RecQ helicases; at the crossroad of genome replication, repair, and recombination (Q37938856)

25 August 2017

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title

RecQ helicases; at the crossroad of genome replication, repair, and recombination (English)

1 reference

25 August 2017

Sarallah Rezazadeh

1

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25 August 2017

23 September 2011

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Molecular Biology Reports

25 August 2017

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25 August 2017

39

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25 August 2017

4527-4543

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25 August 2017

4

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https://scigraph.springernature.com/pub.10.1007/s11033-011-1243-y

25 August 2017

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cites work

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Modularity and specialization in superfamily 1 and 2 helicases

21 January 2018

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Helicases become mechanistically simpler and functionally more complex.

21 January 2018

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RecQ helicases: suppressors of tumorigenesis and premature aging.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Characterization of the helicase activity of the Escherichia coli RecBCD enzyme using a novel helicase assay.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Substrate specificity of the DNA unwinding activity of the RecBC enzyme of Escherichia coli

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Structure and mechanism of helicases and nucleic acid translocases

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Non-hexameric DNA helicases and translocases: mechanisms and regulation

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Structure and mechanism of the RuvB Holliday junction branch migration motor

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

RecQ helicases: caretakers of the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Current advances in unraveling the function of the Werner syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Bloom's syndrome gene product interacts with topoisomerase III

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The N-terminal region of the Schizosaccharomyces pombe RecQ helicase, Rqh1p, physically interacts with Topoisomerase III and is required for Rqh1p function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Topoisomerase III is essential for accurate nuclear division in Schizosaccharomyces pombe

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

A hyper-recombination mutation in S. cerevisiae identifies a novel eukaryotic topoisomerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Mammalian DNA topoisomerase IIIalpha is essential in early embryogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The top3(+) gene is essential in Schizosaccharomyces pombe and the lethality associated with its loss is caused by Rad12 helicase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Purification and characterization of the Sgs1 DNA helicase activity of Saccharomyces cerevisiae.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Werner syndrome protein is a DNA helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

DNA helicase deficiencies associated with cancer predisposition and premature ageing disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Analysis of helicase activity and substrate specificity of Drosophila RECQ5

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Drosophila RecQ4 has a 3'-5' DNA helicase activity that is essential for viability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

RECQ1 helicase interacts with human mismatch repair factors that regulate genetic recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Nuclear import and retention domains in the amino terminus of RECQL4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

RecQ4: the second replicative helicase?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Structure of the human RECQ1 helicase reveals a putative strand-separation pin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Major domain swiveling revealed by the crystal structures of complexes of E. coli Rep helicase bound to single-stranded DNA and ADP

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

UvrD helicase unwinds DNA one base pair at a time by a two-part power stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Crystal structures of complexes of PcrA DNA helicase with a DNA substrate indicate an inchworm mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Domain mapping of Escherichia coli RecQ defines the roles of conserved N- and C-terminal regions in the RecQ family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Point mutations causing Bloom's syndrome abolish ATPase and DNA helicase activities of the BLM protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Structural and functional characterizations reveal the importance of a zinc binding domain in Bloom's syndrome helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Bloom's syndrome helicase promotes the annealing of complementary single-stranded DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The zinc finger motif of Escherichia coli RecQ is implicated in both DNA binding and protein folding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Solution structure of a multifunctional DNA- and protein-binding motif of human Werner syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

DNA binding and nucleotide flipping by the human DNA repair protein AGT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

21 January 2018

Winged helix proteins

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Structure of the winged-helix protein hRFX1 reveals a new mode of DNA binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Crystal structure of a CAP-DNA complex: the DNA is bent by 90 degrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Structural basis for DNA duplex separation by a superfamily-2 helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

A conserved G4 DNA binding domain in RecQ family helicases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Werner syndrome protein contains three structure-specific DNA binding domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Conferring substrate specificity to DNA helicases: role of the RecQ HRDC domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Structure and function of the regulatory C-terminal HRDC domain from Deinococcus radiodurans RecQ

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Crystal structure of the HRDC domain of human Werner syndrome protein, WRN

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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/10.1007%2FS11033-011-1243-Y

Characterization and mutational analysis of the RecQ core of the bloom syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The HRDC domain of BLM is required for the dissolution of double Holliday junctions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Redundancy of DNA helicases in p53-mediated apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Physical and functional interaction between p53 and the Werner's syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Molecular bases of progeroid syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Association and regulation of the BLM helicase by the telomere proteins TRF1 and TRF2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Positionally cloned human disease genes: patterns of evolutionary conservation and functional motifs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Biochemical and kinetic characterization of the DNA helicase and exonuclease activities of werner syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Coordinate action of the helicase and 3' to 5' exonuclease of Werner syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

WRN exonuclease structure and molecular mechanism imply an editing role in DNA end processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

