20167849

Source:http://linkedlifedata.com/resource/pubmed/id/20167849

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0006267, umls-concept:C0016059, umls-concept:C0056889, umls-concept:C0277785, umls-concept:C0439799
pubmed:issue	10
pubmed:dateCreated	2010-5-12
pubmed:abstractText	Although in patients with diffuse bronchiectasis (DB) and a normal sweat test the presence of one mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene is frequently observed, its pathogenic role in the development of DB remains unclear.
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/20167849-20460545
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9421642
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CFTR protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Cystic Fibrosis Transmembrane...
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	1535-4970
pubmed:author	pubmed-author:BassinetLaurenceL, pubmed-author:BienvenuThierryT, pubmed-author:BurgelPierre-RegisPR, pubmed-author:CrestaniBrunoB, pubmed-author:DusserDanielD, pubmed-author:FajacIsabelleI, pubmed-author:HubertDominiqueD, pubmed-author:Sermet-GaudelusIsabelleI
pubmed:issnType	Electronic
pubmed:day	15
pubmed:volume	181
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1078-84
pubmed:meshHeading	pubmed-meshheading:20167849-Adult, pubmed-meshheading:20167849-Aged, pubmed-meshheading:20167849-Bronchiectasis, pubmed-meshheading:20167849-Case-Control Studies, pubmed-meshheading:20167849-Cystic Fibrosis, pubmed-meshheading:20167849-Cystic Fibrosis Transmembrane Conductance Regulator, pubmed-meshheading:20167849-Female, pubmed-meshheading:20167849-Genotype, pubmed-meshheading:20167849-Humans, pubmed-meshheading:20167849-Male, pubmed-meshheading:20167849-Membrane Potentials, pubmed-meshheading:20167849-Middle Aged, pubmed-meshheading:20167849-Mutation, pubmed-meshheading:20167849-Nasal Mucosa, pubmed-meshheading:20167849-Phenotype, pubmed-meshheading:20167849-Pseudomonas Infections, pubmed-meshheading:20167849-Pseudomonas aeruginosa, pubmed-meshheading:20167849-Staphylococcal Infections, pubmed-meshheading:20167849-Staphylococcus aureus, pubmed-meshheading:20167849-Sweat, pubmed-meshheading:20167849-Young Adult
pubmed:year	2010
pubmed:articleTitle	Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis.
pubmed:affiliation	Service d'Explorations Fonctionnelles, Hôpital Cochin, 27 rue du Faubourg St-Jacques, Paris, France.
pubmed:publicationType	Journal Article