| 1 | Extra-pineal melatonin in perisynaptic Schwann cell–muscle fiber cross talk at the regenerating neuromuscular junction | 3.7 | 2 | Citations (PDF) |
| 2 | Hydrogen Peroxide Modulates the Timely Activation of Jun and Erk in Schwann Cells at the Injury Site and Is Required for Motor Axon Regeneration | 3.5 | 3 | Citations (PDF) |
| 3 | An agonist of CXCR4 induces a rapid recovery from the neurotoxic effects of Vipera ammodytes and Vipera aspis venoms | 2.8 | 4 | Citations (PDF) |
| 4 | Agonists of melatonin receptors strongly promote the functional recovery from the neuroparalysis induced by neurotoxic snakes | 2.1 | 6 | Citations (PDF) |
| 5 | Paralysis of Cholinergic Enteric Nerve Terminals in Subclinical Foodborne Botulism | 1.2 | 0 | Citations (PDF) |
| 6 | Facial Neuromuscular Junctions and Selected Brainstem Nuclei Are the Targets of Tetanus Neurotoxin in Cephalic Tetanus | 1.2 | 0 | Citations (PDF) |
| 7 | Fabs From Purified HumAbs Open to the Intrathecal Treatment of Tetanus | 1.2 | 0 | Citations (PDF) |
| 8 | A possible cause and therapy for equine grass sickness | 1.2 | 3 | Citations (PDF) |
| 9 | Local Tetanus Begins with a Neuromuscular Junction Paralysis around the Site of Tetanus Neurotoxin Release due to Cleavage of the Vesicle-Associated Membrane Protein | 2.9 | 2 | Citations (PDF) |
| 10 | Latrotoxin-Induced Neuromuscular Junction Degeneration Reveals Urocortin 2 as a Critical Contributor to Motor Axon Terminal Regeneration | 3.3 | 4 | Citations (PDF) |
| 11 | An agonist of the CXCR4 receptor is therapeutic for the neuroparalysis induced by Bungarus snakes envenoming | 5.5 | 5 | Citations (PDF) |
| 12 | Toxicology and pharmacology of botulinum and tetanus neurotoxins: an update | 6.4 | 72 | Citations (PDF) |
| 13 | Detection of VAMP Proteolysis by Tetanus and Botulinum Neurotoxin Type B In Vivo with a Cleavage-Specific Antibody | 3.3 | 13 | Citations (PDF) |
| 14 | Recovery from the Neuroparalysis Caused by the Micrurus nigrocinctus Venom Is Accelerated by an Agonist of the CXCR4 Receptor | 2.5 | 4 | Citations (PDF) |
| 15 | Melatonin promotes regeneration of injured motor axons via MT1 receptors | 4.4 | 29 | Citations (PDF) |
| 16 | Tetanus and tetanus neurotoxin: From peripheral uptake to central nervous tissue targets | 2.8 | 54 | Citations (PDF) |
| 17 | Exceptionally potent human monoclonal antibodies are effective for prophylaxis and treatment of tetanus in mice | 7.1 | 18 | Citations (PDF) |
| 18 | Novel Small Molecule Inhibitors That Prevent the Neuroparalysis of Tetanus Neurotoxin | 3.4 | 2 | Citations (PDF) |
| 19 | An agonist of the CXCR4 receptor accelerates the recovery from the peripheral neuroparalysis induced by Taipan snake envenomation | 2.1 | 10 | Citations (PDF) |
| 20 | Clinical duration of action of different botulinum toxin types in humans | 1.2 | 36 | Citations (PDF) |
| 21 | An Agonist of the CXCR4 Receptor Strongly Promotes Regeneration of Degenerated Motor Axon Terminals | 3.5 | 22 | Citations (PDF) |
| 22 | The role of the single interchains disulfide bond in tetanus and botulinum neurotoxins and the development of antitetanus and antibotulism drugs | 0.7 | 25 | Citations (PDF) |
| 23 | A CXCR4 receptor agonist strongly stimulates axonal regeneration after damage | 2.4 | 25 | Citations (PDF) |
| 24 | Tables of Toxicity of Botulinum and Tetanus Neurotoxins | 2.5 | 105 | Citations (PDF) |
| 25 | Hydrogen peroxide is a neuronal alarmin that triggers specific RNAs, local translation of Annexin A2, and cytoskeletal remodeling in Schwann cells | 2.6 | 17 | Citations (PDF) |
| 26 | Discovery of novel bacterial toxins by genomics and computational biology | 1.2 | 51 | Citations (PDF) |
| 27 | Hsp90 and Thioredoxin-Thioredoxin Reductase enable the catalytic activity of Clostridial neurotoxins inside nerve terminals | 1.2 | 30 | Citations (PDF) |
| 28 | Detection of Clostridium tetani Neurotoxins Inhibited In Vivo by Botulinum Antitoxin B: Potential for Misleading Mouse Test Results in Food Controls | 2.5 | 4 | Citations (PDF) |
| 29 | Primary resistance of human patients to botulinum neurotoxins A and B | 2.4 | 9 | Citations (PDF) |
| 30 | Schwann cells are activated by ATP released from neurons in an in vitro cellular model of Miller Fisher syndrome | 1.4 | 19 | Citations (PDF) |
| 31 | CXCL12α/SDF‐1 from perisynaptic Schwann cells promotes regeneration of injured motor axon terminals | 4.9 | 57 | Citations (PDF) |
| 32 | Botulinum Neurotoxins: Biology, Pharmacology, and Toxicology | 10.9 | 681 | Citations (PDF) |
| 33 | Animal models for studying motor axon terminal paralysis and recovery | 2.8 | 17 | Citations (PDF) |
| 34 | Identification and characterization of C group III field strains by matrix-assisted laser desorption-ionization time-of-flight mass spectrometry (MALDI-TOF MS) | 2.0 | 18 | Citations (PDF) |
| 35 | Hsp90 is involved in the entry of clostridial neurotoxins into the cytosol of nerve terminals | 0.7 | 42 | Citations (PDF) |
| 36 | Electrophysiological Characterization of the Antarease Metalloprotease from Tityus serrulatus Venom | 2.5 | 14 | Citations (PDF) |
| 37 | High Conservation of Tetanus and Botulinum Neurotoxins Cleavage Sites on Human SNARE Proteins Suggests That These Pathogens Exerted Little or No Evolutionary Pressure on Humans | 2.5 | 11 | Citations (PDF) |
