glycerophosphoinositol 4,5-bisphosphate has been researched along with Long QT Syndrome in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (22.22) | 29.6817 |
| 2010's | 7 (77.78) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abderemane-Ali, F; Amarouch, MY; Baró, I; Brasseur, R; Coyan, FC; Loussouarn, G; Marionneau, C; Mérot, J; Mordel, J; Nicolas, CS; Piron, J; Steenman, M; Thomas, A | 1 |
| Attali, B; Ben-Tal Cohen, I; Dessauer, C; Dvir, M; Haitin, Y; Hirsch, JA; Kass, R; Pongs, O; Sachyani, D; Strulovich, R | 1 |
| Sanders, CR; Taylor, KC | 1 |
| Attali, B; Buki, T; Cui, M; Dvir, M; Haitin, Y; Hirsch, JA; Lebel, G; Logothetis, DE; Marom, M; Peretz, A; Tobelaim, WS | 1 |
| Baró, I; Loussouarn, G | 1 |
| Cui, J; Guan, M; Li, Y; Shi, J; Virgin-Downey, B; Wu, D; Zaydman, MA | 1 |
| Gao, Z; Lan, X; Li, M; Xu, H; Zheng, Y; Zhou, P; Zhu, X | 1 |
| Baró, I; Dahimene, S; Escande, D; Loussouarn, G; Mérot, J; Park, KH; Piron, J | 1 |
| Baró, I; Choveau, F; Loussouarn, G; Mérot, J; Peroz, D; Rodriguez, N | 1 |
3 review(s) available for glycerophosphoinositol 4,5-bisphosphate and Long QT Syndrome
| Article | Year |
|---|---|
Regulation of KCNQ/Kv7 family voltage-gated K
Topics: Amino Acid Sequence; Binding Sites; Cell Membrane; Epilepsy, Benign Neonatal; Fatty Acids, Unsaturated; Hearing Loss, Bilateral; Humans; Hydrophobic and Hydrophilic Interactions; KCNQ1 Potassium Channel; Long QT Syndrome; Membrane Lipids; Models, Molecular; Phosphatidylinositol 4,5-Diphosphate; Protein Binding; Protein Isoforms; Protein Structure, Secondary | 2017 |
Neural modulation of ion channels in cardiac arrhythmias: clinical implications and future investigations.
Topics: Arrhythmias, Cardiac; Caveolin 3; Computer Simulation; Cyclic AMP; Death, Sudden, Cardiac; Humans; Induced Pluripotent Stem Cells; Ion Channels; Long QT Syndrome; Neurotransmitter Agents; Phosphatidylinositol 4,5-Diphosphate; Signal Transduction | 2010 |
Kv7.1 (KCNQ1) properties and channelopathies.
Topics: Atrial Fibrillation; Humans; KCNQ1 Potassium Channel; Long QT Syndrome; Mutation; Myocytes, Cardiac; Patch-Clamp Techniques; Phosphatidylinositol 4,5-Diphosphate | 2008 |
6 other study(ies) available for glycerophosphoinositol 4,5-bisphosphate and Long QT Syndrome
| Article | Year |
|---|---|
A long QT mutation substitutes cholesterol for phosphatidylinositol-4,5-bisphosphate in KCNQ1 channel regulation.
Topics: Animals; Arrhythmias, Cardiac; Brugada Syndrome; Cardiac Conduction System Disease; Cell Line; Chlorocebus aethiops; Cholesterol; COS Cells; Heart Conduction System; KCNQ1 Potassium Channel; Long QT Syndrome; Magnesium; Mutation; Phosphatidylinositol 4,5-Diphosphate | 2014 |
Long QT mutations at the interface between KCNQ1 helix C and KCNE1 disrupt I(KS) regulation by PKA and PIP₂.
Topics: A Kinase Anchor Proteins; Animals; CHO Cells; Cricetinae; Cricetulus; Cyclic AMP; Cyclic AMP-Dependent Protein Kinases; Cytoskeletal Proteins; Humans; KCNQ1 Potassium Channel; Long QT Syndrome; Mutation, Missense; Phosphatidylinositol 4,5-Diphosphate; Phosphorylation; Potassium Channels, Voltage-Gated; Protein Binding; Protein Structure, Secondary | 2014 |
Competition of calcified calmodulin N lobe and PIP2 to an LQT mutation site in Kv7.1 channel.
Topics: Animals; Binding Sites; Binding, Competitive; Calcium Signaling; Calmodulin; CHO Cells; Cricetinae; Cricetulus; Humans; Immobilized Proteins; Long QT Syndrome; Models, Molecular; Molecular Docking Simulation; Molecular Dynamics Simulation; Mutation; Phosphatidylinositol 4,5-Diphosphate; Point Mutation; Potassium; Potassium Channels, Voltage-Gated; Protein Conformation; Protein Domains; Recombinant Proteins; Shaker Superfamily of Potassium Channels; Spectrometry, Fluorescence | 2017 |
KCNE1 enhances phosphatidylinositol 4,5-bisphosphate (PIP2) sensitivity of IKs to modulate channel activity.
Topics: Amino Acid Sequence; Animals; Humans; Ions; KCNQ1 Potassium Channel; Lipids; Long QT Syndrome; Molecular Sequence Data; Mutation; Patch-Clamp Techniques; Phosphatidylinositol 4,5-Diphosphate; Potassium Channels; Potassium Channels, Voltage-Gated; Protein Structure, Tertiary; Sequence Homology, Amino Acid; Xenopus laevis; Xenopus Proteins | 2011 |
Hexachlorophene is a potent KCNQ1/KCNE1 potassium channel activator which rescues LQTs mutants.
Topics: Action Potentials; Animals; Cell Line; CHO Cells; Cricetinae; Heart; Hexachlorophene; KCNQ1 Potassium Channel; Long QT Syndrome; Mutation; Myocytes, Cardiac; Phosphatidylinositol 4,5-Diphosphate | 2012 |
Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndrome.
Topics: Animals; COS Cells; Ethyl Methanesulfonate; Humans; KCNQ Potassium Channels; KCNQ1 Potassium Channel; Long QT Syndrome; Magnesium; Mutation; Phosphatidylinositol 4,5-Diphosphate; Potassium Channels, Voltage-Gated | 2005 |