| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/82_2017_50 |
| P698 | PubMed publication ID | 28879524 |
| P2093 | author name string | Michel R Popoff | |
| Chloé Connan | |||
| P2860 | cites work | Botulism | Q21994439 |
| The genome sequence of Clostridium tetani, the causative agent of tetanus disease | Q22066366 | ||
| GTP-dependent twisting of dynamin implicates constriction and tension in membrane fission | Q24322874 | ||
| Botulinum neurotoxins A and E undergo retrograde axonal transport in primary motor neurons | Q27339199 | ||
| The structures of the H(C) fragment of tetanus toxin with carbohydrate subunit complexes provide insight into ganglioside binding | Q27621792 | ||
| Structural analysis of the catalytic and binding sites of Clostridium botulinum neurotoxin B | Q27626220 | ||
| The crystal structure of tetanus toxin Hc fragment complexed with a synthetic GT1b analogue suggests cross-linking between ganglioside receptors and the toxin | Q27632675 | ||
| Structural analysis by X-ray crystallography and calorimetry of a haemagglutinin component (HA1) of the progenitor toxin from Clostridium botulinum | Q27642756 | ||
| A novel subunit structure of Clostridium botulinum serotype D toxin complex with three extended arms | Q27646127 | ||
| Crystal Structure of Botulinum Neurotoxin Type A in Complex with the Cell Surface Co-Receptor GT1b—Insight into the Toxin–Neuron Interaction | Q27651618 | ||
| Domain organization in Clostridium botulinum neurotoxin type E is unique: its implication in faster translocation | Q27653311 | ||
| Glycosylated SV2 and Gangliosides as Dual Receptors for Botulinum Neurotoxin Serotype F | Q27655649 | ||
| Gangliosides as High Affinity Receptors for Tetanus Neurotoxin | Q27656415 | ||
| Structural and mutational analyses of the receptor binding domain of botulinum D/C mosaic neurotoxin: insight into the ganglioside binding mechanism | Q27670769 | ||
| Botulinum Neurotoxin Is Shielded by NTNHA in an Interlocked Complex | Q27677462 | ||
| Structure of dual receptor binding to botulinum neurotoxin B | Q27678834 | ||
| Structure of a Bimodular Botulinum Neurotoxin Complex Provides Insights into Its Oral Toxicity | Q27680382 | ||
| Molecular basis for disruption of E-cadherin adhesion by botulinum neurotoxin A complex | Q27684403 | ||
| Structural basis for recognition of synaptic vesicle protein 2C by botulinum neurotoxin A | Q27687569 | ||
| Structure of a C. perfringens enterotoxin mutant in complex with a modified Claudin-2 extracellular loop 2 | Q27694542 | ||
| Structure of the receptor binding fragment HC of tetanus neurotoxin | Q27746013 | ||
| Crystal structure of botulinum neurotoxin type A and implications for toxicity | Q27765727 | ||
| Cell adhesion: the molecular basis of tissue architecture and morphogenesis | Q28276573 | ||
| The synaptic vesicle protein 2C mediates the uptake of botulinum neurotoxin A into phrenic nerves | Q28578304 | ||
| Identification of the synaptic vesicle glycoprotein 2 receptor binding site in botulinum neurotoxin A | Q28581589 | ||
| The journey of tetanus and botulinum neurotoxins in neurons | Q28609177 | ||
| Pathways of clathrin-independent endocytosis | Q29620660 | ||
| Intersectin is a negative regulator of dynamin recruitment to the synaptic endocytic zone in the central synapse. | Q30159491 | ||
| Complete subunit structure of the Clostridium botulinum type D toxin complex via intermediate assembly with nontoxic components | Q48228499 | ||
| Traffic of botulinum toxins A and E in excitatory and inhibitory neurons. | Q48301665 | ||
| In vitro reconstitution of the Clostridium botulinum type D progenitor toxin | Q48332411 | ||
| Sorting nexin 9 interacts with dynamin 1 and N-WASP and coordinates synaptic vesicle endocytosis | Q50337378 | ||
| Tetanus toxin is transported in a novel neuronal compartment characterized by a specialized pH regulation. | Q50750090 | ||
| Different time courses of recovery after poisoning with botulinum neurotoxin serotypes A and E in humans. | Q50755840 | ||
| Uptake of botulinum neurotoxin into cultured neurons. | Q52095157 | ||
| The high-affinity binding of Clostridium botulinum type B neurotoxin to synaptotagmin II associated with gangliosides GT1b/GD1a. | Q52312776 | ||
