z-logo
open-access-imgOpen Access
Physical interactions between MCM and Rad51 facilitate replication fork lesion bypass and ssDNA gap filling by non-recombinogenic functions
Author(s) -
María J. Cabello-Lobato,
Cristina GonzálezGarrido,
María I. Cano-Linares,
Ronald P. Wong,
Aurora YáñezVilches,
Macarena MorilloHuesca,
Juan María RoldánRomero,
Marta Vicioso,
Román GonzálezPrieto,
Helle D. Ulrich,
Félix Prado
Publication year - 2021
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2021.109440
Subject(s) - rad51 , rad52 , minichromosome maintenance , homologous recombination , microbiology and biotechnology , helicase , biology , control of chromosome duplication , dna replication , dna repair , scaffold protein , replication protein a , replication factor c , dna , dna binding protein , genetics , gene , transcription factor , rna , signal transduction

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom