tgCRISPRi: efficient gene knock-down using truncated gRNAs and catalytically active Cas9
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
tgCRISPRi: efficient gene knock-down using truncated gRNAs and catalytically active Cas9 ; volume:14 ; number:1 ; day:11 ; month:9 ; year:2023 ; pages:1-14 ; date:12.2023
Nature Communications ; 14, Heft 1 (11.9.2023), 1-14, 12.2023
- Creator
-
Auradkar, Ankush
Guichard, Annabel
Kaduwal, Saluja
Sneider, Marketta
Bier, Ethan
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-023-40836-3
- URN
-
urn:nbn:de:101:1-2024020210244497584257
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:32 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
- Auradkar, Ankush
- Guichard, Annabel
- Kaduwal, Saluja
- Sneider, Marketta
- Bier, Ethan
- SpringerLink (Online service)
Other Objects (12)
Author Correction: tgCRISPRi: efficient gene knock-down using truncated gRNAs and catalytically active Cas9
Untersuchung von TRPM3-Kationenkanälen mit Hilfe von Knock-down- und Knock-out-Methoden
Immune cell function in the Clec6a knock-down mouse
Immune cell function in the Clec16a Knock-down Mouse
RNA interference: learning gene knock-down from cell physiology
Gene silencing based on RNA-guided catalytically inactive Cas9 (dCas9): a new tool for genetic engineering in Leptospira
HIV-1 mRNA knockdown with CRISPR/CAS9 enhances neurocognitive function
An efficient method to enrich for knock-out and knock-in cellular clones using the CRISPR/Cas9 system
Knock-down von Desmoglein 2 durch induzierbare Cre-spezifische Rekombination in der Maus
The inhibition of invasion of human melanoma cells through N-cadherin knock-down
Rapid clonal identification of biallelic CRISPR/Cas9 knock-ins using SNEAK PEEC
CRISPR/Cas9-mediated knock-in in the zebrafish lama5 and lama1 loci
Author Correction: tgCRISPRi: efficient gene knock-down using truncated gRNAs and catalytically active Cas9
Untersuchung von TRPM3-Kationenkanälen mit Hilfe von Knock-down- und Knock-out-Methoden
Immune cell function in the Clec6a knock-down mouse
Immune cell function in the Clec16a Knock-down Mouse
RNA interference: learning gene knock-down from cell physiology
Gene silencing based on RNA-guided catalytically inactive Cas9 (dCas9): a new tool for genetic engineering in Leptospira
HIV-1 mRNA knockdown with CRISPR/CAS9 enhances neurocognitive function
An efficient method to enrich for knock-out and knock-in cellular clones using the CRISPR/Cas9 system
Knock-down von Desmoglein 2 durch induzierbare Cre-spezifische Rekombination in der Maus
The inhibition of invasion of human melanoma cells through N-cadherin knock-down
Rapid clonal identification of biallelic CRISPR/Cas9 knock-ins using SNEAK PEEC
CRISPR/Cas9-mediated knock-in in the zebrafish lama5 and lama1 loci
Author Correction: tgCRISPRi: efficient gene knock-down using truncated gRNAs and catalytically active Cas9
Untersuchung von TRPM3-Kationenkanälen mit Hilfe von Knock-down- und Knock-out-Methoden
Immune cell function in the Clec6a knock-down mouse
Immune cell function in the Clec16a Knock-down Mouse
RNA interference: learning gene knock-down from cell physiology
Gene silencing based on RNA-guided catalytically inactive Cas9 (dCas9): a new tool for genetic engineering in Leptospira
HIV-1 mRNA knockdown with CRISPR/CAS9 enhances neurocognitive function
An efficient method to enrich for knock-out and knock-in cellular clones using the CRISPR/Cas9 system
Knock-down von Desmoglein 2 durch induzierbare Cre-spezifische Rekombination in der Maus
The inhibition of invasion of human melanoma cells through N-cadherin knock-down
Rapid clonal identification of biallelic CRISPR/Cas9 knock-ins using SNEAK PEEC