(Q34554610)

English

Blinded by the UV light: how the focus on transcription-coupled NER has distracted from understanding the mechanisms of Cockayne syndrome neurologic disease

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scholarly article

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Europe PubMed Central

PubMed publication ID

3 August 2017

Blinded by the UV light: how the focus on transcription-coupled NER has distracted from understanding the mechanisms of Cockayne syndrome neurologic disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Cockayne syndrome

1 reference

based on heuristic

inferred from title

author name string

P J Brooks

1

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

publication date

16 May 2013

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

656-671

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells

1 reference

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7 July 2018

Tethering of the conserved piggyBac transposase fusion protein CSB-PGBD3 to chromosomal AP-1 proteins regulates expression of nearby genes in humans.

1 reference

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7 July 2018

Human Cockayne syndrome B protein reciprocally communicates with mitochondrial proteins and promotes transcriptional elongation

1 reference

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7 July 2018

Endogenous formation and repair of oxidatively induced G[8-5 m]T intrastrand cross-link lesion

1 reference

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TFIIH: when transcription met DNA repair.

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7 July 2018

The chromatin remodeling complex NuRD establishes the poised state of rRNA genes characterized by bivalent histone modifications and altered nucleosome positions

1 reference

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7 July 2018

The conserved Cockayne syndrome B-piggyBac fusion protein (CSB-PGBD3) affects DNA repair and induces both interferon-like and innate antiviral responses in CSB-null cells.

1 reference

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Cockayne syndrome group B protein prevents the accumulation of damaged mitochondria by promoting mitochondrial autophagy.

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7 July 2018

Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair

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UV-sensitive syndrome protein UVSSA recruits USP7 to regulate transcription-coupled repair

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Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair

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High-throughput genotoxicity assay identifies antioxidants as inducers of DNA damage response and cell death.

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An altered redox balance mediates the hypersensitivity of Cockayne syndrome primary fibroblasts to oxidative stress.

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Dysmyelination not demyelination causes neurological symptoms in preweaned mice in a murine model of Cockayne syndrome.

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Interaction between the Cockayne syndrome B and p53 proteins: implications for aging

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Pathways for repairing and tolerating the spectrum of oxidative DNA lesions

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Emerging roles of the neuronal nucleolus

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Shining a light on xeroderma pigmentosum

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Age-related neuronal degeneration: complementary roles of nucleotide excision repair and transcription-coupled repair in preventing neuropathology

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Reciprocally regulated chromatin association of Cockayne syndrome protein B and p53 protein

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Brain vascular changes in Cockayne syndrome.

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7 July 2018

The xeroderma pigmentosum pathway: decision tree analysis of DNA quality

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DNA damage response and transcription

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DNA polymerases and repair synthesis in NER in human cells

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A history of TFIIH: two decades of molecular biology on a pivotal transcription/repair factor.

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XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase.

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Quantification of oxidative DNA lesions in tissues of Long-Evans Cinnamon rats by capillary high-performance liquid chromatography-tandem mass spectrometry coupled with stable isotope-dilution method

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Proliferative neural stem cells have high endogenous ROS levels that regulate self-renewal and neurogenesis in a PI3K/Akt-dependant manner

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The phosphorylation of the androgen receptor by TFIIH directs the ubiquitin/proteasome process

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The nucleolus under stress

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A ubiquitin-binding domain in Cockayne syndrome B required for transcription-coupled nucleotide excision repair

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Abasic sites in the transcribed strand of yeast DNA are removed by transcription-coupled nucleotide excision repair

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Cockayne syndrome group B protein promotes mitochondrial DNA stability by supporting the DNA repair association with the mitochondrial membrane

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Mitochondria as a target in treatment

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UV-induced association of the CSB remodeling protein with chromatin requires ATP-dependent relief of N-terminal autorepression.

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Proteins of nucleotide and base excision repair pathways interact in mitochondria to protect from loss of subcutaneous fat, a hallmark of aging

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Differentiation driven changes in the dynamic organization of Basal transcription initiation

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DNA Damage, Aging, and Cancer

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Neuropathology of Cockayne syndrome: Evidence for impaired development, premature aging, and neurodegeneration

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A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage

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7 July 2018

Truncated Cockayne syndrome B protein represses elongation by RNA polymerase I.

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7 July 2018

An abundant evolutionarily conserved CSB-PiggyBac fusion protein expressed in Cockayne syndrome

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Profiling of UV-induced ATM/ATR signaling pathways.

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Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH

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Activation of RNA polymerase I transcription by cockayne syndrome group B protein and histone methyltransferase G9a

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ATM, the Mre11/Rad50/Nbs1 complex, and topoisomerase I are concentrated in the nucleus of Purkinje neurons in the juvenile human brain

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The current evidence for defective repair of oxidatively damaged DNA in Cockayne syndrome

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ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage

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XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients

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New insights into the combined Cockayne/xeroderma pigmentosum complex: human XPG protein can function in transcription factor stability

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Increased apoptosis, p53 up-regulation, and cerebellar neuronal degeneration in repair-deficient Cockayne syndrome mice

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7 July 2018

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7 July 2018

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7 July 2018

Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo

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7 July 2018

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7 July 2018

Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assays

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7 July 2018

Ubiquitin ligase activity of TFIIH and the transcriptional response to DNA damage

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7 July 2018

Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome

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DNA damage stabilizes interaction of CSB with the transcription elongation machinery

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At the crossroads of growth control; making ribosomal RNA.

