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TP53 BRCA1 CRISPR single-cell cancer

Ruttkay-Nedecký(B),Subík(J) Curr Genet 1990-04-20

...rad52-mediated chromosome loss the ogd1 mutation can be assigned to chromosome IX. Tetrad analysis of crosses between og...

White(C I),Haber(J E) EMBO J 1990-04-20

...rad52 strain unable to switch. Surprisingly, the proximal side of the HO cut is protected from degradation; this stabili...

Schiestl(R H),Prakash(S),Prakash(L) Genetics 1990-05-14

...RAD52, RAD54, RAD55 or RAD57 genes. Possible mechanisms by which SRS2 may channel unrepaired DNA lesions into the RAD52 ...

Palmer(R E),Hogan(E),Koshland(D) Genetics 1990-10-18

...RAD52 dependent and RAD52 independent mechanism. These results are discussed in the context of the molecular functions o...

Jeggo(P A) Mutat Res 1990-08-13

...rad52 mutants of S. cerevisiae but contrasts to the majority of the E. coli mutants with defective dsb rejoining. Where ...

Zehfus(B R),McWilliams(A D),Lin(Y H),Hoekstr… Genetics 1990-12-05

...RAD52-dependent, and some requires either RAD1 or RAD52 as suggested by the synergistic interaction found in double muta...

Keszenman-Pereyra(D) Photochem Photobiol 1990-07-20

...rad52-1 and rad54-1 from the RAD52 group. Cells carrying single, double and triple rad alleles were transformed to uraci...

Ager(D D),Haynes(R H) Mutat Res 1990-11-20

...RAD52 function (recombinational repair), but not on RAD3 function (excision repair). On the basis of this analysis, the ...

Ascenzioni(F),Guerrini(A M),Donini(P) Plasmid 1990-07-12

...RAD52 strain were rearranged dimers terminating at both ends with Tetrahymena telomeres, whereas in the rad52 strain two...

Ferguson(L R) Mutat Res 1990-09-06

...rad52 derivative. Experiments were performed in the presence of three DNA-repair inhibitors which are currently in clini...

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