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RUNX-1 haploinsufficiency causes a marked deficiency of megakaryocyte-biased hematopoietic progenitor cells.
Estevez, Brian; Borst, Sara; Jarocha, Danuta; Sudunagunta, Varun; Gonzalez, Michael; Garifallou, James; Hakonarson, Hakon; Gao, Peng; Tan, Kai; Liu, Paul; Bagga, Sumedha; Holdreith, Nicholas; Tong, Wei; Speck, Nancy; French, Deborah L; Gadue, Paul; Poncz, Mortimer.
Afiliação
  • Estevez B; Department of Pediatrics and.
  • Borst S; Department of Pathology, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Jarocha D; Department of Pharmacology, University of Pennsylvania, Philadelphia, PA.
  • Sudunagunta V; Department of Pediatrics and.
  • Gonzalez M; Department of Pediatrics and.
  • Garifallou J; Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Hakonarson H; Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Gao P; Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Tan K; Department of Pediatrics.
  • Liu P; Department of Pediatrics.
  • Bagga S; Department of Cell and Development Biology, and.
  • Holdreith N; Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Tong W; Department of Pediatrics.
  • Speck N; Translational and Functional Genomics, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD; and.
  • French DL; Department of Cell and Development Biology, and.
  • Gadue P; Department of Pediatrics and.
  • Poncz M; Department of Pediatrics and.
Blood ; 137(19): 2662-2675, 2021 05 13.
Article em En | MEDLINE | ID: mdl-33569577
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Células-Tronco Hematopoéticas / Megacariócitos / Subunidade alfa 2 de Fator de Ligação ao Core Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Adult / Humans Idioma: En Revista: Blood Ano de publicação: 2021 Tipo de documento: Article País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Células-Tronco Hematopoéticas / Megacariócitos / Subunidade alfa 2 de Fator de Ligação ao Core Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Adult / Humans Idioma: En Revista: Blood Ano de publicação: 2021 Tipo de documento: Article País de publicação: Estados Unidos