Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway

Human Molecular Genetics

Volumn 13, Issue 24, 2004, Pages 3127-3138

  Alderton, Gemma K ^a   Joenje, Hans ^b   Varon, Raymonda ^c   Børglum, Anders D ^d   Jeggo, Penny A ^a   O'Driscoll, Mark ^a  

^a UNIVERSITY OF SUSSEX   (United Kingdom)

^b VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^c CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^d AARHUS UNIVERSITY   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ATR PROTEIN; COMPLEMENTARY DNA;

ARTICLE; CELL COUNT; CELL CYCLE G2 PHASE; CELL DIVISION; CELL LINE; CENTROSOME; CLINICAL FEATURE; CONTROLLED STUDY; DNA DAMAGE; GENE MUTATION; GENETIC DISORDER; GENETIC IDENTIFICATION; HUMAN; HUMAN CELL; MICRONUCLEUS; MITOSIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; RADIATION EXPOSURE; REGULATORY MECHANISM; SECKEL SYNDROME; SIGNAL TRANSDUCTION; ULTRAVIOLET RADIATION;

CELL CYCLE; CELL CYCLE PROTEINS; CELL LINE; CENTROSOME; HUMANS; MICRONUCLEI, CHROMOSOME-DEFECTIVE; PROTEIN-SERINE-THREONINE KINASES; SIGNAL TRANSDUCTION;

ATAXIA; ATAXIA TELANGIECTASIA;

EID: 11044234004     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/ddh335     Document Type: Article

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