Inoue T - Search Results

1

Intragenic homozygous deletion of the WT1 gene in Wilms' tumor.

Tadokoro K, Fujii H, Ohshima A, Kakizawa Y, Shimizu K, Sakai A, Sumiyoshi K, Inoue T, Hayashi Y, Yamada M. Tadokoro K, et al. Among authors: inoue t. Oncogene. 1992 Jun;7(6):1215-21. Oncogene. 1992. PMID: 1350671

2

PCR detection of 9 polymorphisms in the WT1 gene.

Tadokoro K, Oki N, Sakai A, Fujii H, Ohshima A, Nagafuchi S, Inoue T, Yamada M. Tadokoro K, et al. Among authors: inoue t. Hum Mol Genet. 1993 Dec;2(12):2205-6. doi: 10.1093/hmg/2.12.2205. Hum Mol Genet. 1993. PMID: 8111408 No abstract available.

3

Genomic organization of the human WT1 gene.

Tadokoro K, Oki N, Fujii H, Ohshima A, Inoue T, Yamada M. Tadokoro K, et al. Among authors: inoue t. Jpn J Cancer Res. 1992 Nov;83(11):1198-203. doi: 10.1111/j.1349-7006.1992.tb02745.x. Jpn J Cancer Res. 1992. PMID: 1483934 Free PMC article.

4

Polymerase chain reaction (PCR) for detection of ApaI polymorphism at the insulin like growth factor II gene (IGF2).

Tadokoro K, Fujii H, Inoue T, Yamada M. Tadokoro K, et al. Among authors: inoue t. Nucleic Acids Res. 1991 Dec 25;19(24):6967. doi: 10.1093/nar/19.24.6967. Nucleic Acids Res. 1991. PMID: 1684848 Free PMC article.

5

Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA).

Nagafuchi S, Yanagisawa H, Ohsaki E, Shirayama T, Tadokoro K, Inoue T, Yamada M. Nagafuchi S, et al. Among authors: inoue t. Nat Genet. 1994 Oct;8(2):177-82. doi: 10.1038/ng1094-177. Nat Genet. 1994. PMID: 7842016

6

A unique origin and multistep process for the generation of expanded DRPLA triplet repeats.

Yanagisawa H, Fujii K, Nagafuchi S, Nakahori Y, Nakagome Y, Akane A, Nakamura M, Sano A, Komure O, Kondo I, Jin DK, Sørensen SA, Potter NT, Young SR, Nakamura K, Nukina N, Nagao Y, Tadokoro K, Okuyama T, Miyashita T, Inoue T, Kanazawa I, Yamada M. Yanagisawa H, et al. Among authors: inoue t. Hum Mol Genet. 1996 Mar;5(3):373-9. doi: 10.1093/hmg/5.3.373. Hum Mol Genet. 1996. PMID: 8852663

7

An alternatively spliced form of the human CD94 gene.

Furukawa H, Yabe T, Watanabe K, Miyamoto R, Akaza T, Tadokoro K, Tohma S, Inoue T, Yamamoto K, Juji T. Furukawa H, et al. Among authors: inoue t. Immunogenetics. 1998 Jun;48(1):87-8. doi: 10.1007/s002510050407. Immunogenetics. 1998. PMID: 9601951 No abstract available.

8

Polymorphism of TAPASIN and its linkage disequilibria with HLA class II genes in the Japanese population.

Furukawa H, Kashiwase K, Yabe T, Ishikawa Y, Akaza T, Tadokoro K, Tohma S, Inoue T, Tokunaga K, Yamamoto K, Juji T. Furukawa H, et al. Among authors: inoue t. Tissue Antigens. 1998 Sep;52(3):279-81. doi: 10.1111/j.1399-0039.1998.tb03044.x. Tissue Antigens. 1998. PMID: 9802609

9

Bcl-2 relieves the trans-repressive function of the glucocorticoid receptor and inhibits the activation of CPP32-like cysteine proteases.

Miyashita T, Mami U, Inoue T, Reed JC, Yamada M. Miyashita T, et al. Among authors: inoue t. Biochem Biophys Res Commun. 1997 Apr 28;233(3):781-7. doi: 10.1006/bbrc.1997.6559. Biochem Biophys Res Commun. 1997. PMID: 9168933

10

Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies.

Azuma N, Hirakiyama A, Inoue T, Asaka A, Yamada M. Azuma N, et al. Among authors: inoue t. Hum Mol Genet. 2000 Feb 12;9(3):363-6. doi: 10.1093/hmg/9.3.363. Hum Mol Genet. 2000. PMID: 10655545

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