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Nature Protocols|January 26, 2018
CRISPR/Cas9 genome editing in human hematopoietic stem cellsRasmus O Bak, Daniel P Dever, Matthew H PorteusElife|September 29, 2017
Multiplexed genetic engineering of human hematopoietic stem and progenitor cells using CRISPR/Cas9 and AAV6Rasmus O Bak, Daniel P Dever, Andreas Reinisch, et al.Cell Reports|July 21, 2017
CRISPR-Mediated Integration of Large Gene Cassettes Using AAV Donor VectorsRasmus O Bak, Matthew H PorteusCurrent Opinion in Hematology|August 15, 2017
The changing landscape of gene editing in hematopoietic stem cells: a step towards Cas9 clinical translationDaniel P Dever, Matthew H PorteusTrends in Genetics : TIG|June 18, 2018
Gene Editing on Center StageRasmus O Bak, Natalia Gomez-Ospina, Matthew H PorteusMolecular Therapy. Nucleic Acids|September 10, 2018
Priming Human Repopulating Hematopoietic Stem and Progenitor Cells for Cas9/sgRNA Gene TargetingCarsten T Charlesworth, Joab Camarena, M Kyle Cromer, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|July 15, 2018
Global Transcriptional Response to CRISPR/Cas9-AAV6-Based Genome Editing in CD34+ Hematopoietic Stem and Progenitor CellsM Kyle Cromer, Sriram Vaidyanathan, Daniel E Ryan, et al.Nature|November 8, 2016
CRISPR/Cas9 β-globin gene targeting in human haematopoietic stem cellsDaniel P Dever, Rasmus O Bak, Andreas Reinisch, et al.Cell Stem Cell|April 5, 2024
A simultaneous knockout knockin genome editing strategy in HSPCs potently inhibits CCR5- and CXCR4-tropic HIV-1 infectionAmanda M Dudek, William N Feist, Elena J Sasu, et al.Iscience|May 28, 2019
CRISPR/Cas9 Genome Engineering in Engraftable Human Brain-Derived Neural Stem CellsDaniel P Dever, Samantha G Scharenberg, Joab Camarena, et al.Pageof 20