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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Ngā kaituhi matua:	Karolina Wiśniewska, Lidia Gaffke, Magdalena Żabińska, Grzegorz Węgrzyn, Karolina Pierzynowska
Hōputu:	Artigo
Reo:	Inglês
I whakaputaina:	MDPI AG 2024-03-01
Rangatū:	Current Issues in Molecular Biology
Ngā marau:	mucopolysaccharidosis neurodegeneration organelles organelle-related genes transcriptomics Golgi apparatus fragmentation
Urunga tuihono:	https://www.mdpi.com/1467-3045/46/3/169
Ngā Tūtohu:	Tāpirihia he Tūtohu Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!