Human extracellular matrices can be edited in their composition using the CRISPR/Cas9 system, leading to materials exhibiting tailored regenerative capacities.
为探究 CRISPR/Cas9 技术编辑利什曼原虫(Leishmania major)UMSBP 基因效果,研究人员开展研究,发现其突变株有潜力,意义重大。
This study achieved CRISPR/Cas9-mediated genome editing in grass carp (Ctenopharyngodon idella), China's most economically vital freshwater fish.
Advances in the gene-editing technology known as CRISPR-Cas9 over the past 15 years have yielded important new insights into ...
The Cas9 protein is the most widely used by scientists. This protein can easily be programmed to find and bind to almost any desired target sequence, simply by giving it a piece of RNA to guide it ...
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News-Medical.Net on MSNTransforming genetic deafness treatment with base editingCongenital hearing loss refers to impaired auditory function that occurs due to genetic causes. GJB2 is the gene responsible ...
In their new work, to find novel programmable systems, the team began by zeroing in on a structural feature of the CRISPR Cas9 protein that binds to the enzyme's RNA guide. That is a key feature ...
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