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Lysosomal and mitochondrial liaisons in Niemann-Pick disease
Sandra Torres
,
Elisa Balboa
, Silvana Zanlungo
, Carlos Enrich
, Carmen Garcia-Ruiz
, Jose C. Fernandez-Checa
*
*
Corresponding author for this work
CSIC
Institut d'Investigacions Biomèdiques August Pi i Sunyer
Pontificia Universidad Católica de Chile
University of Barcelona
Southern California Research Center for ALDP and Cirrhosis
Research output
:
Contribution to journal
›
Review article
›
peer-review
66
Scopus citations
Overview
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Keyphrases
Mitochondrium
100%
Mitochondria
100%
Niemann-Pick Disease
100%
Cholesterol
66%
Lysosome
66%
Lysosomal Storage Disease
66%
Specific Lipids
66%
Membrane Contact Sites
66%
Lipid Species
66%
Mitochondrial Dysfunction
33%
NP-C
33%
Niemann-Pick C1-like 1 (NPC1L1)
33%
Disease Progression
33%
Endoplasmic Reticulum
33%
Antioxidant System
33%
Lysosomal Function
33%
Acid Sphingomyelinase
33%
Biochemical Features
33%
Sphingolipids
33%
Intracellular Trafficking
33%
Endolysosome
33%
Lysosomal Homeostasis
33%
Close Proximity
33%
Secondary Accumulation
33%
Functional Defects
33%
Functional Regulation
33%
Loss Function
33%
Niemann-Pick Type C
33%
Niemann-Pick Type
33%
Sterol Lipids
33%
Biochemistry, Genetics and Molecular Biology
Lipid
100%
Niemann-Pick Disease
100%
Mitochondrion
75%
Lysosome
50%
NPC1
25%
Acid Sphingomyelinase
25%
Sterol
25%
Sphingomyelin Phosphodiesterase
25%
Homeostasis
25%
Intracellular Trafficking
25%
Mitochondrial Disorder
25%
Sphingolipid
25%
Neuroscience
Mitochondrion
100%
Pick's Disease
100%
Lysosome
66%
Antioxidant
33%
Sterol
33%
Intracellular Trafficking
33%
Sphingolipid
33%
Sphingomyelin Phosphodiesterase
33%
Endoplasmic Reticulum
33%