Pages that link to "Q36010684"
The following pages link to Noninvasive in vivo fluorescence measurement of airway-surface liquid depth, salt concentration, and pH. (Q36010684):
Displaying 50 items.
- In vitro selection of a sodium-specific DNAzyme and its application in intracellular sensing (Q22066247) (← links)
- Function of the HVCN1 proton channel in airway epithelia and a naturally occurring mutation, M91T (Q24625061) (← links)
- The epithelial anion transporter pendrin is induced by allergy and rhinovirus infection, regulates airway surface liquid, and increases airway reactivity and inflammation in an asthma model (Q24652628) (← links)
- State of the Art: Why do the lungs of patients with cystic fibrosis become infected and why can't they clear the infection? (Q24802489) (← links)
- Microscale imaging of cilia-driven fluid flow (Q26826635) (← links)
- Characterization of defects in ion transport and tissue development in cystic fibrosis transmembrane conductance regulator (CFTR)-knockout rats (Q27316635) (← links)
- Method for quantitative study of airway functional microanatomy using micro-optical coherence tomography (Q27319331) (← links)
- Cystic fibrosis (Q28212180) (← links)
- Evidence of amiloride-sensitive fluid absorption in rat descending colonic crypts from fluorescence recovery of FITC-labelled dextran after photobleaching (Q28361703) (← links)
- Role of aquaporin water channels in airway fluid transport, humidification, and surface liquid hydration (Q28584765) (← links)
- Aquaporin deletion in mice reduces intraocular pressure and aqueous fluid production (Q28584934) (← links)
- Voltage-gated proton channels: molecular biology, physiology, and pathophysiology of the H(V) family (Q28681630) (← links)
- Mitochondria control store-operated Ca2+ entry through Na+ and redox signals (Q30274638) (← links)
- Quantifying the effects of altering ambient humidity on ionic composition of vocal fold surface fluid (Q30435796) (← links)
- Airway surface liquid depth imaged by surface laser reflectance microscopy (Q33659880) (← links)
- Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study (Q33766585) (← links)
- CFTR-mediated halide transport in phagosomes of human neutrophils (Q33806624) (← links)
- Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung (Q33950252) (← links)
- In situ fluorescence measurement of tear film [Na+], [K+], [Cl-], and pH in mice shows marked hypertonicity in aquaporin-5 deficiency (Q33995808) (← links)
- A new role for bicarbonate in mucus formation (Q34212678) (← links)
- Airway surface liquid: end of the controversy? (Q34237588) (← links)
- A functional anatomic defect of the cystic fibrosis airway (Q34425996) (← links)
- The role of inflammation in the pathophysiology of CF lung disease (Q34773499) (← links)
- Abnormal surface liquid pH regulation by cultured cystic fibrosis bronchial epithelium (Q34795536) (← links)
- pH modulates the activity and synergism of the airway surface liquid antimicrobials β-defensin-3 and LL-37 (Q34832018) (← links)
- Regulation of the depth and composition of airway surface liquid (Q34996416) (← links)
- Lung edema clearance: 20 years of progress: invited review: role of aquaporin water channels in fluid transport in lung and airways (Q34998571) (← links)
- An overview of the pathogenesis of cystic fibrosis lung disease (Q35012409) (← links)
- Hyperviscous airway periciliary and mucous liquid layers in cystic fibrosis measured by confocal fluorescence photobleaching (Q35043906) (← links)
- Regulation of chemokine expression by NaCl occurs independently of cystic fibrosis transmembrane conductance regulator in macrophages (Q35221848) (← links)
- Update on pathogenesis of cystic fibrosis lung disease (Q35554386) (← links)
- Pathophysiology and Management of Pulmonary Infections in Cystic Fibrosis (Q35557791) (← links)
- Automated acquisition and analysis of airway surface liquid height by confocal microscopy (Q35639690) (← links)
- Role of aquaporins in lung liquid physiology (Q35860530) (← links)
- From structure to disease: the evolving tale of aquaporin biology (Q35875999) (← links)
- Function of Proton Channels in Lung Epithelia (Q35994631) (← links)
- Transcriptional and posttranscriptional control of cable pilus gene expression in Burkholderia cenocepacia (Q36233411) (← links)
- Soluble mediators, not cilia, determine airway surface liquid volume in normal and cystic fibrosis superficial airway epithelia (Q36295665) (← links)
- Sodium and chloride concentrations, pH, and depth of airway surface liquid in distal airways (Q36436631) (← links)
- Airway surface liquid osmolality measured using fluorophore-encapsulated liposomes (Q36444640) (← links)
- In vivo airway surface liquid Cl- analysis with solid-state electrodes (Q36445272) (← links)
- Submucosal gland secretions in airways from cystic fibrosis patients have normal [Na(+)] and pH but elevated viscosity (Q36541617) (← links)
- Mechanisms of acid and base secretion by the airway epithelium (Q36647815) (← links)
- Contribution of α7 nicotinic receptor to airway epithelium dysfunction under nicotine exposure (Q36673189) (← links)
- Airway acidification initiates host defense abnormalities in cystic fibrosis mice. (Q36857687) (← links)
- Chronic inflammation in the cystic fibrosis lung: alterations in inter- and intracellular signaling (Q36981240) (← links)
- In situ measurement of airway surface liquid [K+] using a ratioable K+-sensitive fluorescent dye (Q37257384) (← links)
- Airway surface liquid depth measured in ex vivo fragments of pig and human trachea: dependence on Na+ and Cl- channel function (Q37475006) (← links)
- Airway drug pharmacokinetics via analysis of exhaled breath condensate (Q37625778) (← links)
- Chloride flux in phagocytes (Q38936533) (← links)