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Gene Therapy
|
October 12, 1999
An adenoviral vector regulated by hypoxia for the treatment of ischaemic disease and cancer
K Binley, S Iqball, A Kingsman, et al.
Gene Therapy
|
March 21, 2003
Hypoxia-mediated tumour targeting
K Binley, Z Askham, L Martin, et al.
Human Gene Therapy
|
September 25, 1999
Characterization of physiologically regulated vectors for the treatment of ischemic disease
K Boast, K Binley, S Iqball, et al.
Gene Therapy
|
May 31, 2003
Hypoxia-regulated transgene expression in experimental retinal and choroidal neovascularization
J W B Bainbridge, A Mistry, K Binley, et al.
Gene Therapy
|
March 1, 2000
The macrophage - a novel system to deliver gene therapy to pathological hypoxia
L Griffiths, K Binley, S Iqball, et al.
The Journal of Gene Medicine
|
November 22, 2005
Stable and efficient intraocular gene transfer using pseudotyped EIAV lentiviral vectors
K S Balaggan, K Binley, M Esapa, et al.
Gene Therapy
|
May 9, 2008
Correction of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapy
J Kong, S-R Kim, K Binley, et al.
Gene Therapy
|
March 31, 2006
EIAV vector-mediated delivery of endostatin or angiostatin inhibits angiogenesis and vascular hyperpermeability in experimental CNV
K S Balaggan, K Binley, M Esapa, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Gene Therapy
|
October 12, 1999
An adenoviral vector regulated by hypoxia for the treatment of ischaemic disease and cancer
K Binley, S Iqball, A Kingsman, et al.
Gene Therapy
|
March 21, 2003
Hypoxia-mediated tumour targeting
K Binley, Z Askham, L Martin, et al.
Human Gene Therapy
|
September 25, 1999
Characterization of physiologically regulated vectors for the treatment of ischemic disease
K Boast, K Binley, S Iqball, et al.
Gene Therapy
|
May 31, 2003
Hypoxia-regulated transgene expression in experimental retinal and choroidal neovascularization
J W B Bainbridge, A Mistry, K Binley, et al.
Gene Therapy
|
March 1, 2000
The macrophage - a novel system to deliver gene therapy to pathological hypoxia
L Griffiths, K Binley, S Iqball, et al.
The Journal of Gene Medicine
|
November 22, 2005
Stable and efficient intraocular gene transfer using pseudotyped EIAV lentiviral vectors
K S Balaggan, K Binley, M Esapa, et al.
Gene Therapy
|
May 9, 2008
Correction of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapy
J Kong, S-R Kim, K Binley, et al.
Gene Therapy
|
March 31, 2006
EIAV vector-mediated delivery of endostatin or angiostatin inhibits angiogenesis and vascular hyperpermeability in experimental CNV
K S Balaggan, K Binley, M Esapa, et al.
Page
of 1