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DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Bettencourt, Conceição; Hensman-Moss, Davina; Flower, Michael; Wiethoff, Sarah; Brice, Alexis; Goizet, Cyril; Stevanin, Giovanni; Koutsis, Georgios; Karadima, Georgia; Panas, Marios; Yescas-Gómez, Petra; García-Velázquez, Lizbeth Esmeralda; Alonso-Vilatela, María Elisa; Lima, Manuela; Raposo, Mafalda; Traynor, Bryan; Sweeney, Mary; Wood, Nicholas; Giunti, Paola; Durr, Alexandra; Holmans, Peter; Houlden, Henry; Tabrizi, Sarah J; Jones, Lesley.
Afiliação
  • Bettencourt C; Department of Molecular Neuroscience, Institute of Neurology, University College London, London WC1N 3BG, United Kingdom.
  • Hensman-Moss D; Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London WC1N 3BG, United Kingdom.
  • Flower M; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London WC1N 3BG, United Kingdom.
  • Wiethoff S; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London WC1N 3BG, United Kingdom.
  • Brice A; Department of Molecular Neuroscience, Institute of Neurology, University College London, London WC1N 3BG, United Kingdom.
  • Goizet C; Center for Neurology and Hertie Institute for Clinical Brain Research, Eberhard-Karls-University, Tübingen, Germany.
  • Stevanin G; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC University Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière (ICM), Paris, France.
  • Koutsis G; APHP, Department of Genetics, University Hospital Pitié-Salpêtrière, 75013 Paris, France.
  • Karadima G; Université Bordeaux, Laboratoire Maladies Rares: Génétique et Métabolisme, INSERM1211, Bordeaux, France.
  • Panas M; CHU Pellegrin, Service de Génétique Médicale, F-33000, Bordeaux, France.
  • Yescas-Gómez P; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC University Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière (ICM), Paris, France.
  • García-Velázquez LE; Ecole Pratique des Hautes Etudes, 75014 Paris, France.
  • Alonso-Vilatela ME; Neurogenetics Unit, 1st Department of Neurology, University of Athens Medical School, Eginition Hospital, 115 28 Athens, Greece.
  • Lima M; Neurogenetics Unit, 1st Department of Neurology, University of Athens Medical School, Eginition Hospital, 115 28 Athens, Greece.
  • Raposo M; Neurogenetics Unit, 1st Department of Neurology, University of Athens Medical School, Eginition Hospital, 115 28 Athens, Greece.
  • Traynor B; Neurogenetics Department, National Institute of Neurology and Neurosurgery, "Manuel Velasco Suárez", Mexico City CP14269, Mexico.
  • Sweeney M; Neurogenetics Department, National Institute of Neurology and Neurosurgery, "Manuel Velasco Suárez", Mexico City CP14269, Mexico.
  • Wood N; Neurogenetics Department, National Institute of Neurology and Neurosurgery, "Manuel Velasco Suárez", Mexico City CP14269, Mexico.
  • Giunti P; Department of Biology, University of the Azores, 9500-321 Ponta Delgada, Portugal.
  • Durr A; Institute for Molecular and Cell Biology (IBMC), University of Porto, 4150-180 Porto, Portugal.
  • Holmans P; Department of Biology, University of the Azores, 9500-321 Ponta Delgada, Portugal.
  • Houlden H; Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4150-180 Porto, Portugal.
  • Tabrizi SJ; Institute for Molecular and Cell Biology (IBMC), University of Porto, 4150-180 Porto, Portugal.
  • Jones L; Laboratory of Neurogenetics, National Institute of Aging, NIH, Bethesda, MD 20892, USA.
Ann Neurol ; 79(6): 983-90, 2016 Jun.
Article em En | MEDLINE | ID: mdl-27044000
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Huntington / Ataxias Espinocerebelares / Reparo do DNA / Exodesoxirribonucleases / Endonuclease PMS2 de Reparo de Erro de Pareamento Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Ann Neurol 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 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Huntington / Ataxias Espinocerebelares / Reparo do DNA / Exodesoxirribonucleases / Endonuclease PMS2 de Reparo de Erro de Pareamento Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Ann Neurol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Reino Unido