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Autor:
Mark Petronczki, Stefan Kubicek, Nara C. Marella, Christoph Bock, André C. Müller, Jung-Ming G. Lin, Sarah Grosche, Danica Drpic, Gerald Hofstätter, Hana Imrichova, Anna Koren, Martin G. Jaeger, André F. Rendeiro, Michael Schuster, Sandra Schick, Georg E. Winter, Katharina Eva Kohl
Publikováno v:
Nature Genetics
Cancer-associated, loss-of-function mutations in genes encoding subunits of the BRG1/BRM-associated factor (BAF) chromatin-remodeling complexes1–8 often cause drastic chromatin accessibility changes, especially in important regulatory regions9–19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76ca62813be8ca4a6654f5bf7c4a16b7
