cohort Studies; Coronary Artery Disease; Coronary Res

2007
Association of CD14, IL1B, IL6, IL10 and TNFA functional gene polymorphisms with symptomatic dental abscesses.
    International endodontic journal, 2007, Volume: 40, Issue:7

    Topics: Abscess; Adenine; Adult; Age Factors; Case-Control Studies; Chromosome Mapping; Cross-Sectional Stud

2007
Evaluation of AC(n) and C(-106)T polymorphisms of the aldose reductase gene in Brazilian patients with DM1 and susceptibility to diabetic retinopathy.
    Molecular vision, 2007, May-23, Volume: 13

    Topics: Adolescent; Adult; Aldehyde Reductase; Brazil; Child; Cytosine; Diabetes Mellitus, Type 1; Diabetic

2007
The endothelial nitric oxide synthase gene -786T/C polymorphism is a predictive factor for reattacks of coronary spasm.
    Pharmacogenetics and genomics, 2007, Volume: 17, Issue:8

    Topics: Adult; Aged; Calcium Channel Blockers; Cause of Death; Coronary Artery Disease; Coronary Vasospasm;

2007
Association of methylenetetrahydrofolate reductase polymorphism and the risk of squamous cell carcinoma in renal transplant patients.
    Transplantation, 2007, Jul-15, Volume: 84, Issue:1

    Topics: Alleles; Carcinoma, Squamous Cell; Cytosine; Female; Genetic Predisposition to Disease; Genotype; Gu

2007
[Metabolic bone disease in premature infants and genetic polymorphisms].
    Orvosi hetilap, 2007, Oct-14, Volume: 148, Issue:41

    Topics: Adenine; Alkaline Phosphatase; Biomarkers; Bone and Bones; Bone Density; Bone Diseases, Metabolic; B

2007
A functional TNFRSF5 gene variant is associated with risk of lymphoma.
    Blood, 2008, Apr-15, Volume: 111, Issue:8

    Topics: Adult; Aged; CD40 Antigens; CD40 Ligand; Confidence Intervals; Cytosine; Dendritic Cells; Genetic Pr

2008
Mutation of the CDKN2A 5' UTR creates an aberrant initiation codon and predisposes to melanoma.
    Nature genetics, 1999, Volume: 21, Issue:1

    Topics: 5' Untranslated Regions; Alleles; Cell Line, Transformed; Codon, Initiator; Cyclin-Dependent Kinase

1999
Oculoleptomeningeal amyloidosis associated with a new transthyretin variant Ser64.
    Archives of neurology, 1999, Volume: 56, Issue:9

    Topics: Adolescent; Adult; Amyloidosis; Autoradiography; Central Nervous System Diseases; Cytosine; Genetic

1999
Mutation screening of the CDKN2A promoter in melanoma families.
    Genes, chromosomes & cancer, 2000, Volume: 28, Issue:1

    Topics: Adolescent; Adult; Aged; Cyclin-Dependent Kinase Inhibitor p16; DNA, Neoplasm; Genetic Predispositio

2000