Lista de obras -

A DNA-PKcs mutation in a radiosensitive T-B- SCID patient inhibits Artemis activation and nonhomologous end-joining.

artículo científico publicado en 2008

A PALB2-interacting domain in RNF168 couples homologous recombination to DNA break-induced chromatin ubiquitylation.

scientific article published on 27 February 2017

A new non-catalytic role for ubiquitin ligase RNF8 in unfolding higher-order chromatin structure

artículo científico publicado en 2012

A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation.

artículo científico publicado en 2005

A novel radiosensitive SCID patient with a pronounced G(2)/M sensitivity

artículo científico publicado en 2010

Ataxin-3 consolidates the MDC1-dependent DNA double-strand break response by counteracting the SUMO-targeted ubiquitin ligase RNF4.

artículo científico publicado en 2017

Brca2 (XRCC11) deficiency results in enhanced mutagenesis ⬇️

artículo científico publicado el 1 de noviembre de 2003

CHD7 and 53BP1 regulate distinct pathways for the re-ligation of DNA double-strand breaks

artículo científico publicado en 2020

Chinese hamster cell mutant, V-C8, a model for analysis of Brca2 function

artículo científico publicado en 2006

ERCC1 mutations impede DNA damage repair and cause liver and kidney dysfunction in patients

artículo científico publicado en 2021

Functional Analysis of Missense Variants in the Putative Breast Cancer Susceptibility Gene XRCC2.

artículo científico publicado en 2016

Functional analysis of genetic variants in the high-risk breast cancer susceptibility gene PALB2

scientific article published on 22 November 2019

Inducibility of nuclear Rad51 foci after DNA damage distinguishes all Fanconi anemia complementation groups from D1/BRCA2.

artículo científico publicado en 2005

Mammalian Rad51C contributes to DNA cross-link resistance, sister chromatid cohesion and genomic stability

artículo científico publicado en 2002

Map of synthetic rescue interactions for the Fanconi anemia DNA repair pathway identifies USP48.

artículo científico publicado en 2018

PARP1 Links CHD2-Mediated Chromatin Expansion and H3.3 Deposition to DNA Repair by Non-homologous End-Joining.

artículo científico publicado en 2016

PHF2 regulates homology-directed DNA repair by controlling the resection of DNA double strand breaks

scientific article published on 30 March 2020

PHF6 promotes non-homologous end joining and G2 checkpoint recovery

artículo científico publicado en 2019

Poly(ADP-ribosyl)ation links the chromatin remodeler SMARCA5/SNF2H to RNF168-dependent DNA damage signaling

artículo científico publicado en 2012

Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrow.

artículo científico publicado en 2002

Remodeling and spacing factor 1 (RSF1) deposits centromere proteins at DNA double-strand breaks to promote non-homologous end-joining

artículo científico publicado en 2013

Role of Artemis in DSB repair and guarding chromosomal stability following exposure to ionizing radiation at different stages of cell cycle.

artículo científico publicado en 2006

Selective Loss of PARG Restores PARylation and Counteracts PARP Inhibitor-Mediated Synthetic Lethality

scientific article published on 01 June 2018

Selective Loss of PARG Restores PARylation and Counteracts PARP Inhibitor-Mediated Synthetic Lethality.

artículo científico publicado en 2019

Suppression of the DNA repair defects of BRCA2-deficient cells with heterologous protein fusions

artículo científico publicado en 2006

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

article

The NuRD chromatin-remodeling complex regulates signaling and repair of DNA damage

artículo científico publicado en 2010

The de-ubiquitylating enzymes USP26 and USP37 regulate homologous recombination by counteracting RAP80

artículo científico publicado en 2015

The de-ubiquitylating enzymes USP26 and USP37 regulate homologous recombination by counteracting RAP80.

