Pages that link to "Q40529951"
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The following pages link to Novel regulation of cystic fibrosis transmembrane conductance regulator (CFTR) channel gating by external chloride (Q40529951):
Displaying 26 items.
- SLC26A9 is a Cl(-) channel regulated by the WNK kinases (Q24336113) (← links)
- Molecular mechanism of pancreatic and salivary gland fluid and HCO3 secretion (Q26852694) (← links)
- Airway Gland Structure and Function (Q28082284) (← links)
- Bestrophin Cl- channels are highly permeable to HCO3- (Q28609348) (← links)
- Functional Cftr in crypt epithelium of organotypic enteroid cultures from murine small intestine (Q30514240) (← links)
- Mechanism and synergism in epithelial fluid and electrolyte secretion (Q33624152) (← links)
- A biophysical model for integration of electrical, osmotic, and pH regulation in the human bronchial epithelium (Q33795623) (← links)
- Cystic fibrosis transmembrane conductance regulator chloride channel blockers: Pharmacological, biophysical and physiological relevance (Q34408604) (← links)
- Modulation of CFTR gating by permeant ions (Q34780305) (← links)
- Slc26a6 regulates CFTR activity in vivo to determine pancreatic duct HCO3- secretion: relevance to cystic fibrosis (Q35121200) (← links)
- Composition of mineralizing incisor enamel in cystic fibrosis transmembrane conductance regulator-deficient mice (Q35554820) (← links)
- Gating the glutamate gate of CLC-2 chloride channel by pore occupancy. (Q36407985) (← links)
- CFTR functions as a bicarbonate channel in pancreatic duct cells (Q37124268) (← links)
- CLC-0 and CFTR: chloride channels evolved from transporters (Q37129332) (← links)
- Interaction between 2 extracellular loops influences the activity of the cystic fibrosis transmembrane conductance regulator chloride channel (Q38953529) (← links)
- Architecture and functional properties of the CFTR channel pore (Q38971502) (← links)
- Pseudohalide anions reveal a novel extracellular site for potentiators to increase CFTR function (Q39345267) (← links)
- Regulation of CFTR chloride channel macroscopic conductance by extracellular bicarbonate (Q39647491) (← links)
- On the origin of asymmetric interactions between permeant anions and the cystic fibrosis transmembrane conductance regulator chloride channel pore (Q40201664) (← links)
- Interactions between impermeant blocking ions in the cystic fibrosis transmembrane conductance regulator chloride channel pore: evidence for anion-induced conformational changes (Q40263455) (← links)
- The cystic fibrosis transmembrane conductance regulator is an extracellular chloride sensor (Q41580343) (← links)
- The effects induced by the sulphonylurea glibenclamide on the neonatal rat spinal cord indicate a novel mechanism to control neuronal excitability and inhibitory neurotransmission (Q41584119) (← links)
- Sendai virus-mediated CFTR gene transfer to the airway epithelium. (Q45402489) (← links)
- A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR. (Q47140243) (← links)
- Evidence that extracellular anions interact with a site outside the CFTR chloride channel pore to modify channel properties (Q47781167) (← links)
- Increases in cytosolic Ca2 induce dynamin- and calcineurin-dependent internalisation of CFTR (Q90470039) (← links)