scholarly article | Q13442814 |
P50 | author | Tony Ng | Q30582909 |
P2093 | author name string | G Schiavo | |
J Herreros | |||
P2860 | cites work | Extraction of cholesterol with methyl-beta-cyclodextrin perturbs formation of clathrin-coated endocytic vesicles | Q24657869 |
Internalization and processing of transferrin and the transferrin receptor in human carcinoma A431 cells | Q24681319 | ||
The structures of the H(C) fragment of tetanus toxin with carbohydrate subunit complexes provide insight into ganglioside binding | Q27621792 | ||
Functional rafts in cell membranes | Q27860768 | ||
Lipid rafts and signal transduction | Q28131735 | ||
Association of GAP-43 with detergent-resistant membranes requires two palmitoylated cysteine residues | Q28285568 | ||
HC fragment (C-terminal portion of the heavy chain) of tetanus toxin activates protein kinase C isoforms and phosphoproteins involved in signal transduction | Q28364243 | ||
Functionally different GPI proteins are organized in different domains on the neuronal surface | Q28580230 | ||
Thymocytes in Thy-1-/- mice show augmented TCR signaling and impaired differentiation | Q28580247 | ||
Structure and function of sphingolipid- and cholesterol-rich membrane rafts | Q29618518 | ||
Lipid domain structure of the plasma membrane revealed by patching of membrane components | Q29620204 | ||
Tissue-specific N-glycosylation, site-specific oligosaccharide patterns and lentil lectin recognition of rat Thy-1 | Q30403136 | ||
Three dimensional image restoration in fluorescence lifetime imaging microscopy | Q30649360 | ||
Cholera toxin is found in detergent-insoluble rafts/domains at the cell surface of hippocampal neurons but is internalized via a raft-independent mechanism | Q31672781 | ||
Looking at lipid rafts? | Q33592628 | ||
Exploitation of major histocompatibility complex class I molecules and caveolae by simian virus 40. | Q33683316 | ||
Neurotoxins affecting neuroexocytosis | Q33881286 | ||
Lipid trafficking and sorting: how cholesterol is filling gaps | Q33954545 | ||
The renaissance of fluorescence resonance energy transfer | Q34019505 | ||
Role of membrane organization and membrane domains in endocytic lipid trafficking | Q34156593 | ||
High-resolution FRET microscopy of cholera toxin B-subunit and GPI-anchored proteins in cell plasma membranes | Q34709520 | ||
High cell sensitivity to Helicobacter pylori VacA toxin depends on a GPI-anchored protein and is not blocked by inhibition of the clathrin-mediated pathway of endocytosis | Q34777823 | ||
Expression of botulinum toxin binding sites in Xenopus oocytes | Q35549101 | ||
SNARE proteins are highly enriched in lipid rafts in PC12 cells: implications for the spatial control of exocytosis. | Q35888471 | ||
Selective binding, uptake, and retrograde transport of tetanus toxin by nerve terminals in the rat iris. An electron microscope study using colloidal gold as a tracer | Q36199087 | ||
Filipin-sensitive caveolae-mediated transport in endothelium: reduced transcytosis, scavenger endocytosis, and capillary permeability of select macromolecules | Q36234903 | ||
Endocytosis of GPI-anchored proteins in human lymphocytes: role of glycolipid-based domains, actin cytoskeleton, and protein kinases | Q36236870 | ||
Filipin-dependent inhibition of cholera toxin: evidence for toxin internalization and activation through caveolae-like domains | Q36255404 | ||
Ganglioside structure dictates signal transduction by cholera toxin and association with caveolae-like membrane domains in polarized epithelia | Q36255410 | ||
Thy-1 is a component common to multiple populations of synaptic vesicles | Q36274886 | ||
A pore-forming toxin interacts with a GPI-anchored protein and causes vacuolation of the endoplasmic reticulum. | Q36274905 | ||
Plasma membrane microdomains act as concentration platforms to facilitate intoxication by aerolysin | Q36310741 | ||
Acute cholesterol depletion inhibits clathrin-coated pit budding | Q36380759 | ||
Exogenous administration of gangliosides displaces GPI-anchored proteins from lipid microdomains in living cells | Q36918308 | ||
Detergent-insoluble GPI-anchored proteins are apically sorted in fischer rat thyroid cells, but interference with cholesterol or sphingolipids differentially affects detergent insolubility and apical sorting | Q38478806 | ||
Endosome to Golgi transport of ricin is regulated by cholesterol | Q38490873 | ||
Clostridial neurotoxins: handling and action at the cellular and molecular level | Q39745477 | ||
Neuronal Cell Thy-1 Glycoprotein: Homology with Immunoglobulin | Q40103416 | ||
