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International Journal of Molecular Sciences|February 11, 2023
Genetics and Molecular Basis of Congenital Heart Defects in Down Syndrome: Role of Extracellular Matrix RegulationNunzia Mollo, Roberta Scognamiglio, Anna Conti, et al.
Journal of Cellular Physiology|November 25, 2015
Rab7 Regulates CDH1 Endocytosis, Circular Dorsal Ruffles Genesis, and Thyroglobulin Internalization in a Thyroid Cell LineAnna Mascia, Flaviana Gentile, Antonella Izzo, et al.
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.
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.
Molecular Medicine (Cambridge, Mass.)|August 24, 2018
Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targetsAntonella Izzo, Nunzia Mollo, Maria Nitti, 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.
Journal of Personalized Medicine|November 19, 2020
Inhibition of 37/67kDa Laminin-1 Receptor Restores APP Maturation and Reduces Amyloid-β in Human Skin Fibroblasts from Familial Alzheimer's DiseaseAntaripa Bhattacharya, Antonella Izzo, Nunzia Mollo, 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.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|October 22, 2019
First trimester ultrasound features of X-linked Opitz syndrome and early molecular diagnosis: case report and review of the literatureLaura Sarno, Giuseppe Maria Maruotti, Antonella Izzo, et al.
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