RecQ helicases: multiple structures for multiple functions?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

MPS1-dependent mitotic BLM phosphorylation is important for chromosome stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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/10.1007%2FS11033-011-1243-Y

Werner syndrome protein phosphorylation by abl tyrosine kinase regulates its activity and distribution

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Werner's syndrome protein is phosphorylated in an ATR/ATM-dependent manner following replication arrest and DNA damage induced during the S phase of the cell cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Intra-nuclear trafficking of the BLM helicase to DNA damage-induced foci is regulated by SUMO modification

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Evidence for BLM and Topoisomerase IIIalpha interaction in genomic stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Human RECQ1 is a DNA damage responsive protein required for genotoxic stress resistance and suppression of sister chromatid exchanges

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The DNA helicase activity of BLM is necessary for the correction of the genomic instability of bloom syndrome cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

A new human topoisomerase III that interacts with SGS1 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Human RecQ5beta, a large isomer of RecQ5 DNA helicase, localizes in the nucleoplasm and interacts with topoisomerases 3alpha and 3beta

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Mut-7 of C. elegans, required for transposon silencing and RNA interference, is a homolog of Werner syndrome helicase and RNaseD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Molecular characterisation of RecQ homologues in Arabidopsis thaliana.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Recql5 and Blm RecQ DNA helicases have nonredundant roles in suppressing crossovers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The N-terminal region of Sgs1, which interacts with Top3, is required for complementation of MMS sensitivity and suppression of hyper-recombination in sgs1 disruptants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Unwinding the molecular basis of the Werner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Human RecQ helicases, BLM and RECQ1, display distinct DNA substrate specificities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Mobile D-loops are a preferred substrate for the Bloom's syndrome helicase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Identification of RecQL1 as a Holliday junction processing enzyme in human cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

RECQL5/Recql5 helicase regulates homologous recombination and suppresses tumor formation via disruption of Rad51 presynaptic filaments

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Novel pro- and anti-recombination activities of the Bloom's syndrome helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Werner syndrome protein participates in a complex with RAD51, RAD54, RAD54B and ATR in response to ICL-induced replication arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Potential role for the BLM helicase in recombinational repair via a conserved interaction with RAD51

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Junction of RecQ helicase biochemistry and human disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

DNA helicases required for homologous recombination and repair of damaged replication forks

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Recombinational repair and restart of damaged replication forks.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Functional interactions between BLM and XRCC3 in the cell

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Mechanism of homologous recombination: mediators and helicases take on regulatory functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Identification and purification of two distinct complexes containing the five RAD51 paralogs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Evidence for simultaneous protein interactions between human Rad51 paralogs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Physical interaction of RECQ5 helicase with RAD51 facilitates its anti-recombinase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Human RECQ5beta helicase promotes strand exchange on synthetic DNA structures resembling a stalled replication fork

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Werner and Bloom syndrome proteins catalyze regression of a model replication fork

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

RecQ helicases and topoisomerases: components of a conserved complex for the regulation of genetic recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Bloom's syndrome helicase stimulates the activity of human topoisomerase IIIalpha

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Bloom syndrome protein interacts and cooperates with p53 in regulation of transcription and cell growth control

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Bloom syndrome helicase BLM interacts with TRF2 in ALT cells and promotes telomeric DNA synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Stimulation of flap endonuclease-1 by the Bloom's syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

ATM-dependent phosphorylation and accumulation of endogenous BLM protein in response to ionizing radiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Bloom's syndrome protein response to ultraviolet-C radiation and hydroxyurea-mediated DNA synthesis inhibition

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Bloom's syndrome protein is required for correct relocalization of RAD50/MRE11/NBS1 complex after replication fork arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Nuclear structure in normal and Bloom syndrome cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Functional interaction of p53 and BLM DNA helicase in apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

BLM, the Bloom's syndrome protein, varies during the cell cycle in its amount, distribution, and co-localization with other nuclear proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

A role for PML and the nuclear body in genomic stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Induced cytoskeletal changes in bovine pulmonary artery endothelial cells by resveratrol and the accompanying modified responses to arterial shear stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Sterility of Drosophila with mutations in the Bloom syndrome gene--complementation by Ku70.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

POT1 stimulates RecQ helicases WRN and BLM to unwind telomeric DNA substrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Rif1 provides a new DNA-binding interface for the Bloom syndrome complex to maintain normal replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Molecular cooperation between the Werner syndrome protein and replication protein A in relation to replication fork blockage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

A functional interaction of Ku with Werner exonuclease facilitates digestion of damaged DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

A novel protein interacts with the Werner's syndrome gene product physically and functionally

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The human Werner syndrome protein stimulates repair of oxidative DNA base damage by the DNA glycosylase NEIL1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Linkage between Werner syndrome protein and the Mre11 complex via Nbs1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