| 38 | Semicarbazone EGA Inhibits Uptake of Diphtheria Toxin into Human Cells and Protects Cells from Intoxication | 2.5 | 11 | Citations (PDF) |
| 39 | EGA Protects Mammalian Cells from Clostridium difficile CDT, Clostridium perfringens Iota Toxin and Clostridium botulinum C2 Toxin | 2.5 | 8 | Citations (PDF) |
| 40 | Top bar navigation | 2.5 | 31 | Citations (PDF) |
| 41 | The first non Clostridial botulinum-like toxin cleaves VAMP within the juxtamembrane domain | 2.8 | 90 | Citations (PDF) |
| 42 | Reform oversight of Italy's science funds | 32.8 | 0 | Citations (PDF) |
| 43 | An animal model of Miller Fisher syndrome: Mitochondrial hydrogen peroxide is produced by the autoimmune attack of nerve terminals and activates Schwann cells | 3.6 | 32 | Citations (PDF) |
| 44 | On the translocation of botulinum and tetanus neurotoxins across the membrane of acidic intracellular compartments | 1.5 | 93 | Citations (PDF) |
| 45 | Thioredoxin reductase inhibitor auranofin prevents membrane transport of diphtheria toxin into the cytosol and protects human cells from intoxication | 1.2 | 21 | Citations (PDF) |
| 46 | A Novel Inhibitor Prevents the Peripheral Neuroparalysis of Botulinum Neurotoxins | 2.8 | 31 | Citations (PDF) |
| 47 | Snake and Spider Toxins Induce a Rapid Recovery of Function of Botulinum Neurotoxin Paralysed Neuromuscular Junction | 2.5 | 26 | Citations (PDF) |
| 48 | Mitochondrial alarmins released by degenerating motor axon terminals activate perisynaptic Schwann cells | 5.4 | 71 | Citations (PDF) |
| 49 | Current gaps in basic science knowledge of botulinum neurotoxin biological actions | 1.2 | 15 | Citations (PDF) |
| 50 | Practical guidance for CD management involving treatment of botulinum toxin: a consensus statement | 2.9 | 70 | Citations (PDF) |
| 51 | The thioredoxin reductase – Thioredoxin redox system cleaves the interchain disulphide bond of botulinum neurotoxins on the cytosolic surface of synaptic vesicles | 1.2 | 29 | Citations (PDF) |
| 52 | Inhibition of botulinum neurotoxins interchain disulfide bond reduction prevents the peripheral neuroparalysis of botulism | 3.9 | 40 | Citations (PDF) |
| 53 | The synaptotagmin juxtamembrane domain is involved in neuroexocytosis | 1.6 | 5 | Citations (PDF) |
| 54 | Thioredoxin and Its Reductase Are Present on Synaptic Vesicles, and Their Inhibition Prevents the Paralysis Induced by Botulinum Neurotoxins | 4.6 | 101 | Citations (PDF) |
| 55 | Diphtheria toxin conformational switching at acidic pH | 3.4 | 28 | Citations (PDF) |
| 56 | Botulinum neurotoxins: genetic, structural and mechanistic insights | 61.3 | 579 | Citations (PDF) |
| 57 | Synergism between Basic Asp49 and Lys49 Phospholipase A2 Myotoxins of Viperid Snake Venom In Vitro and In Vivo | 1.6 | 92 | Citations (PDF) |
| 58 | Botulinum Neurotoxin Type A is Internalized and Translocated from Small Synaptic Vesicles at the Neuromuscular Junction | 3.2 | 77 | Citations (PDF) |
| 59 | The thioredoxin reductase-thioredoxin system is involved in the entry of tetanus and botulinum neurotoxins in the cytosol of nerve terminals | 1.9 | 63 | Citations (PDF) |
| 60 | Botulinum neurotoxins | 1.2 | 40 | Citations (PDF) |
| 61 | Neutralisation of specific surface carboxylates speeds up translocation of botulinum neurotoxin type B enzymatic domain | 1.9 | 41 | Citations (PDF) |
| 62 | Tetanus neurotoxin | 1.2 | 61 | Citations (PDF) |
| 63 | Botulinum neurotoxin serotype D is poorly effective in humans: An electrophysiological study | 0.9 | 41 | Citations (PDF) |
| 64 | Calpains participate in nerve terminal degeneration induced by spider and snake presynaptic neurotoxins | 1.2 | 20 | Citations (PDF) |
| 65 | Why myotoxin-containing snake venoms possess powerful nucleotidases? | 1.5 | 35 | Citations (PDF) |
| 66 | Time course and temperature dependence of the membrane translocation of tetanus and botulinum neurotoxins C and D in neurons | 1.5 | 37 | Citations (PDF) |
| 67 | The Apoptogenic Toxin AIP56 Is a Metalloprotease A-B Toxin that Cleaves NF-κb P65 | 3.0 | 41 | Citations (PDF) |
| 68 | Evidence for a radial SNARE super-complex mediating neurotransmitter release at the Drosophila neuromuscular junction | 1.8 | 32 | Citations (PDF) |
| 69 | Muscle phospholipid hydrolysis by Bothrops asper Asp49 and Lys49 phospholipase A2 myotoxins – distinct mechanisms of action | 3.4 | 54 | Citations (PDF) |
| 70 | The adjuvant MF59 induces ATP release from muscle that potentiates response to vaccination | 5.4 | 148 | Citations (PDF) |
| 71 | The blockade of the neurotransmitter release apparatus by botulinum neurotoxins | 3.7 | 125 | Citations (PDF) |
| 72 | Envenomations by Bothrops and Crotalus Snakes Induce the Release of Mitochondrial Alarmins | 2.1 | 39 | Citations (PDF) |
| 73 | A Lys49-PLA2 myotoxin of Bothrops asper triggers a rapid death of macrophages that involves autocrine purinergic receptor signaling | 7.0 | 22 | Citations (PDF) |
| 74 | Double anchorage to the membrane and intact inter-chain disulfide bond are required for the low pH induced entry of tetanus and botulinum neurotoxins into neurons | 0.7 | 63 | Citations (PDF) |
| 75 | Lipid function at synapses | 3.5 | 62 | Citations (PDF) |
| 76 | Imaging the cell entry of the anthrax oedema and lethal toxins with fluorescent protein chimeras | 0.7 | 52 | Citations (PDF) |
