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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Int J Mol Sci
Egile Nagusiak: Rintz, Estera, Gaffke, Lidia, Podlacha, Magdalena, Brokowska, Joanna, Cyske, Zuzanna, Węgrzyn, Grzegorz, Pierzynowska, Karolina
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: MDPI 2020
Gaiak:
Article
Sarrera elektronikoa: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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