Nakahori Y - Search Results

1

Assignment of cardiac homeobox gene CSX to human chromosome 5q34.

Shiojima I, Komuro I, Inazawa J, Nakahori Y, Matsushita I, Abe T, Nagai R, Yazaki Y. Shiojima I, et al. Among authors: nakahori y. Genomics. 1995 May 1;27(1):204-6. doi: 10.1006/geno.1995.1027. Genomics. 1995. PMID: 7665173

2

Assignment of the human GPAA1 gene, which encodes a product required for the attachment of glycosylphosphatidylinositols to proteins, at 8q24.

Hiroi Y, Komuro I, Matsushita I, Aburatani H, Hosoda T, Nakahori Y, Medof ME, Yazaki Y. Hiroi Y, et al. Among authors: nakahori y. Genomics. 1998 Dec 1;54(2):354-5. doi: 10.1006/geno.1998.5490. Genomics. 1998. PMID: 9828142 No abstract available.

3

A human protective protein gene partially overlaps the gene encoding phospholipid transfer protein on the complementary strand of DNA.

Shimmoto M, Nakahori Y, Matsushita I, Shinka T, Kuroki Y, Itoh K, Sakuraba H. Shimmoto M, et al. Among authors: nakahori y. Biochem Biophys Res Commun. 1996 Mar 27;220(3):802-6. doi: 10.1006/bbrc.1996.0484. Biochem Biophys Res Commun. 1996. PMID: 8607845

4

YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31.

Miyake M, Nakahori Y, Matsushita I, Kobayashi K, Mizuno K, Hirai M, Kanazawa I, Nakagome Y, Tokunaga K, Toda T. Miyake M, et al. Among authors: nakahori y. Genomics. 1997 Mar 1;40(2):284-93. doi: 10.1006/geno.1996.4584. Genomics. 1997. PMID: 9119396

5

Structure and chromosome location of human OGG1.

Ishida T, Hippo Y, Nakahori Y, Matsushita I, Kodama T, Nishimura S, Aburatani H. Ishida T, et al. Among authors: nakahori y. Cytogenet Cell Genet. 1999;85(3-4):232-6. doi: 10.1159/000015299. Cytogenet Cell Genet. 1999. PMID: 10449904

6

11q trisomy detected by fluorescence in situ hybridization.

Takano T, Yamanouchi Y, Kawashima S, Date M, Hashira S, Kida M, Abe T, Nakahori Y, Nakagome Y. Takano T, et al. Among authors: nakahori y. Clin Genet. 1993 Dec;44(6):324-8. doi: 10.1111/j.1399-0004.1993.tb03909.x. Clin Genet. 1993. PMID: 8131305

7

A novel (CA)n polymorphism on 6p21.1-21.2.

Kotliarova SE, Toda T, Matsushita I, Nakagome Y, Nakahori Y. Kotliarova SE, et al. Among authors: nakahori y. Jpn J Hum Genet. 1996 Dec;41(4):423-5. doi: 10.1007/BF01876334. Jpn J Hum Genet. 1996. PMID: 9088114

8

A locus of the candidate gene family for azoospermia factor (YRRM2) is polymorphic with a null allele in Japanese males.

Nakahori Y, Kobayashi K, Komaki R, Matsushita I, Nakagome Y. Nakahori Y, et al. Hum Mol Genet. 1994 Sep;3(9):1709. doi: 10.1093/hmg/3.9.1709. Hum Mol Genet. 1994. PMID: 7833938 No abstract available.

9

Molecular cloning and mapping of 10 new probes on the human Y chromosome.

Nakahori Y, Tamura T, Nagafuchi S, Fujieda K, Minowada S, Fukutani K, Fuse H, Hayashi K, Kuroki Y, Fukushima Y, et al. Nakahori Y, et al. Genomics. 1991 Apr;9(4):765-9. doi: 10.1016/0888-7543(91)90373-m. Genomics. 1991. PMID: 2037302

10

Novel (CA)n marker DXYS241 on the nonrecombinant part of the human Y chromosome.

Kotliarova SE, Toda T, Takenaka O, Matsushita I, Hida A, Shinka T, Goto J, Tokunaga K, Nakagome Y, Nakahori Y. Kotliarova SE, et al. Among authors: nakahori y. Hum Biol. 1999 Apr;71(2):261-75. Hum Biol. 1999. PMID: 10222647

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