Furuta H - Search Results

1

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.

Yasuda K, Miyake K, Horikawa Y, Hara K, Osawa H, Furuta H, Hirota Y, Mori H, Jonsson A, Sato Y, Yamagata K, Hinokio Y, Wang HY, Tanahashi T, Nakamura N, Oka Y, Iwasaki N, Iwamoto Y, Yamada Y, Seino Y, Maegawa H, Kashiwagi A, Takeda J, Maeda E, Shin HD, Cho YM, Park KS, Lee HK, Ng MC, Ma RC, So WY, Chan JC, Lyssenko V, Tuomi T, Nilsson P, Groop L, Kamatani N, Sekine A, Nakamura Y, Yamamoto K, Yoshida T, Tokunaga K, Itakura M, Makino H, Nanjo K, Kadowaki T, Kasuga M. Yasuda K, et al. Among authors: furuta h. Nat Genet. 2008 Sep;40(9):1092-7. doi: 10.1038/ng.207. Nat Genet. 2008. PMID: 18711367

2

Association of the prohormone convertase 2 gene (PCSK2) on chromosome 20 with NIDDM in Japanese subjects.

Yoshida H, Ohagi S, Sanke T, Furuta H, Furuta M, Nanjo K. Yoshida H, et al. Among authors: furuta h, furuta m. Diabetes. 1995 Apr;44(4):389-93. doi: 10.2337/diab.44.4.389. Diabetes. 1995. PMID: 7698505

3

Simple tandem repeat DNA polymorphism in the human glycogen synthase gene is associated with NIDDM in Japanese subjects.

Kuroyama H, Sanke T, Ohagi S, Furuta M, Furuta H, Nanjo K. Kuroyama H, et al. Among authors: furuta h, furuta m. Diabetologia. 1994 May;37(5):536-9. doi: 10.1007/s001250050144. Diabetologia. 1994. PMID: 8056194

4

Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3).

Yamagata K, Oda N, Kaisaki PJ, Menzel S, Furuta H, Vaxillaire M, Southam L, Cox RD, Lathrop GM, Boriraj VV, Chen X, Cox NJ, Oda Y, Yano H, Le Beau MM, Yamada S, Nishigori H, Takeda J, Fajans SS, Hattersley AT, Iwasaki N, Hansen T, Pedersen O, Polonsky KS, Bell GI, et al. Yamagata K, et al. Among authors: furuta h. Nature. 1996 Dec 5;384(6608):455-8. doi: 10.1038/384455a0. Nature. 1996. PMID: 8945470 Free article.

5

Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY.

Furuta H, Iwasaki N, Oda N, Hinokio Y, Horikawa Y, Yamagata K, Yano N, Sugahiro J, Ogata M, Ohgawara H, Omori Y, Iwamoto Y, Bell GI. Furuta H, et al. Diabetes. 1997 Oct;46(10):1652-7. doi: 10.2337/diacare.46.10.1652. Diabetes. 1997. PMID: 9313765

6

Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.

Horikawa Y, Iwasaki N, Hara M, Furuta H, Hinokio Y, Cockburn BN, Lindner T, Yamagata K, Ogata M, Tomonaga O, Kuroki H, Kasahara T, Iwamoto Y, Bell GI. Horikawa Y, et al. Among authors: furuta h. Nat Genet. 1997 Dec;17(4):384-5. doi: 10.1038/ng1297-384. Nat Genet. 1997. PMID: 9398836 No abstract available.

7

Beta-cell transcription factors and diabetes: mutations in the coding region of the BETA2/NeuroD1 (NEUROD1) and Nkx2.2 (NKX2B) genes are not associated with maturity-onset diabetes of the young in Japanese.

Furuta H, Horikawa Y, Iwasaki N, Hara M, Sussel L, Le Beau MM, Davis EM, Ogata M, Iwamoto Y, German MS, Bell GI. Furuta H, et al. Diabetes. 1998 Aug;47(8):1356-8. doi: 10.2337/diab.47.8.1356. Diabetes. 1998. PMID: 9703340 No abstract available.

8

[NIDDM susceptibility genes].

Furuta H, Sanke T, Nanjo K. Furuta H, et al. Nihon Rinsho. 1999 Mar;57(3):545-50. Nihon Rinsho. 1999. PMID: 10199131 Review. Japanese.

9

Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young.

Hinokio Y, Horikawa Y, Furuta H, Cox NJ, Iwasaki N, Honda M, Ogata M, Iwamoto Y, Bell GI. Hinokio Y, et al. Among authors: furuta h. Diabetes. 2000 Feb;49(2):302-5. doi: 10.2337/diabetes.49.2.302. Diabetes. 2000. PMID: 10868948

10

A polymorphic marker in the leptin gene associated with Japanese morbid obesity.

Ohshiro Y, Ueda K, Nishi M, Ishigame M, Wakasaki H, Kawashima H, Furuta H, Sasaki H, Sanke T, Takasu N, Nanjo K. Ohshiro Y, et al. Among authors: furuta h. J Mol Med (Berl). 2000;78(9):516-20. doi: 10.1007/s001090000143. J Mol Med (Berl). 2000. PMID: 11140377

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