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PARP1 and PARP2 stabilise replication forks at base excision repair intermediates through Fbh1-dependent Rad51 regulation

Nature communications, 2018-02, Vol.9 (1), p.746-12, Article 746

2018

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Regulation of DNA-End Resection by hnRNPU-like Proteins Promotes DNA Double-Strand Break Signaling and Repair

Molecular cell, 2012-02, Vol.45 (4), p.505-516

2012

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The hMsh2-hMsh6 Complex Acts in Concert with Monoubiquitinated PCNA and Pol η in Response to Oxidative DNA Damage in Human Cells

Molecular cell, 2011-08, Vol.43 (4), p.649-662

2011

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BOD1L Is Required to Suppress Deleterious Resection of Stressed Replication Forks

Molecular cell, 2015-08, Vol.59 (3), p.462-477

2015

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Solving the RIDDLE of 53BP1 recruitment to sites of damage

Cell cycle (Georgetown, Tex.), 2009-05, Vol.8 (10), p.1532-1538

Stewart, Grant S.

2009

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PRMT5-Dependent Methylation of the TIP60 Coactivator RUVBL1 Is a Key Regulator of Homologous Recombination

Molecular cell, 2017-03, Vol.65 (5), p.900-916.e7

2017

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Actin nucleators safeguard replication forks by limiting nascent strand degradation

Nucleic acids research, 2023-07, Vol.51 (12), p.6337-6354

2023

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53BP1-dependent robust localized KAP-1 phosphorylation is essential for heterochromatic DNA double-strand break repair

Nature cell biology, 2010-02, Vol.12 (2), p.177-184

2010

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DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain

Nature communications, 2020-08, Vol.11 (1), p.3951-3951, Article 3951

2020

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ATRX proximal protein associations boast roles beyond histone deposition

PLoS genetics, 2021-11, Vol.17 (11), p.e1009909-e1009909

2021

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Mutations in the NHEJ Component XRCC4 Cause Primordial Dwarfism

American journal of human genetics, 2015-03, Vol.96 (3), p.412-424

2015

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Localization of Double-Strand Break Repair Proteins to Viral Replication Compartments following Lytic Reactivation of Kaposi's Sarcoma-Associated Herpesvirus

Journal of virology, 2017-11, Vol.91 (22)

2017

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Arginine methylation and ubiquitylation crosstalk controls DNA end-resection and homologous recombination repair

Nature communications, 2021-11, Vol.12 (1), p.6313-6313, Article 6313

2021

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A Hypomorphic PALB2 Allele Gives Rise to an Unusual Form of FA-N Associated with Lymphoid Tumour Development

PLoS genetics, 2016-03, Vol.12 (3), p.e1005945-e1005945

2016

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Excessive transcription-replication conflicts are a vulnerability of BRCA1-mutant cancers

Nucleic acids research, 2023-05, Vol.51 (9), p.4341-4362

2023

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RNF168 ubiquitylates 53BP1 and controls its response to DNA double-strand breaks

Proceedings of the National Academy of Sciences - PNAS, 2013-12, Vol.110 (52), p.20982-20987

2013

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A viral E3 ligase targets RNF8 and RNF168 to control histone ubiquitination and DNA damage responses

The EMBO journal, 2010-03, Vol.29 (5), p.943-955

2010

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Genomic instability, defective spermatogenesis, immunodeficiency, and cancer in a mouse model of the RIDDLE syndrome

PLoS genetics, 2011-04, Vol.7 (4), p.e1001381-e1001381

2011

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Constitutive phosphorylation of MDC1 physically links the MRE11-RAD50-NBS1 complex to damaged chromatin

The Journal of cell biology, 2008-04, Vol.181 (2), p.227-240

2008

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MDC1 is a mediator of the mammalian DNA damage checkpoint

Nature (London), 2003-02, Vol.421 (6926), p.961-966

2003

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RNF168 and USP10 regulate topoisomerase IIα function via opposing effects on its ubiquitylation

Nature communications, 2016-08, Vol.7 (1), p.12638-13, Article 12638

2016

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Identification of Adenovirus E1B-55K Interaction Partners through a Common Binding Motif

Viruses, 2023-11, Vol.15 (12), p.2356

2023

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DONSON: Slding in 2 the limelight

DNA repair, 2024-02, Vol.134, p.103616-103616, Article 103616

Stewart, Grant S.

2024

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Identification of the first ATRIP-deficient patient and novel mutations in ATR define a clinical spectrum for ATR-ATRIP Seckel Syndrome

PLoS genetics, 2012-11, Vol.8 (11), p.e1002945

2012

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PARP1 and PARP2 stabilise replication forks at base excision repair intermediates through Fbh1-dependent Rad51 regulation

Regulation of DNA-End Resection by hnRNPU-like Proteins Promotes DNA Double-Strand Break Signaling and Repair

The hMsh2-hMsh6 Complex Acts in Concert with Monoubiquitinated PCNA and Pol η in Response to Oxidative DNA Damage in Human Cells

BOD1L Is Required to Suppress Deleterious Resection of Stressed Replication Forks

Solving the RIDDLE of 53BP1 recruitment to sites of damage

PRMT5-Dependent Methylation of the TIP60 Coactivator RUVBL1 Is a Key Regulator of Homologous Recombination

Actin nucleators safeguard replication forks by limiting nascent strand degradation

53BP1-dependent robust localized KAP-1 phosphorylation is essential for heterochromatic DNA double-strand break repair

DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain

ATRX proximal protein associations boast roles beyond histone deposition

Mutations in the NHEJ Component XRCC4 Cause Primordial Dwarfism

Localization of Double-Strand Break Repair Proteins to Viral Replication Compartments following Lytic Reactivation of Kaposi's Sarcoma-Associated Herpesvirus

Arginine methylation and ubiquitylation crosstalk controls DNA end-resection and homologous recombination repair

A Hypomorphic PALB2 Allele Gives Rise to an Unusual Form of FA-N Associated with Lymphoid Tumour Development

RNF8 ubiquitylation of XRN2 facilitates R-loop resolution and restrains genomic instability in BRCA1 mutant cells

Excessive transcription-replication conflicts are a vulnerability of BRCA1-mutant cancers

RNF168 ubiquitylates 53BP1 and controls its response to DNA double-strand breaks

A viral E3 ligase targets RNF8 and RNF168 to control histone ubiquitination and DNA damage responses

Genomic instability, defective spermatogenesis, immunodeficiency, and cancer in a mouse model of the RIDDLE syndrome

Constitutive phosphorylation of MDC1 physically links the MRE11-RAD50-NBS1 complex to damaged chromatin

MDC1 is a mediator of the mammalian DNA damage checkpoint

RNF168 and USP10 regulate topoisomerase IIα function via opposing effects on its ubiquitylation

Identification of Adenovirus E1B-55K Interaction Partners through a Common Binding Motif

DONSON: Slding in 2 the limelight

Identification of the first ATRIP-deficient patient and novel mutations in ATR define a clinical spectrum for ATR-ATRIP Seckel Syndrome

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