To the Editor: In their paper describing increased electric potential difference across respiratory epithelia in cystic fibrosis (December 17 issue1) Knowles et al. mentioned that the time course of indomethacin's action on the bioelectric properties of respiratory epithelia was not well documented. This is not correct; we have previously reported details of indomethacin's effect on electrical properties and on transport of sodium and chloride across canine tracheal mucosa in vitro
The macrolide antibiotic azithromycin improves lung function and prognosis among patients with cysti...
Comment in :The yin and yang of cystic fibrosis transmembrane conductance regulator function: implic...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
To the Editor: As reported by Knowles et al. in the issue of December 17, 1981, in vivo measurements...
To investigate respiratory epithelial function in cystic fibrosis, we measured the transepithelial e...
Cystic fibrosis (CF) airway epithelia exhibit defective trans-epithelial electrolyte transport: cAMP...
La réduction de la conductance de Cl−de la membrane cellulaire apicale et l'augmentation de la condu...
A recent study by Leonard, Lebecque, Dingemanse, and Leal [1] tested the effect of Miglustat, an alp...
Loss of cystic fibrosis transmembrane conductance regulator (CFTR) anion channel function causes cys...
The airways are lined with a thin layer of fluid called the airway surface liquid (ASL), whose funct...
tential difference (PD) across respiratory epithelia in cystic fibrosis (CF) has suggested an abnorm...
1. Employing a primary cell culture system and intracellular microelectrodes, we quantitated and com...
Abstract Quantitation of CFTR function in vitro is commonly performed by acutely stimulating then in...
The nasal potential difference test has been used for almost three decades to assist in the diagnosi...
This study compares the effect of three chemically unrelated cystic fibrosis transmembrane conductan...
The macrolide antibiotic azithromycin improves lung function and prognosis among patients with cysti...
Comment in :The yin and yang of cystic fibrosis transmembrane conductance regulator function: implic...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
To the Editor: As reported by Knowles et al. in the issue of December 17, 1981, in vivo measurements...
To investigate respiratory epithelial function in cystic fibrosis, we measured the transepithelial e...
Cystic fibrosis (CF) airway epithelia exhibit defective trans-epithelial electrolyte transport: cAMP...
La réduction de la conductance de Cl−de la membrane cellulaire apicale et l'augmentation de la condu...
A recent study by Leonard, Lebecque, Dingemanse, and Leal [1] tested the effect of Miglustat, an alp...
Loss of cystic fibrosis transmembrane conductance regulator (CFTR) anion channel function causes cys...
The airways are lined with a thin layer of fluid called the airway surface liquid (ASL), whose funct...
tential difference (PD) across respiratory epithelia in cystic fibrosis (CF) has suggested an abnorm...
1. Employing a primary cell culture system and intracellular microelectrodes, we quantitated and com...
Abstract Quantitation of CFTR function in vitro is commonly performed by acutely stimulating then in...
The nasal potential difference test has been used for almost three decades to assist in the diagnosi...
This study compares the effect of three chemically unrelated cystic fibrosis transmembrane conductan...
The macrolide antibiotic azithromycin improves lung function and prognosis among patients with cysti...
Comment in :The yin and yang of cystic fibrosis transmembrane conductance regulator function: implic...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...