Blood-brain barrier–penetrating single CRISPR-Cas9 nanocapsules for effective and safe glioblastoma gene therapy
We designed a unique nanocapsule for efficient single CRISPR-Cas9 capsuling,
noninvasive brain delivery and tumor cell targeting, demonstrating an effective and safe …
noninvasive brain delivery and tumor cell targeting, demonstrating an effective and safe …
Brain-targeted CRISPR/Cas9 nanomedicine for effective glioblastoma therapy
W Ruan, M Jiao, S Xu, M Ismail, X Xie, Y An… - Journal of Controlled …, 2022 - Elsevier
CRISPR/Cas9 gene-editing technology shows great potential for treating a variety of
diseases, such as glioblastoma multiforme (GBM). However, CRISPR components suffer …
diseases, such as glioblastoma multiforme (GBM). However, CRISPR components suffer …
Engineered extracellular vesicle-delivered CRISPR/Cas9 for radiotherapy sensitization of glioblastoma
X Liu, Z Cao, W Wang, C Zou, Y Wang, L Pan, B Jia… - ACS …, 2023 - ACS Publications
Radiotherapy is a mainstay of glioblastoma (GBM) treatment; however, the development of
therapeutic resistance has hampered the efficacy of radiotherapy, suggesting that additional …
therapeutic resistance has hampered the efficacy of radiotherapy, suggesting that additional …
CRISPR-Cas9 genome editing using targeted lipid nanoparticles for cancer therapy
D Rosenblum, A Gutkin, R Kedmi, S Ramishetti… - Science …, 2020 - science.org
Harnessing CRISPR-Cas9 technology for cancer therapeutics has been hampered by low
editing efficiency in tumors and potential toxicity of existing delivery systems. Here, we …
editing efficiency in tumors and potential toxicity of existing delivery systems. Here, we …
[HTML][HTML] Strategies in the delivery of Cas9 ribonucleoprotein for CRISPR/Cas9 genome editing
S Zhang, J Shen, D Li, Y Cheng - Theranostics, 2021 - ncbi.nlm.nih.gov
CRISPR/Cas9 genome editing has gained rapidly increasing attentions in recent years,
however, the translation of this biotechnology into therapy has been hindered by efficient …
however, the translation of this biotechnology into therapy has been hindered by efficient …
A biodegradable nanocapsule delivers a Cas9 ribonucleoprotein complex for in vivo genome editing
Delivery technologies for the CRISPR-Cas9 (CRISPR, clustered regularly interspaced short
palindromic repeats) gene editing system often require viral vectors, which pose safety …
palindromic repeats) gene editing system often require viral vectors, which pose safety …
Engineered nanomaterials to potentiate CRISPR/Cas9 gene editing for cancer therapy
Clustered regularly interspaced short palindromic repeats/associated protein 9
(CRISPR/Cas9) gene‐editing technology shows promise for manipulating single or multiple …
(CRISPR/Cas9) gene‐editing technology shows promise for manipulating single or multiple …
Nanoparticle delivery of CRISPR/Cas9 for genome editing
L Duan, K Ouyang, X Xu, L Xu, C Wen, X Zhou… - Frontiers in …, 2021 - frontiersin.org
The emerging clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-
associated system (Cas) gene-editing system represents a promising tool for genome …
associated system (Cas) gene-editing system represents a promising tool for genome …
CRISPR/Cas9 delivery system engineering for genome editing in therapeutic applications
H Cheng, F Zhang, Y Ding - Pharmaceutics, 2021 - mdpi.com
The clustered regularly interspaced short palindromic repeats (CRISPR)/associated protein
9 (CRISPR/Cas9) systems have emerged as a robust and versatile genome editing platform …
9 (CRISPR/Cas9) systems have emerged as a robust and versatile genome editing platform …
A self-restricted CRISPR system to reduce off-target effects
Y Chen, X Liu, Y Zhang, H Wang, H Ying, M Liu, D Li… - Molecular therapy, 2016 - cell.com
Genome editing technologies, such as clustered regularly interspaced short palindromic
repeats (CRISPR)/CRISPR-associated (Cas) systems, are being widely applied in …
repeats (CRISPR)/CRISPR-associated (Cas) systems, are being widely applied in …