Tomatsu S - Search Results

1

Activity of daily living for Morquio A syndrome.

Yasuda E, Suzuki Y, Shimada T, Sawamoto K, Mackenzie WG, Theroux MC, Pizarro C, Xie L, Miller F, Rahman T, Kecskemethy HH, Nagao K, Morlet T, Shaffer TH, Chinen Y, Yabe H, Tanaka A, Shintaku H, Orii KE, Orii KO, Mason RW, Montaño AM, Fukao T, Orii T, Tomatsu S. Yasuda E, et al. Among authors: tomatsu s. Mol Genet Metab. 2016 Jun;118(2):111-22. doi: 10.1016/j.ymgme.2016.04.005. Epub 2016 Apr 25. Mol Genet Metab. 2016. PMID: 27161890 Free PMC article.

2

Optimization of electroporation for transfection of human fibroblast cell lines with origin-defective SV40 DNA: development of human transformed fibroblast cell lines with mucopolysaccharidoses (I-VII).

Okamoto H, Sukegawa K, Tomatsu S, Suzuki Y, Orii T. Okamoto H, et al. Among authors: tomatsu s. Cell Struct Funct. 1992 Apr;17(2):123-8. doi: 10.1247/csf.17.123. Cell Struct Funct. 1992. PMID: 1318788 Free article.

3

Intermediate form of mucopolysaccharidosis type II (Hunter disease): a C1327 to T substitution in the iduronate sulfatase gene.

Sukegawa K, Tomatsu S, Tamai K, Ikeda M, Sasaki T, Masue M, Fukuda S, Yamada Y, Orii T. Sukegawa K, et al. Among authors: tomatsu s. Biochem Biophys Res Commun. 1992 Mar 16;183(2):809-13. doi: 10.1016/0006-291x(92)90555-y. Biochem Biophys Res Commun. 1992. PMID: 1550586

4

Evidence for a structural mutation (347Ala to Thr) in a German family with 3-ketothiolase deficiency.

Fukao T, Yamaguchi S, Tomatsu S, Orii T, Frauendienst-Egger G, Schrod L, Osumi T, Hashimoto T. Fukao T, et al. Among authors: tomatsu s. Biochem Biophys Res Commun. 1991 Aug 30;179(1):124-9. doi: 10.1016/0006-291x(91)91343-b. Biochem Biophys Res Commun. 1991. PMID: 1715688

5

Morquio disease: isolation, characterization and expression of full-length cDNA for human N-acetylgalactosamine-6-sulfate sulfatase.

Tomatsu S, Fukuda S, Masue M, Sukegawa K, Fukao T, Yamagishi A, Hori T, Iwata H, Ogawa T, Nakashima Y, et al. Tomatsu S, et al. Biochem Biophys Res Commun. 1991 Dec 16;181(2):677-83. doi: 10.1016/0006-291x(91)91244-7. Biochem Biophys Res Commun. 1991. PMID: 1755850

6

Molecular analysis of mucopolysaccharidosis type VII.

Fukuda S, Tomatsu S, Sukegawa K, Sasaki T, Yamada Y, Kuwahara T, Okamoto H, Ikedo Y, Yamaguchi S, Orii T. Fukuda S, et al. Among authors: tomatsu s. J Inherit Metab Dis. 1991;14(5):800-4. doi: 10.1007/BF01799953. J Inherit Metab Dis. 1991. PMID: 1779626 No abstract available.

7

Purification and partial characterization of alpha-N-acetylglucosaminidase from human liver.

Sasaki T, Sukegawa K, Masue M, Fukuda S, Tomatsu S, Orii T. Sasaki T, et al. Among authors: tomatsu s. J Biochem. 1991 Nov;110(5):842-6. doi: 10.1093/oxfordjournals.jbchem.a123668. J Biochem. 1991. PMID: 1783617 Free article.

8

Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection.

Asano J, Tomatsu S, Sukegawa K, Ikedo Y, Minami R, Iida M, Nishimura M, Nakagawa M, Ohshiro M, Orii T. Asano J, et al. Among authors: tomatsu s. Clin Genet. 1991 Jun;39(6):419-24. doi: 10.1111/j.1399-0004.1991.tb03052.x. Clin Genet. 1991. PMID: 1863988

9

Non-existence of a tight association between a 444leucine to proline mutation and phenotypes of Gaucher disease: high frequency of a NciI polymorphism in the non-neuronopathic form.

Masuno M, Tomatsu S, Sukegawa K, Orii T. Masuno M, et al. Among authors: tomatsu s. Hum Genet. 1990 Jan;84(2):203-6. doi: 10.1007/BF00208943. Hum Genet. 1990. PMID: 1967589

10

[Molecular basis of mucopolysaccaridosis type VII (beta-glucuronidase deficiency)].

Tomatsu S, Fukuda S, Sukegawa K, Yamaguchi S, Sasaki T, Ikedo Y, Orii T. Tomatsu S, et al. Rinsho Byori. 1990 Sep;38(9):1027-35. Rinsho Byori. 1990. PMID: 2232263 Japanese.

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