| 77 | Bothrops snake myotoxins induce a large efflux of ATP and potassium with spreading of cell damage and pain | 5.4 | 70 | Citations (PDF) |
| 78 | Arg206 of SNAP-25 is essential for neuroexocytosis at the Drosophila melanogaster neuromuscular junction | 1.8 | 19 | Citations (PDF) |
| 79 | The C-terminal region of a Lys49 myotoxin mediates Ca influx in C2C12 myotubes | 1.2 | 32 | Citations (PDF) |
| 80 | Paralytic activity of lysophosphatidylcholine from saliva of the waterbug Belostoma anurum | 1.5 | 16 | Citations (PDF) |
| 81 | Clinical use of non-a botulinum toxins: Botulinum toxin type C and botulinum toxin type F | 2.6 | 49 | Citations (PDF) |
| 82 | The Adenylate Cyclase Toxins of Bacillus anthracis and Bordetella pertussis Promote Th2 Cell Development by Shaping T Cell Antigen Receptor Signaling | 3.0 | 44 | Citations (PDF) |
| 83 | Assay of diffusion of different botulinum neurotoxin type a formulations injected in the mouse leg | 1.6 | 97 | Citations (PDF) |
| 84 | Calcium imaging of muscle cells treated with snake myotoxins reveals toxin synergism and presence of acceptors | 3.7 | 74 | Citations (PDF) |
| 85 | Mass spectrometry analysis of the phospholipase A(2) activity of snake pre-synaptic neurotoxins in cultured neurons. | 2.8 | 48 | Citations (PDF) |
| 86 | The N-terminal half of the receptor domain of botulinum neurotoxin A binds to microdomains of the plasma membrane | 1.5 | 89 | Citations (PDF) |
| 87 | Different mechanisms of inhibition of nerve terminals by botulinum and snake presynaptic neurotoxins | 1.2 | 27 | Citations (PDF) |
| 88 | Calcium overload in nerve terminals of cultured neurons intoxicated by alpha-latrotoxin and snake PLA2 neurotoxins | 1.2 | 52 | Citations (PDF) |
| 89 | The anthrax lethal factor and its MAPK kinase-specific metalloprotease activity | 7.9 | 77 | Citations (PDF) |
| 90 | Neurotoxicity of inverted-cone shaped lipids | 2.4 | 9 | Citations (PDF) |
| 91 | Cellular pathology induced by snake venom phospholipase A2 myotoxins and neurotoxins: common aspects of their mechanisms of action | 3.7 | 258 | Citations (PDF) |
| 92 | Tetanus, botulinum and snake presynaptic neurotoxins | 0.0 | 3 | Citations (PDF) |
| 93 | The Vibrio cholerae cytolysin promotes activation of mast cell (T helper 2) cytokine production | 0.7 | 10 | Citations (PDF) |
| 94 | : Balancing innocent research with dual-use potential | 1.7 | 36 | Citations (PDF) |
| 95 | Ratio of lethal and edema factors in rabbit systemic anthrax | 1.2 | 45 | Citations (PDF) |
| 96 | Protective activity and immunogenicity of two recombinant anthrax vaccines for veterinary use | 2.1 | 17 | Citations (PDF) |
| 97 | cAMP imaging of cells treated with pertussis toxin, cholera toxin, and anthrax edema toxin | 1.5 | 17 | Citations (PDF) |
| 98 | Snake Phospholipase A2 Neurotoxins Enter Neurons, Bind Specifically to Mitochondria, and Open Their Transition Pores * | 1.4 | 91 | Citations (PDF) |
| 99 | Suppression of T-lymphocyte activation and chemotaxis by the adenylate cyclase toxin of Bordetella pertussis. | 2.0 | 51 | Citations (PDF) |
| 100 | Anthrax Edema Toxin Modulates PKA- and CREB-Dependent Signaling in Two Phases | 1.6 | 21 | Citations (PDF) |
| 101 | Calcium Influx and Mitochondrial Alterations at Synapses Exposed to Snake Neurotoxins or Their Phospholipid Hydrolysis Products* | 1.4 | 63 | Citations (PDF) |
| 102 | Transient Synaptic Silencing of Developing Striate Cortex Has Persistent Effects on Visual Function and Plasticity | 2.5 | 50 | Citations (PDF) |
| 103 | VacA and HP-NAP, of -associated gastric inflammation | 0.7 | 19 | Citations (PDF) |
| 104 | A lysolecithin/fatty acid mixture promotes and then blocks neurotransmitter release at the larval neuromuscular junction | 1.4 | 16 | Citations (PDF) |
| 105 | The crystal structure of CagS from the Helicobacter pylori pathogenicity island | 2.0 | 11 | Citations (PDF) |
| 106 | Glycogen synthase kinase 3 activation is essential for the snake phospholipase A2 neurotoxin-induced secretion in chromaffin cells | 1.7 | 7 | Citations (PDF) |
| 107 | Neuromuscular paralysis and recovery in mice injected with botulinum neurotoxins A and C | 1.7 | 51 | Citations (PDF) |
| 108 | Anthrax toxins inhibit immune cell chemotaxis by perturbing chemokine receptor signalling | 0.7 | 70 | Citations (PDF) |
| 109 | The concerted action of the Helicobacter pylori cytotoxin VacA and of the v-ATPase proton pump induces swelling of isolated endosomes | 0.7 | 48 | Citations (PDF) |
| 110 | Traffic of Botulinum Toxins A and E in Excitatory and Inhibitory Neurons | 1.8 | 94 | Citations (PDF) |
| 111 | Crystal structure of antigen TpF1 from Treponema pallidum | 2.0 | 20 | Citations (PDF) |
| 112 | Reversible skeletal neuromuscular paralysis induced by different lysophospholipids | 1.9 | 34 | Citations (PDF) |
| 113 | induces mast cell degranulation | 1.7 | 21 | Citations (PDF) |
| 114 | Anthrax toxins: a paradigm of bacterial immune suppression | 8.7 | 147 | Citations (PDF) |
| 115 | Cloning, expression, purification, and characterization of IgA1 protease | 1.1 | 16 | Citations (PDF) |
| 116 | A molecular model of the cytolysin transmembrane pore | 1.2 | 12 | Citations (PDF) |
| 117 | Presynaptic enzymatic neurotoxins. | 2.8 | 104 | Citations (PDF) |
| 118 | Cell entry and cAMP imaging of anthrax edema toxin | 5.4 | 71 | Citations (PDF) |
