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Marina Mora

Showing results (61-70 of 122) with videos related to

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BMC Biology|July 18, 2009
Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiationBeatrice Bodega, Gabriella Di Capua Ramirez, Florian Grasser, et al.
Neuromuscular Disorders : NMD|December 3, 2014
A novel homozygous ISPD gene mutation causing phenotype variability in a consanguineous familyGiovanni Baranello, Simona Saredi, Serena Sansanelli, et al.
Orphanet Journal of Rare Diseases|September 6, 2013
Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseasesMirella Filocamo, Chiara Baldo, Stefano Goldwurm, et al.
Biochimica Et Biophysica Acta|November 4, 2008
Identification of novel mutations in five patients with mitochondrial encephalomyopathyLucia Valente, Daniela Piga, Eleonora Lamantea, et al.
Mitochondrion|April 16, 2019
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB geneSilvia Marchet, Federica Invernizzi, Flavia Blasevich, et al.
Cell Reports|December 28, 2018
Engineering an Environment for the Study of Fibrosis: A 3D Human Muscle Model with Endothelium Specificity and EndomysiumSimone Bersini, Mara Gilardi, Giovanni S Ugolini, et al.
Brain : a Journal of Neurology|September 27, 2005
Decorin and biglycan expression is differentially altered in several muscular dystrophiesSimona Zanotti, Tiziana Negri, Cristina Cappelletti, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 13, 2019
Aging-associated genes and <i>let-7</i> microRNAs: a contribution to myogenic program dysregulation in oculopharyngeal muscular dystrophyCristina Cappelletti, Barbara Galbardi, Mirella Bruttini, et al.
Neurobiology of Disease|May 22, 2012
Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperatureOrazio Brunetti, Paola Imbrici, Fabio Massimo Botti, et al.
Molecular Genetics & Genomic Medicine|September 16, 2020
Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophyEdmund S Cauley, Alan Pittman, Swati Mummidivarpu, et al.
Pageof 13

Showing results (61-70 of 122) with videos related to

Sort By:
Pageof 13
BMC Biology|July 18, 2009
Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiationBeatrice Bodega, Gabriella Di Capua Ramirez, Florian Grasser, et al.
Neuromuscular Disorders : NMD|December 3, 2014
A novel homozygous ISPD gene mutation causing phenotype variability in a consanguineous familyGiovanni Baranello, Simona Saredi, Serena Sansanelli, et al.
Orphanet Journal of Rare Diseases|September 6, 2013
Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseasesMirella Filocamo, Chiara Baldo, Stefano Goldwurm, et al.
Biochimica Et Biophysica Acta|November 4, 2008
Identification of novel mutations in five patients with mitochondrial encephalomyopathyLucia Valente, Daniela Piga, Eleonora Lamantea, et al.
Mitochondrion|April 16, 2019
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB geneSilvia Marchet, Federica Invernizzi, Flavia Blasevich, et al.
Cell Reports|December 28, 2018
Engineering an Environment for the Study of Fibrosis: A 3D Human Muscle Model with Endothelium Specificity and EndomysiumSimone Bersini, Mara Gilardi, Giovanni S Ugolini, et al.
Brain : a Journal of Neurology|September 27, 2005
Decorin and biglycan expression is differentially altered in several muscular dystrophiesSimona Zanotti, Tiziana Negri, Cristina Cappelletti, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 13, 2019
Aging-associated genes and <i>let-7</i> microRNAs: a contribution to myogenic program dysregulation in oculopharyngeal muscular dystrophyCristina Cappelletti, Barbara Galbardi, Mirella Bruttini, et al.
Neurobiology of Disease|May 22, 2012
Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperatureOrazio Brunetti, Paola Imbrici, Fabio Massimo Botti, et al.
Molecular Genetics & Genomic Medicine|September 16, 2020
Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophyEdmund S Cauley, Alan Pittman, Swati Mummidivarpu, et al.
Pageof 13