Furuta H - Search Results

1

History of obesity as a risk factor for both carotid atherosclerosis and microangiopathy.

Ogawa K, Ueda K, Sasaki H, Yamasaki H, Okamoto K, Wakasaki H, Matsumoto E, Furuta H, Hanabusa T, Nishi M, Nanjo K. Ogawa K, et al. Among authors: furuta h. Diabetes Res Clin Pract. 2004 Dec;66 Suppl 1:S165-8. doi: 10.1016/j.diabres.2003.09.020. Diabetes Res Clin Pract. 2004. PMID: 15563970

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

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.

7

[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.

8

Nonsense mutation of islet-1 gene (Q310X) found in a type 2 diabetic patient with a strong family history.

Shimomura H, Sanke T, Hanabusa T, Tsunoda K, Furuta H, Nanjo K. Shimomura H, et al. Among authors: furuta h. Diabetes. 2000 Sep;49(9):1597-600. doi: 10.2337/diabetes.49.9.1597. Diabetes. 2000. PMID: 10969846

9

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

10

Single nucleotide polymorphism (D68D, T to C) in the syntaxin 1A gene correlates to age at onset and insulin requirement in Type II diabetic patients.

Tsunoda K, Sanke T, Nakagawa T, Furuta H, Nanjo K. Tsunoda K, et al. Among authors: furuta h. Diabetologia. 2001 Nov;44(11):2092-7. doi: 10.1007/s001250100015. Diabetologia. 2001. PMID: 11719842

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