Shimmoto M - Search Results

1

Immunohistochemical characterization of transgenic mice highly expressing human lysosomal alpha-galactosidase.

Kase R, Shimmoto M, Itoh K, Utsumi K, Kotani M, Taya C, Yonekawa H, Sakuraba H. Kase R, et al. Among authors: shimmoto m. Biochim Biophys Acta. 1998 Apr 28;1406(3):260-6. doi: 10.1016/s0925-4439(98)00012-x. Biochim Biophys Acta. 1998. PMID: 9630664 Free article.

2

Distribution of lysosomal protective protein in human tissues.

Satake A, Itoh K, Shimmoto M, Saido TC, Sakuraba H, Suzuki Y. Satake A, et al. Among authors: shimmoto m. Biochem Biophys Res Commun. 1994 Nov 30;205(1):38-43. doi: 10.1006/bbrc.1994.2626. Biochem Biophys Res Commun. 1994. PMID: 7999052

3

Generation and characterization of transgenic mice expressing a human mutant alpha-galactosidase with an R301Q substitution causing a variant form of Fabry disease.

Shimmoto M, Kase R, Itoh K, Utsumi K, Ishii S, Taya C, Yonekawa H, Sakuraba H. Shimmoto M, et al. FEBS Lett. 1997 Nov 3;417(1):89-91. doi: 10.1016/s0014-5793(97)01263-5. FEBS Lett. 1997. PMID: 9395081 Free article.

4

Hypertrophic cardiomyopathy in late-onset variant of Fabry disease with high residual activity of alpha-galactosidase A.

Nagao Y, Nakashima H, Fukuhara Y, Shimmoto M, Oshima A, Ikari Y, Mori Y, Sakuraba H, Suzuki Y. Nagao Y, et al. Among authors: shimmoto m. Clin Genet. 1991 Mar;39(3):233-7. doi: 10.1111/j.1399-0004.1991.tb03018.x. Clin Genet. 1991. PMID: 1645238

5

Fabry disease: detection of 13-bp deletion in alpha-galactosidase A gene and its application to gene diagnosis of heterozygotes.

Ishii S, Sakuraba H, Shimmoto M, Minamikawa-Tachino R, Suzuki T, Suzuki Y. Ishii S, et al. Among authors: shimmoto m. Ann Neurol. 1991 May;29(5):560-4. doi: 10.1002/ana.410290517. Ann Neurol. 1991. PMID: 1650161

6

Human beta-galactosidase gene mutations in morquio B disease.

Oshima A, Yoshida K, Shimmoto M, Fukuhara Y, Sakuraba H, Suzuki Y. Oshima A, et al. Among authors: shimmoto m. Am J Hum Genet. 1991 Nov;49(5):1091-3. Am J Hum Genet. 1991. PMID: 1928092 Free PMC article.

7

Identification of point mutations in the alpha-galactosidase A gene in classical and atypical hemizygotes with Fabry disease.

Sakuraba H, Oshima A, Fukuhara Y, Shimmoto M, Nagao Y, Bishop DF, Desnick RJ, Suzuki Y. Sakuraba H, et al. Among authors: shimmoto m. Am J Hum Genet. 1990 Nov;47(5):784-9. Am J Hum Genet. 1990. PMID: 2171331 Free PMC article.

8

Protective protein as an endogenous endothelin degradation enzyme in human tissues.

Itoh K, Kase R, Shimmoto M, Satake A, Sakuraba H, Suzuki Y. Itoh K, et al. Among authors: shimmoto m. J Biol Chem. 1995 Jan 13;270(2):515-8. doi: 10.1074/jbc.270.2.515. J Biol Chem. 1995. PMID: 7822272 Free article.

9

[Multifunctional protective protein and its genetic deficiency 'galactosialidosis'].

Sakuraba H, Itoh K, Shimmoto M. Sakuraba H, et al. Among authors: shimmoto m. Seikagaku. 1993 Jul;65(7):561-6. Seikagaku. 1993. PMID: 8370987 Review. Japanese. No abstract available.

10

Protective protein gene mutations in galactosialidosis.

Shimmoto M, Fukuhara Y, Itoh K, Oshima A, Sakuraba H, Suzuki Y. Shimmoto M, et al. J Clin Invest. 1993 Jun;91(6):2393-8. doi: 10.1172/JCI116472. J Clin Invest. 1993. PMID: 8514852 Free PMC article.

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