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A novel IKAROS haploinsufficiency kindred with unexpectedly late and variable B-cell maturation defects.
Bogaert, Delfien J; Kuehn, Hye Sun; Bonroy, Carolien; Calvo, Katherine R; Dehoorne, Joke; Vanlander, Arnaud V; De Bruyne, Marieke; Cytlak, Urszula; Bigley, Venetia; De Baets, Frans; De Baere, Elfride; Rosenzweig, Sergio D; Haerynck, Filomeen; Dullaers, Melissa.
Afiliação
  • Bogaert DJ; Clinical Immunology Research Laboratory, Department of Pulmonary Medicine, Ghent University Hospital, Ghent, Belgium; Department of Pediatrics, Division of Pediatric Immunology and Pulmonology, Ghent University Hospital, Ghent, Belgium; Center for Medical Genetics, Ghent University and Ghent Univers
  • Kuehn HS; Immunology Service, Department of Laboratory Medicine, NIH Clinical Center, National Institutes of Health, Bethesda, Md.
  • Bonroy C; Center for Primary Immunodeficiency, Jeffrey Modell Diagnosis and Research Centre, Ghent University Hospital, Ghent, Belgium; Department of Laboratory Medicine, Ghent University Hospital, Ghent, Belgium.
  • Calvo KR; Hematology Section, Department of Laboratory Medicine, NIH Clinical Center, National Institutes of Health, Bethesda, Md.
  • Dehoorne J; Department of Pediatrics, Division of Pediatric Nephrology and Rheumatology, Ghent University Hospital, Ghent, Belgium.
  • Vanlander AV; Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Ghent University Hospital, Ghent, Belgium.
  • De Bruyne M; Clinical Immunology Research Laboratory, Department of Pulmonary Medicine, Ghent University Hospital, Ghent, Belgium; Department of Pediatrics, Division of Pediatric Immunology and Pulmonology, Ghent University Hospital, Ghent, Belgium; Center for Medical Genetics, Ghent University and Ghent Univers
  • Cytlak U; Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom; Northern Centre for Bone Marrow Transplantation, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.
  • Bigley V; Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom; Northern Centre for Bone Marrow Transplantation, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.
  • De Baets F; Department of Pediatrics, Division of Pediatric Immunology and Pulmonology, Ghent University Hospital, Ghent, Belgium; Center for Primary Immunodeficiency, Jeffrey Modell Diagnosis and Research Centre, Ghent University Hospital, Ghent, Belgium.
  • De Baere E; Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium; Center for Primary Immunodeficiency, Jeffrey Modell Diagnosis and Research Centre, Ghent University Hospital, Ghent, Belgium.
  • Rosenzweig SD; Immunology Service, Department of Laboratory Medicine, NIH Clinical Center, National Institutes of Health, Bethesda, Md.
  • Haerynck F; Clinical Immunology Research Laboratory, Department of Pulmonary Medicine, Ghent University Hospital, Ghent, Belgium; Department of Pediatrics, Division of Pediatric Immunology and Pulmonology, Ghent University Hospital, Ghent, Belgium; Center for Primary Immunodeficiency, Jeffrey Modell Diagnosis a
  • Dullaers M; Clinical Immunology Research Laboratory, Department of Pulmonary Medicine, Ghent University Hospital, Ghent, Belgium; Center for Primary Immunodeficiency, Jeffrey Modell Diagnosis and Research Centre, Ghent University Hospital, Ghent, Belgium; Laboratory of Immunoregulation, VIB Inflammation Researc
J Allergy Clin Immunol ; 141(1): 432-435.e7, 2018 01.
Article em En | MEDLINE | ID: mdl-28927821
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos B / Diferenciação Celular / Predisposição Genética para Doença / Fator de Transcrição Ikaros / Estudos de Associação Genética / Haploinsuficiência Tipo de estudo: Prognostic_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos B / Diferenciação Celular / Predisposição Genética para Doença / Fator de Transcrição Ikaros / Estudos de Associação Genética / Haploinsuficiência Tipo de estudo: Prognostic_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article