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Journal Abstract Search

277 related items for PubMed ID: 7686701

  • 21. Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.
    Dray-Charier N, Paul A, Scoazec JY, Veissière D, Mergey M, Capeau J, Soubrane O, Housset C.
    Hepatology; 1999 Jun; 29(6):1624-34. PubMed ID: 10347100
    [Abstract] [Full Text] [Related]

  • 22. Reaching the diagnosis of cystic fibrosis--the limits of the spectrum.
    Lotem Y, Barak A, Mussaffi H, Shohat M, Wilschanski M, Sivan Y, Blau H.
    Isr Med Assoc J; 2000 Feb; 2(2):94-8. PubMed ID: 10804926
    [Abstract] [Full Text] [Related]

  • 23. [Expression of the cystic fibrosis gene in the lungs].
    Heijerman HG, de Jonge HR.
    Ned Tijdschr Geneeskd; 2004 Apr 24; 148(17):816-9. PubMed ID: 15141646
    [Abstract] [Full Text] [Related]

  • 24. Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.
    De Boeck K, Weren M, Proesmans M, Kerem E.
    Pediatrics; 2005 Apr 24; 115(4):e463-9. PubMed ID: 15772171
    [Abstract] [Full Text] [Related]

  • 25. Relationships between cystic fibrosis transmembrane conductance regulator, extracellular nucleotides and cystic fibrosis.
    Marcet B, Boeynaems JM.
    Pharmacol Ther; 2006 Dec 24; 112(3):719-32. PubMed ID: 16828872
    [Abstract] [Full Text] [Related]

  • 26. [Early bronchial inflammation in cystic fibrosis].
    Puchelle E.
    J Soc Biol; 2002 Dec 24; 196(1):29-35. PubMed ID: 12134630
    [Abstract] [Full Text] [Related]

  • 27. [Cystic fibrosis--review].
    Jonsdottir B, Bergsteinsson H, Baldursson O.
    Laeknabladid; 2008 Dec 24; 94(12):831-7. PubMed ID: 19182319
    [Abstract] [Full Text] [Related]

  • 28. CFTR gene transfer to human cystic fibrosis pancreatic duct cells using a Sendai virus vector.
    Rakonczay Z, Hegyi P, Hasegawa M, Inoue M, You J, Iida A, Ignáth I, Alton EW, Griesenbach U, Ovári G, Vág J, Da Paula AC, Crawford RM, Varga G, Amaral MD, Mehta A, Lonovics J, Argent BE, Gray MA.
    J Cell Physiol; 2008 Feb 24; 214(2):442-55. PubMed ID: 17654517
    [Abstract] [Full Text] [Related]

  • 29. [From the laboratory to the clinic: CFTR and the therapeutic options for cystic fibrosis].
    Mayol J, Alvarez de Arcaya Vicente A, Arbeo Escolar AM, Peña Soria MJ, Alvarez Fernández-Represa J.
    An Med Interna; 2000 Feb 24; 17(2):92-8. PubMed ID: 10829466
    [Abstract] [Full Text] [Related]

  • 30. [Cystic fibrosis modifying genes].
    Knauer N, Ratjen F, Grasemann H.
    Pneumologie; 2005 Jun 24; 59(6):395-404. PubMed ID: 15991075
    [Abstract] [Full Text] [Related]

  • 31. Cystic fibrosis. Chloride channels revisited.
    Higgins C.
    Nature; 1992 Aug 13; 358(6387):536. PubMed ID: 1380127
    [No Abstract] [Full Text] [Related]

  • 32. Defective regulatory volume decrease in human cystic fibrosis tracheal cells because of altered regulation of intermediate conductance Ca2+-dependent potassium channels.
    Vázquez E, Nobles M, Valverde MA.
    Proc Natl Acad Sci U S A; 2001 Apr 24; 98(9):5329-34. PubMed ID: 11309505
    [Abstract] [Full Text] [Related]

  • 33. The changing face of the exocrine pancreas in cystic fibrosis: pancreatic sufficiency, pancreatitis and genotype.
    Walkowiak J, Lisowska A, Blaszczyński M.
    Eur J Gastroenterol Hepatol; 2008 Mar 24; 20(3):157-60. PubMed ID: 18301292
    [Abstract] [Full Text] [Related]

  • 34. [Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].
    Iwańczak F, Smigiel R, Stawarski A, Pawłowicz J, Stembalska A, Mowszet K, Sasiadek M.
    Pol Merkur Lekarski; 2005 Feb 24; 18(104):205-9. PubMed ID: 17877132
    [Abstract] [Full Text] [Related]

  • 35. Lack of association of common cystic fibrosis transmembrane conductance regulator gene mutations with primary sclerosing cholangitis.
    Gallegos-Orozco JF, E Yurk C, Wang N, Rakela J, Charlton MR, Cutting GR, Balan V.
    Am J Gastroenterol; 2005 Apr 24; 100(4):874-8. PubMed ID: 15784035
    [Abstract] [Full Text] [Related]

  • 36. Association of common haplotypes of surfactant protein A1 and A2 (SFTPA1 and SFTPA2) genes with severity of lung disease in cystic fibrosis.
    Choi EH, Ehrmantraut M, Foster CB, Moss J, Chanock SJ.
    Pediatr Pulmonol; 2006 Mar 24; 41(3):255-62. PubMed ID: 16429424
    [Abstract] [Full Text] [Related]

  • 37. [Physiopathology of cystic fibrosis lung disease].
    Chinet T.
    Rev Mal Respir; 1999 Jun 24; 16(3):339-45. PubMed ID: 10472642
    [Abstract] [Full Text] [Related]

  • 38. Molecular pathophysiology of cystic fibrosis based on the rescued knockout mouse model.
    Cohen JC, Morrow SL, Cork RJ, Delcarpio JB, Larson JE.
    Mol Genet Metab; 1998 Jun 24; 64(2):108-18. PubMed ID: 9705235
    [Abstract] [Full Text] [Related]

  • 39. [Genetics and cellular biology of cystic fibrosis].
    Chinet T, Blouquit S.
    Rev Prat; 2003 Jan 15; 53(2):130-4. PubMed ID: 12664842
    [Abstract] [Full Text] [Related]

  • 40. Cystic fibrosis. Sickly channels in mild disease.
    Miller C.
    Nature; 1993 Mar 11; 362(6416):106. PubMed ID: 7680767
    [No Abstract] [Full Text] [Related]

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