scholarly article | Q13442814 |
P50 | author | Amir M. Farnoud | Q92174448 |
Maurizio Del Poeta | Q111269485 | ||
P2093 | author name string | Antonella Rella | |
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Apoptogenic effects of β-sitosterol glucoside from Castanopsis indica leaves | Q86959046 | ||
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Correlation of elastase production by some strains of Aspergillus fumigatus with ability to cause pulmonary invasive aspergillosis in mice | Q24658562 | ||
Virulence factors of medically important fungi | Q24683790 | ||
Cryptococcus neoformans-derived microvesicles enhance the pathogenesis of fungal brain infection | Q27341616 | ||
Functional rafts in cell membranes | Q27860768 | ||
Ergosteryl-β-glucosidase (Egh1) involved in sterylglucoside catabolism and vacuole formation in Saccharomyces cerevisiae | Q27931026 | ||
Plasma membrane proton ATPase Pma1p requires raft association for surface delivery in yeast | Q27932251 | ||
Lipid rafts function in biosynthetic delivery of proteins to the cell surface in yeast | Q27932650 | ||
Cell surface polarization during yeast mating | Q27934709 | ||
Cloning and functional expression of UGT genes encoding sterol glucosyltransferases from Saccharomyces cerevisiae, Candida albicans, Pichia pastoris, and Dictyostelium discoideum | Q27936426 | ||
Ergosterol is required for targeting of tryptophan permease to the yeast plasma membrane | Q27937645 | ||
Cholesterol, inflammation and innate immunity | Q28086912 | ||
Characterization of yeast extracellular vesicles: evidence for the participation of different pathways of cellular traffic in vesicle biogenesis | Q28474369 | ||
Comparative lipidomics in clinical isolates of Candida albicans reveal crosstalk between mitochondria, cell wall integrity and azole resistance | Q28480747 | ||
Dectin-1 is a major beta-glucan receptor on macrophages | Q28593983 | ||
Sorting of GPI-anchored proteins to glycolipid-enriched membrane subdomains during transport to the apical cell surface | Q29547857 | ||
Apical sterol-rich membranes are essential for localizing cell end markers that determine growth directionality in the filamentous fungus Aspergillus nidulans | Q30480990 | ||
Extracellular vesicles from Cryptococcus neoformans modulate macrophage functions | Q30493958 | ||
Phase equilibria of cholesterol/dipalmitoylphosphatidylcholine mixtures: 2H nuclear magnetic resonance and differential scanning calorimetry | Q30571359 | ||
Phylogenetic analysis of the UDP-glycosyltransferase multigene family of Arabidopsis thaliana. | Q31480020 | ||
An A643T mutation in the transcription factor Upc2p causes constitutive ERG11 upregulation and increased fluconazole resistance in Candida albicans | Q33559158 | ||
Evidence for possible involvement of an elastolytic serine protease in aspergillosis. | Q33599272 | ||
Antifungal agents: mode of action, mechanisms of resistance, and correlation of these mechanisms with bacterial resistance | Q33749111 | ||
Potential role of phospholipases in virulence and fungal pathogenesis | Q33812431 | ||
Prevalence of molecular mechanisms of resistance to azole antifungal agents in Candida albicans strains displaying high-level fluconazole resistance isolated from human immunodeficiency virus-infected patients | Q33983022 | ||
A microscopic interaction model of maximum solubility of cholesterol in lipid bilayers | Q34170267 | ||
Glycosyltransferases in secondary plant metabolism: tranquilizers and stimulant controllers | Q34317234 | ||
Lipidomic analysis of extracellular vesicles from the pathogenic phase of Paracoccidioides brasiliensis. | Q34321418 | ||
Lipid raft polarization contributes to hyphal growth in Candida albicans | Q34361022 | ||
Sterol glycosides and cerebrosides accumulate in Pichia pastoris, Rhynchosporium secalis and other fungi under normal conditions or under heat shock and ethanol stress | Q43621887 | ||
