Excitation of rat sympathetic neurons via M muscarinic receptors independently of K7 channels.
- Published in:
- Pflügers Archiv: European Journal of Physiology, 2014, v. 466, n. 12, p. 2289, doi. 10.1007/s00424-014-1487-1
- By:
- Publication type:
- Article
Works by Salzer, Isabella
Results: 15
1
2
δ Subunit-containing GABAA receptors are preferred targets for the centrally acting analgesic flupirtine.
- Published in:
- 2015
- By:
- Publication type:
- journal article
3
Concomitant facilitation of GABAA receptors and KV7 channels by the non-opioid analgesic flupirtine.
- Published in:
- 2012
- By:
- Publication type:
- journal article
4
Concomitant facilitation of GABA<sub>A</sub> receptors and K<sub>V</sub>7 channels by the non-opioid analgesic flupirtine.
- Published in:
- British Journal of Pharmacology, 2012, v. 166, n. 5, p. 1631, doi. 10.1111/j.1476-5381.2011.01821.x
- By:
- Publication type:
- Article
5
Facilitation of transmitter release from rat sympathetic neurons via presynaptic P2Y(1) receptors.
- Published in:
- 2011
- By:
- Publication type:
- journal article
6
Evidence for a Physiological Role of T-Type Ca Channels in Ventricular Cardiomyocytes of Adult Mice.
- Published in:
- Membranes, 2022, v. 12, n. 6, p. 566, doi. 10.3390/membranes12060566
- By:
- Publication type:
- Article
7
Updating In Vivo and In Vitro Phosphorylation and Methylation Sites of Voltage-Gated Kv7.2 Potassium Channels.
- Published in:
- Proteomics, 2017, v. 17, n. 19, p. n/a, doi. 10.1002/pmic.201700015
- By:
- Publication type:
- Article
8
The paracetamol metabolite N‐acetyl‐4‐benzoquinoneimine (NAPQI) prevents modulation of K<sub>V</sub>7 channels via G‐protein coupled receptors by interference with PIP<sub>2</sub> and Ca<sup>2+</sup> sensitivity.
- Published in:
- British Journal of Pharmacology, 2025, v. 182, n. 6, p. 1341, doi. 10.1111/bph.17419
- By:
- Publication type:
- Article
9
The paracetamol metabolite N‐acetyl‐4‐benzoquinoneimine (NAPQI) prevents modulation of K<sub>V</sub>7 channels via G‐protein coupled receptors by interference with PIP<sub>2</sub> and Ca<sup>2+</sup> sensitivity.
- Published in:
- British Journal of Pharmacology, 2025, v. 182, n. 5, p. 1341, doi. 10.1111/bph.17419
- By:
- Publication type:
- Article
10
A triple cysteine motif as major determinant of the modulation of neuronal K<sub>V</sub>7 channels by the paracetamol metabolite N‐acetyl‐p‐benzo quinone imine.
- Published in:
- British Journal of Pharmacology, 2024, v. 181, n. 16, p. 2851, doi. 10.1111/bph.16380
- By:
- Publication type:
- Article
11
Phosphorylation regulates the sensitivity of voltage-gated Kv7.2 channels towards phosphatidylinositol-4,5-bisphosphate.
- Published in:
- Journal of Physiology, 2017, v. 595, n. 3, p. 759, doi. 10.1113/JP273274
- By:
- Publication type:
- Article
12
Gaussian white noise stimulation as an alternative method to excite sensory neurons.
- Published in:
- Frontiers in Pharmacology, 2025, p. 1, doi. 10.3389/fphar.2025.1561905
- By:
- Publication type:
- Article
13
Electrophysiological Investigation of the Subcellular Fine Tuning of Sympathetic Neurons by Hydrogen Sulfide.
- Published in:
- Frontiers in Pharmacology, 2017, p. 1, doi. 10.3389/fphar.2017.00522
- By:
- Publication type:
- Article
14
Analgesic Action of Acetaminophen via Kv7 Channels.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 1, p. 650, doi. 10.3390/ijms24010650
- By:
- Publication type:
- Article
15
Nociceptor Signalling through ion Channel Regulation via GPCRs.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 10, p. 2488, doi. 10.3390/ijms20102488
- By:
- Publication type:
- Article