Miki T - Search Results

1

Molecular and epidemiological studies of Werner syndrome in the Japanese population.

Miki T, Nakura J, Ye L, Mitsuda N, Morishima A, Sato N, Kamino K, Ogihara T. Miki T, et al. Mech Ageing Dev. 1997 Dec;98(3):255-65. doi: 10.1016/s0047-6374(97)00112-7. Mech Ageing Dev. 1997. PMID: 9352494

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: miki t. Genomics. 1995 Aug 10;28(3):566-9. doi: 10.1006/geno.1995.1189. Genomics. 1995. PMID: 7490095

3

Homozygosity mapping of the Werner syndrome locus (WRN).

Nakura J, Wijsman EM, Miki T, Kamino K, Yu CE, Oshima J, Fukuchi K, Weber JL, Piussan C, Melaragno MI, et al. Nakura J, et al. Among authors: miki t. Genomics. 1994 Oct;23(3):600-8. doi: 10.1006/geno.1994.1548. Genomics. 1994. PMID: 7851888

4

Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus.

Kihara K, Nakura J, Ye L, Mitsuda N, Kamino K, Zhao Y, Fujioka Y, Miki T, Ogihara T. Kihara K, et al. Among authors: miki t. Jpn J Hum Genet. 1994 Dec;39(4):403-9. doi: 10.1007/BF01892385. Jpn J Hum Genet. 1994. PMID: 7873752

5

[Werner's syndrome and familial Alzheimer's disease].

Miki T, Nakura J, Kamino K, Ogihara T. Miki T, et al. Tanpakushitsu Kakusan Koso. 1993 Feb;38(3):366-73. Tanpakushitsu Kakusan Koso. 1993. PMID: 8098160 Review. Japanese. No abstract available.

6

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: miki t. Jpn J Hum Genet. 1993 Dec;38(4):391-7. doi: 10.1007/BF01907985. Jpn J Hum Genet. 1993. PMID: 8186416

7

Close linkage of the gene for Werner's syndrome to ANK1 and D8S87 on the short arm of chromosome 8.

Nakura J, Miki T, Nagano K, Kihara K, Ye L, Kamino K, Fujiwara Y, Yoshida S, Murano S, Fukuchi K, et al. Nakura J, et al. Among authors: miki t. Gerontology. 1993;39 Suppl 1:11-5. doi: 10.1159/000213560. Gerontology. 1993. PMID: 8365666

8

Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.

Nakura J, Miki T, Ye L, Mitsuda N, Zhao Y, Kihara K, Yu CE, Oshima J, Fukuchi KI, Wijsman EM, Schellenberg GD, Martin GM, Murano Si, Hashimoto K, Fujiwara Y, Ogihara T. Nakura J, et al. Among authors: miki t. Genomics. 1996 Aug 15;36(1):130-41. doi: 10.1006/geno.1996.0433. Genomics. 1996. PMID: 8812424

9

[Genetic analysis of Werner syndrome in a family].

Morishima A, Mitsuda N, Nakura J, Kamino K, Sato N, Miki T, Ogihara T. Morishima A, et al. Among authors: miki t. Nihon Ronen Igakkai Zasshi. 1995 Dec;32(12):817-21. doi: 10.3143/geriatrics.32.817. Nihon Ronen Igakkai Zasshi. 1995. PMID: 8865743 Free article. Japanese.

10

Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population.

Ye L, Miki T, Nakura J, Oshima J, Kamino K, Rakugi H, Ikegami H, Higaki J, Edland SD, Martin GM, Ogihara T. Ye L, et al. Among authors: miki t. Am J Med Genet. 1997 Feb 11;68(4):494-8. doi: 10.1002/(sici)1096-8628(19970211)68:4<494::aid-ajmg30>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9021029

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