Alteration in Fluidity of Cell Plasma Membrane in Huntington Disease Revealed by Spectral Phasor Analysis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-19160-0.pdf
Reference54 articles.
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2. Arrasate, M. et al. Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death. Nature. 431, 805–810 (2004).
3. Davies, S. W. et al. Formation of Neuronal Intranuclear Inclusions Underlies the Neurological Dysfunction in Mice Transgenic for the HD Mutation. Cell 90, 537–548, https://doi.org/10.1016/S0092-8674(00)80513-9 (1997).
4. Sameni, S., Adeela Syed, J. L Marsh & Digman, M. A. The phasor-FLIM fingerprints reveal shifts from OXPHOS to enhanced glycolysis in Huntington Disease. Nature scientific reports (2016).
5. Block, R. C., Dorsey, E. R., Beck, C. A., Brenna, J. T. & Shoulson, I. Altered Cholesterol and Fatty Acid Metabolism in Huntington Disease. Journal of clinical lipidology 4, 17–23, https://doi.org/10.1016/j.jacl.2009.11.003 (2010).
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