Small molecule inhibitors can influence the choice of repair pathways, enhancing nucleotide substitution and gene integration in CRISPR-mediated genome editing. Here the authors introduce CRISPY, a mix of small molecules that can enhance precise editing with Cpf1 and Cas9D10A in hiPSCs
The CRISPR-Cas9 system is a powerful genome-editing tool that promises application for gene editing ...
The CRISPR-Cas9 system is a powerful genome-editing tool that promises application for gene editing ...
Thesis (Ph.D.)--University of Washington, 2022Clustered regularly interspaced short palindromic repe...
SummaryThe bacterial CRISPR-Cas9 system has emerged as an effective tool for sequence-specific gene ...
SummaryThe bacterial CRISPR-Cas9 system has emerged as an effective tool for sequence-specific gene ...
The bacterial CRISPR-Cas9 system has emerged as an effective tool for sequence-specific gene knockou...
Introduction: Clustered regularly interspaced short palindromic repeat and its associated protein (C...
Kmiec, EricSingle base mutations can be repaired by introducing single stranded DNA oligonucleotides...
Single base mutations can be repaired by introducing single stranded DNA oligonucleotides (ssODN) in...
Genome engineering technologies have been in a rapid series of development over the past decade. The...
BACKGROUND: Precise genetic modifications are preferred products of CRISPR-Cas9 mediated gene editin...
Precision CRISPR gene editing relies on the cellular homology-directed DNA repair (HDR) to introduce...
Gene manipulations of human induced pluripotent stem cells (iPSCs) by CRISPR-Cas9 genome engineering...
Targeted genome editing has become a powerful genetic tool for modification of DNA sequences in thei...
Modification of the human genome has immense potential for preventing or treating disease. Modern ge...
The CRISPR-Cas9 system is a powerful genome-editing tool that promises application for gene editing ...
The CRISPR-Cas9 system is a powerful genome-editing tool that promises application for gene editing ...
Thesis (Ph.D.)--University of Washington, 2022Clustered regularly interspaced short palindromic repe...
SummaryThe bacterial CRISPR-Cas9 system has emerged as an effective tool for sequence-specific gene ...
SummaryThe bacterial CRISPR-Cas9 system has emerged as an effective tool for sequence-specific gene ...
The bacterial CRISPR-Cas9 system has emerged as an effective tool for sequence-specific gene knockou...
Introduction: Clustered regularly interspaced short palindromic repeat and its associated protein (C...
Kmiec, EricSingle base mutations can be repaired by introducing single stranded DNA oligonucleotides...
Single base mutations can be repaired by introducing single stranded DNA oligonucleotides (ssODN) in...
Genome engineering technologies have been in a rapid series of development over the past decade. The...
BACKGROUND: Precise genetic modifications are preferred products of CRISPR-Cas9 mediated gene editin...
Precision CRISPR gene editing relies on the cellular homology-directed DNA repair (HDR) to introduce...
Gene manipulations of human induced pluripotent stem cells (iPSCs) by CRISPR-Cas9 genome engineering...
Targeted genome editing has become a powerful genetic tool for modification of DNA sequences in thei...
Modification of the human genome has immense potential for preventing or treating disease. Modern ge...
The CRISPR-Cas9 system is a powerful genome-editing tool that promises application for gene editing ...
The CRISPR-Cas9 system is a powerful genome-editing tool that promises application for gene editing ...
Thesis (Ph.D.)--University of Washington, 2022Clustered regularly interspaced short palindromic repe...