Lipid composition of microdomains is altered in a cell model of Gaucher disease.
about
Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson diseaseMeasuring brain lipidsGaucher disease and malignancy: a model for cancer pathogenesis in an inborn error of metabolismCharacterization of Gaucher disease bone marrow mesenchymal stromal cells reveals an altered inflammatory secretomeA prospective study of bone marrow hematopoietic and mesenchymal stem cells in type 1 Gaucher disease patientsFunctional diversification and specialization of cytosolic 70-kDa heat shock proteins.Analysis of lipid-composition changes in plasma membrane microdomainsExploring the link between glucocerebrosidase mutations and parkinsonismGlucocerebrosidase is present in α-synuclein inclusions in Lewy body disorders.Risk of death in heart disease is associated with elevated urinary globotriaosylceramide.Sphingolipids: the nexus between Gaucher disease and insulin resistance.Secondary alterations of sphingolipid metabolism in lysosomal storage diseases.Glucocerebrosidase, a new player changing the old rules in Lewy body diseases.Selective reduction of bis(monoacylglycero)phosphate ameliorates the storage burden in a THP-1 macrophage model of Gaucher disease.Abnormal nonstoring capillary endothelium: a novel feature of Gaucher disease. Ultrastructural study of dermal capillaries.Abnormal gangliosides are localized in lipid rafts in Sanfilippo (MPS3a) mouse brain.Peroxisome proliferator-activated receptor gamma-coactivator-1 alpha coordinates sphingolipid metabolism, lipid raft composition and myelin protein synthesis.Distinct lipid compositions of two types of human prostasomes.Alterations in the properties of the cell membrane due to glycosphingolipid accumulation in a model of Gaucher disease.The dipole potential correlates with lipid raft markers in the plasma membrane of living cells.Plasmalogens inhibit APP processing by directly affecting γ-secretase activity in Alzheimer's disease.Glucocerebrosidase deficiency promotes protein aggregation through dysregulation of extracellular vesicles
P2860
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P2860
Lipid composition of microdomains is altered in a cell model of Gaucher disease.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Lipid composition of microdomains is altered in a cell model of Gaucher disease.
@ast
Lipid composition of microdomains is altered in a cell model of Gaucher disease.
@en
type
label
Lipid composition of microdomains is altered in a cell model of Gaucher disease.
@ast
Lipid composition of microdomains is altered in a cell model of Gaucher disease.
@en
prefLabel
Lipid composition of microdomains is altered in a cell model of Gaucher disease.
@ast
Lipid composition of microdomains is altered in a cell model of Gaucher disease.
@en
P2093
P2860
P1476
Lipid composition of microdomains is altered in a cell model of Gaucher disease.
@en
P2093
John J Hopwood
Leanne K Hein
Maria Fuller
Stephen Duplock
P2860
P304
P356
10.1194/JLR.M800092-JLR200
P577
2008-04-21T00:00:00Z