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Benzoquinolines and chloride secretion in murine colonic epitheliumCUTHBERT, Alan W.British journal of pharmacology. 2003, Vol 138, Num 8, pp 1528-1534, issn 0007-1188, 7 p.Article

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

Cystic Fibrosis: Need for Mass Deployable Screening MethodsADITYA SINGH SENGAR; AGARWAL, Anirudh; SINGH, Manish K et al.Applied biochemistry and biotechnology. 2014, Vol 174, Num 3, pp 1127-1136, issn 0273-2289, 10 p.Conference Paper

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

VIP-dependent increase in F508del-CFTR membrane localization is mediated by PKCεALCOLADO, Nicole; CONRAD, Dustin J; RAFFERTY, Sara et al.American journal of physiology. Cell physiology. 2011, Vol 70, Num 1, issn 0363-6143, C53-C65Article

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

La mucoviscidoseRéadaptation (Paris). 1995, Num 424, pp 31-32, issn 0484-0305Article

Discovery of putative oocyte quality markers by comparative ExacTag proteomicsPOWELL, Michael D; MANANDHAR, Gaurishankar; SPATE, Lee et al.Proteomics. Clinical applications (Print). 2010, Vol 4, Num 3, pp 337-351, issn 1862-8346, 15 p.Article

Technology platforms for molecular diagnosis of cystic fibrosisESHAQUE, Bithi; DIXON, Brian.Biotechnology advances. 2006, Vol 24, Num 1, pp 86-93, issn 0734-9750, 8 p.Article

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

Cystic fibrosis diagnosed in an elderly manGILLJAM, Marita; BJÖRCK, Eva.Respiration (Basel). 2004, Vol 71, Num 1, pp 98-100, issn 0025-7931, 3 p.Article

Efficiency of calcium absorption is not compromised in clinically stable prepubertal and pubertal girls with cystic fibrosisSCHULZE, Kerry J; O'BRIEN, Kimberly O; GERMAIN-LEE, Emily L et al.The American journal of clinical nutrition. 2003, Vol 78, Num 1, pp 110-116, issn 0002-9165, 7 p.Article

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

Mannitol-Guided Delivery of Ciprofloxacin in Artificial Cystic Fibrosis Mucus ModelYAN YANG; TSIFANSKY, Michael D; SHIN, Sooyoung et al.Biotechnology and bioengineering. 2011, Vol 108, Num 6, pp 1441-1449, issn 0006-3592, 9 p.Article

Optical detection and discrimination of cystic fibrosis-related genetic mutations using oligonucleotide-nanoparticle conjugatesMURPHY, Deirdre; REDMOND, Gareth.Analytical and bioanalytical chemistry. 2005, Vol 381, Num 6, pp 1122-1129, 8 p.Article

RNA interference targeted to multiple P2X receptor subtypes attenuates zinc-induced calcium entryLIHUA LIANG; ZSEMBERY, Akos; SCHWIEBERT, Erik M et al.American journal of physiology. Cell physiology. 2005, Vol 58, Num 2, pp C388-C396, issn 0363-6143Article

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

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