[Aerosol administration of a replication defective recombinant adenovirus expressing normal human cDNA-CFTR in the respiratory tractus in patients with cystic fibrosis]

Autor: G, Bellon, L, Calmard, D, Thouvenot, H, Levrey, V, Jagneaux, F, Poitevin, C, Malcus, N, Accart, C, Séné, M P, Layani, M, Aymard, J, Bienvenu, M, Courtney, G, Döring, B, Gilly, R, Gilly, D, Lamy, Y, Morel, C, Paulin, F, Perraud, L, Rodillon, S, So, F, Touraine, C, Schatz, A, Pavirani

Publikováno v: Comptes rendus des seances de la Societe de biologie et de ses filiales. 190(1)

At present it is conceivable to think that gene therapy represents a way to treat or even prevent the respiratory manifestations of cystic fibrosis. Consistent to such a concept, there is sufficient evidence that Ad-CFTR, a recombinant replication-de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::800bc9ad46df7a9af604bc86bf3fb1c4
https://pubmed.ncbi.nlm.nih.gov/8881273

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Mechanism of Restriction of Normal and Cystic Fibrosis Transmembrane Conductance Regulator-Deficient Human Tracheal Gland Cells to Adenovirus Infection and Ad-Mediated Gene Transfer.

Autor: Gaden, Florence, Franqueville, Laure, Saw See Hong, Legrand, Valérie, Figarella, Catherine, Boulanger, Pierre

Publikováno v: American Journal of Respiratory Cell & Molecular Biology; 2002, Vol. 27 Issue 5, p628-640, 13p, 1 Black and White Photograph, 3 Charts, 6 Graphs