| Studies on the dissociation of botulinum neurotoxin type A complexes. | Q52606394 | ||
| Interactions between Clostridium perfringens enterotoxin and claudins. | Q52613139 | ||
| Transsynaptic inhibition of spinal transmission by A2 botulinum toxin. | Q53136780 | ||
| Evidence for anterograde transport and transcytosis of botulinum neurotoxin A (BoNT/A). | Q53208463 | ||
| GPI-anchored proteins are delivered to recycling endosomes via a distinct cdc42-regulated, clathrin-independent pinocytic pathway. | Q53973070 | ||
| Rescue of exocytosis in botulinum toxin A-poisoned chromaffin cells by expression of cleavage-resistant SNAP-25. Identification of the minimal essential C-terminal residues. | Q54068444 | ||
| Molecular properties of each subcomponent in Clostridium botulinum type B haemagglutinin complex. | Q54195995 | ||
| Intracellular trafficking of bacterial and plant protein toxins | Q57358628 | ||
| Uptake and transport of Clostridium neurotoxins | Q57358645 | ||
| Gangliosides are the binding substances in neural cells for tetanus and botulinum toxins in mice | Q57539150 | ||
| Dynamics of motor nerve terminal remodeling unveiled using SNARE-cleaving botulinum toxins: the extent and duration are dictated by the sites of SNAP-25 truncation | Q58120767 | ||
| Clostridium botulinum type A haemagglutinin-positive progenitor toxin (HA(+)-PTX) binds to oligosaccharides containing Gal beta1-4GlcNAc through one subcomponent of haemagglutinin (HA1). | Q38302343 | ||
| Intersectin regulates fission and internalization of caveolae in endothelial cells. | Q30164523 | ||
| SH3-domain-containing proteins function at distinct steps in clathrin-coated vesicle formation | Q30175316 | ||
| Toxic and nontoxic components of botulinum neurotoxin complex are evolved from a common ancestral zinc protein | Q30413536 | ||
| Crosstalk between different adhesion molecules | Q30441081 | ||
| Depletion of E-cadherin disrupts establishment but not maintenance of cell junctions in Madin-Darby canine kidney epithelial cells | Q30442081 | ||
| Helicobacter pylori VacA cytotoxin: a probe for a clathrin-independent and Cdc42-dependent pinocytic pathway routed to late endosomes | Q30476218 | ||
| Molecular assembly of botulinum neurotoxin progenitor complexes | Q30538466 | ||
| Substrates and controls for the quantitative detection of active botulinum neurotoxin in protease-containing samples | Q30543272 | ||
| Botulinum toxin A complex exploits intestinal M cells to enter the host and exert neurotoxicity | Q30621197 | ||
| Characterization of nicking of the nontoxic-nonhemagglutinin components of Clostridium botulinum types C and D progenitor toxin. | Q30662229 | ||
| The HCC-domain of botulinum neurotoxins A and B exhibits a singular ganglioside binding site displaying serotype specific carbohydrate interaction | Q31036598 | ||
| Molecular properties of a hemagglutinin purified from type A Clostridium botulinum | Q31220663 | ||
| Sequencing the botulinum neurotoxin gene and related genes in Clostridium botulinum type E strains reveals orfx3 and a novel type E neurotoxin subtype | Q33300918 | ||
| Subunit stoichiometry of the Clostridium botulinum type A neurotoxin complex determined using denaturing capillary electrophoresis | Q33385692 | ||
| Expression of the Clostridium botulinum A2 neurotoxin gene cluster proteins and characterization of the A2 complex | Q33559451 | ||
| Co-regulation of caveolar and Cdc42-dependent fluid phase endocytosis by phosphocaveolin-1. | Q33832662 | ||
| Botulinum neurotoxin D uses synaptic vesicle protein SV2 and gangliosides as receptors | Q33869062 | ||
| Characterization of botulinum progenitor toxins by mass spectrometry | Q33913243 | ||
| Cdc42-dependent modulation of tight junctions and membrane protein traffic in polarized Madin-Darby canine kidney cells | Q33944040 | ||
| Membrane traffic in polarized epithelial cells | Q33954492 | ||
| Molecular studies of the intestinal mucosal barrier physiopathology using cocultures of epithelial and immune cells: a technical update | Q34019996 | ||
| Retrograde trans-synaptic transfer of green fluorescent protein allows the genetic mapping of neuronal circuits in transgenic mice | Q34099258 | ||
