Saito S - Search Results

1

Screening of Fabry disease in patients with chronic kidney disease in Japan.

Nagata A, Nasu M, Kaida Y, Nakayama Y, Kurokawa Y, Nakamura N, Shibata R, Hazama T, Tsukimura T, Togawa T, Saito S, Sakuraba H, Fukami K. Nagata A, et al. Among authors: saito s. Nephrol Dial Transplant. 2021 Dec 31;37(1):115-125. doi: 10.1093/ndt/gfaa324. Nephrol Dial Transplant. 2021. PMID: 34282462 Free PMC article.

2

Fabry-database.org: database of the clinical phenotypes, genotypes and mutant α-galactosidase A structures in Fabry disease.

Saito S, Ohno K, Sakuraba H. Saito S, et al. J Hum Genet. 2011 Jun;56(6):467-8. doi: 10.1038/jhg.2011.31. Epub 2011 Mar 17. J Hum Genet. 2011. PMID: 21412250

3

High-throughput screening identified disease-causing mutants and functional variants of α-galactosidase A gene in Japanese male hemodialysis patients.

Doi K, Noiri E, Ishizu T, Negishi K, Suzuki Y, Hamasaki Y, Honda K, Fujita T, Tsukimura T, Togawa T, Saito S, Sakuraba H. Doi K, et al. Among authors: saito s. J Hum Genet. 2012 Sep;57(9):575-9. doi: 10.1038/jhg.2012.68. Epub 2012 Jun 14. J Hum Genet. 2012. PMID: 22695894

4

Erratum to: Screening of Fabry disease in patients with chronic kidney disease in Japan.

Nagata A, Nasu M, Kaida Y, Nakayama Y, Kurokawa Y, Nakamura N, Shibata R, Hazama T, Tsukimura T, Togawa T, Saito S, Sakuraba H, Fukami K. Nagata A, et al. Among authors: saito s. Nephrol Dial Transplant. 2021 Nov 9;36(11):2155-2159. doi: 10.1093/ndt/gfab234. Nephrol Dial Transplant. 2021. PMID: 34535801 Free PMC article. No abstract available.

5

Structural characterization of mutant alpha-galactosidases causing Fabry disease.

Sugawara K, Ohno K, Saito S, Sakuraba H. Sugawara K, et al. Among authors: saito s. J Hum Genet. 2008;53(9):812-824. doi: 10.1007/s10038-008-0316-9. Epub 2008 Jul 17. J Hum Genet. 2008. PMID: 18633574

6

Molecular interaction of imino sugars with human alpha-galactosidase: Insight into the mechanism of complex formation and pharmacological chaperone action in Fabry disease.

Sugawara K, Tajima Y, Kawashima I, Tsukimura T, Saito S, Ohno K, Iwamoto K, Kobayashi T, Itoh K, Sakuraba H. Sugawara K, et al. Among authors: saito s. Mol Genet Metab. 2009 Apr;96(4):233-8. doi: 10.1016/j.ymgme.2008.12.017. Epub 2009 Jan 31. Mol Genet Metab. 2009. PMID: 19181556

7

Prediction of the clinical phenotype of Fabry disease based on protein sequential and structural information.

Saito S, Ohno K, Sese J, Sugawara K, Sakuraba H. Saito S, et al. J Hum Genet. 2010 Mar;55(3):175-8. doi: 10.1038/jhg.2010.5. Epub 2010 Feb 5. J Hum Genet. 2010. PMID: 20139917

8

Molecular mechanism for stabilization of a mutant α-galactosidase A involving M51I amino acid substitution by imino sugars.

Tsukimura T, Chiba Y, Ohno K, Saito S, Tajima Y, Sakuraba H. Tsukimura T, et al. Among authors: saito s. Mol Genet Metab. 2011 May;103(1):26-32. doi: 10.1016/j.ymgme.2011.01.013. Epub 2011 Feb 2. Mol Genet Metab. 2011. PMID: 21353612

9

Fabry disease: biochemical, pathological and structural studies of the α-galactosidase A with E66Q amino acid substitution.

Togawa T, Tsukimura T, Kodama T, Tanaka T, Kawashima I, Saito S, Ohno K, Fukushige T, Kanekura T, Satomura A, Kang DH, Lee BH, Yoo HW, Doi K, Noiri E, Sakuraba H. Togawa T, et al. Among authors: saito s. Mol Genet Metab. 2012 Apr;105(4):615-20. doi: 10.1016/j.ymgme.2012.01.010. Epub 2012 Jan 18. Mol Genet Metab. 2012. PMID: 22305854

10

Mutant α-galactosidase A with M296I does not cause elevation of the plasma globotriaosylsphingosine level.

Mitobe S, Togawa T, Tsukimura T, Kodama T, Tanaka T, Doi K, Noiri E, Akai Y, Saito Y, Yoshino M, Takenaka T, Saito S, Ohno K, Sakuraba H. Mitobe S, et al. Among authors: saito s, saito y. Mol Genet Metab. 2012 Nov;107(3):623-6. doi: 10.1016/j.ymgme.2012.07.003. Epub 2012 Jul 14. Mol Genet Metab. 2012. PMID: 22841442

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