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Table of Contents
Part I: Maintaining proteostasis; 1: Structural allostery and protein-protein interactions of Sin3
2: Protein post-translational modifications: role in protein structure, function and stability
3: Small molecule osmolytes can modulate proteostasis
Part II: Proteopathy: failure of proteostasis; 4: Protein folding and aggregation: a revisit of basic conception
5: Protein folding: from normal cellular function to pathophysiology
6: Protein misfolding diseases: in perspective of gain and loss of function
7: Protein misfolding and amyloid formation in alzheimer's disease
Part III: Chaperone surveillance of proteopathy; 8: Proteopathies: biological, molecular and clinical perspectives
9: Pharmacological chaperones in protein aggregation disorders.
2: Protein post-translational modifications: role in protein structure, function and stability
3: Small molecule osmolytes can modulate proteostasis
Part II: Proteopathy: failure of proteostasis; 4: Protein folding and aggregation: a revisit of basic conception
5: Protein folding: from normal cellular function to pathophysiology
6: Protein misfolding diseases: in perspective of gain and loss of function
7: Protein misfolding and amyloid formation in alzheimer's disease
Part III: Chaperone surveillance of proteopathy; 8: Proteopathies: biological, molecular and clinical perspectives
9: Pharmacological chaperones in protein aggregation disorders.