Detalhe da pesquisa
1.
The Long Road to Understanding RNAPII Transcription Initiation and Related Syndromes.
Annu Rev Biochem
; 90: 193-219, 2021 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34153211
2.
Nucleotide Excision Repair and Transcriptional Regulation: TFIIH and Beyond.
Annu Rev Biochem
; 85: 265-90, 2016 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27294439
3.
Transcription without XPB Establishes a Unified Helicase-Independent Mechanism of Promoter Opening in Eukaryotic Gene Expression.
Mol Cell
; 65(3): 504-514.e4, 2017 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28157507
4.
Cockayne's Syndrome A and B Proteins Regulate Transcription Arrest after Genotoxic Stress by Promoting ATF3 Degradation.
Mol Cell
; 68(6): 1054-1066.e6, 2017 12 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29225035
5.
TFIIH: when transcription met DNA repair.
Nat Rev Mol Cell Biol
; 13(6): 343-54, 2012 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22572993
6.
CDK7 and MITF repress a transcription program involved in survival and drug tolerance in melanoma.
EMBO Rep
; 22(9): e51683, 2021 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34296805
7.
Revisiting the Function of CDK7 in Transcription by Virtue of a Recently Described TFIIH Kinase Inhibitor.
Mol Cell
; 59(4): 513-4, 2015 Aug 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-26295956
8.
The Cockayne syndrome group A and B proteins are part of a ubiquitin-proteasome degradation complex regulating cell division.
Proc Natl Acad Sci U S A
; 117(48): 30498-30508, 2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33199595
9.
XPG and XPF endonucleases trigger chromatin looping and DNA demethylation for accurate expression of activated genes.
Mol Cell
; 47(4): 622-32, 2012 Aug 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-22771116
10.
Poly (ADP-ribose) glycohydrolase regulates retinoic acid receptor-mediated gene expression.
Mol Cell
; 48(5): 785-98, 2012 Dec 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23102699
11.
MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression.
Hum Mol Genet
; 26(11): 2062-2075, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28369444
12.
Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect.
Genet Med
; 21(11): 2663, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31267042
13.
Variants in MED12L, encoding a subunit of the mediator kinase module, are responsible for intellectual disability associated with transcriptional defect.
Genet Med
; 21(12): 2713-2722, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31155615
14.
TFIIH subunit alterations causing xeroderma pigmentosum and trichothiodystrophy specifically disturb several steps during transcription.
Am J Hum Genet
; 96(2): 194-207, 2015 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25620205
15.
NER factors are recruited to active promoters and facilitate chromatin modification for transcription in the absence of exogenous genotoxic attack.
Mol Cell
; 38(1): 54-66, 2010 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-20385089
16.
A ubiquitin-binding domain in Cockayne syndrome B required for transcription-coupled nucleotide excision repair.
Mol Cell
; 38(5): 637-48, 2010 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-20541997
17.
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin.
Proc Natl Acad Sci U S A
; 112(5): 1499-504, 2015 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25605938
18.
Influenza virus NS1 protein binds cellular DNA to block transcription of antiviral genes.
Biochim Biophys Acta
; 1859(11): 1440-1448, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27664935
19.
In TFIIH, XPD helicase is exclusively devoted to DNA repair.
PLoS Biol
; 12(9): e1001954, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25268380
20.
Dynamic partnership between TFIIH, PGC-1α and SIRT1 is impaired in trichothiodystrophy.
PLoS Genet
; 10(10): e1004732, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25340339