Furuta H - Search Results

1

Association of TCF7L2 polymorphisms with susceptibility to type 2 diabetes in 4,087 Japanese subjects.

Miyake K, Horikawa Y, Hara K, Yasuda K, Osawa H, Furuta H, Hirota Y, Yamagata K, Hinokio Y, Oka Y, Iwasaki N, Iwamoto Y, Yamada Y, Seino Y, Maegawa H, Kashiwagi A, Yamamoto K, Tokunaga K, Takeda J, Makino H, Nanjo K, Kadowaki T, Kasuga M. Miyake K, et al. Among authors: furuta h. J Hum Genet. 2008;53(2):174-180. doi: 10.1007/s10038-007-0231-5. Epub 2007 Dec 21. J Hum Genet. 2008. PMID: 18097733

2

Islet amyloid polypeptide (IAPP/amylin) causes insulin resistance in perfused rat hindlimb muscle.

Tabata H, Hirayama J, Sowa R, Furuta H, Negoro T, Sanke T, Nanjo K. Tabata H, et al. Among authors: furuta h. Diabetes Res Clin Pract. 1992 Jan;15(1):57-61. doi: 10.1016/0168-8227(92)90068-3. Diabetes Res Clin Pract. 1992. PMID: 1541236

3

Islet amyloid polypeptide amide causes peripheral insulin resistance in vivo in dogs.

Sowa R, Sanke T, Hirayama J, Tabata H, Furuta H, Nishimura S, Nanjo K. Sowa R, et al. Among authors: furuta h. Diabetologia. 1990 Feb;33(2):118-20. doi: 10.1007/BF00401051. Diabetologia. 1990. PMID: 2184060

4

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

5

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

6

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

7

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.

8

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.

9

Characterization of the promoter of the mouse prohormone convertase PC2 gene.

Ohagi S, Tatsuta H, Sanke T, Furuta H, Furuta M, Hanabusa T, Nanjo K. Ohagi S, et al. Among authors: furuta h, furuta m. Endocr J. 1998 Aug;45(4):569-73. doi: 10.1507/endocrj.45.569. Endocr J. 1998. PMID: 9881908 Free article.

10

[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.

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