Pages that link to "Q33763425"
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The following pages link to Molecular pharmacology of the CFTR Cl- channel (Q33763425):
Displaying 50 items.
- Identification of resveratrol oligomers as inhibitors of cystic fibrosis transmembrane conductance regulator by high-throughput screening of natural products from chinese medicinal plants (Q28537590) (← links)
- Curcumin and genistein: the combined effects on disease-associated CFTR mutants and their clinical implications (Q28830793) (← links)
- Direct block of the cystic fibrosis transmembrane conductance regulator Cl(-) channel by butyrate and phenylbutyrate (Q31869423) (← links)
- 4'-Methyl-4,5'-bithiazole-based correctors of defective delta F508-CFTR cellular processing (Q33327200) (← links)
- Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening. (Q33925348) (← links)
- Direct effects of 9-anthracene compounds on cystic fibrosis transmembrane conductance regulator gating (Q33947514) (← links)
- Glucose-sensing neurons: are they physiologically relevant? (Q33960169) (← links)
- CFTR and calcium-activated chloride channels in primary cultures of human airway gland cells of serous or mucous phenotype (Q34212692) (← links)
- Non-synaptic ion channels in insects--basic properties of currents and their modulation in neurons and skeletal muscles (Q34217875) (← links)
- On the mechanism of CFTR inhibition by a thiazolidinone derivative (Q34368505) (← 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)
- Potent stimulation and inhibition of the CFTR Cl(-) current by phloxine B. (Q35042745) (← links)
- Probing Conformational Rescue Induced by a Chemical Corrector of F508del-Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutant (Q35107406) (← links)
- Stimulation of Airway and Intestinal Mucosal Secretion by Natural Coumarin CFTR Activators (Q35233627) (← links)
- Interaction non grata between CFTR's correctors and potentiators (Q35561343) (← links)
- Molecular basis for the chloride channel activity of cystic fibrosis transmembrane conductance regulator and the consequences of disease-causing mutations (Q35749944) (← links)
- Cystic fibrosis transmembrane conductance regulator: a molecular model defines the architecture of the anion conduction path and locates a "bottleneck" in the pore (Q35862414) (← links)
- Nanomolar CFTR inhibition by pore-occluding divalent polyethylene glycol-malonic acid hydrazides (Q35878231) (← links)
- Divergent CFTR orthologs respond differently to the channel inhibitors CFTRinh-172, glibenclamide, and GlyH-101 (Q35895699) (← links)
- An Optimised Human Cell Culture Model for Alveolar Epithelial Transport. (Q36174165) (← links)
- Mechanism of chloride permeation in the cystic fibrosis transmembrane conductance regulator chloride channel (Q36255649) (← links)
- G551D and G1349D, two CF-associated mutations in the signature sequences of CFTR, exhibit distinct gating defects (Q36296010) (← links)
- Modulation of Chloride Channel Functions by the Plant Lignan Compounds Kobusin and Eudesmin. (Q36316757) (← links)
- Locating a plausible binding site for an open-channel blocker, GlyH-101, in the pore of the cystic fibrosis transmembrane conductance regulator. (Q36412828) (← links)
- Voltage-dependent Gating of the Cystic Fibrosis Transmembrane Conductance Regulator Cl− Channel (Q36436627) (← links)
- Prolonged treatment of cells with genistein modulates the expression and function of the cystic fibrosis transmembrane conductance regulator. (Q36510038) (← links)
- Vx-770 potentiates CFTR function by promoting decoupling between the gating cycle and ATP hydrolysis cycle (Q36692979) (← links)
- Inhibition of histone deacetylase 6 activity reduces cyst growth in polycystic kidney disease (Q37017182) (← links)
- Acute inhibition of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel by thyroid hormones involves multiple mechanisms (Q37234590) (← links)
- Molecular modeling of the heterodimer of human CFTR's nucleotide-binding domains using a protein-protein docking approach (Q37378641) (← links)
- Therapeutics Development for Cystic Fibrosis: A Successful Model for a Multisystem Genetic Disease (Q37827865) (← links)
- Pharmacological therapy for cystic fibrosis: from bench to bedside (Q37887169) (← links)
- Functional architecture of the CFTR chloride channel (Q38171539) (← links)
- CFTR potentiators partially restore channel function to A561E-CFTR, a cystic fibrosis mutant with a similar mechanism of dysfunction as F508del-CFTR (Q38987933) (← links)
- Revisiting CFTR inhibition: a comparative study of CFTRinh -172 and GlyH-101 inhibitors (Q39001744) (← links)
- Revertant mutants modify, but do not rescue, the gating defect of the cystic fibrosis mutant G551D-CFTR. (Q39018857) (← links)
- Role of the juxtamembrane region of cytoplasmic loop 3 in the gating and conductance of the cystic fibrosis transmembrane conductance regulator chloride channel (Q39356403) (← links)
- Mutation-induced blocker permeability and multiion block of the CFTR chloride channel pore (Q39388172) (← links)
- Alternating access to the transmembrane domain of the ATP-binding cassette protein cystic fibrosis transmembrane conductance regulator (ABCC7). (Q39401986) (← links)
- Benzbromarone Stabilizes ΔF508 CFTR at the Cell Surface (Q39552649) (← links)
- CFTR directly mediates nucleotide-regulated glutathione flux. (Q39756358) (← links)
- Cysteine-independent inhibition of the CFTR chloride channel by the cysteine-reactive reagent sodium (2-sulphonatoethyl) methanethiosulphonate (Q39847523) (← links)
- A quantitative description of the activation and inhibition of CFTR by potentiators: Genistein. (Q40401974) (← links)
- Two mechanisms of genistein inhibition of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in murine cell line (Q40886609) (← links)
- Nutrient Sensing: Another Chemosensitivity of the Olfactory System (Q40987474) (← links)
- CFTR in K562 human leukemic cells. (Q42169019) (← links)
- CFTR activation in human bronchial epithelial cells by novel benzoflavone and benzimidazolone compounds (Q42438647) (← links)
- Relative contribution of different transmembrane segments to the CFTR chloride channel pore. (Q42614303) (← links)
- Voltage-dependent flickery block of an open cystic fibrosis transmembrane conductance regulator (CFTR) channel pore (Q42647604) (← links)