Works matching AU BETT, John S.
Results: 9
Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington's disease mice: exclusion of proteasome activator REGγ as a therapeutic target.
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- Human Molecular Genetics, 2006, v. 15, n. 4, p. 665, doi. 10.1093/hmg/ddi488
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- Article
Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington’s disease mice: exclusion of proteasome activator REGγ as a therapeutic target.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 33, doi. 10.1093/hmg/ddi423
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- Article
The polyubiquitin Ubc gene modulates histone H2A monoubiquitylation in the R6/2 mouse model of Huntington's disease.
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- Journal of Cellular & Molecular Medicine, 2009, v. 13, n. 8b, p. 2645, doi. 10.1111/j.1582-4934.2008.00543.x
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- Article
Ubiquitin C-terminal hydrolases cleave isopeptide- and peptide-linked ubiquitin from structured proteins but do not edit ubiquitin homopolymers.
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- Biochemical Journal, 2015, v. 466, n. 3, p. 489, doi. 10.1042/BJ20141349
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The P-body component USP52/PAN2 is a novel regulator of HIF1A mRNA stability.
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- Biochemical Journal, 2013, v. 451, n. 2, p. 185, doi. 10.1042/BJ20130026
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- Article
Proteostasis regulation by the ubiquitin system.
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- Essays in Biochemistry, 2016, v. 60, n. 2, p. 143, doi. 10.1042/EBC20160001
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The Inherited Blindness Protein AIPL1 Regulates the Ubiquitin-Like FAT10 Pathway.
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- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0030866
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- Article
The Ubiquitin-Proteasome Reporter GFPu Does Not Accumulate in Neurons of the R6/2 Transgenic Mouse Model of Huntington's Disease.
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- PLoS ONE, 2009, v. 4, n. 4, p. 1, doi. 10.1371/journal.pone.0005128
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- Article
Suppression of protein aggregation by chaperone modification of high molecular weight complexes.
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- Brain: A Journal of Neurology, 2012, v. 135, n. 4, p. 1180, doi. 10.1093/brain/aws022
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- Article