Mucopolysaccharidoses: Cellular Consequences of Glycosaminoglycans Accumulation and Potential Targets
Mucopolysaccharidoses (MPSs) constitute a heterogeneous group of lysosomal storage disorders characterized by the lysosomal accumulation of glycosaminoglycans (GAGs). Although lysosomal dysfunction is mainly affected, several cellular organelles such as mitochondria, endoplasmic reticulum, Golgi app...
Main Authors: | Andrés Felipe Leal, Eliana Benincore-Flórez, Estera Rintz, Angélica María Herreño-Pachón, Betul Celik, Yasuhiko Ago, Carlos Javier Alméciga-Díaz, Shunji Tomatsu |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-12-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/24/1/477 |
Similar Items
-
Glycosaminoglycans as Biomarkers for Mucopolysaccharidoses and Other Disorders
by: Paige C. Amendum, et al.
Published: (2021-08-01) -
Diagnosis of Mucopolysaccharidoses and Mucolipidosis by Assaying Multiplex Enzymes and Glycosaminoglycans
by: Nivethitha Arunkumar, et al.
Published: (2021-07-01) -
Epidemiology of Mucopolysaccharidoses Update
by: Betul Celik, et al.
Published: (2021-02-01) -
Establishment of Glycosaminoglycan Assays for Mucopolysaccharidoses
by: Shunji Tomatsu, et al.
Published: (2014-08-01) -
Use of a commercial agarose gel for analysis of urinary glycosaminoglycans in mucopolysaccharidoses
by: Ana Carolina Breier, et al.