Replication timing is regulated by the number of MCMs loaded at origins

Genome Research

Volumn 25, Issue 12, 2015, Pages 1886-1892

  Das, Shankar P ^a   Borrman, Tyler ^a   Liu, Victor W T ^a   Yang, Scott C H ^b,c   Bechhoefer, John ^b   Rhind, Nicholas ^a  

^a UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

^b SIMON FRASER UNIVERSITY   (Canada)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA BINDING PROTEIN; HELICASE; MCM HELICASE; UNCLASSIFIED DRUG; MINICHROMOSOME MAINTENANCE PROTEIN; PROTEIN BINDING;

ARTICLE; CELL CYCLE S PHASE; CHROMATIN STRUCTURE; DNA REPAIR; DNA REPLICATION ORIGIN; DNA REPLICATION TIMING; EVOLUTION; GENE EXPRESSION; GENETIC ENGINEERING; GENETIC REGULATION; GENOME; HETEROCHROMATIN; IN VIVO STUDY; NONHUMAN; PRIORITY JOURNAL; PROTEIN PURIFICATION; CELL CYCLE; CHROMATIN IMMUNOPRECIPITATION; DNA REPLICATION; GENETICS; HIGH THROUGHPUT SEQUENCING; METABOLISM; SACCHAROMYCES CEREVISIAE;

CELL CYCLE; CHROMATIN IMMUNOPRECIPITATION; DNA REPLICATION; DNA REPLICATION TIMING; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; MINICHROMOSOME MAINTENANCE PROTEINS; PROTEIN BINDING; REPLICATION ORIGIN; SACCHAROMYCES CEREVISIAE;

EID: 84956605207     PISSN: 10889051     EISSN: 15495469     Source Type: Journal    
DOI: 10.1101/gr.195305.115     Document Type: Article

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