| scholarly article | Q13442814 |
| P2093 | author name string | Jung-Ja P Kim | |
| Andrew P-A Karalewitz | |||
| Joseph T Barbieri | |||
| Michael R Baldwin | |||
| Zhuji Fu | |||
| P2860 | cites work | 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 of the receptor-binding sites in the carboxyl-terminal half of the heavy chain of botulinum neurotoxin types C and D. | Q46777601 | ||
| Mosaic structures of neurotoxins produced from Clostridium botulinum types C and D organisms | Q46880568 | ||
| Translocation of botulinum neurotoxin light chain protease through the heavy chain channel | Q46942366 | ||
| Protection with recombinant Clostridium botulinum C1 and D binding domain subunit (Hc) vaccines against C and D neurotoxins | Q48080473 | ||
| Association of botulinum neurotoxin serotypes a and B with synaptic vesicle protein complexes. | Q53570184 | ||
| How do tetanus and botulinum toxins bind to neuronal membranes? | Q56226691 | ||
| A readily retrievable pool of synaptic vesicles | Q57949867 | ||
| GM1 structure determines SV40-induced membrane invagination and infection | Q58830543 | ||
| The origin, structure, and pharmacological activity of botulinum toxin | Q72518481 | ||
| Universal template plasmid for introduction of the triple-HA epitope sequence into cloned genes | Q73613459 | ||
| Botulinum neurotoxin B-host receptor recognition: it takes two receptors to tango | Q79487898 | ||
| Synaptic vesicles interchange their membrane proteins with a large surface reservoir during recycling | Q79921374 | ||
| Induced domain formation in endocytic invagination, lipid sorting, and scission | Q84772653 | ||
| Botulinum Toxin as a Biological Weapon: Medical and Public Health Management | Q23832736 | ||
| A general method of in vitro preparation and specific mutagenesis of DNA fragments: study of protein and DNA interactions | Q24597783 | ||
| Processing of X-ray diffraction data collected in oscillation mode | Q26778468 | ||
| Structural basis of cell surface receptor recognition by botulinum neurotoxin B | Q27643302 | ||
| Botulinum neurotoxin B recognizes its protein receptor with high affinity and specificity | Q27643303 | ||
| Crystal Structure of Botulinum Neurotoxin Type A in Complex with the Cell Surface Co-Receptor GT1b—Insight into the Toxin–Neuron Interaction | Q27651618 | ||
| Glycosylated SV2 and Gangliosides as Dual Receptors for Botulinum Neurotoxin Serotype F | Q27655649 | ||
| Gangliosides as High Affinity Receptors for Tetanus Neurotoxin | Q27656415 | ||
| Botulinum neurotoxin serotype D attacks neurons via two carbohydrate-binding sites in a ganglioside-dependent manner | Q27664044 | ||
| Identification of a Unique Ganglioside Binding Loop within Botulinum Neurotoxins C and D-SA, | Q27664131 | ||
| The biological activity of botulinum neurotoxin type C is dependent upon novel types of ganglioside binding sites | Q27667683 | ||
| Novel Ganglioside-mediated Entry of Botulinum Neurotoxin Serotype D into Neurons | Q27668123 | ||
| Structural and mutational analyses of the receptor binding domain of botulinum D/C mosaic neurotoxin: insight into the ganglioside binding mechanism | Q27670769 | ||
| Unique Ganglioside Recognition Strategies for Clostridial Neurotoxins | Q27671814 | ||
| Coot: model-building tools for molecular graphics | Q27860505 | ||
| Version 1.2 of the Crystallography and NMR system | Q27860583 | ||
| Phasercrystallographic software | Q27860930 | ||
| SNAREs--engines for membrane fusion | Q29547230 | ||
| Tetanus and botulinum-B neurotoxins block neurotransmitter release by proteolytic cleavage of synaptobrevin | Q29619130 | ||
| STED microscopy reveals that synaptotagmin remains clustered after synaptic vesicle exocytosis | Q34513459 | ||
| Shiga toxin induces tubular membrane invaginations for its uptake into cells | Q34719609 | ||
| Genetic diversity among Botulinum Neurotoxin-producing clostridial strains | Q35634548 | ||
| Glycosphingolipids-sweets for botulinum neurotoxin | Q35932883 | ||
| Botulinum neurotoxin A blocks synaptic vesicle exocytosis but not endocytosis at the nerve terminal | Q36313397 | ||
| Mechanism of botulinum neurotoxin B and G entry into hippocampal neurons | Q36639118 | ||
