The Bloom's syndrome helicase interacts directly with the human DNA mismatch repair protein hMSH6. (Q40634607)

22 September 2017

title

The Bloom's syndrome helicase interacts directly with the human DNA mismatch repair protein hMSH6. (English)

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22 September 2017

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Graziella Pedrazzi

1

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22 September 2017

Csanád Z Bachrati

2

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22 September 2017

Nives Selak

3

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22 September 2017

Ingrid Studer

4

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22 September 2017

Maja Petkovic

5

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22 September 2017

Ian D Hickson

6

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22 September 2017

Josef Jiricny

7

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22 September 2017

Igor Stagljar

8

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22 September 2017

publication date

1 August 2003

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22 September 2017

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22 September 2017

volume

384

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22 September 2017

issue

8

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22 September 2017

page(s)

1155-1164

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Functional interactions and signaling properties of mammalian DNA mismatch repair proteins

22 September 2017

cites work

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https://api.crossref.org/works/10.1515%2FBC.2003.128

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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/10.1515%2FBC.2003.128

Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

Roles for mismatch repair factors in regulating genetic recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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/10.1515%2FBC.2003.128

DNA mismatch repair and genetic instability

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSalpha

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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/10.1515%2FBC.2003.128

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

hMSH3 and hMSH6 interact with PCNA and colocalize with it to replication foci

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

The Bloom's syndrome protein (BLM) interacts with MLH1 but is not required for DNA mismatch repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

Cancer predisposition caused by elevated mitotic recombination in Bloom mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

'Saccharomyces cerevisiae MSH2/6 complex interacts with Holliday junctions and facilitates their cleavage by phage resolution enzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

Mismatch repair in replication fidelity, genetic recombination, and cancer biology

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

The recQ gene of Escherichia coli K12: molecular cloning and isolation of insertion mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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/10.1515%2FBC.2003.128

Identification of hMutLbeta, a heterodimer of hMLH1 and hPMS1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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/10.1515%2FBC.2003.128

BLM helicase-dependent transport of p53 to sites of stalled DNA replication forks modulates homologous recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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/10.1515%2FBC.2003.128

rqh1+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

Functional interaction of p53 and BLM DNA helicase in apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

Sgs1: a eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

The Bloom's syndrome gene product interacts with topoisomerase III

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

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/10.1515%2FBC.2003.128

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/10.1515%2FBC.2003.128

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

Nuclear structure in normal and Bloom syndrome cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

Positional cloning of the Werner's syndrome gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2003.128

21 January 2018

Identifiers

DOI

10.1515/BC.2003.128

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22 September 2017

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