Transcriptomic Changes Related to Cellular Processes with Particular Emphasis on Cell Activation in Lysosomal Storage Diseases from the Group of Mucopolysaccharidoses

Although mucopolysaccharidoses (MPS), inherited metabolic diseases from the group of lysosomal storage diseases (LSD), are monogenic disorders, recent studies indicated that their molecular mechanisms are complicated. Storage of glycosaminoglycans (GAGs), arising from a deficiency in one of the enzy...

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Detalles Bibliográficos
Publicado en:Int J Mol Sci
Main Authors: Rintz, Estera, Gaffke, Lidia, Podlacha, Magdalena, Brokowska, Joanna, Cyske, Zuzanna, Węgrzyn, Grzegorz, Pierzynowska, Karolina
Formato: Artigo
Idioma:Inglês
Publicado: MDPI 2020
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7246638/
https://ncbi.nlm.nih.gov/pubmed/32366041
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21093194
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