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Agnès Gouble

Researcher at Royal Holloway, University of London

Publications -  56
Citations -  2153

Agnès Gouble is an academic researcher from Royal Holloway, University of London. The author has contributed to research in topics: Immunotherapy & Chimeric antigen receptor. The author has an hindex of 18, co-authored 51 publications receiving 1959 citations.

Papers
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Journal ArticleDOI

Multiplex Genome-Edited T-cell Manufacturing Platform for “Off-the-Shelf” Adoptive T-cell Immunotherapies

TL;DR: The applicability of TALEN-mediated genome editing to a scalable process enables the manufacturing of third-party CAR T-cell immunotherapies against arbitrary targets and can therefore be used in an "off-the-shelf" manner akin to other biologic immunopharmaceuticals.
Patent

Custom-made meganuclease and use thereof

TL;DR: In this paper, custom-made meganucleases, which recognize and cleave a specific nucleotide sequence, derived polynucleotide sequences, recombinant vector cell, animal, or plant comprising said polyn nucleotide sequences are used for genetic engineering, antiviral therapy and gene therapy.
Journal ArticleDOI

Engineered I-CreI Derivatives Cleaving Sequences from the Human XPC Gene can Induce Highly Efficient Gene Correction in Mammalian Cells

TL;DR: Tailored I- CreI derivatives cleaving sequences from the XPC gene were found to induce high levels of gene targeting, similar to the I-CreI scaffold or theI-SceI "gold standard", the first time an engineered homing endonuclease has been used to modify a chromosomal locus.
Patent

Use of meganucleases for inducing homologous recombination ex vivo and in toto in vertebrate somatic tissues and application thereof.

TL;DR: Use of meganucleases for inducing homologous recombination ex vivo and in toto in vertebrate somatic tissues and its application for genome engineering and gene therapy as discussed by the authors.
Patent

Methods for engineering allogeneic and immunosuppressive resistant t cell for immunotherapy

TL;DR: This article used rare cutting endonucleases, in particular TALE-nucleases (TAL effector endonuclease) and polynucleotides encoding such polypeptides, to precisely target a selection of key genes in T-cells.