Type C Niemann-Pick disease: use of hydrophobic amines to study defective cholesterol transport.
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Cholesterol trafficking is required for mTOR activation in endothelial cellsDeficiency of niemann-pick type C-1 protein impairs release of human immunodeficiency virus type 1 and results in Gag accumulation in late endosomal/lysosomal compartmentsAccumulation of glycosphingolipids in Niemann-Pick C disease disrupts endosomal transportAmyloid-β metabolism in Niemann-Pick C disease models and patients.ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism.Fluorescence image screening for chemical compounds modifying cholesterol metabolism and distribution.Itraconazole suppresses the growth of glioblastoma through induction of autophagy: involvement of abnormal cholesterol trafficking.Secondary lipid accumulation in lysosomal disease.Mucolipidosis IV consists of one complementation groupCationic amphiphilic drugs cause a marked expansion of apparent lysosomal volume: implications for an intracellular distribution-based drug interaction.Traffic, polarity, and detergent solubility of a glycosylphosphatidylinositol-anchored protein after LDL-deprivation of MDCK cells.Toxoplasma gondii exploits host low-density lipoprotein receptor-mediated endocytosis for cholesterol acquisitionIncreased Expression of RhoA in Epithelium and Smooth Muscle of Obese Mouse Models: Implications for Isoprenoid Control of Airway Smooth Muscle and Fibroblasts.Cholesterol sensor ORP1L contacts the ER protein VAP to control Rab7-RILP-p150 Glued and late endosome positioning.The potential of histone deacetylase inhibitors in Niemann - Pick type C disease.Ultra high performance liquid chromatography-high resolution mass spectrometry plasma lipidomics can distinguish between canine breeds despite uncontrolled environmental variability and non-standardized diets.Sequestration of cholesterol within the host late endocytic pathway restricts liver-stage Plasmodium development.Drug-drug interactions involving lysosomes: mechanisms and potential clinical implications.Complex lipid trafficking in Niemann-Pick disease type C.Cholesterol accumulation by macrophages impairs phagosome maturation.Polarized membrane traffic and cell polarity development is dependent on dihydroceramide synthase-regulated sphinganine turnoverImipramine blocks acute silicosis in a mouse model.Lipoproteins, lipid droplets, lysosomes, and adrenocortical steroid hormone synthesis: morphological studies.Relating toxicity to transfection: using sphingosine to maintain prolonged expression in vitro.Niemann-Pick C1 functions in regulating lysosomal amine content.Modulation of protein kinase C by endogenous sphingosine: inhibition of phorbol dibutyrate binding in Niemann-Pick C fibroblasts.
P2860
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P2860
Type C Niemann-Pick disease: use of hydrophobic amines to study defective cholesterol transport.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 1991
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Type C Niemann-Pick disease: u ...... fective cholesterol transport.
@en
Type C Niemann-Pick disease: u ...... fective cholesterol transport.
@nl
type
label
Type C Niemann-Pick disease: u ...... fective cholesterol transport.
@en
Type C Niemann-Pick disease: u ...... fective cholesterol transport.
@nl
prefLabel
Type C Niemann-Pick disease: u ...... fective cholesterol transport.
@en
Type C Niemann-Pick disease: u ...... fective cholesterol transport.
@nl
P2093
P356
P1476
Type C Niemann-Pick disease: u ...... fective cholesterol transport.
@en
P2093
Pentchev PG
P304
P356
10.1159/000112179
P577
1991-01-01T00:00:00Z