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Journal Abstract Search

199 related items for PubMed ID: 21349786

  • 1. Molecular repair of a defective CFTR protein in cystic fibrosis.
    Erlinger S.
    Clin Res Hepatol Gastroenterol; 2011 Apr; 35(4):254-6. PubMed ID: 21349786
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  • 9. [From gene to disease; from defective chloride ion transport to cystic fibrosis].
    Scheffer H, van den Ouweland AM, Veeze HJ.
    Ned Tijdschr Geneeskd; 2001 Apr 07; 145(14):686-7. PubMed ID: 11530706
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  • 12. Rescue of DeltaF508-CFTR (cystic fibrosis transmembrane conductance regulator) by curcumin: involvement of the keratin 18 network.
    Lipecka J, Norez C, Bensalem N, Baudouin-Legros M, Planelles G, Becq F, Edelman A, Davezac N.
    J Pharmacol Exp Ther; 2006 May 07; 317(2):500-5. PubMed ID: 16424149
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  • 13. Rescuing cystic fibrosis transmembrane conductance regulator (CFTR)-processing mutants by transcomplementation.
    Cormet-Boyaka E, Jablonsky M, Naren AP, Jackson PL, Muccio DD, Kirk KL.
    Proc Natl Acad Sci U S A; 2004 May 25; 101(21):8221-6. PubMed ID: 15141088
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  • 16. [Cystic fibrosis: molecular update and clinical implications].
    Orozco L, Chávez M, Saldaña Y, Velázquez R, Carnevale A, González-del Angel A, Jiménez S.
    Rev Invest Clin; 2006 May 25; 58(2):139-52. PubMed ID: 16827266
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  • 17. [Cystic fibrosis].
    Yoshimura K, Anzai C.
    Nihon Rinsho; 1996 Mar 25; 54(3):825-33. PubMed ID: 8904244
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  • 19. 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 25; 29(6):1624-34. PubMed ID: 10347100
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