Protein Misfolding in Neurodegenerative Diseases
Autor Neha Gogia, Sandeep Kumar Singh, Vidyadhara Devarunda Jaganathen Limba Engleză Paperback – mar 2025
- Discusses underlying cellular and molecular mechanisms altered in protein-associated neurodegenerative disorders
- Describes methods for detection and analysis of protein aggregates
- Features advancements in therapeutics and emerging techniques to treat these disorders
- Covers implications in a variety of neurodegenerative diseases, including Alzheimer's, Parkinson’s, ALS, Creutzfeldt-Jakob disease, Cystic fibrosis, Gaucher's disease, and Polyglutamine diseases, including Huntington’s and other related proteinopathies
Preț: 867.74 lei
Preț vechi: 1126.93 lei
-23% Nou
Puncte Express: 1302
Preț estimativ în valută:
166.08€ • 172.71$ • 138.97£
166.08€ • 172.71$ • 138.97£
Carte nepublicată încă
Doresc să fiu notificat când acest titlu va fi disponibil:
Se trimite...
Preluare comenzi: 021 569.72.76
Specificații
ISBN-13: 9780443187162
ISBN-10: 0443187169
Pagini: 300
Dimensiuni: 152 x 229 mm
Editura: ELSEVIER SCIENCE
ISBN-10: 0443187169
Pagini: 300
Dimensiuni: 152 x 229 mm
Editura: ELSEVIER SCIENCE
Cuprins
1. Maintenance of balanced proteome homeostasis
2. Determinants of protein misfolding, aggregation in neuronal cell death
3. Classification, structure, and function of protein aggregates in proteinopathies
4. Protein aggregation and cellular and molecular mechanisms in neurodegenerative disease
5. Advances in methods to detect and study protein aggregation
6. Organelle specific protein quality control
7. Molecular chaperones and co-chaperones in proteostasis
8. The ubiquitin-Proteasome System (UPS) and Autophagy lysosomal proteolytic pathways
9. Alterations in protein quality control
10. Alternate mechanisms to maintain proteome homeostasis
11. Advances in developing novel therapeutics, strategies, approaches and use of emerging techniques
12. Challenges in translating laboratory findings to drug development
13. Advancements in drug delivery technologies for protein misfolding diseases
2. Determinants of protein misfolding, aggregation in neuronal cell death
3. Classification, structure, and function of protein aggregates in proteinopathies
4. Protein aggregation and cellular and molecular mechanisms in neurodegenerative disease
5. Advances in methods to detect and study protein aggregation
6. Organelle specific protein quality control
7. Molecular chaperones and co-chaperones in proteostasis
8. The ubiquitin-Proteasome System (UPS) and Autophagy lysosomal proteolytic pathways
9. Alterations in protein quality control
10. Alternate mechanisms to maintain proteome homeostasis
11. Advances in developing novel therapeutics, strategies, approaches and use of emerging techniques
12. Challenges in translating laboratory findings to drug development
13. Advancements in drug delivery technologies for protein misfolding diseases