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Biophysical and pharmacological properties of the voltage-gated potassium current of human pancreatic β-cells.
- Published in:
- Journal of Physiology, 2005, v. 567, n. 1, p. 159, doi. 10.1113/jphysiol.2005.089375
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- Article
A Cell-Sparing Electric Field Stimulation Technique forHigh-Throughput Screening of Voltage-Gated Ion Channels.
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- Assay & Drug Development Technologies, 2006, v. 4, n. 1, p. 21
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- Article
Highly Parallelized, Multicolor Optogenetic Recordings of Cellular Activity for Therapeutic Discovery Applications in Ion Channels and Disease-Associated Excitable Cells.
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- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.896320
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- Article
Suppression of Kv3.3 channels by antisense oligonucleotides reverses biochemical effects and motor impairment in spinocerebellar ataxia type 13 mice.
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- FASEB Journal, 2021, v. 35, n. 12, p. 1, doi. 10.1096/fj.202101356R
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- Article
Profiling Diverse Compounds by Flux- and Electrophysiology-Based Primary Screens for Inhibition of Human Ether-à-go-goRelated Gene Potassium Channels.
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- Assay & Drug Development Technologies, 2010, v. 8, n. 6, p. 743, doi. 10.1089/adt.2010.0339
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- Article
A High-Throughput Assay for Evaluating State Dependence and Subtype Selectivity of Cav2 Calcium Channel Inhibitors.
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- Assay & Drug Development Technologies, 2008, v. 6, n. 2, p. 195, doi. 10.1089/adt.2008.136
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- Article
An Automated Electrophysiology Serum Shift Assay for KVChannels.
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- Assay & Drug Development Technologies, 2008, v. 6, n. 2, p. 243, doi. 10.1089/adt.2008.128
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- Article
Blockers of the Delayed-Rectifier Potassium Current in Pancreatic β-Cells Enhance Glucose-Dependent Insulin Secretion.
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- Diabetes, 2006, v. 55, n. 4, p. 1034, doi. 10.2337/diabetes.55.04.06.db05-0788
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- Article
Identification and optimization of 2-aminobenzimidazole derivatives as novel inhibitors of TRPC4 and TRPC5 channels.
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- British Journal of Pharmacology, 2015, v. 172, n. 14, p. 3495, doi. 10.1111/bph.13140
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- Article
Discovery and Characterization of 2-(Cyclopropanesulfonamido)- N-(2-ethoxyphenyl)benzamide, ML382: a Potent and Selective Positive Allosteric Modulator of MrgX1.
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- ChemMedChem, 2015, v. 10, n. 1, p. 57, doi. 10.1002/cmdc.201402277
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- Article