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Cellular Organelle-Related Transcriptomic Profile Abnormalities in Neuronopathic Types of Mucopolysaccharidosis: A Comparison with Other Neurodegenerative Diseases

Mucopolysaccharidoses (MPS) are a group of diseases caused by mutations in genes encoding lysosomal enzymes that catalyze reactions of glycosaminoglycan (GAG) degradation. As a result, GAGs accumulate in lysosomes, impairing the proper functioning of entire cells and tissues. There are 14 types/subt...

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Principais autores: Karolina Wiśniewska, Lidia Gaffke, Magdalena Żabińska, Grzegorz Węgrzyn, Karolina Pierzynowska
Format: Artigo
Sprog:Inglês
Udgivet: MDPI AG 2024-03-01
Serier:Current Issues in Molecular Biology
Fag:
mucopolysaccharidosis
neurodegeneration
organelles
organelle-related genes
transcriptomics
Golgi apparatus fragmentation
Online adgang:https://www.mdpi.com/1467-3045/46/3/169
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