| High sensitivity of mouse neuronal cells to tetanus toxin requires a GPI-anchored protein | Q34102597 | ||
| Evaluation of the therapeutic usefulness of botulinum neurotoxin B, C1, E, and F compared with the long lasting type A. Basis for distinct durations of inhibition of exocytosis in central neurons | Q34154552 | ||
| Clostridium botulinum in the post-genomic era. | Q34164135 | ||
| Preferential entry of botulinum neurotoxin A Hc domain through intestinal crypt cells and targeting to cholinergic neurons of the mouse intestine | Q34205889 | ||
| The toxins of Bacteroides fragilis | Q34398297 | ||
| Tetanus toxin entry. Nidogens are therapeutic targets for the prevention of tetanus | Q34449930 | ||
| Botulinum neurotoxin subtype A2 enters neuronal cells faster than subtype A1 | Q34583087 | ||
| Evidence That Botulinum Toxin Receptors on Epithelial Cells and Neuronal Cells Are Not Identical: Implications for Development of a Non-Neurotropic Vaccine | Q34702285 | ||
| Inhalational poisoning by botulinum toxin and inhalation vaccination with its heavy-chain component | Q34713991 | ||
| Long lasting dysautonomia due to botulinum toxin B poisoning: clinical-laboratory follow up and difficulties in initial diagnosis | Q35028885 | ||
| Identification of the protein receptor binding site of botulinum neurotoxins B and G proves the double-receptor concept. | Q35250681 | ||
| Dynamin inhibition blocks botulinum neurotoxin type A endocytosis in neurons and delays botulism | Q35371760 | ||
| Clostridium botulinum type A progenitor toxin binds to Intestine-407 cells via N-acetyllactosamine moiety | Q38327528 | ||
| Interaction between the two subdomains of the C-terminal part of the botulinum neurotoxin A is essential for the generation of protective antibodies. | Q38337915 | ||
| Involvement of sialic acid in transport of serotype C1 botulinum toxins through rat intestinal epithelial cells | Q38344130 | ||
| The long journey of botulinum neurotoxins into the synapse | Q38561450 | ||
| Clostridium botulinum type C hemagglutinin affects the morphology and viability of cultured mammalian cells via binding to the ganglioside GM3. | Q38863848 | ||
| Lipid rafts act as specialized domains for tetanus toxin binding and internalization into neurons | Q39226359 | ||
| HA-33 facilitates transport of the serotype D botulinum toxin across a rat intestinal epithelial cell monolayer | Q39610189 | ||
| Botulinum hemagglutinin disrupts the intercellular epithelial barrier by directly binding E-cadherin | Q39705548 | ||
| Clathrin-mediated endocytosis is the dominant mechanism of vesicle retrieval at hippocampal synapses. | Q39751968 | ||
| Sialic acid-dependent binding and transcytosis of serotype D botulinum neurotoxin and toxin complex in rat intestinal epithelial cells. | Q39794198 | ||
| Disruption of the epithelial barrier by botulinum haemagglutinin (HA) proteins - differences in cell tropism and the mechanism of action between HA proteins of types A or B, and HA proteins of type C. | Q39899515 | ||
| A novel function of botulinum toxin-associated proteins: HA proteins disrupt intestinal epithelial barrier to increase toxin absorption | Q39906568 | ||
| Differential entry of botulinum neurotoxin A into neuronal and intestinal cells | Q39915110 | ||
| Cholesterol-sensitive Cdc42 activation regulates actin polymerization for endocytosis via the GEEC pathway | Q40140638 | ||
| Disruption of lipid rafts enhances activity of botulinum neurotoxin serotype A. | Q40219347 | ||
| Gangliosides that associate with lipid rafts mediate transport of cholera and related toxins from the plasma membrane to endoplasmic reticulm | Q40286860 | ||
| SV2 is the protein receptor for botulinum neurotoxin A. | Q40303506 | ||
| Visualization of binding and transcytosis of botulinum toxin by human intestinal epithelial cells | Q40376633 | ||
| Structural features of the botulinum neurotoxin molecule that govern binding and transcytosis across polarized human intestinal epithelial cells | Q40556533 | ||
| Novel targets and catalytic activities of bacterial protein toxins | Q40733108 | ||
