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KCNQ2 Potassium Channel

A very slow opening and closing voltage-gated potassium channel that is expressed in NEURONS and is commonly mutated in BENIGN FAMILIAL NEONATAL CONVULSIONS.
Also Known As:
KCNQ2 Protein; Kv7.2 Potassium Channel; Voltage-Gated K+ Channel KCNQ2; Potassium Channel, KCNQ2; Potassium Channel, Kv7.2; Voltage Gated K+ Channel KCNQ2
Networked: 12 relevant articles (0 outcomes, 2 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Hui, Zhi-Yan: 2 articles (10/2012 - 08/2011)
2. Liu, Li: 2 articles (10/2012 - 08/2011)
3. Shi, Rui-Ming: 2 articles (10/2012 - 08/2011)
4. Song, Hong-Xia: 2 articles (10/2012 - 08/2011)
5. Zhang, Wei: 2 articles (10/2012 - 08/2011)
6. Zhou, Xi-Hui: 2 articles (10/2012 - 08/2011)
7. Ambrosino, Paolo: 1 article (01/2022)
8. Binda, Anna: 1 article (01/2022)
9. Castellotti, Barbara: 1 article (01/2022)
10. DiFrancesco, Jacopo C: 1 article (01/2022)

Related Diseases

1. Epilepsy (Aura)
2. Brain Diseases (Brain Disorder)
3. Benign Neonatal Epilepsy (Benign Familial Neonatal Convulsions)
4. Seizures (Absence Seizure)

Related Drugs and Biologics

1. Sodium
2. Ligands
3. Calmodulin (Calcium-Dependent Activator Protein)