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Page 1
A low-frequency GLIS3 variant associated with resistance to Japanese type 1 diabetes.
Awata T, Yamashita H, Kurihara S, Morita-Ohkubo T, Miyashita Y, Katayama S, Kawasaki E, Tanaka S, Ikegami H, Maruyama T, Shimada A, Takahashi K, Kawabata Y, Kobayashi T, Nishida N, Mawatari Y. Awata T, et al. Among authors: kurihara s. Biochem Biophys Res Commun. 2013 Aug 9;437(4):521-5. doi: 10.1016/j.bbrc.2013.06.102. Epub 2013 Jul 13. Biochem Biophys Res Commun. 2013. PMID: 23856252
Functional VEGF C-634G polymorphism is associated with development of diabetic macular edema and correlated with macular retinal thickness in type 2 diabetes.
Awata T, Kurihara S, Takata N, Neda T, Iizuka H, Ohkubo T, Osaki M, Watanabe M, Nakashima Y, Inukai K, Inoue I, Kawasaki I, Mori K, Yoneya S, Katayama S. Awata T, et al. Among authors: kurihara s. Biochem Biophys Res Commun. 2005 Aug 5;333(3):679-85. doi: 10.1016/j.bbrc.2005.05.167. Biochem Biophys Res Commun. 2005. PMID: 15963467
Insulin gene/IDDM2 locus in Japanese type 1 diabetes: contribution of class I alleles and influence of class I subdivision in susceptibility to type 1 diabetes.
Awata T, Kawasaki E, Ikegami H, Kobayashi T, Maruyama T, Nakanishi K, Shimada A, Iizuka H, Kurihara S, Osaki M, Uga M, Kawabata Y, Tanaka S, Kanazawa Y, Katayama S. Awata T, et al. Among authors: kurihara s. J Clin Endocrinol Metab. 2007 May;92(5):1791-5. doi: 10.1210/jc.2006-2242. Epub 2007 Mar 6. J Clin Endocrinol Metab. 2007. PMID: 17341563
Association of type 1 diabetes with two Loci on 12q13 and 16p13 and the influence coexisting thyroid autoimmunity in Japanese.
Awata T, Kawasaki E, Tanaka S, Ikegami H, Maruyama T, Shimada A, Nakanishi K, Kobayashi T, Iizuka H, Uga M, Kawabata Y, Kanazawa Y, Kurihara S, Osaki M, Katayama S; Japanese Study Group on Type 1 Diabetes Genetics. Awata T, et al. Among authors: kurihara s. J Clin Endocrinol Metab. 2009 Jan;94(1):231-5. doi: 10.1210/jc.2008-0718. Epub 2008 Oct 21. J Clin Endocrinol Metab. 2009. PMID: 18940880
Analysis of the HLA and non-HLA susceptibility loci in Japanese type 1 diabetes.
Yamashita H, Awata T, Kawasaki E, Ikegami H, Tanaka S, Maruyama T, Shimada A, Nakanishi K, Takahashi K, Kobayashi T, Kawabata Y, Miyashita Y, Kurihara S, Morita-Ohkubo T, Katayama S; Japanese Study Group on Type 1 Diabetes Genetics. Yamashita H, et al. Among authors: kurihara s. Diabetes Metab Res Rev. 2011 Nov;27(8):844-8. doi: 10.1002/dmrr.1234. Diabetes Metab Res Rev. 2011. PMID: 22069271
Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis.
Awata T, Inoue K, Kurihara S, Ohkubo T, Inoue I, Abe T, Takino H, Kanazawa Y, Katayama S. Awata T, et al. Among authors: kurihara s. Biochem Biophys Res Commun. 2000 Feb 16;268(2):612-6. doi: 10.1006/bbrc.2000.2169. Biochem Biophys Res Commun. 2000. PMID: 10679252
The association of CTLA4 polymorphism with type 1 diabetes is concentrated in patients complicated with autoimmune thyroid disease: a multicenter collaborative study in Japan.
Ikegami H, Awata T, Kawasaki E, Kobayashi T, Maruyama T, Nakanishi K, Shimada A, Amemiya S, Kawabata Y, Kurihara S, Tanaka S, Kanazawa Y, Mochizuki M, Ogihara T. Ikegami H, et al. Among authors: kurihara s. J Clin Endocrinol Metab. 2006 Mar;91(3):1087-92. doi: 10.1210/jc.2005-1407. Epub 2005 Dec 13. J Clin Endocrinol Metab. 2006. PMID: 16352685
Systematic search for single nucleotide polymorphisms in a lymphoid tyrosine phosphatase gene (PTPN22): association between a promoter polymorphism and type 1 diabetes in Asian populations.
Kawasaki E, Awata T, Ikegami H, Kobayashi T, Maruyama T, Nakanishi K, Shimada A, Uga M, Kurihara S, Kawabata Y, Tanaka S, Kanazawa Y, Lee I, Eguchi K. Kawasaki E, et al. Among authors: kurihara s. Am J Med Genet A. 2006 Mar 15;140(6):586-93. doi: 10.1002/ajmg.a.31124. Am J Med Genet A. 2006. PMID: 16470599
736 results