[HTML][HTML] Mosaicism in CRISPR/Cas9-mediated genome editing
The CRISPR/Cas9 system is a rapid, simple, and often extremely efficient gene editing
method. This method has been used in a variety of organisms and cell types over the past …
method. This method has been used in a variety of organisms and cell types over the past …
Whole-body and whole-organ clearing and imaging techniques with single-cell resolution: toward organism-level systems biology in mammals
Organism-level systems biology aims to identify, analyze, control and design cellular circuits
in organisms. Many experimental and computational approaches have been developed …
in organisms. Many experimental and computational approaches have been developed …
Liver-derived signals sequentially reprogram myeloid enhancers to initiate and maintain Kupffer cell identity
Tissue environment plays a powerful role in establishing and maintaining the distinct
phenotypes of resident macrophages, but the underlying molecular mechanisms remain …
phenotypes of resident macrophages, but the underlying molecular mechanisms remain …
Easi-CRISPR: a robust method for one-step generation of mice carrying conditional and insertion alleles using long ssDNA donors and CRISPR ribonucleoproteins
RM Quadros, H Miura, DW Harms, H Akatsuka, T Sato… - Genome biology, 2017 - Springer
Background Conditional knockout mice and transgenic mice expressing recombinases,
reporters, and inducible transcriptional activators are key for many genetic studies and …
reporters, and inducible transcriptional activators are key for many genetic studies and …
High Efficiency, Homology-Directed Genome Editing in Caenorhabditis elegans Using CRISPR-Cas9 Ribonucleoprotein Complexes
Homology-directed repair (HDR) of breaks induced by the RNA-programmed nuclease
Cas9 has become a popular method for genome editing in several organisms. Most HDR …
Cas9 has become a popular method for genome editing in several organisms. Most HDR …
Easi-CRISPR for creating knock-in and conditional knockout mouse models using long ssDNA donors
H Miura, RM Quadros, CB Gurumurthy, M Ohtsuka - Nature protocols, 2018 - nature.com
CRISPR/Cas9-based genome editing can easily generate knockout mouse models by
disrupting the gene sequence, but its efficiency for creating models that require either …
disrupting the gene sequence, but its efficiency for creating models that require either …
Cathepsin G inhibition by Serpinb1 and Serpinb6 prevents programmed necrosis in neutrophils and monocytes and reduces GSDMD-driven inflammation
Neutrophil granule serine proteases contribute to immune responses through cleavage of
microbial toxins and structural proteins. They induce tissue damage and modulate …
microbial toxins and structural proteins. They induce tissue damage and modulate …
Synaptic pruning through glial synapse engulfment upon motor learning
YM Morizawa, M Matsumoto, Y Nakashima… - Nature …, 2022 - nature.com
Synaptic pruning is a fundamental process of neuronal circuit refinement in learning and
memory. Accumulating evidence suggests that glia participates in sculpting the neuronal …
memory. Accumulating evidence suggests that glia participates in sculpting the neuronal …
Site-directed mutagenesis in Petunia × hybrida protoplast system using direct delivery of purified recombinant Cas9 ribonucleoproteins
S Subburaj, SJ Chung, C Lee, SM Ryu, DH Kim… - Plant cell reports, 2016 - Springer
Key message Site-directed mutagenesis of nitrate reductase genes using direct delivery of
purified Cas9 protein preassembled with guide RNA produces mutations efficiently in …
purified Cas9 protein preassembled with guide RNA produces mutations efficiently in …
[HTML][HTML] Electroporation of Cas9 protein/sgRNA into early pronuclear zygotes generates non-mosaic mutants in the mouse
M Hashimoto, Y Yamashita, T Takemoto - Developmental biology, 2016 - Elsevier
The CRISPR/Cas9 system is a powerful tool for elucidating the roles of genes in a wide
variety of organisms including mice. To obtain genetically modified embryos or mice by this …
variety of organisms including mice. To obtain genetically modified embryos or mice by this …