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Gene Expression-Related Changes in Morphologies of Organelles and Cellular Component Organization in Mucopolysaccharidoses

Mucopolysaccharidoses (MPS) are inherited metabolic diseases characterized by accumulation of incompletely degraded glycosaminoglycans (GAGs) in lysosomes. Although primary causes of these diseases are mutations in genes coding for enzymes involved in lysosomal GAG degradation, it was demonstrated t...

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書目詳細資料
發表在:Int J Mol Sci
Main Authors: Gaffke, Lidia, Pierzynowska, Karolina, Rintz, Estera, Cyske, Zuzanna, Giecewicz, Izabela, Węgrzyn, Grzegorz
格式: Artigo
語言:Inglês
出版: MDPI 2021
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC7967209/
https://ncbi.nlm.nih.gov/pubmed/33803318
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22052766
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