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International Journal of Molecular Sciences|October 3, 2013
Non-coding RNAs in muscle dystrophiesDaniela Erriquez, Giovanni Perini, Alessandra FerliniFrontiers in Oncology|March 14, 2013
MYCN-mediated transcriptional repression in neuroblastoma: the other side of the coinSamuele Gherardi, Emanuele Valli, Daniela Erriquez, et al.Plos One|October 3, 2012
The DMD locus harbours multiple long non-coding RNAs which orchestrate and control transcription of muscle dystrophin mRNA isoformsMatteo Bovolenta, Daniela Erriquez, Emanuele Valli, et al.Biochimica Et Biophysica Acta|August 28, 2012
CDKL5, a novel MYCN-repressed gene, blocks cell cycle and promotes differentiation of neuronal cellsEmanuele Valli, Stefania Trazzi, Claudia Fuchs, et al.BMC Medical Genetics|March 30, 2012
The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathyMarcella Neri, Emanuele Valli, Giovanna Alfano, et al.Methods in Molecular Biology (Clifton, N.J.)|March 29, 2012
Exon skipping quantification by real-time PCRAlessandra Ferlini, Paola RimessiJournal of Neuromuscular Diseases|August 7, 2023
Biomarkers in Duchenne Muscular Dystrophy: Current Status and Future DirectionsFernanda Fortunato, Alessandra FerliniBiochimica Et Biophysica Acta. Gene Regulatory Mechanisms|February 7, 2018
MAX to MYCN intracellular ratio drives the aggressive phenotype and clinical outcome of high risk neuroblastomaFrancesca Ferrucci, Roberto Ciaccio, Sara Monticelli, et al.Journal of Clinical Medicine|May 11, 2019
Urinary Stem Cells as Tools to Study Genetic Disease: Overview of the LiteratureMaria Sofia Falzarano, Alessandra FerliniNeuromuscular Disorders : NMD|November 3, 2012
The medical genetics of dystrophinopathies: molecular genetic diagnosis and its impact on clinical practiceAlessandra Ferlini, Marcella Neri, Francesca GualandiPageof 26