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L-Proline induces a mesenchymal-like invasive program in embryonic stem cells by remodeling H3K9 and H3K36 methylation.
Comes S, Gagliardi M, Laprano N, Fico A, Cimmino A, Palamidessi A, De Cesare D, De Falco S, Angelini C, Scita G, Patriarca EJ, Matarazzo MR, Minchiotti G. Comes S, et al. Among authors: angelini c. Stem Cell Reports. 2013 Oct 10;1(4):307-21. doi: 10.1016/j.stemcr.2013.09.001. eCollection 2013. Stem Cell Reports. 2013. PMID: 24319666 Free PMC article.
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells.
Anvar Z, Cammisa M, Riso V, Baglivo I, Kukreja H, Sparago A, Girardot M, Lad S, De Feis I, Cerrato F, Angelini C, Feil R, Pedone PV, Grimaldi G, Riccio A. Anvar Z, et al. Among authors: angelini c. Nucleic Acids Res. 2016 Feb 18;44(3):1118-32. doi: 10.1093/nar/gkv1059. Epub 2015 Oct 19. Nucleic Acids Res. 2016. PMID: 26481358 Free PMC article.
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells.
Riso V, Cammisa M, Kukreja H, Anvar Z, Verde G, Sparago A, Acurzio B, Lad S, Lonardo E, Sankar A, Helin K, Feil R, Fico A, Angelini C, Grimaldi G, Riccio A. Riso V, et al. Among authors: angelini c. Nucleic Acids Res. 2016 Sep 30;44(17):8165-78. doi: 10.1093/nar/gkw505. Epub 2016 Jun 1. Nucleic Acids Res. 2016. PMID: 27257070 Free PMC article.
Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus.
Valente FM, Sparago A, Freschi A, Hill-Harfe K, Maas SM, Frints SGM, Alders M, Pignata L, Franzese M, Angelini C, Carli D, Mussa A, Gazzin A, Gabbarini F, Acurzio B, Ferrero GB, Bliek J, Williams CA, Riccio A, Cerrato F. Valente FM, et al. Among authors: angelini c. Genet Med. 2019 Aug;21(8):1808-1820. doi: 10.1038/s41436-018-0416-7. Epub 2019 Jan 12. Genet Med. 2019. PMID: 30635621 Free PMC article.
HiCeekR: A Novel Shiny App for Hi-C Data Analysis.
Di Filippo L, Righelli D, Gagliardi M, Matarazzo MR, Angelini C. Di Filippo L, et al. Among authors: angelini c. Front Genet. 2019 Nov 4;10:1079. doi: 10.3389/fgene.2019.01079. eCollection 2019. Front Genet. 2019. PMID: 31749839 Free PMC article.
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype.
Sparago A, Verma A, Patricelli MG, Pignata L, Russo S, Calzari L, De Francesco N, Del Prete R, Palumbo O, Carella M, Mackay DJG, Rezwan FI, Angelini C, Cerrato F, Cubellis MV, Riccio A. Sparago A, et al. Among authors: angelini c. Clin Epigenetics. 2019 Dec 11;11(1):190. doi: 10.1186/s13148-019-0760-8. Clin Epigenetics. 2019. PMID: 31829238 Free PMC article.
1,028 results