Riccio A - Search Results

1

Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice.

Freschi A, Hur SK, Valente FM, Ideraabdullah FY, Sparago A, Gentile MT, Oneglia A, Di Nucci D, Colucci-D'Amato L, Thorvaldsen JL, Bartolomei MS, Riccio A, Cerrato F. Freschi A, et al. Among authors: riccio a. PLoS Genet. 2018 Feb 22;14(2):e1007243. doi: 10.1371/journal.pgen.1007243. eCollection 2018 Feb. PLoS Genet. 2018. PMID: 29470501 Free PMC article.

2

Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes.

Pedone PV, Pikaart MJ, Cerrato F, Vernucci M, Ungaro P, Bruni CB, Riccio A. Pedone PV, et al. Among authors: riccio a. FEBS Lett. 1999 Sep 10;458(1):45-50. doi: 10.1016/s0014-5793(99)01124-2. FEBS Lett. 1999. PMID: 10518931 Free article.

3

Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.

Sperandeo MP, Ungaro P, Vernucci M, Pedone PV, Cerrato F, Perone L, Casola S, Cubellis MV, Bruni CB, Andria G, Sebastio G, Riccio A. Sperandeo MP, et al. Among authors: riccio a. Am J Hum Genet. 2000 Mar;66(3):841-7. doi: 10.1086/302811. Am J Hum Genet. 2000. PMID: 10712200 Free PMC article.

4

The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis.

Vernucci M, Cerrato F, Besnard N, Casola S, Pedone PV, Bruni CB, Riccio A. Vernucci M, et al. Among authors: riccio a. Oncogene. 2000 Dec 14;19(54):6376-85. doi: 10.1038/sj.onc.1204024. Oncogene. 2000. PMID: 11175353

5

The 5' end of the KCNQ1OT1 gene is hypomethylated in the Beckwith-Wiedemann syndrome.

Cerrato F, Vernucci M, Pedone PV, Chiariotti L, Sebastio G, Bruni CB, Riccio A. Cerrato F, et al. Among authors: riccio a. Hum Genet. 2002 Jul;111(1):105-7. doi: 10.1007/s00439-002-0751-1. Epub 2002 Jun 14. Hum Genet. 2002. PMID: 12136243 No abstract available.

6

Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA.

Cerrato F, Dean W, Davies K, Kagotani K, Mitsuya K, Okumura K, Riccio A, Reik W. Cerrato F, et al. Among authors: riccio a. Hum Mol Genet. 2003 Dec 1;12(23):3123-32. doi: 10.1093/hmg/ddg338. Epub 2003 Oct 7. Hum Mol Genet. 2003. PMID: 14532328

7

Developmentally regulated functions of the H19 differentially methylated domain.

Vernucci M, Cerrato F, Pedone PV, Dandolo L, Bruni CB, Riccio A. Vernucci M, et al. Among authors: riccio a. Hum Mol Genet. 2004 Feb 1;13(3):353-61. doi: 10.1093/hmg/ddh028. Epub 2003 Dec 17. Hum Mol Genet. 2004. PMID: 14681296

8

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

Sparago A, Cerrato F, Vernucci M, Ferrero GB, Silengo MC, Riccio A. Sparago A, et al. Among authors: riccio a. Nat Genet. 2004 Sep;36(9):958-60. doi: 10.1038/ng1410. Epub 2004 Aug 15. Nat Genet. 2004. PMID: 15314640

9

The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster.

Cerrato F, Sparago A, Di Matteo I, Zou X, Dean W, Sasaki H, Smith P, Genesio R, Bruggemann M, Reik W, Riccio A. Cerrato F, et al. Among authors: riccio a. Hum Mol Genet. 2005 Feb 15;14(4):503-11. doi: 10.1093/hmg/ddi047. Epub 2005 Jan 7. Hum Mol Genet. 2005. PMID: 15640248

10

Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.

Sparago A, Russo S, Cerrato F, Ferraiuolo S, Castorina P, Selicorni A, Schwienbacher C, Negrini M, Ferrero GB, Silengo MC, Anichini C, Larizza L, Riccio A. Sparago A, et al. Among authors: riccio a. Hum Mol Genet. 2007 Feb 1;16(3):254-64. doi: 10.1093/hmg/ddl448. Epub 2006 Dec 11. Hum Mol Genet. 2007. PMID: 17158821

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