Nishizawa M - Search Results

1

Human placental sialidase: further purification and characterization.

Hiraiwa M, Nishizawa M, Uda Y, Nakajima T, Miyatake T. Hiraiwa M, et al. Among authors: nishizawa m. J Biochem. 1988 Jan;103(1):86-90. doi: 10.1093/oxfordjournals.jbchem.a122245. J Biochem. 1988. PMID: 3360767 Free article.

2

Molecular cloning of a full-length cDNA for human alpha-N-acetylgalactosaminidase (alpha-galactosidase B).

Tsuji S, Yamauchi T, Hiraiwa M, Isobe T, Okuyama T, Sakimura K, Takahashi Y, Nishizawa M, Uda Y, Miyatake T. Tsuji S, et al. Among authors: nishizawa m. Biochem Biophys Res Commun. 1989 Sep 29;163(3):1498-504. doi: 10.1016/0006-291x(89)91149-2. Biochem Biophys Res Commun. 1989. PMID: 2551294

3

Human placental sialidase: partial purification and characterization.

Hiraiwa M, Uda Y, Nishizawa M, Miyatake T. Hiraiwa M, et al. Among authors: nishizawa m. J Biochem. 1987 May;101(5):1273-9. doi: 10.1093/oxfordjournals.jbchem.a121991. J Biochem. 1987. PMID: 3654592 Free article.

4

Activation of human lysosomal sialidase.

Hiraiwa M, Yamauchi T, Tsuji S, Nishizawa M, Miyatake T, Oyanagi K, Ikuta F, Uda Y. Hiraiwa M, et al. Among authors: nishizawa m. J Biochem. 1993 Dec;114(6):901-5. doi: 10.1093/oxfordjournals.jbchem.a124274. J Biochem. 1993. PMID: 8138549 Free article.

5

Biochemical and clinical analysis of accumulated glycolipids in symptomatic heterozygotes of angiokeratoma corporis diffusum (Fabry's disease) in comparison with hemizygotes.

Hozumi I, Nishizawa M, Ariga T, Miyatake T. Hozumi I, et al. Among authors: nishizawa m. J Lipid Res. 1990 Feb;31(2):335-40. J Lipid Res. 1990. PMID: 2157788 Free article.

6

Accumulation of glycosphingolipids in spinal and sympathetic ganglia of a symptomatic heterozygote of Fabry's disease.

Hozumi I, Nishizawa M, Ariga T, Inoue Y, Ohnishi Y, Yokoyama A, Shibata A, Miyatake T. Hozumi I, et al. Among authors: nishizawa m. J Neurol Sci. 1989 May;90(3):273-80. doi: 10.1016/0022-510x(89)90113-5. J Neurol Sci. 1989. PMID: 2500499

7

Alterations of oligodendrocytes and demyelination in the spinal cord of patients with mitochondrial encephalomyopathy.

Ohara S, Ohama E, Takahashi H, Ikuta F, Nishizawa M, Tanaka K, Miyatake T. Ohara S, et al. Among authors: nishizawa m. J Neurol Sci. 1988 Aug;86(1):19-29. doi: 10.1016/0022-510x(88)90004-4. J Neurol Sci. 1988. PMID: 3171595

8

[Mitochondrial angiopathy in the cerebral blood vessels of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes)].

Ohama E, Ohara S, Ikuta F, Tanaka K, Nishizawa M, Miyatake T. Ohama E, et al. Among authors: nishizawa m. No To Shinkei. 1988 Feb;40(2):109-18. No To Shinkei. 1988. PMID: 3370163 Japanese.

9

Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy.

Ohama E, Ohara S, Ikuta F, Tanaka K, Nishizawa M, Miyatake T. Ohama E, et al. Among authors: nishizawa m. Acta Neuropathol. 1987;74(3):226-33. doi: 10.1007/BF00688185. Acta Neuropathol. 1987. PMID: 3673514

10

Close kinship of human 20alpha-hydroxysteroid dehydrogenase gene with three aldo-keto reductase genes.

Nishizawa M, Nakajima T, Yasuda K, Kanzaki H, Sasaguri Y, Watanabe K, Ito S. Nishizawa M, et al. Genes Cells. 2000 Feb;5(2):111-25. doi: 10.1046/j.1365-2443.2000.00310.x. Genes Cells. 2000. PMID: 10672042 Free article.

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