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cystic fibrosis transmembrane conductance regulator delta F508

CFTR - Cystic Fibrosis Transmembrane conductance regulator (a plasma membrane chloride channel); has mutation deletion of phenylalanine at residue 508; associated with cystic fibrosis
Also Known As:
deltaF508-CFTR; deltaF508-CFTR protein
Networked: 24 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Verkman, A S: 5 articles (01/2010 - 09/2004)
2. Kurth, Mark J: 2 articles (01/2010 - 10/2008)
3. Yang, Baoxue: 2 articles (01/2010 - 10/2008)
4. Becq, Frédéric: 2 articles (05/2007 - 05/2006)
5. Galietta, Luis J V: 2 articles (01/2006 - 09/2004)
6. Haston, Christina K: 1 article (07/2010)
7. Paradis, Josée: 1 article (07/2010)
8. Wilke, Martina: 1 article (07/2010)
9. Butler, Jeffrey D: 1 article (01/2010)
10. Mills, Aaron D: 1 article (01/2010)

Related Diseases

1. Cystic Fibrosis (Mucoviscidosis)
2. Pancreatic Diseases (Pancreatic Disease)
3. Inflammation (Inflammations)
4. Infections
5. Bone Diseases (Bone Disease)

Related Drugs and Biologics

1. Proteins (Proteins, Gene)
2. Curcumin
3. Mutant Proteins (Protein, Mutant)
4. Casein Kinase II (Casein Kinase 2)
5. Ubiquitin
6. Genistein
7. Cystic Fibrosis Transmembrane Conductance Regulator (Protein, CFTR)
8. NF-kappa B (NF-kB)
9. Phenylalanine (L-Phenylalanine)
10. Isoflavones

Related Therapies and Procedures

1. Therapeutics