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Physiological Genomics|February 19, 2009
Muscle genome-wide expression profiling during disease evolution in mdx miceMario Marotta, Claudia Ruiz-Roig, Yaris Sarria, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|August 16, 2014
The role of subscapularis muscle denervation in the pathogenesis of shoulder internal rotation contracture after neonatal brachial plexus palsy: a study in a rat modelVasco V Mascarenhas, Marcelo Casaccia, Alejandra Fernandez-Martin, et al.
Surgical Endoscopy|May 15, 2013
Single-Access Fetal Endoscopy (SAFE) for myelomeningocele in sheep model I: amniotic carbon dioxide gas approachJose L Peiro, Cesar G Fontecha, Rodrigo Ruano, et al.
Frontiers in Pediatrics|March 14, 2022
Fetal Tracheal Occlusion Increases Lung Basal Cells via Increased Yap SignalingVincent Serapiglia, Chad A Stephens, Rashika Joshi, et al.
Prenatal Diagnosis|February 7, 2016
Myocardial effects of fetal endoscopic tracheal occlusion in lambs with CDHElisa Zambaiti, Rossana Bussani, Valeria Calcaterra, et al.
Journal of Shoulder and Elbow Surgery|January 7, 2014
The role of muscle imbalance in the pathogenesis of shoulder contracture after neonatal brachial plexus palsy: a study in a rat modelFrancisco Soldado, Cesar G Fontecha, Mario Marotta, et al.
American Journal of Physiology. Cell Physiology|May 18, 2005
Impact on fatty acid metabolism and differential localization of FATP1 and FAT/CD36 proteins delivered in cultured human muscle cellsCèlia García-Martínez, Mario Marotta, Rodrigo Moore-Carrasco, et al.
International Journal of Molecular Sciences|June 19, 2024
A Novel Minimally Invasive Surgically Induced Skeletal Muscle Injury Model in SheepLaura Vidal, Ingrid Vila, Vanesa Venegas, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|September 28, 2018
Proteomic profiling of tracheal fluid in an ovine model of congenital diaphragmatic hernia and fetal tracheal occlusionJose Luis Peiro, Marc Oria, Emrah Aydin, et al.
Mitochondrion|September 4, 2010
A novel mutation in the mitochondrial tRNA(Ala) gene (m.5636T>C) in a patient with progressive external ophthalmoplegiaTomàs Pinós, Mario Marotta, Eduard Gallardo, et al.
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