| Spinal Central Effects of Peripherally Applied Botulinum Neurotoxin A in Comparison between Its Subtypes A1 and A2. | Q40983059 | ||
| Translocation and dissemination to target neurons of botulinum neurotoxin type B in the mouse intestinal wall | Q41040621 | ||
| Conversion by Peyer's patch lymphocytes of human enterocytes into M cells that transport bacteria | Q41094317 | ||
| Botulinum versus tetanus neurotoxins: why is botulinum neurotoxin but not tetanus neurotoxin a food poison? | Q41160070 | ||
| Identification and characterization of a novel botulinum neurotoxin. | Q41245604 | ||
| Genomic characterization of Italian Clostridium botulinum group I strains | Q41407289 | ||
| Sequence homology and structural analysis of the clostridial neurotoxins | Q41695875 | ||
| Sequence diversity of genes encoding botulinum neurotoxin type F. | Q41773499 | ||
| Independent evolution of neurotoxin and flagellar genetic loci in proteolytic Clostridium botulinum | Q41970504 | ||
| Botulinum neurotoxin type B uses a distinct entry pathway mediated by CDC42 into intestinal cells versus neuronal cells. | Q42506921 | ||
| Poliovirus transcytosis through M-like cells | Q42524958 | ||
| The botulinum toxin complex meets E-cadherin on the way to its destination | Q42598307 | ||
| Neurotoxin Gene Clusters in Clostridium botulinum Type A Strains: Sequence Comparison and Evolutionary Implications | Q42598657 | ||
| Rab5 and Rab7 control endocytic sorting along the axonal retrograde transport pathway | Q42600951 | ||
| Botulinum neurotoxin A impairs neurotransmission following retrograde transynaptic transport. | Q42644905 | ||
| Molecular construction of Clostridium botulinum type C progenitor toxin and its gene organization | Q42687098 | ||
| Analysis of retrograde transport in motor neurons reveals common endocytic carriers for tetanus toxin and neurotrophin receptor p75NTR. | Q42951910 | ||
| Botulinum neurotoxins C, E and F bind gangliosides via a conserved binding site prior to stimulation-dependent uptake with botulinum neurotoxin F utilising the three isoforms of SV2 as second receptor | Q43299518 | ||
| Membrane Interaction of botulinum neurotoxin A translocation (T) domain. The belt region is a regulatory loop for membrane interaction. | Q43960895 | ||
| Identification of the interaction region between hemagglutinin components of the botulinum toxin complex | Q44138273 | ||
| 2.3 A crystal structure of tetanus neurotoxin light chain | Q44333513 | ||
| Synaptotagmins I and II act as nerve cell receptors for botulinum neurotoxin G. | Q44881077 | ||
| Molecular characterization of binding subcomponents of Clostridium botulinum type C progenitor toxin for intestinal epithelial cells and erythrocytes | Q44888205 | ||
| Tetanus toxin receptor. Specific cross-linking of tetanus toxin to a protein of NGF-differentiated PC 12 cells. | Q44928968 | ||
| Botulinum neurotoxin G binds synaptotagmin-II in a mode similar to that of serotype B: tyrosine 1186 and lysine 1191 cause its lower affinity | Q45345429 | ||
| The haemagglutinin of Clostridium botulinum type C progenitor toxin plays an essential role in binding of toxin to the epithelial cells of guinea pig small intestine, leading to the efficient absorption of the toxin | Q46266554 | ||
| Molecular basis for tetanus toxin coreceptor interactions | Q46547987 | ||
| Binding of Clostridium botulinum type C and D neurotoxins to ganglioside and phospholipid. Novel insights into the receptor for clostridial neurotoxins | Q46663715 | ||
| Identification and characterization of functional subunits of Clostridium botulinum type A progenitor toxin involved in binding to intestinal microvilli and erythrocytes | Q46954550 | ||
| The receptor and transporter for internalization of Clostridium botulinum type C progenitor toxin into HT-29 cells | Q47393038 | ||
| Glycosphingolipids internalized via caveolar-related endocytosis rapidly merge with the clathrin pathway in early endosomes and form microdomains for recycling | Q47614765 | ||
| Binding and transcytosis of botulinum neurotoxin by polarized human colon carcinoma cells | Q47681886 | ||
| Diverse binding modes, same goal: The receptor recognition mechanism of botulinum neurotoxin. | Q35563112 | ||
