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DNMT3B PWWP mutations cause hypermethylation of heterochromatin.
EMBO Rep. 2024 Mar;25(3):1130-1155. doi: 10.1038/s44319-024-00061-5. Epub 2024 Jan 30.
EMBO Rep. 2024.
PMID: 38291337
Free PMC article.
Genome-wide single-molecule analysis of long-read DNA methylation reveals heterogeneous patterns at heterochromatin that reflect nucleosome organisation.
Kerr L, Kafetzopoulos I, Grima R, Sproul D.
Kerr L, et al. Among authors: kafetzopoulos i.
PLoS Genet. 2023 Oct 2;19(10):e1010958. doi: 10.1371/journal.pgen.1010958. eCollection 2023 Oct.
PLoS Genet. 2023.
PMID: 37782664
Free PMC article.
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Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
Sherwood K, Ward JC, Soriano I, Martin L, Campbell A, Rahbari R, Kafetzopoulos I, Sproul D, Green A, Sampson JR, Donaldson A, Ong KR, Heinimann K, Nielsen M, Thomas H, Latchford A, Palles C, Tomlinson I.
Sherwood K, et al. Among authors: kafetzopoulos i.
Nat Commun. 2023 Jun 28;14(1):3836. doi: 10.1038/s41467-023-39587-y.
Nat Commun. 2023.
PMID: 37380644
Free PMC article.
No abstract available.
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Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
Sherwood K, Ward JC, Soriano I, Martin L, Campbell A, Rahbari R, Kafetzopoulos I, Sproul D, Green A, Sampson JR, Donaldson A, Ong KR, Heinimann K, Nielsen M, Thomas H, Latchford A, Palles C, Tomlinson I.
Sherwood K, et al. Among authors: kafetzopoulos i.
Nat Commun. 2023 Jun 19;14(1):3636. doi: 10.1038/s41467-023-39248-0.
Nat Commun. 2023.
PMID: 37336879
Free PMC article.
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De novo DNA methyltransferase activity in colorectal cancer is directed towards H3K36me3 marked CpG islands.
Masalmeh RHA, Taglini F, Rubio-Ramon C, Musialik KI, Higham J, Davidson-Smith H, Kafetzopoulos I, Pawlicka KP, Finan HM, Clark R, Wills J, Finch AJ, Murphy L, Sproul D.
Masalmeh RHA, et al. Among authors: kafetzopoulos i.
Nat Commun. 2021 Jan 29;12(1):694. doi: 10.1038/s41467-020-20716-w.
Nat Commun. 2021.
PMID: 33514701
Free PMC article.
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