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In Vitro Differentiation of Human Neural Progenitor Cells Into Striatal GABAergic Neurons
Huntington’s disease (HD) results from a CAG repeat expansion in the gene encoding the huntingtin protein. This inherited disorder is characterized by progressive neurodegeneration. In particular, HD progression involves the loss of striatal projection neurons. The limited availability of reliable s...
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| Pubblicato in: | Stem Cells Transl Med |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
AlphaMed Press
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4479615/ https://ncbi.nlm.nih.gov/pubmed/25972145 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5966/sctm.2014-0083 |
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