Iduronate-2-sulfatase interactome: validation by yeast two-hybrid assay
Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is a rare X-linked recessive disease caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase (IDS), which activates intracellular accumulation of nonmetabolized glycosaminoglycans such as heparan sulfate and dermatan...
- Autores:
-
Benincore Flórez, Eliana
El-Azaz, Jorge
Solarte, Gabriela Alejandra
Rodríguez, Alexander
Reyes, Luis
Alméciga-Díaz, Carlos Javier
Ramírez, Carolina Cardona
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2022
- Institución:
- Universidad de Ciencias Aplicadas y Ambientales U.D.C.A
- Repositorio:
- Repositorio Institucional UDCA
- Idioma:
- eng
- OAI Identifier:
- oai:repository.udca.edu.co:11158/4612
- Palabra clave:
- Mucopolisacaridosis II
Lisosomas
Proteómica
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode.es