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Christopher D. Guzman

Researcher at Yale University

Publications -  10
Citations -  2209

Christopher D. Guzman is an academic researcher from Yale University. The author has contributed to research in topics: CRISPR & Gene. The author has an hindex of 6, co-authored 10 publications receiving 1558 citations. Previous affiliations of Christopher D. Guzman include Massachusetts Institute of Technology & Wyss Institute for Biologically Inspired Engineering.

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Highly efficient Cas9-mediated transcriptional programming

TL;DR: An improved transcriptional regulator obtained through the rational design of a tripartite activator, VP64-p65-Rta (VPR), fused to nuclease-null Cas9 is described and demonstrated in activating endogenous coding and noncoding genes and stimulating neuronal differentiation of human induced pluripotent stem cells (iPSCs).

Highly efficient Cas9-mediated transcriptional programming

TL;DR: In this article, the authors describe the development of an improved transcriptional regulator through the rational design of a tripartite activator, VP64-p65-Rta (VPR), fused to Cas9 and demonstrate its utility in activating expression of endogenous coding and non-coding genes, targeting several genes simultaneously and stimulating neuronal differentiation of induced pluripotent stem cells (iPSCs).
Posted ContentDOI

Highly-efficient Cas9-mediated transcriptional programming

TL;DR: The development of an improved transcriptional regulator through the rational design of a tripartite activator, VP64-p65-Rta (VPR), fused to Cas9 is described and its utility in activating expression of endogenous coding and non-coding genes, targeting several genes simultaneously and stimulating neuronal differentiation of induced pluripotent stem cells (iPSCs).
Journal ArticleDOI

Synthetic biosensors for precise gene control and real-time monitoring of metabolites

TL;DR: This work applies a characterization pipeline to four genetically encoded sensors that respond to acrylate, glucarate, erythromycin and naringenin, and shows that activation of each sensor is orthogonal to the other sensors, and to other common inducible systems.