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

3

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: ogihara t. Jpn J Hum Genet. 1994 Dec;39(4):403-9. doi: 10.1007/BF01892385. Jpn J Hum Genet. 1994. PMID: 7873752

4

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

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

5

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: ogihara t. Genomics. 1996 Aug 15;36(1):130-41. doi: 10.1006/geno.1996.0433. Genomics. 1996. PMID: 8812424

6

[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: ogihara 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.

7

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: ogihara 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

8

The locus for Japanese myotonic dystrophy is also linked to D19S19 on the long arm of chromosome 19.

Takemoto Y, Miki T, Nishikawa K, Nakura J, Kamino K, Takai S, Honjo T, Ogihara T. Takemoto Y, et al. Among authors: ogihara t. Genomics. 1990 Jan;6(1):195-6. doi: 10.1016/0888-7543(90)90468-a. Genomics. 1990. PMID: 2303261 No abstract available.

9

Dinucleotide repeat polymorphism at the D8S1054.

Mitsuda N, Nakura J, Ye L, Takahashi-Fujii A, Ishino Y, Miki T, Ogihara T. Mitsuda N, et al. Among authors: ogihara t. Jpn J Hum Genet. 1995 Jun;40(2):215-6. doi: 10.1007/BF01883580. Jpn J Hum Genet. 1995. PMID: 7663003 No abstract available.

10

Identification of a single base polymorphism in intron 2 of the c-fos gene and its detection by mismatched PCR-RFLP.

Kamino K, Miki T, Ogihara T. Kamino K, et al. Among authors: ogihara t. Jpn J Hum Genet. 1994 Dec;39(4):439-40. doi: 10.1007/BF01892390. Jpn J Hum Genet. 1994. PMID: 7873757

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