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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 2
2008 2
2010 3
2011 2
2012 2
2013 1
2014 4
2015 4
2016 11
2017 3
2018 4
2019 7
2020 1
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42 results
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Page 1
Uncovering the complexity of transcriptomes with RNA-Seq.
Costa V, Angelini C, De Feis I, Ciccodicola A. Costa V, et al. Among authors: Angelini C. J Biomed Biotechnol. 2010;2010:853916. doi: 10.1155/2010/853916. Epub 2010 Jun 27. J Biomed Biotechnol. 2010. PMID: 20625424 Free PMC article. Review.
Preface to the BMC-CIBB 2015-16 special issue.
Angelini C, Bracciali A, Gilbert D, Rizzo R. Angelini C, et al. BMC Bioinformatics. 2018 Jul 9;19(Suppl 7):201. doi: 10.1186/s12859-018-2176-4. BMC Bioinformatics. 2018. PMID: 30066660 Free PMC article. No abstract available.
Rebalancing gene haploinsufficiency in vivo by targeting chromatin.
Fulcoli FG, Franzese M, Liu X, Zhang Z, Angelini C, Baldini A. Fulcoli FG, et al. Among authors: Angelini C. Nat Commun. 2016 Jun 3;7:11688. doi: 10.1038/ncomms11688. Nat Commun. 2016. PMID: 27256596 Free PMC article.
Cripto is essential to capture mouse epiblast stem cell and human embryonic stem cell pluripotency.
Fiorenzano A, Pascale E, D'Aniello C, Acampora D, Bassalert C, Russo F, Andolfi G, Biffoni M, Francescangeli F, Zeuner A, Angelini C, Chazaud C, Patriarca EJ, Fico A, Minchiotti G. Fiorenzano A, et al. Among authors: Angelini C. Nat Commun. 2016 Sep 2;7:12589. doi: 10.1038/ncomms12589. Nat Commun. 2016. PMID: 27586544 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. Version 2. 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.
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.
Interactome mapping defines BRG1, a component of the SWI/SNF chromatin remodeling complex, as a new partner of the transcriptional regulator CTCF.
Marino MM, Rega C, Russo R, Valletta M, Gentile MT, Esposito S, Baglivo I, De Feis I, Angelini C, Xiao T, Felsenfeld G, Chambery A, Pedone PV. Marino MM, et al. Among authors: Angelini C. J Biol Chem. 2019 Jan 18;294(3):861-873. doi: 10.1074/jbc.RA118.004882. Epub 2018 Nov 20. J Biol Chem. 2019. PMID: 30459231 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.
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