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Human Gene Therapy|September 23, 2014
Biodistribution studies of polymeric nanoparticles for drug delivery in miceMaria Sofia Falzarano, Elena Bassi, Chiara Passarelli, et al.Current Pharmaceutical Design|January 11, 2018
Nanodiagnostics and Nanodelivery Applications in Genetic AlterationsMaria Sofia Falzarano, Cristina Flesia, Roberta Cavalli, et al.Plos Computational Biology|February 10, 2012
Novel approach to meta-analysis of microarray datasets reveals muscle remodeling-related drug targets and biomarkers in Duchenne muscular dystrophyEkaterina Kotelnikova, Maria A Shkrob, Mikhail A Pyatnitskiy, et al.Journal of Molecular Evolution|March 11, 2004
Tempo and mode of evolution of a primate-specific retrotransposon belonging to the LINE 1 familyBarbara Cardazzo, Luca Bargelloni, Luisa Toffolatti, et al.Journal of Child Neurology|April 13, 2010
Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patientCarlo Fusco, Daniele Frattini, Francesco Pisani, et al.Human Molecular Genetics|January 7, 2009
Paroxysmal non-kinesigenic dyskinesia is caused by mutations of the MR-1 mitochondrial targeting sequenceDaniele Ghezzi, Carlo Viscomi, Alessandra Ferlini, et al.Cardiology|June 13, 2017
A Clinical Case of Catecholaminergic Polymorphic Ventricular Tachycardia: The Clinical Suspicious and the Need of GeneticsAnnamaria Del Franco, Francesca Gualandi, Michele Malagù, et al.Breast Cancer Research and Treatment|July 16, 2010
Association of CYP1B1 with hypersensitivity induced by taxane therapy in breast cancer patientsRoberta Rizzo, Federica Spaggiari, Monica Indelli, et al.Pediatrics|October 3, 2018
Neurology Care, Diagnostics, and Emerging Therapies of the Patient With Duchenne Muscular DystrophyFawn Leigh, Alessandra Ferlini, Doug Biggar, et al.European Journal of Human Genetics : EJHG|May 20, 2020
EMQN best practice guidelines for genetic testing in dystrophinopathiesCarl Fratter, Raymond Dalgleish, Stephanie K Allen, et al.Pageof 19