Amyloid, Prions, and Other Protein Aggregates, Part C

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Author :
Publisher : Elsevier
ISBN 13 : 0080468977
Total Pages : 412 pages
Book Rating : 4.0/5 (84 download)

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Book Synopsis Amyloid, Prions, and Other Protein Aggregates, Part C by :

Download or read book Amyloid, Prions, and Other Protein Aggregates, Part C written by and published by Elsevier. This book was released on 2006-10-06 with total page 412 pages. Available in PDF, EPUB and Kindle. Book excerpt: The ability of polypeptides to form alternatively folded, polymeric structures such as amyloids and related aggregates is being increasingly recognized as a major new frontier in protein research. This new volume of Methods in Enzymology along with Part B (volume 412) on Amyloid, Prions and other Protein Aggregates continue in the tradition of the first volume (309) in containing detailed protocols and methodological insights, provided by leaders in the field, into the latest methods for investigating the structures, mechanisms of formation, and biological activities of this important class of protein assemblies. Presents detailed protocols Includes troubleshooting tips Provides coverage on structural biology, computational methods, and biology

Amyloid, Prions, and Other Protein Aggregates

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Author :
Publisher : Elsevier
ISBN 13 : 0080496679
Total Pages : 861 pages
Book Rating : 4.0/5 (84 download)

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Book Synopsis Amyloid, Prions, and Other Protein Aggregates by :

Download or read book Amyloid, Prions, and Other Protein Aggregates written by and published by Elsevier. This book was released on 1999-09-22 with total page 861 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume includes a core of methodologies to attack the unique experimental problems presented by protein misassembly. Emphasis is on human biology applications, the area in which there is the most interest, in which most of the work has already been done, and in which there is the best evidence for the structural sophisitication of the protein aggregates.The critically acclaimed laboratory standard for more than forty years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Since 1955, each volume has been eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with more than 300 volumes (all of them still in print), the series contains much material still relevant today--truly an essential publication for researchers in all fields of life sciences.

Amyloid, Prions, and Other Protein Aggregates, Part C.

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Publisher :
ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (76 download)

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Book Synopsis Amyloid, Prions, and Other Protein Aggregates, Part C. by :

Download or read book Amyloid, Prions, and Other Protein Aggregates, Part C. written by and published by . This book was released on 2006 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Amyloid, Prions, and Other Protein Aggregates, Part B

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Publisher :
ISBN 13 :
Total Pages : 0 pages
Book Rating : 4.:/5 (878 download)

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Book Synopsis Amyloid, Prions, and Other Protein Aggregates, Part B by : Indu Kheterpal

Download or read book Amyloid, Prions, and Other Protein Aggregates, Part B written by Indu Kheterpal and published by . This book was released on 2006 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Amyloid, Prions, and Other Protein Aggregates

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Author :
Publisher : Academic Press
ISBN 13 : 9780121822101
Total Pages : 820 pages
Book Rating : 4.8/5 (221 download)

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Book Synopsis Amyloid, Prions, and Other Protein Aggregates by :

Download or read book Amyloid, Prions, and Other Protein Aggregates written by and published by Academic Press. This book was released on 1999-09-28 with total page 820 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume includes a core of methodologies to attack the unique experimental problems presented by protein misassembly. Emphasis is on human biology applications, the area in which there is the most interest, in which most of the work has already been done, and in which there is the best evidence for the structural sophisitication of the protein aggregates. The critically acclaimed laboratory standard for more than forty years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Since 1955, each volume has been eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with more than 300 volumes (all of them still in print), the series contains much material still relevant today--truly an essential publication for researchers in all fields of life sciences.

Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease

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Author :
Publisher : Springer Science & Business Media
ISBN 13 : 9400754167
Total Pages : 654 pages
Book Rating : 4.4/5 (7 download)

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Book Synopsis Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease by : J. Robin Harris

Download or read book Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease written by J. Robin Harris and published by Springer Science & Business Media. This book was released on 2012-12-09 with total page 654 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume of the Subcellular Biochemistry series is the result of the long-standing research interest of the editor in the molecular mechanism underlying Alzheimer’s disease and other amyloid diseases, indicated also by the earlier book in the series (Volume 38), devoted to Alzheimer’s disease. The broad coverage within the present amyloidogenesis book represents an attempt to collate current knowledge relating to the proteins and peptides involved in most of the known amyloid diseases, together with some amyloid/fibril-forming proteins and peptides that are not involved in diseases. Thus, the range of topics included is comprehensive and furthermore it was thought appropriate to include both basic science and clinical presentation of the subjects under discussion.

