Kamino K - 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: kamino k. Jpn J Hum Genet. 1993 Dec;38(4):391-7. doi: 10.1007/BF01907985. Jpn J Hum Genet. 1993. PMID: 8186416

2

[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: kamino k. 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.

3

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: kamino k. 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

4

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: kamino k. Mech Ageing Dev. 1997 Dec;98(3):255-65. doi: 10.1016/s0047-6374(97)00112-7. Mech Ageing Dev. 1997. PMID: 9352494

5

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: kamino k. Genomics. 1994 Oct;23(3):600-8. doi: 10.1006/geno.1994.1548. Genomics. 1994. PMID: 7851888

6

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

7

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. Jpn J Hum Genet. 1994 Dec;39(4):439-40. doi: 10.1007/BF01892390. Jpn J Hum Genet. 1994. PMID: 7873757

8

Dinucleotide repeat polymorphism at the D8S1055.

Ye L, Kihara K, Nakura J, Kamino K, Mitsuda N, Takahashi-Fujii A, Ishino Y, Miki T, Ogihara T. Ye L, et al. Among authors: kamino k. Jpn J Hum Genet. 1994 Dec;39(4):441-3. doi: 10.1007/BF01892391. Jpn J Hum Genet. 1994. PMID: 7873758 No abstract available.

9

Dinucleotide repeat polymorphism at D7S813.

Ye L, Nakura J, Miki T, Kihara K, Nagano K, Mitsuda N, Kamino K, Ogihara T, Takahashi-Fujii A, Ishino Y. Ye L, et al. Among authors: kamino k. Hum Mol Genet. 1994 Feb;3(2):385. doi: 10.1093/hmg/3.2.385. Hum Mol Genet. 1994. PMID: 8004121 No abstract available.

10

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

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

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