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Systemic delivery of antagomirs during blood-brain barrier disruption is disease-modifying in experimental epilepsy
Oligonucleotide therapies offer precision treatments for a variety of neurological diseases, including epilepsy, but their deployment is hampered by the blood-brain barrier (BBB). Previous studies showed that intracerebroventricular injection of an antisense oligonucleotide (antagomir) targeting mic...
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| Vydáno v: | Mol Ther |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society of Gene & Cell Therapy
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8178478/ https://ncbi.nlm.nih.gov/pubmed/33609732 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymthe.2021.02.021 |
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