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Molecular and Cellular Endocrinology|January 23, 2010
Genetics and phenomics of hypothyroidism and goiter due to thyroglobulin mutationsHéctor M Targovnik, Sebastián A Esperante, Carina M Rivolta
ACS Omega|December 18, 2018
Mechanism of Tetramer Dissociation, Unfolding, and Oligomer Assembly of Pneumovirus M2-1 Transcription AntiterminatorsSebastián A Esperante, Damián Alvarez-Paggi, Mariano Salgueiro, et al.
Molecular and Cellular Probes|July 26, 2008
Identification and characterization of new variants of three associated SNPs and a microsatellite in the TSH receptor gene which are useful for genetic studiesSebastián A Esperante, Carina M Rivolta, Mariela Caputo, et al.
Scientific Reports|July 16, 2017
Plasticity in the Oxidative Folding Pathway of the High Affinity Nerita Versicolor Carboxypeptidase Inhibitor (NvCI)Sebastián A Esperante, Giovanni Covaleda, Sebastián A Trejo, et al.
Human Mutation|August 26, 2003
Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defectCarina M Rivolta, Sebastián A Esperante, Laura Gruñeiro-Papendieck, et al.
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