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Protein misfolding and aggregation A defining feature of many NDDs is the accumulation of misfolded, aggregation-prone proteins (A and tau in AD, -synuclein in PD, SOD1/TDP-43 in ALS, etc.) [53]

In over 90% of individuals with cEDS a dominant pathogenic variant in either COL5A1 or COL5A2 is identified

DSIP is a peptide studied in controlled research environments as a model compound in investigations involving peptide structure, signalling pathways, and experimental biological systems

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