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Volumn 3, Issue 1, 2018, Pages
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Development of an airway mucus defect in the cystic fibrosis rat
a,b a a b a c c,d,e f g a,b,h,i |
Author keywords
Cell Biology; Epithelial transport of ions and water; Pulmonology
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Indexed keywords
BICARBONATE;
CFTR PROTEIN, RAT;
CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;
ANIMAL;
CYSTIC FIBROSIS;
DISEASE MODEL;
FEMALE;
GENE KNOCKOUT;
GENETICS;
ION TRANSPORT;
MALE;
METABOLISM;
MUCOCILIARY CLEARANCE;
MUCUS;
PATHOLOGY;
RAT;
RESPIRATORY MUCOSA;
SURFACE PROPERTY;
TRANSPORT AT THE CELLULAR LEVEL;
ANIMALS;
BICARBONATES;
BIOLOGICAL TRANSPORT;
CYSTIC FIBROSIS;
CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;
DISEASE MODELS, ANIMAL;
FEMALE;
GENE KNOCKOUT TECHNIQUES;
ION TRANSPORT;
MALE;
MUCOCILIARY CLEARANCE;
MUCUS;
RATS;
RESPIRATORY MUCOSA;
SURFACE PROPERTIES;
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EID: 85051635109
PISSN: None
EISSN: 23793708
Source Type: Journal
DOI: 10.1172/jci.insight.97199 Document Type: Article |
Times cited : (86)
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References (0)
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