The yeast gene ERG6 is required for normal membrane function but is not essential for biosynthesis of the cell-cycle-sparking sterol
about
Folding-competent and folding-defective forms of ricin A chain have different fates after retrotranslocation from the endoplasmic reticulumA Simple Chemical Method for Rendering Wild-Type Yeast Permeable to Brefeldin A That Does Not Require the Presence of anerg6MutationHigh rates of actin filament turnover in budding yeast and roles for actin in establishment and maintenance of cell polarity revealed using the actin inhibitor latrunculin-A.Yeast osmosensor Sln1 and plant cytokinin receptor Cre1 respond to changes in turgor pressure.Dual targeting of Osh1p, a yeast homologue of oxysterol-binding protein, to both the Golgi and the nucleus-vacuole junction.Regulation of iron homeostasis mediated by the heme-binding protein Dap1 (damage resistance protein 1) via the P450 protein Erg11/Cyp51.Cell surface polarization during yeast mating.Overlapping functions of the yeast oxysterol-binding protein homologues.Dual localization of squalene epoxidase, Erg1p, in yeast reflects a relationship between the endoplasmic reticulum and lipid particlesA genetic analysis of glucocorticoid receptor signaling. Identification and characterization of ligand-effect modulators in Saccharomyces cerevisiae.Ergosterol is required for targeting of tryptophan permease to the yeast plasma membrane.Saccharomyces cerevisiae Na+/H+ antiporter Nha1p associates with lipid rafts and requires sphingolipid for stable localization to the plasma membrane.Kes1p shares homology with human oxysterol binding protein and participates in a novel regulatory pathway for yeast Golgi-derived transport vesicle biogenesis.Mutagenesis of the putative sterol-sensing domain of yeast Niemann Pick C-related protein reveals a primordial role in subcellular sphingolipid distribution.Comparison of in vitro activities of camptothecin and nitidine derivatives against fungal and cancer cellsSterol methyltransferase 1 controls the level of cholesterol in plantsA Screen for Germination Mutants in Saccharomyces cerevisiae.Global screening of genes essential for growth in high-pressure and cold environments: searching for basic adaptive strategies using a yeast deletion libraryComparative genomics allowed the identification of drug targets against human fungal pathogens.Discovery of a small molecule targeting IRA2 deletion in budding yeast and neurofibromin loss in malignant peripheral nerve sheath tumor cellsDirect selection for mutants with increased K+ transport in Saccharomyces cerevisiae.BFR1, a multicopy suppressor of brefeldin A-induced lethality, is implicated in secretion and nuclear segregation in Saccharomyces cerevisiae.Calcineurin is essential for survival during membrane stress in Candida albicans.Selective ATP-competitive inhibitors of TOR suppress rapamycin-insensitive function of TORC2 in Saccharomyces cerevisiae.Diversity in genetic in vivo methods for protein-protein interaction studies: from the yeast two-hybrid system to the mammalian split-luciferase system.Identification of cDNA clones encoding valosin-containing protein and other plant plasma membrane-associated proteins by a general immunoscreening strategy.A specific structural requirement for ergosterol in long-chain fatty acid synthesis mutants important for maintaining raft domains in yeast.Puromycin- and methotrexate-resistance cassettes and optimized Cre-recombinase expression plasmids for use in yeastDual effects of plant steroidal alkaloids on Saccharomyces cerevisiae.Distribution and functions of sterols and sphingolipids.Cumulative mutations affecting sterol biosynthesis in the yeast Saccharomyces cerevisiae result in synthetic lethality that is suppressed by alterations in sphingolipid profiles.Molecular cloning, characterization, and overexpression of ERG7, the Saccharomyces cerevisiae gene encoding lanosterol synthase.Naturally azole-resistant Leishmania braziliensis promastigotes are rendered susceptible in the presence of terbinafine: comparative study with azole-susceptible Leishmania mexicana promastigotes.Yeast synthetic biology platform generates novel chemical structures as scaffolds for drug discovery.Candida albicans mutations in the ergosterol biosynthetic pathway and resistance to several antifungal agents.Aerobic isolation of an ERG24 null mutant of Saccharomyces cerevisiae.DNA repair functions that control sensitivity to topoisomerase-targeting drugsFenpropimorph affects uptake of uracil and cytosine in Saccharomyces cerevisiaeMethylation of glycosylated sphingolipid modulates membrane lipid topography and pathogenicity of Cryptococcus neoformans.Tension-dependent nucleosome remodeling at the pericentromere in yeast
P2860
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P2860
The yeast gene ERG6 is required for normal membrane function but is not essential for biosynthesis of the cell-cycle-sparking sterol
description
1989 nî lūn-bûn
@nan
1989 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
The yeast gene ERG6 is require ...... the cell-cycle-sparking sterol
@ast
The yeast gene ERG6 is require ...... the cell-cycle-sparking sterol
@en
The yeast gene ERG6 is require ...... he cell-cycle-sparking sterol.
@nl
type
label
The yeast gene ERG6 is require ...... the cell-cycle-sparking sterol
@ast
The yeast gene ERG6 is require ...... the cell-cycle-sparking sterol
@en
The yeast gene ERG6 is require ...... he cell-cycle-sparking sterol.
@nl
prefLabel
The yeast gene ERG6 is require ...... the cell-cycle-sparking sterol
@ast
The yeast gene ERG6 is require ...... the cell-cycle-sparking sterol
@en
The yeast gene ERG6 is require ...... he cell-cycle-sparking sterol.
@nl
P2093
P2860
P356
P1476
The yeast gene ERG6 is require ...... the cell-cycle-sparking sterol
@en
P2093
P2860
P304
P356
10.1128/MCB.9.8.3447
P407
P577
1989-08-01T00:00:00Z