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Items: 1 to 20 of 28

1.

Report on Abstracts of the 15th Meeting of IIM, the Interuniversity Institute of Myology - Assisi (Italy), October 11-14, 2018.

Gabellini D, MusarĂ² A.

Eur J Transl Myol. 2018 Nov 30;28(4):7957. doi: 10.4081/ejtm.2018.7957. eCollection 2018 Nov 2.

2.

The Trithorax protein Ash1L promotes myoblast fusion by activating Cdon expression.

Castiglioni I, Caccia R, Garcia-Manteiga JM, Ferri G, Caretti G, Molineris I, Nishioka K, Gabellini D.

Nat Commun. 2018 Nov 28;9(1):5026. doi: 10.1038/s41467-018-07313-8.

3.

Amino acid deprivation triggers a novel GCN2-independent response leading to the transcriptional reactivation of non-native DNA sequences.

De Vito A, Lazzaro M, Palmisano I, Cittaro D, Riba M, Lazarevic D, Bannai M, Gabellini D, Schiaffino MV.

PLoS One. 2018 Jul 18;13(7):e0200783. doi: 10.1371/journal.pone.0200783. eCollection 2018.

4.

Diversification of the muscle proteome through alternative splicing.

Nakka K, Ghigna C, Gabellini D, Dilworth FJ.

Skelet Muscle. 2018 Mar 6;8(1):8. doi: 10.1186/s13395-018-0152-3. Review.

5.

Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy.

Casa V, Runfola V, Micheloni S, Aziz A, Dilworth FJ, Gabellini D.

Hum Mol Genet. 2017 Feb 15;26(4):753-767. doi: 10.1093/hmg/ddw426.

6.

Noncoding RNA Interplay with the Genome.

Gabellini D.

Methods Mol Biol. 2016;1480:69-72. doi: 10.1007/978-1-4939-6380-5_6.

PMID:
27659975
7.

A Human Pluripotent Stem Cell Model of Facioscapulohumeral Muscular Dystrophy-Affected Skeletal Muscles.

Caron L, Kher D, Lee KL, McKernan R, Dumevska B, Hidalgo A, Li J, Yang H, Main H, Ferri G, Petek LM, Poellinger L, Miller DG, Gabellini D, Schmidt U.

Stem Cells Transl Med. 2016 Sep;5(9):1145-61. doi: 10.5966/sctm.2015-0224. Epub 2016 May 23.

8.

Rbfox proteins regulate tissue-specific alternative splicing of Mef2D required for muscle differentiation.

Runfola V, Sebastian S, Dilworth FJ, Gabellini D.

J Cell Sci. 2015 Feb 15;128(4):631-7. doi: 10.1242/jcs.161059. Epub 2015 Jan 20.

9.

DNA methylation analysis of the macrosatellite repeat associated with FSHD muscular dystrophy at single nucleotide level.

Huichalaf C, Micheloni S, Ferri G, Caccia R, Gabellini D.

PLoS One. 2014 Dec 29;9(12):e115278. doi: 10.1371/journal.pone.0115278. eCollection 2014. Erratum in: PLoS One. 2015;10(3):e0119742.

10.

Direct interplay between two candidate genes in FSHD muscular dystrophy.

Ferri G, Huichalaf CH, Caccia R, Gabellini D.

Hum Mol Genet. 2015 Mar 1;24(5):1256-66. doi: 10.1093/hmg/ddu536. Epub 2014 Oct 17.

11.

Long noncoding RNAs, emerging players in muscle differentiation and disease.

Neguembor MV, Jothi M, Gabellini D.

Skelet Muscle. 2014 Mar 31;4(1):8. doi: 10.1186/2044-5040-4-8.

12.

FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis.

Neguembor MV, Xynos A, Onorati MC, Caccia R, Bortolanza S, Godio C, Pistoni M, Corona DF, Schotta G, Gabellini D.

J Mol Cell Biol. 2013 Oct;5(5):294-307. doi: 10.1093/jmcb/mjt018. Epub 2013 May 29.

PMID:
23720823
13.

Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells.

Xynos A, Neguembor MV, Caccia R, Licastro D, Nonis A, Di Serio C, Stupka E, Gabellini D.

J Cell Sci. 2013 May 15;126(Pt 10):2236-45. doi: 10.1242/jcs.121533. Epub 2013 Mar 22.

14.

Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD).

Pistoni M, Shiue L, Cline MS, Bortolanza S, Neguembor MV, Xynos A, Ares M Jr, Gabellini D.

PLoS Genet. 2013;9(1):e1003186. doi: 10.1371/journal.pgen.1003186. Epub 2013 Jan 3.

15.

A repetitive elements perspective in Polycomb epigenetics.

Casa V, Gabellini D.

Front Genet. 2012 Oct 8;3:199. doi: 10.3389/fgene.2012.00199. eCollection 2012.

16.

A novel molecular mechanism in human genetic disease: a DNA repeat-derived lncRNA.

Cabianca DS, Casa V, Gabellini D.

RNA Biol. 2012 Oct;9(10):1211-7. doi: 10.4161/rna.21922. Epub 2012 Oct 1.

17.

Hmgb3 is regulated by microRNA-206 during muscle regeneration.

Maciotta S, Meregalli M, Cassinelli L, Parolini D, Farini A, Fraro GD, Gandolfi F, Forcato M, Ferrari S, Gabellini D, Bicciato S, Cossu G, Torrente Y.

PLoS One. 2012;7(8):e43464. doi: 10.1371/journal.pone.0043464. Epub 2012 Aug 17.

18.

Amino acid starvation induces reactivation of silenced transgenes and latent HIV-1 provirus via down-regulation of histone deacetylase 4 (HDAC4).

Palmisano I, Della Chiara G, D'Ambrosio RL, Huichalaf C, Brambilla P, Corbetta S, Riba M, Piccirillo R, Valente S, Casari G, Mai A, Martinelli Boneschi F, Gabellini D, Poli G, Schiaffino MV.

Proc Natl Acad Sci U S A. 2012 Aug 21;109(34):E2284-93. doi: 10.1073/pnas.1202174109. Epub 2012 Jul 23.

19.

A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy.

Cabianca DS, Casa V, Bodega B, Xynos A, Ginelli E, Tanaka Y, Gabellini D.

Cell. 2012 May 11;149(4):819-31. doi: 10.1016/j.cell.2012.03.035. Epub 2012 Apr 26.

20.

AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy.

Bortolanza S, Nonis A, Sanvito F, Maciotta S, Sitia G, Wei J, Torrente Y, Di Serio C, Chamberlain JR, Gabellini D.

Mol Ther. 2011 Nov;19(11):2055-64. doi: 10.1038/mt.2011.153. Epub 2011 Aug 9.

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