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Molecular Genetics & Genomic Medicine|March 13, 2021
Ex vivo model predicted in vivo efficacy of CFTR modulator therapy in a child with rare genotypeVito Terlizzi, Felice Amato, Chiara Castellani, et al.Biochimica Et Biophysica Acta|November 13, 2007
The kelch protein NS1-BP interacts with alpha-enolase/MBP-1 and is involved in c-Myc gene transcriptional controlGiovanni Perconti, Arianna Ferro, Felice Amato, et al.The Journal of Molecular Diagnostics : JMD|October 25, 2011
Extensive molecular analysis of patients bearing CFTR-related disordersFelice Amato, Chiara Bellia, Giuseppe Cardillo, et al.Lung|November 10, 2020
ACE2: The Major Cell Entry Receptor for SARS-CoV-2Filippo Scialo, Aurora Daniele, Felice Amato, et al.The Journal of Molecular Diagnostics : JMD|September 3, 2011
A novel DHPLC-based procedure for the analysis of COL1A1 and COL1A2 mutations in osteogenesis imperfectaAntonella Fuccio, Mariangela Iorio, Felice Amato, et al.International Journal of Molecular Sciences|June 28, 2023
Comparative Analysis of a Human Neutralizing mAb Specific for SARS-CoV-2 Spike-RBD with Cilgavimab and Tixagevimab for the Efficacy on the Omicron Variant in Neutralizing and Detection AssaysMargherita Passariello, Speranza Esposito, Lorenzo Manna, et al.International Journal of Molecular Sciences|June 28, 2023
Theratyping of the Rare CFTR Genotype A559T in Rectal Organoids and Nasal Cells Reveals a Relevant Response to Elexacaftor (VX-445) and Tezacaftor (VX-661) CombinationKarina Kleinfelder, Valeria Rachela Villella, Anca Manuela Hristodor, et al.Journal of Clinical Medicine|December 11, 2022
Cystic Fibrosis Patients with F508del/Minimal Function Genotype: Laboratory and Nutritional Evaluations after One Year of Elexacaftor/Tezacaftor/Ivacaftor TreatmentVincenzo Carnovale, Filippo Scialò, Monica Gelzo, et al.International Journal of Molecular Sciences|May 19, 2012
Congenital diarrheal disorders: an updated diagnostic approachGianluca Terrin, Rossella Tomaiuolo, Annalisa Passariello, et al.Clinical Case Reports|December 20, 2018
Two cases of microvillous inclusion disease caused by novel mutations in <i>MYO5B</i> geneMarika Comegna, Felice Amato, Renato Liguori, et al.Pageof 6