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

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

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

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

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

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

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

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

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

Faut-il avoir peur du génie génétique ?LA RECHERCHE. 1994, Vol 25, Num 270, pp 1106-1141Article

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

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

Click-based synthesis of triazolobithiazole ΔF508-CFTR correctors for cystic fibrosisDONALD, Michael B; RODRIGUEZ, Kevin X; SHAY, Hannah et al.Bioorganic & medicinal chemistry. 2012, Vol 20, Num 17, pp 5247-5253, issn 0968-0896, 7 p.Article

Pathway prediction by bioinformatic analysis of the untranslated regions of the CFTR mRNASPENCE, Jean.Genomics (San Diego, Calif.). 2009, Vol 94, Num 1, pp 39-47, issn 0888-7543, 9 p.Article

Cystic fibrosis in neonates and infantsMINASIAN, Caro; MCCULLAGH, Angela; BUSH, Andrew et al.Early human development. 2005, Vol 81, Num 12, pp 997-1004, issn 0378-3782, 8 p.Conference Paper

Expression of Intestinal and Lung Alkaline Sphingomyelinase and Neutral Ceramidase in Cystic Fibrosis F508del Transgenic MiceOHLSSON, Lena; HJELTE, Lena; HÜHN, Michael et al.Journal of pediatric gastroenterology and nutrition. 2008, Vol 47, Num 5, pp 547-554, issn 0277-2116, 8 p.Article

Cystic fibrosis heterozygotes do not have increased platelet activationTARNOW, Inge; MICHELSON, Alan D; FRELINGER, Andrew L et al.Thrombosis research. 2007, Vol 121, Num 2, pp 159-162, issn 0049-3848, 4 p.Article

Rapid detection of the ΔF508 mutation in single cells using DHPLC: Implications for preimplantation genetic diagnosisGIRARDET, Anne; CATHALA, Philippe; CLAUSTRES, Mireille et al.Journal of assisted reproduction and genetics. 2003, Vol 20, Num 4, pp 153-156, issn 1058-0468, 4 p.Article

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