Synaptobrevin binding to synaptophysin: a potential mechanism for controlling the exocytotic fusion machine. | Q40805470 | ||
Invasion of epithelial cells by Shigella flexneri induces tyrosine phosphorylation of cortactin by a pp60c-src-mediated signalling pathway | Q40806872 | ||
GAP43, MARCKS, and CAP23 modulate PI(4,5)P(2) at plasmalemmal rafts, and regulate cell cortex actin dynamics through a common mechanism | Q40871328 | ||
Tetanus toxin fragment C binds to a protein present in neuronal cell lines and motoneurons. | Q40881492 | ||
B-50/GAP-43 potentiates cytoskeletal reorganization in raft domains. | Q40921617 | ||
Neurospecific binding, internalization, and retrograde axonal transport. | Q40935938 | ||
Microdomains of GPI-anchored proteins in living cells revealed by crosslinking | Q41011350 | ||
Clostridial neurotoxins: new tools for dissecting exocytosis | Q41033673 | ||
Regulated internalization of caveolae | Q41418184 | ||
Characterization of tetanus toxin binding to rat brain membranes. Evidence for a high-affinity proteinase-sensitive receptor | Q41452280 | ||
Selective inhibition of neurite outgrowth on mature astrocytes by Thy-1 glycoprotein | Q41639350 | ||
Nerve growth factor signaling in caveolae-like domains at the plasma membrane | Q41706850 | ||
Sequestration of GPI-anchored proteins in caveolae triggered by cross-linking | Q42797660 | ||
C-terminal half of tetanus toxin fragment C is sufficient for neuronal binding and interaction with a putative protein receptor. | Q42996274 | ||
Tetanus toxin receptor. Specific cross-linking of tetanus toxin to a protein of NGF-differentiated PC 12 cells. | Q44928968 | ||
Functional characterisation of tetanus and botulinum neurotoxins binding domains | Q47945260 | ||
Neuronal sensitivity to tetanus toxin requires gangliosides | Q48131477 | ||
Identification of protein receptor for Clostridium botulinum type B neurotoxin in rat brain synaptosomes. | Q48141244 | ||
Affinity-purified tetanus neurotoxin interaction with synaptic membranes: properties of a protease-sensitive receptor component | Q48277488 | ||
Isolation of synaptotagmin as a receptor for types A and E botulinum neurotoxin and analysis of their comparative binding using a new microtiter plate assay. | Q48369928 | ||
Tetanus toxin receptors on nerve cells contain a trypsin-sensitive component | Q48385775 | ||
Botulinum neurotoxin type B. Its purification, radioiodination and interaction with rat-brain synaptosomal membranes | Q48385813 | ||
Normal spatial learning despite regional inhibition of LTP in mice lacking Thy-1. | Q49110272 | ||
GPI-anchored proteins are organized in submicron domains at the cell surface. | Q52531693 | ||
Involvement of cellular caveolae in bacterial entry into mast cells. | Q52540262 | ||
Clostridium septicum alpha toxin uses glycosylphosphatidylinositol-anchored protein receptors. | Q54079548 | ||
Landing on lipid rafts. | Q55033078 | ||
Jamming the endosomal system: lipid rafts and lysosomal storage diseases. | Q55034334 | ||
Differential Targeting of Shaker-like Potassium Channels to Lipid Rafts | Q57371812 | ||
Sphingolipid-enriched Membrane Domains from Rat Cerebellar Granule Cells Differentiated in Culture | Q57371827 | ||
Survival of FimH-expressing enterobacteria in macrophages relies on glycolipid traffic | Q57962356 | ||
Expression of synaptobrevin II, cellubrevin and syntaxin but not SNAP-25 in cultured astrocytes | Q57979052 | ||
High resolution labeling of cholinergic nerve terminals using a specific fully active biotinylated botulinum neurotoxin type A | Q58493576 | ||
Activation of signal transduction pathways involving trkA, PLCγ-1, PKC isoforms and ERK-1/2 by tetanus toxin | Q61948827 | ||
Placental alkaline phosphatase, a GPI-anchored protein, is clustered in clathrin-coated vesicles | Q68077567 | ||
Intramolecular crosslinking of gamma-glutamyl transpeptidase | Q69900613 | ||
A study of the mechanism of internalisation of tetanus toxin by primary mouse spinal cord cultures | Q70356136 | ||
Intracellular trafficking of cholesterol monitored with a cyclodextrin | Q71246519 | ||
Productive and non-productive binding of botulinum neurotoxin A to motor nerve endings are distinguished by its heavy chain | Q71302857 | ||
Quaternary structure of botulinum and tetanus neurotoxins as probed by chemical cross-linking and native gel electrophoresis | Q72359526 | ||
At least three sequential steps are involved in the tetanus toxin-induced block of neuromuscular transmission | Q72518098 | ||