Early Stage Protein Misfolding and Amyloid Aggregation

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Publisher : Academic Press
ISBN 13 : 0128122528
Total Pages : 320 pages
Book Rating : 4.1/5 (281 download)

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Book Synopsis Early Stage Protein Misfolding and Amyloid Aggregation by :

Download or read book Early Stage Protein Misfolding and Amyloid Aggregation written by and published by Academic Press. This book was released on 2017-02-01 with total page 320 pages. Available in PDF, EPUB and Kindle. Book excerpt: Early Stage Protein Misfolding and Amyloid Aggregation, Volume 329, the latest in the International Review of Cell and Molecular Biology series presents comprehensive reviews and current advances in cell and molecular biology, including articles that address the structure and control of gene expression, nucleocytoplasmic interactions, control of cell development and differentiation, and cell transformation and growth. The series has a worldwide readership and maintains a high standard by publishing invited articles on important and timely topics as authored by prominent cell and molecular biologists. Provides comprehensive reviews and current advances Presents a wide range of perspectives on specific subjects Includes valuable reference material for advanced undergraduates, graduate students, and professional scientists

Fibrous Proteins: Amyloids, Prions and Beta Proteins

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Publisher : Elsevier
ISBN 13 : 0080468950
Total Pages : 328 pages
Book Rating : 4.0/5 (84 download)

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Book Synopsis Fibrous Proteins: Amyloids, Prions and Beta Proteins by : John M. Squire

Download or read book Fibrous Proteins: Amyloids, Prions and Beta Proteins written by John M. Squire and published by Elsevier. This book was released on 2006-12-12 with total page 328 pages. Available in PDF, EPUB and Kindle. Book excerpt: Amyloids, Prions and Beta Proteins is the last volume of the three-part thematic series on Fibrous Proteins in the Advances in Protein Chemistry serial. Fibrous proteins act as molecular scaffolds in cells providing the supporting structures of our skeletons, bones, tendons, cartilage, and skin. They define the mechanical properties of our internal hollow organs such as the intestines, heart, and blood vessels. This volume covers such topics as Beta-Structures in Fibrous Proteins; B-Silks: Enhancing and Controlling Aggregation; Beta-Rolls, Beta-Helices and Other Beta-Solenoid Proteins; Natural Triple B-Stranded Fibrous Folds; Structure, Function and Amyloidogenesis of Fungal Prions: Filament Polymorphism and Prion Variants; X-Ray Fiber and powder Diffraction of PRP Prion Peptides; From the Polymorphism of Amyloid Fibrils to Their Assembly Mechanism and Cytotoxicity; Structural Models of Amyloid-like Fibrils.

Methods in Enzymology

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Publisher :
ISBN 13 :
Total Pages : 403 pages
Book Rating : 4.:/5 (475 download)

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Book Synopsis Methods in Enzymology by :

Download or read book Methods in Enzymology written by and published by . This book was released on 2006 with total page 403 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Amyloid Fibrils and Prefibrillar Aggregates

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Publisher : John Wiley & Sons
ISBN 13 : 3527654208
Total Pages : 496 pages
Book Rating : 4.5/5 (276 download)

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Book Synopsis Amyloid Fibrils and Prefibrillar Aggregates by : Daniel Erik Otzen

Download or read book Amyloid Fibrils and Prefibrillar Aggregates written by Daniel Erik Otzen and published by John Wiley & Sons. This book was released on 2013-06-04 with total page 496 pages. Available in PDF, EPUB and Kindle. Book excerpt: Summing up almost a decade of biomedical research, this topical and eagerly awaited handbook is the first reference on the topic to incorporate recent breakthroughs in amyloid research. The first part covers the structural biology of amyloid fibrils and pre-fibrillar assemblies, including a description of current models for amyloid formation. The second part looks at the diagnosis and biomedical study of amyloid in humans and in animal models, while the final section discusses pharmacological approaches to manipulating amyloid and also looks at its physiological roles in lower and higher organisms. For Biochemists, Molecular Biologists, Neurobiologists, Neurophysiologists and those working in the Pharmaceutical Industry.

