Sulfated glycosaminoglycans in protein aggregation diseases

Protein aggregation diseases are characterized by intracellular or extracellular deposition of misfolded and aggregated proteins. These aggregated deposits contain multiple proteinaceous and non-protein components that are thought to play critical roles in the etiology and pathogenesis of protein ag...

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Veröffentlicht in:	Glycoconjugate journal 2017-08, Vol.34 (4), p.453-466
Hauptverfasser:	Nishitsuji, Kazuchika, Uchimura, Kenji
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Biochemistry Biomedical and Life Sciences Cell Communication Chemical Sciences Chondroitin sulfate Deposits Disease Diseases Etiology Glycosaminoglycans Glycosaminoglycans - metabolism Heparan sulfate Humans Keratan sulfate Life Sciences Ligands or physical chemistry Pathogenesis Pathology Protein Aggregates Protein Aggregation, Pathological - metabolism Protein folding Protein interaction Proteins Review Sulfates Sulfates - metabolism Sulfation Theoretical and Tissues
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