(Q30983796)

5 November 2017

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

1 reference

5 November 2017

7

1 reference

5 November 2017

A Constantinou

1

1 reference

5 November 2017

M Tarsounas

2

1 reference

5 November 2017

J K Karow

3

1 reference

5 November 2017

R M Brosh

4

1 reference

5 November 2017

V A Bohr

5

1 reference

5 November 2017

I D Hickson

6

1 reference

5 November 2017

1 July 2000

1 reference

5 November 2017

1 reference

5 November 2017

1

1 reference

5 November 2017

80-84

1 reference

5 November 2017

1

1 reference

The Bloom's syndrome gene product promotes branch migration of holliday junctions

5 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Replication fork pausing and recombination or "gimme a break"

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Enzymatic and DNA binding properties of purified WRN protein: high affinity binding to single-stranded DNA but not to DNA damage induced by 4NQO.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

DNA recombination: the replication connection.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Defending genome integrity during DNA replication: a proposed role for RecQ family helicases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Functional and physical interaction between WRN helicase and human replication protein A

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Binding specificity determines polarity of DNA unwinding by the Sgs1 protein of S. cerevisiae.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Replication focus-forming activity 1 and the Werner syndrome gene product

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Nucleolar localization of the Werner syndrome protein in human cells

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Proliferating cell nuclear antigen: more than a clamp for DNA polymerases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Bloom syndrome: a mendelian prototype of somatic mutational disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Replicative life-span of cultivated human cells. Effects of donor's age, tissue, and genotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Mutator phenotype of Werner syndrome is characterized by extensive deletions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Unusual stability of recombination intermediates made by Escherichia coli RecA protein.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Interaction of Escherichia coli RuvA and RuvB proteins with synthetic Holliday junctions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

Purification and properties of the RuvA and RuvB proteins of Escherichia coli

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1083680

In vitro reconstitution of the late steps of genetic recombination in E. coli.

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FEMBO-REPORTS%2FKVD004

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FEMBO-REPORTS%2FKVD004

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEMBO-REPORTS%2FKVD004

Werner syndrome protein. II. Characterization of the integral 3' --> 5' DNA exonuclease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11256630

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11256630

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/EMBO-REPORTS/KVD004

1 reference

5 November 2017

1 reference

5 November 2017

1 reference