Sato W - Search Results

1

Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene.

Hayasaka K, Himoro M, Sato W, Takada G, Uyemura K, Shimizu N, Bird TD, Conneally PM, Chance PF. Hayasaka K, et al. Among authors: sato w. Nat Genet. 1993 Sep;5(1):31-4. doi: 10.1038/ng0993-31. Nat Genet. 1993. PMID: 7693129

2

Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin.

Hayasaka K, Nanao K, Tahara M, Sato W, Takada G, Miura M, Uyemura K. Hayasaka K, et al. Among authors: sato w. Biochem Biophys Res Commun. 1991 Oct 31;180(2):515-8. doi: 10.1016/s0006-291x(05)81094-0. Biochem Biophys Res Commun. 1991. PMID: 1719967

3

Isolation and sequence determination of cDNA encoding PMP-22 (PAS-II/SR13/Gas-3) of human peripheral myelin.

Hayasaka K, Himoro M, Nanao K, Sato W, Miura M, Uyemura K, Takahashi E, Takada G. Hayasaka K, et al. Among authors: sato w. Biochem Biophys Res Commun. 1992 Jul 31;186(2):827-31. doi: 10.1016/0006-291x(92)90820-b. Biochem Biophys Res Commun. 1992. PMID: 1497668

4

Isolation and sequence determination of cDNA encoding P2 protein of human peripheral myelin.

Hayasaka K, Nanao K, Tahara M, Sato W, Takada G, Miura M, Uyemura K. Hayasaka K, et al. Among authors: sato w. Biochem Biophys Res Commun. 1991 Nov 27;181(1):204-7. doi: 10.1016/s0006-291x(05)81402-0. Biochem Biophys Res Commun. 1991. PMID: 1720307

5

Isolation of cDNA encoding the human liver phosphorylase kinase alpha subunit (PHKA2) and identification of a missense mutation of the PHKA2 gene in a family with liver phosphorylase kinase deficiency.

Hirono H, Hayasaka K, Sato W, Takahashi T, Takada G. Hirono H, et al. Among authors: sato w. Biochem Mol Biol Int. 1995 Jul;36(3):505-11. Biochem Mol Biol Int. 1995. PMID: 7549948

6

A T-to-C substitution at nucleotide 12311 in tRNA(Leu(CUN)) gene may be a mtDNA polymorphism.

Sato W, Hayasaka K. Sato W, et al. J Neurol Sci. 1994 Dec 20;127(2):236. doi: 10.1016/0022-510x(94)90079-5. J Neurol Sci. 1994. PMID: 7707084 No abstract available.

7

Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

Shoji Y, Sato W, Hayasaka K, Takada G. Shoji Y, et al. Among authors: sato w. J Inherit Metab Dis. 1993;16(1):27-30. doi: 10.1007/BF00711311. J Inherit Metab Dis. 1993. PMID: 8487499

8

A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

Sato W, Hayasaka K, Shoji Y, Takahashi T, Takada G, Saito M, Fukawa O, Wachi E. Sato W, et al. Biochem Mol Biol Int. 1994 Aug;33(6):1055-61. Biochem Mol Biol Int. 1994. PMID: 7804130

9

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) decrease in diastolic left ventricular function assessed by echocardiography.

Suzuki Y, Harada K, Miura Y, Sato W, Hayasaka K, Kawamura K, Takada G. Suzuki Y, et al. Among authors: sato w. Pediatr Cardiol. 1993 Jul;14(3):162-6. doi: 10.1007/BF00795646. Pediatr Cardiol. 1993. PMID: 8415219

10

Identification and expression of a missense mutation (Y446C) in the acid sphingomyelinase gene from a Japanese patient with type A Niemann-Pick disease.

Takahashi T, Suchi M, Sato W, Ten SB, Sakuragawa N, Desnick RJ, Schuchman EH, Takada G. Takahashi T, et al. Among authors: sato w. Tohoku J Exp Med. 1995 Oct;177(2):117-23. doi: 10.1620/tjem.177.117. Tohoku J Exp Med. 1995. PMID: 8693491 Free article.

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