[HTML][HTML] Exploiting botulinum neurotoxins for the study of brain physiology and pathology
Botulinum neurotoxins are metalloproteases that specifically cleave N-ethylmaleimide-
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
Exploiting Botulinum Neurotoxins for the Study of Brain Physiology and Pathology
M Caleo, L Restani - Toxins, 2018 - pubmed.ncbi.nlm.nih.gov
Botulinum neurotoxins are metalloproteases that specifically cleave N-ethylmaleimide-
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
Exploiting Botulinum Neurotoxins for the Study of Brain Physiology and Pathology.
M Caleo, L Restani - Toxins, 2018 - europepmc.org
Botulinum neurotoxins are metalloproteases that specifically cleave N-ethylmaleimide-
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
[HTML][HTML] Exploiting Botulinum Neurotoxins for the Study of Brain Physiology and Pathology
M Caleo, L Restani - Toxins, 2018 - ncbi.nlm.nih.gov
Botulinum neurotoxins are metalloproteases that specifically cleave N-ethylmaleimide-
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
Exploiting Botulinum Neurotoxins for the Study of Brain Physiology and Pathology
M Caleo, L Restani - 2018 - hero.epa.gov
Botulinum neurotoxins are metalloproteases that specifically cleave N-ethylmaleimide-
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
Exploiting Botulinum Neurotoxins for the Study of Brain Physiology and Pathology
M Caleo, L Restani - Toxins, 2018 - search.proquest.com
Botulinum neurotoxins are metalloproteases that specifically cleave N-ethylmaleimide-
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
Exploiting Botulinum Neurotoxins for the Study of Brain Physiology and Pathology
M Caleo, L Restani - Toxins, 2018 - agris.fao.org
Botulinum neurotoxins are metalloproteases that specifically cleave N-ethylmaleimide-
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
[HTML][HTML] Exploiting Botulinum Neurotoxins for the Study of Brain Physiology and Pathology
M Caleo, L Restani - … and Nervous System: Future Challenges for …, 2020 - books.google.com
Botulinum neurotoxins are metalloproteases that specifically cleave N-ethylmaleimide-
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
Exploiting Botulinum Neurotoxins for the Study of Brain Physiology and Pathology.
M Caleo, L Restani - Toxins, 2018 - search.ebscohost.com
Botulinum neurotoxins are metalloproteases that specifically cleave < italic>
N</italic>-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins …
N</italic>-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins …
[PDF][PDF] Exploiting Botulinum Neurotoxins for the Study of Brain Physiology and Pathology
M Caleo, L Restani - pdfs.semanticscholar.org
Botulinum neurotoxins are metalloproteases that specifically cleave N-ethylmaleimide-
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …
sensitive factor attachment protein receptor (SNARE) proteins in synaptic terminals, resulting …