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Molecular Therapy : the Journal of the American Society of Gene Therapy|September 13, 2012
Muscle function recovery in golden retriever muscular dystrophy after AAV1-U7 exon skippingAdeline Vulin, Inès Barthélémy, Aurélie Goyenvalle, et al.Human Molecular Genetics|August 14, 2003
Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased alpha 7 integrin, utrophin and associated glycoproteinsBehzad Moghadaszadeh, Reidar Albrechtsen, Ling T Guo, et al.Journal of Pediatric Gastroenterology and Nutrition|December 31, 2004
Removal of metabolites, cytokines and hepatic growth factors by extracorporeal liver support in childrenMarcus K H Auth, Hyun Soo Kim, Mechthild Beste, et al.The Journal of Pediatrics|July 25, 2006
Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe diseasePriya Sunil Kishnani, Marc Nicolino, Thomas Voit, et al.Nutrients|April 27, 2024
Effects of Different Types of Intermittent Fasting Interventions on Metabolic Health in Healthy Individuals (EDIF): A Randomised Trial with a Controlled-Run in PhaseDaniel Herz, Sebastian Karl, Johannes Weiß, et al.Journal of Neuroimmunology|April 13, 2010
Differential integrin expression by T lymphocytes: potential role in DMD muscle damageFernanda Pinto-Mariz, Luciana Rodrigues Carvalho, Wallace de Mello, et al.Human Gene Therapy|June 27, 2013
scAAV9 intracisternal delivery results in efficient gene transfer to the central nervous system of a feline model of motor neuron diseaseThomas Bucher, Marie-Anne Colle, Erin Wakeling, et al.The Journal of Cell Biology|May 7, 2014
Actin scaffolding by clathrin heavy chain is required for skeletal muscle sarcomere organizationStéphane Vassilopoulos, Christel Gentil, Jeanne Lainé, et al.Annals of Neurology|July 12, 2002
A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 geneAna Ferreiro, Nicole Monnier, Norma B Romero, et al.Epigenomics|March 23, 2018
Downregulation of miRNA-29, -23 and -21 in urine of Duchenne muscular dystrophy patientsFrancesco Catapano, Joana Domingos, Mark Perry, et al.Pageof 16