| Q37954286 | Bacterial toxins and the nervous system: neurotoxins and multipotential toxins interacting with neuronal cells |
| Q40242526 | Biophysical comparison of diphtheria and tetanus toxins with the formaldehyde-detoxified toxoids, the main components of diphtheria and tetanus vaccines. |
| Q37954285 | Clostridial neurotoxins: mechanism of SNARE cleavage and outlook on potential substrate specificity reengineering |
| Q37613674 | Clostridial toxins |
| Q61807386 | Evolutionary Features in the Structure and Function of Bacterial Toxins |
| Q91069899 | Identification of Formaldehyde-Induced Modifications in Diphtheria Toxin |
| Q60310521 | Identity, Structure and Compositional Analysis of Aluminum Phosphate Adsorbed Pediatric Quadrivalent and Pentavalent Vaccines |
| Q33994987 | Liposomes containing monophosphoryl lipid A: a potent adjuvant system for inducing antibodies to heroin hapten analogs. |
| Q53575621 | Mechanism of substrate recognition by botulinum neurotoxin serotype A. |
| Q46294932 | Molecular architecture of botulinum neurotoxin E revealed by single particle electron microscopy |
| Q37876965 | Molecular structures and functional relationships in clostridial neurotoxins |
| Q37408530 | Receptor and substrate interactions of clostridial neurotoxins |
| Q52655358 | Structural characterisation of the catalytic domain of botulinum neurotoxin X - high activity and unique substrate specificity. |
| Q38113138 | The blockade of the neurotransmitter release apparatus by botulinum neurotoxins |
| Q41597441 | The structure of the tetanus toxin reveals pH-mediated domain dynamics |
| Q48124277 | Uptake of Clostridial Neurotoxins into Cells and Dissemination |