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Cre-dependent selection yields AAV variants for widespread gene transfer to the adult brain

TL;DR: This work uses Cre recombination–based AAV targeted evolution (CREATE) to generate AAV variants that efficiently and widely transduce the adult mouse central nervous system (CNS) after intravenous injection and demonstrates the potential of CREATE to produce customized AAV vectors for biomedical applications.
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Ischemic stroke: experimental models and reality

TL;DR: The two models mimicking human stroke most closely are various embolic stroke models and spontaneous stroke models, which more closely mimics the therapeutic situation of mechanical thrombectomy which is expected to be increasingly applied to stroke patients.
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A comprehensive transcriptional map of primate brain development

Trygve E. Bakken, +98 more
- 21 Jul 2016 - 
TL;DR: A high-resolution transcriptional atlas of rhesus monkey (Macaca mulatta) brain development is described that combines dense temporal sampling of prenatal and postnatal periods with fine anatomical division of cortical and subcortical regions associated with human neuropsychiatric disease.
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Spatiotemporal transcriptomic divergence across human and macaque brain development.

TL;DR: This study provides insights into the evolution of gene expression in the developing human brain and may shed some light on potentially human-specific underpinnings of certain neuropsychiatric disorders.
References
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Journal ArticleDOI

Neural Mechanisms of Selective Visual Attention

TL;DR: The two basic phenomena that define the problem of visual attention can be illustrated in a simple example and selectivity-the ability to filter out un­ wanted information is illustrated.
Journal ArticleDOI

The new frontier of genome engineering with CRISPR-Cas9

TL;DR: The power of the CRISPR-Cas9 technology to systematically analyze gene functions in mammalian cells, study genomic rearrangements and the progression of cancers or other diseases, and potentially correct genetic mutations responsible for inherited disorders is illustrated.
Journal ArticleDOI

One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering.

TL;DR: The CRISPR/Cas system allows the one-step generation of animals carrying mutations in multiple genes, an approach that will greatly accelerate the in vivo study of functionally redundant genes and of epistatic gene interactions.
Journal ArticleDOI

High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells.

TL;DR: It is found that single and double mismatches are tolerated to varying degrees depending on their position along the guide RNA (gRNA)-DNA interface, and off-target cleavage of CRISPR-associated (Cas)9-based RGNs is characterized.
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