Cargando…

High-efficiency nonviral CRISPR/Cas9-mediated gene editing of human T cells using plasmid donor DNA

Genome engineering of T lymphocytes, the main effectors of antitumor adaptive immune responses, has the potential to uncover unique insights into their functions and enable the development of next-generation adoptive T cell therapies. Viral gene delivery into T cells, which is currently used to gene...

Descripción completa

Detalles Bibliográficos
Autores principales:	Oh, Soyoung A., Senger, Kate, Madireddi, Shravan, Akhmetzyanova, Ilseyar, Ishizuka, Isabel E., Tarighat, Somayeh, Lo, Jerry H., Shaw, David, Haley, Benjamin, Rutz, Sascha
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Rockefeller University Press 2022
Materias:	Technical Advances and Resources
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040063/ https://www.ncbi.nlm.nih.gov/pubmed/35452075 http://dx.doi.org/10.1084/jem.20211530

Ejemplares similares

Systematic genome editing of the genes on zebrafish Chromosome 1 by CRISPR/Cas9
por: Sun, Yonghua, et al.
Publicado: (2020)

Recent advances in the delivery and applications of nonviral CRISPR/Cas9 gene editing
por: Sinclair, Frazer, et al.
Publicado: (2023)

Computational Tools and Resources for CRISPR/Cas Genome Editing
por: Li, Chao, et al.
Publicado: (2023)

Efficient gene knockout in primary human and murine myeloid cells by non-viral delivery of CRISPR-Cas9
por: Freund, Emily C., et al.
Publicado: (2020)

Transcriptome networks identify mechanisms of viral and nonviral asthma exacerbations in children
por: Altman, Matthew C., et al.
Publicado: (2019)

Precise and efficient genome editing in zebrafish using the CRISPR/Cas9 system
por: Irion, Uwe, et al.
Publicado: (2014)

Homozygous might be hemizygous: CRISPR/Cas9 editing in iPSCs results in detrimental on-target defects that escape standard quality controls
por: Simkin, Dina, et al.
Publicado: (2022)

Nonviral gene editing via CRISPR/Cas9 delivery by membrane-disruptive and endosomolytic helical polypeptide
por: Wang, Hong-Xia, et al.
Publicado: (2018)

CRISPR-Cas systems are widespread accessory elements across bacterial and archaeal plasmids
por: Pinilla-Redondo, Rafael, et al.
Publicado: (2021)

Plasmid Sequence and Availability for an Improved Clostridioides difficile CRISPR-Cas9 Mutagenesis System
por: Brehm, Joshua N., et al.
Publicado: (2022)

Engineering T cell receptor fusion proteins using nonviral CRISPR/Cas9 genome editing for cancer immunotherapy
por: Shu, Runzhe, et al.
Publicado: (2023)

Repurposing CRISPR/Cas9 for in situ functional assays
por: Malina, Abba, et al.
Publicado: (2013)

Poly(Beta-Amino Ester) Nanoparticles Enable Nonviral Delivery of CRISPR-Cas9 Plasmids for Gene Knockout and Gene Deletion
por: Rui, Yuan, et al.
Publicado: (2020)

Modeling invasive lobular breast carcinoma by CRISPR/Cas9-mediated somatic genome editing of the mammary gland
por: Annunziato, Stefano, et al.
Publicado: (2016)

ORANGE: A CRISPR/Cas9-based genome editing toolbox for epitope tagging of endogenous proteins in neurons
por: Willems, Jelmer, et al.
Publicado: (2020)

Highly Efficient Targeted Mutagenesis of Drosophila with the CRISPR/Cas9 System
por: Bassett, Andrew R., et al.
Publicado: (2013)

CRISPR Explorer: A fast and intuitive tool for designing guide RNA for genome editing
por: Chen, Kenian, et al.
Publicado: (2016)

Pancreatic cancer modeling using retrograde viral vector delivery and in vivo CRISPR/Cas9-mediated somatic genome editing
por: Chiou, Shin-Heng, et al.
Publicado: (2015)