Endocytic mechanisms responsible for uptake of GPI-linked diphtheria toxin receptor | Q73146748 | ||
Cholesterol and sphingolipid enhance the Triton X-100 insolubility of glycosylphosphatidylinositol-anchored proteins by promoting the formation of detergent-insoluble ordered membrane domains | Q74016377 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | membrane raft | Q424178 |
P304 | page(s) | 2947-2960 | |
P577 | publication date | 2001-10-01 | |
P1433 | published in | Molecular Biology of the Cell | Q2338259 |
P1476 | title | Lipid rafts act as specialized domains for tetanus toxin binding and internalization into neurons | |
P478 | volume | 12 |
Q35694587 | A New Membrane Lipid Raft Gene SpFLT-1 Facilitating the Endocytosis of Vibrio alginolyticus in the Crab Scylla paramamosain |
Q37779726 | A hitchhiker's guide to the nervous system: the complex journey of viruses and toxins. |
Q45861738 | A non-viral vector for targeting gene therapy to motoneurons in the CNS. |
Q44007678 | A novel PKC-regulated mechanism controls CD44 ezrin association and directional cell motility |
Q33897001 | Accuracy of regenerating motor neurons: influence of diffusion in denervated nerve |
Q42951910 | Analysis of retrograde transport in motor neurons reveals common endocytic carriers for tetanus toxin and neurotrophin receptor p75NTR. |
Q44066924 | Association of Helicobacter pylori vacuolating toxin (VacA) with lipid rafts |
Q35620222 | Axonal transport and neuronal transcytosis of trophic factors, tracers, and pathogens |
Q36624085 | Bacterial protein toxins and lipids: role in toxin targeting and activity |
Q37954286 | Bacterial toxins and the nervous system: neurotoxins and multipotential toxins interacting with neuronal cells |
Q57374189 | Bacterial-associated cholera toxin and GM1 binding are required for transcytosis of classical biotype Vibrio cholerae through an in vitro M cell model system |
Q28775841 | Binding and internalization of Clostridium perfringens iota-toxin in lipid rafts |
Q34212823 | Biological activities and pore formation of Clostridium perfringens beta toxin in HL 60 cells |
Q45177751 | Botulinum neurotoxin type D enables cytosolic delivery of enzymatically active cargo proteins to neurones via unfolded translocation intermediates |
Q44188182 | Botulism: the agent, mode of action of the botulinum neurotoxins, forms of acquisition, treatment and prevention |
Q48412198 | Brain-derived neurotrophic factor facilitates in vivo internalization of tetanus neurotoxin C-terminal fragment fusion proteins in mature mouse motor nerve terminals. |
Q63408250 | CLOSTRIDIAL NEUROTOXINS |
Q37613674 | Clostridial toxins |
Q34290711 | Comparative in vitro and in vivo assessment of toxin neutralization by anti-tetanus toxin monoclonal antibodies. |
Q39915110 | Differential entry of botulinum neurotoxin A into neuronal and intestinal cells |
Q34468288 | Dynamics of the gel to fluid phase transformation in unilamellar DPPC vesicles |
Q30481106 | Elastic membrane heterogeneity of living cells revealed by stiff nanoscale membrane domains |
Q37686075 | Endocytosis unplugged: multiple ways to enter the cell |
Q34609707 | Endocytosis via caveolae |
Q89844345 | Endocytosis, trafficking and exocytosis of intact full-length botulinum neurotoxin type a in cultured rat neurons |
Q37546383 | Entry of a recombinant, full-length, atoxic tetanus neurotoxin into Neuro-2a cells |
Q36494859 | Experimental and computational studies investigating trehalose protection of HepG2 cells from palmitate-induced toxicity |
Q37959958 | FRET in Membrane Biophysics: An Overview. |
Q40003065 | Flotillin-dependent clustering of the amyloid precursor protein regulates its endocytosis and amyloidogenic processing in neurons. |
Q38030004 | Fragment C of tetanus toxin: new insights into its neuronal signaling pathway |
Q27656415 | Gangliosides as High Affinity Receptors for Tetanus Neurotoxin |
Q35932883 | Glycosphingolipids-sweets for botulinum neurotoxin |
Q35250681 | Identification of the protein receptor binding site of botulinum neurotoxins B and G proves the double-receptor concept. |
Q40620329 | Inhibition of chemokine receptor function by membrane cholesterol oxidation |
Q42170081 | Internalization and retrograde axonal trafficking of tetanus toxin in motor neurons and trans-synaptic propagation at central synapses exceed those of its C-terminal-binding fragments. |
Q24676056 | Kidins220/ARMS is transported by a kinesin-1-based mechanism likely to be involved in neuronal differentiation |
Q28201387 | Ligand-induced internalization of the p75 neurotrophin receptor: a slow route to the signaling endosome |
