Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Jacobo Cepeda Del Castillo"'
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/
Autor:
Carlos J. Alméciga-Díaz, Jacobo Cepeda Del Castillo, Edwin Alexander Rodriguez-López, Juan Camilo Losada Díaz
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 1, p 232 (2019)
International Journal of Molecular Sciences, Vol 21, Iss 1, p 232 (2019)
The mucopolysaccharidoses (MPS) are a group of 11 lysosomal storage diseases (LSDs) produced by mutations in the enzymes involved in the lysosomal catabolism of glycosaminoglycans. Most of the mutations affecting these enzymes may lead to changes in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10092ec2be3252b219537120db8a3115
https://pubmed.ncbi.nlm.nih.gov/31905715
https://pubmed.ncbi.nlm.nih.gov/31905715
