The Fanconi anemia protein FANCM is controlled by FANCD2 and the ATR/ATM pathways

Journal of Biological Chemistry

Volumn 284, Issue 38, 2009, Pages 25560-25568

  Sobeck, Alexandra ^a,b   Stone, Stacie ^a   Landais, Igor ^a   de Graaf, Bendert ^a   Hoatlin, Maureen E ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL CYCLE; CORE COMPLEX; DNA DAMAGE RESPONSE; DNA DAMAGES; DNA STRUCTURE; DOWNSTREAM TARGET; FANCONI ANEMIAS; GENOMIC STABILITY; PROCESSING ACTIVITY; XENOPUS;

CELL MEMBRANES; DNA; NUCLEIC ACIDS; PHOSPHORYLATION;

GENES;

ATM PROTEIN; ATR PROTEIN; FANCONI ANEMIA GROUP C PROTEIN; FANCONI ANEMIA GROUP D2 PROTEIN; ATR PROTEIN, XENOPUS; CELL CYCLE PROTEIN; DNA BINDING PROTEIN; FANCM PROTEIN, XENOPUS; HELICASE; PROTEIN SERINE THREONINE KINASE; TUMOR SUPPRESSOR PROTEIN; XENOPUS PROTEIN;

ARTICLE; CHROMATIN ASSEMBLY AND DISASSEMBLY; CONTROLLED STUDY; DNA DAMAGE; DNA STRUCTURE; GENOMIC INSTABILITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; UBIQUITINATION; ANIMAL; CHROMATIN; CYTOLOGY; DNA REPLICATION; GENETICS; METABOLISM; OOCYTE; PHOSPHORYLATION; PHYSIOLOGY; XENOPUS LAEVIS;

ANIMALS; CELL CYCLE PROTEINS; CHROMATIN; DNA DAMAGE; DNA HELICASES; DNA REPLICATION; DNA-BINDING PROTEINS; FANCONI ANEMIA COMPLEMENTATION GROUP D2 PROTEIN; OOCYTES; PHOSPHORYLATION; PROTEIN-SERINE-THREONINE KINASES; TUMOR SUPPRESSOR PROTEINS; XENOPUS LAEVIS; XENOPUS PROTEINS;

EID: 70350007132     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M109.007690     Document Type: Article

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