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George H. Silva

Researcher at University of Giessen

Publications -  29
Citations -  1308

George H. Silva is an academic researcher from University of Giessen. The author has contributed to research in topics: Transcription activator-like effector nuclease & Genome engineering. The author has an hindex of 14, co-authored 29 publications receiving 1238 citations. Previous affiliations of George H. Silva include University of Copenhagen & University at Albany, SUNY.

Papers
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Journal ArticleDOI

Meganucleases and other tools for targeted genome engineering: perspectives and challenges for gene therapy.

TL;DR: These alternative approaches based on non-viral vectorization and/or targeted insertion aimed at achieving safer gene transfer are reviewed, with a special emphasis on megan nucleases, a family of naturally occurring rare-cutting endonucleases, and speculate on their current and future potential.
Patent

Method for the generation of compact tale-nucleases and uses thereof

TL;DR: In this paper, a method for the generation of compact Transcription Activator-Like Effector Nucleases (TALENs) that can efficiently target and process double-stranded DNA is presented.
Journal ArticleDOI

Compact designer TALENs for efficient genome engineering

TL;DR: A significant improvement to the standard transcription activator-like effector nuclease architecture is reported by leveraging the partially specific I-TevI catalytic domain to create a new class of monomeric, DNA-cleaving enzymes.
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Crystal structure of the thermostable archaeal intron-encoded endonuclease I-DmoI

TL;DR: The overall fold of I-DmoI is similar to that of two other LAGLIDADG proteins for which the structures are known, I-CreI and the endonuclease domain of PI-SceI, but the loops connecting the beta-strands differ most in the loops connected to the respective DNA target site sizes and geometries.
Journal ArticleDOI

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.