| 119 | Entering neurons: botulinum toxins and synaptic vesicle recycling | 3.6 | 83 | Citations (PDF) |
| 120 | Botulinum neurotoxins and formalin-induced pain: Central vs. peripheral effects in mice | 1.9 | 76 | Citations (PDF) |
| 121 | Interaction with CagF is required for translocation of CagA into the host via the Helicobacter pylori type IV secretion system. | 2.0 | 73 | Citations (PDF) |
| 122 | The Helicobacter pylori VacA cytotoxin activates RBL-2H3 cells by inducing cytosolic calcium oscillations | 0.7 | 40 | Citations (PDF) |
| 123 | SNARE complexes and neuroexocytosis: how many, how close? | 7.6 | 181 | Citations (PDF) |
| 124 | Antiepileptic Effects of Botulinum Neurotoxin E | 2.5 | 87 | Citations (PDF) |
| 125 | Anthrax Edema Toxin Cooperates with Lethal Toxin to Impair Cytokine Secretion during Infection of Dendritic Cells1 | 0.8 | 132 | Citations (PDF) |
| 126 | Taipoxin Induces Synaptic Vesicle Exocytosis and Disrupts the Interaction of Synaptophysin I with VAMP2 | 2.4 | 29 | Citations (PDF) |
| 127 | Equivalent Effects of Snake PLA2 Neurotoxins and Lysophospholipid-Fatty Acid Mixtures | 26.9 | 181 | Citations (PDF) |
| 128 | Internalization and Mechanism of Action of Clostridial Toxins in Neurons | 2.4 | 97 | Citations (PDF) |
| 129 | Botulinal neurotoxins: revival of an old killer | 2.9 | 299 | Citations (PDF) |
| 130 | Central injection of botulinum neurotoxins: behavioural effects in mice | 1.8 | 28 | Citations (PDF) |
| 131 | Potent inhibitors of anthrax lethal factor from green tea | 3.6 | 69 | Citations (PDF) |
| 132 | Stop the killer: how to inhibit the anthrax lethal factor metalloprotease | 7.6 | 33 | Citations (PDF) |
| 133 | Different types of botulinum toxin in humans | 3.3 | 105 | Citations (PDF) |
| 134 | Snake presynaptic neurotoxins with phospholipase A2 activity induce punctate swellings of neurites and exocytosis of synaptic vesicles | 1.8 | 63 | Citations (PDF) |
| 135 | Different mechanism of blockade of neuroexocytosis by presynaptic neurotoxins | 0.4 | 31 | Citations (PDF) |
| 136 | Tyrosine-728 and glutamic acid-735 are essential for the metalloproteolytic activity of the lethal factor of | 1.5 | 45 | Citations (PDF) |
| 137 | Comparison of the pH-induced conformational change of different clostridial neurotoxins | 1.5 | 34 | Citations (PDF) |
| 138 | Presynaptic receptor arrays for clostridial neurotoxins | 8.9 | 154 | Citations (PDF) |
| 139 | The multiple cellular activities of the VacA cytotoxin of | 1.7 | 32 | Citations (PDF) |
| 140 | Comparison of the pH-induced conformational change of different clostridial neurotoxins | 1.5 | 0 | Citations (PDF) |
| 141 | The neutrophil-activating protein of Helicobacter pylori (HP-NAP) activates the MAPK pathway in human neutrophils | 2.4 | 39 | Citations (PDF) |
| 142 | Molecular and cellular mechanisms of action of the vacuolating cytotoxin (VacA) and neutrophil-activating protein (HP-NAP) virulence factors of | 1.8 | 87 | Citations (PDF) |
| 143 | Taipoxin induces F-actin fragmentation and enhances release of catecholamines in bovine chromaffin cells | 2.8 | 38 | Citations (PDF) |
| 144 | VAMP/synaptobrevin cleavage by tetanus and botulinum neurotoxins is strongly enhanced by acidic liposomes | 1.9 | 36 | Citations (PDF) |
| 145 | Toxicity of botulinum neurotoxins in central nervous system of mice | 1.2 | 42 | Citations (PDF) |
| 146 | G-CSF–stimulated Neutrophils Are a Prominent Source of Functional BLyS | 6.2 | 280 | Citations (PDF) |
| 147 | The Metalloproteolytic Activity of the Anthrax Lethal Factor Is Substrate-inhibited* | 1.4 | 47 | Citations (PDF) |
| 148 | Structure of Two Iron-binding Proteins from Bacillus anthracis* | 1.4 | 113 | Citations (PDF) |
| 149 | Characterization and immunogenicity of the CagF protein of the cag pathogenicity island of Helicobacter pylori. | 2.0 | 9 | Citations (PDF) |
| 150 | 16 Bacterial toxins: Intracellular trafficking and target identification | 0.3 | 0 | Citations (PDF) |
| 151 | Botulinum neurotoxin serotypes A and C do not affect motor units survival in humans: an electrophysiological study by motor units counting | 0.9 | 42 | Citations (PDF) |
| 152 | Anthrax toxin: a tripartite lethal combination1 | 1.9 | 127 | Citations (PDF) |
| 153 | Structure of the Neutrophil-activating Protein from | 3.0 | 124 | Citations (PDF) |
| 154 | The neutrophil-activating protein (HP-NAP) of Helicobacter pylori is a potent stimulant of mast cells | 2.4 | 37 | Citations (PDF) |
| 155 | The role of gustatory flushing in Frey's syndrome and its treatment with botulinum toxin type A | 1.7 | 50 | Citations (PDF) |
| 156 | Cell vacuolization induced by Helicobacter pylori VacA cytotoxin does not depend on late endosomal SNAREs† | 0.7 | 29 | Citations (PDF) |
| 157 | The Vibrio cholerae haemolysin anion channel is required for cell vacuolation and death | 0.7 | 37 | Citations (PDF) |
| 158 | Internalization and Proteolytic Action of Botulinum Toxins in CNS Neurons and Astrocytes | 2.8 | 64 | Citations (PDF) |
| 159 | Botulinum Neurotoxin E-Insensitive Mutants of SNAP-25 Fail to Bind VAMP but Support Exocytosis | 2.8 | 25 | Citations (PDF) |
| 160 | Screening inhibitors of anthrax lethal factor | 32.8 | 106 | Citations (PDF) |