Sphingolipids are required for the stable membrane association of glycosylphosphatidylinositol-anchored proteins in yeast | Q44189953 | ||
Cholesteryl glucoside-induced protection against gastric ulcer | Q44570775 | ||
Synthesis of steryl glucoside in Bakers yeast | Q44581639 | ||
Amphotericin B nephrotoxicity: the adverse consequences of altered membrane properties. | Q45103287 | ||
Disruption of the sphingolipid Delta8-desaturase gene causes a delay in morphological changes in Candida albicans | Q45413575 | ||
The role of flotillin FloA and stomatin StoA in the maintenance of apical sterol-rich membrane domains and polarity in the filamentous fungus Aspergillus nidulans. | Q46526736 | ||
beta-Sitosterol and beta-sitosterol glucoside stimulate human peripheral blood lymphocyte proliferation: implications for their use as an immunomodulatory vitamin combination | Q46819655 | ||
Glucosylceramide synthase is essential for alfalfa defensin-mediated growth inhibition but not for pathogenicity of Fusarium graminearum. | Q46972707 | ||
Defensins from insects and plants interact with fungal glucosylceramides | Q47398270 | ||
Glucosylceramide synthases, a gene family responsible for the biosynthesis of glucosphingolipids in animals, plants, and fungi | Q48354725 | ||
Sec6-dependent sorting of fungal extracellular exosomes and laccase of Cryptococcus neoformans. | Q50603104 | ||
Purification of a Membrane-Bound UDP-Glucose:Sterol [beta]-D-Glucosyltransferase Based on Its Solubility in Diethyl Ether. | Q50770217 | ||
Immunoregulatory activity by daucosterol, a beta-sitosterol glycoside, induces protective Th1 immune response against disseminated Candidiasis in mice. | Q53576625 | ||
Resistance to polyene antibiotics and correlated sterol changes in two isolates of Candida tropicalis from a patient with an amphotericin B-resistant funguria. | Q53743852 | ||
Membrane fluidity affects functions of Cdr1p, a multidrug ABC transporter of Candida albicans. | Q54097600 | ||
Cholesterol glucosylation promotes immune evasion by Helicobacter pylori | Q56984433 | ||
Lipid Rafts in Protein Sorting and Cell Polarity in Budding Yeast Saccharomyces cerevisiae | Q57375641 | ||
Phase equilibria in the phosphatidylcholine-cholesterol system | Q69441432 | ||
Isolation and wall analysis of dimorphic mutants of Paracoccidioides brasiliensis | Q70298843 | ||
Evidence for the involvement of a 66 kDa membrane protein in the synthesis of sterolglucoside in Saccharomyces cerevisiae | Q70969461 | ||
Amphotericin B resistant isolates of Cryptococcus neoformans without alteration in sterol biosynthesis | Q71523746 | ||
Composition and distribution of lipids within cells of Saccharomyces cerevisiae | Q71683331 | ||
Mixed monolayers of phospholipids and cholesterol | Q72535754 | ||
Biosynthesis of the core region of yeast mannoproteins. Formation of a glucosylated dolichol-bound oligosaccharide precursor, its transfer to protein and subsequent modification | Q72615447 | ||
Resistance to fluconazole and cross-resistance to amphotericin B in Candida albicans from AIDS patients caused by defective sterol delta5,6-desaturation | Q72989562 | ||
A randomised placebo-controlled trial of the efficacy of beta-sitosterol and its glucoside as adjuvants in the treatment of pulmonary tuberculosis | Q74259175 | ||
Simvastatin reduces ergosterol levels, inhibits growth and causes loss of mtDNA in Candida glabrata | Q79673045 | ||
PAK kinases Ste20 and Pak1 govern cell polarity at different stages of mating in Cryptococcus neoformans | Q37537946 | ||
The functions of steryl glycosides come to those who wait: Recent advances in plants, fungi, bacteria and animals | Q37688647 | ||
Fungal Biofilms: Relevance in the Setting of Human Disease | Q37887512 | ||
Role of phospholipases in fungal fitness, pathogenicity, and drug development - lessons from cryptococcus neoformans | Q37891813 | ||
Fungal glucosylceramides: from structural components to biologically active targets of new antimicrobials | Q37949339 | ||
