- ES
- EN
15th National Research Competition in Life and Earth Sciences
Rare diseases
Research Centre or Institution : Facultad de Química. Universidad de Sevilla
This project aims to explore therapeutic strategies for treating lysosomal storage disorders based on the development of compounds capable of acting as pharmacological chaperones, that is, binding strongly to the mutant protein in the endoplasmic reticulum, promoting the correct folding and facilitating transport to the lysosome. In particular, we will focus on the study of sp2 iminosugars as they have a high selectivity and are capable of adapting to the active site of different lysosomal enzymes by controlled modification of its structure. As proof of concept, it has been proposed to develop pharmacological chaperones for Gaucher's disease, Fabry disease and GM1 gangliosidosis.
Activities related
Projects related
News related
Publications related
International Symposium Understanding and reprogramming developmental visual disorders: from anophthalmia to cortical impairments Madrid, Thursday and Friday, 30 and 31 January 2020, 9:30 hours
Panel Discussion Mundo de las prótesis, los nuevos materiales, sus complicaciones y su futuro Madrid , Lunes, 8 de abril 2024. 17.00 horas
Session Situación actual de las Enfermedades Raras en España Madrid, Martes, 23 de abril de 2024, 10:00 horas


La Fundación Ramón Areces refuerza su compromiso con las enfermedades raras
Published on 04/23/2024