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Volumn 103, Issue 1, 2007, Pages 413-
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The role of cystic fibrosis transmembrane conductance regulator chloride channel in β-receptor-mediated regulation of alveolar fluid clearance [2]
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Author keywords
[No Author keywords available]
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Indexed keywords
ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM);
BETA ADRENERGIC RECEPTOR;
BETA ADRENERGIC RECEPTOR STIMULATING AGENT;
CHLORIDE CHANNEL;
SODIUM CHANNEL;
SODIUM ION;
TRANSMEMBRANE CONDUCTANCE REGULATOR;
AIRWAY;
ANALYTICAL PARAMETERS;
BIOACCUMULATION;
COMPARATIVE STUDY;
GENOTYPE;
HUMAN;
IN VITRO STUDY;
ION TRANSPORT;
LETTER;
LUNG ALVEOLUS;
LUNG ALVEOLUS EPITHELIUM;
LUNG CLEARANCE;
LUNG FLUID;
MUTATION;
PRIORITY JOURNAL;
PSEUDOHYPOALDOSTERONISM;
RECEPTOR DENSITY;
SALIVARY GLAND;
SODIUM TRANSPORT;
STIMULATION;
SWEAT;
VOLUNTEER;
ANIMALS;
BODY FLUIDS;
CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;
EPITHELIAL SODIUM CHANNEL;
HUMANS;
MICE;
MICE, INBRED CFTR;
NA(+)-K(+)-EXCHANGING ATPASE;
PULMONARY ALVEOLI;
PULMONARY EDEMA;
RECEPTORS, ADRENERGIC, BETA;
WATER-ELECTROLYTE BALANCE;
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EID: 34447640964
PISSN: 87507587
EISSN: 15221601
Source Type: Journal
DOI: 10.1152/japplphysiol.00280.2007 Document Type: Letter |
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Times cited : (2)
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References (6)
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