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Jennifer R. Deuis
Jennifer R. Deuis
Verified email at uq.edu.au
Title
Cited by
Cited by
Year
Methods used to evaluate pain behaviors in rodents
JR Deuis, LS Dvorakova, I Vetter
Frontiers in molecular neuroscience 10, 284, 2017
11172017
An animal model of oxaliplatin-induced cold allodynia reveals a crucial role for Nav1. 6 in peripheral pain pathways
JR Deuis, K Zimmermann, AA Romanovsky, LD Possani, PJ Cabot, ...
Pain® 154 (9), 1749-1757, 2013
1992013
Pharmacological characterisation of the highly NaV1.7 selective spider venom peptide Pn3a
JR Deuis, Z Dekan, JS Wingerd, JJ Smith, NR Munasinghe, RF Bhola, ...
Scientific reports 7 (1), 40883, 2017
1492017
NaV1. 7 as a pain target–from gene to pharmacology
I Vetter, JR Deuis, A Mueller, MR Israel, H Starobova, A Zhang, LD Rash, ...
Pharmacology & therapeutics 172, 73-100, 2017
1442017
Burn pain: a systematic and critical review of epidemiology, pathophysiology, and treatment
M Morgan, JR Deuis, M Frøsig-Jørgensen, RJ Lewis, PJ Cabot, PD Gray, ...
Pain medicine 19 (4), 708-734, 2018
1212018
Analgesic Effects of GpTx-1, PF-04856264 and CNV1014802 in a Mouse Model of NaV1.7-Mediated Pain
JR Deuis, JS Wingerd, Z Winter, T Durek, Z Dekan, SR Sousa, ...
Toxins 8 (3), 78, 2016
1192016
Identification and characterization of ProTx-III [μ-TRTX-Tp1a], a new voltage-gated sodium channel inhibitor from venom of the tarantula Thrixopelma pruriens
FC Cardoso, Z Dekan, KJ Rosengren, A Erickson, I Vetter, JR Deuis, ...
Molecular pharmacology 88 (2), 291-303, 2015
952015
Multiple sodium channel isoforms mediate the pathological effects of Pacific ciguatoxin-1
MC Inserra, MR Israel, A Caldwell, J Castro, JR Deuis, AM Harrington, ...
Scientific reports 7 (1), 42810, 2017
842017
The pharmacology of voltage-gated sodium channel activators
JR Deuis, A Mueller, MR Israel, I Vetter
Neuropharmacology 127, 87-108, 2017
752017
The thermal probe test: A novel behavioral assay to quantify thermal paw withdrawal thresholds in mice
JR Deuis, I Vetter
Temperature 3 (2), 199-207, 2016
742016
Sodium channels and venom peptide pharmacology
MR Israel, B Tay, JR Deuis, I Vetter
Advances in pharmacology 79, 67-116, 2017
722017
The snake with the scorpion’s sting: Novel three-finger toxin sodium channel activators from the venom of the long-glanded blue coral snake (Calliophis bivirgatus)
DC Yang, JR Deuis, D Dashevsky, J Dobson, TNW Jackson, A Brust, ...
Toxins 8 (10), 303, 2016
712016
Transcriptomic and behavioural characterisation of a mouse model of burn pain identify the cholecystokinin 2 receptor as an analgesic target
K Yin, JR Deuis, RJ Lewis, I Vetter
Molecular pain 12, 1744806916665366, 2016
712016
Analgesic treatment of ciguatoxin-induced cold allodynia
K Zimmermann, JR Deuis, MC Inserra, LS Collins, B Namer, PJ Cabot, ...
Pain 154 (10), 1999-2006, 2013
632013
Antiallodynic effects of the selective NaV1. 7 inhibitor Pn3a in a mouse model of acute postsurgical pain: evidence for analgesic synergy with opioids and baclofen
A Mueller, H Starobova, M Morgan, Z Dekan, O Cheneval, CI Schroeder, ...
Pain 160 (8), 1766-1780, 2019
562019
Analgesic effects of clinically used compounds in novel mouse models of polyneuropathy induced by oxaliplatin and cisplatin
JR Deuis, YL Lim, S Rodrigues de Sousa, RJ Lewis, PF Alewood, ...
Neuro-oncology 16 (10), 1324-1332, 2014
552014
Modulatory features of the novel spider toxin μ‐TRTX‐Df1a isolated from the venom of the spider Davus fasciatus
FC Cardoso, Z Dekan, JJ Smith, JR Deuis, I Vetter, V Herzig, PF Alewood, ...
British journal of pharmacology 174 (15), 2528-2544, 2017
532017
Inflammatory and neuropathic gene expression signatures of chemotherapy-induced neuropathy induced by vincristine, cisplatin, and oxaliplatin in C57BL/6J mice
H Starobova, A Mueller, JR Deuis, DA Carter, I Vetter
The journal of pain 21 (1-2), 182-194, 2020
482020
The structure, dynamics and selectivity profile of a NaV1.7 potency-optimised huwentoxin-IV variant
S Rahnama, JR Deuis, FC Cardoso, V Ramanujam, RJ Lewis, LD Rash, ...
PLoS one 12 (3), e0173551, 2017
462017
Development of a μO-conotoxin analogue with improved lipid membrane interactions and potency for the analgesic sodium channel NaV1. 8
JR Deuis, Z Dekan, MC Inserra, TH Lee, MI Aguilar, DJ Craik, RJ Lewis, ...
Journal of Biological Chemistry 291 (22), 11829-11842, 2016
442016
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