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Did you mean vaglini f[Author] (97 results)?
DNMT3B PWWP mutations cause hypermethylation of heterochromatin.
Taglini F, Kafetzopoulos I, Rolls W, Musialik KI, Lee HY, Zhang Y, Marenda M, Kerr L, Finan H, Rubio-Ramon C, Gautier P, Wapenaar H, Kumar D, Davidson-Smith H, Wills J, Murphy LC, Wheeler A, Wilson MD, Sproul D. Taglini F, et al. 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.
Global regulation of heterochromatin spreading by Leo1.
Verrier L, Taglini F, Barrales RR, Webb S, Urano T, Braun S, Bayne EH. Verrier L, et al. Among authors: taglini f. Open Biol. 2015 May;5(5):150045. doi: 10.1098/rsob.150045. Open Biol. 2015. PMID: 25972440 Free PMC article.
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions.
Heyn P, Logan CV, Fluteau A, Challis RC, Auchynnikava T, Martin CA, Marsh JA, Taglini F, Kilanowski F, Parry DA, Cormier-Daire V, Fong CT, Gibson K, Hwa V, Ibáñez L, Robertson SP, Sebastiani G, Rappsilber J, Allshire RC, Reijns MAM, Dauber A, Sproul D, Jackson AP. Heyn P, et al. Among authors: taglini f. Nat Genet. 2019 Jan;51(1):96-105. doi: 10.1038/s41588-018-0274-x. Epub 2018 Nov 26. Nat Genet. 2019. PMID: 30478443 Free PMC article.
The Gcm/Glide molecular and cellular pathway: new actors and new lineages.
Laneve P, Delaporte C, Trebuchet G, Komonyi O, Flici H, Popkova A, D'Agostino G, Taglini F, Kerekes I, Giangrande A. Laneve P, et al. Among authors: taglini f. Dev Biol. 2013 Mar 1;375(1):65-78. doi: 10.1016/j.ydbio.2012.12.014. Epub 2012 Dec 28. Dev Biol. 2013. PMID: 23276603 Free article.