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Boglárka Kántás
Boglárka Kántás
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Title
Cited by
Cited by
Year
Novel drug-like somatostatin receptor 4 agonists are potential analgesics for neuropathic pain
B Kántás, R Börzsei, É Szőke, P Bánhegyi, Á Horváth, Á Hunyady, ...
International journal of molecular sciences 20 (24), 6245, 2019
352019
Analgesic effects of lipid raft disruption by sphingomyelinase and myriocin via transient receptor potential vanilloid 1 and transient receptor potential ankyrin 1 ion channel …
Á Horváth, M Payrits, A Steib, B Kántás, T Biró-Süt, J Erostyák, G Makkai, ...
Frontiers in Pharmacology 11, 593319, 2021
112021
Antinociceptive effects of lipid raft disruptors, a novel carboxamido-steroid and methyl β-cyclodextrin, in mice by inhibiting transient receptor potential vanilloid 1 and …
Á Horváth, T Biró-Sütő, B Kántás, M Payrits, R Skoda-Földes, ...
Frontiers in Physiology 11, 559109, 2020
112020
In Silico, In Vitro and In Vivo Pharmacodynamic Characterization of Novel Analgesic Drug Candidate Somatostatin SST4 Receptor Agonists
B Kántás, É Szőke, R Börzsei, P Bánhegyi, J Asghar, L Hudhud, A Steib, ...
Frontiers in Pharmacology 11, 601887, 2021
92021
The heptapeptide somatostatin analogue TT-232 exerts analgesic and anti-inflammatory actions via SST4 receptor activation: In silico, in vitro and in vivo evidence in mice
R Börzsei, É Borbély, B Kántás, L Hudhud, Á Horváth, É Szőke, C Hetényi, ...
Biochemical Pharmacology 209, 115419, 2023
22023
The Epigenetics of Neuropathic Pain: A Systematic Update
G Pethő, B Kántás, Á Horváth, E Pintér
International Journal of Molecular Sciences 24 (24), 17143, 2023
12023
Anti-Nociceptive Effects of Sphingomyelinase and Methyl-Beta-Cyclodextrin in the Icilin-Induced Mouse Pain Model
Á Horváth, A Steib, A Nehr-Majoros, B Kántás, Á Király, M Racskó, BI Tóth, ...
International Journal of Molecular Sciences 25 (9), 4637, 2024
2024
Characterization of novel somatostatin 4 receptor agonists in different pain models
B Kántás, Z Helyes, É Borbély
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