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PLoS ONE, ISSN 1932-6203, 03/2015, Volume 10, Issue 3, p. e0121089
The involvement of the ubiquitin-proteasome system (UPS) in the course of various age-associated neurodegenerative diseases is well established. The single... 
SPINOCEREBELLAR ATAXIA TYPE-2 | DROSOPHILA HOMOLOG | PROTEIN | GENE | RNA | MULTIDISCIPLINARY SCIENCES | SCA2 | F-BOX | INTRANUCLEAR INCLUSIONS | LENGTH POLYGLUTAMINE EXPANSIONS | TRINUCLEOTIDE REPEAT | Up-Regulation | Humans | Middle Aged | Male | Ataxin-2 - genetics | Young Adult | F-Box Proteins - blood | Peptides - metabolism | Ataxin-2 - metabolism | Proteolysis | Adult | Female | Fibroblasts - metabolism | F-Box Proteins - metabolism | Cerebellum - metabolism | F-Box Proteins - chemistry | Gene Expression Regulation | Solubility | Ubiquitin-Protein Ligases - metabolism | Spinocerebellar Ataxias - blood | Spinocerebellar Ataxias - pathology | Ubiquitin-Protein Ligases - chemistry | Gene Knock-In Techniques | Protein Transport | Animals | Aged | Mice | HeLa Cells | Ubiquitin-Protein Ligases - genetics | F-Box Proteins - genetics | Ubiquitin | Amyotrophic lateral sclerosis | Nervous system diseases | Ligases | Cerebellum | Huntingtons disease | Neurosciences | Parkinson's disease | Transcription | Laboratories | Biochemistry | Blood | Medical schools | Degradation | Proteins | Motor neuron diseases | Neurodegeneration | Spinocerebellar ataxia | Animal tissues | Fibroblasts | Ataxia | Physiology | Levodopa | Localization | Trinucleotide repeat diseases | Ubiquitin-protein ligase | Age | Movement disorders | Polyglutamine | Neurodegenerative diseases | Neurons | Neurological diseases | Studies | Neurology | DNA microarrays | Proteasomes | Skin | Diabetes | Mutation | Molecular biology
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by Mathew, N.R and Baumgartner, F and Braun, L and O'Sullivan, D and Thomas, S and Waterhouse, M and Muller, T.A and Hanke, K and Taromi, S and Apostolova, P and Illert, A.L and Melchinger, W and Duquesne, S and Schmitt-Graeff, A and Osswald, L and Yan, K.L and Weber, A and Tugues, S and Spath, S and Pfeifer, D and Follo, M and Claus, R and Lubbert, M and Rummelt, C and Bertz, H and Wasch, R and Haag, J and Schmidts, A and Schultheiss, M and Bettinger, D and Thimme, R and Ullrich, E and Tanriver, Y and Vuong, G.L and Arnold, R and Hemmati, P and Wolf, D and Ditschkowski, M and Jilg, C and Wilhelm, K and Leiber, C and Gerull, S and Halter, J and Lengerke, C and Pabst, T and Schroeder, T and Kobbe, G and Rosler, W and Doostkam, S and Meckel, S and Stabla, K and Metzelder, S.K and Halbach, S and Brummer, T and Hu, Z and Dengjel, J and Hackanson, B and Schmid, C and Holtick, U and Scheid, C and Spyridonidis, A and Stolzel, F and Ordemann, R and Muller, L.P and Sicre-de-Fontbrune, F and Ihorst, G and Kuball, J and Ehlert, J.E and Feger, D and Wagner, E.M and Cahn, J.Y and Schnell, J and Kuchenbauer, F and Bunjes, D and Chakraverty, R and Richardson, S and Gill, S and Kroger, N and Ayuk, F and Vago, L and Ciceri, F and Muller, A.M and Kondo, T and Teshima, T and Klaeger, S and Kuster, B and Kim, D.D.H and Weisdorf, D and Velden, W.J. van der and Dorfel, D and Bethge, W and Hilgendorf, I and Hochhaus, A and Anieux, G and Borries, M and Busch, H and Magenau, J and Reddy, P and Labopin, M and Antin, J.H., et al
Nature Medicine, ISSN 1078-8956, 2018, Volume 24, Issue 3, pp. 282 - 291
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The American Journal of Human Genetics, ISSN 0002-9297, 06/2012, Volume 90, Issue 6, pp. 1014 - 1027
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New York Times, ISSN 0362-4331, 01/2009
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