L
Len Seymour
Researcher at University of Oxford
Publications - 51
Citations - 4055
Len Seymour is an academic researcher from University of Oxford. The author has contributed to research in topics: Oncolytic virus & Oncolytic adenovirus. The author has an hindex of 26, co-authored 51 publications receiving 3767 citations. Previous affiliations of Len Seymour include Kumamoto University & Keele University.
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Journal ArticleDOI
Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial
Robert E MacLaren,Robert E MacLaren,Markus Groppe,Markus Groppe,Alun R. Barnard,Charles L Cottriall,Tanya Tolmachova,Len Seymour,K. Reed Clark,Matthew J. During,Frans P.M. Cremers,Graeme C.M. Black,Andrew J. Lotery,Susan M. Downes,Andrew R. Webster,Andrew R. Webster,Miguel C. Seabra,Miguel C. Seabra +17 more
TL;DR: The initial results of this retinal gene therapy trial are consistent with improved rod and cone function that overcome any negative effects of retinal detachment, and lend support to further assessment of gene therapy in the treatment of choroideremia and other diseases, such as age-related macular degeneration, for which intervention should ideally be applied before the onset ofretinal thinning.
Journal ArticleDOI
Conjugates of anticancer agents and polymers: advantages of macromolecular therapeutics in vivo.
Journal ArticleDOI
Key issues in non-viral gene delivery
Colin W. Pouton,Len Seymour +1 more
TL;DR: Present knowledge of the biodistribution and cellular interactions of gene delivery systems are summarized and how improvements in gene delivery will be accomplished in the future are considered.
Journal ArticleDOI
Extended plasma circulation time and decreased toxicity of polymer-coated adenovirus.
N K Green,C Herbert,Sarah Hale,A B Hale,Vivien Mautner,Richard N. Harkins,Terry Hermiston,Karel Ulbrich,Kerry D. Fisher,Len Seymour +9 more
TL;DR: An increase in the bioavailability of adenovirus, coupled with substantial decreases in toxicity and unwanted transgene expression is an important step towards producing systemically available tumour-targeted viruses.
Journal ArticleDOI
Preclinical evaluation of polymer-bound doxorubicin
Ruth Duncan,Len Seymour,K.B. O'Hare,Pauline A. Flanagan,Stephen R. Wedge,I.C. Hume,Karel Ulbrich,Jiří Strohalm,V. Šubr,Federico Spreafico,M. Grandi,M. Ripamonti,M. Farao,A. Suarato +13 more
TL;DR: These macromolecular produgs have the ability to concentrate drug in solid tumours, and with incorporation of targeting residues can promote organ-specific or tumour-specific uptake, and covalent conjugation markedly reduces all aspects of DOX-associated toxicity.