Shimizu N - Search Results

1

Detailed deletion mapping of chromosome band 14q32 in human neuroblastoma defines a 1.1-Mb region of common allelic loss.

Hoshi M, Otagiri N, Shiwaku HO, Asakawa S, Shimizu N, Kaneko Y, Ohi R, Hayashi Y, Horii A. Hoshi M, et al. Among authors: shimizu n. Br J Cancer. 2000 Jun;82(11):1801-7. doi: 10.1054/bjoc.2000.1108. Br J Cancer. 2000. PMID: 10839294 Free PMC article.

2

The organization of the human immunoglobulin lambda gene locus.

Kawasaki K, Minoshima S, Schooler K, Kudoh J, Asakawa S, de Jong PJ, Shimizu N. Kawasaki K, et al. Among authors: shimizu n. Genome Res. 1995 Sep;5(2):125-35. doi: 10.1101/gr.5.2.125. Genome Res. 1995. PMID: 9132267 Free article.

3

Assignment of the human poly(A) polymerase (PAP) gene to chromosome 14q32.1-q32.2 and isolation of a polymorphic CA repeat sequence.

Yamauchi T, Sugimoto J, Hatakeyama T, Asakawa S, Shimizu N, Isobe M. Yamauchi T, et al. Among authors: shimizu n. J Hum Genet. 1999;44(4):253-5. doi: 10.1007/s100380050154. J Hum Genet. 1999. PMID: 10429366

4

A 2-Mb sequence-ready contig map and a novel immunoglobulin superfamily gene IGSF4 in the LOH region of chromosome 11q23.2.

Gomyo H, Arai Y, Tanigami A, Murakami Y, Hattori M, Hosoda F, Arai K, Aikawa Y, Tsuda H, Hirohashi S, Asakawa S, Shimizu N, Soeda E, Sakaki Y, Ohki M. Gomyo H, et al. Among authors: shimizu n. Genomics. 1999 Dec 1;62(2):139-46. doi: 10.1006/geno.1999.6001. Genomics. 1999. PMID: 10610705

5

Isolation of cDNA for a novel human protein KNP-I that is homologous to the E. coli SCRP-27A protein from the autoimmune polyglandular disease type I (APECED) region of chromosome 21q22.3.

Nagamine K, Kudoh J, Minoshima S, Kawasaki K, Asakawa S, Ito F, Shimizu N. Nagamine K, et al. Among authors: shimizu n. Biochem Biophys Res Commun. 1996 Aug 14;225(2):608-16. doi: 10.1006/bbrc.1996.1218. Biochem Biophys Res Commun. 1996. PMID: 8753807

6

Chromosomal mapping of a family of human glutamine synthetase genes: functional gene (GLUL) on 1q25, pseudogene (GLULP) on 9p13, and three related genes (GLULL1, GLULL2, GLULL3) on 5q33, 11p15, and 11q24.

Wang Y, Kudoh J, Kubota R, Asakawa S, Minoshima S, Shimizu N. Wang Y, et al. Among authors: shimizu n. Genomics. 1996 Oct 15;37(2):195-9. doi: 10.1006/geno.1996.0542. Genomics. 1996. PMID: 8921392

7

Human retina-specific amine oxidase (RAO): cDNA cloning, tissue expression, and chromosomal mapping.

Imamura Y, Kubota R, Wang Y, Asakawa S, Kudoh J, Mashima Y, Oguchi Y, Shimizu N. Imamura Y, et al. Among authors: shimizu n. Genomics. 1997 Mar 1;40(2):277-83. doi: 10.1006/geno.1996.4570. Genomics. 1997. PMID: 9119395

8

A novel myosin-like protein (myocilin) expressed in the connecting cilium of the photoreceptor: molecular cloning, tissue expression, and chromosomal mapping.

Kubota R, Noda S, Wang Y, Minoshima S, Asakawa S, Kudoh J, Mashima Y, Oguchi Y, Shimizu N. Kubota R, et al. Among authors: shimizu n. Genomics. 1997 May 1;41(3):360-9. doi: 10.1006/geno.1997.4682. Genomics. 1997. PMID: 9169133

9

Mapping of the human HPC-1/syntaxin 1A gene (STX1A) to chromosome 7 band q11.2.

Nakayama T, Fujiwara T, Miyazawa A, Asakawa S, Shimizu N, Shimizu Y, Mikoshiba K, Akagawa K. Nakayama T, et al. Among authors: shimizu y, shimizu n. Genomics. 1997 May 15;42(1):173-6. doi: 10.1006/geno.1997.4650. Genomics. 1997. PMID: 9177791

10

Localization of 16 exons to a 450-kb region involved in the autoimmune polyglandular disease type I (APECED) on human chromosome 21q22.3.

Kudoh J, Nagamine K, Asakawa S, Abe I, Kawasaki K, Maeda H, Tsujimoto S, Minoshima S, Ito F, Shimizu N. Kudoh J, et al. Among authors: shimizu n. DNA Res. 1997 Feb 28;4(1):45-52. doi: 10.1093/dnares/4.1.45. DNA Res. 1997. PMID: 9179495 Free article.

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