Sakuraba H - Search Results

1

Lyso-GM2 ganglioside: a possible biomarker of Tay-Sachs disease and Sandhoff disease.

Kodama T, Togawa T, Tsukimura T, Kawashima I, Matsuoka K, Kitakaze K, Tsuji D, Itoh K, Ishida Y, Suzuki M, Suzuki T, Sakuraba H. Kodama T, et al. Among authors: sakuraba h. PLoS One. 2011;6(12):e29074. doi: 10.1371/journal.pone.0029074. Epub 2011 Dec 20. PLoS One. 2011. PMID: 22205997 Free PMC article.

2

[Degradation of glycoconjugates in lysosomes and its disorders].

Itoh K, Sakuraba H. Itoh K, et al. Among authors: sakuraba h. Tanpakushitsu Kakusan Koso. 1992 Aug;37(11 Suppl):1951-6. Tanpakushitsu Kakusan Koso. 1992. PMID: 1410488 Review. Japanese. No abstract available.

3

Characterization and purification of human beta-galactosidase overexpressed in recombinant baculovirus-infected Spodoptera frugiperda cells.

Itoh K, Oshima A, Sakuraba H, Suzuki Y. Itoh K, et al. Among authors: sakuraba h. J Inherit Metab Dis. 1991;14(5):813-8. doi: 10.1007/BF01799955. J Inherit Metab Dis. 1991. PMID: 1779628 No abstract available.

4

Expression, glycosylation, and intracellular distribution of human beta-galactosidase in recombinant baculovirus-infected Spodoptera frugiperda cells.

Itoh K, Oshima A, Sakuraba H, Suzuki Y. Itoh K, et al. Among authors: sakuraba h. Biochem Biophys Res Commun. 1990 Mar 16;167(2):746-53. doi: 10.1016/0006-291x(90)92088-h. Biochem Biophys Res Commun. 1990. PMID: 2108671

5

Beta-galactosidase-deficient human fibroblasts: uptake and processing of the exogenous precursor enzyme expressed by stable transformant COS cells.

Oshima A, Itoh K, Nagao Y, Sakuraba H, Suzuki Y. Oshima A, et al. Among authors: sakuraba h. Hum Genet. 1990 Oct;85(5):505-8. doi: 10.1007/BF00194225. Hum Genet. 1990. PMID: 2121639

6

[Partial deletion of alpha-galactosidase A gene in a Japanese mutant of Fabry disease].

Sakuraba H, Bishop DF, Suzuki T, Suzuki Y, Desnick RJ. Sakuraba H, et al. No To Hattatsu. 1990 May;22(3):247-52. No To Hattatsu. 1990. PMID: 2163664 Japanese.

7

Galactosialidosis: simultaneous deficiency of esterase, carboxy-terminal deamidase and acid carboxypeptidase activities.

Kase R, Itoh K, Takiyama N, Oshima A, Sakuraba H, Suzuki Y. Kase R, et al. Among authors: sakuraba h. Biochem Biophys Res Commun. 1990 Nov 15;172(3):1175-9. doi: 10.1016/0006-291x(90)91572-a. Biochem Biophys Res Commun. 1990. PMID: 2244901

8

A novel missense mutation (C522Y) is present in the beta-hexosaminidase beta-subunit gene of a Japanese patient with infantile Sandhoff disease.

Kuroki Y, Itoh K, Nadaoka Y, Tanaka T, Sakuraba H. Kuroki Y, et al. Among authors: sakuraba h. Biochem Biophys Res Commun. 1995 Jul 17;212(2):564-71. doi: 10.1006/bbrc.1995.2007. Biochem Biophys Res Commun. 1995. PMID: 7626071

9

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: sakuraba h. 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.

10

Evidence for direct binding of intracellularly distributed ganglioside GM2 to isolated vimentin intermediate filaments in normal and Tay-Sachs disease human fibroblasts.

Kotani M, Hosoya H, Kubo H, Itoh K, Sakuraba H, Kusubata M, Inagaki M, Yazaki S, Suzuki Y, Tai T. Kotani M, et al. Among authors: sakuraba h. Cell Struct Funct. 1994 Apr;19(2):81-7. doi: 10.1247/csf.19.81. Cell Struct Funct. 1994. PMID: 7923401 Free article.

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