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KCNQ Potassium Channels

A family of delayed rectifier voltage-gated potassium channels that share homology with their founding member, KCNQ1 PROTEIN. KCNQ potassium channels have been implicated in a variety of diseases including LONG QT SYNDROME; DEAFNESS; and EPILEPSY.
Also Known As:
KvLQT Potassium Channels; Potassium Channels, KCNQ; Potassium Channels, KvLQT
Networked: 9 relevant articles (0 outcomes, 2 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Cheng, Jun: 1 article (01/2018)
2. Fu, Xiaodong: 1 article (01/2018)
3. Wei, Xiaohong: 1 article (01/2018)
4. Wen, Jing: 1 article (01/2018)
5. Yin, Benlan: 1 article (01/2018)
6. Zhang, Yujiao: 1 article (01/2018)
7. Bøtker, Hans Erik: 1 article (04/2016)
8. Hedegaard, Elise R: 1 article (04/2016)
9. Jespersen, Nichlas R: 1 article (04/2016)
10. Johnsen, Jacob: 1 article (04/2016)

Related Diseases

1. Epilepsy (Aura)
2. Channelopathies
3. Stroke (Strokes)
4. Pre-Eclampsia (Preeclampsia)
5. Nervous System Diseases (Neurological Disorders)

Related Drugs and Biologics

1. Anticonvulsants (Antiepileptic Drugs)
2. ezogabine (retigabine)
3. Phosphatidylinositols (Phosphatidylinositol)

Related Therapies and Procedures

1. Drug Therapy (Chemotherapy)