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Brain microvascular endothelial cell dysfunction in an isogenic juvenile iPSC model of Huntington’s disease
Huntington’s disease (HD) is an inherited neurodegenerative disease caused by expansion of cytosine–adenine–guanine (CAG) repeats in the huntingtin gene, which leads to neuronal loss and decline in cognitive and motor function. Increasing evidence suggests that blood–brain barrier (BBB) dysfunction...
Autores principales: | Linville, Raleigh M., Nerenberg, Renée F., Grifno, Gabrielle, Arevalo, Diego, Guo, Zhaobin, Searson, Peter C. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245306/ https://www.ncbi.nlm.nih.gov/pubmed/35773691 http://dx.doi.org/10.1186/s12987-022-00347-7 |
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