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Journal Abstract Search

349 related items for PubMed ID: 7511616

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive.
    Denning GM, Anderson MP, Amara JF, Marshall J, Smith AE, Welsh MJ.
    Nature; 1992 Aug 27; 358(6389):761-4. PubMed ID: 1380673
    [Abstract] [Full Text] [Related]

  • 3. The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.
    Li C, Ramjeesingh M, Reyes E, Jensen T, Chang X, Rommens JM, Bear CE.
    Nat Genet; 1993 Apr 27; 3(4):311-6. PubMed ID: 7526932
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.
    Rich DP, Anderson MP, Gregory RJ, Cheng SH, Paul S, Jefferson DM, McCann JD, Klinger KW, Smith AE, Welsh MJ.
    Nature; 1990 Sep 27; 347(6291):358-63. PubMed ID: 1699126
    [Abstract] [Full Text] [Related]

  • 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; 1990 Sep 27; 354(6354):526-8. PubMed ID: 1722027
    [Abstract] [Full Text] [Related]

  • 7. Generation and characterization of a delta F508 cystic fibrosis mouse model.
    Colledge WH, Abella BS, Southern KW, Ratcliff R, Jiang C, Cheng SH, MacVinish LJ, Anderson JR, Cuthbert AW, Evans MJ.
    Nat Genet; 1995 Aug 27; 10(4):445-52. PubMed ID: 7545494
    [Abstract] [Full Text] [Related]

  • 8. A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.
    French PJ, van Doorninck JH, Peters RH, Verbeek E, Ameen NA, Marino CR, de Jonge HR, Bijman J, Scholte BJ.
    J Clin Invest; 1996 Sep 15; 98(6):1304-12. PubMed ID: 8823295
    [Abstract] [Full Text] [Related]

  • 9.
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  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Functional activation of the cystic fibrosis trafficking mutant delta F508-CFTR by overexpression.
    Cheng SH, Fang SL, Zabner J, Marshall J, Piraino S, Schiavi SC, Jefferson DM, Welsh MJ, Smith AE.
    Am J Physiol; 1995 Apr 27; 268(4 Pt 1):L615-24. PubMed ID: 7733303
    [Abstract] [Full Text] [Related]

  • 13. 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 27; 29(6):1624-34. PubMed ID: 10347100
    [Abstract] [Full Text] [Related]

  • 14. Mislocalization of delta F508 CFTR in cystic fibrosis sweat gland.
    Kartner N, Augustinas O, Jensen TJ, Naismith AL, Riordan JR.
    Nat Genet; 1992 Aug 27; 1(5):321-7. PubMed ID: 1284548
    [Abstract] [Full Text] [Related]

  • 15. Cystic fibrosis patients with mutation 1949del84 in exon 13 of the CFTR gene have a similar clinical severity as delta F508 homozygotes.
    Nunes V, Casals T, Gaona A, Antiñolo G, Ferrer-Calvete J, Pérez-Frias J, Tardío E, Molano J, Estivill X.
    Hum Mutat; 1992 Aug 27; 1(5):375-9. PubMed ID: 1284539
    [Abstract] [Full Text] [Related]

  • 16. A frame-shift mutation in the cystic fibrosis gene.
    White MB, Amos J, Hsu JM, Gerrard B, Finn P, Dean M.
    Nature; 1990 Apr 12; 344(6267):665-7. PubMed ID: 1691449
    [Abstract] [Full Text] [Related]

  • 17. [The cystic fibrosis gene: mutation and the function of CFTR protein].
    Goossens M.
    Ann Pediatr (Paris); 1991 Nov 12; 38(9):591-4. PubMed ID: 1721508
    [Abstract] [Full Text] [Related]

  • 18. Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium.
    Puchelle E, Gaillard D, Ploton D, Hinnrasky J, Fuchey C, Boutterin MC, Jacquot J, Dreyer D, Pavirani A, Dalemans W.
    Am J Respir Cell Mol Biol; 1992 Nov 12; 7(5):485-91. PubMed ID: 1384582
    [Abstract] [Full Text] [Related]

  • 19. Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.
    Sheppard DN, Rich DP, Ostedgaard LS, Gregory RJ, Smith AE, Welsh MJ.
    Nature; 1993 Mar 11; 362(6416):160-4. PubMed ID: 7680769
    [Abstract] [Full Text] [Related]

  • 20. [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 11; 177(3):371-80; discussion 380-1. PubMed ID: 7689915
    [Abstract] [Full Text] [Related]

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