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pmid: 28643256
Gene-modified monkey models would be particularly valuable in biomedical and neuroscience research. Virus-based transgenic and programmable nucleases-based site-specific gene editing methods (TALEN, CRISPR-cas9) enable the generation of gene-modified monkeys with gain or loss of function of specific genes. Here, we describe the generation of transgenic and knock-out (KO) monkeys with high efficiency by lentivirus and programmable nucleases.
Animals, Genetically Modified, Gene Editing, Gene Knockout Techniques, Animals, Female, Haplorhini, Sperm Injections, Intracytoplasmic, CRISPR-Cas Systems, Endonucleases
Animals, Genetically Modified, Gene Editing, Gene Knockout Techniques, Animals, Female, Haplorhini, Sperm Injections, Intracytoplasmic, CRISPR-Cas Systems, Endonucleases
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 2 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |