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03493nam a22003495i 4500 |
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978-0-387-25919-2 |
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20191029032517.0 |
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cr nn 008mamaa |
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100301s2006 xxu| s |||| 0|eng d |
| 020 |
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|a 9780387259192
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| 024 |
7 |
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|a 10.1007/b136464
|2 doi
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| 040 |
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|a Sistema de Bibliotecas del Tecnológico de Costa Rica
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| 245 |
1 |
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|a Protein Misfolding, Aggregation and Conformational Diseases
|b Part A: Protein Aggregation and Conformational Diseases /
|c edited by Vladimir N. Uversky, Anthony Fink.
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| 250 |
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|a 1st ed. 2006.
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| 260 |
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|a New York, NY :
|b Springer US :
|b Imprint: Springer,
|c 2006.
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| 300 |
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|a XVIII, 420 p. 104 illus., 46 illus. in color.
|b online resource.
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| 336 |
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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| 490 |
1 |
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|a Protein Reviews ;
|v 4
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| 505 |
0 |
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|a Structural and Conformational Prerequisites of Amyloidogenesis -- Structural and Conformational Prerequisites of Amyloidogenesis -- The Generic Nature of Protein Folding and Misfolding -- The Generic Nature of Protein Folding and Misfolding -- Relative Importance of Hydrophobicity, Net Charge, and Secondary Structure Propensities in Protein Aggregation -- Relative Importance of Hydrophobicity, Net Charge, and Secondary Structure Propensities in Protein Aggregation -- Cytotoxic Intermediates in the Fibrillation Pathway: A? Oligomers in Alzheimer's Disease as a Case Study -- Cytotoxic Intermediates in the Fibrillation Pathway: A? Oligomers in Alzheimer's Disease as a Case Study -- Glycosaminoglycans, Proteoglycans, and Conformational Disorders -- Glycosaminoglycans, Proteoglycans, and Conformational Disorders -- Apolipoproteins in Different Amyloidoses -- Apolipoproteins in Different Amyloidoses -- Oxidative Stress and Protein Deposition Diseases -- Oxidative Stress and Protein Deposition Diseases -- Chaperone and Conformational Disorders -- Chaperone Suppression of Aggregated Protein Toxicity -- Mechanisms of Active Solubilization of Stable Protein Aggregates by Molecular Chaperones -- The Aggresome: Proteasomes, Inclusion Bodies, and Protein Aggregation -- The Aggresome: Proteasomes, Inclusion Bodies, and Protein Aggregation -- Protein Aggregation, Ion Channel Formation, and Membrane Damage -- Protein Aggregation, Ion Channel Formation, and Membrane Damage -- Visualization of Protein Deposits In Vivo -- Congo Red Staining of Amyloid: Improvements and Practical Guide for a More Precise Diagnosis of Amyloid and the Different Amyloidoses -- Immunohistological Study of Experimental Murine AA Amyloidosis -- Visualization of Protein Deposits In Vitro -- Reporters of Amyloid Structure -- Three-Dimensional Structural Analysis of Amyloid Fibrils by Electron Microscopy -- Atomic Force Microscopy -- Direct Observation of Amyloid Fibril Growth Monitored by Total Internal Reflection Fluorescence Microscopy -- Animal and Cell Models of Human Neurodegenerative Disorders -- Drosophila and C. elegans Models of Human Age-Associated Neurodegenerative Diseases -- Genetically Engineered Mouse Models of Neurodegenerative Disorders.
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| 650 |
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0 |
|a Life sciences.
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| 650 |
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0 |
|a Immunology.
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| 650 |
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0 |
|a Cell biology.
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| 650 |
1 |
4 |
|a Life Sciences, general.
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| 650 |
2 |
4 |
|a Immunology.
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| 650 |
2 |
4 |
|a Cell Biology.
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| 700 |
1 |
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|a Uversky, Vladimir N.
|e editor.
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| 700 |
1 |
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|a Fink, Anthony.
|e editor.
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| 710 |
2 |
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|a SpringerLink (Online service)
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| 773 |
0 |
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|t Springer eBooks
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| 856 |
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|u https://doi.org/10.1007/b136464
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