Publications by authors named "Davide Gabellini"

31Publications

16th Meeting of the Interuniversity Institute of Myology (IIM) - Assisi (Italy), October 17-20, 2019: Foreword, Program and Abstracts.

Eur J Transl Myol 2020 Sep 15;30(3):9345. Epub 2020 Sep 15.

DAHFMO-Unit of Histology and Medical Embryology, Laboratory Affiliated to "Istituto Pasteur Italia - Fondazione Cenci Bolognetti", Sapienza University of Rome, Rome, Italy.

View Article and Find Full Text PDF
September 2020

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

Eur J Transl Myol 2018 Nov 30;28(4):7957. Epub 2018 Nov 30.

DAHFMO-Unit of Histology and Medical Embryology, Laboratory Affiliated to Istituto Pasteur Italia - Fondazione Cenci Bolognetti, Sapienza University of Rome, Rome, Italy.

View Article and Find Full Text PDF
November 2018

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

Nat Commun 2018 11 28;9(1):5026. Epub 2018 Nov 28.

Division of Genetics and Cell Biology, IRCCS San Raffaele Scientific Institute, via Olgettina 60, Milano, 20132, Italy.

View Article and Find Full Text PDF
November 2018

Diversification of the muscle proteome through alternative splicing.

Skelet Muscle 2018 03 6;8(1). Epub 2018 Mar 6.

Sprott Centre for Stem Cell Research, Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON, K1H 8L6, Canada.

View Article and Find Full Text PDF
March 2018

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

Hum Mol Genet 2017 02;26(4):753-767

Gene Expression and Muscular Dystrophy Unit, Division of Regenerative Medicine, IRCCS San Raffaele Scientific Institute, Milan 20132, Italy.

View Article and Find Full Text PDF
February 2017

Noncoding RNA Interplay with the Genome.

Authors:
Davide Gabellini

Methods Mol Biol 2016 ;1480:69-72

Dulbecco Telethon Institute and Division of Regenerative Medicine, San Raffaele Scientific Institute, Milano, Italy.

View Article and Find Full Text PDF
January 2018

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

J Cell Sci 2015 Feb 20;128(4):631-7. Epub 2015 Jan 20.

Dulbecco Telethon Institute and Division of Regenerative Medicine, San Raffaele Scientific Institute, 20132 Milan, Italy

View Article and Find Full Text PDF
February 2015

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

PLoS One 2014 29;9(12):e115278. Epub 2014 Dec 29.

Dulbecco Telethon Institute at San Raffaele Scientific Institute, Division of Regenerative Medicine, Stem Cells, and Gene Therapy, DIBIT2, 5A3, Via Olgettina 58, 20132, Milano, Italy.

View Article and Find Full Text PDF
September 2015

Direct interplay between two candidate genes in FSHD muscular dystrophy.

Hum Mol Genet 2015 Mar 17;24(5):1256-66. Epub 2014 Oct 17.

Division of Regenerative Medicine, Stem Cells, and Gene Therapy, Dulbecco Telethon Institute at San Raffaele Scientific Institute, DIBIT2, 5A3, Via Olgettina 58, 20132 Milan, Italy

View Article and Find Full Text PDF
March 2015

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

Skelet Muscle 2014 Mar 31;4(1). Epub 2014 Mar 31.

Dulbecco Telethon Institute at San Raffaele Scientific Institute, Division of Regenerative Medicine, Stem cells, and Gene therapy, DIBIT2, 5A3, Via Olgettina 58, 20132 Milano, Italy.

View Article and Find Full Text PDF
March 2014

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

J Mol Cell Biol 2013 Oct 29;5(5):294-307. Epub 2013 May 29.

Dulbecco Telethon Institute and Division of Regenerative Medicine, San Raffaele Scientific Institute, 20132 Milano, Italy.

View Article and Find Full Text PDF
October 2013

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

J Cell Sci 2013 May 22;126(Pt 10):2236-45. Epub 2013 Mar 22.

Dulbecco Telethon Institute and Division of Regenerative Medicine, San Raffaele Scientific Institute, 20132 Milano, Italy.

View Article and Find Full Text PDF
May 2013

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

PLoS Genet 2013 3;9(1):e1003186. Epub 2013 Jan 3.

Dulbecco Telethon Institute and Division of Regenerative Medicine, San Raffaele Scientific Institute, Milano, Italy.

View Article and Find Full Text PDF
May 2013

A repetitive elements perspective in Polycomb epigenetics.

Front Genet 2012 8;3:199. Epub 2012 Oct 8.

Division of Regenerative Medicine, Stem Cells, and Gene Therapy, Dulbecco Telethon Institute and San Raffaele Scientific Institute Milano, Italy ; Università Vita-Salute San Raffaele Milano, Italy.

View Article and Find Full Text PDF
October 2012

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

RNA Biol 2012 Oct 1;9(10):1211-7. Epub 2012 Oct 1.

Dulbecco Telethon Institute and Division of Regenerative Medicine, Stem cells, and Gene therapy, San Raffaele Scientific Institute, Milan, Italy.

View Article and Find Full Text PDF
October 2012

Hmgb3 is regulated by microRNA-206 during muscle regeneration.

PLoS One 2012 17;7(8):e43464. Epub 2012 Aug 17.

Stem Cell Laboratory, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Centro Dino Ferrari, Milano, Italy.

View Article and Find Full Text PDF
March 2013

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

Cell 2012 May 26;149(4):819-31. Epub 2012 Apr 26.

Dulbecco Telethon Institute at San Raffaele Scientific Institute, Division of Regenerative Medicine, Stem Cells, and Gene Therapy, Milan, Italy.

View Article and Find Full Text PDF
May 2012

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

Mol Ther 2011 Nov 9;19(11):2055-64. Epub 2011 Aug 9.

Dulbecco Telethon Institute and Division of Regenerative Medicine, San Raffaele Scientific Institute, Milano, Italy.

View Article and Find Full Text PDF
November 2011

The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophy.

J Cell Biol 2010 Dec;191(6):1049-60

International PhD Program in Cellular and Molecular Biology, Vita-Salute San Raffaele University, 20132 Milan, Italy.

View Article and Find Full Text PDF
December 2010

Alternative splicing and muscular dystrophy.

RNA Biol 2010 Jul-Aug;7(4):441-52. Epub 2010 Jul 1.

Division of Regenerative Medicine, San Raffaele Scientific Institute, Milan, Italy.

View Article and Find Full Text PDF
January 2011

In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy.

Epigenomics 2010 Apr;2(2):271-87

International PhD Program in Cellular & Molecular Biology, Vita-Salute San Raffaele University, Milan, Italy.

View Article and Find Full Text PDF
April 2010

Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1.

Nature 2006 Feb 11;439(7079):973-7. Epub 2005 Dec 11.

Howard Hughes Medical Institute, Programs in Gene Function and Expression and Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.

View Article and Find Full Text PDF
February 2006

When enough is enough: genetic diseases associated with transcriptional derepression.

Curr Opin Genet Dev 2004 Jun;14(3):301-7

Howard Hughes Medical Institute, Programs in Gene Function and Expression and Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.

View Article and Find Full Text PDF
June 2004

Transcriptional derepression as a cause of genetic diseases.

Curr Opin Genet Dev 2003 Jun;13(3):239-45

Howard Hughes Medical Institute, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.

View Article and Find Full Text PDF
June 2003

Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle.

Cell 2002 Aug;110(3):339-48

Howard Hughes Medical Institute, Program in Gene Function and Expression, Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.

View Article and Find Full Text PDF
August 2002