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Regulation of ultraviolet light-induced gene expression by gene size

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

The comings and goings of nucleotide excision repair factors on damaged DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Aging: a theory based on free radical and radiation chemistry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Malondialdehyde, a product of lipid peroxidation, is mutagenic in human cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

The ubiquitin ligase activity in the DDB2 and CSA complexes is differentially regulated by the COP9 signalosome in response to DNA damage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

The transcriptional response after oxidative stress is defective in Cockayne syndrome group B cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Neurodegeneration: what is it and where are we?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

CSB is a component of RNA pol I transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Requirement of yeast RAD2, a homolog of human XPG gene, for efficient RNA polymerase II transcription. implications for Cockayne syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

TFIIH plays an essential role in RNA polymerase I transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

WRN helicase accelerates the transcription of ribosomal RNA as a component of an RNA polymerase I-associated complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Xeroderma pigmentosum/cockayne syndrome complex: first neuropathological study and review of eight other cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Inherited neurodegenerative diseases: the one-hit model of neurodegeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Trichothiodystrophy, a transcription syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Defective interplay of activators and repressors with TFIH in xeroderma pigmentosum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

UV-induced inhibition of transcription involves repression of transcription initiation and phosphorylation of RNA polymerase II.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Terminally differentiated human neurons repair transcribed genes but display attenuated global DNA repair and modulation of repair gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Oligodendrocyte development and thyroid hormone.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

The Werner syndrome protein is involved in RNA polymerase II transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Neurodegeneration in hereditary nucleotide repair disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

In vitro repair of oxidative DNA damage by human nucleotide excision repair system: possible explanation for neurodegeneration in xeroderma pigmentosum patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Cockayne syndrome: defective repair of transcription?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Substrate specificity of the cdk-activating kinase (CAK) is altered upon association with TFIIH

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

TFIIH: a key component in multiple DNA transactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Reconstitution of human DNA repair excision nuclease in a highly defined system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Nucleotide excision repair syndromes: molecular basis and clinical symptoms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Defective Repair Replication of DNA in Xeroderma Pigmentosum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Complementation of the xeroderma pigmentosum DNA repair defect in cell-free extracts.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Neurological disease in xeroderma pigmentosum. Documentation of a late onset type of the juvenile onset form

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Rapid postanoxic calcification of the basal ganglia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Lethal cytomegalovirus infection in preterm infants: Clinical, radiological, and neuropathological findings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Cockayne syndrome: Review of 140 cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

7 July 2018

XPD mutations in trichothiodystrophy hamper collagen VI expression and reveal a role of TFIIH in transcription derepression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

Neuroimaging in Cockayne syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

Activation of an endogenous suicide response after perturbation of rRNA synthesis leads to neurodegeneration in mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

Response of motor complications in Cockayne syndrome to carbidopa-levodopa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

Transcription arrest at an abasic site in the transcribed strand of template DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

Transcriptional inhibition by an oxidized abasic site in DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

Host cell reactivation of plasmids containing oxidative DNA lesions is defective in Cockayne syndrome but normal in UV-sensitive syndrome fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

UVB radiation-induced cancer predisposition in Cockayne syndrome group A (Csa) mutant mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

Rapid switching of TFIIH between RNA polymerase I and II transcription and DNA repair in vivo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

Transcription-coupled DNA repair is genomic context-dependent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

Oxygen free radical damage to DNA. Translesion synthesis by human DNA polymerase eta and resistance to exonuclease action at cyclopurine deoxynucleoside residues.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

A one-hit model of cell death in inherited neuronal degenerations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

Intracerebral calcification in systemic sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

The yeast RAD2, but not RAD1, gene is involved in the transcription-coupled repair of thymine glycols.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240003

27 October 2018

A comprehensive description of the severity groups in Cockayne syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23683874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multistep damage recognition, pathway coordination and connections to transcription, damage signaling, chromatin structure, cancer and aging: current perspectives on the nucleotide excision repair pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/23683874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nucleotide excision repair of DNA: The very early history

1 reference

https://pubmed.ncbi.nlm.nih.gov/23683874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stimulation of RAR alpha activation function AF-1 through binding to the general transcription factor TFIIH and phosphorylation by CDK7

1 reference

https://pubmed.ncbi.nlm.nih.gov/23683874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retraction notice to "The yeast RAD2, but not RAD1, gene is involved in the transcription-coupled repair of thymine glycols" [Mutat. Res. 337 (1995) 169-178]

1 reference

https://pubmed.ncbi.nlm.nih.gov/23683874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The oxidative DNA lesion 8,5'-(S)-cyclo-2'-deoxyadenosine is repaired by the nucleotide excision repair pathway and blocks gene expression in mammalian cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/23683874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adult-onset neurological degeneration in a patient with Cockayne syndrome and a null mutation in the CSB gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/23683874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Measurement of (5'R)- and (5'S)-8,5'-cyclo-2'-deoxyadenosines in DNA in vivo by liquid chromatography/isotope-dilution tandem mass spectrometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/23683874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse CSB protein is important for gene expression in the presence of a single-strand break in the non-transcribed DNA strand

1 reference

https://pubmed.ncbi.nlm.nih.gov/23683874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum

1 reference

https://pubmed.ncbi.nlm.nih.gov/23683874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.DNAREP.2013.04.018

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

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