Skip to search formSkip to main contentSkip to account menu

Cockayne Syndrome, Type II

Known as: Cockayne Syndrome, Type B, Cockayne Syndrome, Group B, Group B Cockayne Syndrome 
Caused by mutations of gene ERCC6.
National Institutes of Health

Related topics

Related topics

40 relations
AnhidrosisAtaxiaAtrophicAutosomal recessive inheritance

Broader (1)

Cockayne Syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
Treating Compulsive Sexual Behavior
Purpose of ReviewHere we review potential therapeutic approaches for treating compulsive sexual behaviors (CSB; also known as… 
Highly Cited
2014
Highly Cited
2014
Mitochondrial reactive oxygen species are scavenged by Cockayne syndrome B protein in human fibroblasts without nuclear DNA damage
Significance Mitochondria are often considered a source of reactive oxygen species (ROS) that cause damage to cellular components… 
Highly Cited
2012
Highly Cited
2012
Nucleotide excision repair–initiating proteins bind to oxidative DNA lesions in vivo
In vivo imaging reveals that CSB and XPC promote the repair of oxidative DNA lesions independent of the canonical nucleotide… 
Highly Cited
2009
Highly Cited
2009
The C-terminal Repeat Domain of Spt5 Plays an Important Role in Suppression of Rad26-independent Transcription Coupled Repair*
In eukaryotic cells, transcription coupled nucleotide excision repair (TCR) is believed to be initiated by RNA polymerase II (Pol… 
Highly Cited
2007
Highly Cited
2007
Activation of RNA polymerase I transcription by cockayne syndrome group B protein and histone methyltransferase G9a.
Highly Cited
2005
Highly Cited
2005
Relationship between UV-induced mutant p53 patches and skin tumours, analysed by mutation spectra and by induction kinetics in various DNA-repair-deficient mice.
Clusters of p53 immunopositive epidermal keratinocytes (so-called p53 patches, clones or foci) are found in sun or ultraviolet… 
Highly Cited
2002
Highly Cited
2002
Mitochondrial repair of 8-oxoguanine is deficient in Cockayne syndrome group B
Reactive oxygen species, which are prevalent in mitochondria, cause oxidative DNA damage including the mutagenic DNA lesion 7,8… 
Highly Cited
2001
Highly Cited
2001
Loss of heterozygosity of nucleotide excision repair factors in sporadic ovarian, colon and lung carcinomas: implication for their roles of carcinogenesis in human solid tumors.
Highly Cited
2000
Highly Cited
2000
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.
Cerebro-oculo-facio-skeletal (COFS) syndrome is a rapidly progressive neurological disorder leading to brain atrophy with… 
Highly Cited
1996
Highly Cited
1996
Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein.
The human basal transcription factor TFIIH plays a central role in two distinct processes. TFIIH is an obligatory component of… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)