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Volumn 99, Issue 2, 1997, Pages 191-193

Analysis of helicase gene mutations in Japanese Werner's syndrome patients

Author keywords

[No Author keywords available]

Indexed keywords

HELICASE;

EID: 0031018953     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050336     Document Type: Article
Times cited : (79)

References (8)
  • 1
    • 0013907774 scopus 로고
    • Werner's syndrome: A review of its symptomatology, natural history, pathologic factors, genetics and relationship to the natural aging process
    • Epstein CJ, Martin GM, Schulltz AL, Motulsky AG (1966) Werner's syndrome: a review of its symptomatology, natural history, pathologic factors, genetics and relationship to the natural aging process. Medicine 45: 177-221
    • (1966) Medicine , vol.45 , pp. 177-221
    • Epstein, C.J.1    Martin, G.M.2    Schulltz, A.L.3    Motulsky, A.G.4
  • 2
    • 0029971818 scopus 로고    scopus 로고
    • Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotypes: Lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers
    • Goddard KAB, Yu C-E, Oshima J, Miki T, Nakura J, Piussan C, Martin GM, et al. (1996) Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotypes: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers. Am J Hum Genet 58: 1286-1302
    • (1996) Am J Hum Genet , vol.58 , pp. 1286-1302
    • Goddard, K.A.B.1    Yu, C.-E.2    Oshima, J.3    Miki, T.4    Nakura, J.5    Piussan, C.6    Martin, G.M.7
  • 3
    • 0019507754 scopus 로고
    • Family analysis of Werner's syndrome: A survey of 42 Japanese families with a review of the literature
    • Goto M, Tanimoto K, Horiuchi Y, Sasazuki T (1981) Family analysis of Werner's syndrome: a survey of 42 Japanese families with a review of the literature. Clin Genet 19: 8-15
    • (1981) Clin Genet , vol.19 , pp. 8-15
    • Goto, M.1    Tanimoto, K.2    Horiuchi, Y.3    Sasazuki, T.4
  • 4
    • 0026502062 scopus 로고
    • Genetic linkage of Werner's syndrome to five markers on chromosome 8
    • Goto M, Rubenstein M, Weber J, Woods K, Drayna D (1992) Genetic linkage of Werner's syndrome to five markers on chromosome 8. Nature 355: 735-738
    • (1992) Nature , vol.355 , pp. 735-738
    • Goto, M.1    Rubenstein, M.2    Weber, J.3    Woods, K.4    Drayna, D.5
  • 5
    • 33846289198 scopus 로고    scopus 로고
    • Excess of rare cancers in Werner syndrome (adult progeria)
    • Goto M, Miller RW, Ishikawa Y, Sugano H (1996) Excess of rare cancers in Werner syndrome (adult progeria). Can Epi Bio Prev 5: 239-246
    • (1996) Can Epi Bio Prev , vol.5 , pp. 239-246
    • Goto, M.1    Miller, R.W.2    Ishikawa, Y.3    Sugano, H.4
  • 6
    • 0002542639 scopus 로고
    • Genetic syndrome in man with potential relevance to the pathology of aging
    • Bergsma D, Harrison DE (eds) Liss, New York
    • Martin GM (1978) Genetic syndrome in man with potential relevance to the pathology of aging. In: Bergsma D, Harrison DE (eds) Genetic effects on aging. Liss, New York, pp 3-39
    • (1978) Genetic Effects on Aging , pp. 3-39
    • Martin, G.M.1
  • 8
    • 15844409553 scopus 로고    scopus 로고
    • Positional cloning of the Werner's syndrome gene
    • Yu C-E, Oshima J, Fu Y-H, et al. (1996) Positional cloning of the Werner's syndrome gene. Science 272: 258-262
    • (1996) Science , vol.272 , pp. 258-262
    • Yu, C.-E.1    Oshima, J.2    Fu, Y.-H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.