Molecular Chaperones in Human Disorders

<p>1. Functional principles and regulation of molecular chaperones<br>Johannes Buchner<br>2. Chaperones and retinal disorders<br>Nikolai O. Artemyev<br>3. Protein misfolding and degradation in genetic diseases<br>Rasmus Hartmann-Petersen<br>4. Chaperone dysfunction in hereditary myopathic diseases<br>Andreas Roos<br>5. Diseases caused by functional disorder of molecular chaperones residing in the endoplasmic reticulum<br>Masafumi Sakono<br>6. Structural and functional insights on the roles of molecular chaperones in the mistargeting and aggregation phenotypes associated with primary hyperoxaluria type I<br>Angel Luis Pey<br>7. Inflammatory response and its relation to sphingolipid metabolism proteins: Targeting inflammation with molecular chaperones<br>Elif Ozkirimli<br>8. When safeguarding goes wrong: impact of oxidative stress on proteins homeostasis in health and neurodegenerative disorders<br>Dana Reichmann<br>9. Computational approach to unravel the misfolding mechanism of Glucosylceramidase mutations in Gaucher Disease<br>George Priya Doss P. C<br>10. Cytosolic quality control proteins, SGTA and the Bag6 complex, in disease<br>Rivka L. Isaacson</p>