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Rare and private spliceosomal gene mutations drive partial, complete, and dual phenocopies of hotspot alterations.
Pangallo, Joseph; Kiladjian, Jean-Jacques; Cassinat, Bruno; Renneville, Aline; Taylor, Justin; Polaski, Jacob T; North, Khrystyna; Abdel-Wahab, Omar; Bradley, Robert K.
Afiliação
  • Pangallo J; Computational Biology Program, Public Health Sciences Division, and.
  • Kiladjian JJ; Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Cassinat B; Assistance Publique-Hôpitaux de Paris and INSERM Unité Mixte de Recherche en Santé 1131, Institut Universitaire d'Hématologie, Hôpital Saint-Louis, Paris, France.
  • Renneville A; Assistance Publique-Hôpitaux de Paris and INSERM Unité Mixte de Recherche en Santé 1131, Institut Universitaire d'Hématologie, Hôpital Saint-Louis, Paris, France.
  • Taylor J; Hematology Laboratory, Biology and Pathology Center, Centre Hospitalier Universitaire, Lille, France; University of Lille Nord de France, Lille, France; UMR-S 1172, Team 3, Cancer Research Institute of Lille, Lille, France.
  • Polaski JT; Human Oncology and Pathogenesis Program and Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, NY; and.
  • North K; Computational Biology Program, Public Health Sciences Division, and.
  • Abdel-Wahab O; Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Bradley RK; Computational Biology Program, Public Health Sciences Division, and.
Blood ; 135(13): 1032-1043, 2020 03 26.
Article em En | MEDLINE | ID: mdl-31961934
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Spliceossomos / Penetrância / Estudos de Associação Genética / Mutação Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Blood Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Spliceossomos / Penetrância / Estudos de Associação Genética / Mutação Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Blood Ano de publicação: 2020 Tipo de documento: Article