The RNA-binding protein FUS/TLS is a common aggregate-interacting protein in polyglutamine diseases
Author:
Publisher
Elsevier BV
Subject
General Medicine,General Neuroscience
Reference10 articles.
1. Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma;Crozat;Nature,1993
2. Identification of ubiquitin-interacting proteins in purified polyglutamine aggregates;Doi;FEBS Lett.,2004
3. RNA-binding protein TLS is a major nuclear aggregate-interacting protein in huntingtin exon 1 with expanded polyglutamine-expressing cells;Doi;J. Biol. Chem.,2008
4. The RNA binding protein TLS is translocated to dendritic spines by mGluR5 activation and regulates spine morphology;Fujii;Curr. Biol.,2005
5. Cross-seeding fibrillation of Q/N-rich proteins offers new pathomechanism of polyglutamine diseases;Furukawa;J. Neurosci.,2009
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1. TDP43 and huntingtin Exon-1 undergo a conformationally specific interaction that strongly alters the fibril formation of both proteins;Journal of Biological Chemistry;2024-09
2. From the disruption of RNA metabolism to the targeting of RNA‐binding proteins: The case of polyglutamine spinocerebellar ataxias;Journal of Neurochemistry;2023-11-22
3. Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations;Disease Models & Mechanisms;2023-10-01
4. Mutant FUS induces chromatin reorganization in the hippocampus and alters memory processes;Progress in Neurobiology;2023-08
5. RNA binding proteins in senescence: A potential common linker for age-related diseases?;Ageing Research Reviews;2023-07
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