glyburide and sodium azide

glyburide has been researched along with sodium azide in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ashford, ML; Campbell, CM; Kinsella, JM; McKay, NG1
Chen, M; Dong, Y; Simard, JM1
Cannone, G; Carbonara, G; Cippone, V; Conte Camerino, D; Fracchiolla, G; Laghezza, A; Loiodice, F; Mele, A; Rolland, JF; Tortorella, P; Tricarico, D1

Other Studies

3 other study(ies) available for glyburide and sodium azide

ArticleYear
Sensitivity of Kir6.2-SUR1 currents, in the absence and presence of sodium azide, to the K(ATP) channel inhibitors, ciclazindol and englitazone.
    British journal of pharmacology, 2000, Volume: 130, Issue:4

    Topics: Adenosine Triphosphate; Animals; ATP-Binding Cassette Transporters; Benzopyrans; Cell Line; Dose-Response Relationship, Drug; Female; Glyburide; Humans; Indoles; Membrane Potentials; Mice; Microinjections; Oocytes; Potassium Channels; Potassium Channels, Inwardly Rectifying; Receptors, Drug; RNA, Complementary; Sodium Azide; Sulfonylurea Receptors; Thiazoles; Thiazolidinediones; Tolbutamide; Xenopus laevis

2000
Functional coupling between sulfonylurea receptor type 1 and a nonselective cation channel in reactive astrocytes from adult rat brain.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003, Sep-17, Volume: 23, Issue:24

    Topics: Adenosine Triphosphate; Animals; Antibodies; Astrocytes; ATP-Binding Cassette Transporters; Binding, Competitive; Brain; Brain Injuries; Cell Size; Cells, Cultured; Diazoxide; Gliosis; Glyburide; Ion Channels; Membrane Potentials; Patch-Clamp Techniques; Potassium Channels; Potassium Channels, Inwardly Rectifying; Rats; Rats, Wistar; Receptors, Drug; Reverse Transcriptase Polymerase Chain Reaction; Sodium Azide; Sulfonylurea Compounds; Sulfonylurea Receptors; Tolbutamide; Trypsin

2003
Structural nucleotide analogs are potent activators/inhibitors of pancreatic β cell KATP channels: an emerging mechanism supporting their use as antidiabetic drugs.
    The Journal of pharmacology and experimental therapeutics, 2012, Volume: 340, Issue:2

    Topics: Animals; Area Under Curve; Benzoxazines; Blood Glucose; Dose-Response Relationship, Drug; Electrophysiological Phenomena; Fasting; Glucose; Glucose Tolerance Test; Glyburide; HEK293 Cells; Humans; Hypoglycemic Agents; Insulin; Insulin Secretion; Insulin-Secreting Cells; KATP Channels; Membrane Potentials; Mice; Mice, Inbred Strains; Patch-Clamp Techniques; Potassium Channels, Inwardly Rectifying; Sodium Azide; Tolbutamide

2012