A Scaled Framework for CRISPR Editing of Human Pluripotent Stem Cells to Study Psychiatric Disease
por: Hazelbaker, Dane Z., et al.
Publicado: (2017)

A CRISPR/Cas-Mediated Selection-free Knockin Strategy in Human Embryonic Stem Cells
por: Zhu, Zengrong, et al.
Publicado: (2015)

CRISPR/Cas9 gene editing for the creation of an MGAT1-deficient CHO cell line to control HIV-1 vaccine glycosylation
por: Byrne, Gabriel, et al.
Publicado: (2018)

One‐step CRISPR/Cas9 method for the rapid generation of human antibody heavy chain knock‐in mice
por: Lin, Ying‐Cing, et al.
Publicado: (2018)

Modeling High-Grade Serous Ovarian Carcinoma Using a Combination of In Vivo Fallopian Tube Electroporation and CRISPR-Cas9–Mediated Genome Editing
por: Teng, Katie, et al.
Publicado: (2021)

Efficient CRISPR/Cas9 Plasmids for Rapid and Versatile Genome Editing in Drosophila
por: Gokcezade, Joseph, et al.
Publicado: (2014)

Plasmid-Based CRISPR-Cas9 Gene Editing in Multiple Candida Species
por: Lombardi, Lisa, et al.
Publicado: (2019)

Highly efficient genome editing in Xanthomonas oryzae pv. oryzae through repurposing the endogenous type I‐C CRISPR‐Cas system
por: Jiang, Dandan, et al.
Publicado: (2021)

Efficient Recreation of t(11;22) EWSR1-FLI1(+) in Human Stem Cells Using CRISPR/Cas9
por: Torres-Ruiz, Raul, et al.
Publicado: (2017)

Essential Functions of Glycans in Human Epithelia Dissected by a CRISPR-Cas9-Engineered Human Organotypic Skin Model
por: Dabelsteen, Sally, et al.
Publicado: (2020)

Highly efficient CRISPR-mediated gene editing in a rotifer
por: Feng, Haiyang, et al.
Publicado: (2023)

Precise Correction of the Dystrophin Gene in Duchenne Muscular Dystrophy Patient Induced Pluripotent Stem Cells by TALEN and CRISPR-Cas9
por: Li, Hongmei Lisa, et al.
Publicado: (2014)

Multiplexed CRISPR/CAS9‐mediated engineering of pre‐clinical mouse models bearing native human B cell receptors
por: Wang, Xuesong, et al.
Publicado: (2020)

A robust platform for expansion and genome editing of primary human natural killer cells
por: Huang, Rih-Sheng, et al.
Publicado: (2021)

HPV Oncogene Manipulation Using Nonvirally Delivered CRISPR/Cas9 or Natronobacterium gregoryi Argonaute
por: Lao, Yeh‐Hsing, et al.
Publicado: (2018)

Efficient ssODN-Mediated Targeting by Avoiding Cellular Inhibitory RNAs through Precomplexed CRISPR-Cas9/sgRNA Ribonucleoprotein
por: Kagita, Akihiro, et al.
Publicado: (2021)

Efficient genetic editing of human intestinal organoids using ribonucleoprotein-based CRISPR
por: Skoufou-Papoutsaki, Nefeli, et al.
Publicado: (2023)

A single-plasmid approach for genome editing coupled with long-term lineage analysis in chick embryos
por: Gandhi, Shashank, et al.
Publicado: (2021)

Rapid detection of SARS-CoV-2 with CRISPR-Cas12a
por: Xiong, Dan, et al.
Publicado: (2020)

CRISPR-Cas-Guided Mutagenesis of Chromosome and Virulence Plasmid in Shigella flexneri by Cytosine Base Editing
por: Sharma, Atin, et al.
Publicado: (2022)

A Universal, Genomewide GuideFinder for CRISPR/Cas9 Targeting in Microbial Genomes
por: Spoto, Michelle, et al.
Publicado: (2020)

Functional dissection of human mitotic genes using CRISPR–Cas9 tiling screens
por: Herman, Jacob A., et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_9a96mhf4tbdsnh8ikjjkfn41qt