Vesicular transport systems in fungi | Q37955954 | ||
Immunological functions of steryl glycosides | Q38039373 | ||
Vesicular mechanisms of traffic of fungal molecules to the extracellular space | Q38102803 | ||
Where do they come from and where do they go: candidates for regulating extracellular vesicle formation in fungi | Q38104257 | ||
Raft-like membrane domains in pathogenic microorganisms. | Q38503879 | ||
Macrophage cholesterol depletion and its effect on the phagocytosis of Cryptococcus neoformans | Q38924500 | ||
Human antibodies against a purified glucosylceramide from Cryptococcus neoformans inhibit cell budding and fungal growth | Q39517451 | ||
Multiple molecular mechanisms contribute to a stepwise development of fluconazole resistance in clinical Candida albicans strains. | Q39559578 | ||
Role of host glycosphingolipids on Paracoccidioides brasiliensis adhesion | Q39634663 | ||
In vitro low-level resistance to azoles in Candida albicans is associated with changes in membrane lipid fluidity and asymmetry | Q39651398 | ||
Paracoccidioides brasileensis: Cell wall structure and virulence | Q39715050 | ||
Fluconazole resistance due to energy-dependent drug efflux in Candida glabrata | Q39780155 | ||
Interaction of epithelial cell membrane rafts with Paracoccidioides brasiliensis leads to fungal adhesion and Src-family kinase activation | Q39993221 | ||
Virulence factors of Cryptococcus neoformans | Q40927145 | ||
Sterols in yeast subcellular fractions | Q40969998 | ||
Sterylglucoside catabolism in Cryptococcus neoformans with endoglycoceramidase-related protein 2 (EGCrP2), the first steryl-β-glucosidase identified in fungi | Q41681725 | ||
Vesicular transport in Histoplasma capsulatum: an effective mechanism for trans-cell wall transfer of proteins and lipids in ascomycetes | Q41809998 | ||
Extracellular vesicles produced by Cryptococcus neoformans contain protein components associated with virulence. | Q41913077 | ||
Multidrug transporters CaCdr1p and CaMdr1p of Candida albicans display different lipid specificities: both ergosterol and sphingolipids are essential for targeting of CaCdr1p to membrane rafts | Q41915187 | ||
Yeast lipids can phase-separate into micrometer-scale membrane domains | Q41965289 | ||
The pathogenic fungus Paracoccidioides brasiliensis exports extracellular vesicles containing highly immunogenic α-Galactosyl epitopes. | Q41984033 | ||
The cell-envelope glycolipids of baker's yeast | Q42003841 | ||
The lipid composition and permeability to azole of an azole- and polyene-resistant mutant of Candida albicans | Q42217506 | ||
Inositol phosphosphingolipid phospholipase C1 regulates plasma membrane ATPase (Pma1) stability in Cryptococcus neoformans | Q42266243 | ||
Correction: synthesis and biological properties of fungal glucosylceramide. | Q42539343 | ||
Characterization of UDP-glucose:ceramide glucosyltransferases from different organisms | Q42641945 | ||
Mannosylinositol phosphorylceramide is a major sphingolipid component and is required for proper localization of plasma-membrane proteins in Schizosaccharomyces pombe | Q43101001 | ||
Candida albicans sphingolipid C9-methyltransferase is involved in hyphal elongation | Q43216785 | ||
Bioactive compounds from sour orange inhibit colon cancer cell proliferation and induce cell cycle arrest. | Q43226167 | ||
Simvastatin inhibits Candida albicans biofilm in vitro | Q43286148 | ||
The role of phytosterols and phytosterolins in immune modulation: a review of the past 10 years | Q34436867 | ||
Lipid rafts in Cryptococcus neoformans concentrate the virulence determinants phospholipase B1 and Cu/Zn superoxide dismutase | Q34442091 | ||
Cell wall composition of two strains of Blastomyces dermatitidis exhibiting differences in virulence for mice | Q34470484 | ||
Glucosylceramide synthase is an essential regulator of pathogenicity of Cryptococcus neoformans | Q34628045 | ||
