Hashiramoto M - Search Results

1

Mitochondrial mutation in diabetic patient with gastrointestinal symptoms.

Kishimoto M, Hashiramoto M, Kanda F, Tanaka M, Kasuga M. Kishimoto M, et al. Among authors: hashiramoto m. Lancet. 1995 Feb 18;345(8947):452. doi: 10.1016/s0140-6736(95)90433-6. Lancet. 1995. PMID: 7853969 No abstract available.

2

Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene.

Kishimoto M, Hashiramoto M, Araki S, Ishida Y, Kazumi T, Kanda E, Kasuga M. Kishimoto M, et al. Among authors: hashiramoto m. Diabetologia. 1995 Feb;38(2):193-200. doi: 10.1007/BF00400094. Diabetologia. 1995. PMID: 7713314

3

[Insulin receptor Arg1131-->Gln: a novel mutation in the catalytic loop of insulin receptor observed in insulin resistant diabetes].

Kasuga M, Kishimoto M, Hashiramoto M, Yonezawa K, Kazumi T, Hagino H, Shii K. Kasuga M, et al. Among authors: hashiramoto m. Nihon Geka Gakkai Zasshi. 1992 Sep;93(9):968-71. Nihon Geka Gakkai Zasshi. 1992. PMID: 1470163 Japanese.

4

Amino acid polymorphisms of the insulin receptor substrate-1 in Japanese noninsulin-dependent diabetes mellitus.

Mori H, Hashiramoto M, Kishimoto M, Kasuga M. Mori H, et al. Among authors: hashiramoto m. J Clin Endocrinol Metab. 1995 Sep;80(9):2822-6. doi: 10.1210/jcem.80.9.7673430. J Clin Endocrinol Metab. 1995. PMID: 7673430

5

[The structure function relationship in the human insulin receptor].

Kishimoto M, Hashiramoto M, Kasuga M. Kishimoto M, et al. Among authors: hashiramoto m. Nihon Rinsho. 1994 Oct;52(10):2616-22. Nihon Rinsho. 1994. PMID: 7983787 Review. Japanese.

6

Hypertrophic cardiomyopathy in patients with diabetes mellitus associated with mitochondrial tRNA(Leu)(UUR) gene mutation.

Yoshida R, Ishida Y, Abo K, Hozumi T, Ueno H, Shiotani H, Kishimoto-Hashiramoto M, Hashiramoto M, Matsunaga K, Kasuga M, et al. Yoshida R, et al. Among authors: hashiramoto m. Intern Med. 1995 Oct;34(10):953-8. doi: 10.2169/internalmedicine.34.953. Intern Med. 1995. PMID: 8563095 Free article.

7

Substitution of glutamine for arginine 1131. A newly identified mutation in the catalytic loop of the tyrosine kinase domain of the human insulin receptor.

Kishimoto M, Hashiramoto M, Yonezawa K, Shii K, Kazumi T, Kasuga M. Kishimoto M, et al. Among authors: hashiramoto m. J Biol Chem. 1994 Apr 15;269(15):11349-55. J Biol Chem. 1994. PMID: 7512563 Free article.

8

[Mutations in the insulin receptor gene].

Hashiramoto M, Kasuga M. Hashiramoto M, et al. Nihon Rinsho. 2002 Jul;60 Suppl 7:642-7. Nihon Rinsho. 2002. PMID: 12238112 Review. Japanese. No abstract available.

9

Identification of a single nucleotide polymorphism showing no insulin-mediated suppression of the promoter activity in the human insulin receptor substrate 2 gene.

Iwamoto K, Mori H, Okazawa H, Hashiramoto M, Kasuga M. Iwamoto K, et al. Among authors: hashiramoto m. Diabetologia. 2002 Aug;45(8):1182-95. doi: 10.1007/s00125-002-0871-0. Epub 2002 Jun 19. Diabetologia. 2002. PMID: 12189449

10

A polymorphism in the 5' untranslated region and a Met229-->Leu variant in exon 5 of the human UCP1 gene are associated with susceptibility to type II diabetes mellitus.

Mori H, Okazawa H, Iwamoto K, Maeda E, Hashiramoto M, Kasuga M. Mori H, et al. Among authors: hashiramoto m. Diabetologia. 2001 Mar;44(3):373-6. doi: 10.1007/s001250051629. Diabetologia. 2001. PMID: 11317671

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