Related references
Note: Only part of the references are listed.The fellowship of the RING: The RING-B-box linker region interacts with the RING in TRIM21/Ro52, contains a native autoantigenic epitope in Sjogren syndrome, conserved region and is an integral and in TRIM proteins
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Alterations in the solubility and intracellular localization of parkin by several familial Parkinson's disease-linked point mutations
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Parkin mediates nonclassical, proteasomal-independent ubiquitination of synphilin-1: Implications for Lewy body formation
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Parkin increases dopamine uptake by enhancing the cell surface expression of dopamine transporter
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Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology
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S-nitrosylation of Parkin regulates ubiquitination and compromises Parkin's protective function
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Parkin-associated Parkinson's disease
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How much phenotypic variation can be attributed to parkin genotype?
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Parkin facilitates the elimination of expanded polyglutamine proteins and leads to preservation of proteasome function
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A potential proteasome-interacting motif within the ubiquitin-like domain of parkin and other proteins
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Parkin mutations are frequent in patients with isolated early-onset parkinsonism
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Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease
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NMR structure of ubiquitin-like domain in PARKIN: Gene product of familial Parkinson's disease
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Parkin suppresses unfolded protein stress-induced cell death through its E3 ubiquitin-protein ligase activity
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Association between early-onset Parkinson's disease and mutations in the parkin gene
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