Cystic fibrosis transmembrane conductance regulator and Na⁺ channel subunits mRNA transcripts, and Cl^- efflux, show a different distribution in rat duodenum and colonODES, H. S; SMIRNOFF, P; GUBERMAN, R et al.Acta physiologica scandinavica. 2003, Vol 178, Num 3, pp 231-240, issn 0001-6772, 10 p.Article

Role of the scaffold protein RACK1 in apical expression of CFTRAUERBACH, Michael; LIEDTKE, Carole M.American journal of physiology. Cell physiology. 2007, Vol 62, Num 1, issn 0363-6143, C294-C304Article

Influence of cell background on pharmacological rescue of mutant CFTRPEDEMONTE, Nicoletta; TOMATI, Valeria; SONDO, Elvira et al.American journal of physiology. Cell physiology. 2010, Vol 67, Num 4, issn 0363-6143, C866-C874Article

Rescue of the mutant CFTR chloride channel by pharmacological correctors and low temperature analyzed by gene expression profilingSONDO, Elvira; TOMATI, Valeria; CACI, Emanuela et al.American journal of physiology. Cell physiology. 2011, Vol 70, Num 4, issn 0363-6143, C872-C885Article

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Spiperone, identified through compound screening, activates calcium-dependent chloride secretion in the airwayLIHUA LIANG; MACDONALD, Kelvin; SCHWIEBERT, Erik M et al.American journal of physiology. Cell physiology. 2009, Vol 65, Num 1, issn 0363-6143, C131-C141Article

PKC phosphorylation modulates PKA-dependent binding of the R domain to other domains of CFTRSEAVILLEKLEIN, Gage; AMER, Noha; EVAGELIDIS, Alexandra et al.American journal of physiology. Cell physiology. 2008, Vol 64, Num 5, issn 0363-6143, C1366-C1375Article

Cor pulmonale in cystic fibrosisECKLES, Michael; ANDERSON, Paula.Seminars in respiratory and critical care medicine. 2003, Vol 24, Num 3, pp 323-330, issn 1069-3424, 8 p.Article

Dépistage de la mucoviscidose : conséquences attenduesSARLES, J.LES DOSSIERS DE L'OBSTETRIQUE. 1998, Num 263, pp 35-36Article

Development of primary human nasal epithelial cell cultures for the study of cystic fibrosis pathophysiologyDE COURCEY, F; ZHOLOS, A. V; ATHERTON-WATSON, H et al.American journal of physiology. Cell physiology. 2012, Vol 72, Num 6, issn 0363-6143, C1173-C1179Article

Paper based point-of-care testing disc for multiplex whole cell bacteria analysisLI, Chen-Zhong; VANDENBERG, Katherine; PRABHULKAR, Shradha et al.Biosensors & bioelectronics. 2011, Vol 26, Num 11, pp 4342-4348, issn 0956-5663, 7 p.Article

Normal nasal mucociliary clearance in CF children: evidence against a CFTR-related defectMCSHANE, D; DAVIES, J. C; WODEHOUSE, T et al.The European respiratory journal. 2004, Vol 24, Num 1, pp 95-100, issn 0903-1936, 6 p.Article

Abnormal regulatory interactions of I148t-CFTR and the epithelial Na⁺ channel in Xenopus oocytesSUAUD, Laurence; WUSHENG YAN; RUBENSTEIN, Ronald C et al.American journal of physiology. Cell physiology. 2007, Vol 61, Num 1, issn 0363-6143, C603-C611Article

Characterization of Burkholderia cepacia complex from cystic fibrosis patients in China and their chitosan susceptibilityYUAN FANG; LOU, Miao-Miao; BIN LI et al.World journal of microbiology & biotechnology. 2010, Vol 26, Num 3, pp 443-450, issn 0959-3993, 8 p.Article

Early determination of cystic fibrosis by electrochemical chloride quantification in sweatGONZALO-RUIZ, Javier; MAS, Roser; DE HARO, Carmen et al.Biosensors & bioelectronics. 2009, Vol 24, Num 6, pp 1788-1791, issn 0956-5663, 4 p.Article

Inflammatory markers of lung disease in adult patients with cystic fibrosisLEVY, Hara; KALISH, Leslie A; HUNTINGTON, Ian et al.Pediatric pulmonology. 2007, Vol 42, Num 3, pp 256-262, issn 8755-6863, 7 p.Article

S-nitrosothiol signaling in respiratory biologyGASTON, Benjamin; SINGEL, David; DOCTOR, Allan et al.American journal of respiratory and critical care medicine. 2006, Vol 173, Num 11, pp 1186-1193, issn 1073-449X, 8 p.Article

Mucoviscidose : approches thérapeutiques : mémorandum d'une réunion conjointe OMS/AILMLA LETTRE DES NOUVELLES PHARMACEUTIQUES : BULLETIN DE L'ORDRE DES PHARMACIENS. 1994, Vol 72, Num 4, pp 553-567Article

Je vous ai tous aimésHEUCHEL, Johann.1998, 350 p., isbn 2-020-34766-0Book

Mucoviscidose : approches thérapeutiques : mémorandum d'une réunion conjointe OMS/AILMLA LETTRE DES NOUVELLES PHARMACEUTIQUES : BULLETIN DE L'ORDRE DES PHARMACIENS. 1994, Vol 72, Num 4, pp 553-567Article

A role for CFTR in the elevation of glutathione levels in the lung by oral glutathione administrationKARIYA, Chirag; LEITNER, Heather; MIN, Elysia et al.American journal of physiology. Lung cellular and molecular physiology. 2007, Vol 36, Num 6, issn 1040-0605, L1590-L1597Article

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Chemical conjugation of AF508-CFTR corrector deoxyspergualin to transporter human serum albumin enhances its ability to rescue Cl^- channel functionsNOREZ, Caroline; PASETTO, Matteo; CABRINI, Giulio et al.American journal of physiology. Lung cellular and molecular physiology. 2008, Vol 39, Num 2, issn 1040-0605, L336-L347Article

Clinical manifestations of cystic fibrosis among patients with diagnosis in adulthoodGILLJAM, Marita; ELLIS, Lynda; COREY, Mary et al.Chest. 2004, Vol 126, Num 4, pp 1215-1224, issn 0012-3692, 10 p.Article

Efficacy and Safety of Ivacaftor in Patients Aged 6 to 11 Years with Cystic Fibrosis with a G551D MutationDAVIES, Jane C; WAINWRIGHT, Claire E; ORDONEZ, Claudia L et al.American journal of respiratory and critical care medicine. 2013, Vol 187, Num 11, pp 1219-1225, issn 1073-449X, 7 p.Article