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International Journal of Molecular Sciences|May 6, 2020
Targeting Mitochondrial Network Architecture in Down Syndrome and AgingNunzia Mollo, Rita Cicatiello, Miriam Aurilia, et al.
Frontiers in Genetics|March 31, 2022
Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 CellsNunzia Mollo, Miriam Aurilia, Roberta Scognamiglio, et al.
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.
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.
Human Molecular Genetics|April 5, 2014
NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndromeAntonella Izzo, Rosanna Manco, Ferdinando Bonfiglio, et al.
Journal of the Peripheral Nervous System : JPNS|November 11, 2019
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCsFiore Manganelli, Silvia Parisi, Maria Nolano, et al.
Human Molecular Genetics|January 15, 2017
Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cellsAntonella Izzo, Maria Nitti, Nunzia Mollo, et al.
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