Detalhe da pesquisa
1.
The aberrant epigenome of DNMT3B-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory.
Genome Res
; 33(2): 169-183, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36828588
2.
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing.
Nucleic Acids Res
; 45(10): 5739-5756, 2017 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28334849
3.
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming.
Biomolecules
; 13(12)2023 11 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38136588
4.
Interplay between DNA and RNA Modifications: A Constantly Evolving Process.
Epigenomes
; 4(4)2020 Nov 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34968305
5.
MeCP2 and Major Satellite Forward RNA Cooperate for Pericentric Heterochromatin Organization.
Stem Cell Reports
; 15(6): 1317-1332, 2020 12 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33296675
6.
DDX11L: a novel transcript family emerging from human subtelomeric regions.
BMC Genomics
; 10: 250, 2009 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-19476624
7.
Building up the inactive X chromosome.
Biol Cell
; 100(1): 63-70, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18072943
8.
Persistent epigenetic memory impedes rescue of the telomeric phenotype in human ICF iPSCs following DNMT3B correction.
Elife
; 82019 11 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31738163
9.
Collagen Prolyl Hydroxylation-Dependent Metabolic Perturbation Governs Epigenetic Remodeling and Mesenchymal Transition in Pluripotent and Cancer Cells.
Cancer Res
; 79(13): 3235-3250, 2019 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31061065
10.
DNMT3B Functions: Novel Insights From Human Disease.
Front Cell Dev Biol
; 6: 140, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30406101
11.
Editorial: DNA methylation: The aging clock.
Front Cell Dev Biol
; 11: 1164429, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37009473
12.
RIP: RNA Immunoprecipitation.
Methods Mol Biol
; 1480: 73-86, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27659976
13.
De novo DNMTs and DNA methylation: novel insights into disease pathogenesis and therapy from epigenomics.
Curr Pharm Des
; 20(11): 1812-8, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-23888951
14.
Non-coding RNAs in chromatin disease involving neurological defects.
Front Cell Neurosci
; 8: 54, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24616662
15.
L-Proline induces a mesenchymal-like invasive program in embryonic stem cells by remodeling H3K9 and H3K36 methylation.
Stem Cell Reports
; 1(4): 307-21, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24319666
16.
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient.
Epigenetics
; 7(6): 542-50, 2012 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22595875
17.
Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype.
Epigenetics
; 6(10): 1242-7, 2011 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21931280
18.
Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome.
Epigenetics
; 5(5): 427-43, 2010 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20448464
19.
Chromosome territory reorganization in a human disease with altered DNA methylation.
Proc Natl Acad Sci U S A
; 104(42): 16546-51, 2007 Oct 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-17923676
20.
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2).
Genome Res
; 13(2): 281-6, 2003 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-12566406