WRN interacts physically and functionally with the recombination mediator protein RAD52

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Collaboration of Werner syndrome protein and BRCA1 in cellular responses to DNA interstrand cross-links

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

DNA damage-induced translocation of the Werner helicase is regulated by acetylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Central Role for the Werner Syndrome Protein/Poly(ADP-Ribose) Polymerase 1 Complex in the Poly(ADP-Ribosyl)ation Pathway after DNA Damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Physical and functional interaction between the Bloom's syndrome gene product and the largest subunit of chromatin assembly factor 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Werner syndrome protein is required for recruitment of chromatin assembly factor 1 following DNA damage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Analysis of the unwinding activity of the dimeric RECQ1 helicase in the presence of human replication protein A

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Characterization of the DNA-unwinding activity of human RECQ1, a helicase specifically stimulated by human replication protein A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The molecular role of the Rothmund-Thomson-, RAPADILINO- and Baller-Gerold-gene product, RECQL4: recent progress

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The N-terminal noncatalytic region of Xenopus RecQ4 is required for chromatin binding of DNA polymerase alpha in the initiation of DNA replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Roles of Werner syndrome protein in protection of genome integrity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Direct and indirect roles of RECQL4 in modulating base excision repair capacity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

A RECQ5-RNA polymerase II association identified by targeted proteomic analysis of human chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

RECQ5 helicase associates with the C-terminal repeat domain of RNA polymerase II during productive elongation phase of transcription.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Mapping the DNA topoisomerase III binding domain of the Sgs1 DNA helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Bloom's syndrome helicase can promote the regression of a model replication fork.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Saccharomyces cerevisiae WRN homolog Sgs1p participates in telomere maintenance in cells lacking telomerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

p53 Modulates the exonuclease activity of Werner syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Displacement of DNA-PKcs from DNA ends by the Werner syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Ku heterodimer binds to both ends of the Werner protein and functional interaction occurs at the Werner N-terminus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

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/10.1007%2FS11033-011-1243-Y

Cloning of a cDNA encoding a novel importin-alpha homologue, Qip1: discrimination of Qip1 and Rch1 from hSrp1 by their ability to interact with DNA helicase Q1/RecQL

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Helicases: amino acid sequence comparisons and structure-function relationships

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Human homologues of yeast helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Multiple Mechanisms Control Chromosome Integrity after Replication Fork Uncoupling and Restart at Irreparable UV Lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

Branch Migrating Sister Chromatid Junctions Form at Replication Origins through Rad51/Rad52-Independent Mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1243-Y

The Bloom's syndrome helicase unwinds G4 DNA

21 January 2018

1 reference

12 December 2020

Role for BLM in replication-fork restart and suppression of origin firing after replicative stress

1 reference

12 December 2020

1 reference

12 December 2020

Ku complex interacts with and stimulates the Werner protein

1 reference

12 December 2020

Bloom's syndrome gene suppresses premature ageing caused by Sgs1 deficiency in yeast

1 reference

12 December 2020

Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)n trinucleotide repeat sequence

1 reference

12 December 2020

Bipartite structure of the SGS1 DNA helicase in Saccharomyces cerevisiae

1 reference

12 December 2020

Three HRDC domains differentially modulate Deinococcus radiodurans RecQ DNA helicase biochemical activity

1 reference

12 December 2020

Werner syndrome protein is regulated and phosphorylated by DNA-dependent protein kinase

1 reference

12 December 2020

AAA+: A class of chaperone-like ATPases associated with the assembly, operation, and disassembly of protein complexes

1 reference

12 December 2020

The C-terminal domain of the Bloom syndrome DNA helicase is essential for genomic stability

1 reference

12 December 2020

Association of the Bloom syndrome protein with topoisomerase IIIalpha in somatic and meiotic cells

1 reference

12 December 2020

The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability

1 reference

12 December 2020

BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures

1 reference

12 December 2020

Functional link between BLM defective in Bloom's syndrome and the ataxia-telangiectasia-mutated protein, ATM

1 reference

12 December 2020

Crystal structure of the Holliday junction migration motor protein RuvB from Thermus thermophilus HB8

1 reference

12 December 2020

The galvanization of biology: a growing appreciation for the roles of zinc

1 reference

12 December 2020

Elevation of sister chromatid exchange in Saccharomyces cerevisiae sgs1 disruptants and the relevance of the disruptants as a system to evaluate mutations in Bloom's syndrome gene

1 reference

12 December 2020

Biochemical characterization of the WRN-FEN-1 functional interaction

1 reference

12 December 2020

10.1007/S11033-011-1243-Y

Identifiers

DOI

1 reference

release_pkfs53phczgmleflpl5oyfqisa

25 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/pkfs53phczgmleflpl5oyfqisa

24 November 2022

mapped directly with Wikidata item

PubMed ID

21947842

1 reference

PubMed ID

21947842