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Leukemia|May 10, 2018
Single-cell sequencing reveals the origin and the order of mutation acquisition in T-cell acute lymphoblastic leukemiaJolien De Bie, Sofie Demeyer, Llucia Alberti-Servera, et al.Blood|February 18, 2011
JAK2 rearrangements, including the novel SEC31A-JAK2 fusion, are recurrent in classical Hodgkin lymphomaKatrien Van Roosbroeck, Luk Cox, Thomas Tousseyn, et al.Molecular Cell|July 11, 2008
Kinase activation and transformation by NUP214-ABL1 is dependent on the context of the nuclear poreKim De Keersmaecker, Jennifer L Rocnik, Rafael Bernad, et al.Genes, Chromosomes & Cancer|May 25, 2022
Primary mediastinal large B-cell lymphoma is characterized by large-scale copy-neutral loss of heterozygosityStefania Tuveri, Koen Debackere, Lukas Marcelis, et al.Blood|August 20, 2020
Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemiaLlucia Albertí-Servera, Sofie Demeyer, Inge Govaerts, et al.Blood|May 10, 2011
PTPN2 negatively regulates oncogenic JAK1 in T-cell acute lymphoblastic leukemiaMaria Kleppe, Jean Soulier, Vahid Asnafi, et al.Cancer Research|November 29, 2017
miR-139-5p Modulates Radiotherapy Resistance in Breast Cancer by Repressing Multiple Gene Networks of DNA Repair and ROS DefenseMarina Pajic, Danielle Froio, Sheridan Daly, et al.Hemasphere|February 13, 2025
Single-cell DNA and surface protein characterization of high hyperdiploid acute lymphoblastic leukemia at diagnosis and during treatmentMargo Aertgeerts, Sarah Meyers, Olga Gielen, et al.Blood|May 10, 2021
Overexpression of wild-type IL-7Rα promotes T-cell acute lymphoblastic leukemia/lymphomaAna Silva, Afonso R M Almeida, Ana Cachucho, et al.Nature Genetics|August 21, 2007
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotypeHilde Brems, Magdalena Chmara, Mourad Sahbatou, et al.Pageof 18