Detalhe da pesquisa
1.
DNMT3B PWWP mutations cause hypermethylation of heterochromatin.
EMBO Rep
; 25(3): 1130-1155, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38291337
2.
Genome-wide single-molecule analysis of long-read DNA methylation reveals heterogeneous patterns at heterochromatin that reflect nucleosome organisation.
PLoS Genet
; 19(10): e1010958, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37782664
3.
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
Nat Commun
; 14(1): 3636, 2023 06 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37336879
4.
De novo DNA methyltransferase activity in colorectal cancer is directed towards H3K36me3 marked CpG islands.
Nat Commun
; 12(1): 694, 2021 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33514701
5.
Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
Nat Commun
; 14(1): 3836, 2023 Jun 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37380644