000 04549nam a22004455i 4500
001 978-0-387-25919-2
003 DE-He213
005 20250710083935.0
007 cr nn 008mamaa
008 100301s2006 xxu| s |||| 0|eng d
020 _a9780387259192
_a99780387259192
024 7 _a10.1007/b136464
_2doi
082 0 4 _a616.079
_223
100 1 _aUversky, Vladimir N.
_eeditor.
245 1 0 _aProtein Misfolding, Aggregation, and Conformational Diseases
_h[recurso electrónico] :
_bPart A: Protein Aggregation and Conformational Diseases /
_cedited by Vladimir N. Uversky, Anthony L. Fink.
264 1 _aBoston, MA :
_bSpringer US,
_c2006.
300 _aXVIII, 419 p.
_bonline resource.
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _arecurso en línea
_bcr
_2rdacarrier
347 _atext file
_bPDF
_2rda
490 1 _aProtein Reviews ;
_v4
505 0 _aStructural 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.
520 _aProtein Misfolding, Aggregation, and Conformational Disease, is the first book to discuss significant achievements in protein structure-function relationships in the areas of biochemistry, molecular biology and molecular medicine. This volume summarizes recent achievements in the understanding of the relationships between protein misfolding, aggregation and development of protein deposition disorders. Research indicates that various human disorders, including most neurodegenerative diseases, systemic amyloidoses and many others, arise from the misfolding and aggregation of an underlying protein. Protein Misfolding, Aggregation and Conformational Diseases is an ideal book for biochemists, protein scientists, immunologists, pharmaceutical scientists, and molecular and cellular biologists.
650 0 _aMEDICINE.
650 0 _aIMMUNOLOGY.
650 0 _aCYTOLOGY.
650 1 4 _aBIOMEDICINE.
650 2 4 _aIMMUNOLOGY.
650 2 4 _aCELL BIOLOGY.
700 1 _aFink, Anthony L.
_eeditor.
710 2 _aSpringerLink (Online service)
773 0 _tSpringer eBooks
776 0 8 _iPrinted edition:
_z9780387259185
830 0 _aProtein Reviews ;
_v4
856 4 0 _uhttp://dx.doi.org/10.1007/b136464
_zVer el texto completo en las instalaciones del CICY
912 _aZDB-2-SBL
942 _2ddc
_cER
999 _c56508
_d56508