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The Biological Clock and the Molecular Basis of Lysosomal Storage Diseases

The lysosomal storage disorders encompass nearly fifty diseases provoked by lack or deficiency of enzymes essential for the breakdown of complex molecules and hallmarked by accumulation in the lysosomes of metabolic residues. Histochemistry and cytochemistry studies evidenced patterns of circadian v...

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Podrobná bibliografie
Vydáno v:JIMD Rep
Hlavní autoři: Mazzoccoli, Gianluigi, Mazza, Tommaso, Vinciguerra, Manlio, Castellana, Stefano, Scarpa, Maurizio
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer Berlin Heidelberg 2015
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4361918/
https://ncbi.nlm.nih.gov/pubmed/25583520
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2014_354
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