Tajima Y - Search Results

1

Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathies.

Taniguchi M, Kurahashi H, Noguchi S, Fukudome T, Okinaga T, Tsukahara T, Tajima Y, Ozono K, Nishino I, Nonaka I, Toda T. Taniguchi M, et al. Among authors: tajima y. Hum Mol Genet. 2006 Apr 15;15(8):1279-89. doi: 10.1093/hmg/ddl045. Epub 2006 Mar 10. Hum Mol Genet. 2006. PMID: 16531417

2

Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.

Kanagawa M, Nishimoto A, Chiyonobu T, Takeda S, Miyagoe-Suzuki Y, Wang F, Fujikake N, Taniguchi M, Lu Z, Tachikawa M, Nagai Y, Tashiro F, Miyazaki J, Tajima Y, Takeda S, Endo T, Kobayashi K, Campbell KP, Toda T. Kanagawa M, et al. Among authors: tajima y. Hum Mol Genet. 2009 Feb 15;18(4):621-31. doi: 10.1093/hmg/ddn387. Epub 2008 Nov 18. Hum Mol Genet. 2009. PMID: 19017726 Free PMC article.

3

Comparison of the effects of agalsidase alfa and agalsidase beta on cultured human Fabry fibroblasts and Fabry mice.

Sakuraba H, Murata-Ohsawa M, Kawashima I, Tajima Y, Kotani M, Ohshima T, Chiba Y, Takashiba M, Jigami Y, Fukushige T, Kanzaki T, Itoh K. Sakuraba H, et al. Among authors: tajima y. J Hum Genet. 2006;51(3):180-188. doi: 10.1007/s10038-005-0342-9. Epub 2005 Dec 22. J Hum Genet. 2006. PMID: 16372133

4

Use of a modified alpha-N-acetylgalactosaminidase in the development of enzyme replacement therapy for Fabry disease.

Tajima Y, Kawashima I, Tsukimura T, Sugawara K, Kuroda M, Suzuki T, Togawa T, Chiba Y, Jigami Y, Ohno K, Fukushige T, Kanekura T, Itoh K, Ohashi T, Sakuraba H. Tajima Y, et al. Am J Hum Genet. 2009 Nov;85(5):569-80. doi: 10.1016/j.ajhg.2009.09.016. Epub 2009 Oct 22. Am J Hum Genet. 2009. PMID: 19853240 Free PMC article.

5

Biochemical and structural study on a S529V mutant acid α-glucosidase responsive to pharmacological chaperones.

Tajima Y, Saito S, Ohno K, Tsukimura T, Tsujino S, Sakuraba H. Tajima Y, et al. J Hum Genet. 2011 Jun;56(6):440-6. doi: 10.1038/jhg.2011.36. Epub 2011 Apr 7. J Hum Genet. 2011. PMID: 21471980

6

Establishment of immortalized Schwann cells from Fabry mice and their low uptake of recombinant alpha-galactosidase.

Kawashima I, Watabe K, Tajima Y, Fukushige T, Kanzaki T, Kanekura T, Sugawara K, Ohyanagi N, Suzuki T, Togawa T, Sakuraba H. Kawashima I, et al. Among authors: tajima y. J Hum Genet. 2007;52(12):1018-1025. doi: 10.1007/s10038-007-0210-x. Epub 2007 Oct 27. J Hum Genet. 2007. PMID: 17965825

7

Corrective effect on Fabry mice of yeast recombinant human alpha-galactosidase with N-linked sugar chains suitable for lysosomal delivery.

Sakuraba H, Chiba Y, Kotani M, Kawashima I, Ohsawa M, Tajima Y, Takaoka Y, Jigami Y, Takahashi H, Hirai Y, Shimada T, Hashimoto Y, Ishii K, Kobayashi T, Watabe K, Fukushige T, Kanzaki T. Sakuraba H, et al. Among authors: tajima y. J Hum Genet. 2006;51(4):341-352. doi: 10.1007/s10038-006-0369-6. Epub 2006 Mar 11. J Hum Genet. 2006. PMID: 16532254

8

Establishment of immortalized Schwann cells from Sandhoff mice and corrective effect of recombinant human beta-hexosaminidase A on the accumulated GM2 ganglioside.

Ohsawa M, Kotani M, Tajima Y, Tsuji D, Ishibashi Y, Kuroki A, Itoh K, Watabe K, Sango K, Yamanaka S, Sakuraba H. Ohsawa M, et al. Among authors: tajima y. J Hum Genet. 2005;50(9):460-467. doi: 10.1007/s10038-005-0278-0. Epub 2005 Sep 23. J Hum Genet. 2005. PMID: 16180049

9

Clinical, biochemical, and cytochemical studies on a Japanese Salla disease case associated with a renal disorder.

Ishiwari K, Kotani M, Suzuki M, Pumbo E, Suzuki A, Kobayashi T, Ueno T, Fukushige T, Kanzaki T, Imada M, Itoh K, Akioka S, Tajima Y, Sakuraba H. Ishiwari K, et al. Among authors: tajima y. J Hum Genet. 2004;49(12):656-663. doi: 10.1007/s10038-004-0203-y. Epub 2004 Nov 13. J Hum Genet. 2004. PMID: 15635485

10

Structural and biochemical studies on Pompe disease and a "pseudodeficiency of acid alpha-glucosidase".

Tajima Y, Matsuzawa F, Aikawa SI, Okumiya T, Yoshimizu M, Tsukimura T, Ikekita M, Tsujino S, Tsuji A, Edmunds T, Sakuraba H. Tajima Y, et al. J Hum Genet. 2007;52(11):898-906. doi: 10.1007/s10038-007-0191-9. Epub 2007 Sep 6. J Hum Genet. 2007. PMID: 17805474

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