Detalhe da pesquisa
1.
LBR and lamin A/C sequentially tether peripheral heterochromatin and inversely regulate differentiation.
Cell
; 152(3): 584-98, 2013 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-23374351
2.
Transcription factor IID parks and drives preinitiation complexes at sharp or broad promoters.
Trends Biochem Sci
; 48(10): 839-848, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37574371
3.
De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features.
Brain
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38753057
4.
Transcription of Nearly All Yeast RNA Polymerase II-Transcribed Genes Is Dependent on Transcription Factor TFIID.
Mol Cell
; 68(1): 118-129.e5, 2017 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28918900
5.
SAGA Is a General Cofactor for RNA Polymerase II Transcription.
Mol Cell
; 68(1): 130-143.e5, 2017 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28918903
6.
SUPT3H-less SAGA coactivator can assemble and function without significantly perturbing RNA polymerase II transcription in mammalian cells.
Nucleic Acids Res
; 50(14): 7972-7990, 2022 08 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35871303
7.
The SAGA coactivator complex acts on the whole transcribed genome and is required for RNA polymerase II transcription.
Genes Dev
; 28(18): 1999-2012, 2014 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25228644
8.
SAGA-Dependent Histone H2Bub1 Deubiquitination Is Essential for Cellular Ubiquitin Balance during Embryonic Development.
Int J Mol Sci
; 23(13)2022 Jul 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35806465
9.
SAGA Is a General Cofactor for RNA Polymerase II Transcription.
Mol Cell
; 70(6): 1163-1164, 2018 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29932906
10.
Homozygous TAF8 mutation in a patient with intellectual disability results in undetectable TAF8 protein, but preserved RNA polymerase II transcription.
Hum Mol Genet
; 27(12): 2171-2186, 2018 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29648665
11.
Morphological features in juvenile Huntington disease associated with cerebellar atrophy - magnetic resonance imaging morphometric analysis.
Pediatr Radiol
; 48(10): 1463-1471, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29926145
12.
Gcn5 and SAGA regulate shelterin protein turnover and telomere maintenance.
Mol Cell
; 35(3): 352-64, 2009 Aug 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-19683498
13.
H2B mono-ubiquitylation facilitates fork stalling and recovery during replication stress by coordinating Rad53 activation and chromatin assembly.
PLoS Genet
; 10(10): e1004667, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25275495
14.
DNA binding by Sgf11 protein affects histone H2B deubiquitination by Spt-Ada-Gcn5-acetyltransferase (SAGA).
J Biol Chem
; 289(13): 8989-99, 2014 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-24509845
15.
The human TREX-2 complex is stably associated with the nuclear pore basket.
J Cell Sci
; 126(Pt 12): 2656-67, 2013 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23591820
16.
Histone H2B ubiquitination: signaling not scrapping.
Drug Discov Today Technol
; 12: e19-27, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25027370
17.
Zinc-finger UBPs: regulators of deubiquitylation.
Trends Biochem Sci
; 33(8): 369-75, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18603431
18.
The structural plasticity of SCA7 domains defines their differential nucleosome-binding properties.
EMBO Rep
; 11(8): 612-8, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20634802
19.
Juvenile Huntington disease in an 18-month-old boy revealed by global developmental delay and reduced cerebellar volume.
Am J Med Genet A
; 155A(4): 815-8, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21412977
20.
ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia.
Am J Med Genet A
; 155A(1): 98-105, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21204215