(Q34667168)

3 August 2017

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title

Human premature aging syndromes and genomic instability (English)

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3 August 2017

Vilhelm A Bohr

1

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3 August 2017

publication date

1 April 2002

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Mechanisms of Ageing and Development

3 August 2017

published in

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3 August 2017

volume

123

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3 August 2017

issue

8

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3 August 2017

page(s)

987-993

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Reduced RNA polymerase II transcription in intact and permeabilized Cockayne syndrome group B cells

3 August 2017

cites work

1 reference

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7 January 2021

The Werner syndrome protein is involved in RNA polymerase II transcription

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7 January 2021

Genomic heterogeneity of nucleotide excision repair

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7 January 2021

DNA repair and mutagenesis in Werner syndrome.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

p53 Modulates the exonuclease activity of Werner syndrome protein

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7 January 2021

Unwinding of a DNA triple helix by the Werner and Bloom syndrome helicases

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7 January 2021

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

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7 January 2021

Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G

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7 January 2021

Repair pathways for processing of 8-oxoguanine in DNA by mammalian cell extracts

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7 January 2021

Repair of 8-oxoguanine in DNA is deficient in Cockayne syndrome group B cells

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7 January 2021

Cockayne syndrome--a primary defect in DNA repair, transcription, both or neither?

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7 January 2021

Mutator phenotype of Werner syndrome is characterized by extensive deletions

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7 January 2021

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7 January 2021

The Werner syndrome protein is a DNA helicase

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7 January 2021

RecQ DNA helicase is a suppressor of illegitimate recombination in Escherichia coli

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7 January 2021

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

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7 January 2021

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

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7 January 2021

Covalent modification of the Werner's syndrome gene product with the ubiquitin-related protein, SUMO-1

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7 January 2021

DNA damage and repair in telomeres: relation to aging

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7 January 2021

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

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7 January 2021

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

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7 January 2021

An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants

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7 January 2021

The human CSB (ERCC6) gene corrects the transcription-coupled repair defect in the CHO cell mutant UV61

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7 January 2021

SWI2/SNF2 and related proteins: ATP-driven motors that disrupt protein-DNA interactions?

1 reference

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7 January 2021

Impaired S-phase transit of Werner syndrome cells expressed in lymphoblastoid cell lines

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7 January 2021

Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cells

1 reference

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7 January 2021

Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II

1 reference

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7 January 2021

RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair

1 reference

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7 January 2021

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

1 reference

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7 January 2021

p53-mediated apoptosis is attenuated in Werner syndrome cells

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7 January 2021

Genetic instability as the primary cause of human aging

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7 January 2021

Deletional mutations are the basic cause of aging: historical perspectives.

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2802%2900039-8

7 January 2021

Werner protein recruits DNA polymerase delta to the nucleolus

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2802%2900039-8

7 January 2021

Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2802%2900039-8

7 January 2021

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2802%2900039-8

7 January 2021

The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2802%2900039-8

7 January 2021

The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2802%2900039-8

7 January 2021

Telomerase prevents the accelerated cell ageing of Werner syndrome fibroblasts

1 reference

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7 January 2021

10.1016/S0047-6374(02)00039-8

Identifiers

DOI

1 reference

3 August 2017

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