Complementation of chromosomal aberrations in AT/NBS hybrids: Inadequacy of RDS as an endpoint in complementation studies with immortal NBS cells

Mutation Research - DNA Repair

Volumn 485, Issue 3, 2001, Pages 177-185

  Kraakman Van Der Zwet, Maria ^a,b   Overkamp, Wilhelmina J I ^a   Jaspers, Nicolaas G J ^c   Natarajan, Adayapalam T ^a   Lohman, Paul H M ^b   Zdzienicka, Małgorzata Z ^a,b  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b JA Cohen Institute Interuniversity Research Institute for Radiopathology and Radiation Protection   (Netherlands)

^c ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

Ataxia telangiectasia; Chromosomal aberrations; Functional complementation; Nijmegen breakage syndrome; Radioresistant DNA synthesis

Indexed keywords

ARTICLE; ATAXIA TELANGIECTASIA; CANCER; CELL HYBRIDIZATION; CELL KILLING; CELL PROLIFERATION; CHROMOSOME 8; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CONTROLLED STUDY; DISEASE PREDISPOSITION; DNA SYNTHESIS; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; IMMUNE DEFICIENCY; IONIZING RADIATION; LYMPHOBLAST; NIJMEGEN BREAKAGE SYNDROME; PRIORITY JOURNAL; RADIOSENSITIVITY; X RAY;

ABNORMALITIES, MULTIPLE; ANIMALS; ATAXIA TELANGIECTASIA; CELL CYCLE PROTEINS; CELL DEATH; CHROMOSOME ABERRATIONS; DNA REPLICATION; DNA-BINDING PROTEINS; DOSE-RESPONSE RELATIONSHIP, RADIATION; GENETIC COMPLEMENTATION TEST; GENETIC PREDISPOSITION TO DISEASE; HUMANS; HYBRID CELLS; MICE; NUCLEAR PROTEINS; PROTEIN-SERINE-THREONINE KINASES; RADIATION TOLERANCE; SYNDROME; TUMOR SUPPRESSOR PROTEINS; X-RAYS;

ATAXIA; ATAXIA TELANGIECTASIA; GENETTA;

EID: 0035804778     PISSN: 09218777     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0921-8777(00)00078-1     Document Type: Article

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