Browse by UCL people
Group by: Type | Date
Number of items: 7.
Article
Bainbridge, JWB;
Mehat, MS;
Sundaram, V;
Robbie, SJ;
Barker, SE;
Ripamonti, C;
Georgiadis, A;
... Ali, RR; + view all
(2015)
Long-Term Effect of Gene Therapy on Leber's Congenital Amaurosis.
New England Journal of Medicine
, 372
(20)
pp. 1887-1897.
10.1056/NEJMoa1414221.
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Georgiadis, A;
Duran, Y;
Ribeiro, J;
Abelleira-Hervas, L;
Robbie, SJ;
Sünkel-Laing, B;
Fourali, S;
... Ali, RR; + view all
(2016)
Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65.
Gene Therapy
, 23
(12)
pp. 857-862.
10.1038/gt.2016.66.
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Kampik, D;
Basche, M;
Luhmann, UFO;
Nishiguchi, KM;
Williams, JAE;
Greenwood, J;
Moss, SE;
... Ali, RR; + view all
(2017)
In situ regeneration of retinal pigment epithelium by gene transfer of E2F2: a potential strategy for treatment of macular degenerations.
Gene Therapy
, 24
pp. 810-818.
10.1038/gt.2017.89.
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Luhmann, UF;
Lange, CA;
Robbie, S;
Munro, PM;
Cowing, JA;
Armer, HE;
Luong, V;
... Ali, RR; + view all
(2012)
Differential modulation of retinal degeneration by Ccl2 and Cx3cr1 chemokine signalling.
PLoS One
, 7
(4)
, Article e35551. 10.1371/journal.pone.0035551.
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Mihelec, M;
Pearson, RA;
Robbie, SJ;
Buch, PK;
Azam, SA;
Bainbridge, JWB;
Smith, AJ;
(2011)
Long-Term Preservation of Cones and Improvement in Visual Function Following Gene Therapy in a Mouse Model of Leber Congenital Amaurosis Caused by Guanylate Cyclase-1 Deficiency.
Human Gene Therapy
, 22
(10)
1179 - 1190.
10.1089/hum.2011.069.
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Ripamonti, C;
Henning, B;
Ali, RR;
Bainbridge, JW;
Robbie, SJ;
Sundaram, V;
Luong, V;
... Stockman, A; + view all
(2014)
Nature of the visual loss in observers with Leber's congenital amaurosis caused by mutations in RPE65.
Invest Ophthalmol Vis Sci
, 55
(10)
6817 - 6828.
10.1167/iovs.14-14923.
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Thesis
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Robbie, S.J.;
(2012)
The role of innate immune cells in ocular ageing and pathological neovascularisation.
Doctoral thesis , UCL (University College London).
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