Published in Mech Ageing Dev on April 03, 2013
DNA repair diseases: What do they tell us about cancer and aging? Genet Mol Biol (2014) 0.98
The sequence-specific transcription factor c-Jun targets Cockayne syndrome protein B to regulate transcription and chromatin structure. PLoS Genet (2014) 0.96
Dysregulation of gene expression as a cause of Cockayne syndrome neurological disease. Proc Natl Acad Sci U S A (2014) 0.85
The cockayne syndrome B protein is essential for neuronal differentiation and neuritogenesis. Cell Death Dis (2014) 0.83
ERCC6L2 mutations link a distinct bone-marrow-failure syndrome to DNA repair and mitochondrial function. Am J Hum Genet (2014) 0.82
Cockayne syndrome-derived neurons display reduced synapse density and altered neural network synchrony. Hum Mol Genet (2016) 0.81
Cockayne syndrome group B protein regulates DNA double-strand break repair and checkpoint activation. EMBO J (2015) 0.81
Identification of two missense mutations of ERCC6 in three Chinese sisters with Cockayne syndrome by whole exome sequencing. PLoS One (2014) 0.79
Reversal of mitochondrial defects with CSB-dependent serine protease inhibitors in patient cells of the progeroid Cockayne syndrome. Proc Natl Acad Sci U S A (2015) 0.79
The Cellular Response to Oxidatively Induced DNA Damage and Polymorphism of Some DNA Repair Genes Associated with Clinicopathological Features of Bladder Cancer. Oxid Med Cell Longev (2015) 0.77
The C-terminal Region and SUMOylation of Cockayne Syndrome Group B Protein Play Critical Roles in Transcription-coupled Nucleotide Excision Repair. J Biol Chem (2015) 0.77
Regulation of active genome integrity and expression by Rad26p. Nucleus (2014) 0.75
Mutations in Cockayne Syndrome-Associated Genes (Csa and Csb) Predispose to Cisplatin-Induced Hearing Loss in Mice. J Neurosci (2016) 0.75
Cockayne syndrome B protein regulates recruitment of the Elongin A ubiquitin ligase to sites of DNA damage. J Biol Chem (2017) 0.75
Pharmacological Bypass of Cockayne Syndrome B Function in Neuronal Differentiation. Cell Rep (2016) 0.75
TFIIH transcription factor, a target for the Rift Valley hemorrhagic fever virus. Cell (2004) 3.39
The comings and goings of nucleotide excision repair factors on damaged DNA. EMBO J (2003) 2.89
A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A. Nat Genet (2004) 2.54
XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients. Mol Cell (2007) 2.41
Basal transcription defect discriminates between xeroderma pigmentosum and trichothiodystrophy in XPD patients. Mol Cell (2003) 2.12
Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair. Mol Cell (2007) 1.85
A ubiquitin-binding domain in Cockayne syndrome B required for transcription-coupled nucleotide excision repair. Mol Cell (2010) 1.79
TFIIH contains a PH domain involved in DNA nucleotide excision repair. Nat Struct Mol Biol (2004) 1.78
MED23 mutation links intellectual disability to dysregulation of immediate early gene expression. Science (2011) 1.74
TFIIH: when transcription met DNA repair. Nat Rev Mol Cell Biol (2012) 1.63
When transcription and repair meet: a complex system. Trends Genet (2006) 1.62
Phosphorylation of human estrogen receptor alpha at serine 118 by two distinct signal transduction pathways revealed by phosphorylation-specific antisera. Oncogene (2002) 1.62
New functions of XPC in the protection of human skin cells from oxidative damage. EMBO J (2006) 1.60
Ordered conformational changes in damaged DNA induced by nucleotide excision repair factors. J Biol Chem (2004) 1.59
Rescue of progeria in trichothiodystrophy by homozygous lethal Xpd alleles. PLoS Biol (2006) 1.54
Reduced level of the repair/transcription factor TFIIH in trichothiodystrophy. Hum Mol Genet (2002) 1.46
Initiation of DNA repair mediated by a stalled RNA polymerase IIO. EMBO J (2006) 1.44
DNA damage stabilizes interaction of CSB with the transcription elongation machinery. J Cell Biol (2004) 1.42
