Chloride conductance and genetic background modulate the cystic fibrosis phenotype of ΔF508 homozygous twins and siblings

To investigate the impact of chloride (Cl(–)) permeability, mediated by residual activity of the cystic fibrosis transmembrane conductance regulator (CFTR) or by other Cl(–) channels, on the manifestations of cystic fibrosis (CF), we determined Cl(–) transport properties of the respiratory and intes...

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Xehetasun bibliografikoak
Egile Nagusiak: Bronsveld, Inez, Mekus, Frauke, Bijman, Jan, Ballmann, Manfred, de Jonge, Hugo R., Laabs, Ulrike, Halley, Dicky J., Ellemunter, Helmut, Mastella, Gianni, Thomas, Stephen, Veeze, Henk J., Tümmler, Burkhard
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society for Clinical Investigation 2001
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC200980/
https://ncbi.nlm.nih.gov/pubmed/11733566
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