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University of Cambridge > Talks.cam > Babraham Seminar > Nucleosomal Asymmetry Shapes Histone Mark Binding at Bivalent Domains
Nucleosomal Asymmetry Shapes Histone Mark Binding at Bivalent DomainsAdd to your list(s) Download to your calendar using vCal
If you have a question about this talk, please contact Bobbie Claxton. If you would like to attend this seminar, please contact us to arrange site access. Philipp Voigt is a Sir Henry Dale Fellow at the Wellcome Centre for Cell Biology. Work in his lab aims to determine how different histone modifications interact to regulate gene expression in embryonic stem cells, focusing on Polycomb and trithorax group protein complexes. His lab is taking a multidisciplinary approach, combining biochemistry with proteomic, genomic, cell-biological, and systems biology-inspired techniques. Philipp received both his undergraduate and graduate degree in Biochemistry from Freie Universität Berlin, Germany. His PhD work focused on phosphoinositide kinase signalling pathways in lymphocytes. In 2008, he joined the laboratory of Danny Reinberg at NYU School of Medicine, New York, for his postdoctoral studies. There, he studied molecular mechanisms of Polycomb-mediated gene silencing, revealing that sister histones within single nucleosomes can carry different histone modifications in an asymmetric fashion. He moved to Edinburgh in November 2014 to start his own research group as a Sir Henry Dale Fellow and ERC Starting Grant holder. This talk is part of the Babraham Seminar series. This talk is included in these lists:
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