Shimizu T - Search Results

1

Mutation spectrum of the retinoblastoma gene in osteosarcomas.

Wadayama B, Toguchida J, Shimizu T, Ishizaki K, Sasaki MS, Kotoura Y, Yamamuro T. Wadayama B, et al. Among authors: shimizu t. Cancer Res. 1994 Jun 1;54(11):3042-8. Cancer Res. 1994. PMID: 8187094

2

Delayed development of retinoblastoma associated with loss of a maternal allele on chromosome 13.

Kato MV, Ishizaki K, Shimizu T, Toguchida J, Kaneko A, Sasaki MS. Kato MV, et al. Among authors: shimizu t. Int J Cancer. 1995 Feb 20;64(1):3-8. doi: 10.1002/ijc.2910640103. Int J Cancer. 1995. PMID: 7665245

3

Parental origin of germ-line and somatic mutations in the retinoblastoma gene.

Kato MV, Ishizaki K, Shimizu T, Ejima Y, Tanooka H, Takayama J, Kaneko A, Toguchida J, Sasaki MS. Kato MV, et al. Among authors: shimizu t. Hum Genet. 1994 Jul;94(1):31-8. doi: 10.1007/BF02272838. Hum Genet. 1994. PMID: 8034292

4

Mutations in the retinoblastoma gene and their expression in somatic and tumor cells of patients with hereditary retinoblastoma.

Kato MV, Ishizaki K, Toguchida J, Kaneko A, Takayama J, Tanooka H, Kato T, Shimizu T, Sasaki MS. Kato MV, et al. Among authors: shimizu t. Hum Mutat. 1994;3(1):44-51. doi: 10.1002/humu.1380030108. Hum Mutat. 1994. PMID: 8118465

5

Detection of mutations of the RB1 gene in retinoblastoma patients by using exon-by-exon PCR-SSCP analysis.

Shimizu T, Toguchida J, Kato MV, Kaneko A, Ishizaki K, Sasaki MS. Shimizu T, et al. Am J Hum Genet. 1994 May;54(5):793-800. Am J Hum Genet. 1994. PMID: 8178820 Free PMC article.

6

Loss of heterozygosity on chromosome 17 and mutation of the p53 gene in retinoblastoma.

Kato MV, Shimizu T, Ishizaki K, Kaneko A, Yandell DW, Toguchida J, Sasaki MS. Kato MV, et al. Among authors: shimizu t. Cancer Lett. 1996 Aug 23;106(1):75-82. doi: 10.1016/0304-3835(96)04305-4. Cancer Lett. 1996. PMID: 8827049

7

The FANCA gene in Japanese Fanconi anemia: reports of eight novel mutations and analysis of sequence variability.

Tachibana A, Kato T, Ejima Y, Yamada T, Shimizu T, Yang L, Tsunematsu Y, Sasaki MS. Tachibana A, et al. Among authors: shimizu t. Hum Mutat. 1999;13(3):237-44. doi: 10.1002/(SICI)1098-1004(1999)13:3<237::AID-HUMU8>3.0.CO;2-F. Hum Mutat. 1999. PMID: 10090479

8

A high prevalence of functional inactivation by methylation modification of p16INK4A/CDKN2/MTS1 gene in primary urothelial cancers.

Akao T, Kakehi Y, Itoh N, Ozdemir E, Shimizu T, Tachibana A, Sasaki MS, Yoshida O. Akao T, et al. Among authors: shimizu t. Jpn J Cancer Res. 1997 Nov;88(11):1078-86. doi: 10.1111/j.1349-7006.1997.tb00332.x. Jpn J Cancer Res. 1997. PMID: 9439683 Free PMC article.

9

Coordinated regulation of radioadaptive response by protein kinase C and p38 mitogen-activated protein kinase.

Shimizu T, Kato T Jr, Tachibana A, Sasaki MS. Shimizu T, et al. Exp Cell Res. 1999 Sep 15;251(2):424-32. doi: 10.1006/excr.1999.4582. Exp Cell Res. 1999. PMID: 10471327

10

Novel mutations of the FANCG gene causing alternative splicing in Japanese Fanconi anemia.

Yamada T, Tachibana A, Shimizu T, Mugishima H, Okubo M, Sasaki MS. Yamada T, et al. Among authors: shimizu t. J Hum Genet. 2000;45(3):159-66. doi: 10.1007/s100380050203. J Hum Genet. 2000. PMID: 10807541

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