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Loss of Hsp70 Exacerbates Pathogenesis But Not Levels of Fibrillar Aggregates in a Mouse Model of Huntington's Disease.
- Published in:
- Journal of Neuroscience, 2009, v. 29, n. 28, p. 9104, doi. 10.1523/JNEUROSCI.2250-09.2009
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- Article
Functional characterization of endogenous GPR54 mutants.
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- FASEB Journal, 2007, v. 21, n. 5, p. A422, doi. 10.1096/fasebj.21.5.a422-a
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- Article
Green tea (−)-epigallocatechin-gallate modulates early events in huntingtin misfolding and reduces toxicity in Huntington's disease models.
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- Human Molecular Genetics, 2006, v. 15, n. 18, p. 2743, doi. 10.1093/hmg/ddl210
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- Article
Modulation of neurodegeneration by molecular chaperones.
- Published in:
- Nature Reviews Neuroscience, 2005, v. 6, n. 1, p. 11, doi. 10.1038/nrn1587
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- Article
Hsp70 and Hsp40 attenuate formation of spherical and annular polyglutamine oligomers by partitioning monomer.
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- Nature Structural & Molecular Biology, 2004, v. 11, n. 12, p. 1215, doi. 10.1038/nsmb860
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- Article