scispace - formally typeset
B

Benjamin Steyer

Researcher at University of Wisconsin-Madison

Publications -  11
Citations -  292

Benjamin Steyer is an academic researcher from University of Wisconsin-Madison. The author has contributed to research in topics: Gene & Induced pluripotent stem cell. The author has an hindex of 6, co-authored 11 publications receiving 229 citations. Previous affiliations of Benjamin Steyer include Wisconsin Alumni Research Foundation & University of California, Riverside.

Papers
More filters
Journal ArticleDOI

Electrochemical oxidation of ferrocene: a strong dependence on the concentration of the supporting electrolyte for nonpolar solvents.

TL;DR: The dependence of the oxidation potential of ferrocene on the electrolyte concentration for differentsolvents revealed that the abovementioned approximation in the Born correction term indeed introduces a significant error in the estimation of the charge-transfer driving force from redox data collected using relatively nonpolar solvents.
Journal ArticleDOI

Scarless Genome Editing of Human Pluripotent Stem Cells via Transient Puromycin Selection

TL;DR: A robust method for rapid, scarless introduction or correction of disease-associated variants in hPSCs using CRISPR/Cas9 is presented and characterized.
Journal ArticleDOI

Human iPSC Modeling Reveals Mutation-Specific Responses to Gene Therapy in a Genotypically Diverse Dominant Maculopathy

TL;DR: The results suggest that gene augmentation is a viable first-line approach for some individuals with dominant Best disease and that non-responders are candidates for alternate approaches such as gene editing, however, testing gene editing strategies for on-target efficiency and off-target events using personalized iPSC-RPE model systems is warranted.
Journal ArticleDOI

High content analysis platform for optimization of lipid mediated CRISPR-Cas9 delivery strategies in human cells ☆

TL;DR: An innovative platform to generate and screen many formulations of synthetic biomaterials and components of the CRISPR-Cas9 system in parallel and identify formulation parameters for Cas9-material complexes that can optimize gene-editing in a specific human cell type is described.
Journal ArticleDOI

Drug-loaded nanoparticles induce gene expression in human pluripotent stem cell derivatives

TL;DR: The results demonstrate that the PEG-H40-DXC nanoparticle system provides an effective tool to controlling gene expression in human stem cell derivatives and maintains higher fibroblast proliferation levels and MMP activity.