Advancing Epigenetics Towards Systems Biology

List of EpiGeneSys publications

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Group Leader:
Davide Gabellini9 Publications.


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

J Cell Sci 2015 Jan 20;

Runfola V, Sebastian S, Dilworth FJ, Gabellini D

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DNA Methylation Analysis of the Macrosatellite Repeat Associated with FSHD Muscular Dystrophy at Single Nucleotide Level.

PLoS One 2014;9(12):e115278

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

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Direct Interplay Between Two Candidate Genes in FSHD Muscular Dystrophy.

Hum Mol Genet 2014 Oct 17;

Ferri G, Huichalaf CH, Caccia R, Gabellini D

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

Skelet Muscle 2014 Mar 31;4(1):8

Neguembor MV, Jothi M, Gabellini D

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

J Mol Cell Biol 2013 Jun 26;

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

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Facioscapulohumeral muscular dystrophy region gene 1 over-expression causes primary defects of myogenic stem cells.

J Cell Sci 2013 Mar 22;

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

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

PLoS Genet 2013 Jan;9(1):e1003186

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

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A repetitive elements perspective in Polycomb epigenetics.

Front Genet 2012;3:199

Casa V, Gabellini D

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

RNA Biol 2012 Oct;9(10):1211-7

Cabianca DS, Casa V, Gabellini D

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Latest publications


The Histone Acetyltransferase Mst2 Protects Active Chromatin from Epigenetic Silencing by Acetylating the Ubiquitin Ligase Brl1.

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Proliferation Drives Aging-Related Functional Decline in a Subpopulation of the Hematopoietic Stem Cell Compartment.

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The impact of rare and low-frequency genetic variants in common disease.

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