Detalhe da pesquisa
1.
Sound of silence: the properties and functions of repressive Lys methyltransferases.
Nat Rev Mol Cell Biol
; 16(8): 499-513, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26204160
2.
Epigenetic control of muscle stem cells: time for a new dimension.
Trends Genet
; 38(5): 501-513, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35078651
3.
Synaptic alterations as a neurodevelopmental trait of Duchenne muscular dystrophy.
Neurobiol Dis
; 168: 105718, 2022 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35390481
4.
Identification and in vitro characterization of a new series of potent and highly selective G9a inhibitors as novel anti-fibroadipogenic agents.
Bioorg Med Chem Lett
; 72: 128858, 2022 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35718104
5.
The histone H3 lysine 9 methyltransferases G9a and GLP regulate polycomb repressive complex 2-mediated gene silencing.
Mol Cell
; 53(2): 277-89, 2014 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-24389103
6.
HDAC-regulated myomiRs control BAF60 variant exchange and direct the functional phenotype of fibro-adipogenic progenitors in dystrophic muscles.
Genes Dev
; 28(8): 841-57, 2014 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24682306
7.
Statins interfere with the attachment of S. cerevisiae mtDNA to the inner mitochondrial membrane.
J Enzyme Inhib Med Chem
; 35(1): 129-137, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31694426
8.
HDAC inhibitors as pharmacological treatment for Duchenne muscular dystrophy: a discovery journey from bench to patients.
Trends Mol Med
; 30(3): 278-294, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38408879
9.
Preclinical studies in the mdx mouse model of duchenne muscular dystrophy with the histone deacetylase inhibitor givinostat.
Mol Med
; 19: 79-87, 2013 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-23552722
10.
The m6A reader YTHDC1 and the RNA helicase DDX5 control the production of rhabdomyosarcoma-enriched circRNAs.
Nat Commun
; 14(1): 1898, 2023 04 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37019933
11.
The RNA helicase DDX5 cooperates with EHMT2 to sustain alveolar rhabdomyosarcoma growth.
Cell Rep
; 40(9): 111267, 2022 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36044855
12.
Muscle Damage in Dystrophic mdx Mice Is Influenced by the Activity of Ca2+-Activated KCa3.1 Channels.
Life (Basel)
; 12(4)2022 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35455028
13.
Histone deacetylase inhibitors in the treatment of muscular dystrophies: epigenetic drugs for genetic diseases.
Mol Med
; 17(5-6): 457-65, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21308150
14.
HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment.
Proc Natl Acad Sci U S A
; 105(49): 19183-7, 2008 Dec 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-19047631
15.
Targeting the Expression of Long Noncoding RNAs in Murine Satellite Cells from Single Myofibers.
Bio Protoc
; 11(21): e4209, 2021 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34859124
16.
Epigenetic regulation of Wnt7b expression by the cis-acting long noncoding RNA Lnc-Rewind in muscle stem cells.
Elife
; 102021 01 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33432928
17.
Prdm16-mediated H3K9 methylation controls fibro-adipogenic progenitors identity during skeletal muscle repair.
Sci Adv
; 7(23)2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34078594
18.
Nitric oxide deficiency determines global chromatin changes in Duchenne muscular dystrophy.
FASEB J
; 23(7): 2131-41, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19264835
19.
Single Myofiber Isolation and Culture from a Murine Model of Emery-Dreifuss Muscular Dystrophy in Early Post-Natal Development.
J Vis Exp
; (161)2020 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32716379
20.
Dysfunctional polycomb transcriptional repression contributes to lamin A/C-dependent muscular dystrophy.
J Clin Invest
; 130(5): 2408-2421, 2020 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31999646