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Whole-genome optical mapping to elucidate myeloid/lymphoid neoplasms with eosinophilia and tyrosine kinase gene fusions.

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第一作者： Benjamin,Podvin

第一单位： CHU Lille, Institute of Medical Genetics, France. Electronic address: benjamin.podvin@chru-lille.fr.

作者： Benjamin,Podvin ^[1] ; Pauline,Roynard ^[2] ; Augustin,Boudry ^[3] ; Hélène,Guermouche ^[2] ; Agnès,Daudignon ^[2] ; Louis,Terriou ^[4] ; Walid,Bouabdelli ^[5] ; Maha,Salameh ^[6] ; Nathalie,Grardel ^[3] ; Nicolas,Duployez ^[7] ; Catherine,Roche-Lestienne ^[8]

作者单位： CHU Lille, Institute of Medical Genetics, France. Electronic address: benjamin.podvin@chru-lille.fr. ^[1] CHU Lille, Institute of Medical Genetics, France. ^[2] CHU Lille, Laboratory of Hematology, France. ^[3] CHU Lille, Internal Medicine and Immunology, Centre de reference des maladies autoimmunes systémiques rares du Nord et Nord-Ouest de France (CeRAINO), France; U1286 - INFINITE - Institute for Translational Research in Inflammation, F-59000 Lille, France. ^[4] CH Arras, Hematology Department, France. ^[5] CH Arras, Laboratory of Hematology, France. ^[6] CHU Lille, Laboratory of Hematology, France; Univ. Lille, CNRS, Inserm, CHU Lille, IRCL, UMR9020 - UMR1277 - Canther - Cancer Heterogeneity, Plasticity and Resistance to Therapies, F-59000 Lille, France. ^[7] CHU Lille, Institute of Medical Genetics, France; Univ. Lille, CNRS, Inserm, CHU Lille, IRCL, UMR9020 - UMR1277 - Canther - Cancer Heterogeneity, Plasticity and Resistance to Therapies, F-59000 Lille, France. ^[8]

关键词 Hypereosinophilia Karyotype Optical Genome Mapping PDGFRB

主题词人类(Humans);蛋白酪氨酸激酶类(Protein-Tyrosine Kinases);骨髓增殖性疾病(Myeloproliferative Disorders);嗜酸粒细胞增多(Eosinophilia);基因融合(Gene Fusion);肿瘤(Neoplasms);癌基因蛋白质类, 融合(Oncogene Proteins, Fusion)

DOI 10.1016/j.leukres.2022.106972

PMID 36306722

发布时间 2022-12-27

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