Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects.Pierre-M Girard, Penelope A. Jeggo, Nicolas Foray et al.|PubMed|2000Cited by 71
A DNA double-strand break defective fibroblast cell line (180BR) derived from a radiosensitive patient represents a new mutant phenotype.Christophe Badie, E.P. Malaise, Penelope A. Jeggo et al.|PubMed|1997Cited by 51
A novel splice variant of the DNA-PKcs gene is associated with clinical and cellular radiosensitivity in a patient with xeroderma pigmentosumFatemeh Abbaszadeh, Christopher N. Parris, Michael Themis et al.|Journal of Medical Genetics|2009Cited by 35
The effect of variable serum factors and clonal morphology on the ability to detect hypoxanthine guanine phosphoribosyl transferase (HPRT) deficient variants in cultured Chinese hamster cellsRobert F. Newbold, Brian Dean, P. Brookes et al.|Mutation research. Fundamental and molecular mechanisms of mutagenesis|1975Cited by 23