Overcoming lentiviral delivery limitations in hard-to-transduce suspension cells for genome-wide CRISPR screening.
- DOI
- 10.1016/j.omta.2026.201678
- Published
- 2026 Mar 12
- Container
- Molecular therapy. Advances
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1016/j.omta.2026.201678,
title = {Overcoming lentiviral delivery limitations in hard-to-transduce suspension cells for genome-wide CRISPR screening.},
author = {Napoleone A and Sebastian IR and De Marco F and Molin A and Hussein M and Kramer L and Jostock T and Kelly T and Borth N},
year = {2026},
journal = {Molecular therapy. Advances},
doi = {10.1016/j.omta.2026.201678},
url = {https://doi.org/10.1016/j.omta.2026.201678}
}RIS
TY - JOUR TI - Overcoming lentiviral delivery limitations in hard-to-transduce suspension cells for genome-wide CRISPR screening. AU - Napoleone A AU - Sebastian IR AU - De Marco F AU - Molin A AU - Hussein M AU - Kramer L AU - Jostock T AU - Kelly T AU - Borth N PY - 2026 JO - Molecular therapy. Advances DO - 10.1016/j.omta.2026.201678 UR - https://doi.org/10.1016/j.omta.2026.201678 ER -
APA
A, N., IR, S., F, D. M., A, M., M, H., L, K., T, J., T, K., & N, B. (2026). Overcoming lentiviral delivery limitations in hard-to-transduce suspension cells for genome-wide CRISPR screening.. Molecular therapy. Advances. https://doi.org/10.1016/j.omta.2026.201678
Source records
- pubmed · retrieved 2026-09-25T18:12:45.167Z