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In vivo cell-autonomous transcriptional abnormalities revealed in mice expressing mutant huntingtin in striatal but not cortical neurons

Huntington's disease (HD), caused by a CAG repeat expansion in the huntingtin (HTT) gene, is characterized by abnormal protein aggregates and motor and cognitive dysfunction. Htt protein is ubiquitously expressed, but the striatal medium spiny neuron (MSN) is most susceptible to dysfunction and...

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Bibliografiset tiedot
Päätekijät: Thomas, Elizabeth A., Coppola, Giovanni, Tang, Bin, Kuhn, Alexandre, Kim, SoongHo, Geschwind, Daniel H., Brown, Timothy B., Luthi-Carter, Ruth, Ehrlich, Michelle E.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2011
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3043657/
https://ncbi.nlm.nih.gov/pubmed/21177255
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq548
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