| 161 | Site-Directed Mutagenesis Identifies Active-Site Residues of the Light Chain of Botulinum Neurotoxin Type A | 1.5 | 63 | Citations (PDF) |
| 162 | The neutrophil-activating protein of | 1.7 | 45 | Citations (PDF) |
| 163 | How the Loop and Middle Regions Influence the Properties of Helicobacter pylori VacA Channels | 1.6 | 15 | Citations (PDF) |
| 164 | Detoxification of a bacterial toxin by the toxin itself | 11.4 | 4 | Citations (PDF) |
| 165 | Virulence factors of | 1.7 | 47 | Citations (PDF) |
| 166 | Tetanus and botulinum neurotoxins: turning bad guys into good by research | 1.2 | 182 | Citations (PDF) |
| 167 | Active-site mutagenesis of tetanus neurotoxin implicates TYR-375 and GLU-271 in metalloproteolytic activity | 1.2 | 47 | Citations (PDF) |
| 168 | The Design of Vaccines Against Helicobacter Pylori and Their Development | 23.5 | 196 | Citations (PDF) |
| 169 | Helicobacter pylori cytotoxin VacA increases alkaline secretion in gastric epithelial cells | 1.9 | 27 | Citations (PDF) |
| 170 | Neutrophil-activating protein (HP-NAP) versus ferritin (Pfr): comparison of synthesis in Helicobacter pylori. | 1.2 | 34 | Citations (PDF) |
| 171 | Living dangerously: how Helicobacter pylori survives in the human stomach | 72.9 | 445 | Citations (PDF) |
| 172 | Helicobacter pylori neutrophil-activating protein stimulates tissue factor and plasminogen activator inhibitor-2 production by human blood mononuclear cells. | 2.3 | 51 | Citations (PDF) |
| 173 | Expression, crystallization and preliminary X-ray diffraction studies of recombinant Bacillus anthracis lethal factor | 3.2 | 6 | Citations (PDF) |
| 174 | How do presynaptic PLA2 neurotoxins block nerve terminals? | 7.6 | 105 | Citations (PDF) |
| 175 | The VacA toxin of Helicobacter pylori identifies a new intermediate filament‐interacting protein | 5.4 | 52 | Citations (PDF) |
| 176 | Neurotoxins Affecting Neuroexocytosis | 20.6 | 1,203 | Citations (PDF) |
| 177 | The Neutrophil-Activating Protein (Hp-Nap) of Helicobacter pylori Is a Protective Antigen and a Major Virulence Factor | 6.2 | 262 | Citations (PDF) |
| 178 | Lethal factor of cleaves the N-terminus of MAPKKs: analysis of the intracellular consequences in macrophages | 1.7 | 62 | Citations (PDF) |
| 179 | Bacterial toxins with intracellular protease activity | 0.7 | 28 | Citations (PDF) |
| 180 | Tetanus Toxin Fragment C Binds to a Protein Present in Neuronal Cell Lines and Motoneurons | 2.8 | 72 | Citations (PDF) |
| 181 | Susceptibility of mitogen-activated protein kinase kinase family members to proteolysis by anthrax lethal factor | 2.3 | 277 | Citations (PDF) |
| 182 | Tetanus Toxin Blocks the Exocytosis of Synaptic Vesicles Clustered at Synapses But Not of Synaptic Vesicles in Isolated Axons | 2.5 | 85 | Citations (PDF) |
| 183 | Anthrax lethal factor cleaves the N-terminus of MAPKKS and induces tyrosine/threonine phosphorylation of MAPKS in cultured macrophages | 1.8 | 70 | Citations (PDF) |
| 184 | The Helicobacter pylori neutrophil-activating protein is an iron-binding protein with dodecameric structure | 1.9 | 155 | Citations (PDF) |
| 185 | Towards deciphering the Helicobacter pylori cytotoxin | 1.9 | 60 | Citations (PDF) |
| 186 | Formation of anion‐selective channels in the cell plasma membrane by the toxin VacA of Helicobacter pylori is required for its biological activity | 5.4 | 239 | Citations (PDF) |
| 187 | Molecular and cellular activities of Helicobacter pylori pathogenic factors | 1.9 | 47 | Citations (PDF) |
| 188 | Inhibition of the vacuolating and anion channel activities of the VacA toxin of Helicobacter pylori | 1.9 | 65 | Citations (PDF) |
| 189 | Anthrax lethal factor cleaves MKK3 in macrophages and inhibits the LPS/IFNγ-induced release of NO and TNFα | 1.9 | 261 | Citations (PDF) |
| 190 | Tetanus and botulinum neurotoxins: mechanism of action and therapeutic uses | 5.1 | 284 | Citations (PDF) |
| 191 | Helicobacter pylori Vacuolating Toxin Forms Anion-Selective Channels in Planar Lipid Bilayers: Possible Implications for the Mechanism of Cellular Vacuolation | 1.6 | 142 | Citations (PDF) |
| 192 | Recombinant and Truncated Tetanus Neurotoxin Light Chain: Cloning, Expression, Purification, and Proteolytic Activity | 1.1 | 24 | Citations (PDF) |
| 193 | Helicobacter pylori VacA cytotoxin associated with the bacteria increases epithelial permeability independently of its vacuolating activity | 2.4 | 69 | Citations (PDF) |
| 194 | Functional characterisation of tetanus and botulinum neurotoxins binding domains | 1.8 | 164 | Citations (PDF) |
| 195 | On the action of botulinum neurotoxins A and E at cholinergic terminals | 1.7 | 20 | Citations (PDF) |
| 196 | Action site and cellular effects of cytotoxin VacA produced byHelicobacter pylori | 1.9 | 15 | Citations (PDF) |
| 197 | Different time courses of recovery after poisoning with botulinum neurotoxin serotypes A and E in humans | 1.4 | 194 | Citations (PDF) |
| 198 | Protein toxins and membrane transport | 3.8 | 44 | Citations (PDF) |
| 199 | TPA and butyrate increase cell sensitivity to the vacuolating toxin of Helicobacter pylori | 1.9 | 10 | Citations (PDF) |
| 200 | The Acid Activation ofToxin VacA: Structural and Membrane Binding Studies | 1.5 | 84 | Citations (PDF) |
| 201 | Anthrax Lethal Factor Cleaves the N-Terminus of MAPKKs and Induces Tyrosine/Threonine Phosphorylation of MAPKs in Cultured Macrophages | 1.5 | 398 | Citations (PDF) |
