HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

human GJB3 protein

defects in GJB3 are a cause of erythrokeratodermia variabilis (EKV), RefSeq NM_024009
Also Known As:
GJB3 protein, human; Gap junction beta-3 protein, human; connexin 31; connexin Cx31; connexin-31
Networked: 31 relevant articles (1 outcomes, 2 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Pan, Qian: 5 articles (11/2015 - 06/2005)
2. Xia, Kun: 5 articles (10/2011 - 03/2002)
3. Zhang, Zhuohua: 3 articles (11/2015 - 10/2010)
4. Wang, Danling: 3 articles (11/2015 - 10/2010)
5. Kelsell, David P: 3 articles (03/2006 - 05/2002)
6. Richard, G: 3 articles (04/2003 - 02/2000)
7. Tang, Chengyuan: 2 articles (11/2015 - 01/2012)
8. Liu, Mujun: 2 articles (11/2015 - 01/2012)
9. Chi, Jingwei: 2 articles (11/2015 - 01/2012)
10. Tan, Zhi-Ping: 2 articles (08/2005 - 03/2002)

Related Diseases

1. Deafness (Deaf Mutism)
2. Hearing Loss (Hearing Impairment)
3. Erythrokeratodermia Variabilis
4. Skin Diseases
5. Peripheral Nervous System Diseases (PNS Diseases)

Related Drugs and Biologics

1. connexin 26
2. Sodium-Potassium-Chloride Symporters
3. Adenosine Triphosphatases (ATPase)
4. Connexins
5. Voltage-Gated Potassium Channels (Voltage-Gated Potassium Channel)
6. connexin 30.3
7. 5' Untranslated Regions (5' UTR)
8. Peptides
9. connexin 32