| Analysis of Clostridium botulinum serotype E strains by using multilocus sequence typing, amplified fragment length polymorphism, variable-number tandem-repeat analysis, and botulinum neurotoxin gene sequencing | Q35599226 | ||
| Genetic diversity among Botulinum Neurotoxin-producing clostridial strains | Q35634548 | ||
| Rafts: scale-dependent, active lipid organization at the cell surface | Q35696755 | ||
| Botulinum Neurotoxins Can Enter Cultured Neurons Independent of Synaptic Vesicle Recycling | Q35710270 | ||
| Tetanus toxin and botulinum toxin a utilize unique mechanisms to enter neurons of the central nervous system | Q35944001 | ||
| Comparative genomic analyses reveal broad diversity in botulinum-toxin-producing Clostridia | Q35945124 | ||
| The Translocation Domain of Botulinum Neurotoxin A Moderates the Propensity of the Catalytic Domain to Interact with Membranes at Acidic pH | Q35987067 | ||
| Regulatory mechanisms of dynamin-dependent endocytosis | Q36088968 | ||
| Tetanus toxin is internalized by a sequential clathrin-dependent mechanism initiated within lipid microdomains and independent of epsin1. | Q36118391 | ||
| Translocation of botulinum neurotoxin serotype A and associated proteins across the intestinal epithelia | Q36176597 | ||
| Botulinum neurotoxin A blocks synaptic vesicle exocytosis but not endocytosis at the nerve terminal | Q36313397 | ||
| Synaptotagmins I and II mediate entry of botulinum neurotoxin B into cells | Q36325534 | ||
| Molecular Assembly of Clostridium botulinum progenitor M complex of type E | Q36350322 | ||
| Analysis of the mechanisms that underlie absorption of botulinum toxin by the inhalation route | Q36396775 | ||
| A Novel Botulinum Neurotoxin, Previously Reported as Serotype H, Has a Hybrid-Like Structure With Regions of Similarity to the Structures of Serotypes A and F and Is Neutralized With Serotype A Antitoxin | Q36440215 | ||
| The type F6 neurotoxin gene cluster locus of group II clostridium botulinum has evolved by successive disruption of two different ancestral precursors. | Q36905232 | ||
| Adherens and tight junctions: structure, function and connections to the actin cytoskeleton | Q36940193 | ||
| Glycosylated SV2A and SV2B mediate the entry of botulinum neurotoxin E into neurons. | Q36992893 | ||
| N-linked glycosylation of SV2 is required for binding and uptake of botulinum neurotoxin A. | Q37276819 | ||
| Antibody protection against botulinum neurotoxin intoxication in mice | Q37355925 | ||
| Translocation of botulinum neurotoxin light chain protease by the heavy chain protein-conducting channel | Q37359166 | ||
| A reappraisal of the central effects of botulinum neurotoxin type A: by what mechanism? | Q37372753 | ||
| Central effects of tetanus and botulinum neurotoxins | Q37407393 | ||
| Multifaceted role of Rho, Rac, Cdc42 and Ras in intercellular junctions, lessons from toxins | Q37444292 | ||
| Entry of a recombinant, full-length, atoxic tetanus neurotoxin into Neuro-2a cells | Q37546383 | ||
| Botulinum neurotoxin A complex recognizes host carbohydrates through its hemagglutinin component | Q37617806 | ||
| Historical Perspectives and Guidelines for Botulinum Neurotoxin Subtype Nomenclature. | Q37641175 | ||
| Botulinum neurotoxin: a marvel of protein design | Q37710092 | ||
| Molecular structures and functional relationships in clostridial neurotoxins | Q37876965 | ||
| Bacterial toxins and the nervous system: neurotoxins and multipotential toxins interacting with neuronal cells | Q37954286 | ||
| Assembly and function of the botulinum neurotoxin progenitor complex | Q38067346 | ||
| Molecular dissection of botulinum neurotoxin reveals interdomain chaperone function | Q38080382 | ||
| The life history of a botulinum toxin molecule | Q38091815 | ||
| Historical and current perspectives on Clostridium botulinum diversity | Q38259821 | ||
| P304 | page(s) | 39-78 | |
| P577 | publication date | 2017-09-07 | |
| P1433 | published in | Current Topics in Microbiology and Immunology | Q15752446 |
| P1476 | title | Uptake of Clostridial Neurotoxins into Cells and Dissemination | |
| P478 | volume | 406 |
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