Tsc13p is required for fatty acid elongation and localizes to a novel structure at the nuclear-vacuolar interface in Saccharomyces cerevisiae
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SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorderDisruptions 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 vesiclesGlobal analysis of the yeast lipidome by quantitative shotgun mass spectrometryFunctional characterization of the Arabidopsis beta-ketoacyl-coenzyme A reductase candidates of the fatty acid elongaseA conserved ER targeting motif in three families of lipid binding proteins and in Opi1p binds VAPMetabolism and regulation of glycerolipids in the yeast Saccharomyces cerevisiaeLcb4p is a key regulator of ceramide synthesis from exogenous long chain sphingoid base in Saccharomyces cerevisiae.Obese yeast: triglyceride lipolysis is functionally conserved from mammals to yeast.C26-CoA-dependent ceramide synthesis of Saccharomyces cerevisiae is operated by Lag1p and Lac1pDual targeting of Osh1p, a yeast homologue of oxysterol-binding protein, to both the Golgi and the nucleus-vacuole junction.Membrane topology and essential amino acid residues of Phs1, a 3-hydroxyacyl-CoA dehydratase involved in very long-chain fatty acid elongation.Csg1p and newly identified Csh1p function in mannosylinositol phosphorylceramide synthesis by interacting with Csg2p.The Saccharomyces cerevisiae YBR159w gene encodes the 3-ketoreductase of the microsomal fatty acid elongase.Piecemeal microautophagy of nucleus in Saccharomyces cerevisiae.Effects on vesicular transport pathways at the late endosome in cells with limited very long-chain fatty acids.Probing the membrane environment of the TOR kinases reveals functional interactions between TORC1, actin, and membrane trafficking in Saccharomyces cerevisiaeStorage reserve accumulation in Arabidopsis: metabolic and developmental control of seed fillingA Chemogenomic Screen Reveals Novel Snf1p/AMPK Independent Regulators of Acetyl-CoA CarboxylaseMannosyl-diinositolphospho-ceramide, the major yeast plasma membrane sphingolipid, governs toxicity of Kluyveromyces lactis zymocin.Inheritance of yeast nuclear pore complexes requires the Nsp1p subcomplexThe spatial organization of lipid synthesis in the yeast Saccharomyces cerevisiae derived from large scale green fluorescent protein tagging and high resolution microscopy.A split-ubiquitin two-hybrid screen for proteins physically interacting with the yeast amino acid transceptor Gap1 and ammonium transceptor Mep2.A Saccharomyces cerevisiae gene required for heterologous fatty acid elongase activity encodes a microsomal beta-keto-reductase.Characterization of the early response of the orchid, Phalaenopsis amabilis, to Erwinia chrysanthemi infection using expression profiling.Dual functions of the trans-2-enoyl-CoA reductase TER in the sphingosine 1-phosphate metabolic pathway and in fatty acid elongation.Microbial type I fatty acid synthases (FAS): major players in a network of cellular FAS systems.Yeast nuclear envelope subdomains with distinct abilities to resist membrane expansion.Lipid metabolism and vesicle trafficking: more than just greasing the transport machinery.A post-genomic approach to understanding sphingolipid metabolism in Arabidopsis thalianaYeast sphingolipids: recent developments in understanding biosynthesis, regulation, and function.Thematic review series: sphingolipids. New insights into sphingolipid metabolism and function in budding yeast.The very-long-chain hydroxy fatty acyl-CoA dehydratase PASTICCINO2 is essential and limiting for plant development.Yeast sphingolipid metabolism: clues and connections.Oxysterol binding proteins: in more than one place at one time?Lipid partitioning at the nuclear envelope controls membrane biogenesisPolyunsaturated fatty acids: biotechnology.Novel type II fatty acid biosynthesis (FAS II) inhibitors as multistage antimalarial agentsPlant surface lipid biosynthetic pathways and their utility for metabolic engineering of waxes and hydrocarbon biofuels.Characterization of two cotton cDNAs encoding trans-2-enoyl-CoA reductase reveals a putative novel NADPH-binding motif.
P2860
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P2860
Tsc13p is required for fatty acid elongation and localizes to a novel structure at the nuclear-vacuolar interface in Saccharomyces cerevisiae
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2001 nî lūn-bûn
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2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
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2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Tsc13p is required for fatty a ...... ce in Saccharomyces cerevisiae
@ast
Tsc13p is required for fatty a ...... ce in Saccharomyces cerevisiae
@en
Tsc13p is required for fatty a ...... ce in Saccharomyces cerevisiae
@nl
type
label
Tsc13p is required for fatty a ...... ce in Saccharomyces cerevisiae
@ast
Tsc13p is required for fatty a ...... ce in Saccharomyces cerevisiae
@en
Tsc13p is required for fatty a ...... ce in Saccharomyces cerevisiae
@nl
prefLabel
Tsc13p is required for fatty a ...... ce in Saccharomyces cerevisiae
@ast
Tsc13p is required for fatty a ...... ce in Saccharomyces cerevisiae
@en
Tsc13p is required for fatty a ...... ce in Saccharomyces cerevisiae
@nl
P2093
P2860
P921
P1476
Tsc13p is required for fatty a ...... ce in Saccharomyces cerevisiae
@en
P2093
C E Martin
D Bacikova
S D Kohlwein
P2860
P304
P356
10.1128/MCB.21.1.109-125.2001
P407
P577
2001-01-01T00:00:00Z