Cara-lin Lonetree

Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors

Klaus N. Lovendahl, Walker S. Lahr, Beau R. Webber, 2018, Nature Communications.

A Pan-RNase Inhibitor Enabling CRISPR-mRNA Platforms for Engineering of Primary Human Monocytes

Walker S. Lahr, Beau R. Webber, B. Moriarity, 2022, International journal of molecular sciences.

Evaluation of TCR Gene Editing Achieved by TALENs, CRISPR/Cas9, and megaTAL Nucleases.

Christof von Kalle, Jakub Tolar, Richard Gabriel, 2016, Molecular therapy : the journal of the American Society of Gene Therapy.

CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary and immortalized cells

Walker S. Lahr, Beau R. Webber, Mitchell G. Kluesner, 2021, Nature Communications.

CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary cells

Walker S. Lahr, Beau R. Webber, Mitchell G. Kluesner, 2020, bioRxiv.

A New Immuno‐, Dystrophin‐Deficient Model, the NSG‐mdx4Cv Mouse, Provides Evidence for Functional Improvement Following Allogeneic Satellite Cell Transplantation

M. Kyba, R. Perlingeiro, D. Lowe, 2013, Stem cells.

CRISPR/Cas9-based genetic correction for recessive dystrophic epidermolysis bullosa

Beau R. Webber, J. Tolar, C. Eide, 2016, npj Regenerative Medicine.

CRISPR/Cas9 Targeted Gene Editing and Cellular Engineering in Fanconi Anemia.

Beau R. Webber, J. Wagner, J. Tolar, 2016, Stem cells and development.

Multiplex Human T Cell Engineering without Double-Strand Break Induction Using the Cas9 Base Editor System

Walker S. Lahr, Beau R. Webber, B. Moriarity, 2018, Blood.