Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick
Por um escritor misterioso
Last updated 20 setembro 2024
Mitochondrial biogenesis is transcriptionally repressed in lysosomal lipid storage diseases
Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium
Mitochondrial dysfunction in fibroblasts derived from patients with Niemann- Pick type C disease - ScienceDirect
Correction of Niemann-Pick type C1 disease with the histone deacetylase inhibitor valproic acid
PDF) Acid ceramidase improves mitochondrial function and oxidative stress in Niemann-Pick type C disease by repressing STARD1 expression and mitochondrial cholesterol accumulation
Correction of Niemann-Pick type C1 trafficking and activity with the histone deacetylase inhibitor valproic acid - ScienceDirect
Niemann-Pick Type C Disease Reveals a Link between Lysosomal Cholesterol and PtdIns(4,5)P2 That Regulates Neuronal Excitability - ScienceDirect
Finding pathogenic commonalities between Niemann-Pick type C and other lysosomal storage disorders: Opportunities for shared therapeutic interventions - ScienceDirect
Lipid-mediated motor-adaptor sequestration impairs axonal lysosome delivery leading to autophagic stress and dystrophy in Niemann-Pick type C - ScienceDirect
The pathogenesis of Niemann–Pick type C disease: a role for autophagy?, Expert Reviews in Molecular Medicine
Oxidative damage of lysosomes in regulated cell death systems: Pathophysiology and pharmacologic interventions - ScienceDirect
Mitochondrial biogenesis is transcriptionally repressed in lysosomal lipid storage diseases
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