Cargando…
Intra-embryo Gene Cassette Knockin by CRISPR/Cas9-Mediated Genome Editing with Adeno-Associated Viral Vector
Intra-embryo genome editing by CRISPR/Cas9 enables easy generation of gene-modified animals by non-homologous end joining (NHEJ)-mediated frameshift mutations or homology-directed repair (HDR)-mediated point mutations. However, large modifications, such as gene replacement or gene fusions, are still...
Autores principales: | Mizuno, Naoaki, Mizutani, Eiji, Sato, Hideyuki, Kasai, Mariko, Ogawa, Aki, Suchy, Fabian, Yamaguchi, Tomoyuki, Nakauchi, Hiromitsu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240711/ https://www.ncbi.nlm.nih.gov/pubmed/30447647 http://dx.doi.org/10.1016/j.isci.2018.10.030 |
Ejemplares similares
-
Generation of Vascular Endothelial Cells and Hematopoietic Cells by Blastocyst Complementation
por: Hamanaka, Sanae, et al.
Publicado: (2018) -
Removal of sperm tail using trypsin and pre-activation of oocyte facilitates intracytoplasmic sperm injection in mice and rats
por: TORIKAI, Kohei, et al.
Publicado: (2022) -
Generation of a tyrosine hydroxylase-2A-Cre knockin non-human primate model by homology-directed-repair-biased CRISPR genome editing
por: Yoshimatsu, Sho, et al.
Publicado: (2023) -
A humanized knockin mouse model of Duchenne muscular dystrophy and its correction by CRISPR-Cas9 therapeutic gene editing
por: Zhang, Yu, et al.
Publicado: (2022) -
Exome sequencing in the knockin mice generated using the CRISPR/Cas system
por: Nakajima, Kazuo, et al.
Publicado: (2016)