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KCNQ3 Potassium Channel

A very slow opening and closing voltage-gated potassium channel that is expressed in NEURONS and is closely related to KCNQ2 POTASSIUM CHANNEL. It is commonly mutated in BENIGN FAMILIAL NEONATAL CONVULSIONS.
Also Known As:
KCNQ3 Protein; Kv7.3 Potassium Channel; Voltage-Gated K+ Channel KCNQ3; Potassium Channel, KCNQ3; Potassium Channel, Kv7.3; Voltage Gated K+ Channel KCNQ3
Networked: 5 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Shioya, Takao: 1 article (03/2008)
2. Nakamura, Yuki: 1 article (03/2008)
3. Uehara, Akira: 1 article (03/2008)
4. Hirose, Shinichi: 1 article (03/2008)
5. Yasukochi, Midori: 1 article (03/2008)
6. Uehara, Kiyoko: 1 article (03/2008)
7. Li, Min: 1 article (05/2007)
8. Sun, Haiyan: 1 article (05/2007)
9. Xiong, Qiaojie: 1 article (05/2007)
10. Hu, Hua: 1 article (01/2005)

Related Diseases

1. Benign Neonatal Epilepsy (Benign Familial Neonatal Convulsions)
2. Epilepsy (Aura)

Related Drugs and Biologics

1. Potassium Channels (Potassium Channel)