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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: 6 relevant articles (0 outcomes, 1 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Yamashita, Sayaka: 1 article (01/2014)
2. Araki, Kimi: 1 article (01/2014)
3. Takano, Yukio: 1 article (01/2014)
4. Deshimaru, Masanobu: 1 article (01/2014)
5. Kakita, Akiyoshi: 1 article (01/2014)
6. Itoh, Masayuki: 1 article (01/2014)
7. Hirose, Shinichi: 1 article (01/2014)
8. Ueno, Shinya: 1 article (01/2014)
9. Kitamura, Haruna: 1 article (01/2014)
10. Tanaka, Yasuyoshi: 1 article (01/2014)

Related Diseases

1. Epilepsy (Aura)
2. Seizures (Seizure)
3. Benign Neonatal Epilepsy (Benign Familial Neonatal Convulsions)

Related Drugs and Biologics

1. Sodium
2. Ligands