Kishino T - Search Results

1

Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q32.

Yamada T, Mitsuya K, Kayashima T, Yamasaki K, Ohta T, Yoshiura K, Matsumoto N, Yamada H, Minakami H, Oshimura M, Niikawa N, Kishino T. Yamada T, et al. Among authors: kishino t. Genomics. 2004 Mar;83(3):402-12. doi: 10.1016/j.ygeno.2003.08.016. Genomics. 2004. PMID: 14962666

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

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.

5

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

6

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

7

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

8

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

9

Molecular cloning, tissue distribution, and chromosomal localization of human cationic amino acid transporter 2 (HCAT2).

Hoshide R, Ikeda Y, Karashima S, Matsuura T, Komaki S, Kishino T, Niikawa N, Endo F, Matsuda I. Hoshide R, et al. Among authors: kishino t. Genomics. 1996 Dec 1;38(2):174-8. doi: 10.1006/geno.1996.0613. Genomics. 1996. PMID: 8954799

10

Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32.

Hayashida S, Yamasaki K, Asada Y, Soeda E, Niikawa N, Kishino T. Hayashida S, et al. Among authors: kishino t. Genomics. 2000 Jun 1;66(2):221-5. doi: 10.1006/geno.2000.6206. Genomics. 2000. PMID: 10860668

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