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Journal Abstract Search

186 related items for PubMed ID: 9696826

  • 21. "Stealth" adenoviruses blunt cell-mediated and humoral immune responses against the virus and allow for significant gene expression upon readministration in the lung.
    Croyle MA, Chirmule N, Zhang Y, Wilson JM.
    J Virol; 2001 May; 75(10):4792-801. PubMed ID: 11312351
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  • 22. [Aerosol administration of a replication defective recombinant adenovirus expressing normal human cDNA-CFTR in the respiratory tractus in patients with cystic fibrosis].
    Bellon G, Calmard L, Thouvenot D, Levrey H, Jagneaux V, Poitevin F, Malcus C, Accart N, Séné C, Layani MP, Aymard M, Bienvenu J, Courtney M, Döring G, Gilly B, Gilly R, Lamy D, Morel Y, Paulin C, Perraud F, Rodillon L, So S, Touraine F, Schatz C, Pavirani A.
    C R Seances Soc Biol Fil; 1996 May; 190(1):109-42. PubMed ID: 8881273
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  • 24. A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis.
    Knowles MR, Hohneker KW, Zhou Z, Olsen JC, Noah TL, Hu PC, Leigh MW, Engelhardt JF, Edwards LJ, Jones KR.
    N Engl J Med; 1995 Sep 28; 333(13):823-31. PubMed ID: 7544439
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  • 25. In Vitro Validation of a CRISPR-Mediated CFTR Correction Strategy for Preclinical Translation in Pigs.
    Zhou ZP, Yang LL, Cao H, Chen ZR, Zhang Y, Wen XY, Hu J.
    Hum Gene Ther; 2019 Sep 28; 30(9):1101-1116. PubMed ID: 31099266
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  • 26. Development and analysis of recombinant adenoviruses for gene therapy of cystic fibrosis.
    Rich DP, Couture LA, Cardoza LM, Guiggio VM, Armentano D, Espino PC, Hehir K, Welsh MJ, Smith AE, Gregory RJ.
    Hum Gene Ther; 1993 Aug 28; 4(4):461-76. PubMed ID: 7691187
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  • 34. Readministration of helper-dependent adenoviral vectors to mouse airway mediated via transient immunosuppression.
    Cao H, Yang T, Li XF, Wu J, Duan C, Coates AL, Hu J.
    Gene Ther; 2011 Feb 28; 18(2):173-81. PubMed ID: 20882053
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  • 36. Ability of adenovirus vectors containing different CFTR transcriptional cassettes to correct ion transport defects in CF cells.
    Jiang C, O'Connor SP, Armentano D, Berthelette PB, Schiavi SC, Jefferson DM, Smith AE, Wadsworth SC, Cheng SH.
    Am J Physiol; 1996 Oct 28; 271(4 Pt 1):L527-37. PubMed ID: 8897899
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  • 37. Gene therapy for the respiratory manifestations of cystic fibrosis.
    Korst RJ, McElvaney NG, Chu CS, Rosenfeld MA, Mastrangeli A, Hay J, Brody SL, Eissa NT, Danel C, Jaffe HA.
    Am J Respir Crit Care Med; 1995 Mar 28; 151(3 Pt 2):S75-87. PubMed ID: 7533609
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  • 38. Novel role for E4 region genes in protection of adenovirus vectors from lysis by cytotoxic T lymphocytes.
    Kaplan JM, Armentano D, Scaria A, Woodworth LA, Pennington SE, Wadsworth SC, Smith AE, Gregory RJ.
    J Virol; 1999 May 28; 73(5):4489-92. PubMed ID: 10196353
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  • 40. Generation and characterization of E1/E2a/E3/E4-deficient adenoviral vectors encoding human factor VIII.
    Andrews JL, Kadan MJ, Gorziglia MI, Kaleko M, Connelly S.
    Mol Ther; 2001 Mar 28; 3(3):329-36. PubMed ID: 11273775
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