Flux of Fatty Acids through NPC1 Lysosomes
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference21 articles.
1. The Metabolic and Molecular Bases for Inherited Diseases;Patterson,2000
2. Niemann–Pick C1 Is a Late Endosome-Resident Protein That Transiently Associates with Lysosomes and the Trans-Golgi Network
3. Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis
4. Mutations in NPC1 Highlight a Conserved NPC1-Specific Cysteine-Rich Domain
5. Identification of 58 novel mutations in Niemann-Pick disease type C: Correlation with biochemical phenotype and importance ofPTC1-like domains inNPC1
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3. Treatment with fibrates is associated with higher LAL activity in dyslipidemic patients;Pharmacological Research;2019-09
4. Lysosomal Acid Lipase: From Cellular Lipid Handler to Immunometabolic Target;Trends in Pharmacological Sciences;2019-02
5. Niemann-Pick C1-deficient mice lacking sterol O-acyltransferase 2 have less hepatic cholesterol entrapment and improved liver function;American Journal of Physiology-Gastrointestinal and Liver Physiology;2018-10-01
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