Lipid rafts have different sizes depending on membrane composition: a time-resolved fluorescence resonance energy transfer study.
about
Fluorophores, environments, and quantification techniques in the analysis of transmembrane helix interaction using FRETTime-resolved fluorescence in lipid bilayers: selected applications and advantages over steady stateA fluorescent glycolipid-binding peptide probe traces cholesterol dependent microdomain-derived trafficking pathwaysCaveolae contribute to the apoptosis resistance induced by the alpha(1A)-adrenoceptor in androgen-independent prostate cancer cellsPhase diagrams of lipid mixtures relevant to the study of membrane rafts.Membrane domain formation, interdigitation, and morphological alterations induced by the very long chain asymmetric C24:1 ceramide.Phase diagram of a polyunsaturated lipid mixture: Brain sphingomyelin/1-stearoyl-2-docosahexaenoyl-sn-glycero-3-phosphocholine/cholesterol.Hepatitis C virus core protein binding to lipid membranes: the role of domains 1 and 2.Phase diagrams and lipid domains in multicomponent lipid bilayer mixtures.Development of fluorophore dynamics imaging as a probe for lipid domains in model vesicles and cell membranes.Use of dansyl-cholestanol as a probe of cholesterol behavior in membranes of living cells.Reconstituting ring-rafts in bud-mimicking topography of model membranes.Relationship between CYP1A2 localization and lipid microdomain formation as a function of lipid composition.Fluorescence-quenching and resonance energy transfer studies of lipid microdomains in model and biological membranes.Illuminating the lateral organization of cell-surface CD24 and CD44 through plasmon coupling between Au nanoparticle immunolabels.Gel domains in the plasma membrane of Saccharomyces cerevisiae: highly ordered, ergosterol-free, and sphingolipid-enriched lipid rafts.Shear rheology of lipid monolayers and insights on membrane fluidity.Nanoparticle-induced surface reconstruction of phospholipid membranes.Temperature and composition dependence of the interaction of delta-lysin with ternary mixtures of sphingomyelin/cholesterol/POPC.Lipid peroxides promote large rafts: effects of excitation of probes in fluorescence microscopy and electrochemical reactions during vesicle formation.Material properties of matrix lipids determine the conformation and intermolecular reactivity of diacetylenic phosphatidylcholine in the lipid bilayer.Sphingomyelin and sphingomyelin synthase (SMS) in the malignant transformation of glioma cells and in 2-hydroxyoleic acid therapy.Investigation of domain formation in sphingomyelin/cholesterol/POPC mixtures by fluorescence resonance energy transfer and Monte Carlo simulations.Toward a mathematical model of the assembly and disassembly of membrane microdomains: comparison with experimental models.Effect of membrane microheterogeneity and domain size on fluorescence resonance energy transfer.Imaging and shape analysis of GUVs as model plasma membranes: effect of trans DOPC on membrane propertiesInhibition of cytokine signaling in human retinal endothelial cells through modification of caveolae/lipid rafts by docosahexaenoic acidVisualization of membrane rafts using a perylene monoimide derivative and fluorescence lifetime imagingLipid rafts, fluid/fluid phase separation, and their relevance to plasma membrane structure and function.DHA-fluorescent probe is sensitive to membrane order and reveals molecular adaptation of DHA in ordered lipid microdomainsVisualization of detergent solubilization of membranes: implications for the isolation of raftsLipid rafts: contentious only from simplistic standpointsPhase behavior and domain size in sphingomyelin-containing lipid bilayers.Role of ganglioside metabolism in the pathogenesis of Alzheimer's disease--a reviewLipid mediators in membrane rafts are important determinants of human health and disease.Lipids and lipid modifications in the regulation of membrane traffic.Cholesterol interactions with fluid-phase phospholipids: effect on the lateral organization of the bilayer.Phenomenological model and phase behavior of saturated and unsaturated lipids and cholesterolRas acylation, compartmentalization and signaling nanoclusters (Review).Changes in membrane biophysical properties induced by sphingomyelinase depend on the sphingolipid N-acyl chain.