| Identification of a ganglioside recognition domain of tetanus toxin using a novel ganglioside photoaffinity ligand. | Q36891826 | ||
| Glycosylated SV2A and SV2B mediate the entry of botulinum neurotoxin E into neurons. | Q36992893 | ||
| Cell entry strategy of clostridial neurotoxins | Q37490213 | ||
| Molecular circuitry of endocytosis at nerve terminals. | Q37540209 | ||
| Sphingolipids and gangliosides of the nervous system in membrane function and dysfunction | Q37652733 | ||
| Botulinum neurotoxin: a marvel of protein design | Q37710092 | ||
| Retargeted clostridial neurotoxins as novel agents for treating chronic diseases. | Q39449111 | ||
| SV2 is the protein receptor for botulinum neurotoxin A. | Q40303506 | ||
| Molecular diversity of neurotoxins from Clostridium botulinum type D strains | Q40428135 | ||
| Substrate recognition of VAMP-2 by botulinum neurotoxin B and tetanus neurotoxin | Q40642361 | ||
| 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 | ||
| Synaptotagmins I and II act as nerve cell receptors for botulinum neurotoxin G. | Q44881077 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 48 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cell biology | Q7141 |
| P304 | page(s) | 40806-16 | |
| P577 | publication date | 2012-11-23 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Botulinum Neurotoxin Serotype C Associates with Dual Ganglioside Receptors to Facilitate Cell Entry | |
| P478 | volume | 287 |
| Q35745530 | A Heterologous Reporter Defines the Role of the Tetanus Toxin Interchain Disulfide in Light-Chain Translocation |
| Q52803571 | A lipid-binding loop of botulinum neurotoxin serotypes B, DC and G is an essential feature to confer their exquisite potency. |
| Q58615344 | Botulinum and Tetanus Neurotoxins |
| Q38224215 | Botulinum neurotoxins: genetic, structural and mechanistic insights. |
| Q35692529 | CRISPR/Cas9-Mediated Genomic Deletion of the Beta-1, 4 N-acetylgalactosaminyltransferase 1 Gene in Murine P19 Embryonal Carcinoma Cells Results in Low Sensitivity to Botulinum Neurotoxin Type C. |
| Q90390390 | Characterization of a membrane binding loop leads to engineering botulinum neurotoxin B with improved therapeutic efficacy |
| Q27679493 | Crystal Structures of Botulinum Neurotoxin DC in Complex with Its Protein Receptors Synaptotagmin I and II |
| Q26778129 | Current status and future directions of botulinum neurotoxins for targeting pain processing |
| Q38847565 | Detection, differentiation, and identification of botulinum neurotoxin serotypes C, CD, D, and DC by highly specific immunoassays and mass spectrometry. |
| Q38587703 | Dissecting the Role of Anti-ganglioside Antibodies in Guillain-Barré Syndrome: an Animal Model Approach. |
| Q35563112 | Diverse binding modes, same goal: The receptor recognition mechanism of botulinum neurotoxin. |
| Q37654972 | Engineering Botulinum Neurotoxin C1 as a Molecular Vehicle for Intra-Neuronal Drug Delivery. |
| Q57177243 | Engineering Botulinum Toxins to Improve and Expand Targeting and SNARE Cleavage Activity |
| Q37546383 | Entry of a recombinant, full-length, atoxic tetanus neurotoxin into Neuro-2a cells |
| Q45364853 | Identification of the SV2 protein receptor-binding site of botulinum neurotoxin type E. |
| Q98176846 | Intracellular G-actin targeting of peripheral sensory neurons by the multifunctional engineered protein C2C confers relief from inflammatory pain |
| Q39648919 | Retargeting the Clostridium botulinum C2 toxin to the neuronal cytosol |
| Q47093993 | Structural basis for the unique ganglioside and cell membrane recognition mechanism of botulinum neurotoxin DC. |
| Q87698566 | Synaptotagmin II and gangliosides bind independently with botulinum neurotoxin B but each restrains the other |
| Q34070484 | Tetanus neurotoxin utilizes two sequential membrane interactions for channel formation. |
| Q45316693 | Toxicity of botulinum toxin type C (botC) |
| Q48026258 | Two Feet on the Membrane: Uptake of Clostridial Neurotoxins |
| Q57808978 | Variations in the Botulinum Neurotoxin Binding Domain and the Potential for Novel Therapeutics |
| Q50289594 | botC HC:LC binds GT1b on the target cell surface |
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