Furuta H - Search Results

1

A missense mutation of Pax4 gene (R121W) is associated with type 2 diabetes in Japanese.

Shimajiri Y, Sanke T, Furuta H, Hanabusa T, Nakagawa T, Fujitani Y, Kajimoto Y, Takasu N, Nanjo K. Shimajiri Y, et al. Among authors: furuta h. Diabetes. 2001 Dec;50(12):2864-9. doi: 10.2337/diabetes.50.12.2864. Diabetes. 2001. PMID: 11723072

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

[A case of so-called neoplastic angioendotheliosis with fever of unknown origin and temporary loss of consciousness].

Takeuchi K, Nisimura S, Furuta H, Satogami E, Ekawa K, Sanke T, Kondo M, Nanjyo K, Miyamura K, Morikawa Y, et al. Takeuchi K, et al. Among authors: furuta h. Rinsho Ketsueki. 1991 Feb;32(2):127-31. Rinsho Ketsueki. 1991. PMID: 2027239 Japanese.

4

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

5

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

6

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

7

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

8

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.

9

[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.

10

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

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