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A huntingtin knock-in pig model recapitulates features of selective neurodegeneration in Huntington’s disease
Huntington’s disease (HD) is characterized by the preferential loss of the medium spiny neurons in the striatum. Using CRISPR-Cas9 and somatic nuclear transfer technology, we established a knock-in (KI) pig model of HD that endogenously expresses full-length mutant huntingtin (HTT). By breeding this...
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| Pubblicato in: | Cell |
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| Autori principali: | , , , , , , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5935586/ https://ncbi.nlm.nih.gov/pubmed/29606351 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2018.03.005 |
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