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A missense single nucleotide polymorphism, V114I of the Werner syndrome gene, is associated with risk of osteoporosis and femoral fracture in the Japanese population.
Zhou, Heying; Mori, Seijiro; Tanaka, Masashi; Sawabe, Motoji; Arai, Tomio; Muramatsu, Masaaki; Mieno, Makiko Naka; Shinkai, Shoji; Yamada, Yoshiji; Miyachi, Motohiko; Murakami, Haruka; Sanada, Kiyoshi; Ito, Hideki.
Afiliação
  • Zhou H; Center for Promotion of Clinical Investigation, Tokyo Metropolitan Geriatric Hospital, 35-2 Sakae, Itabashi, Tokyo, 173-0015, Japan.
  • Mori S; Center for Promotion of Clinical Investigation, Tokyo Metropolitan Geriatric Hospital, 35-2 Sakae, Itabashi, Tokyo, 173-0015, Japan. mori_seijiro@tmghig.jp.
  • Tanaka M; Department of Genomics for Longevity and Health, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
  • Sawabe M; Section of Molecular Pathology, Graduate School of Health Care Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
  • Arai T; Department of Pathology, Tokyo Metropolitan Geriatric Hospital, Tokyo, Japan.
  • Muramatsu M; Department of Molecular Epidemiology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
  • Mieno MN; Department of Medical Informatics, Center for Information, Jichi Medical University, Shimotsuke, Tochigi, Japan.
  • Shinkai S; Research Team for Social Participation and Community Health, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
  • Yamada Y; Department of Human Functional Genomics, Life Science Research Center, Mie University, Tsu, Mie, Japan.
  • Miyachi M; Department of Health Promotion and Exercise, National Institute of Health and Nutrition, Tokyo, Japan.
  • Murakami H; Department of Health Promotion and Exercise, National Institute of Health and Nutrition, Tokyo, Japan.
  • Sanada K; Faculty of Sport and Health Science, Ritsumeikan University, Kita, Shiga, Japan.
  • Ito H; President, Local Independent Administrative Agency, Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology, Tokyo, Japan.
J Bone Miner Metab ; 33(6): 694-700, 2015 Nov.
Article em En | MEDLINE | ID: mdl-25637295
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Osteoporose / Predisposição Genética para Doença / Mutação de Sentido Incorreto / Polimorfismo de Nucleotídeo Único / Povo Asiático / Exodesoxirribonucleases / RecQ Helicases / Fraturas do Fêmur Tipo de estudo: Etiology_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male Idioma: En Revista: J Bone Miner Metab Assunto da revista: METABOLISMO Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Osteoporose / Predisposição Genética para Doença / Mutação de Sentido Incorreto / Polimorfismo de Nucleotídeo Único / Povo Asiático / Exodesoxirribonucleases / RecQ Helicases / Fraturas do Fêmur Tipo de estudo: Etiology_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male Idioma: En Revista: J Bone Miner Metab Assunto da revista: METABOLISMO Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão