Kishino T - Search Results

1

Duplication of 8p23.2: a benign cytogenetic variant?

Harada N, Takano J, Kondoh T, Ohashi H, Hasegawa T, Sugawara H, Ida T, Yoshiura K, Ohta T, Kishino T, Kajii T, Niikawa N, Matsumoto N. Harada N, et al. Among authors: kishino t. Am J Med Genet. 2002 Aug 15;111(3):285-8. doi: 10.1002/ajmg.10584. Am J Med Genet. 2002. PMID: 12210324

2

A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.

Tonoki H, Kishino T, Niikawa N. Tonoki H, et al. Among authors: kishino t. Am J Med Genet. 1990 May;36(1):89-93. doi: 10.1002/ajmg.1320360117. Am J Med Genet. 1990. PMID: 2333912

3

Molecular cloning of a human protein that binds to the retinoblastoma protein and chromosomal mapping.

Saijo M, Sakai Y, Kishino T, Niikawa N, Matsuura Y, Morino K, Tamai K, Taya Y. Saijo M, et al. Among authors: kishino t. Genomics. 1995 Jun 10;27(3):511-9. doi: 10.1006/geno.1995.1084. Genomics. 1995. PMID: 7558034

4

Skewed X-inactivation in a tumor tissue from a female patient with leiomyomatosis.

Kishino T, Jinno Y, Niikawa N, Hashida T. Kishino T, et al. Am J Med Genet. 1995 Jul 17;57(4):637-8. doi: 10.1002/ajmg.1320570425. Am J Med Genet. 1995. PMID: 7573145 No abstract available.

5

Isolation of microdissection clones from rat chromosome 10.

Kobayashi T, Kawaguchi T, Kishino T, Matsumoto N, Niikawa N, Mori M, Levan G, Klinga-Levan K, Hino O. Kobayashi T, et al. Among authors: kishino t. Mamm Genome. 1995 Mar;6(3):216-8. doi: 10.1007/BF00293019. Mamm Genome. 1995. PMID: 7749234 No abstract available.

6

Isolation and characterization of mutations in the human holocarboxylase synthetase cDNA.

Suzuki Y, Aoki Y, Ishida Y, Chiba Y, Iwamatsu A, Kishino T, Niikawa N, Matsubara Y, Narisawa K. Suzuki Y, et al. Among authors: kishino t. Nat Genet. 1994 Oct;8(2):122-8. doi: 10.1038/ng1094-122. Nat Genet. 1994. PMID: 7842009

7

Assignment of the human moesin gene (MSN) to chromosome region Xq11.2-->q12.

Kishino T, Ariga T, Soejima H, Tamura T, Ohta T, Jinno Y, Yonemura S, Sato N, Tsukita S, Tsukita S, et al. Kishino T, et al. Cytogenet Cell Genet. 1994;66(3):167-9. doi: 10.1159/000133692. Cytogenet Cell Genet. 1994. PMID: 8125014

8

Assignment of the human PAX4 gene to chromosome band 7q32 by fluorescence in situ hybridization.

Tamura T, Izumikawa Y, Kishino T, Soejima H, Jinno Y, Niikawa N. Tamura T, et al. Among authors: kishino t. Cytogenet Cell Genet. 1994;66(2):132-4. doi: 10.1159/000133684. Cytogenet Cell Genet. 1994. PMID: 8287686

9

Mapping of the bone morphogenetic protein 1 gene (BMP1) to 8p21: removal of BMP1 from candidacy for the bone disorder in Langer-Giedion syndrome.

Yoshiura K, Tamura T, Hong HS, Ohta T, Soejima H, Kishino T, Jinno Y, Niikawa N. Yoshiura K, et al. Among authors: kishino t. Cytogenet Cell Genet. 1993;64(3-4):208-9. doi: 10.1159/000133577. Cytogenet Cell Genet. 1993. PMID: 8404039

10

cDNA sequence and chromosomal localization of a novel human protein, RBQ-1 (RBBP6), that binds to the retinoblastoma gene product.

Sakai Y, Saijo M, Coelho K, Kishino T, Niikawa N, Taya Y. Sakai Y, et al. Among authors: kishino t. Genomics. 1995 Nov 1;30(1):98-101. doi: 10.1006/geno.1995.0017. Genomics. 1995. PMID: 8595913

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