Niikawa N - Search Results

1

Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2-p22.

Nagano K, Nakura J, Kihara K, Ye L, Kamino K, Mitsuda N, Ohta T, Jinno Y, Niikawa N, Miki T, et al. Nagano K, et al. Among authors: niikawa n. Jpn J Hum Genet. 1993 Dec;38(4):391-7. doi: 10.1007/BF01907985. Jpn J Hum Genet. 1993. PMID: 8186416

2

Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): chromosome microdissection and homozygosity mapping.

Ye L, Nakura J, Mitsuda N, Fujioka Y, Kamino K, Ohta T, Jinno Y, Niikawa N, Miki T, Ogihara T. Ye L, et al. Among authors: niikawa n. Genomics. 1995 Aug 10;28(3):566-9. doi: 10.1006/geno.1995.1189. Genomics. 1995. PMID: 7490095

3

Six dinucleotide repeat polymorphisms on chromosome 7.

Nakura J, Miki T, Ye L, Mitsuda N, Ogihara T, Ohta T, Jinno Y, Niikawa N, Takahashi-Fujii A, Ishino Y. Nakura J, et al. Among authors: niikawa n. Jpn J Hum Genet. 1994 Dec;39(4):447-9. doi: 10.1007/BF01892393. Jpn J Hum Genet. 1994. PMID: 7873760 No abstract available.

4

Cosmid clones from microdissected human chromosomal region 15q11-q13.

Tohma T, Tamura T, Ohta T, Soejima H, Kubota T, Jinno Y, Tsukamoto K, Nakamura Y, Naritomi K, Niikawa N. Tohma T, et al. Among authors: niikawa n. Jpn J Hum Genet. 1993 Sep;38(3):267-75. doi: 10.1007/BF01874137. Jpn J Hum Genet. 1993. PMID: 8260719

5

Population variation in the dinucleotide repeat polymorphism at the D8S360 locus.

Kamino K, Nakura J, Kihara K, Ye L, Nagano K, Ohta T, Jinno Y, Niikawa N, Miki T, Ogihara T. Kamino K, et al. Among authors: niikawa n. Hum Mol Genet. 1993 Oct;2(10):1751. doi: 10.1093/hmg/2.10.1751. Hum Mol Genet. 1993. PMID: 8268949 No abstract available.

6

The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.

Ohta T, Tohma T, Soejima H, Fukushima Y, Nagai T, Yoshiura K, Jinno Y, Niikawa N. Ohta T, et al. Among authors: niikawa n. Hum Genet. 1993 Aug;92(1):1-5. doi: 10.1007/BF00216136. Hum Genet. 1993. PMID: 8365720

7

Two polymorphic AvaI and HhaI sites in a differentially methylated region of the human H19 gene.

Miyatake S, Ikeda Y, Jinno Y, Niikawa N. Miyatake S, et al. Among authors: niikawa n. Jpn J Hum Genet. 1996 Jun;41(2):253-5. doi: 10.1007/BF01875986. Jpn J Hum Genet. 1996. PMID: 8771991

8

Physical map of a YAC contig containing the region of the human gene (HYRC) complementing hyper-radiosensitivity of the scid mouse mutation.

Watanabe Y, Matsumoto N, Ohta T, Tsujita T, Niikawa N. Watanabe Y, et al. Among authors: niikawa n. Jpn J Hum Genet. 1996 Mar;41(1):149-58. doi: 10.1007/BF01892622. Jpn J Hum Genet. 1996. PMID: 8914630

9

Isolation of 2 novel RFLP markers and their localization at 2q35 by microdissection and subsequent enzymatic amplification.

Kibe T, Tsukamoto K, Hirota T, Yoshiura K, Ohta T, Tohma T, Tamura T, Jinno Y, Niikawa N. Kibe T, et al. Among authors: niikawa n. Jpn J Hum Genet. 1992 Dec;37(4):263-70. doi: 10.1007/BF01883317. Jpn J Hum Genet. 1992. PMID: 1284292

10

Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool.

Deng HX, Yoshiura K, Dirks RW, Harada N, Hirota T, Tsukamoto K, Jinno Y, Niikawa N. Deng HX, et al. Among authors: niikawa n. Hum Genet. 1992 Apr;89(1):13-7. doi: 10.1007/BF00207034. Hum Genet. 1992. PMID: 1577461

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