(Q38358620)

2 September 2017

title

Functional crosstalk between hOgg1 and the helicase domain of Cockayne syndrome group B protein (English)

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2 September 2017

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5

Vilhelm A Bohr

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2 September 2017

Jingsheng Tuo

1

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2 September 2017

Catheryne Chen

series ordinal

2

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2 September 2017

Xianmin Zeng

series ordinal

3

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2 September 2017

Mette Christiansen

series ordinal

4

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2 September 2017

publication date

1 November 2002

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2 September 2017

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2 September 2017

volume

1

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2 September 2017

issue

11

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2 September 2017

page(s)

913-927

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

2 September 2017

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7 January 2021

Cockayne syndrome: Review of 140 cases

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7 January 2021

The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH

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7 January 2021

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

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7 January 2021

Genomic heterogeneity of nucleotide excision repair

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7 January 2021

Recognition of DNA adducts by human nucleotide excision repair. Evidence for a thermodynamic probing mechanism

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7 January 2021

Preferential DNA repair of an active gene in human cells

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7 January 2021

Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells

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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.

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7 January 2021

Progeroid syndromes: probing the molecular basis of aging?

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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

DNA repair. Engagement with transcription

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7 January 2021

The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex

1 reference

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7 January 2021

Cockayne syndrome group B protein enhances elongation by RNA polymerase II

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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7 January 2021

Molecular cloning of the human DNA excision repair gene ERCC-6

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7 January 2021

Evolution of the SNF2 family of proteins: subfamilies with distinct sequences and functions

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Efficient immortalization and morphological transformation of human fibroblasts by transfection with SV40 DNA linked to a dominant marker

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7 January 2021

Phenotypic consequences of mutations in the conserved motifs of the putative helicase domain of the human Cockayne syndrome group B gene.

1 reference

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7 January 2021

Biochemical and biological characterization of wild-type and ATPase-deficient Cockayne syndrome B repair protein.

1 reference

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7 January 2021

Preferential recognition of I·T base-pairs in the initiation of excision-repair by hypoxanthine-DNA glycosylase

1 reference

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7 January 2021

In vitro transcription: whole-cell extract

1 reference

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7 January 2021

Opposite base-dependent reactions of a human base excision repair enzyme on DNA containing 7,8-dihydro-8-oxoguanine and abasic sites

1 reference

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7 January 2021

Location of calcium transporters at presynaptic terminals

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7 January 2021

A repair system for 8-oxo-7,8-dihydrodeoxyguanine

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7 January 2021

The presence of two distinct 8-oxoguanine repair enzymes in human cells: their potential complementary roles in preventing mutation

1 reference

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7 January 2021

Cloning and characterization of hOGG1, a human homolog of the OGG1 gene of Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

Cloning and characterization of a mammalian 8-oxoguanine DNA glycosylase

1 reference

https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

Human MMH (OGG1) type 1a protein is a major enzyme for repair of 8-hydroxyguanine lesions in human cells

1 reference

https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

Relationships between DNA repair and transcription

1 reference

https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

Transcriptional healing

1 reference

https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

The nucleosome remodeling complex, Snf/Swi, is required for the maintenance of transcription in vivo and is partially redundant with the histone acetyltransferase, Gcn5.

1 reference

https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

The Swi/Snf family nucleosome-remodeling complexes and transcriptional control

1 reference

https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor.

1 reference

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7 January 2021

8-hydroxyguanine (7,8-dihydro-8-oxoguanine) DNA glycosylase and AP lyase activities of hOGG1 protein and their substrate specificity

1 reference

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7 January 2021

Functional sites of interaction between release factor RF1 and the ribosome

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7 January 2021

The human OGG1 gene: structure, functions, and its implication in the process of carcinogenesis

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7 January 2021

Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA

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https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

Helicase motifs: the engine that powers DNA unwinding

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https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

Helicase motifs V and VI of the Escherichia coli UvrB protein of the UvrABC endonuclease are essential for the formation of the preincision complex.

1 reference

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7 January 2021

Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene

1 reference

https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

Human 8-oxoguanine DNA glycosylase 1 mRNA expression as an oxidative stress exposure biomarker of cooking oil fumes

1 reference

https://api.crossref.org/works/10.1016%2FS1568-7864%2802%2900116-7

7 January 2021

10.1016/S1568-7864(02)00116-7

Identifiers

DOI

1 reference

2 September 2017

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