, Hum Mol Genet, vol.10, pp.741-747, 2001.
The Werner syndrome gene: the molecular basis of RecQ helicasedeficiency diseases, Trends Genet, vol.16, pp.213-233, 2000. ,
Mutator phenotype of Werner syndrome is characterized by extensive deletions, Proc Natl Acad Sci, vol.86, pp.5893-5900, 1989. ,
Loss of Werner syndrome protein function promotes aberrant mitotic recombination, Genes Dev, vol.15, pp.933-941, 2001. ,
Homologous recombinational repair of DNA ensures mammalian chromosome stability, Mutat Res, vol.477, pp.131-53, 2001. ,
Branch migration and Holliday junction resolution catalyzed by activities from mammalian cells ,