Rossen Donev
Molecular Chaperones in Human Disorders
Gebonden Engels 2019 9780128155578Levertijd ongeveer 9 werkdagen
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Samenvatting
Molecular Chaperones in Human Disorders, Volume 114 in the Advances in Protein Chemistry and Structural Biology series, provides an overview of current developments in mechanisms underlying DNA repair and their involvement in maintaining chromatin repair, the balance between chromosomal repair pathways, tumorigenesis, immune signaling and infection-induced inflammation. Chapters in this new release cover Functional principles and regulation of molecular chaperones, Chaperones and retinal disorders, Protein misfolding and degradation in genetic diseases, Chaperone dysfunction in hereditary myopathic diseases, Diseases caused by functional disorder of molecular chaperones residing in the endoplasmic reticulum, and many other timely topics.
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Inhoudsopgave
1. Functional principles and regulation of molecular chaperones
Johannes Buchner
2. Chaperones and retinal disorders
Nikolai O. Artemyev
3. Protein misfolding and degradation in genetic diseases
Rasmus Hartmann-Petersen
4. Chaperone dysfunction in hereditary myopathic diseases
Andreas Roos
5. Diseases caused by functional disorder of molecular chaperones residing in the endoplasmic reticulum
Masafumi Sakono
6. Structural and functional insights on the roles of molecular chaperones in the mistargeting and aggregation phenotypes associated with primary hyperoxaluria type I
Angel Luis Pey
7. Inflammatory response and its relation to sphingolipid metabolism proteins: Targeting inflammation with molecular chaperones
Elif Ozkirimli
8. When safeguarding goes wrong: impact of oxidative stress on proteins homeostasis in health and neurodegenerative disorders
Dana Reichmann
9. Computational approach to unravel the misfolding mechanism of Glucosylceramidase mutations in Gaucher Disease
George Priya Doss P. C
10. Cytosolic quality control proteins, SGTA and the Bag6 complex, in disease
Rivka L. Isaacson
Johannes Buchner
2. Chaperones and retinal disorders
Nikolai O. Artemyev
3. Protein misfolding and degradation in genetic diseases
Rasmus Hartmann-Petersen
4. Chaperone dysfunction in hereditary myopathic diseases
Andreas Roos
5. Diseases caused by functional disorder of molecular chaperones residing in the endoplasmic reticulum
Masafumi Sakono
6. Structural and functional insights on the roles of molecular chaperones in the mistargeting and aggregation phenotypes associated with primary hyperoxaluria type I
Angel Luis Pey
7. Inflammatory response and its relation to sphingolipid metabolism proteins: Targeting inflammation with molecular chaperones
Elif Ozkirimli
8. When safeguarding goes wrong: impact of oxidative stress on proteins homeostasis in health and neurodegenerative disorders
Dana Reichmann
9. Computational approach to unravel the misfolding mechanism of Glucosylceramidase mutations in Gaucher Disease
George Priya Doss P. C
10. Cytosolic quality control proteins, SGTA and the Bag6 complex, in disease
Rivka L. Isaacson
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