Exploiting the Potential of <i>Drosophila</i> Models in Lysosomal Storage Disorders: Pathological Mechanisms and Drug Discovery

Lysosomal storage disorders (LSDs) represent a complex and heterogeneous group of rare genetic diseases due to mutations in genes coding for lysosomal enzymes, membrane proteins or transporters. This leads to the accumulation of undegraded materials within lysosomes and a broad range of severe clini...

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Hlavní autoři:	Laura Rigon, Concetta De Filippis, Barbara Napoli, Rosella Tomanin, Genny Orso
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	MDPI AG 2021-03-01
Edice:	Biomedicines
Témata:	lysosomal storage disorders <i>Drosophila melanogaster</i> animal model mucopolysaccharidosis sphingolipidosis mucolipidosis
On-line přístup:	https://www.mdpi.com/2227-9059/9/3/268
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