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MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria.
Dalla Rosa, Ilaria; Cámara, Yolanda; Durigon, Romina; Moss, Chloe F; Vidoni, Sara; Akman, Gokhan; Hunt, Lilian; Johnson, Mark A; Grocott, Sarah; Wang, Liya; Thorburn, David R; Hirano, Michio; Poulton, Joanna; Taylor, Robert W; Elgar, Greg; Martí, Ramon; Voshol, Peter; Holt, Ian J; Spinazzola, Antonella.
Afiliação
  • Dalla Rosa I; MRC Mill Hill Laboratory, London, United Kingdom.
  • Cámara Y; Laboratory of Mitochondrial Disorders, Vall d'Hebron Institut de Recerca, Universitat Autònoma de Barcelona, Barcelona, Catalonia.
  • Durigon R; Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III, Madrid, Spain.
  • Moss CF; MRC Mill Hill Laboratory, London, United Kingdom.
  • Vidoni S; MRC Mill Hill Laboratory, London, United Kingdom.
  • Akman G; MRC Mitochondrial Biology Unit, Wellcome Trust-MRC Building, Cambridge, United Kingdom.
  • Hunt L; MRC Mill Hill Laboratory, London, United Kingdom.
  • Johnson MA; MRC Mill Hill Laboratory, London, United Kingdom.
  • Grocott S; MRC Mitochondrial Biology Unit, Wellcome Trust-MRC Building, Cambridge, United Kingdom.
  • Wang L; Mitochondrial Genetics Group, Nuffield Department of Obstetrics and Gynaecology, Women's Centre, The John Radcliffe Hospital, Oxford, United Kingdom.
  • Thorburn DR; Department of Anatomy, Physiology and Biochemistry, The Swedish University of Agricultural Sciences, Biomedical Center, Uppsala, Sweden.
  • Hirano M; Murdoch Childrens Research Institute and University of Melbourne Department of Paediatrics, Royal Children's Hospital, Flemington Road, Parkville, Victoria, Australia.
  • Poulton J; Department of Neurology, Columbia University Medical Center, New York, New York, United States of America.
  • Taylor RW; Mitochondrial Genetics Group, Nuffield Department of Obstetrics and Gynaecology, Women's Centre, The John Radcliffe Hospital, Oxford, United Kingdom.
  • Elgar G; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, The Medical School, Newcastle upon Tyne, United Kingdom.
  • Martí R; MRC Mill Hill Laboratory, London, United Kingdom.
  • Voshol P; Laboratory of Mitochondrial Disorders, Vall d'Hebron Institut de Recerca, Universitat Autònoma de Barcelona, Barcelona, Catalonia.
  • Holt IJ; Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III, Madrid, Spain.
  • Spinazzola A; Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.
PLoS Genet ; 12(1): e1005779, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26760297
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Mitocôndrias Hepáticas / Replicação do DNA / Proteínas de Membrana Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Mitocôndrias Hepáticas / Replicação do DNA / Proteínas de Membrana Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Reino Unido