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Nature Structural & Molecular Biology|October 2, 2012
Association of UHRF1 with methylated H3K9 directs the maintenance of DNA methylationScott B Rothbart, Krzysztof Krajewski, Nataliya Nady, et al.ACS Chemical Biology|August 9, 2023
SETDB1 Triple Tudor Domain Ligand, (R,R)-59, Promotes Methylation of Akt1 in CellsMélanie Uguen, Yu Deng, Fengling Li, et al.The Biochemical Journal|August 26, 2009
A survey of proteins encoded by non-synonymous single nucleotide polymorphisms reveals a significant fraction with altered stability and activityAbdellah Allali-Hassani, Gregory A Wasney, Irene Chau, et al.Nature Reviews. Cancer|June 30, 2021
MYC protein interactors in gene transcription and cancerCorey Lourenco, Diana Resetca, Cornelia Redel, et al.Scientific Reports|April 27, 2019
Discovery of selective activators of PRC2 mutant EED-I363MJunghyun L Suh, Kimberly D Barnash, Tigran M Abramyan, et al.Nucleic Acids Research|December 14, 2020
Identification of lysine isobutyrylation as a new histone modification markZhesi Zhu, Zhen Han, Levon Halabelian, et al.Journal of Molecular Biology|July 5, 2005
A structure-based model of the c-Myc/Bin1 protein interaction shows alternative splicing of Bin1 and c-Myc phosphorylation are key binding determinantsAntonio Pineda-Lucena, Cynthia S W Ho, Daniel Y L Mao, et al.Journal of Medicinal Chemistry|July 26, 2011
Optimization of cellular activity of G9a inhibitors 7-aminoalkoxy-quinazolinesFeng Liu, Dalia Barsyte-Lovejoy, Abdellah Allali-Hassani, et al.Proceedings of the National Academy of Sciences of the United States of America|July 20, 2005
NMR data collection and analysis protocol for high-throughput protein structure determinationGaohua Liu, Yang Shen, Hanudatta S Atreya, et al.Journal of Medicinal Chemistry|March 1, 2013
Exploiting an allosteric binding site of PRMT3 yields potent and selective inhibitorsFeng Liu, Fengling Li, Anqi Ma, et al.Pageof 39