Jennifer L. Gori, Ph.D.
Affiliations: | 2008 | Microbiology, Immunology and Cancer Biology | University of Minnesota, Twin Cities, Minneapolis, MN |
Area:
Molecular Biology, Virology Biology, Microbiology BiologyGoogle:
"Jennifer Gori"Parents
Sign in to add mentorDavid A. Largaespada | grad student | 2008 | UMN | |
(Methotrexate resistance gene transfer in stem cells.) |
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Publications
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Shamah S, Elpek K, Ezell T, et al. (2020) Abstract 6604: Drug responsive domain regulation of IL15-engineered T cells provides pharmacological control over antigen-independent cell expansion Immunology |
Suri V, Gori JL. (2018) Small Molecule Regulated Cytokine Expression Enables Potent and Durable Responses to Engineered T-Cell Therapy Blood. 132: 2045-2045 |
Gori JL, Butler JM, Kunar B, et al. (2017) Endothelial Cells Promote Expansion of Long-Term Engrafting Marrow Hematopoietic Stem and Progenitor Cells in Primates. Stem Cells Translational Medicine. 6: 864-876 |
Gori JL, Butler JM, Kunar B, et al. (2016) Endothelial Cells Promote Expansion of Long-Term Engrafting Marrow Hematopoietic Stem and Progenitor Cells in Primates. Stem Cells Translational Medicine |
Heath JM, Chalishazar A, Lee CS, et al. (2016) Precise and Efficient Crispr/Cas9 Mediated Gene Editing in Long-Term Engrafting Human Hematopoietic Stem/Progenitor Cells Blood. 128: 2312-2312 |
Heath JM, Chalishazar A, Lee CS, et al. (2016) 732. CRISPR/Cas9 Mediates Highly Efficient Gene Editing in Long-Term Engrafting Human Hematopoietic Stem/Progenitor Cells Molecular Therapy. 24: S288-S289 |
Gori JL, Hsu PD, Maeder ML, et al. (2015) Delivery and Specificity of CRISPR-Cas9 Genome Editing Technologies for Human Gene Therapy. Human Gene Therapy. 26: 443-51 |
Gori JL, Butler JM, Chan YY, et al. (2015) Vascular niche promotes hematopoietic multipotent progenitor formation from pluripotent stem cells. The Journal of Clinical Investigation. 125: 1243-54 |
Rafii S, Butler JM, Michael G, et al. (2015) Vascular Niche-Derived Angiocrine Factors Specify and Maintain Hematopoietic Stem Cells Blood. 126: SCI-25-SCI-25 |
Grant Welstead G, Gori J, Fang J, et al. (2015) 348. Characterization of Cas9-Mediated Genome Editing in Human T Cells Molecular Therapy. 23: S138 |