Development of an in vivo cleavable donor plasmid for targeted transgene integration by CRISPR-Cas9 and CRISPR-Cas12a
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2045-2322
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Development of an in vivo cleavable donor plasmid for targeted transgene integration by CRISPR-Cas9 and CRISPR-Cas12a ; volume:12 ; number:1 ; day:22 ; month:10 ; year:2022 ; pages:1-12 ; date:12.2022
Scientific reports ; 12, Heft 1 (22.10.2022), 1-12, 12.2022
- Creator
-
Ishibashi, Riki
Maki, Ritsuko
Kitano, Satsuki
Miyachi, Hitoshi
Toyoshima, Fumiko
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41598-022-22639-6
- URN
-
urn:nbn:de:101:1-2023010621041561685154
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:37 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Ishibashi, Riki
- Maki, Ritsuko
- Kitano, Satsuki
- Miyachi, Hitoshi
- Toyoshima, Fumiko
- SpringerLink (Online service)
Other Objects (12)
Ratiometric nonfluorescent CRISPR assay utilizing Cas12a-induced plasmid supercoil relaxation
Gene targeting in adult organs using in vivo cleavable donor plasmids for CRISPR-Cas9 and CRISPR-Cas12a
CRISPR-Cas12a-assisted nucleic acid detection
Programmable RNA detection with CRISPR-Cas12a
Fabrication and characterization of PLGA nanoparticles encapsulating large CRISPR–Cas9 plasmid
A versatile one-step CRISPR-Cas9 based approach to plasmid-curing
CRISPR/Cas9 in Gastrointestinal Malignancies
CRISPR-Cas9 and T cells
Genome editing with TALEN, CRISPR-Cas9 and CRISPR-Cas12a in combination with AAV6 homology donor restores T cell function for XLP
Exploiting anti-CRISPR proteins for conditional activation of CRISPR-Cas9
Improving CRISPR–Cas9 directed faithful transgene integration outcomes by reducing unwanted random DNA integration
CRISPR-Cas12a-assisted gene tagging in mammalian cells
Ratiometric nonfluorescent CRISPR assay utilizing Cas12a-induced plasmid supercoil relaxation
Gene targeting in adult organs using in vivo cleavable donor plasmids for CRISPR-Cas9 and CRISPR-Cas12a
CRISPR-Cas12a-assisted nucleic acid detection
Programmable RNA detection with CRISPR-Cas12a
Fabrication and characterization of PLGA nanoparticles encapsulating large CRISPR–Cas9 plasmid
A versatile one-step CRISPR-Cas9 based approach to plasmid-curing
CRISPR/Cas9 in Gastrointestinal Malignancies
CRISPR-Cas9 and T cells
Genome editing with TALEN, CRISPR-Cas9 and CRISPR-Cas12a in combination with AAV6 homology donor restores T cell function for XLP
Exploiting anti-CRISPR proteins for conditional activation of CRISPR-Cas9
Improving CRISPR–Cas9 directed faithful transgene integration outcomes by reducing unwanted random DNA integration
CRISPR-Cas12a-assisted gene tagging in mammalian cells
Ratiometric nonfluorescent CRISPR assay utilizing Cas12a-induced plasmid supercoil relaxation
Gene targeting in adult organs using in vivo cleavable donor plasmids for CRISPR-Cas9 and CRISPR-Cas12a
CRISPR-Cas12a-assisted nucleic acid detection
Programmable RNA detection with CRISPR-Cas12a
Fabrication and characterization of PLGA nanoparticles encapsulating large CRISPR–Cas9 plasmid
A versatile one-step CRISPR-Cas9 based approach to plasmid-curing
CRISPR/Cas9 in Gastrointestinal Malignancies
CRISPR-Cas9 and T cells
Genome editing with TALEN, CRISPR-Cas9 and CRISPR-Cas12a in combination with AAV6 homology donor restores T cell function for XLP
Exploiting anti-CRISPR proteins for conditional activation of CRISPR-Cas9
Improving CRISPR–Cas9 directed faithful transgene integration outcomes by reducing unwanted random DNA integration