Functional characterization of ETV6 and ETV6/CBFA2 in the regulation of the MCSFR proximal promoter
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference33 articles.
1. Nonrandom involvement of the 12p12 breakpoint in chromosome abnormalities of childhood acute lymphoblastic leukemia
2. Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1
3. Molecular characterization of 12p abnormalities in hematologic malignancies: deletion of KIP1, rearrangement of TEL, and amplification of CCND2
4. The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberrations in different hematological malignancies
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1. Therapeutic targeting of RBPJ, an upstream regulator of ETV6 gene, abrogates ETV6-NTRK3 fusion gene transformations in glioblastoma;Cancer Letters;2022-09
2. Germline ETV6 mutation promotes inflammation and disrupts lymphoid development of early hematopoietic progenitors;Experimental Hematology;2022-08
3. ETV6-RUNX1 and RUNX1 directly regulate RAG1 expression: one more step in the understanding of childhood B-cell acute lymphoblastic leukemia leukemogenesis;Leukemia;2021-09-17
4. Reduction of RUNX1 transcription factor activity by a CBFA2T3-mimicking peptide: application to B cell precursor acute lymphoblastic leukemia;Journal of Hematology & Oncology;2021-03-20
5. Diagnosis and treatment of mixed phenotype (T-myeloid/lymphoid) acute leukemia with novel ETV6-FGFR2 rearrangement;Blood Advances;2020-10-13
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