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Molecular Genetics and Metabolism|April 9, 2013
Enzyme replacement therapy started at birth improves outcome in difficult-to-treat organs in mucopolysaccharidosis I miceGuilherme Baldo, Fabiana Q Mayer, Bárbara Z Martinelli, et al.Chemosphere|August 28, 2020
Cellular response to chemicals present in air pollution in occupationally exposed workers and its potential cancer susceptibilityBruna Gauer, Elisa Sauer, Sabrina Nascimento, et al.International Journal of Pharmaceutics|June 26, 2018
Intra-articular nonviral gene therapy in mucopolysaccharidosis I miceJuliana Bidone, Roselena Silvestri Schuh, Mirian Farinon, et al.Journal of Neurochemistry|April 17, 2004
Induction of motor neuron apoptosis by free 3-nitro-L-tyrosineHugo Peluffo, John J Shacka, Karina Ricart, et al.Inflammation|October 23, 2015
Fc Gamma Receptor IIA (CD32A) R131 Polymorphism as a Marker of Genetic Susceptibility to SepsisJaqueline Beppler, Patrícia Koehler-Santos, Gabriela Pasqualim, et al.Genetics and Molecular Biology|April 16, 2019
Sensitivity, advantages, limitations, and clinical utility of targeted next-generation sequencing panels for the diagnosis of selected lysosomal storage disordersDiana Rojas Málaga, Ana Carolina Brusius-Facchin, Marina Siebert, et al.Clinical Biochemistry|April 12, 2005
Ontogenetic changes in serum S100B in Down syndrome patientsCristina B O Netto, Luis V Portela, Cristina T Ferreira, et al.Journal of Molecular Graphics & Modelling|December 3, 2014
Lessons from molecular modeling human α-L-iduronidaseDanieli Forgiarini Figueiredo, Dinler A Antunes, Maurício M Rigo, et al.Journal of the Neurological Sciences|December 17, 2017
Clinical and molecular characterization of hereditary spastic paraplegias: A next-generation sequencing panel approachDaniela Burguez, Márcia Polese-Bonatto, Laís Alves Jacinto Scudeiro, et al.Meta Gene|January 22, 2015
Pitfalls in the prenatal diagnosis of mucolipidosis II alpha/beta: A case reportTaciane Alegra, Tiago Koppe, Angelina Acosta, et al.Pageof 19