WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair (Q34224821)

31 July 2017

title

WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair (English)

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31 July 2017

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6

Judith Campisi

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31 July 2017

Lishan Chen

1

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31 July 2017

Shurong Huang

2

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31 July 2017

Lin Lee

3

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31 July 2017

Albert Davalos

4

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31 July 2017

Robert H Schiestl

5

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31 July 2017

Junko Oshima

7

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31 July 2017

publication date

1 August 2003

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31 July 2017

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31 July 2017

volume

2

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31 July 2017

issue

4

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31 July 2017

page(s)

191-199

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One-sided invasion events in homologous recombination at double-strand breaks

31 July 2017

cites work

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https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Regulation and localization of the Bloom syndrome protein in response to DNA damage

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Roles of the Werner syndrome protein in pathways required for maintenance of genome stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

p53 Modulates the exonuclease activity of Werner syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Werner helicase is localized to transcriptionally active nucleoli of cycling cells

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Ku70-deficient embryonic stem cells have increased ionizing radiosensitivity, defective DNA end-binding activity, and inability to support V(D)J recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Growth retardation and leaky SCID phenotype of Ku70-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Characterization of the human and mouse WRN 3'-->5' exonuclease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

The premature ageing syndrome protein, WRN, is a 3'-->5' exonuclease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Werner and Bloom helicases are involved in DNA repair in a complementary fashion

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

PML is critical for ND10 formation and recruits the PML-interacting protein daxx to this nuclear structure when modified by SUMO-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Differential regulation of human RecQ family helicases in cell transformation and cell cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Functional interaction between Ku and the werner syndrome protein in DNA end processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Requirements for the nucleolytic processing of DNA ends by the Werner syndrome protein-Ku70/80 complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

The Werner syndrome protein: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Werner helicase relocates into nuclear foci in response to DNA damaging agents and co-localizes with RPA and Rad51.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

The V(D)J recombination activating gene, RAG-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Characterization of Werner syndrome protein DNA helicase activity: directionality, substrate dependence and stimulation by replication protein A

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Werner syndrome exonuclease catalyzes structure-dependent degradation of DNA.

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

Potential targets for autosomal SCID mutations

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

The processing of Holliday junctions by BLM and WRN helicases is regulated by p53

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

V(D)J rearrangement in Nijmegen breakage syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

A role for PML and the nuclear body in genomic stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1474-9728.2003.00052.X

10.1046/J.1474-9728.2003.00052.X

21 January 2018

Identifiers

DOI

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31 July 2017

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