(Q38327669)

2 September 2017

RecQ family members combine strand pairing and unwinding activities to catalyze strand exchange (English)

1 reference

2 September 2017

Amrita Machwe

1

1 reference

2 September 2017

Liren Xiao

2

1 reference

2 September 2017

Joanna Groden

3

1 reference

2 September 2017

Steven W Matson

4

1 reference

2 September 2017

David K Orren

5

1 reference

2 September 2017

language of work or name

English

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publication date

20 April 2005

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Journal of Biological Chemistry

2 September 2017

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2 September 2017

280

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2 September 2017

23397-23407

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2 September 2017

24

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The Bloom's syndrome gene product is homologous to RecQ helicases

2 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Positional cloning of the Werner's syndrome gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Lessons from human progeroid syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

DNA helicases, genomic instability, and human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Homologous recombination resolution defect in werner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

RecQ helicases: caretakers of the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Bloom syndrome cells undergo p53-dependent apoptosis and delayed assembly of BRCA1 and NBS1 repair complexes at stalled replication forks

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

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/10.1074%2FJBC.M414130200

Binding and melting of D-loops by the Bloom syndrome helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Werner syndrome exonuclease catalyzes structure-dependent degradation of DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

The Werner syndrome helicase/exonuclease (WRN) disrupts and degrades D-loops in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Analysis of helicase activity and substrate specificity of Drosophila RECQ5

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

A putative nucleic acid-binding domain in Bloom's and Werner's syndrome helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

The three-dimensional structure of the HRDC domain and implications for the Werner and Bloom syndrome proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

High-resolution structure of the E.coli RecQ helicase catalytic core

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Werner syndrome protein contains three structure-specific DNA binding domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

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 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Escherichia coli DNA helicase II is active as a monomer

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Biochemical characterization of the small isoform of Drosophila melanogaster RECQ5 helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

The Bloom's syndrome gene product is a 3'-5' DNA helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

The helicase from hepatitis C virus is active as an oligomer

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

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/10.1074%2FJBC.M414130200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Replication protein A physically interacts with the Bloom's syndrome protein and stimulates its helicase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

The Bloom's syndrome helicase suppresses crossing over during homologous recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

Human RECQ5beta, a protein with DNA helicase and strand-annealing activities in a single polypeptide

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M414130200

21 January 2018

Identifiers

DOI

10.1074/JBC.M414130200

1 reference

2 September 2017

1 reference