Bioactive sphingolipids: metabolism and function | Q34883222 | ||
Polyene-resistant mutants of Aspergillus fennelliae: sterol content and genetics | Q34912480 | ||
Resistance of cell membranes to different detergents | Q35022104 | ||
Recently discovered functions of glucosylceramides in plants and fungi | Q35162993 | ||
Mechanism of fluconazole resistance in Candida albicans biofilms: phase-specific role of efflux pumps and membrane sterols | Q35164903 | ||
Invasion of Cryptococcus neoformans into human brain microvascular endothelial cells is mediated through the lipid rafts-endocytic pathway via the dual specificity tyrosine phosphorylation-regulated kinase 3 (DYRK3) | Q35266439 | ||
Vesicular polysaccharide export in Cryptococcus neoformans is a eukaryotic solution to the problem of fungal trans-cell wall transport | Q35641043 | ||
Quality control of fungus-specific glucosylceramide in Cryptococcus neoformans by endoglycoceramidase-related protein 1 (EGCrP1) | Q35643688 | ||
Identification of an N-acetylglucosamine transporter that mediates hyphal induction in Candida albicans. | Q35650752 | ||
Identification of a New Class of Antifungals Targeting the Synthesis of Fungal Sphingolipids | Q35672458 | ||
Fungal biofilm resistance | Q35821475 | ||
Methylation of glycosylated sphingolipid modulates membrane lipid topography and pathogenicity of Cryptococcus neoformans | Q35827998 | ||
Role of Sterylglucosidase 1 (Sgl1) on the pathogenicity of Cryptococcus neoformans: potential applications for vaccine development | Q35938253 | ||
Lipidomics of Candida albicans biofilms reveals phase-dependent production of phospholipid molecular classes and role for lipid rafts in biofilm formation | Q35960269 | ||
Biosynthesis and immunogenicity of glucosylceramide in Cryptococcus neoformans and other human pathogens | Q36095320 | ||
Soluble glucan is internalized and trafficked to the Golgi apparatus in macrophages via a clathrin-mediated, lipid raft-regulated mechanism | Q36174179 | ||
Candida biofilm: a well-designed protected environment | Q36190737 | ||
How principles of domain formation in model membranes may explain ambiguities concerning lipid raft formation in cells | Q36286604 | ||
Monoclonal antibody to fungal glucosylceramide protects mice against lethal Cryptococcus neoformans infection | Q36313467 | ||
Gangliosides as components of lipid membrane domains. | Q36597110 | ||
UDP-glucose:sterol glucosyltransferase: cloning and functional expression in Escherichia coli | Q36888372 | ||
Isolation and characterization of an elastinolytic proteinase from Aspergillus flavus | Q36986733 | ||
Cell walls from avirulent variants of Histoplasma capsulatum lack alpha-(1,3)-glucan | Q37001114 | ||
MesA, a novel fungal protein required for the stabilization of polarity axes in Aspergillus nidulans | Q37031693 | ||
Determination of campesterol, stigmasterol, and beta-sitosterol in saw palmetto raw materials and dietary supplements by gas chromatography: collaborative study | Q37037570 | ||
The impact of proteomics on the understanding of functions and biogenesis of fungal extracellular vesicles | Q37100258 | ||
Lipophilic dye staining of Cryptococcus neoformans extracellular vesicles and capsule | Q37355720 | ||
Activated dectin-1 localizes to lipid raft microdomains for signaling and activation of phagocytosis and cytokine production in dendritic cells. | Q37372186 | ||
Lipid signalling in pathogenic fungi | Q37482149 | ||
Fluorescence Studies of the Binding of the Polyene Antibiotics Filipin III, Amphotericin B, Nystatin, and Lagosin to Cholesterol | Q37504058 | ||
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 63-72 | |
P577 | publication date | 2015-12-15 | |
P1433 | published in | Progress in Lipid Research | Q15757018 |
P1476 | title | Plasma membrane lipids and their role in fungal virulence | |
P478 | volume | 61 |
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