Pages that link to "Q36051784"
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The following pages link to In vivo activation of the cystic fibrosis transmembrane conductance regulator mutant deltaF508 in murine nasal epithelium (Q36051784):
Displaying 43 items.
- The human DnaJ homologue (Hdj)-1/heat-shock protein (Hsp) 40 co-chaperone is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70 (Q24534481) (← links)
- Pathophysiology of gene-targeted mouse models for cystic fibrosis (Q28295602) (← links)
- INO-4995 therapeutic efficacy is enhanced with repeat dosing in cystic fibrosis knockout mice and human epithelia (Q33601898) (← links)
- Compartmentalized cyclic adenosine 3',5'-monophosphate at the plasma membrane clusters PDE3A and cystic fibrosis transmembrane conductance regulator into microdomains (Q33721181) (← links)
- Improved Growth Patterns in Cystic Fibrosis Mice after Loss of Histone Deacetylase 6. (Q33807836) (← links)
- DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis (Q33854446) (← links)
- Pharmacotherapy of the ion transport defect in cystic fibrosis. (Q34434649) (← links)
- Marked repression of CFTR mRNA in the transgenic Cftr(tm1kth) mouse model (Q34989078) (← links)
- Therapeutic approaches to repair defects in deltaF508 CFTR folding and cellular targeting. (Q35012417) (← links)
- Processing and function of CFTR-DeltaF508 are species-dependent (Q35991100) (← links)
- Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings (Q36042699) (← links)
- Targeted therapy for cystic fibrosis: cystic fibrosis transmembrane conductance regulator mutation-specific pharmacologic strategies (Q36615230) (← links)
- Role of oxygen availability in CFTR expression and function (Q36951832) (← links)
- Generation of a conditional null allele for Cftr in mice (Q37263623) (← links)
- Inducible nitric oxide synthase expression is reduced in cystic fibrosis murine and human airway epithelial cells (Q37387553) (← links)
- Mis-trafficking of bicarbonate transporters: implications to human diseases (Q37860156) (← links)
- Transcriptional adaptation to cystic fibrosis transmembrane conductance regulator deficiency (Q38359766) (← links)
- In vivo alterations of IFN regulatory factor-1 and PIAS1 protein levels in cystic fibrosis epithelium (Q40431922) (← links)
- Adenosine receptors and phosphodiesterase inhibitors stimulate Cl- secretion in Calu-3 cells (Q40591756) (← links)
- A(2) adenosine receptors regulate CFTR through PKA and PLA(2). (Q40763901) (← links)
- What happens to deltaF508 in vivo? (Q40851360) (← links)
- Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells. (Q40870168) (← links)
- Cystic fibrosis transmembrane conductance regulator-dependent regulation of epithelial inducible nitric oxide synthase expression (Q40909336) (← links)
- Activation of ΔF508 CFTR in an epithelial monolayer (Q41020011) (← links)
- Defective function of the cystic fibrosis-causing missense mutation G551D is recovered by genistein (Q41695434) (← links)
- Identification of transport abnormalities in duodenal mucosa and duodenal enterocytes from patients with cystic fibrosis (Q41738688) (← links)
- PDE5 Inhibitors as Potential Tools in the Treatment of Cystic Fibrosis (Q42325938) (← links)
- Activation of the cystic fibrosis transmembrane conductance regulator by the flavonoid quercetin: potential use as a biomarker of ΔF508 cystic fibrosis transmembrane conductance regulator rescue (Q42385588) (← links)
- Regulation of amiloride-sensitive sodium absorption in murine airway epithelium by C-type natriuretic peptide (Q42456057) (← links)
- A cyclic nucleotide PDE5 inhibitor corrects defective mucin secretion in submandibular cells containing antibody directed against the cystic fibrosis transmembrane conductance regulator protein (Q42481546) (← links)
- Examining basal chloride transport using the nasal potential difference response in a murine model (Q42511337) (← links)
- Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation (Q44200339) (← links)
- CFTR involvement in nasal potential differences in mice and pigs studied using a thiazolidinone CFTR inhibitor (Q44972948) (← links)
- Role of Cftr genotype in the response to chronic Pseudomonas aeruginosa lung infection in mice (Q44972950) (← links)
- Defective respiratory amiloride-sensitive sodium transport predisposes to pulmonary oedema and delays its resolution in mice (Q45016713) (← links)
- Pharmacology of CFTR chloride channel activity. (Q53938452) (← links)
- Cystic fibrosis (Q56084190) (← links)
- THERAPIES DIRECTED AT THE BASIC DEFECT IN CYSTIC FIBROSIS (Q57952421) (← links)
- In vivo activation of CFTR-dependent chloride transport in murine airway epithelium by CNP (Q73890791) (← links)
- Type II protein kinase A regulates CFTR in airway, pancreatic, and intestinal cells (Q74408446) (← links)
- Distinct Nuclear Localization and Activity of Tissue Transglutaminase (Q74516745) (← links)
- [Mucoviscidosis: therapeutic strategies are multiplying] (Q77681664) (← links)
- Electrochemical measurement of membrane cholesterol correlates with CFTR function and is HDAC6-dependent (Q89238951) (← links)