Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease [electronic resource] / edited by J. Robin Harris.
By: Harris, J. Robin [editor.].
Contributor(s): SpringerLink (Online service).
Material type:
BookSeries: Subcellular Biochemistry: 65Publisher: Dordrecht : Springer Netherlands : Imprint: Springer, 2012Description: XVII, 648 p. 114 illus., 41 illus. in color. online resource.Content type: text Media type: computer Carrier type: online resourceISBN: 9789400754164.Subject(s): Medicine | Entomology | Biomedicine | Biomedicine general | Entomology | Medicine/Public Health, generalDDC classification: 610 Online resources: Click here to access online
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Springer eBooksSummary: This volume of the Subcellular Biochemistry series is devoted to the aggregation and fibrillogenesis of the amyloid-forming peptides and proteins, including emphasis on oligomer formation as well as fibril formation. The diverse topics included here are presented within 22 chapters, covering many of the relevant topics from both a basic science and clinical perspective. The authorship of these chapters is thoroughly international, with authoritative contributions from active researchers. Fundamental structural and cellular studies using many different technical approaches are presented, leading through to clinical and therapeutic aspects of the amyloid diseases, considered from both pharmaceutical and natural product view points. It is hoped that this book will be of use to both biomedical scientists and clinicians wishing to keep abreast of this rapidly advancing field, of direct importance to the understanding of cerebral neurodegenerative disease and systemic amyloid disease.
This volume of the Subcellular Biochemistry series is devoted to the aggregation and fibrillogenesis of the amyloid-forming peptides and proteins, including emphasis on oligomer formation as well as fibril formation. The diverse topics included here are presented within 22 chapters, covering many of the relevant topics from both a basic science and clinical perspective. The authorship of these chapters is thoroughly international, with authoritative contributions from active researchers. Fundamental structural and cellular studies using many different technical approaches are presented, leading through to clinical and therapeutic aspects of the amyloid diseases, considered from both pharmaceutical and natural product view points. It is hoped that this book will be of use to both biomedical scientists and clinicians wishing to keep abreast of this rapidly advancing field, of direct importance to the understanding of cerebral neurodegenerative disease and systemic amyloid disease.
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