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Proceedings of the National Academy of Sciences of the United States of America

Volumn 98, Issue 9, 2001, Pages 5329-5334

Defective regulatory volume decrease in human cystic fibrosis tracheal cells because of altered regulation of intermediate conductance Ca2+-dependent potassium channels

(3) Vázquez, Esther a Nobles, Muriel b Valverde, Miguel A a

a UNIVERSITAT POMPEU FABRA (Spain)

b MEDICAL RESEARCH COUNCIL (United Kingdom)

Author keywords

F508; Airways; CFTR; Chloride secretion; HIKK

Indexed keywords

CALCIUM; CHLORIDE CHANNEL; POTASSIUM; POTASSIUM CHANNEL; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARTICLE; CALCIUM CONDUCTANCE; CELL VOLUME; CYSTIC FIBROSIS; GENE EXPRESSION; HUMAN; HUMAN CELL; LUNG INSUFFICIENCY; MALE INFERTILITY; MECONIUM ILEUS; PANCREAS INSUFFICIENCY; POTASSIUM CONDUCTANCE; POTASSIUM CURRENT; PRIORITY JOURNAL; TRACHEA MUCOSA;

CALCIUM; CELL LINE; CELL SIZE; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; ELECTRIC CONDUCTIVITY; HUMANS; HYPOTONIC SOLUTIONS; INTERMEDIATE-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNELS; ION TRANSPORT; PHENOTYPE; POTASSIUM; POTASSIUM CHANNEL BLOCKERS; POTASSIUM CHANNELS; POTASSIUM CHANNELS, CALCIUM-ACTIVATED; TRACHEA;

MURINAE;

EID: 0035942218 PISSN: 00278424 EISSN: None Source Type: Journal
DOI: 10.1073/pnas.091096498 Document Type: Article

Times cited : (57)

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