Human 100-kDa homologous DNA-pairing protein is the splicing factor PSF and promotes DNA strand invasion

по Akhmedov, Alexandre T., Lopez, Bernard S.
Опубликовано 2000

Characterization of mammalian RAD51 double strand break repair using non-lethal dominant-negative forms

по Lambert, Sarah, Lopez, Bernard S.
Опубликовано 2000

Is Non-Homologous End-Joining Really an Inherently Error-Prone Process?

по Bétermier, Mireille, Bertrand, Pascale, Lopez, Bernard S.
Опубликовано 2014

Replication Stress in Mammalian Cells and Its Consequences for Mitosis

по Gelot, Camille, Magdalou, Indiana, Lopez, Bernard S.
Опубликовано в: Genes (Basel) (2015)

AKT1/BRCA1 in the control of homologous recombination and genetic stability: the missing link between hereditary and sporadic breast cancers

по Guirouilh-Barbat, Josée, Wilhelm, Therese, Lopez, Bernard S.
Опубликовано 2010

The cohesin complex prevents the end-joining of distant DNA double-strand ends in S phase: Consequences on genome stability maintenance

по Gelot, Camille, Guirouilh-Barbat, Josée, Lopez, Bernard S.
Опубликовано в: Nucleus (2016)

The Cohesion complex maintains genome stability by preventing end joining of distant DNA ends in S phase

по Gelot, Camille, Guirouilh-Barbat, Josée, Lopez, Bernard S.
Опубликовано в: Mol Cell Oncol (2018)

Replication Stress, DNA Damage, Inflammatory Cytokines and Innate Immune Response

по Ragu, Sandrine, Matos-Rodrigues, Gabriel, Lopez, Bernard S.
Опубликовано в: Genes (Basel) (2020)

Mouse Models for Deciphering the Impact of Homologous Recombination on Tumorigenesis

по Matos-Rodrigues, Gabriel, Martini, Emmanuelle, Lopez, Bernard S.
Опубликовано в: Cancers (Basel) (2021)

A novel role for the Bcl-2 protein family: specific suppression of the RAD51 recombination pathway

по Saintigny, Yannick, Dumay, Anne, Lambert, Sarah, Lopez, Bernard S.
Опубликовано 2001

Initiation of DNA double strand break repair: signaling and single-stranded resection dictate the choice between homologous recombination, non-homologous end-joining and alternativ...

по Grabarz, Anastazja, Barascu, Aurélia, Guirouilh-Barbat, Josée, Lopez, Bernard S
Опубликовано 2012

Is homologous recombination really an error-free process?

по Guirouilh-Barbat, Josée, Lambert, Sarah, Bertrand, Pascale, Lopez, Bernard S.
Опубликовано 2014

Role of the double-strand break repair pathway in the maintenance of genomic stability

по Le Guen, Tangui, Ragu, Sandrine, Guirouilh-Barbat, Josée, Lopez, Bernard S
Опубликовано в: Mol Cell Oncol (2014)

Homologous recombination, cancer and the ‘RAD51 paradox’

по Matos-Rodrigues, Gabriel, Guirouilh-Barbat, Josée, Martini, Emmanuelle, Lopez, Bernard S
Опубликовано в: NAR Cancer (2021)

An xrcc4 defect or Wortmannin stimulates homologous recombination specifically induced by double-strand breaks in mammalian cells

по Delacôte, Fabien, Han, Mingguang, Stamato, Thomas D., Jasin, Maria, Lopez, Bernard S.
Опубликовано 2002

Defects in XRCC4 and KU80 differentially affect the joining of distal nonhomologous ends

по Guirouilh-Barbat, Josée, Rass, Emilie, Plo, Isabelle, Bertrand, Pascale, Lopez, Bernard S.
Опубликовано 2007

Terminal deoxynucleotidyl transferase requires KU80 and XRCC4 to promote N-addition at non-V(D)J chromosomal breaks in non-lymphoid cells

по Boubakour-Azzouz, Imenne, Bertrand, Pascale, Claes, Aurélie, Lopez, Bernard S., Rougeon, François
Опубликовано 2012

Chromosome translocation based on illegitimate recombination in human tumors

по Zucman-Rossi, Jessica, Legoix, Patricia, Victor, Jean-Marc, Lopez, Bernard, Thomas, Gilles
Опубликовано 1998

Spontaneous slow replication fork progression elicits mitosis alterations in homologous recombination-deficient mammalian cells

по Wilhelm, Therese, Magdalou, Indiana, Barascu, Aurélia, Técher, Hervé, Debatisse, Michelle, Lopez, Bernard S.
Опубликовано 2014

53BP1 Protects against CtIP-Dependent Capture of Ectopic Chromosomal Sequences at the Junction of Distant Double-Strand Breaks

по Guirouilh-Barbat, Josée, Gelot, Camille, Xie, Anyong, Dardillac, Elodie, Scully, Ralph, Lopez, Bernard S.
Опубликовано в: PLoS Genet (2016)