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.
Dynamic aqueous multiphase reaction system for simple, sensitive and quantitative one-pot CRISPR-Cas12a based molecular diagnosis
Targeted genome editing in Nicotiana tabacum using inducible CRISPR/Cas9 system
Arrayed CRISPRi and Quantitative Imaging Describe the Morphotypic Landscape of Essential Mycobacterial Genes
Targeted mutagenesis of ∆5 and ∆6 fatty acyl desaturases induce multiplex-mutagenesis and lipogenesis in Atlantic salmon (Salmo salar)
Start codon disruption with CRISPR/Cas9 prevents murine Fuchs' endothelial corneal dystrophy
Fuse to defuse: a self-limiting ribonuclease-ring nuclease fusion for type III CRISPR defence
Evolutionary Changes in Left-Right Visceral Asymmetry in Astyanax Cavefish
Efficient Generation of Isogenic Primary Human Myeloid Cells using CRISPR-Cas9 Ribonucleoproteins
Development of CRISPR as a prophylactic strategy to combat novel coronavirus and influenza
Rapid Detection of 2019 Novel Coronavirus SARS-CoV-2 Using a CRISPR-based DETECTR Lateral Flow Assay
Bar-seq strategies for the LeishGEdit toolbox
Sequential CRISPR gene editing in human iPSCs charts the clonal evolution of leukemia
Non-canonical open reading frames encode functional proteins essential for cancer cell survival
Optimization of multiplexed CRISPR/Cas9 system for highly efficient genome editing in Setaria viridis
Rapid and accurate detection of novel coronavirus SARS-CoV-2 using CRISPR-Cas3
HIV-1 promoter is gradually silenced when integrated into BACH2
Enhancement of trans-cleavage activity of Cas12a with engineered crRNA enables amplified nucleic acid detection
Sox2 controls neural stem cell self-renewal through a Fos-centered gene regulatory network
A heterodimeric SNX4:SNX7 SNX-BAR autophagy complex coordinates ATG9A trafficking for efficient autophagosome assembly
Genome editing in mammals using CRISPR type I-D nuclease
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