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The Journal of Biological Chemistry|November 10, 2011
Protein aggregates are recruited to aggresome by histone deacetylase 6 via unanchored ubiquitin C terminiHui Ouyang, Yousuf O Ali, Mani Ravichandran, et al.
Nature Reviews. Drug Discovery|September 22, 2015
Tackling reproducibility in academic preclinical drug discoveryStephen V Frye, Michelle R Arkin, Cheryl H Arrowsmith, et al.
Journal of Molecular Biology|September 8, 2001
Solution structure and dynamics of yeast elongin C in complex with a von Hippel-Lindau peptideM V Botuyan, G Mer, G S Yi, et al.
The Journal of Biological Chemistry|August 25, 2011
Anti-Ro52 autoantibodies from patients with Sjögren's syndrome inhibit the Ro52 E3 ligase activity by blocking the E3/E2 interfaceAlexander Espinosa, Janosch Hennig, Aurélie Ambrosi, et al.
Organic & Biomolecular Chemistry|November 7, 2015
Design of a fluorescent ligand targeting the S-adenosylmethionine binding site of the histone methyltransferase MLL1Yepeng Luan, Levi L Blazer, Hao Hu, et al.
Journal of Biomolecular Screening|December 17, 2009
Screening for inhibitors of low-affinity epigenetic peptide-protein interactions: an AlphaScreen-based assay for antagonists of methyl-lysine binding proteinsTim J Wigle, J Martin Herold, Guillermo A Senisterra, et al.
Molecular Cell|March 25, 2015
Cbx2 targets PRC1 to constitutive heterochromatin in mouse zygotes in a parent-of-origin-dependent mannerMathieu Tardat, Mareike Albert, Rico Kunzmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 3, 2022
Dissecting the stability determinants of a challenging de novo protein fold using massively parallel design and experimentationTae-Eun Kim, Kotaro Tsuboyama, Scott Houliston, et al.
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