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Page 1
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 CTLA-4 gene A-G polymorphism (IDDM12 locus) with acute-onset and insulin-depleted IDDM as well as autoimmune thyroid disease (Graves' disease and Hashimoto's thyroiditis) in the Japanese population.
Awata T, Kurihara S, Iitaka M, Takei S, Inoue I, Ishii C, Negishi K, Izumida T, Yoshida Y, Hagura R, Kuzuya N, Kanazawa Y, Katayama S. Awata T, et al. Among authors: kurihara s. Diabetes. 1998 Jan;47(1):128-9. doi: 10.2337/diab.47.1.128. Diabetes. 1998. PMID: 9421386 No abstract available.
Efficacy of glimepiride in Japanese type 2 diabetic subjects.
Inukai K, Watanabe M, Nakashima Y, Sawa T, Takata N, Tanaka M, Kashiwabara H, Yokota K, Suzuki M, Kurihara S, Awata T, Katayama S. Inukai K, et al. Among authors: kurihara s. Diabetes Res Clin Pract. 2005 Jun;68(3):250-7. doi: 10.1016/j.diabres.2004.10.002. Epub 2004 Nov 19. Diabetes Res Clin Pract. 2005. PMID: 15936468 Clinical Trial.
Adiponectin upregulates ferritin heavy chain in skeletal muscle cells.
Ikegami Y, Inukai K, Imai K, Sakamoto Y, Katagiri H, Kurihara S, Awata T, Katayama S. Ikegami Y, et al. Among authors: kurihara s. Diabetes. 2009 Jan;58(1):61-70. doi: 10.2337/db07-0690. Epub 2008 Oct 17. Diabetes. 2009. PMID: 18931039 Free PMC article.
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
A novel missense mutation in the homeodomain of the hepatocyte nuclear factor-1alpha/maturity-onset diabetes of the young 3 in a Japanese early-onset type 2 diabetic patient and time-course of glucose-stimulated insulin secretion.
Awata T, Kurihara S, Inoue K, Inoue I, Takei S, Ishii C, Negishi K, Namai K, Kanazawa Y, Kuzuya T, Katayama S. Awata T, et al. Among authors: kurihara s. Diabetes Care. 1998 Sep;21(9):1569-71. doi: 10.2337/diacare.21.9.1569. Diabetes Care. 1998. PMID: 9727913 No abstract available.
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
733 results