Ubiquilin 2: A component of the ubiquitin–proteasome system with an emerging role in neurodegeneration
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Biochemistry
Reference28 articles.
1. Recognition of tandem PxxP motifs as a unique Src homology 3-binding mode triggers pathogen-driven actin assembly;Aitio;Proc Natl Acad Sci USA,2010
2. Pattern of ubiquilin pathology in ALS and FTLD indicates presence of C9ORF72 hexanucleotide expansion;Brettschneider;Acta Neuropathol,2012
3. Ubiquilin-2 (UBQLN2) binds with high affinity to the C-terminal region of TDP-43 and modulates TDP-43 levels in H4 cells: characterization of inhibition by nucleic acids and 4-aminoquinolines;Cassel;Biochim Biophys Acta,2013
4. UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis;Daoud;Neurobiol Aging,2012
5. Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia;Deng;Nature,2011
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2. Wild-type and pathogenic forms of ubiquilin 2 differentially modulate components of the autophagy-lysosome pathways;Journal of Pharmacological Sciences;2023-07
3. Ubiquilin-2 regulates pathological alpha-synuclein;Scientific Reports;2023-01-06
4. Mitochondrial proteotoxicity: implications and ubiquitin-dependent quality control mechanisms;Cellular and Molecular Life Sciences;2022-10-29
5. TDP-43 pathology: From noxious assembly to therapeutic removal;Progress in Neurobiology;2022-04
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