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Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurological disease characterized by autosomal recessive mutations in the sacsin gene (SACS), that cause in patients progressive cerebellar atrophy, damage of the peripheral nerves, and significant retinal changes and cognitive...
ORGANISM(S): Homo sapiens (Human) 
2021-11-03 | PXD025718 | Pride
Glioblastoma (GBM) is a highly aggressive brain tumor known for its resistance to standard treatments. Despite surgery being a primary option, its invasive nature often leads to incomplete removal and high recurrence rates. Photodynamic therapy (PDT) holds promise as an adjunctive treatment, but saf...
ORGANISM(S): Homo sapiens (Human) 
2024-10-02 | PXD053482 | Pride
Upon entering in contact with the biological environment, nanostructures are immediately covered by biomolecules, and in particular proteins forming the so-called “protein corona” (PC). The phenomenon of PC formation has gained great attention in recent years due to its implication for the use of na...
ORGANISM(S): Mus musculus (Mouse) 
2022-10-14 | PXD031034 | Pride
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