Publications by authors named "Giuliana Galluzzi"

15Publications

Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2.

J Med Genet 2016 05 1;53(5):348-55. Epub 2016 Feb 1.

Institute of Cell Biology and Neurobiology, National Research Council of Italy, Monterotondo (Rome), Italy.

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May 2016

The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure.

BMC Med Genet 2007 Mar 2;8. Epub 2007 Mar 2.

Department of Neuroscience, Institute of Neurology, Catholic University of Sacred Heart, L,go A, Gemelli 8, 00168 Rome, Italy.

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March 2007

Pulse field gel electrophoresis for the detection of facioscapulohumeral muscular dystrophy gene rearrangements.

Methods Mol Biol 2003 ;217:153-64

Institute of Neurology, Faculty of Medicine, Catholic University, Rome, Italy.

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April 2003

Chimeric snRNA molecules carrying antisense sequences against the splice junctions of exon 51 of the dystrophin pre-mRNA induce exon skipping and restoration of a dystrophin synthesis in Delta 48-50 DMD cells.

Proc Natl Acad Sci U S A 2002 Jul 20;99(14):9456-61. Epub 2002 Jun 20.

Institute Pasteur Fondazione Cenci-Bolognetti, Department of Genetics and Molecular Biology, University La Sapienza, P.le Aldo Moro 5, 00185 Rome, Italy.

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July 2002