Transforming activities of the <i>NUP98-KMT2A</i> fusion gene associated with myelodysplasia and acute myeloid leukemia.

Fisher, James N; Thanasopoulou, Angeliki; Juge, Sabine; Tzankov, Alexandar; Bagger, Frederik O; Mendez, Max A; Peters, Antoine H F M; Schwaller, Juerg

Transforming activities of the NUP98-KMT2A fusion gene associated with myelodysplasia and acute myeloid leukemia.

Fisher, James N; Thanasopoulou, Angeliki; Juge, Sabine; Tzankov, Alexandar; Bagger, Frederik O; Mendez, Max A; Peters, Antoine H F M; Schwaller, Juerg.

Afiliação

Fisher JN; University Children's Hospital Basel (UKBB).
Thanasopoulou A; Department of Biomedicine, University of Basel.
Juge S; University Children's Hospital Basel (UKBB).
Tzankov A; Department of Biomedicine, University of Basel.
Bagger FO; University Children's Hospital Basel (UKBB).
Mendez MA; Department of Biomedicine, University of Basel.
Peters AHFM; Institute for Pathology, University of Basel.
Schwaller J; University Children's Hospital Basel (UKBB).

Haematologica ; 105(7): 1857-1867, 2020 07.

Article em En | MEDLINE | ID: mdl-31558671

Assuntos

Leucemia Mieloide Aguda; Síndromes Mielodisplásicas; Animais; Fibroblastos; Humanos; Leucemia Mieloide Aguda/genética; Camundongos; Síndromes Mielodisplásicas/genética; Proteína de Leucina Linfoide-Mieloide; Complexo de Proteínas Formadoras de Poros Nucleares/genética; Proteínas de Fusão Oncogênica/genética

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Leucemia Mieloide Aguda Tipo de estudo: Risk_factors_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

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