Uncovering genetic relationships using small molecules that selectively target yeast cell cycle mutants

Chemical Biology and Drug Design

Volumn 69, Issue 4, 2007, Pages 258-264

  Nehil, Michael T ^a   Tamble, Craig M ^b   Combs, David J ^c   Kellogg, Douglas R ^b   Scott Lokey, R ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Cell cycle; Chemical genetics; Chemical genomics; High throughput screening; Yeast

Indexed keywords

1,4 NAPHTHOQUINONE DERIVATIVE; BENZENE DERIVATIVE; CYCLIN G1; MITOGEN ACTIVATED PROTEIN KINASE; PICOLINE DERIVATIVE; PROTEIN KINASE C; PYRIDINE DERIVATIVE; PYRIMIDINE DERIVATIVE;

ARTICLE; CELL CYCLE ARREST; CONTROLLED STUDY; DRUG EFFECT; DRUG IDENTIFICATION; DRUG SCREENING; DRUG SELECTIVITY; FUNGUS MUTANT; GENE DELETION; GENE IDENTIFICATION; GENE TARGETING; GENETIC ANALYSIS; LETHALITY; NONHUMAN; PRIORITY JOURNAL; WILD TYPE; YEAST;

CELL CYCLE; MOLECULAR STRUCTURE; MUTATION; PHARMACEUTICAL PREPARATIONS; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS;

EUKARYOTA; SACCHAROMYCETALES;

EID: 34247472032     PISSN: 17470277     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1747-0285.2007.00496.x     Document Type: Article

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