Pages that link to "Q41695007"
Jump to navigation
Jump to search
The following pages link to Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance (Q41695007):
Displaying 50 items.
- Molecular cloning, expression analysis, and chromosomal localization of human syntaxin 8 (STX8) (Q22009359) (← links)
- Differential function of the two nucleotide binding domains on cystic fibrosis transmembrane conductance regulator (Q22010873) (← links)
- Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasome (Q24533430) (← links)
- Identification of a protein that confers calcitonin gene-related peptide responsiveness to oocytes by using a cystic fibrosis transmembrane conductance regulator assay (Q24567952) (← links)
- Volume-regulated chloride channels associated with the human multidrug-resistance P-glycoprotein (Q28186115) (← links)
- Cystic fibrosis. Channelling our thoughts (Q28276216) (← 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)
- A chloride channel widely expressed in epithelial and non-epithelial cells (Q28581891) (← links)
- Mouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting duct (Q28941235) (← links)
- Lung infections associated with cystic fibrosis (Q30080000) (← links)
- Perturbation of the pore of the cystic fibrosis transmembrane conductance regulator (CFTR) inhibits its atpase activity (Q31743298) (← links)
- Abnormal secretagogue-induced intracellular free Ca2+ regulation in cystic fibrosis nasal epithelial cells (Q33209490) (← links)
- Isolation and expression of a guanylate cyclase-coupled heat stable enterotoxin receptor cDNA from a human colonic cell line (Q33267240) (← links)
- Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung disease (Q33594335) (← links)
- CFTR transcripts are undetectable in lymphocytes and respiratory epithelial cells of a CF patient homozygous for the nonsense mutation R553X (Q33595872) (← links)
- Regulation of CFTR Cl- ion channels by phosphorylation and dephosphorylation. (Q33602315) (← links)
- The regulation of epithelial cell cAMP- and calcium-dependent chloride channels (Q33637654) (← links)
- Cystic fibrosis: exploiting its genetic basis in the hunt for new therapies (Q33664918) (← links)
- Phenotypic profiling of CFTR modulators in patient-derived respiratory epithelia (Q33825789) (← links)
- Cystic fibrosis transmembrane conductance regulator interacts with multiple immunoglobulin domains of filamin A. (Q33883521) (← links)
- Nonsense mutation R1162X of the cystic fibrosis transmembrane conductance regulator gene does not reduce messenger RNA expression in nasal epithelial tissue (Q33909657) (← links)
- Phosphorylation of CFTR by PKA promotes binding of the regulatory domain (Q33910924) (← links)
- Regulation of CFTR expression and function during differentiation of intestinal epithelial cells (Q33938002) (← links)
- How cystic fibrosis affects pancreatic ductal bicarbonate secretion (Q33953482) (← links)
- Cystic fibrosis transmembrane conductance regulator (CFTR) potentiator VX-770 (ivacaftor) opens the defective channel gate of mutant CFTR in a phosphorylation-dependent but ATP-independent manner (Q34033437) (← links)
- Structural and functional similarities between the nucleotide-binding domains of CFTR and GTP-binding proteins (Q34047787) (← links)
- The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation (Q34088939) (← links)
- A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis (Q34141568) (← links)
- Interaction between permeation and gating in a putative pore domain mutant in the cystic fibrosis transmembrane conductance regulator (Q34173438) (← links)
- The cystic fibrosis transmembrane conductance regulator impedes proteolytic stimulation of the epithelial Na+ channel (Q34186468) (← links)
- Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel (Q34205844) (← links)
- Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis (Q34213495) (← links)
- Non-synaptic ion channels in insects--basic properties of currents and their modulation in neurons and skeletal muscles (Q34217875) (← links)
- Molecular Biology of Cystic Fibrosis (Q34306869) (← links)
- Disulphonic stilbene block of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in a mammalian cell line and its regulation by a critical pore residue (Q34408228) (← links)
- Activation of ion transport pathways by changes in cell volume (Q34573926) (← links)
- Molecular analysis of the ovine cystic fibrosis transmembrane conductance regulator gene (Q34583768) (← links)
- Interleukin-13 (IL-13)/IL-13 receptor alpha1 (IL-13Ralpha1) signaling regulates intestinal epithelial cystic fibrosis transmembrane conductance regulator channel-dependent Cl- secretion. (Q34787194) (← links)
- Abnormal surface liquid pH regulation by cultured cystic fibrosis bronchial epithelium (Q34795536) (← links)
- Transfer of a constitutive viral promoter-cystic fibrosis transmembrane conductance regulator cDNA to human epithelial cells conveys resistance to down-regulation of cAMP-regulated Cl- secretion in the presence of inflammatory stimuli (Q34889409) (← links)
- Identification of an ion channel-forming motif in the primary structure of CFTR, the cystic fibrosis chloride channel (Q35054035) (← links)
- Expression of the human cystic fibrosis transmembrane conductance regulator gene in the mouse lung after in vivo intratracheal plasmid-mediated gene transfer (Q35072251) (← links)
- Genetic determination of exocrine pancreatic function in cystic fibrosis (Q35195369) (← links)
- Identification of a nonframeshift 84-bp deletion in exon 13 of the cystic fibrosis gene (Q35195536) (← links)
- Evolution of an ion-translocating ATPase (Q35238872) (← links)
- Altered protein folding may be the molecular basis of most cases of cystic fibrosis (Q35344873) (← links)
- Energy metabolism in cystic fibrosis (Q35531229) (← links)
- Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells (Q35554260) (← links)
- Update on pathogenesis of cystic fibrosis lung disease (Q35554386) (← links)