Detalhe da pesquisa
1.
Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.
Am J Hum Genet
; 106(3): 356-370, 2020 03 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32109418
2.
Regulation of telomeric function by DNA methylation differs between humans and mice.
Hum Mol Genet
; 29(19): 3197-3210, 2020 11 25.
Artigo
Inglês
| MEDLINE | ID: mdl-32916696
3.
Centromeres Transcription and Transcripts for Better and for Worse.
Prog Mol Subcell Biol
; 60: 169-201, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34386876
4.
Interplay between Histone and DNA Methylation Seen through Comparative Methylomes in Rare Mendelian Disorders.
Int J Mol Sci
; 22(7)2021 Apr 03.
Artigo
Inglês
| MEDLINE | ID: mdl-33916664
5.
Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome.
Hum Mol Genet
; 27(20): 3568-3581, 2018 10 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30010917
6.
Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state.
Hum Mol Genet
; 27(14): 2409-2424, 2018 07 15.
Artigo
Inglês
| MEDLINE | ID: mdl-29659838
7.
Multiple information carried by RNAs: total eclipse or a light at the end of the tunnel?
RNA Biol
; 17(12): 1707-1720, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-32559119
8.
Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.
Am J Hum Genet
; 108(6): 1161-1163, 2021 Jun 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34087165
9.
Genetics meets DNA methylation in rare diseases.
Clin Genet
; 95(2): 210-220, 2019 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30456829
10.
Short intron-derived ncRNAs.
Nucleic Acids Res
; 45(8): 4768-4781, 2017 05 05.
Artigo
Inglês
| MEDLINE | ID: mdl-28053119
11.
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
Inglês
| MEDLINE | ID: mdl-28334849
12.
Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey.
J Clin Immunol
; 36(2): 149-59, 2016 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-26851945
13.
Mammalian introns: when the junk generates molecular diversity.
Int J Mol Sci
; 16(3): 4429-52, 2015 Feb 20.
Artigo
Inglês
| MEDLINE | ID: mdl-25710723
14.
Tunable DNMT1 degradation reveals DNMT1/DNMT3B synergy in DNA methylation and genome organization.
J Cell Biol
; 223(4)2024 04 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38376465
15.
Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients.
J Hum Genet
; 58(7): 455-60, 2013 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-23739126
16.
Steroid receptor RNA activator protein binds to and counteracts SRA RNA-mediated activation of MyoD and muscle differentiation.
Nucleic Acids Res
; 39(2): 513-25, 2011 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-20855289
17.
Dnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissues.
Proc Natl Acad Sci U S A
; 107(20): 9281-6, 2010 May 18.
Artigo
Inglês
| MEDLINE | ID: mdl-20439742
18.
A Tool to Design Bridging Oligos Used to Detect Pseudouridylation Sites on RNA after CMC Treatment.
Noncoding RNA
; 8(5)2022 Sep 23.
Artigo
Inglês
| MEDLINE | ID: mdl-36287115
19.
Proteasome inhibition alters mitotic progression through the upregulation of centromeric α-Satellite RNAs.
FEBS J
; 289(7): 1858-1875, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-34739170
20.
Non-coding murine centromeric transcripts associate with and potentiate Aurora B kinase.
Nucleic Acids Res
; 37(15): 5071-80, 2009 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-19542185