Intraretinal regeneration of axotomised retinal ganglion cells after AAV mediated CNTF delivery von Ali, R, Maclaren, R, Buch, P, Balaggan, K, Schlichtenbrede, F, Smith, A

In contrast to AAV-mediated Cntf expression, AAV-mediated Gdnf expression enhances gene replacement therapy in rodent models of retinal degeneration. von Buch, P, Maclaren, R, Durán, Y, Balaggan, K, MacNeil, A, Schlichtenbrede, F, Smith, A, Ali, R

CNTF gene transfer protects ganglion cells in rat retinae undergoing focal injury and branch vessel occlusion. von Maclaren, R, Buch, P, Smith, A, Balaggan, K, MacNeil, A, Taylor, J, Osborne, N, Ali, R

Autologous transplantation of the retinal pigment epithelium and choroid in the treatment of neovascular age-related macular degeneration. von Maclaren, R, Uppal, G, Balaggan, K, Tufail, A, Munro, P, Milliken, AB, Ali, R, Rubin, G, Aylward, G, da Cruz, L

Subretinal delivery of adeno-associated virus serotype 2 results in minimal immune responses that allow repeat vector administration in immunocompetent mice. von Barker, SE, Broderick, C, Robbie, S, Duran, Y, Natkunarajah, M, Buch, P, Balaggan, K, Maclaren, R, Bainbridge, J, Smith, A, Ali, R

EIAV vector-mediated delivery of endostatin or angiostatin inhibits angiogenesis and vascular hyperpermeability in experimental CNV. von Balaggan, K, Binley, K, Esapa, M, Maclaren, R, Iqball, S, Duran, Y, Pearson, R, Kan, O, Barker, SE, Smith, A, Bainbridge, J, Naylor, S, Ali, R

Effective gene therapy with nonintegrating lentiviral vectors. von Yáñez-Muñoz, R, Balaggan, K, MacNeil, A, Howe, S, Schmidt, M, Smith, A, Buch, P, Maclaren, R, Anderson, P, Barker, SE, Duran, Y, Bartholomae, C, von Kalle, C, Heckenlively, JR, Kinnon, C, Ali, R, Thrasher, A