CRISPR for Genome Editing (Preprints)

Genome editing technologies enable the editing of genes to create or correct mutations. Clustered regularly interspaced short palindromic repeats (CRISPR) are DNA sequences in the genome that are recognized and cleaved by CRISPR-associated proteins (Cas). Here are the latest preprints on the use of CRISPR-Cas system in gene editing.

March 14, 2020
Preprint
Open Access

Targeted genome editing in Nicotiana tabacum using inducible CRISPR/Cas9 system

bioRxiv
Chong RenZhenchang Liang
March 22, 2020
Preprint
Open Access

Arrayed CRISPRi and Quantitative Imaging Describe the Morphotypic Landscape of Essential Mycobacterial Genes

bioRxiv
Timothy Jack de WetDigby Francis Warner
March 20, 2020
Preprint
Open Access

Start codon disruption with CRISPR/Cas9 prevents murine Fuchs' endothelial corneal dystrophy

bioRxiv
Hironori UeharaBalamurali K Ambati
March 12, 2020
Preprint
Open Access

Fuse to defuse: a self-limiting ribonuclease-ring nuclease fusion for type III CRISPR defence

bioRxiv
Aleksei SamolygoMalcolm F White
May 16, 2020
Preprint
Open Access

Evolutionary Changes in Left-Right Visceral Asymmetry in Astyanax Cavefish

bioRxiv
L. MaWilliam R. Jeffery
March 20, 2020
Preprint
Open Access

Bar-seq strategies for the LeishGEdit toolbox

bioRxiv
Tom Beneke, Eva Gluenz
April 22, 2020
Preprint
Open Access

Sequential CRISPR gene editing in human iPSCs charts the clonal evolution of leukemia

bioRxiv
T. WangEirini P Papapetrou
March 30, 2020
Preprint
Open Access

HIV-1 promoter is gradually silenced when integrated into BACH2

bioRxiv
Anne InderbitzinKarin J Metzner
March 18, 2020
Preprint
Open Access

Sox2 controls neural stem cell self-renewal through a Fos-centered gene regulatory network

bioRxiv
Miriam PaginSilvia Kirsten Nicolis
March 15, 2020
Preprint
Open Access

Genome editing in mammals using CRISPR type I-D nuclease

bioRxiv
Keishi OsakabeYuriko Osakabe

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