The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4

DNA Repair

Volumn 3, Issue 11, 2004, Pages 1493-1502

  Clements, Paula M ^a   Breslin, Claire ^a   Deeks, Emma D ^b   Byrd, Philip J ^b   Ju, Limei ^a   Bieganowski, Pawel ^c   Brenner, Charles ^c   Moreira, Maria Céu ^d   Taylor, A Malcolm R ^b   Caldecott, Keith W ^a  

^a UNIVERSITY OF SUSSEX   (United Kingdom)

^b UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^c DARTMOUTH MEDICAL SCHOOL   (United States)

^d CNRS   (France)

Author keywords

Ataxia oculomotor apraxia 1; Double strand break; Single strand break

Indexed keywords

APRATAXIN; ATAXIA OCULOMOTOR APRAXIA 1 PROTEIN; ATM PROTEIN; COMPLEMENTARY DNA; DOUBLE STRANDED DNA; GENE PRODUCT; HYDROGEN PEROXIDE; MESYLIC ACID METHYL ESTER; POLYNUCLEOTIDE 5' HYDROXYL KINASE; PROTEIN; UNCLASSIFIED DRUG; XRCC1 PROTEIN; XRCC4 PROTEIN;

ARTICLE; ATAXIA OCULOMOTOR APRAXIA; ATAXIA TELANGIECTASIA; AUTOSOMAL RECESSIVE DISORDER; CELL CYCLE; CELL LINE; CONTROLLED STUDY; DEGENERATIVE DISEASE; DNA DAMAGE; DNA REPAIR; DNA STRAND; DNA STRAND BREAKAGE; DNA SYNTHESIS; FIBROBLAST; GENE MUTATION; HUMAN; HUMAN CELL; IONIZING RADIATION; PHOSPHORYLATION; PRIORITY JOURNAL; PROTEIN DNA INTERACTION;

APRAXIAS; ATAXIA; ATAXIA TELANGIECTASIA; CELL LINE; DNA DAMAGE; DNA REPAIR; DNA-BINDING PROTEINS; HUMANS; NUCLEAR PROTEINS; OCULOMOTOR NERVE DISEASES; RADIATION TOLERANCE; RECOMBINANT PROTEINS; TWO-HYBRID SYSTEM TECHNIQUES;

ATAXIA; ATAXIA TELANGIECTASIA;

EID: 4544341920     PISSN: 15687864     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dnarep.2004.06.017     Document Type: Article

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