Results 81 to 90 of about 194,133 (208)

CRISPR–Cas9 genome editing induces a p53-mediated DNA damage response

open access: yesNature Network Boston, 2018
Here, we report that genome editing by CRISPR–Cas9 induces a p53-mediated DNA damage response and cell cycle arrest in immortalized human retinal pigment epithelial cells, leading to a selection against cells with a functional p53 pathway.
E. Haapaniemi   +4 more
semanticscholar   +1 more source

Fast Antibiotic resistance-Based gene editing of mammalian cells with CRISPR-Cas9 (FAB-CRISPR) [PDF]

open access: yesarXiv
Protein tagging with CRISPR-Cas9 enables the investigation of protein function in its native environment but is limited by low homology-directed repair (HDR) efficiency causing low knock-in rates. We present a detailed pipeline using HDR donor plasmids containing antibiotic resistance cassettes for rapid selection of gene-edited cells.
arxiv  

Cas-OFFinder: a fast and versatile algorithm that searches for potential off-target sites of Cas9 RNA-guided endonucleases

open access: yesBioinform., 2014
Summary: The Type II clustered regularly interspaced short palindromic repeats (CRISPR)/Cas system is an adaptive immune response in prokaryotes, protecting host cells against invading phages or plasmids by cleaving these foreign DNA species in a ...
Sangsu Bae, Jeongbin Park, Jin-Soo Kim
semanticscholar   +1 more source

Single step production of Cas9 mRNA for zygote injection

open access: yesBioTechniques, 2018
Production of Cas9 mRNA in vitro typically requires the addition of a 5´ cap and 3´ polyadenylation. A plasmid was constructed that harbored the T7 promoter followed by the EMCV IRES and a Cas9 coding region.
Bethany K Redel   +8 more
doaj   +1 more source

Genome Engineering ofDrosophilawith the CRISPR RNA-Guided Cas9 Nuclease [PDF]

open access: bronze, 2013
Scott J. Gratz   +7 more
openalex   +1 more source

Development and testing of a versatile genome editing application reporter (V-GEAR) system

open access: yesMolecular Therapy: Methods & Clinical Development
CRISPR-Cas9 and novel cas fusion proteins leveraging specific DNA targeting ability combined with deaminases or reverse transcriptases have revolutionized genome editing.
Evan W. Kleinboehl   +7 more
doaj  

Target search in the CRISPR/Cas9 system: Facilitated diffusion with target cues [PDF]

open access: yesarXiv
We study how Cas9, a central component of the CRISPR/Cas9 system, searches for a target sequence on the DNA. We propose a model that includes as key ingredients 3D diffusion, 1D sliding along the DNA, and the effect of short binding sequences preceding the target (protospacer adjacent sequences -- PAMs).
arxiv  

Correction of a Genetic Disease in Mouse via Use of CRISPR-Cas9 [PDF]

open access: hybrid, 2013
Yuxuan Wu   +8 more
openalex   +1 more source

Recent Advances in Genome Editing Using CRISPR/Cas9

open access: yesFrontiers in Plant Science, 2016
The CRISPR (clustered regularly interspaced short palindromic repeat)-Cas9 (CRISPR-associated nuclease 9) system is a versatile tool for genome engineering that uses a guide RNA (gRNA) to target Cas9 to a specific sequence.
Yuduan eDing   +6 more
doaj   +1 more source

DeepFM-Crispr: Prediction of CRISPR On-Target Effects via Deep Learning [PDF]

open access: yesarXiv
Since the advent of CRISPR-Cas9, a groundbreaking gene-editing technology that enables precise genomic modifications via a short RNA guide sequence, there has been a marked increase in the accessibility and application of this technology across various fields.
arxiv  

Home - About - Disclaimer - Privacy