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Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.
Kaneb, Hannah M; Folkmann, Andrew W; Belzil, Véronique V; Jao, Li-En; Leblond, Claire S; Girard, Simon L; Daoud, Hussein; Noreau, Anne; Rochefort, Daniel; Hince, Pascale; Szuto, Anna; Levert, Annie; Vidal, Sabrina; André-Guimont, Catherine; Camu, William; Bouchard, Jean-Pierre; Dupré, Nicolas; Rouleau, Guy A; Wente, Susan R; Dion, Patrick A.
Afiliación
  • Kaneb HM; Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada H3A 2B4, Department of Neurology and Neurosurgery, McGill University, Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Université de Montréal, Montréal, QC, Canada H2L 2W5.
  • Folkmann AW; Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
  • Belzil VV; Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Université de Montréal, Montréal, QC, Canada H2L 2W5, Department of Physiology, Université de Montréal.
  • Jao LE; Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
  • Leblond CS; Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada H3A 2B4, Department of Human Genetics, McGill University, Montreal, QC, Canada H3A 0G4.
  • Girard SL; Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Université de Montréal, Montréal, QC, Canada H2L 2W5, Department of Molecular Biology, Université de Montréal.
  • Daoud H; Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Université de Montréal, Montréal, QC, Canada H2L 2W5, Department of Medicine, Université de Montréal.
  • Noreau A; Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Université de Montréal, Montréal, QC, Canada H2L 2W5, Department of Pathology and Cellular Biology, Université de Montréal.
  • Rochefort D; Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada H3A 2B4.
  • Hince P; Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada H3A 2B4.
  • Szuto A; Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Université de Montréal, Montréal, QC, Canada H2L 2W5.
  • Levert A; Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada H3A 2B4.
  • Vidal S; Department of Biochemistry, Université de Montréal.
  • André-Guimont C; Department of Biological Sciences, Université de Montréal, Montréal, QC, Canada H2L 4M1.
  • Camu W; Unité de Neurologie Comportementale et Dégénérative, Institute of Biology, Montpellier 34967, France.
  • Bouchard JP; Department of Neurological Sciences and Faculty of Medicine, Centre Hospitalier Universitaire de Québec, Laval University, Quebec City, QC, Canada G1J 1Z4.
  • Dupré N; Department of Neurological Sciences and Faculty of Medicine, Centre Hospitalier Universitaire de Québec, Laval University, Quebec City, QC, Canada G1J 1Z4.
  • Rouleau GA; Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada H3A 2B4, Department of Neurology and Neurosurgery, McGill University.
  • Wente SR; Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
  • Dion PA; Montreal Neurological Institute and Hospital, McGill University, Montreal, QC, Canada H3A 2B4, Department of Neurology and Neurosurgery, McGill University, Department of Pathology and Cellular Biology, Université de Montréal, patrick.a.dion@mcgill.ca.
Hum Mol Genet ; 24(5): 1363-73, 2015 Mar 01.
Article en En | MEDLINE | ID: mdl-25343993
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Codón sin Sentido / Mutación Missense / Proteínas de Transporte Nucleocitoplasmático / Esclerosis Amiotrófica Lateral Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2015 Tipo del documento: Article Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Codón sin Sentido / Mutación Missense / Proteínas de Transporte Nucleocitoplasmático / Esclerosis Amiotrófica Lateral Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2015 Tipo del documento: Article Pais de publicación: Reino Unido