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Gwendoline Dubois

Researcher at University of Toulouse

Publications -  9
Citations -  705

Gwendoline Dubois is an academic researcher from University of Toulouse. The author has contributed to research in topics: Transcription activator-like effector nuclease & Genome editing. The author has an hindex of 6, co-authored 8 publications receiving 566 citations. Previous affiliations of Gwendoline Dubois include University of Copenhagen & Centre national de la recherche scientifique.

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Genome engineering empowers the diatom Phaeodactylum tricornutum for biotechnology

TL;DR: The generation of an enhanced lipid-producing strain through the disruption of the UDP-glucose pyrophosphorylase gene exemplifies the power of genome engineering to harness diatoms for biofuel production.
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One-step generation of multiple gene knock-outs in the diatom Phaeodactylum tricornutum by DNA-free genome editing.

TL;DR: A highly efficient multiplex genome-editing method in the diatom Phaeodactylum tricornutum, relying on the biolistic delivery of CRISPR-Cas9 ribonucleoproteins coupled with the identification of two endogenous counter-selectable markers, PtUMPS and PtAPT is reported.
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Comprehensive analysis of the specificity of transcription activator-like effector nucleases

TL;DR: It is reported that TALEN can only accommodate a relatively small number of position-dependent mismatches while maintaining a detectable activity at endogenous loci in vivo, demonstrating the high specificity of these molecular tools.
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Production of Medium Chain Fatty Acids by Yarrowia lipolytica: Combining Molecular Design and TALEN to Engineer the Fatty Acid Synthase

TL;DR: TALEN (transcription activator-like effector nucleases)-based genome editing technology was applied for the first time to Yarrowia lipolytica and proved to be very efficient for inducing targeted genome modifications.
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BurrH: a new modular DNA binding protein for genome engineering

TL;DR: BurgerH as discussed by the authors is a new DNA binding protein from Burkholderia rhizoxinica that is composed of highly polymorphic DNA targeting modules and can be used to efficiently induce in vivo targeted mutagenesis and targeted gene insertion at a desired locus.