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Oncology Letters|November 9, 2017
Germline cytotoxic lymphocytes defective mutations in Chinese patients with lymphomaXue Chen, Yang Zhang, Fang Wang, et al.Haematologica|May 28, 2026
Novel tripartite CPSF7::RARG::CPSF7 fusion confers primary ATRA resistance in atypical acute promyelocytic leukemiaXiaosu Zhou, Zhanglin Zhang, Fang Xu, et al.Haematologica|April 9, 2026
Bipartite NUP98::RARA-E412* fusion with a cis-aligned ligand binding domain truncation mutation in atypical acute promyelocytic leukemiaQinqin Liu, Jiaqi Chen, Xiaosu Zhou, et al.British Journal of Cancer|April 4, 2026
TCF3::HLF-positive B-ALL: integrated clinical and molecular characterization of 34 cases from a single-center cohortXue Chen, Xiaoli Ma, Lili Yuan, et al.Hematological Oncology|May 3, 2023
Report of PRPF19 as a novel partner of RARG and the recurrence of interposition-type fusion in variant acute promyelocytic leukemiaHuanling Wu, Hongjun Li, Xiaosu Zhou, et al.Frontiers in Oncology|January 2, 2023
Torque teno mini virus driven childhood acute promyelocytic leukemia: The third case report and sequence analysisXue Chen, Fang Wang, Xiaosu Zhou, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 9, 2021
[Identification of TCF3-ZNF384 fusion by transcriptome sequencing in B cell acute lymphoblastic leukemia and its laboratory and clinical characteristics]Qisheng Wu, Fang Wang, Junfang Yang, et al.American Journal of Hematology|February 7, 2024
Advances towards genome-based acute myeloid leukemia classification: A comparative analysis of WHO-HAEM4R, WHO-HAEM5, and International Consensus ClassificationXue Chen, Lili Yuan, Yang Zhang, et al.Annals of Hematology|July 18, 2025
Clinical features and fusion gene analysis of two Torque Teno Mini virus associated acute promyelocytic leukemia casesDeyan Liu, Jiaqi Chen, Yu Luo, et al.Heliyon|March 4, 2024
Case report of pediatric TTMV-related acute promyelocytic leukemia with central nervous system infiltration and rapid accumulation of RARA-LBD mutationsLinya Wang, Jiaqi Chen, Bei Hou, et al.Pageof 6