A specific structural requirement for ergosterol in long-chain fatty acid synthesis mutants important for maintaining raft domains in yeast.
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Disruptions of the Arabidopsis Enoyl-CoA reductase gene reveal an essential role for very-long-chain fatty acid synthesis in cell expansion during plant morphogenesisTargeting of Tsc13p to nucleus-vacuole junctions: a role for very-long-chain fatty acids in the biogenesis of microautophagic vesiclesA heritable switch in carbon source utilization driven by an unusual yeast prionDifferential regulation of ceramide synthase components LAC1 and LAG1 in Saccharomyces cerevisiae.Mathematical modeling and validation of the ergosterol pathway in Saccharomyces cerevisiaeThe spatial organization of lipid synthesis in the yeast Saccharomyces cerevisiae derived from large scale green fluorescent protein tagging and high resolution microscopy.A genome-wide visual screen reveals a role for sphingolipids and ergosterol in cell surface delivery in yeastA multi-level study of recombinant Pichia pastoris in different oxygen conditions.Defects in very long chain fatty acid synthesis enhance alpha-synuclein toxicity in a yeast model of Parkinson's disease.The impact of oxygen on the transcriptome of recombinant S. cerevisiae and P. pastoris - a comparative analysis.A split-ubiquitin two-hybrid screen for proteins physically interacting with the yeast amino acid transceptor Gap1 and ammonium transceptor Mep2.The effect of ergosterol on dipalmitoylphosphatidylcholine bilayers: a deuterium NMR and calorimetric study.The yeast sphingolipid signaling landscape.Gel domains in the plasma membrane of Saccharomyces cerevisiae: highly ordered, ergosterol-free, and sphingolipid-enriched lipid rafts.The plasma membrane proton pump PMA-1 is incorporated into distal parts of the hyphae independently of the Spitzenkörper in Neurospora crassa.Segregation of sphingolipids and sterols during formation of secretory vesicles at the trans-Golgi network.Cumulative mutations affecting sterol biosynthesis in the yeast Saccharomyces cerevisiae result in synthetic lethality that is suppressed by alterations in sphingolipid profiles.Evidence for coupled biogenesis of yeast Gap1 permease and sphingolipids: essential role in transport activity and normal control by ubiquitinationLight-induced recruitment of INAD-signaling complexes to detergent-resistant lipid rafts in Drosophila photoreceptors.Identification of Yeast Mutants Exhibiting Altered Sensitivity to Valinomycin and Nigericin Demonstrate Pleiotropic Effects of Ionophores on Cellular Processes.Functional interactions between sphingolipids and sterols in biological membranes regulating cell physiologyHopanoids are not essential for growth of Streptomyces scabies 87-22.Roles for sphingolipids in Saccharomyces cerevisiae.Protein trafficking, ergosterol biosynthesis and membrane physics impact recombinant protein secretion in Pichia pastoris.Yeast sphingolipids do not need to contain very long chain fatty acids.Loss of hydroxyl groups from the ceramide moiety can modify the lateral diffusion of membrane proteins in S. cerevisiae.Synthetically lethal interactions involving loss of the yeast ERG24: the sterol C-14 reductase geneYeast lipids can phase-separate into micrometer-scale membrane domains.Regulation of telomere length by fatty acid elongase 3 in yeast. Involvement of inositol phosphate metabolism and Ku70/80 functionInositol phosphosphingolipid phospholipase C1 regulates plasma membrane ATPase (Pma1) stability in Cryptococcus neoformans.The equilibria of sphingolipid-cholesterol and sphingolipid-sphingolipid in monolayers at the air-water interface.Membrane rafts are involved in intracellular miconazole accumulation in yeast cells.The order of rafts. Conference on microdomains, lipid rafts and caveolae.Lipid-based membrane domains: physics meets immunology.Synthesis of sphingolipids with very long chain fatty acids but not ergosterol is required for routing of newly synthesized plasma membrane ATPase to the cell surface of yeast.Sphingolipid C4 hydroxylation influences properties of yeast detergent-insoluble glycolipid-enriched membranes.TMD1 domain and CRAC motif determine the association and disassociation of MxIRT1 with detergent-resistant membranes.Very long-chain fatty acid-containing lipids rather than sphingolipids per se are required for raft association and stable surface transport of newly synthesized plasma membrane ATPase in yeast.Pdr18 is involved in yeast response to acetic acid stress counteracting the decrease of plasma membrane ergosterol content and order.Cytotoxicity of an Anti-cancer Lysophospholipid through Selective Modification of Lipid Raft Composition
P2860
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P2860
A specific structural requirement for ergosterol in long-chain fatty acid synthesis mutants important for maintaining raft domains in yeast.
description
2002 nî lūn-bûn
@nan
2002 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
A specific structural requirem ...... taining raft domains in yeast.
@ast
A specific structural requirem ...... taining raft domains in yeast.
@en
A specific structural requirem ...... taining raft domains in yeast.
@nl
type
label
A specific structural requirem ...... taining raft domains in yeast.
@ast
A specific structural requirem ...... taining raft domains in yeast.
@en
A specific structural requirem ...... taining raft domains in yeast.
@nl
prefLabel
A specific structural requirem ...... taining raft domains in yeast.
@ast
A specific structural requirem ...... taining raft domains in yeast.
@en
A specific structural requirem ...... taining raft domains in yeast.
@nl
P2093
P2860
P356
P1476
A specific structural requirem ...... taining raft domains in yeast.
@en
P2093
Christoph Zenzmaier
Erich Leitner
Marlis Eisenkolb
Roger Schneiter
P2860
P304
P356
10.1091/MBC.E02-02-0116
P577
2002-12-01T00:00:00Z