Niemann–Pick type C (NPC) disease is a lysosomal storage disorder arising from mutations in the cholesterol-trafficking protein NPC1 (95%) or NPC2 (5%). These mutations result in accumulation of low-density lipoprotein-derived cholesterol in late endosomes/lysosomes, disruption of endocytic trafficking, and stalled autophagic flux. Additionally, NPC disease results in sphingolipid accumulation, yet it is unique among the sphingolipidoses because of the absence of mutations in the enzymes responsible for sphingolipid degradation. In this work, we examined the cause for sphingosine and sphingolipid accumulation in multiple cellular models of NPC disease and observed that the activity of sphingosine kinase 1 (SphK1), one of the two isoenzymes ...
Niemann-Pick type C1 (NPC1) disease is a neurodegenerative lysosomal storage disorder caused by muta...
Niemann-Pick type C disease (NPCD) is a ruinous condition that mostly affects children. Although ste...
AbstractNiemann–Pick disease type C (NP-C) is an autosomal recessive disorder characterized by the s...
Niemann-Pick disease type C (NPC) is a fatal, autosomal recessive lipidosis characterized by lysosom...
Activation of protein kinase C (PKC) has previously been shown to ameliorate the cholesterol transpo...
AbstractNiemann–Pick type C disease (NPC) is a neurovisceral (or, extremely rarely, only visceral) l...
Niemann-Pick Type C (NPC) disease is a fatal pediatric cholesterol storage disease that is caused by...
Niemann–Pick type C1 (NPC1) is a lysosomal storage disorder, inherited as an autosomal-recessive tra...
Membrane contact sites (MCS), close membrane apposition between organelles, are platforms for intero...
Niemann-Pick disease type C (NPC) is characterized by the accumulation of cholesterol and sphingolip...
Cholesterol and phosphoinositides (PI) are two critically important lipids that are found in cellula...
AbstractPathways of intracellular cholesterol trafficking are poorly understood at the molecular lev...
Sphingosine-1-phosphate (S1P) lyase irreversibly cleaves S1P, thereby catalysing the ultimate step o...
Studying the biosynthesis, utilization and transport of cholesterol as well as the balance between t...
In Niemann-Pick type C disease, the most prevalent I1061T mutation inhibits folding and trafficking ...
Niemann-Pick type C1 (NPC1) disease is a neurodegenerative lysosomal storage disorder caused by muta...
Niemann-Pick type C disease (NPCD) is a ruinous condition that mostly affects children. Although ste...
AbstractNiemann–Pick disease type C (NP-C) is an autosomal recessive disorder characterized by the s...
Niemann-Pick disease type C (NPC) is a fatal, autosomal recessive lipidosis characterized by lysosom...
Activation of protein kinase C (PKC) has previously been shown to ameliorate the cholesterol transpo...
AbstractNiemann–Pick type C disease (NPC) is a neurovisceral (or, extremely rarely, only visceral) l...
Niemann-Pick Type C (NPC) disease is a fatal pediatric cholesterol storage disease that is caused by...
Niemann–Pick type C1 (NPC1) is a lysosomal storage disorder, inherited as an autosomal-recessive tra...
Membrane contact sites (MCS), close membrane apposition between organelles, are platforms for intero...
Niemann-Pick disease type C (NPC) is characterized by the accumulation of cholesterol and sphingolip...
Cholesterol and phosphoinositides (PI) are two critically important lipids that are found in cellula...
AbstractPathways of intracellular cholesterol trafficking are poorly understood at the molecular lev...
Sphingosine-1-phosphate (S1P) lyase irreversibly cleaves S1P, thereby catalysing the ultimate step o...
Studying the biosynthesis, utilization and transport of cholesterol as well as the balance between t...
In Niemann-Pick type C disease, the most prevalent I1061T mutation inhibits folding and trafficking ...
Niemann-Pick type C1 (NPC1) disease is a neurodegenerative lysosomal storage disorder caused by muta...
Niemann-Pick type C disease (NPCD) is a ruinous condition that mostly affects children. Although ste...
AbstractNiemann–Pick disease type C (NP-C) is an autosomal recessive disorder characterized by the s...