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Clinical Case Reports|April 12, 2018
Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case reportRita Genesio, Giuseppe Maria Maruotti, Gabriele Saccone, et al.Medical Sciences (Basel, Switzerland)|March 2, 2019
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal TranslucencyRita Cicatiello, Piero Pignataro, Antonella Izzo, et al.American Journal of Medical Genetics. Part A|December 21, 2013
Complex chromosomal rearrangements causing Langer-Giedion syndrome atypical phenotype: genotype-phenotype correlation and literature reviewGerarda Cappuccio, Rita Genesio, Valentina Ronga, et al.International Journal of Genomics|October 24, 2017
Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome FetusesAntonella Izzo, Rosanna Manco, Tiziana de Cristofaro, et al.Molecular Medicine (Cambridge, Mass.)|August 24, 2018
Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targetsAntonella Izzo, Nunzia Mollo, Maria Nitti, et al.Epigenetics|September 21, 2011
Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotypeRita Genesio, Daniela Melis, Sole Gatto, et al.Human Molecular Genetics|April 5, 2014
NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndromeAntonella Izzo, Rosanna Manco, Ferdinando Bonfiglio, et al.Stem Cell Research|December 25, 2013
Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modificationsAntonietta Coppola, Antonio Romito, Christelle Borel, et al.Cells|February 15, 2022
Activation of Non-Canonical Autophagic Pathway through Inhibition of Non-Integrin Laminin Receptor in Neuronal CellsAdriana Limone, Iolanda Veneruso, Antonella Izzo, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 4, 2025
Targeting RPSA to modulate endosomal trafficking and amyloidogenesis in genetic Alzheimer's diseaseAdriana Limone, Clelia Di Napoli, Filomena Napolitano, et al.Pageof 4