| 202 | Cell vacuolization induced by VacA toxin: cell line sensitivity and quantitative estimation | 0.4 | 32 | Citations (PDF) |
| 203 | In vitro biological activity and toxicity of tetanus and botulinum neurotoxins | 0.4 | 10 | Citations (PDF) |
| 204 | SepA, the 110 kDa protein secreted by Shigella flexneri: two-domain structure and proteolytic activity | 2.4 | 60 | Citations (PDF) |
| 205 | Identification of the Helicobacter pylori VacA toxin domain active in the cell cytosol. | 2.0 | 96 | Citations (PDF) |
| 206 | Selective increase of the permeability of polarized epithelial cell monolayers by Helicobacter pylori vacuolating toxin. | 7.1 | 211 | Citations (PDF) |
| 207 | The therapeutic use of botulinum toxin | 2.5 | 31 | Citations (PDF) |
| 208 | Effect of Helicobacter pylori Vacuolating Toxin on Maturation and Extracellular Release of Procathepsin D and on Epidermal Growth Factor Degradation * | 1.4 | 106 | Citations (PDF) |
| 209 | Vacuoles Induced by Helicobacter pylori Toxin Contain Both Late Endosomal and Lysosomal Markers* | 1.4 | 165 | Citations (PDF) |
| 210 | Metal substitution of tetanus neurotoxin | 2.3 | 24 | Citations (PDF) |
| 211 | The interaction of synaptic vesicle-associated membrane protein/synaptobrevin with botulinum neurotoxins D and F | 1.9 | 46 | Citations (PDF) |
| 212 | Botulinum neurotoxin types A and E require the SNARE motif in SNAP-25 for proteolysis | 1.9 | 120 | Citations (PDF) |
| 213 | Botulinum neurotoxin serotype C: a novel effective botulinum toxin therapy in human | 1.4 | 132 | Citations (PDF) |
| 214 | Peroxynitrite and Nitric Oxide Donors Induce Neuronal Apoptosis by Eliciting Autocrine Excitotoxicity | 1.7 | 127 | Citations (PDF) |
| 215 | The small GTP binding protein rab7 is essential for cellular vacuolation induced by Helicobacter pylori cytotoxin | 5.4 | 200 | Citations (PDF) |
| 216 | Helicobacter pylori toxin VacA induces vacuole formation by acting in the cell cytosol | 1.9 | 116 | Citations (PDF) |
| 217 | Clostridial Neurotoxins and Substrate Proteolysis in Intact NeuronsBOTULINUM NEUROTOXIN C ACTS ON SYNAPTOSOMAL-ASSOCIATED PROTEIN OF 25 kDa (∗) | 1.4 | 213 | Citations (PDF) |
| 218 | The vacuolar ATPase proton pump is required for the cytotoxicity of Bacillus anthracis lethal toxin | 1.9 | 46 | Citations (PDF) |
| 219 | Substrate residues N-terminal to the cleavage site of botulinum type B neurotoxin play a role in determining the specificity of its endopeptidase activity | 1.9 | 34 | Citations (PDF) |
| 220 | The cytotoxic activity of Bacillus anthracis lethal factor is inhibited by leukotriene A4 hydrolase and metallopeptidase inhibitors | 2.3 | 44 | Citations (PDF) |
| 221 | Synaptic vesicle endocytosis mediates the entry of tetanus neurotoxin into hippocampal neurons | 5.4 | 133 | Citations (PDF) |
| 222 | Botulinum neurotoxins: mechanism of action and therapeutic applications | 2.7 | 87 | Citations (PDF) |
| 223 | Bacterial protein toxins and cell vesicle trafficking | 0.3 | 16 | Citations (PDF) |
| 224 | X-ray Absorption Spectroscopy Study of Zinc Coordination in Tetanus Neurotoxin, Astacin, Alkaline Protease and Thermolysin | 0.2 | 18 | Citations (PDF) |
| 225 | Common and distinct fusion proteins in axonal growth and transmitter release | 1.3 | 189 | Citations (PDF) |
| 226 | VAMP/synaptobrevin isoforms 1 and 2 are widely and differentially expressed in nonneuronal tissues. | 3.7 | 127 | Citations (PDF) |
| 227 | The vacuolar ATPase proton pump is present on intracellular vacuoles induced by Helicobacter pylori | 1.4 | 43 | Citations (PDF) |
| 228 | Structural Determinants of the Specificity for Synaptic Vesicle-associated Membrane Protein/Synaptobrevin of Tetanus and Botulinum Type B and G Neurotoxins* | 1.4 | 110 | Citations (PDF) |
| 229 | Botulinum Neurotoxin Type C Cleaves a Single Lys-Ala Bond within the Carboxyl-terminal Region of Syntaxins * | 1.4 | 257 | Citations (PDF) |
| 230 | Vesicle-associated membrane protein-2 (synaptobrevin-2) forms a complex with synaptophysin | 2.3 | 118 | Citations (PDF) |
| 231 | Structural Studies on the Zinc-endopeptidase Light Chain of Tetanus Neurotoxin | 0.2 | 4 | Citations (PDF) |
| 232 | Lipid Interaction of the 37-kDa and 58-kDa Fragments of the Helicobacter Pylori Cytotoxin | 0.2 | 53 | Citations (PDF) |
| 233 | Similarities between the lethal factor of Bacillus anthracis and leukotriene A4 hydrolase | 1.9 | 6 | Citations (PDF) |
| 234 | The metallo-proteinase activity of tetanus and botulism neurotoxins | 1.7 | 43 | Citations (PDF) |
| 235 | VAMP‐2 and cellubrevin are expressed in pancreatic beta‐cells and are essential for Ca(2+)‐but not for GTP gamma S‐induced insulin secretion. | 5.4 | 206 | Citations (PDF) |
| 236 | Low pH Activates the Vacuolating Toxin of Helicobacter pylori, Which Becomes Acid and Pepsin Resistant (∗) | 1.4 | 188 | Citations (PDF) |
| 237 | SNAP-25 is expressed in islets of Langerhans and is involved in insulin release. | 3.7 | 228 | Citations (PDF) |
| 238 | Insertion of Diphtheria Toxin in Lipid Bilayers Studied by Spin Label ESR | 1.8 | 18 | Citations (PDF) |
| 239 | Different requirements for NSF, SNAP, and Rab proteins in apical and basolateral transport in MDCK cells. | 24.4 | 229 | Citations (PDF) |
