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Trends in Molecular Medicine|December 9, 2022
Proteome balance in ciliopathies: the OFD1 protein exampleManuela Morleo, Nunziana Pezzella, Brunella FrancoHuman Molecular Genetics|December 7, 2005
CDKL5/Stk9 kinase inactivation is associated with neuronal developmental disordersClark Lin, Brunella Franco, Marsha Rich RosnerGenes|July 29, 2023
Cilia and Cancer: From Molecular Genetics to Therapeutic StrategiesPietro Carotenuto, Sergio A Gradilone, Brunella FrancoAmerican Journal of Medical Genetics. Part A|October 30, 2007
Oral-facial-digital syndromes: review and diagnostic guidelinesFiorella Gurrieri, Brunella Franco, Helga Toriello, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 3, 2022
OFD1: One gene, several disordersNunziana Pezzella, Guglielmo Bove, Roberta Tammaro, et al.Indian Pediatrics|December 7, 2007
Oral-facial digital syndrome type 1Ercan Mihci, Sukran Tacoy, Gulay Ozbilim, et al.Frontiers in Neuroscience|October 19, 2020
Mutation-Independent Therapies for Retinal Diseases: Focus on Gene-Based ApproachesSabrina Carrella, Alessia Indrieri, Brunella Franco, et al.Frontiers in Neuroscience|November 16, 2020
Dopamine, Alpha-Synuclein, and Mitochondrial Dysfunctions in Parkinsonian EyesAlessia Indrieri, Rocco Pizzarelli, Brunella Franco, et al.Wiley Interdisciplinary Reviews. RNA|January 30, 2023
New insights into the centrosome-associated spliceosome components as regulators of ciliogenesis and tissue identityJohan Busselez, Rustem E Uzbekov, Brunella Franco, et al.American Journal of Medical Genetics. Part A|December 8, 2006
Terminal osseous dysplasia with pigmentary defects: clinical description of a new familyAnna Baroncini, Pia Castelluccio, Manuela Morleo, et al.Pageof 10