P2860
Q26851539-9F2C4758-76DA-4492-AC22-350C0708F028Q27007127-E78616BB-773D-4654-9788-913C929B76B7Q27300755-DF4C2797-48A5-4D43-84DB-335DEC55BFB0Q28476183-26C54BA0-7EEB-4186-A513-A68B57524F91Q30485547-0BD65446-066E-4548-8C2C-C43D340FA5DFQ30486627-D4DAF6BB-8DCA-4BAD-95A7-E18E76E4D3BEQ30683916-E392C912-C197-4F54-A442-E39C3D5E7485Q33313498-FCE5290D-4B0F-4919-AAA3-F35E42C26713Q33370820-9AE97EB2-2FE0-4113-8E83-A58F1B705D83Q33720810-74A567FC-6ED7-4350-9235-4B1766180756Q33784523-345E99E9-5AAD-48B9-8BF1-B06A03AF71FCQ34014645-AFFD5C62-5DE3-4C4E-8C67-0A4C98DC3E01Q34365496-8290C80C-67E3-4A8C-8362-2AA0B33CE71EQ34513225-FD13391C-DD6C-4CBF-8812-485C51A28C1CQ34548478-9FFCCEDB-C2C0-44B3-BD9E-6BC356E0B739Q34568292-C4948A16-7EEE-4708-B63C-DCD15A0E3C67Q34794494-9E7CA1E1-0004-43DD-8DEF-9DE4A51598FEQ34881067-48C8A19C-8CEE-4E5D-AA6D-621F959A3EA0Q35012281-A4FF209D-29EF-4A78-9DFC-AEFC749BC9EAQ35012324-7D1055AA-8514-457A-921C-5DBCE4D17F51Q35613391-EAB87457-E58D-4A83-9264-87AF167C98FFQ35621265-64933D6E-C87A-414D-A750-C57D273263BEQ35781213-D552F52C-0442-4D35-AF7C-CF0B6EA4DF29Q35812285-9318E9FA-1F3B-44C3-A9DD-2BE44E4B09D5Q35850985-F32B2C2E-8134-45FF-AD18-202161F5A515Q35963341-F4211BB7-5276-41D0-B3EE-1B95A79C3CA3Q35989359-2A33F6D8-5D79-44A1-8DF5-8C699A2318C6Q36008685-5FAFBE83-5C18-47C9-A7ED-829A294C564CQ36287389-A9B3291A-DEBC-4AD9-9770-5B4F3CA4F541Q36360840-C6843D04-0668-4B19-B3B0-FEBC182A9E3EQ36402293-32222468-CBD2-494E-9980-8DCC3B1DA981Q36453789-55A14400-CA86-40D5-A460-10D5D4AE7EF0Q36639938-831426AF-5CA4-46F2-BA28-14650AC98D80Q36662671-C5ED7363-C5DF-40CC-B205-282CFA4E1E3BQ36825607-3BED95F9-3090-45D4-80B6-E7538DE5FD08Q36891287-792B9E7F-E540-4CEF-9D81-FB50B328C316Q36908352-A4D7D221-7145-4679-9356-02AFC5C00387Q36957349-57FDDC38-6849-4703-8A55-8B174DFED1B2Q37359986-3E21037A-240F-4EF8-B8EF-CCEC41A405DBQ37590278-FCE224F1-52D3-4C78-A8E1-16C2D0D467B8
P2860
Lipid rafts have different sizes depending on membrane composition: a time-resolved fluorescence resonance energy transfer study.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Lipid rafts have different siz ...... sonance energy transfer study.
@en
Lipid rafts have different siz ...... sonance energy transfer study.
@nl
type
label
Lipid rafts have different siz ...... sonance energy transfer study.
@en
Lipid rafts have different siz ...... sonance energy transfer study.
@nl
prefLabel
Lipid rafts have different siz ...... sonance energy transfer study.
@en
Lipid rafts have different siz ...... sonance energy transfer study.
@nl
P50
P1476
Lipid rafts have different siz ...... esonance energy transfer study
@en
P2093
Luís M S Loura
Rodrigo F M de Almeida
P304
P356
10.1016/J.JMB.2004.12.026
P407
P577
2005-01-12T00:00:00Z