| 240 | Phosphorylation of VAMP/synaptobrevin in synaptic vesicles | 6.7 | 0 | Citations (PDF) |
| 241 | Cell penetration of bacterial protein toxins | 8.9 | 6 | Citations (PDF) |
| 242 | The Mechanism of Action of Tetanus and Botulinum Neurotoxins | 0.4 | 0 | Citations (PDF) |
| 243 | Phosphorylation of VAMP/Synaptobrevin in Synaptic Vesicles by Endogenous Protein Kinases | 2.8 | 88 | Citations (PDF) |
| 244 | Clostridial neurotoxins as tools to investigate the molecular events of neurotransmitter release | 3.3 | 95 | Citations (PDF) |
| 245 | Unravelling the pathogenic role of in peptic ulcer: Potential new therapies and vaccines | 8.2 | 70 | Citations (PDF) |
| 246 | Zinc content of the Bacillus anthracis lethal factor. | 1.2 | 52 | Citations (PDF) |
| 247 | SNARE motif and neurotoxins | 32.8 | 204 | Citations (PDF) |
| 248 | Eurotox-6 Conference: old bacterial toxins reveal new cell machineries | 1.9 | 0 | Citations (PDF) |
| 249 | Mechanism of action of tetanus and botulinum neurotoxins | 1.9 | 516 | Citations (PDF) |
| 250 | Tetanus and Botulinum Neurotoxins Are Zinc Proteases Specific for Components of the Neuroexocytosis Apparatusa | 2.7 | 140 | Citations (PDF) |
| 251 | Bacterial protein toxins penetrate cells via a four-step mechanism | 1.9 | 203 | Citations (PDF) |
| 252 | Molecular mechanisms of action of bacterial protein toxins | 7.9 | 81 | Citations (PDF) |
| 253 | Cellular vacuoles induced by Helicobacter pylori originate from late endosomal compartments. | 5.4 | 211 | Citations (PDF) |
| 254 | Botulinum G neurotoxin cleaves VAMP/synaptobrevin at a single Ala-Ala peptide bond. | 1.4 | 181 | Citations (PDF) |
| 255 | Neurotransmission and secretion | 32.8 | 45 | Citations (PDF) |
| 256 | Bafilomycin A1 inhibits Helicobacter pylori-induced vacuolization of HeLa cells | 1.9 | 111 | Citations (PDF) |
| 257 | Antibodies Against Rat Brain Vesicle-Associated Membrane Protein (Synaptobrevin) Prevent Inhibition of Acetylcholine Release by Tetanus Toxin or Botulinum Neurotoxin Type B | 2.8 | 41 | Citations (PDF) |
| 258 | Botulinum A Like Type B and Tetanus Toxins Fulfils Criteria for Being a Zinc-Dependent Protease | 2.8 | 67 | Citations (PDF) |
| 259 | Cell vacuolization induced by Helicobacter pylori: inhibition by bafilomycins A1, B1, C1 and D. | 1.2 | 24 | Citations (PDF) |
| 260 | The sensitivity of cystic fibrosis cells to diphtheria toxin | 1.2 | 3 | Citations (PDF) |
| 261 | Botulinum neurotoxins serotypes A and E cleave SNAP-25 at distinct COOH-terminal peptide bonds | 1.9 | 422 | Citations (PDF) |
| 262 | Novel targets and catalytic activities of bacterial protein toxins | 8.9 | 35 | Citations (PDF) |
| 263 | Tetanus and botulism neurotoxins: a new group of zinc proteases | 7.6 | 250 | Citations (PDF) |
| 264 | Cell penetration of diphtheria toxin. Reduction of the interchain disulfide bridge is the rate-limiting step of translocation in the cytosol. | 1.4 | 118 | Citations (PDF) |
| 265 | Botulinum neurotoxin serotype F is a zinc endopeptidase specific for VAMP/synaptobrevin | 1.4 | 289 | Citations (PDF) |
| 266 | Identification of the nerve terminal targets of botulinum neurotoxin serotypes A, D, and E. | 1.4 | 424 | Citations (PDF) |
| 267 | Surface topography of histidine residues of tetanus toxin probed by immobilized-metal-ion affinity chromatography | 2.3 | 36 | Citations (PDF) |
| 268 | Lipid interaction of Tetanus neurotoxin A calorimetric and fluorescence spectroscopy study | 1.9 | 15 | Citations (PDF) |
| 269 | Tetanus toxin is a zinc protein and its inhibition of neurotransmitter release and protease activity depend on zinc. | 5.4 | 271 | Citations (PDF) |
| 270 | Tetanus and botulinum-B neurotoxins block neurotransmitter release by proteolytic cleavage of synaptobrevin | 32.8 | 1,699 | Citations (PDF) |
| 271 | Ion channel and membrane translocation of diphtheria toxin. | 0.9 | 20 | Citations (PDF) |
| 272 | Botulinum neurotoxins are zinc proteins. | 1.4 | 258 | Citations (PDF) |
| 273 | Tetanus toxin receptor Specific cross-linking of tetanus toxin to a protein of NGF-differentiated PC 12 cells | 1.9 | 38 | Citations (PDF) |
| 274 | Computer modelling of the NAD binding site of ADP-ribosylating toxins: active-site structure and mechanism of NAD binding | 1.9 | 66 | Citations (PDF) |
| 275 | Lipid interaction of diphtheria toxin and mutants | 0.2 | 16 | Citations (PDF) |
| 276 | On the role of polysialoglycosphingolipids as tetanus toxin receptors | 0.2 | 31 | Citations (PDF) |
| 277 | Tyrosine 65 is photolabeled by 8-azidoadenine and 8-azidoadenosine at the NAD binding site of diphtheria toxin | 1.4 | 29 | Citations (PDF) |
| 278 | Histidine-21 is involved in diphtheria toxin NAD binding | 1.2 | 20 | Citations (PDF) |
| 279 | An intact interchain disulfide bond is required for the neurotoxicity of tetanus toxin. | 2.0 | 131 | Citations (PDF) |
| 280 | Effect of pH on the interaction of botulinum neurotoxins A, B and E with liposomes | 2.3 | 79 | Citations (PDF) |
| 281 | Histidine 21 Is at the NAD+ Binding Site of Diphtheria Toxin | 1.4 | 56 | Citations (PDF) |
| 282 | Selective extraction of haemagglutinin and matrix protein from Sendai virions by employing trifluoperazine as a detergent | 1.9 | 5 | Citations (PDF) |
| 283 | MP17, a fiber-specific intrinsic membrane protein from mammalian eye lens | 1.4 | 54 | Citations (PDF) |
