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Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor level.
Scott, Caroline; Bartolovic, Kerol; Clark, Sally-Ann; Waithe, Dominic; Hill, Quentin A; Okoli, Steven; Renella, Raffaele; Ryan, Kate; Cahill, Mary R; Higgs, Douglas R; Roy, Noémi B A; Buckle, Veronica; Roberts, Irene; Babbs, Christian.
Afiliação
  • Scott C; MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Bartolovic K; MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Clark SA; Flow Cytometry Facility, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Waithe D; Wolfson Imaging Centre, MRC Weatherall Institute of Molecular Medicine, Oxford, UK.
  • Hill QA; Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Okoli S; Imperial College, The Commonwealth Building, Hammersmith Hospital, London, UK.
  • Renella R; Pediatric Hematology-Oncology Research Laboratory, CHUV-UNIL, Lausanne, Switzerland.
  • Ryan K; Department of Haematology, Manchester Royal Infirmary, Manchester, UK.
  • Cahill MR; Department of Haematology, Cork University Hospital, Cork, Ireland.
  • Higgs DR; MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Roy NBA; MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Buckle V; Department of Haematology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Roberts I; BRC Blood Theme and BRC/NHS Translational Molecular Diagnostics Centre, John Radcliffe Hospital, Oxford, UK.
  • Babbs C; MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
Br J Haematol ; 198(1): e10-e14, 2022 07.
Article em En | MEDLINE | ID: mdl-35417566
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eritropoese / Anemia Diseritropoética Congênita Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Eritropoese / Anemia Diseritropoética Congênita Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article