Vissers, C.J.( C.J. Vissers)
1*292 ercc 1*292 mice repair ercc 1-mutant mice ercc 1 wild-type 1-mutant mouse knockout analysis ercc 1 knockout protein liver probe mutation ercc 1-mutant mefs fragment cycle level abnormality ercc 1 gene ercc 1*292 mefs +/+ life span recombination cross-link xpa / mice p 21cip kidney defect ercc 1*292 mutation cell cycle arrest survival control fibroblast figure bamhi allele nuclei ercc 1 protein background ercc 1*292 blot analysis syndrome cross-link repair *292 senescence group clone offspring function region sensitivity replicative senescence effect vol 7 ercc 1mutant mice mcwhir ercc 1*292 allele result mice weeda 30 g dmba treatment tissue mutant addition number section growth arrest 21cip lesion phenotype c 57bl agent disruption wild-type litter-mates genomic dna repair culture
1 Most Recent Publications
Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence.
Weeda, G. Donker, I. Wit, J. de Morreau, H. Janssens, R. Vissers, C.J. Nigg, A. Steeg, H. van Bootsma, D. Hoeijmakers, J.H.J.