000 01233 a2200361 4500
005 20250515010450.0
264 0 _c20060523
008 200605s 0 0 eng d
022 _a0950-9232
024 7 _a10.1038/sj.onc.1209277
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCampbell, M R
245 0 0 _aMsh2 deficiency leads to chromosomal abnormalities, centrosome amplification, and telomere capping defect.
_h[electronic resource]
260 _bOncogene
_cApr 2006
300 _a2531-6 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
650 0 4 _aAnimals
650 0 4 _aCentrosome
650 0 4 _aChromosome Aberrations
650 0 4 _aDNA Repair
650 0 4 _aEmbryo, Mammalian
_xcytology
650 0 4 _aFibroblasts
_xcytology
650 0 4 _aGene Amplification
650 0 4 _aMice
650 0 4 _aMice, Knockout
650 0 4 _aMutS Homolog 2 Protein
_xdeficiency
650 0 4 _aTelomere
_xphysiology
700 1 _aWang, Y
700 1 _aAndrew, S E
700 1 _aLiu, Y
773 0 _tOncogene
_gvol. 25
_gno. 17
_gp. 2531-6
856 4 0 _uhttps://doi.org/10.1038/sj.onc.1209277
_zAvailable from publisher's website
999 _c15952732
_d15952732