Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Andrés Felipe Rojas-Rodriguez"'
Autor:
Carlos J. Alméciga-Díaz, Esteban Guzman, Wei Zheng, Oscar A. Hidalgo, María Alejandra Puentes-Tellez, Andrés Felipe Rojas-Rodriguez, Alexander Rodríguez-López, Kirill Gorshkov, Luisa N. Pimentel-Vera, Rafael Garzon, Rong Li, Sergio Olarte-Avellaneda
Publikováno v:
Journal of Medicinal Chemistry. 62:6175-6189
Mucopolysaccharidosis type IVA (MPS IVA) is a rare disease caused by mutations in the gene encoding the lysosomal enzyme N-acetylgalactosamine-6-sulfate sulfatase (GALNS). We report here two GALNS pharmacological chaperones, ezetimibe and pranlukast,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8993f8dc366cec0e3508ad82e3488ab
https://doi.org/10.1021/acs.jmedchem.9b00428
https://doi.org/10.1021/acs.jmedchem.9b00428
Autor:
Diego A. Suárez García, Carlos J. Alméciga-Díaz, Andrés Felipe Rojas-Rodriguez, Luz Mary Salazar Pulido, Sergio Olarte-Avellaneda, Oscar F. Sánchez, Jacobo Cepeda Del Castillo, Alexander Rodríguez-López
Publikováno v:
ACS Med Chem Lett
[Image: see text] Mucopolysaccharidosis IVA (MPS IVA) is a lysosomal storage disease caused by mutations in the gene encoding for the enzyme N-acetylgalactosamine-6-sulfate sulfatase (GALNS), leading to lysosomal accumulation of keratan sulfate (KS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d60a63a19d84eb255ca6794c49d58b
https://europepmc.org/articles/PMC7356376/
https://europepmc.org/articles/PMC7356376/
