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Recent advances in the molecular basis of Lafora’s progressive myoclonus epilepsy.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 1, p. 1, doi. 10.1007/s10038-005-0321-1
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- Article
Correction to: Interdependence of laforin and malin proteins for their stability and functions could underlie the molecular basis of locus heterogeneity in Lafora disease.
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- 2018
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- Correction Notice
Interdependence of laforin and malin proteins for their stability and functions could underlie the molecular basis of locus heterogeneity in Lafora disease.
- Published in:
- Journal of Biosciences, 2015, v. 40, n. 5, p. 863, doi. 10.1007/s12038-015-9570-0
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- Article
The malin–laforin complex suppresses the cellular toxicity of misfolded proteins by promoting their degradation through the ubiquitin–proteasome system.
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- Human Molecular Genetics, 2009, v. 18, n. 4, p. 688, doi. 10.1093/hmg/ddn398
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- Article
Lafora disease proteins malin and laforin are recruited to aggresomes in response to proteasomal impairment.
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- Human Molecular Genetics, 2007, v. 16, n. 7, p. 753, doi. 10.1093/hmg/ddm006
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- Article
A Feed-Forward Circuit of Endogenous PGC-1α and Estrogen Related Receptor α Regulates the Neuronal Electron Transport Chain.
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- Parkinson's Disease (20420080), 2016, p. 1, doi. 10.1155/2016/2405176
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- Article
NF-kappaB Signaling Pathways in Neurological Inflammation: A Mini Review.
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- Frontiers in Molecular Neuroscience, 2015, p. 1, doi. 10.3389/fnmol.2015.00077
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- Article