37 results on '"Partiseti, Michel"'
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2. The grapefruit polyphenol naringenin inhibits multiple cardiac ion channels
3. In vitro ion channel profile and ex vivo cardiac electrophysiology properties of the R(-) and S(+) enantiomers of hydroxychloroquine
4. The atypic antipsychotic clozapine inhibits multiple cardiac ion channels
5. Transforming TRP Channel Drug Discovery Using Medium-Throughput Electrophysiological Assays
6. Automated Patch-Clamp Methods for the hERG Cardiac Potassium Channel
7. The Grapefruit Flavonoid Naringenin Inhibits Multiple Cardiac Ion Channels
8. Cross-Linking of IgG Receptors Inhibits Membrane Immunoglobulin-Stimulated Calcium Influx in B Lymphocytes
9. Fluorescent‐ and tagged‐protoxin II peptides: potent markers of the Na v 1.7 channel pain target
10. Multichannel inhibitory profile of (−)-Cannabidiol on cardiac ion channels
11. Lysophosphatidic Acid Receptor Agonism: Discovery of Potent Nonlipid Benzofuran Ethanolamine Structures
12. A PHARMACOLOGICAL SYNOPSIS OF SMALL MOLECULES, TOXINS AND CiPA COMPOUNDS TARGETING HUMAN CARDIAC Kv4.3 CHANNELS
13. Fluorescent- and tagged-protoxin II peptides: potent markers of the Nav 1.7 channel pain target.
14. From identification to functional characterization of cyriotoxin‐1a, an antinociceptive toxin from the spiderCyriopagopus schioedtei
15. Electrophysiological and Pharmacological Characterization of Human Inwardly Rectifying Kir2.1 Channels on an Automated Patch-Clamp Platform
16. Corrigendum: The NaV1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons
17. The NaV1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons
18. D peptide, a promising toxin as potential antinociceptive agent targeting the Nav1.7 subtype of voltage-gated sodium channels
19. A non-invasive method to appraise time-dependent effects of venom toxins on the mouse neuromuscular excitability in vivo
20. A multiscale functional approach to assess pharmacologocal interactions between huwentoxin-IV spider peptide and sodium channel subtypes
21. Direct evidence for high affinity blockade of NaV1.6 channel subtype by huwentoxin-IV spider peptide, using multiscale functional approaches
22. Validation of an Automated Patch-Clamp Screening Assay on Human Kir2.1 Cardiac Ion Channels
23. Functional Studies of Sodium Channels: From Target to Compound Identification
24. From identification to functional characterization of cyriotoxin-1a, an antinociceptive toxin from the spider Cyriopagopus schioedtei.
25. Electrophysiological and Pharmacological Characterization of Human Inwardly Rectifying Kir2.1 Channels on an Automated Patch-Clamp Platform.
26. Direct evidence for high affinity blockade of NaV1.6 channel subtype by huwentoxin-IV spider peptide, using multiscale functional approaches.
27. Design and validation of a homogeneous time-resolved fluorescence cell-based assay targeting the ligand-gated ion channel 5-HT3A
28. Cloning and characterization of a novel human inwardly rectifying potassium channel predominantly expressed in small intestine
29. Corrigendum: The NaV1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons.
30. A Primary T-Cell Immunodeficiency Associated With Defective Transmembrane Calcium Influx
31. A new potent peptide blocker, from Poecilotheria subfusca spider, of the human Cav1.2 channel subtype.
32. Cannabidiol inhibits multiple cardiac ion channels and shortens ventricular action potential duration in vitro.
33. Electrophysiological and Pharmacological Characterization of Human Inwardly Rectifying K ir 2.1 Channels on an Automated Patch-Clamp Platform.
34. Corrigendum: The Na V 1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons.
35. The Na V 1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons.
36. Direct evidence for high affinity blockade of Na V 1.6 channel subtype by huwentoxin-IV spider peptide, using multiscale functional approaches.
37. Automated Patch-Clamp Methods for the hERG Cardiac Potassium Channel.
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