The neglected ion: HCO3-

Nature Medicine

Volumn 7, Issue 3, 2001, Pages 292-293

  Quinton, P M ^a  

^a UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BICARBONATE; CHLORIDE; TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR PROTEIN, HUMAN;

CHLORIDE TRANSPORT; CONTROLLED STUDY; CYSTIC FIBROSIS; GENE MUTATION; GENETIC TRANSFECTION; GENOTYPE; HUMAN; HUMAN CELL; PANCREAS SECRETION; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN PROCESSING; SHORT SURVEY; ARTICLE; ION TRANSPORT; METABOLISM; PANCREAS;

BICARBONATES; CHLORIDES; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; HUMANS; ION TRANSPORT; PANCREAS;

EID: 0034745438     PISSN: 10788956     EISSN: None     Source Type: Journal    
DOI: 10.1038/85429     Document Type: Short Survey

References (14)

1. Genotype and phenotype in cystic fibrosis
2. Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
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4. Genetics, diagnosis, and clinical phenotype
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6. Quantitative assessment of exocrine pancreatic function in infants and children
7. The exocrine pancreas
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9. Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland
10. Biosynthesis and degradation of CFTR
11. Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive
12. pH- and protein-dependent buffer capacity and viscosity of respiratory mucus. Their interrelationships and influence on health
13. - conductance through CFTR in human airway epithelia
14. Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions