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Azadeh Shahsavar

Showing results (11-20 of 21) with videos related to

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Molecular Pharmacology|July 17, 2015
Acetylcholine-Binding Protein Engineered to Mimic the α4-α4 Binding Pocket in α4β2 Nicotinic Acetylcholine Receptors Reveals Interface Specific Interactions Important for Binding and ActivityAzadeh Shahsavar, Philip K Ahring, Jeppe A Olsen, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 25, 2013
Crystal structures of a pentameric ligand-gated ion channel provide a mechanism for activationLudovic Sauguet, Azadeh Shahsavar, Frédéric Poitevin, et al.
Nature Communications|January 29, 2026
Structural basis for selective inhibition of human GABA transporter GAT3Jonas Sigurd Mortensen, Francesco Bavo, Malene Hall Jensen, et al.
The Journal of Biological Chemistry|August 4, 2022
The Na<sup>+</sup>,K<sup>+</sup>-ATPase in complex with beryllium fluoride mimics an ATPase phosphorylated stateMarlene U Fruergaard, Ingrid Dach, Jacob L Andersen, et al.
Nature Communications|May 26, 2016
A conserved leucine occupies the empty substrate site of LeuT in the Na(+)-free return stateLina Malinauskaite, Saida Said, Caglanur Sahin, et al.
Nature|March 4, 2021
Structural insights into the inhibition of glycine reuptakeAzadeh Shahsavar, Peter Stohler, Gleb Bourenkov, et al.
Neuropharmacology|January 18, 2015
Engineered α4β2 nicotinic acetylcholine receptors as models for measuring agonist binding and effect at the orthosteric low-affinity α4-α4 interfacePhilip K Ahring, Jeppe A Olsen, Elsebet Ø Nielsen, et al.
Journal of Neurochemistry|July 16, 2024
Cryo-EM structure of the dopamine transporter with a novel atypical non-competitive inhibitor bound to the orthosteric siteClara Nautrup Pedersen, Fuyu Yang, Samantha Ita, et al.
Biorxiv : the Preprint Server for Biology|December 3, 2025
A reversible allosteric inhibitor of GlyT2 alleviates neuropathic pain without on-target side effectsRyan P Cantwell Chater, Julian Peiser-Oliver, Tanmay K Pati, et al.
Nature Communications|February 16, 2026
A reversible allosteric inhibitor of GlyT2 for neuropathic pain without on-target side effectsRyan P Cantwell Chater, Julian Peiser-Oliver, Tanmay K Pati, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Molecular Pharmacology|July 17, 2015
Acetylcholine-Binding Protein Engineered to Mimic the α4-α4 Binding Pocket in α4β2 Nicotinic Acetylcholine Receptors Reveals Interface Specific Interactions Important for Binding and ActivityAzadeh Shahsavar, Philip K Ahring, Jeppe A Olsen, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 25, 2013
Crystal structures of a pentameric ligand-gated ion channel provide a mechanism for activationLudovic Sauguet, Azadeh Shahsavar, Frédéric Poitevin, et al.
Nature Communications|January 29, 2026
Structural basis for selective inhibition of human GABA transporter GAT3Jonas Sigurd Mortensen, Francesco Bavo, Malene Hall Jensen, et al.
The Journal of Biological Chemistry|August 4, 2022
The Na<sup>+</sup>,K<sup>+</sup>-ATPase in complex with beryllium fluoride mimics an ATPase phosphorylated stateMarlene U Fruergaard, Ingrid Dach, Jacob L Andersen, et al.
Nature Communications|May 26, 2016
A conserved leucine occupies the empty substrate site of LeuT in the Na(+)-free return stateLina Malinauskaite, Saida Said, Caglanur Sahin, et al.
Nature|March 4, 2021
Structural insights into the inhibition of glycine reuptakeAzadeh Shahsavar, Peter Stohler, Gleb Bourenkov, et al.
Neuropharmacology|January 18, 2015
Engineered α4β2 nicotinic acetylcholine receptors as models for measuring agonist binding and effect at the orthosteric low-affinity α4-α4 interfacePhilip K Ahring, Jeppe A Olsen, Elsebet Ø Nielsen, et al.
Journal of Neurochemistry|July 16, 2024
Cryo-EM structure of the dopamine transporter with a novel atypical non-competitive inhibitor bound to the orthosteric siteClara Nautrup Pedersen, Fuyu Yang, Samantha Ita, et al.
Biorxiv : the Preprint Server for Biology|December 3, 2025
A reversible allosteric inhibitor of GlyT2 alleviates neuropathic pain without on-target side effectsRyan P Cantwell Chater, Julian Peiser-Oliver, Tanmay K Pati, et al.
Nature Communications|February 16, 2026
A reversible allosteric inhibitor of GlyT2 for neuropathic pain without on-target side effectsRyan P Cantwell Chater, Julian Peiser-Oliver, Tanmay K Pati, et al.
Pageof 3