Pages that link to "Q33970197"
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The following pages link to Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR) (Q33970197):
Displaying 50 items.
- Differential function of the two nucleotide binding domains on cystic fibrosis transmembrane conductance regulator (Q22010873) (← links)
- Cystic Fibrosis Heterozygote Resistance to Cholera Toxin in the Cystic Fibrosis Mouse Model (Q22299398) (← links)
- Sodium channel blockers for cystic fibrosis (Q24197477) (← links)
- Sodium channel blockers for cystic fibrosis (Q24200975) (← links)
- Sodium channel blockers for cystic fibrosis (Q24245081) (← links)
- Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosa (Q24310215) (← links)
- An excitatory amino-acid transporter with properties of a ligand-gated chloride channel (Q24323343) (← links)
- The relevance of sweat testing for the diagnosis of cystic fibrosis in the genomic era. (Q24535769) (← links)
- Defective regulation of gap junctional coupling in cystic fibrosis pancreatic duct cells (Q24563188) (← links)
- Cooperative, ATP-dependent association of the nucleotide binding cassettes during the catalytic cycle of ATP-binding cassette transporters (Q24602798) (← links)
- The ABC protein turned chloride channel whose failure causes cystic fibrosis (Q24657572) (← links)
- Patterns of GI disease in adulthood associated with mutations in the CFTR gene (Q24673570) (← links)
- Mechanisms of lipid malabsorption in Cystic Fibrosis: the impact of essential fatty acids deficiency (Q24806288) (← links)
- New and emerging targeted therapies for cystic fibrosis (Q26749278) (← links)
- Cystic fibrosis in young children: A review of disease manifestation, progression, and response to early treatment (Q26784611) (← links)
- Airway hydration and COPD (Q28082617) (← links)
- Retinal stimulates ATP hydrolysis by purified and reconstituted ABCR, the photoreceptor-specific ATP-binding cassette transporter responsible for Stargardt disease (Q28138732) (← links)
- pCLCA1 becomes a cAMP-dependent chloride conductance mediator in Caco-2 cells (Q28212490) (← links)
- Membrane insertion, processing, and topology of cystic fibrosis transmembrane conductance regulator (CFTR) in microsomal membranes (Q28237929) (← links)
- Regulation of CFTR chloride channels by syntaxin and Munc18 isoforms (Q28255553) (← links)
- Molecular physiology of bestrophins: multifunctional membrane proteins linked to best disease and other retinopathies (Q28275211) (← links)
- The CLCA gene locus as a modulator of the gastrointestinal basic defect in cystic fibrosis (Q28288390) (← links)
- Pathophysiology of gene-targeted mouse models for cystic fibrosis (Q28295602) (← links)
- Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy (Q28297851) (← links)
- Chloride channels: an emerging molecular picture (Q28304402) (← links)
- Protein kinase C-mediated phosphorylation of the human multidrug resistance P-glycoprotein regulates cell volume-activated chloride channels (Q28910230) (← links)
- Lung infections associated with cystic fibrosis (Q30080000) (← links)
- Multiple forms of casein kinase from rabbit erythrocytes (Q30110841) (← links)
- Inhibition of CFTR Cl- channel function caused by enzymatic hydrolysis of sphingomyelin (Q30444368) (← links)
- The ΔF508-CFTR mutation inhibits wild-type CFTR processing and function when co-expressed in human airway epithelia and in mouse nasal mucosa (Q31099925) (← links)
- Cystic fibrosis transmembrane conductance regulator gating requires cytosolic electrolytes (Q31668598) (← links)
- Perturbation of the pore of the cystic fibrosis transmembrane conductance regulator (CFTR) inhibits its atpase activity (Q31743298) (← links)
- A divergent CFTR homologue: highly regulated salt transport in the euryhaline teleost F. heteroclitus (Q32074473) (← links)
- Evaluation of the membrane-spanning domain of ClC-2 (Q33235938) (← links)
- Calnexin Delta 185-520 partially reverses the misprocessing of the Delta F508 cystic fibrosis transmembrane conductance regulator. (Q33292065) (← links)
- Biokinetics of nanoparticles and susceptibility to particulate exposure in a murine model of cystic fibrosis (Q33560161) (← links)
- Syntaxin 1A inhibits CFTR chloride channels by means of domain-specific protein-protein interactions (Q33567267) (← links)
- Quality of life in cystic fibrosis (Q33569482) (← links)
- Molecular insights into the physiology of the 'thin film' of airway surface liquid (Q33592224) (← links)
- Regulation of CFTR Cl- ion channels by phosphorylation and dephosphorylation. (Q33602315) (← links)
- Gene therapy for cystic fibrosis (Q33623207) (← links)
- The regulation of epithelial cell cAMP- and calcium-dependent chloride channels (Q33637654) (← links)
- Genetic Variation and Clinical Heterogeneity in Cystic Fibrosis (Q33645546) (← links)
- CFTR and TNR-CFTR expression and function in the kidney (Q33659294) (← links)
- Cystic fibrosis: exploiting its genetic basis in the hunt for new therapies (Q33664918) (← links)
- Genotype-phenotype relationship in 12 patients carrying cystic fibrosis mutation R334W (Q33678356) (← links)
- Structure and function of the cystic fibrosis transmembrane conductance regulator (Q33716379) (← links)
- Compartmentalized cyclic adenosine 3',5'-monophosphate at the plasma membrane clusters PDE3A and cystic fibrosis transmembrane conductance regulator into microdomains (Q33721181) (← links)
- Are mutations in the cystic fibrosis gene important in chronic pancreatitis? (Q33724438) (← links)
- Non-specific activation of the epithelial sodium channel by the CFTR chloride channel (Q33757239) (← links)