Takahashi K - Search Results

1

Mutation and polymorphic marker analyses of 65K- and 67K-glutamate decarboxylase genes in two families with pyridoxine-dependent epilepsy.

Kure S, Sakata Y, Miyabayashi S, Takahashi K, Shinka T, Matsubara Y, Hoshino H, Narisawa K. Kure S, et al. Among authors: takahashi k. J Hum Genet. 1998;43(2):128-31. doi: 10.1007/s100380050053. J Hum Genet. 1998. PMID: 9621518

2

Molecular analysis of holocarboxylase synthetase deficiency: a missense mutation and a single base deletion are predominant in Japanese patients.

Aoki Y, Suzuki Y, Sakamoto O, Li X, Takahashi K, Ohtake A, Sakuta R, Ohura T, Miyabayashi S, Narisawa K. Aoki Y, et al. Among authors: takahashi k. Biochim Biophys Acta. 1995 Dec 12;1272(3):168-74. doi: 10.1016/0925-4439(95)00082-8. Biochim Biophys Acta. 1995. PMID: 8541348 Free article.

3

Mutation detection by TaqMan-allele specific amplification: application to molecular diagnosis of glycogen storage disease type Ia and medium-chain acyl-CoA dehydrogenase deficiency.

Fujii K, Matsubara Y, Akanuma J, Takahashi K, Kure S, Suzuki Y, Imaizumi M, Iinuma K, Sakatsume O, Rinaldo P, Narisawa K. Fujii K, et al. Among authors: takahashi k. Hum Mutat. 2000;15(2):189-96. doi: 10.1002/(SICI)1098-1004(200002)15:2<189::AID-HUMU8>3.0.CO;2-H. Hum Mutat. 2000. PMID: 10649496

4

Glycogen storage disease type Ia: molecular diagnosis of 51 Japanese patients and characterization of splicing mutations by analysis of ectopically transcribed mRNA from lymphoblastoid cells.

Akanuma J, Nishigaki T, Fujii K, Matsubara Y, Inui K, Takahashi K, Kure S, Suzuki Y, Ohura T, Miyabayashi S, Ogawa E, Iinuma K, Okada S, Narisawa K. Akanuma J, et al. Among authors: takahashi k. Am J Med Genet. 2000 Mar 13;91(2):107-12. Am J Med Genet. 2000. PMID: 10748407

5

Heterogeneous mutations in the glucose-6-phosphatase gene in Japanese patients with glycogen storage disease type Ia.

Takahashi K, Akanuma J, Matsubara Y, Fujii K, Kure S, Suzuki Y, Wataya K, Sakamoto O, Aoki Y, Ogasawara M, Ohura T, Miyabayashi S, Narisawa K. Takahashi K, et al. Am J Med Genet. 2000 May 15;92(2):90-4. Am J Med Genet. 2000. PMID: 10797430

6

Complete suppression of insulitis and diabetes in NOD mice lacking interferon regulatory factor-1.

Nakazawa T, Satoh J, Takahashi K, Sakata Y, Ikehata F, Takizawa Y, Bando SI, Housai T, Li Y, Chen C, Masuda T, Kure S, Kato I, Takasawa S, Taniguchi T, Okamoto H, Toyota T. Nakazawa T, et al. Among authors: takahashi k. J Autoimmun. 2001 Sep;17(2):119-25. doi: 10.1006/jaut.2001.0531. J Autoimmun. 2001. PMID: 11591120

7

Reversal of hypopigmentation in phenylketonuria mice by adenovirus-mediated gene transfer.

Nagasaki Y, Matsubara Y, Takano H, Fujii K, Senoo M, Akanuma J, Takahashi K, Kure S, Hara M, Kanegae Y, Saito I, Narisawa K. Nagasaki Y, et al. Among authors: takahashi k. Pediatr Res. 1999 Apr;45(4 Pt 1):465-73. doi: 10.1203/00006450-199904010-00003. Pediatr Res. 1999. PMID: 10203136

8

Microsatellite polymorphism in the human heme oxygenase-1 gene promoter and its application in association studies with Alzheimer and Parkinson disease.

Kimpara T, Takeda A, Watanabe K, Itoyama Y, Ikawa S, Watanabe M, Arai H, Sasaki H, Higuchi S, Okita N, Takase S, Saito H, Takahashi K, Shibahara S. Kimpara T, et al. Among authors: takahashi k. Hum Genet. 1997 Jul;100(1):145-7. doi: 10.1007/s004390050480. Hum Genet. 1997. PMID: 9225984

9

Inhibitory effect of troglitazone on diabetic neuropathy in streptozotocin-induced diabetic rats.

Qiang X, Satoh J, Sagara M, Fukuzawa M, Masuda T, Sakata Y, Muto G, Muto Y, Takahashi K, Toyota T. Qiang X, et al. Among authors: takahashi k. Diabetologia. 1998 Nov;41(11):1321-6. doi: 10.1007/s001250051072. Diabetologia. 1998. PMID: 9833940

10

[Current concept of the pathogenesis of autoimmune type 1 diabetes mellitus].

Satoh J, Takahashi K, Nakazawa T, Sakata Y, Toyota T. Satoh J, et al. Among authors: takahashi k. Nihon Rinsho. 1999 Mar;57(3):528-33. Nihon Rinsho. 1999. PMID: 10199128 Review. Japanese.

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