de Garibay(Gorka Ruiz),Díaz(Avellaneda),Gavi… Eur J Hum Genet 2013-10-29

...SLX4 have been demonstrated to cause a previously unknown FA subtype (FA-P). We address the role of SLX4/FANCP in breast...

Haitjema(Anneke),Brandt(Bernd W),Ameziane(Na… PLoS One 2013-11-11

...SLX4, and XRCC2 displayed scores in the range of the already known FA proteins. Likewise, a prime candidate FA gene base...

Pardo(Benjamin),Aguilera(Andrés) PLoS Genet 2013-03-14

...Slx4, also promote template switching during BIR. Altogether, our study provides evidence for a role of SSEs at multiple...

Kim(Yonghwan),Spitz(Gabriella S),Veturi(Uma)… Blood 2013-02-25

...SLX4 function is unclear. Here, by complementing a null FA-P Fanconi anemia cell line with SLX4 mutants that specificall...

Schuster(Beatrice),Knies(Kerstin),Stoepker(C… Hum Mutat 2013-07-01

...SLX4/FANCP. Whole exome sequencing (WES) revealed a nonsense mutation and an unusual splice site mutation resulting in t...

Ohouo(Patrice Y),Bastos de Oliveira(Francisc… Nature 2013-02-06

...Slx4 or Rtt107. We propose that the Slx4-Rtt107 complex modulates Rad53 activation by a competition-based mechanism that...

McHugh(Peter J),Ward(Thomas A),Chovanec(Miro… Cell Cycle 2013-03-01

...Slx4, respectively) as well as of the FANCM-associated proteins MHF1 and MHF2 (Mhf1 and Mhf2), the corresponding mutants...

Salewsky(Bastian),Schmiester(Maren),Schindle… Hum Mol Genet 2013-03-26

...SLX4, a protein recently identified as a new FA protein, FANCP, and known to interact with several structure-specific nu...

Beck(Halfdan),Nähse-Kumpf(Viola),Larsen(Mari… Mol Cell Biol 2013-01-03

...SLX4/MUS81-mediated DNA double-strand breakage. Fork speed is normalized and DNA double-strand break (DSB) formation is ...

Bakker(Janine L),van Mil(Saskia E),Crossan(G… Hum Mutat 2013-07-01

...SLX4 mutation in breast cancer patients, our data indicate that germline mutations in SLX4 are very rare and are unlikel...