The role of PR-Set7 in replication licensing depends on Suv4-20h

Genes and Development

Volumn 26, Issue 23, 2012, Pages 2580-2589

  Beck, David B ^a   Burton, Adam ^b   Oda, Hisanobu ^a   Ziegler Birling, Céline ^b   Torres Padilla, Maria Elena ^b   Reinberg, Danny ^a  

^a NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

Author keywords

Cell cycle; Chromatin; H4K20; ORC; PR Set7; Suv4 20

Indexed keywords

BIOLOGICAL FACTOR; BIOLOGICAL FACTOR CRL4 CDT2; CELL CYCLE PROTEIN; HISTONE H4; METHYLTRANSFERASE; ORIGIN RECOGNITION COMPLEX; UNCLASSIFIED DRUG;

ARTICLE; CELL CYCLE PROGRESSION; CELL DIFFERENTIATION; CONTROLLED STUDY; DNA DAMAGE; DNA REPLICATION; EMBRYO; FLOW CYTOMETRY; GENE; GENE EXPRESSION; H4K20 GENE; METHYLATION; MOUSE; NONHUMAN; PR SET7 GENE; PRIORITY JOURNAL; PROTEIN BINDING; TOXICITY;

ANIMALS; CELL CYCLE; CELL DIFFERENTIATION; CELL LINE, TUMOR; CELL PROLIFERATION; DNA DAMAGE; DNA REPLICATION; EMBRYO, MAMMALIAN; FIBROBLASTS; HELA CELLS; HISTONE-LYSINE N-METHYLTRANSFERASE; HUMANS; MICE; ORIGIN RECOGNITION COMPLEX; PROTEIN BINDING; UBIQUITIN-PROTEIN LIGASES;

EUKARYOTA;

EID: 84870529834     PISSN: 08909369     EISSN: 15495477     Source Type: Journal    
DOI: 10.1101/gad.195636.112     Document Type: Article

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