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154 related items for PubMed ID: 7689915

  • 1. [The cystic fibrosis gene, its product CFTR protein and its mutations].
    Goossens M, Fanen P, Costes B, Ghanem N.
    Bull Acad Natl Med; 1993 Mar; 177(3):371-80; discussion 380-1. PubMed ID: 7689915
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  • 3. [The cystic fibrosis gene: mutation and the function of CFTR protein].
    Goossens M.
    Ann Pediatr (Paris); 1991 Nov; 38(9):591-4. PubMed ID: 1721508
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  • 4. 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
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  • 5. CFTR!
    Fuller CM, Benos DJ.
    Am J Physiol; 1992 Aug; 263(2 Pt 1):C267-86. PubMed ID: 1381146
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  • 6. Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation.
    Dalemans W, Barbry P, Champigny G, Jallat S, Dott K, Dreyer D, Crystal RG, Pavirani A, Lecocq JP, Lazdunski M.
    Nature; 1992 Aug; 354(6354):526-8. PubMed ID: 1722027
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  • 7. A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein.
    Cutting GR, Kasch LM, Rosenstein BJ, Zielenski J, Tsui LC, Antonarakis SE, Kazazian HH.
    Nature; 1990 Jul 26; 346(6282):366-9. PubMed ID: 1695717
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  • 8. [Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].
    Radivojević D, Guć-Sćekić M, Djurisić M, Lalić T, Minić P, Kanavakis E.
    Srp Arh Celok Lek; 2001 Jul 26; 129 Suppl 1():6-9. PubMed ID: 15637983
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  • 9. Cystic fibrosis transmembrane conductance regulator (CFTR) and renal function.
    Stanton BA.
    Wien Klin Wochenschr; 1997 Jun 27; 109(12-13):457-64. PubMed ID: 9261986
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  • 10. Dysfunction of CFTR bearing the delta F508 mutation.
    Welsh MJ, Denning GM, Ostedgaard LS, Anderson MP.
    J Cell Sci Suppl; 1993 Jun 27; 17():235-9. PubMed ID: 7511616
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  • 11. [CFTR protein and molecular mechanisms of pulmonary involvement in cystic fibrosis].
    Chinet T.
    Rev Pneumol Clin; 1995 Jun 27; 51(3):122-9. PubMed ID: 7569573
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  • 12. Expression and characterization of the cystic fibrosis transmembrane conductance regulator.
    Gregory RJ, Cheng SH, Rich DP, Marshall J, Paul S, Hehir K, Ostedgaard L, Klinger KW, Welsh MJ, Smith AE.
    Nature; 1990 Sep 27; 347(6291):382-6. PubMed ID: 1699127
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  • 13. Turnover of the cystic fibrosis transmembrane conductance regulator (CFTR): slow degradation of wild-type and delta F508 CFTR in surface membrane preparations of immortalized airway epithelial cells.
    Wei X, Eisman R, Xu J, Harsch AD, Mulberg AE, Bevins CL, Glick MC, Scanlin TF.
    J Cell Physiol; 1996 Aug 27; 168(2):373-84. PubMed ID: 8707873
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  • 16. [Cystic fibrosis modifying genes].
    Knauer N, Ratjen F, Grasemann H.
    Pneumologie; 2005 Jun 27; 59(6):395-404. PubMed ID: 15991075
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  • 17. Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- conductances.
    Reddy MM, Quinton PM.
    JOP; 2001 Jul 27; 2(4 Suppl):212-8. PubMed ID: 11875262
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  • 18. [Frequency of delta F508 mutation in Venezuelan patients with cystic fibrosis].
    Morales-Machin A, Borjas-Fajardo L, Pineda L, González S, Delgado W, Zabala W, Fernández E.
    Invest Clin; 2004 Jun 27; 45(2):121-30. PubMed ID: 15211979
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