| 284 | Interaction of botulinum and tetanus toxins with the lipid bilayer surface | 2.3 | 50 | Citations (PDF) |
| 285 | On the membrane translocation of diphtheria toxin: at low pH the toxin induces ion channels on cells. | 5.4 | 81 | Citations (PDF) |
| 286 | On the enzymatic activity of tetanus toxin | 1.2 | 2 | Citations (PDF) |
| 287 | Does tetanus toxin have a sequence homology with the haemagglutinin of influenza virus? | 1.2 | 2 | Citations (PDF) |
| 288 | Diphtheria toxin and its mutant crm 197 differ in their interaction with lipids | 1.9 | 32 | Citations (PDF) |
| 289 | Photolabeling of the integral proteins of skeletal muscle sarcoplasmic reticulum: Comparison of junctional and nonjunctional membrane fractions | 2.2 | 16 | Citations (PDF) |
| 290 | Isolation and characterization of cytochrome oxidase from bird and fish heart mitochondria | 0.5 | 6 | Citations (PDF) |
| 291 | Diphtheria toxin membrane translocation: an open question | 7.6 | 15 | Citations (PDF) |
| 292 | Lipid interaction of diphtheria toxin and mutants with altered fragment B | 0.2 | 37 | Citations (PDF) |
| 293 | Lipid interaction of diphtheria toxin and mutants with altered fragment B | 0.2 | 63 | Citations (PDF) |
| 294 | ATP induces conformational changes in mitochondrial cytochrome c oxidase. Effect on the cytochrome c binding site. | 1.4 | 70 | Citations (PDF) |
| 295 | Multiple lipid interactions of the Sendai virus fusogenic protein. | 1.4 | 15 | Citations (PDF) |
| 296 | Hydrophobic photolabelling of pertussis toxin subunits interacting with lipids | 1.9 | 16 | Citations (PDF) |
| 297 | How do tetanus and botulinum toxins bind to neuronal membranes? | 7.6 | 412 | Citations (PDF) |
| 298 | Comparative biochemistry of the ubiquinolcytochrome oxidoreductase (EC 1.10.2.2) isolated from different heart mitochondria | 0.5 | 15 | Citations (PDF) |
| 299 | Tetanus toxin is labeled with photoactivatable phospholipids at low pH | 1.8 | 52 | Citations (PDF) |
| 300 | ATP binding to bovine heart cytochrome c oxidase. A photoaffinity labelling study | 2.3 | 56 | Citations (PDF) |
| 301 | 1-Palmitoyl-2-(p-benzoyl)benzoyl phosphatidylcholine, a photoactive phospholipid for the labelling of membrane components | 2.3 | 13 | Citations (PDF) |
| 302 | pH-dependence of the phospholipid interaction of diphtheria-toxin fragments | 2.3 | 88 | Citations (PDF) |
| 303 | Helical packing in the hydrophobic sector of cytochrome oxidase | 2.4 | 8 | Citations (PDF) |
| 304 | Hydrophobic photolabelling of sarcoplasmic reticulum with [I]TID | 1.0 | 2 | Citations (PDF) |
| 305 | Transmembrane topology of acetylcholine receptor subunits probed with photoreactive phospholipids | 1.8 | 85 | Citations (PDF) |
| 306 | Labelling of the integral proteins of sarcoplasmic-reticulum membranes | 2.3 | 8 | Citations (PDF) |
| 307 | Membrane Topology of ATP Synthase from Bovine Heart Mitochondira and Escherichia coli | 0.2 | 50 | Citations (PDF) |
| 308 | Labeling of subunit b of the ATP synthase from Escherichia coli with a photoreactive phospholipid analogue. | 1.4 | 60 | Citations (PDF) |
| 309 | Micellar gangliosides mediate the lipid insertion of cholera toxin protomer A | 1.5 | 14 | Citations (PDF) |
| 310 | Bilayer thickness and enzymatic activity in the mitochondrial cytochrome c oxidase and ATPase complex | 1.9 | 72 | Citations (PDF) |
| 311 | Different polypeptides of bovine heart cytochrome c oxidase are in contact with cytochrome c | 1.9 | 36 | Citations (PDF) |
| 312 | Labelling of the hydrophobic domain of the Na+,K+-ATPase | 1.9 | 21 | Citations (PDF) |
| 313 | Hydrophobic photolabelling of the yeast cytochrome oxidase subunits in contact with lipids | 0.7 | 21 | Citations (PDF) |
| 314 | Effect of local anaesthetics on lymphocyte capping and energy metabolism | 3.9 | 14 | Citations (PDF) |
| 315 | Photolabelling of membrane proteins with photoactive phospholipids | 2.3 | 64 | Citations (PDF) |
| 316 | Membrane topology of beef-heart ubiquinone-cytochrome c reductase (complex III). | 1.4 | 33 | Citations (PDF) |
| 317 | Lipid insertion of cholera toxin after binding to GM1-containing liposomes. | 1.4 | 80 | Citations (PDF) |
| 318 | Interaction of the mitochondrial ATPase complex with phospholipids. | 1.4 | 26 | Citations (PDF) |
| 319 | Interaction of membranous cytochrome b 5 with arylazidophospholipids | 1.9 | 21 | Citations (PDF) |
| 320 | Cytochrome c oxidase subunits in contact with phospholipids. Hydrophobic photolabeling with azidophospholipids. | 1.4 | 66 | Citations (PDF) |
| 321 | Isotopic labeling of phosphatidylcholine in the choline moiety | 1.0 | 48 | Citations (PDF) |
| 322 | Covalent binding of arylazido derivatives of cytochrome c to cytochrome oxidase | 1.9 | 35 | Citations (PDF) |
| 323 | Probes for energy transduction in membranes | 2.2 | 11 | Citations (PDF) |
| 324 | The use of acetylated ferricytochrome C for the detection of superoxide radicals produced in biological membranes | 1.5 | 314 | Citations (PDF) |
| 325 | Molecular interactions of adenosine triphosphatase with the mitochondrial membrane as revealed by a spin label study. | 1.4 | 20 | Citations (PDF) |
| 326 | Treatment of Frey Syndrome With Botulinum Toxin Type F | 2.0 | 4 | Citations (PDF) |
| 327 | Enteric botulinum neurotoxins facilitate infection by Salmonella and Shigella. | 8.3 | 0 | Citations (PDF) |
