Huntington’s Chorea—a Rare Neurodegenerative Autosomal Dominant Disease: Insight into Molecular Genetics, Prognosis and Diagnosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Applied Microbiology and Biotechnology,Biochemistry,General Medicine,Bioengineering,Biotechnology
Link
https://link.springer.com/content/pdf/10.1007/s12010-021-03523-x.pdf
Reference82 articles.
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2. Bae, B. I., Xu, H., Igarashi, S., Fujimuro, M., Agrawal, N., Taya, Y., et al. (2005). p53 mediates cellular dysfunction and behavioral abnormalities in Huntington’s disease. Neuron, 47(1), 29–41. https://doi.org/10.1016/j.neuron.2005.06.005.
3. Ghose, J., Sinha, M., Das, E., Jana, N. R., & Bhattacharyya, N. P. (2011). Regulation of miR-146a by RelA/NFkB and p53 in STHdhQ111/HdhQ111 cells, a cell model of Huntington’s disease. PloS ONE, 6(8), e23837. https://doi.org/10.1371/journal.pone.0023837.
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5. Gingras, A. C., Gygi, S. P., Raught, B., Polakiewicz, R. D., Abraham, R. T., Hoekstra, M. F., Aebersold, R., & Sonenberg, N. (1999). Regulation of 4E-BP1 phosphorylation: a novel two-step mechanism. Genes & development, 13(11), 1422–1437.
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