Molecular Insights into Proteinopathies: Increased Scope from Neurodegeneration to other Pathologies of the Brain
Editat de Eva Žerovnik, Robert Layfielden Limba Engleză Paperback – aug 2026
- Investigates proteostasis dysfunction across a range of proteinopathies including Alzheimer's disease and Parkinson’s disease
- Considers biophysical techniques, molecular dynamics and machine learning to study molecular mechanisms
- Explores small molecules as modulators of the key processes in proteinopathies
- Provides a basis for further study on potential therapeutic intervention to treat proteinopathies
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Specificații
ISBN-13: 9780443341762
ISBN-10: 0443341761
Pagini: 350
Dimensiuni: 191 x 235 mm
Greutate: 0.45 kg
Editura: ELSEVIER SCIENCE
ISBN-10: 0443341761
Pagini: 350
Dimensiuni: 191 x 235 mm
Greutate: 0.45 kg
Editura: ELSEVIER SCIENCE
Cuprins
Part 1. Protein aggregation in different proteinopathies
1. Amyloid-pore hypothesis: prefibrillar oligomers interaction with membranes; a generic cause of neurodegeneration?
2. In vivo molecular brain imaging of metabolic (dys)function and protein accumulation in neurodegenerative disease
3. Amyotrophic lateral sclerosis: Relevance of protein aggregation of TDP-43 and mechanisms of toxicity
4. Cystatin C amyloid angiopathy (CAA) and AD: Interaction of cystatins oligomers with A-beta
5. Protein aggregation and disturbed proteostasis in mental illness, stress on shizophrenia
6. Protein aggregation in progressive myoclonus epilepsies, in particular EPM1
7. Model amyloid proteins: What are the lessons to understand proteinopathies
Part 2. Common signaling pathways and biomarkers of disease
8. The integrated stress response: from mechanism to disease
9. Comparison of AD and schizophrenia: From signaling to biomarkers
10. Oxidative stress and mitochondrial decline in common to several proteinopathies
11. Irisin reduces amyloid-b by inducing the release of neprilysin from astrocytes following down regulation of ERK-STAT3 signaling
12. Dysregulated molecular pathways in amyotrophic lateral sclerosis–frontotemporal dementia spectrum disorder
Part 3. Small molecules as modulators of the key processes in proteinopathies
13. Trem2 signaling modulators to treat neurodegenerative disease
14. Small molecules modulators of protein aggregation and toxicity: antioxidants and polyphenol compounds
15. Therapeutic Strategies to Mitigate the Toxicity of α-Synuclein Oligomers in Parkinson's Disease
16. Repurposed drugs that modulate proteinopathies
17. Future of metal chelators in AD therapy
18. Novel dual-acting hybrids targeting type-2 cannabinoid receptors and cholinesterase activity show neuroprotective effects in vitro and amelioration of cognitive impairment in vivo
19. Role of autophagy in neurodegeneration and aging; small molecule modulators
20. NEW treatments on the horizon for Alzheimer’s and other neurodegenerative diseases
Part 4. Modern biophysical methods, molecular dynamics and machine learning
21. Intrinsically unfolded proteins and the role of protein condensation
22. A-beta: Structure and interaction with membranes as revealed by NMR
23. Oligomers formation by amyloid beta as studied by coarse-grain MD
24. Machine learning in prediction of protein aggregation and/or condensation states
1. Amyloid-pore hypothesis: prefibrillar oligomers interaction with membranes; a generic cause of neurodegeneration?
2. In vivo molecular brain imaging of metabolic (dys)function and protein accumulation in neurodegenerative disease
3. Amyotrophic lateral sclerosis: Relevance of protein aggregation of TDP-43 and mechanisms of toxicity
4. Cystatin C amyloid angiopathy (CAA) and AD: Interaction of cystatins oligomers with A-beta
5. Protein aggregation and disturbed proteostasis in mental illness, stress on shizophrenia
6. Protein aggregation in progressive myoclonus epilepsies, in particular EPM1
7. Model amyloid proteins: What are the lessons to understand proteinopathies
Part 2. Common signaling pathways and biomarkers of disease
8. The integrated stress response: from mechanism to disease
9. Comparison of AD and schizophrenia: From signaling to biomarkers
10. Oxidative stress and mitochondrial decline in common to several proteinopathies
11. Irisin reduces amyloid-b by inducing the release of neprilysin from astrocytes following down regulation of ERK-STAT3 signaling
12. Dysregulated molecular pathways in amyotrophic lateral sclerosis–frontotemporal dementia spectrum disorder
Part 3. Small molecules as modulators of the key processes in proteinopathies
13. Trem2 signaling modulators to treat neurodegenerative disease
14. Small molecules modulators of protein aggregation and toxicity: antioxidants and polyphenol compounds
15. Therapeutic Strategies to Mitigate the Toxicity of α-Synuclein Oligomers in Parkinson's Disease
16. Repurposed drugs that modulate proteinopathies
17. Future of metal chelators in AD therapy
18. Novel dual-acting hybrids targeting type-2 cannabinoid receptors and cholinesterase activity show neuroprotective effects in vitro and amelioration of cognitive impairment in vivo
19. Role of autophagy in neurodegeneration and aging; small molecule modulators
20. NEW treatments on the horizon for Alzheimer’s and other neurodegenerative diseases
Part 4. Modern biophysical methods, molecular dynamics and machine learning
21. Intrinsically unfolded proteins and the role of protein condensation
22. A-beta: Structure and interaction with membranes as revealed by NMR
23. Oligomers formation by amyloid beta as studied by coarse-grain MD
24. Machine learning in prediction of protein aggregation and/or condensation states