When are the BET factors the most sensitive to bromodomain inhibitors?
Author:
Publisher
Informa UK Limited
Subject
Genetics,Biochemistry,Biotechnology
Link
http://www.tandfonline.com/doi/pdf/10.4161/trns.23191
Reference18 articles.
1. Structure and ligand of a histone acetyltransferase bromodomain
2. Histone Recognition and Large-Scale Structural Analysis of the Human Bromodomain Family
3. Bromodomains as therapeutic targets
4. You bet-cha: a novel family of transcriptional regulators
5. BET domain co-regulators in obesity, inflammation and cancer
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1. Structural modification of 4, 5-dihydro-[1, 2, 4] triazolo [4, 3-f] pteridine derivatives as BRD4 inhibitors using 2D/3D-QSAR and molecular docking analysis;Molecular Diversity;2021-01-03
2. Blocking the Bromodomains Function Contributes to Disturbances in Alga Chara vulgaris Spermatids Differentiation;Cells;2020-05-29
3. Whole-exome sequencing identified a homozygous BRDT mutation in a patient with acephalic spermatozoa;Oncotarget;2017-02-10
4. The Role of Bromodomain Testis-Specific Factor, BRDT, in Cancer: A Biomarker and A Possible Therapeutic Target;CELL J;2017
5. The bromodomain inhibitor JQ1 triggers growth arrest and apoptosis in testicular germ cell tumoursin vitroandin vivo;Journal of Cellular and Molecular Medicine;2016-12-27
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