Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2004-10-6
pubmed:abstractText
Loss of cystic fibrosis transmembrane conductance regulator (CFTR) function in cystic fibrosis (CF) causes dysregulation of multiple ion channels, water channels, and acid-base transporters in epithelia. As such, we hypothesized that dysregulation of many critical ion channels and transporters may cause defects in human airway epithelial cell volume regulation.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1569-1993
pubmed:author
pubmed:issnType
Print
pubmed:volume
3
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
99-117
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:15463893-Adenosine Triphosphate, pubmed-meshheading:15463893-Autocrine Communication, pubmed-meshheading:15463893-Bronchi, pubmed-meshheading:15463893-Calcium, pubmed-meshheading:15463893-Cell Line, pubmed-meshheading:15463893-Chlorides, pubmed-meshheading:15463893-Cystic Fibrosis, pubmed-meshheading:15463893-Cystic Fibrosis Transmembrane Conductance Regulator, pubmed-meshheading:15463893-Epithelial Cells, pubmed-meshheading:15463893-Gene Expression, pubmed-meshheading:15463893-Humans, pubmed-meshheading:15463893-Hypotonic Solutions, pubmed-meshheading:15463893-Isotonic Solutions, pubmed-meshheading:15463893-Receptors, Purinergic P2, pubmed-meshheading:15463893-Respiratory Mucosa, pubmed-meshheading:15463893-Signal Transduction, pubmed-meshheading:15463893-Transfection, pubmed-meshheading:15463893-Water-Electrolyte Balance
pubmed:year
2004
pubmed:articleTitle
Purinergic signaling underlies CFTR control of human airway epithelial cell volume.
pubmed:affiliation
Department of Physiology and Biophysics, University of Alabama at Birmingham, Birmingham, AL 35294-0005, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.