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Epigenetics & Chromatin|May 20, 2016
Setdb1-mediated H3K9 methylation is enriched on the inactive X and plays a role in its epigenetic silencingAndrew Keniry, Linden J Gearing, Natasha Jansz, et al.Proceedings of the National Academy of Sciences of the United States of America|June 21, 2015
Genome-wide binding and mechanistic analyses of Smchd1-mediated epigenetic regulationKelan Chen, Jiang Hu, Darcy L Moore, et al.The Biochemical Journal|October 11, 2013
A robust methodology to subclassify pseudokinases based on their nucleotide-binding propertiesJames M Murphy, Qingwei Zhang, Samuel N Young, et al.Nature Communications|September 25, 2023
SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in diseaseAndres Tapia Del Fierro, Bianca den Hamer, Natalia Benetti, et al.Nature Genetics|January 10, 2017
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal developmentChristopher T Gordon, Shifeng Xue, Gökhan Yigit, et al.Pageof 2