Shiomi T - Search Results

1

Purkinje cell degeneration in mice lacking the xeroderma pigmentosum group G gene.

Sun XZ, Harada YN, Takahashi S, Shiomi N, Shiomi T. Sun XZ, et al. Among authors: shiomi t, shiomi n. J Neurosci Res. 2001 May 15;64(4):348-54. doi: 10.1002/jnr.1085. J Neurosci Res. 2001. PMID: 11340641

2

Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene.

Harada YN, Shiomi N, Koike M, Ikawa M, Okabe M, Hirota S, Kitamura Y, Kitagawa M, Matsunaga T, Nikaido O, Shiomi T. Harada YN, et al. Among authors: shiomi t, shiomi n. Mol Cell Biol. 1999 Mar;19(3):2366-72. doi: 10.1128/MCB.19.3.2366. Mol Cell Biol. 1999. PMID: 10022922 Free PMC article.

3

An ERCC5 gene with homology to yeast RAD2 is involved in group G xeroderma pigmentosum.

Shiomi T, Harada Y, Saito T, Shiomi N, Okuno Y, Yamaizumi M. Shiomi T, et al. Among authors: shiomi n. Mutat Res. 1994 Mar;314(2):167-75. doi: 10.1016/0921-8777(94)90080-9. Mutat Res. 1994. PMID: 7510366

4

Complementary DNA sequence and chromosomal localization of xpg, the mouse counterpart of human repair gene XPG/ERCC5.

Harada YN, Matsuda Y, Shiomi N, Shiomi T. Harada YN, et al. Among authors: shiomi t, shiomi n. Genomics. 1995 Jul 1;28(1):59-65. doi: 10.1006/geno.1995.1106. Genomics. 1995. PMID: 7590748

5

Chromosomal localization of the mouse and rat DNA double-strand break repair genes Ku p70 and Ku p80/XRCC5 and their mRNA expression in various mouse tissues.

Koike M, Matsuda Y, Mimori T, Harada YN, Shiomi N, Shiomi T. Koike M, et al. Among authors: shiomi t, shiomi n. Genomics. 1996 Nov 15;38(1):38-44. doi: 10.1006/geno.1996.0589. Genomics. 1996. PMID: 8954777

6

Disruption of Xpg increases spontaneous mutation frequency, particularly A:T to C:G transversion.

Shiomi N, Hayashi E, Sasanuma S, Mita K, Shiomi T. Shiomi N, et al. Among authors: shiomi t. Mutat Res. 2001 Dec 19;487(3-4):127-35. doi: 10.1016/s0921-8777(01)00111-2. Mutat Res. 2001. PMID: 11738939

7

DNA methylation in xeroderma pigmentosum.

Sano H, Shiomi N, Imanishi K, Maie O, Shiomi T. Sano H, et al. Among authors: shiomi t, shiomi n. Mutat Res. 1989 Mar;217(2):141-51. doi: 10.1016/0921-8777(89)90066-9. Mutat Res. 1989. PMID: 2918867

8

Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A.

Itoh T, Shiomi T, Shiomi N, Harada Y, Wakasugi M, Matsunaga T, Nikaido O, Friedberg EC, Yamaizumi M. Itoh T, et al. Among authors: shiomi t, shiomi n. Mutat Res. 1996 Feb 15;362(2):167-74. doi: 10.1016/0921-8777(95)00046-1. Mutat Res. 1996. PMID: 8596535

9

Precise localization of the excision repair gene, ERCC5, to human chromosome 13q32.3-q33.1 by direct R-banding fluorescence in situ hybridization.

Takahashi E, Shiomi N, Shiomi T. Takahashi E, et al. Among authors: shiomi t, shiomi n. Jpn J Cancer Res. 1992 Nov;83(11):1117-9. doi: 10.1111/j.1349-7006.1992.tb02731.x. Jpn J Cancer Res. 1992. PMID: 1483924 Free PMC article.

10

Location of the mouse complement factor H gene (cfh) by FISH analysis and replication R-banding.

Matsuda Y, Harada YN, Natsuume-Sakai S, Lee K, Shiomi T, Chapman VM. Matsuda Y, et al. Among authors: shiomi t. Cytogenet Cell Genet. 1992;61(4):282-5. doi: 10.1159/000133423. Cytogenet Cell Genet. 1992. PMID: 1486806

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