artículo científico publicado en 2015

The yeast Fun30 and human SMARCAD1 chromatin remodellers promote DNA end resection

artículo científico publicado en 2012

WWP2 ubiquitylates RNA polymerase II for DNA-PK-dependent transcription arrest and repair at DNA breaks

artículo científico publicado en 2019

ZMYND8 Co-localizes with NuRD on Target Genes and Regulates Poly(ADP-Ribose)-Dependent Recruitment of GATAD2A/NuRD to Sites of DNA Damage.

artículo científico publicado en 2016

Zinc finger protein ZNF384 is an adaptor of Ku to DNA during classical non-homologous end-joining

artículo científico publicado en 2021

Lista de obras de

A DNA-PKcs mutation in a radiosensitive T-B- SCID patient inhibits Artemis activation and nonhomologous end-joining.

A PALB2-interacting domain in RNF168 couples homologous recombination to DNA break-induced chromatin ubiquitylation.

A new non-catalytic role for ubiquitin ligase RNF8 in unfolding higher-order chromatin structure

A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation.

A novel radiosensitive SCID patient with a pronounced G(2)/M sensitivity

Ataxin-3 consolidates the MDC1-dependent DNA double-strand break response by counteracting the SUMO-targeted ubiquitin ligase RNF4.

Brca2 (XRCC11) deficiency results in enhanced mutagenesis ⬇️

CHD7 and 53BP1 regulate distinct pathways for the re-ligation of DNA double-strand breaks

Chinese hamster cell mutant, V-C8, a model for analysis of Brca2 function

ERCC1 mutations impede DNA damage repair and cause liver and kidney dysfunction in patients

Functional Analysis of Missense Variants in the Putative Breast Cancer Susceptibility Gene XRCC2.

Functional analysis of genetic variants in the high-risk breast cancer susceptibility gene PALB2

Inducibility of nuclear Rad51 foci after DNA damage distinguishes all Fanconi anemia complementation groups from D1/BRCA2.

Mammalian Rad51C contributes to DNA cross-link resistance, sister chromatid cohesion and genomic stability

Map of synthetic rescue interactions for the Fanconi anemia DNA repair pathway identifies USP48.

PARP1 Links CHD2-Mediated Chromatin Expansion and H3.3 Deposition to DNA Repair by Non-homologous End-Joining.

PHF2 regulates homology-directed DNA repair by controlling the resection of DNA double strand breaks

PHF6 promotes non-homologous end joining and G2 checkpoint recovery

Poly(ADP-ribosyl)ation links the chromatin remodeler SMARCA5/SNF2H to RNF168-dependent DNA damage signaling

Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrow.

Remodeling and spacing factor 1 (RSF1) deposits centromere proteins at DNA double-strand breaks to promote non-homologous end-joining

Role of Artemis in DSB repair and guarding chromosomal stability following exposure to ionizing radiation at different stages of cell cycle.

Selective Loss of PARG Restores PARylation and Counteracts PARP Inhibitor-Mediated Synthetic Lethality

Selective Loss of PARG Restores PARylation and Counteracts PARP Inhibitor-Mediated Synthetic Lethality.

Suppression of the DNA repair defects of BRCA2-deficient cells with heterologous protein fusions

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

The NuRD chromatin-remodeling complex regulates signaling and repair of DNA damage

The de-ubiquitylating enzymes USP26 and USP37 regulate homologous recombination by counteracting RAP80

The de-ubiquitylating enzymes USP26 and USP37 regulate homologous recombination by counteracting RAP80.

The yeast Fun30 and human SMARCAD1 chromatin remodellers promote DNA end resection

WWP2 ubiquitylates RNA polymerase II for DNA-PK-dependent transcription arrest and repair at DNA breaks

ZMYND8 Co-localizes with NuRD on Target Genes and Regulates Poly(ADP-Ribose)-Dependent Recruitment of GATAD2A/NuRD to Sites of DNA Damage.

Zinc finger protein ZNF384 is an adaptor of Ku to DNA during classical non-homologous end-joining