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ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13.
Zhang, Yihan; Huang, Haigen; Zhao, Gexin; Yokoyama, Tadafumi; Vega, Hugo; Huang, Yan; Sood, Raman; Bishop, Kevin; Maduro, Valerie; Accardi, John; Toro, Camilo; Boerkoel, Cornelius F; Lyons, Karen; Gahl, William A; Duan, Xiaohong; Malicdan, May Christine V; Lin, Shuo.
Afiliação
  • Zhang Y; Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen China.
  • Huang H; Department of Molecular, Cell, and Developmental Biology, University of California Los Angeles, Los Angeles, California, United States of America.
  • Zhao G; Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen China.
  • Yokoyama T; Department of Molecular, Cell, and Developmental Biology, University of California Los Angeles, Los Angeles, California, United States of America.
  • Vega H; Department of Orthopaedic Surgery and Orthopaedic Institute for Children, David Geffen School of Medicine, University of California, Los Angeles, California, United States of America.
  • Huang Y; Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
  • Sood R; NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH and National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
  • Bishop K; NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH and National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
  • Maduro V; Zebrafish core, Translational and Functional Genomics Branch, National Human Genome Research Institute/NIH, Bethesda, Maryland, United States of America.
  • Accardi J; Zebrafish core, Translational and Functional Genomics Branch, National Human Genome Research Institute/NIH, Bethesda, Maryland, United States of America.
  • Toro C; NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH and National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
  • Boerkoel CF; NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH and National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
  • Lyons K; NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH and National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
  • Gahl WA; NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH and National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
  • Duan X; Department of Molecular, Cell, and Developmental Biology, University of California Los Angeles, Los Angeles, California, United States of America.
  • Malicdan MC; Department of Orthopaedic Surgery and Orthopaedic Institute for Children, David Geffen School of Medicine, University of California, Los Angeles, California, United States of America.
  • Lin S; Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
PLoS Genet ; 13(2): e1006481, 2017 02.
Article em En | MEDLINE | ID: mdl-28158191
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoporose / Desenvolvimento Ósseo / Metaloproteinase 9 da Matriz / ATPases Vacuolares Próton-Translocadoras / Metaloproteinase 13 da Matriz Limite: Adult / Animals / Humans Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoporose / Desenvolvimento Ósseo / Metaloproteinase 9 da Matriz / ATPases Vacuolares Próton-Translocadoras / Metaloproteinase 13 da Matriz Limite: Adult / Animals / Humans Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2017 Tipo de documento: Article