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Friedrich Fauser

Researcher at Carnegie Institution for Science

Publications -  25
Citations -  2301

Friedrich Fauser is an academic researcher from Carnegie Institution for Science. The author has contributed to research in topics: CRISPR & Genome engineering. The author has an hindex of 13, co-authored 23 publications receiving 1835 citations. Previous affiliations of Friedrich Fauser include BASF Plant Science & Karlsruhe Institute of Technology.

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Journal ArticleDOI

Both CRISPR/Cas-based nucleases and nickases can be used efficiently for genome engineering in Arabidopsis thaliana.

TL;DR: It is shown that only the nuclease but not the nickase is an efficient tool for NHEJ-mediated mutagenesis in plants and the Cas9 nickase has the potential to become an important tool for genome engineering in plants.
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The CRISPR/Cas system can be used as nuclease for in planta gene targeting and as paired nickases for directed mutagenesis in Arabidopsis resulting in heritable progeny

TL;DR: It is demonstrated that this Cas9 paired nickase strategy has a mutagenic potential comparable with that of the nuclease, while the resulting mutations are mostly deletions, and the stable inheritance of such mutations in A. thaliana is demonstrated.
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Highly efficient heritable plant genome engineering using Cas9 orthologues from Streptococcus thermophilus and Staphylococcus aureus.

TL;DR: Codon-optimised Cas9 orthologues from Streptococcus thermophilus and Staphylococcus aureus can both be used to induce error-prone non-homologous end-joining-mediated targeted mutagenesis in the model plant Arabidopsis thaliana at frequencies at least comparable to those that have previously been reported for the S. pyogenes CRISPR/Cas system.
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Synthetic nucleases for genome engineering in plants: prospects for a bright future.

TL;DR: The recently discovered RNA-based CRISPR/Cas system, a new tool to induce multiple DSBs, and sophisticated technical applications, such as the in planta gene targeting system, are further steps in this development.
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In planta gene targeting

TL;DR: A highly efficient GT system that is suitable for all transformable plants regardless of transformation efficiency is described, achieved in Arabidopsis thaliana by expression of a site-specific endonuclease that not only cuts within the target but also the chromosomal transgenic donor, leading to an excised targeting vector.