Mutagenesis of the putative sterol-sensing domain of yeast Niemann Pick C-related protein reveals a primordial role in subcellular sphingolipid distribution.
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The pathogenesis of Niemann-Pick type C disease: a role for autophagy?The 'permeome' of the malaria parasite: an overview of the membrane transport proteins of Plasmodium falciparum.Iron, glucose and intrinsic factors alter sphingolipid composition as yeast cells enter stationary phase.Trans-Golgi network and endosome dynamics connect ceramide homeostasis with regulation of the unfolded protein response and TOR signaling in yeast.Saccharomyces cerevisiae Npc2p is a functionally conserved homologue of the human Niemann-Pick disease type C 2 protein, hNPC2.Accumulation of glycosphingolipids in Niemann-Pick C disease disrupts endosomal transportEfficacy and ototoxicity of different cyclodextrins in Niemann-Pick C diseaseA novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations.Adaptations to High Salt in a Halophilic Protist: Differential Expression and Gene Acquisitions through Duplications and Gene TransfersDeficiency of a Niemann-Pick, type C1-related protein in toxoplasma is associated with multiple lipidoses and increased pathogenicity.Niemann-Pick type C disease and intracellular cholesterol trafficking.Global regulation of a differentiation MAPK pathway in yeast.A role for oxysterol-binding protein-related protein 5 in endosomal cholesterol trafficking.Niemann-Pick type C pathogenesis and treatment: from statins to sugars.Loss of subcellular lipid transport due to ARV1 deficiency disrupts organelle homeostasis and activates the unfolded protein responseThe Hog1 mitogen-activated protein kinase mediates a hypoxic response in Saccharomyces cerevisiae.An "exacerbate-reverse" strategy in yeast identifies histone deacetylase inhibition as a correction for cholesterol and sphingolipid transport defects in human Niemann-Pick type C disease.Endosomal/lysosomal processing of gangliosides affects neuronal cholesterol sequestration in Niemann-Pick disease type C.9-O-butyl-13-(4-isopropylbenzyl)berberine, KR-72, is a potent antifungal agent that inhibits the growth of Cryptococcus neoformans by regulating gene expression.Sterol-rich plasma membrane domains in fungi.Sterol transport in yeast and the oxysterol binding protein homologue (OSH) familyLipid imbalance in the neurological disorder, Niemann-Pick C disease.Mechanisms for cellular cholesterol transport: defects and human disease.Niemann-Pick type C disease proteins: orphan transporters or membrane rheostats?Binding between the Niemann-Pick C1 protein and a photoactivatable cholesterol analog requires a functional sterol-sensing domain.Sphingolipid signalling mediates mitochondrial dysfunctions and reduced chronological lifespan in the yeast model of Niemann-Pick type C1.Sphingolipids and mitochondrial function, lessons learned from yeastCholesterol in Niemann-Pick Type C disease.Sterols and sphingolipids: dynamic duo or partners in crime?The yeast protein sorting pathway as an experimental model for lysosomal trafficking.Yeast as a model system for studying lipid homeostasis and function.Cell polarization in budding and fission yeasts.Yeast lipid metabolism at a glance.Sphingolipids and mitochondrial function in budding yeast.Candida albicans phospholipomannan: a sweet spot for controlling host response/inflammation.Niemann-Pick type C proteins promote microautophagy by expanding raft-like membrane domains in the yeast vacuoleExploring the power of yeast to model aging and age-related neurodegenerative disorders.Exacerbating and reversing lysosomal storage diseases: from yeast to humans.Sphingolipids regulate telomere clustering by affecting the transcription of genes involved in telomere homeostasis.Misexpression of the Niemann-Pick disease type C1 (NPC1)-like protein in Arabidopsis causes sphingolipid accumulation and reproductive defects.
P2860
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P2860
Mutagenesis of the putative sterol-sensing domain of yeast Niemann Pick C-related protein reveals a primordial role in subcellular sphingolipid distribution.
description
2004 nî lūn-bûn
@nan
2004 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Mutagenesis of the putative st ...... lar sphingolipid distribution.
@ast
Mutagenesis of the putative st ...... lar sphingolipid distribution.
@en
Mutagenesis of the putative st ...... lar sphingolipid distribution.
@nl
type
label
Mutagenesis of the putative st ...... lar sphingolipid distribution.
@ast
Mutagenesis of the putative st ...... lar sphingolipid distribution.
@en
Mutagenesis of the putative st ...... lar sphingolipid distribution.
@nl
prefLabel
Mutagenesis of the putative st ...... lar sphingolipid distribution.
@ast
Mutagenesis of the putative st ...... lar sphingolipid distribution.
@en
Mutagenesis of the putative st ...... lar sphingolipid distribution.
@nl
P2093
P2860
P3181
P356
P1476
Mutagenesis of the putative st ...... lar sphingolipid distribution.
@en
P2093
Arthur H Tinkelenberg
Dina A Balderes
Dorca Almanzar-Paramio
Eugene D Carstea
Francis Redican
Frederick Alcantara
Jill A Morris
Katsumi Higaki
Krishnamurthy Malathi
Lisa J Wilcox
P2860
P304
P3181
P356
10.1083/JCB.200310046
P407
P577
2004-02-16T00:00:00Z