The phosphorylation of the androgen receptor by TFIIH directs the ubiquitin/proteasome process. EMBO J (2010) 1.39
Cockayne syndrome B protein regulates the transcriptional program after UV irradiation. EMBO J (2006) 1.34
Dysregulation of the peroxisome proliferator-activated receptor target genes by XPD mutations. Mol Cell Biol (2005) 1.32
The human DNA repair factor XPC-HR23B distinguishes stereoisomeric benzo[a]pyrenyl-DNA lesions. EMBO J (2007) 1.28
XPG and XPF endonucleases trigger chromatin looping and DNA demethylation for accurate expression of activated genes. Mol Cell (2012) 1.24
p8/TTD-A as a repair-specific TFIIH subunit. Mol Cell (2006) 1.16
Selective regulation of vitamin D receptor-responsive genes by TFIIH. Mol Cell (2004) 1.16
Molecular insights into the recruitment of TFIIH to sites of DNA damage. EMBO J (2009) 1.16
CSB protein is (a direct target of HIF-1 and) a critical mediator of the hypoxic response. EMBO J (2008) 1.13
Deletion of 5' sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome. Eur J Hum Genet (2008) 1.12
Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH. Nat Neurosci (2007) 1.08
Promoter of FGF8 reveals a unique regulation by unliganded RARalpha. J Mol Biol (2002) 1.07
Fate of RNA polymerase II stalled at a cisplatin lesion. J Biol Chem (2003) 1.06
Transcription activities at 8-oxoG lesions in DNA. DNA Repair (Amst) (2004) 1.06
TFIIH enzymatic activities in transcription and nucleotide excision repair. Methods Enzymol (2006) 1.00
Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients. J Exp Med (2009) 0.99
Tools to study DNA repair: what's in the box? Trends Genet (2008) 0.99
DNA repair and transcriptional deficiencies caused by mutations in the Drosophila p52 subunit of TFIIH generate developmental defects and chromosome fragility. Mol Cell Biol (2007) 0.98
Structural basis for group A trichothiodystrophy. Nat Struct Mol Biol (2008) 0.98
Phosphorylation of XPB helicase regulates TFIIH nucleotide excision repair activity. EMBO J (2004) 0.96
True lies: the double life of the nucleotide excision repair factors in transcription and DNA repair. J Nucleic Acids (2010) 0.94
ARCH domain of XPD, an anchoring platform for CAK that conditions TFIIH DNA repair and transcription activities. Proc Natl Acad Sci U S A (2013) 0.91
p52 Mediates XPB function within the transcription/repair factor TFIIH. J Biol Chem (2002) 0.91
XPF-dependent DNA breaks and RNA polymerase II arrest induced by antitumor DNA interstrand crosslinking-mimetic alkaloids. Chem Biol (2011) 0.91
Histone methyltransferase DOT1L drives recovery of gene expression after a genotoxic attack. PLoS Genet (2013) 0.88
Poly (ADP-ribose) glycohydrolase regulates retinoic acid receptor-mediated gene expression. Mol Cell (2012) 0.87
Myo-InositolTrisPyroPhosphate treatment leads to HIF-1α suppression and eradication of early hepatoma tumors in rats. Chembiochem (2011) 0.86
Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells. Proc Natl Acad Sci U S A (2012) 0.86
Interacting partners of the Tfb2 subunit from yeast TFIIH. DNA Repair (Amst) (2009) 0.81
Solution structure and self-association properties of the p8 TFIIH subunit responsible for trichothiodystrophy. J Mol Biol (2007) 0.80
Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosum. Eur J Hum Genet (2012) 0.80
Regulatory interplay of Cockayne syndrome B ATPase and stress-response gene ATF3 following genotoxic stress. Proc Natl Acad Sci U S A (2013) 0.78
Design and in vivo evaluation of a robotized needle insertion system for small animals. IEEE Trans Biomed Eng (2013) 0.76
Mechanics of the IL2RA gene activation revealed by modeling and atomic force microscopy. PLoS One (2011) 0.75
[Early gene expression dysregulation and intellectual disability]. Med Sci (Paris) (2012) 0.75
[Neurological disorders and trichothiodystrophy: when the transcription process is impaired]. Med Sci (Paris) (2007) 0.75