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Developing gene therapy for use in the central nervous system has been hampered by the lack of an efficient vector for gene delivery. We report an adeno-associated virus vector with an
enhanced ability to cross the blood–brain barrier in both rodents and non-human primates, and use it to develop systemic anti-tumour gene therapies for glioblastoma. Access through your
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calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our FAQs * Contact customer support REFERENCES * Mendell, J. R. et al.
Single-dose gene-replacement therapy for spinal muscular atrophy. _N. Engl. J. Med._ 377, 1713–1722 (2017). AN ARTICLE THAT PRESENTS THE FIRST CLINICAL SUCCESS OF AAV9-MEDIATED GENE THERAPY.
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transgene expression and decreased liver targeting after intravenous delivery in mouse and marmoset. _Nat. Neurosci._ 25, 106–115 (2021). USING A DIRECTED REVOLUTION SCREENING METHOD, THIS
ARTICLE IDENTIFIES AAV CAPSIDS THAT PENETRATE THE BBB IN MICE AND MARMOSETS. Article PubMed Google Scholar Download references ADDITIONAL INFORMATION PUBLISHER’S NOTE Springer Nature
remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. THIS IS A SUMMARY OF: Yao, Y. et al. Variants of the adeno-associated virus serotype 9
with enhanced penetration of the blood–brain barrier in rodents and primates. _Nat. Biomed. Eng_. https://doi.org/10.1038/s41551-022-00938-7 (2022). RIGHTS AND PERMISSIONS Reprints and
permissions ABOUT THIS ARTICLE CITE THIS ARTICLE An adeno-associated virus vector penetrates the blood–brain barrier in non-human primates. _Nat. Biomed. Eng_ 6, 1201–1202 (2022).
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