Tumor cell-targeted delivery of CRISPR/Cas9 by aptamer-functionalized lipopolymer for therapeutic genome editing of VEGFA in osteosarcoma
Osteosarcoma (OS) is a highly aggressive pediatric cancer, characterized by frequent lung
metastasis and pathologic bone destruction. Vascular endothelial growth factor A (VEGFA) …
metastasis and pathologic bone destruction. Vascular endothelial growth factor A (VEGFA) …
Lipid nanoparticle-mediated efficient delivery of CRISPR/Cas9 for tumor therapy
The emerging CRISPR/Cas9 system represents a promising platform for genome editing.
However, its low transfection efficiency is a major problem hampering the application of the …
However, its low transfection efficiency is a major problem hampering the application of the …
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 …
Non-viral delivery systems for CRISPR/Cas9-based genome editing: Challenges and opportunities
L Li, S Hu, X Chen - Biomaterials, 2018 - Elsevier
In recent years, CRISPR (clustered regularly interspaced short palindromic repeat)/Cas
(CRISPR-associated) genome editing systems have become one of the most robust …
(CRISPR-associated) genome editing systems have become one of the most robust …
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 …
Biomaterial-assisted targeted and controlled delivery of CRISPR/Cas9 for precise gene editing
RISPR-Cas9 has exhibited enormous potential in gene therapy. It can perform genome
editing with single-nucleotide precision in various types of cell and tissue, providing a …
editing with single-nucleotide precision in various types of cell and tissue, providing a …
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 …
Effective PEI-mediated delivery of CRISPR-Cas9 complex for targeted gene therapy
The-state-of-art CRISPR/Cas9 is one of the most powerful among the approaches being
developed to rescue fundamental causes of gene-based inheritable diseases. Several …
developed to rescue fundamental causes of gene-based inheritable diseases. Several …
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 …
Tropism-facilitated delivery of CRISPR/Cas9 system with chimeric antigen receptor-extracellular vesicles against B-cell malignancies
Q Xu, Z Zhang, L Zhao, Y Qin, H Cai, Z Geng… - Journal of Controlled …, 2020 - Elsevier
The CRISPR/Cas9 system is an efficient genome-editing system that has been successfully
applied in the field of gene therapy. However, clinical applications of the CRISPR/Cas9 …
applied in the field of gene therapy. However, clinical applications of the CRISPR/Cas9 …
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