Zobrazeno 1 - 10
of 45
pro vyhledávání: '"F. Sorgi"'
Publikováno v:
Methods in molecular medicine. 7
Development of safe and effective technology for delivering functional DNA into cells in an intact organism is crucial to broad applications of gene therapy to human disease. Both viral and nonviral vectors have been developed. Of the technologies cu
Autor:
Natasha J. Caplen, Peter G. Middleton, F. Sorgi, Duncan M. Geddes, Leaf Huang, M Stern, SJ Farr, DC Gruenert, JE Browning, C Hughes, Ewfw Alton
Publikováno v:
Gene Therapy. 5:583-593
Nebulisation is currently the most acceptable and practical delivery system for repeated applications of gene therapy to the lower airways of cystic fibrosis (CF) patients. We have assessed whether this route of administration offers other benefits w
Autor:
M Stern, Felix M. Munkonge, Leaf Huang, Natasha J. Caplen, T. Pitt, Ann Dewar, Andrew Bush, Duncan M. Geddes, Eric W.F.W. Alton, Jane C. Davies, F. Sorgi
Publikováno v:
American Journal of Respiratory Cell and Molecular Biology. 16:657-663
Much of the morbidity and mortality seen in cystic fibrosis (CF) is related to chronic infection of the respiratory tract with Pseudomonas aeruginosa. Some studies have attributed the strong relationship between CF and Pseudomonas colonization to the
Autor:
William H. Colledge, Martin J. Evans, Gooi Hc, Leaf Huang, Egan Jj, SE Smyth, C. A. Goddard, Deborah R. Gill, A K Webb, EM Fitzjohn, F. Sorgi, Alan W. Cuthbert, BE Waddell, KA Mofford, Uzi Gileadi, Kevin W Southern, S C Hyde, Hannavy K, Christopher F. Higgins
Publikováno v:
Scopus-Elsevier
The major cause of mortality in patients with cystic fibrosis (CF) is lung disease. Expression of the cystic fibrosis transmembrane conductance regulator (CFTR) gene product in the airways is a potential treatment. Clinical studies in which the CFTR
Autor:
P, Leone, C G, Janson, L, Bilaniuk, Z, Wang, F, Sorgi, L, Huang, R, Matalon, R, Kaul, Z, Zeng, A, Freese, S W, McPhee, E, Mee, M J, During, L, Bilianuk
Publikováno v:
Annals of neurology. 48(1)
With the ultimate goal of developing safe and effective in vivo gene therapy for the treatment of Canavan disease and other neurological disorders, we developed a non-viral lipid-entrapped, polycation-condensed delivery system (LPD) for central nervo
Autor:
Leaf Huang, Ronald G. Crystal, F. Sorgi, JE Browning, C Marriot, Ewfw Alton, Duncan M. Geddes, Dieter C. Gruenert, Natasha J. Caplen, M Stern, Uta Griesenbach
Publikováno v:
Gene therapy. 5(1)
Trials of gene transfer for cystic fibrosis (CF) are currently underway. However, direct application to the airways may be impeded by the presence of airway secretions. We have therefore assessed the effect of CF sputum on the expression of the repor
The effect of cationic liposome pretreatment and centrifugation on retrovirus-mediated gene transfer
Publikováno v:
Gene therapy. 4(12)
Pretreatment of retroviral supernatants with the cationic liposomes DOTMA-DOPE (Lipofectin), DC-Chol-DOPE and DOSPA-DOPE (Lipofectamine) was found to enhance static transductions of TF-1 target cells. The relative effectiveness at increasing transduc
Publikováno v:
Gene therapy. 4(9)
A polycationic peptide, protamine sulfate, USP, has been shown to be able to condense plasmid DNA efficiently for delivery into several different types of cells in vitro by several different types of cationic liposomes. The monovalent cationic liposo
Autor:
Stephen C. Hyde, William H. Colledge, L J MacVinish, Mathew J. Evans, Peter G. Middleton, Leaf Huang, D Bilton, K A Mofford, A K Webb, K W Southern, Alan W. Cuthbert, Christopher F. Higgins, A Thomson, Deborah R. Gill, D J Lane, T Seddon, J M Littlewood, F. Sorgi, Rosemary Ratcliff
Publikováno v:
Scopus-Elsevier
Cystic fibrosis (CF) is a common, serious, inherited disease. The major cause of mortality in CF is lung disease, due to the failure of airway epithelial cells to express a functional product of the cystic fibrosis transmembrane conductance regulator
Publikováno v:
Gene therapy. 3(7)
The human interleukin-2 (IL-2) gene was successfully delivered into established human tumor xenografts in SCID (severe combined immunodeficient) mice by cationic liposome-mediated DNA delivery. A bicistronic mammalian expression vector containing a r