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haplotype DRB1 * 034-DQB1 * 02-DQA1 * 0501. Clin. Endocrinol. (Oxf) , 51 , 115-118. John, S., Worthington, J. (2001). Genetic epidemiology. Approaches to the genetic analysis of rheumatoid arthritis. Arthritis Res. , 3 , 216-220. Kalis, M., Sjakste, T., Sjakste, N., Luthman, H., Groop, L. (2002). Association study between (TG) repeat polymorphism in PSMA6 gene and type II dibetes mellitus in Botnia. Biologija , 2 , 12-14. Kamnasaran, D., Cox, D.W. (2002). Current Status of Human Chromosome 14. J. Med. Genet. , 39 , 81-91. Kozak, M. (1997). Recognition of AUG and

, Nozaki Y, Yukawa W, Nakashige R, Yamaguchi D, Ishibashi H, Yonekura M, Nakami Y, Takayama S, Endo T, Saruwatari T, Yagura M, Yoshikawa Y, Fujimoto K, Oka A, Chiku S, Linsen SE, Giphart MJ, Kulski JK, Fukazawa T, Hashimoto H, Kimura M, Hoshina Y, Suzuki Y, Hotta T, Mochida J, Minezaki T, Komai K, Shiozawa S, Taniguchi A, Yamanaka H, Kamatani N, Gojobori T, Bahram S, Inoko H. Whole genome association study of rheumatoid arthritis using 27 039 microsatellites. Hum Mol Genet 2005; 14(16): 2305-2321. Thorisson GA, Stein LD. The SNP Consortium website: past, present and

PF, et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 2009; 460: 748-52. 10. Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, et al. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Mol Psychiatry 2009; 14: 774-85. 11. Li J, Zhou G, Ji W, Feng G, Zhao Q, Liu J, et al. Common variants in the BCL9 gene conferring risk of schizophrenia. Arch Gen Psychiatry 2011; 68: 232-40. 12. Zandi PP, Belmonte PL, Willour VL, Goes FS, Badner JA, Simpson SG, et al. Association study of Wnt signaling

. A genome-wide association study and metaanalysis indicate that over 40 loci affect risk of type 1 diabetes. Nat Genet. 2009; 41(6): 703-707. 12. Chen Y, Zhao S, Xiang R. RTN3 and RTN4: candidate modulators in vascular cell apoptosis and atherosclerosis. J Cell Biochem. 2010; 111(4): 797-800. 13. Jitoku D, Hattori E, Iwayama Y, Yamada K, Toyota T, Kikuchi M, et al. Association study of Nogo-related genes with schizophrenia in a Japanese case-control sample. Am J Med Genet B Neuropsychiatr Genet. 2011; 156B(5): 581-592. 14. Kathiresan S, Manning AK, Demissie S, D

is modulated by stimulation of ADRB2s with endogenous and exogenous agonists that have a potential to affect cervical tone and resistance to mechanical stretching [ 29 ]. Therefore, we hypothesized that genetic variability in the ADRB2 gene modulates uterine contractility and might be consequently associated with SPTB. Several association studies have linked ADRB2 polymorphism rs1042713 and SPTB, but the results were found to be inconsistent [ 30 , 31 , 32 , 33 ]. Selected polymorphism is a missense polymorphism that results in amino acid change R (Arg

References Abdoli R., Mirhoseini S.Z., Ghavi Hossein-Zadeh N., Zamani P., Gondro C. (2018). Genome-wide association study to identify genomic regions affecting prolificacy in Lori-Bakhtiari sheep. Anim. Genet., 49: 488–491. Abdoli R., Mirhoseini S.Z., Ghavi Hossein-Zadeh N., Zamani P., Moradi M.H., Ferdosi M.H., Gondro, C. (2019). Genome-wide association study of first lambing age and lambing interval in sheep. Small Rumin. Res., 178: 43–45. Abdoli R., Zamani P., Mirhoseini S.Z., Ghavi Hossein-Zadeh N., Nadri S. (2016). A review on prolificacy genes in sheep

References Abdoli R, Mirhoseini S.Z., Ghavi Hossein-Zadeh N., Zamani P., Ferdosi M.H., Gondro C. (2019a). Genome-wide association study of four composite reproductive traits in Iranian fat-tailed sheep. Reprod Fert Develop., 31(6): 1127-1133. Abdoli R, Mirhoseini S.Z., Ghavi Hossein-Zadeh N., Zamani P., Gondro C. (2018). Genome-wide association study to identify genomic regions affecting prolificacy in Lori-Bakhtiari sheep. Anim. Genet., 49: 488-491. Abdoli R, Mirhoseini S.Z., Ghavi Hossein-Zadeh N., Zamani P., Moradi M.H., Ferdosi M.H., Gondro C. (2019b). Genome

beta cell proliferation. J Biol Chem 283, 8723–8735, 2008. Long J, Edwards T, Signorello LB, Cai Q, Zheng W, Shu XO, Blot WJ. Evaluation of genome-wide association study-identified type 2 diabetes loci in African Americans. Am J Epidemiol 176, 995–1001, 2012. Lyssenko V, Lupi R, Marchetti P, Del Guerra S, Orho-Melander M, Almgren P, Sjogren M, Ling C, Eriksson KF, Lethagen AL, Mancarella R, Berglund G, Tuomi T, Nilsson P, Del Prato S, Groop L. Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes. J Clin Invest 117, 2155–2163, 2007

genetic contribution to adult psychiatric disorders. Int Rev Psychiatry. 2004; 16:260-83. 5. Craddock N, Davé S, Greening J. Association studies of bipolar disorder. Bipolar Disord. 2001; 3:284-98. 6. Lesch KP, Balling U, Gross J, Strauss K, Wolozin BL, Murphy DL, et al. Organization of the human serotonin transporter gene. J Neural Transm Gen Sect. 1994; n95: 157-62. 7. Heils A, Teufel A, Petri S, Stöber G, Riederer P, Bengel D, et al. Allelic variation of human serotonin transporter gene expression. J Neurochem. 1996; 66:2621-4. 8. Lesch KP, Bengel D, Heils A, Sabol

E, Mishra A, Deepak D, Singh B, Rahman I, et al. CYP1A1, CYP1A2 and CYBA gene polymorphisms associated with oxidative stress in COPD. Clin Chim Acta 2010; 411: 474-80. 26. Silverman EK, Palmer LJ. Case-control association studies for the genetics of complex respiratory diseases. Am J Respir Cell Mol Biol 2000; 22: 645-8. 27. Arif E, Vibhuti A, Alam P, Deepak D, Singh B, Athar M, et al. Association of CYP2E1 and NAT2 gene polymorphisms with chronic obstructive pulmonary disease. Clin Chim Acta 2007; 382: 37-42. 28. Korytina GF, Yanbaeva DG, Babenkova LI, Etkina EI