Q44851101 | Lipid raft disruption triggers protein kinase C and Src-dependent protein kinase D activation and Kidins220 phosphorylation in neuronal cells |
Q28253198 | Lipids in host-pathogen interactions: pathogens exploit the complexity of the host cell lipidome |
Q35911455 | Multi-tasking by the p75 neurotrophin receptor: sortilin things out? |
Q40316155 | Multiphoton-FLIM quantification of the EGFP-mRFP1 FRET pair for localization of membrane receptor-kinase interactions |
Q37079198 | Neuron-specific delivery of nucleic acids mediated by Tet1-modified poly(ethylenimine). |
Q36362330 | Neurotrophin receptor p75 mediates the uptake of the amyloid beta (Aβ) peptide, guiding it to lysosomes for degradation in basal forebrain cholinergic neurons. |
Q35183159 | Pathogens: raft hijackers |
Q38711761 | Perturbation to Cholesterol at the Neuromuscular Junction confers botulinum neurotoxin A sensitivity to neonatal mice |
Q35031390 | Presynaptic quantal plasticity: Katz's original hypothesis revisited |
Q42151944 | Production and characterization of recombinant light chain and carboxyterminal heavy chain fragments of tetanus toxin |
Q65001074 | Protein Toxins That Utilize Gangliosides as Host Receptors. |
Q42692486 | Quantitative proteomics analysis of detergent-resistant membranes from chemical synapses: evidence for cholesterol as spatial organizer of synaptic vesicle cycling |
Q37408530 | Receptor and substrate interactions of clostridial neurotoxins |
Q28219128 | Reversible translocation and activity-dependent localization of the calcium-myristoyl switch protein VILIP-1 to different membrane compartments in living hippocampal neurons |
Q40835741 | Roles of the Mevalonate Pathway and Cholesterol Trafficking in Pulmonary Host Defense. |
Q21090499 | SV2 mediates entry of tetanus neurotoxin into central neurons |
Q24537649 | Site-directed perturbation of protein kinase C- integrin interaction blocks carcinoma cell chemotaxis. |
Q40457910 | Spatially distinct binding of Cdc42 to PAK1 and N-WASP in breast carcinoma cells |
Q30583252 | Specific retrograde transduction of spinal motor neurons using lentiviral vectors targeted to presynaptic NMJ receptors |
Q37624377 | Streptococcal pyrogenic exotoxin B-induced apoptosis in a549 cells is mediated by a receptor- and mitochondrion-dependent pathway |
Q36325534 | Synaptotagmins I and II mediate entry of botulinum neurotoxin B into cells |
Q34797732 | Tetanus Toxin Hc Fragment Induces the Formation of Ceramide Platforms and Protects Neuronal Cells against Oxidative Stress |
Q35155645 | Tetanus toxin C-fragment: the courier and the cure? |
Q35944001 | Tetanus toxin and botulinum toxin a utilize unique mechanisms to enter neurons of the central nervous system |
Q34449930 | Tetanus toxin entry. Nidogens are therapeutic targets for the prevention of tetanus |
Q36118391 | Tetanus toxin is internalized by a sequential clathrin-dependent mechanism initiated within lipid microdomains and independent of epsin1. |
Q43578360 | The C-terminal domain of tetanus toxin protects motoneurons against acute excitotoxic damage on spinal cord organotypic cultures. |
Q31036598 | The HCC-domain of botulinum neurotoxins A and B exhibits a singular ganglioside binding site displaying serotype specific carbohydrate interaction |
Q27667683 | The biological activity of botulinum neurotoxin type C is dependent upon novel types of ganglioside binding sites |
Q24305325 | The dystonia-associated protein torsinA modulates synaptic vesicle recycling |
Q41943328 | The fate of SPE B after internalization and its implication in SPEB-induced apoptosis |
Q36164122 | The immunobiology of Guillain-Barré syndromes |
Q28609177 | The journey of tetanus and botulinum neurotoxins in neurons |
Q35076697 | The roles of membrane microdomains (rafts) in T cell activation |
Q35148875 | Therapy and prophylaxis of inhaled biological toxins |
Q44306444 | Transganglionic transport of choleragenoid by capsaicin-sensitive C-fibre afferents to the substantia gelatinosa of the spinal dorsal horn after peripheral nerve section |
Q48026258 | Two Feet on the Membrane: Uptake of Clostridial Neurotoxins |
Q44312023 | Two carbohydrate binding sites in the H(CC)-domain of tetanus neurotoxin are required for toxicity |
Q48124277 | Uptake of Clostridial Neurotoxins into Cells and Dissemination |
Q36008685 | Visualization of membrane rafts using a perylene monoimide derivative and fluorescence lifetime imaging |
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