Molecular Chaperones in Health and Disease

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Publisher : Springer Science & Business Media
ISBN 13 : 9783540258759
Total Pages : 464 pages
Book Rating : 4.2/5 (587 download)

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Book Synopsis Molecular Chaperones in Health and Disease by : Matthias Gaestel

Download or read book Molecular Chaperones in Health and Disease written by Matthias Gaestel and published by Springer Science & Business Media. This book was released on 2005-09-27 with total page 464 pages. Available in PDF, EPUB and Kindle. Book excerpt: Molecular chaperones are involved in a wide variety of essential cellular processes in living cells. A subset of molecular chaperones have been initially described as heat shock proteins protecting cells from stress damage by keeping cellular proteins in a folding competent state and preventing them from irreversible aggregation. Later it became obvious that molecular chaperones are also expressed constitutively in the cell and are involved in complex processes such as protein synthesis, intracellular protein transport, post-translational modification and secretion of proteins as well as receptor signalling. Hence, it is not surprising that molecular chaperones are implicated in the pathogenesis of many relevant diseases and could be regarded as potential pharmacological targets. Starting with the analysis of the mode of action of chaperones at the molecular, cellular and organismic level, this book will then describe specific aspects where modulation of chaperone action could be of pharmacological and therapeutic interest.

Biophysics And Biochemistry Of Protein Aggregation: Experimental And Theoretical Studies On Folding, Misfolding, And Self-assembly Of Amyloidogenic Peptides

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Author :
Publisher : World Scientific
ISBN 13 : 9813202394
Total Pages : 328 pages
Book Rating : 4.8/5 (132 download)

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Book Synopsis Biophysics And Biochemistry Of Protein Aggregation: Experimental And Theoretical Studies On Folding, Misfolding, And Self-assembly Of Amyloidogenic Peptides by : Yuan Jian-min

Download or read book Biophysics And Biochemistry Of Protein Aggregation: Experimental And Theoretical Studies On Folding, Misfolding, And Self-assembly Of Amyloidogenic Peptides written by Yuan Jian-min and published by World Scientific. This book was released on 2017-06-02 with total page 328 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book reviews current research on the important processes involved in neurodegenerative diseases (e.g. Alzheimer's disease) and the peptides and proteins involved in the amyloidogenic processes. It covers the design and developments of anti-amyloid inhibitors, and gives readers a fundamental understanding of the underlying oligomerization and aggregation processes of these diseases from both computational and experimental points of view.

The Hidden World of Protein Aggregation

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Publisher : Elsevier
ISBN 13 : 0443293406
Total Pages : 528 pages
Book Rating : 4.4/5 (432 download)

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Book Synopsis The Hidden World of Protein Aggregation by : David B. Teplow

Download or read book The Hidden World of Protein Aggregation written by David B. Teplow and published by Elsevier. This book was released on 2024-08 with total page 528 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Hidden World of Protein Aggregation, Volume 206 provides a comprehensive exploration of protein aggregation, uncovering the factors behind the formation of amorphous aggregates and ordered structures called amyloid fibrils. It delves into the advantages and disadvantages of protein aggregates, addressing topics such as cytotoxicity and disorders linked to misfolding. Specific chapters in this release include Protein Aggregation: An Overview, Pathways of Amyloid Fibril Formation and Aggregation, Factors Influencing Amyloid Fibril Formation, Morphological Features and Types of Aggregated Structures, Each big journey starts with a first step: Importance of Oligomerization, Liquid-Liquid Phase Separation as Triggering Factor of Fibril Formation, and more. Additional sections cover Experimental Techniques for Detecting and Evaluating the Amyloid Fibrils, Prediction of Protein Aggregation, Amyloid Fibril Cytotoxicity and Associated Disorders, Inhibitors of Amyloid Fibril Formation, Therapeutic Approaches in Proteinopathies, Functional Amyloids, Biotechnological Applications of Amyloid Fibrils, and The Hidden World of Protein Aggregation.

Amyloid, Prions, and Other Protein Aggregates

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Author :
Publisher : Academic Press
ISBN 13 : 9780121828172
Total Pages : 430 pages
Book Rating : 4.8/5 (281 download)

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Book Synopsis Amyloid, Prions, and Other Protein Aggregates by :

Download or read book Amyloid, Prions, and Other Protein Aggregates written by and published by Academic Press. This book was released on 2006-10-20 with total page 430 pages. Available in PDF, EPUB and Kindle. Book excerpt: The ability of polypeptides to form alternatively folded, polymeric structures such as amyloids and related aggregates is being increasingly recognized as a major new frontier in protein research. This new volume of Methods in Enzymology along with Part C (volume 413) on Amyloid, Prions and other Protein Aggregates continue in the tradition of the first volume (309) in containing detailed protocols and methodological insights, provided by leaders in the field, into the latest methods for investigating the structures, mechanisms of formation, and biological activities of this important class of protein assemblies. Presents detailed protocols Includes troubleshooting tips Provides coverage on structural biology, computational methods, and biology

Protein Misfolding, Aggregation and Conformational Diseases

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Publisher : Springer Science & Business Media
ISBN 13 : 0387259198
Total Pages : 419 pages
Book Rating : 4.3/5 (872 download)

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Book Synopsis Protein Misfolding, Aggregation and Conformational Diseases by : Vladimir N. Uversky

Download or read book Protein Misfolding, Aggregation and Conformational Diseases written by Vladimir N. Uversky and published by Springer Science & Business Media. This book was released on 2007-11-24 with total page 419 pages. Available in PDF, EPUB and Kindle. Book excerpt: Research indicates that most neurodegenerative diseases, systemic amyloidoses and many others, arise from the misfolding and aggregation of an underlying protein. This is the first book to discuss significant achievements in protein structure-function relationships in biochemistry, molecular biology and molecular medicine. The authors summarize recent progress in the understanding of the relationships between protein misfolding, aggregation and development of protein deposition disorders.

Neurodegeneration

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Publisher : National Academies Press
ISBN 13 : 9780309285674
Total Pages : 0 pages
Book Rating : 4.2/5 (856 download)

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Book Synopsis Neurodegeneration by : Forum on Neuroscience and Nervous System Disorders

Download or read book Neurodegeneration written by Forum on Neuroscience and Nervous System Disorders and published by National Academies Press. This book was released on 2013-12-26 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Neurodegeneration: Exploring Commonalities Across Diseases is the summary of a workshop hosted by the Institute of Medicine\'s (IOM\'s) Forum on Neuroscience and Nervous System Disorders in Spring 2012 to explore commonalities across neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis (ALS), and frontotemporal dementia (FTD). Participants from academia; pharmaceutical and biotechnology industries; government agencies such as the National Institutes of Health and the U.S. Department of Veterans Affairs (VA); patient advocacy groups; and private foundations presented and identified potential opportunities for collaboration across the respective research and development communities. This report identifies and discusses commonalities related to genetic and cellular mechanisms, identifies areas of fundamental science needed to facilitate therapeutics development, and explores areas of potential collaboration among the respective research communities. Neurodegenerative diseases, such as Alzheimer\'s disease, Parkinson\'s disease, ALS, and FTD, are becoming increasingly prevalent in the United States due to an aging population. Implications are grave for quality of life and health care costs. Research on neurodegenerative diseases has expanded greatly over the past four decades. Nevertheless, fundamental questions remain about the biology of these diseases, and further insights into the mechanisms of these diseases would help to inform the development of effective means to prevent and to efficiently treat them. Recent findings have revealed certain commonalities in genetic and cellular mechanisms across neurodegenerative diseases. These findings suggest that it might be valuable - at least in some cases - to change the traditional way of studying these diseases by no longer seeing each as an independent entity, but rather as clinical variants of common cellular and molecular biological defects. This approach could help enhance basic scientific understanding of neurodegenerative disease, and could help with the development of biomarkers and new therapeutics.

The Nature and Origin of Amyloid Fibrils

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Publisher : John Wiley & Sons
ISBN 13 : 0470514930
Total Pages : 266 pages
Book Rating : 4.4/5 (75 download)

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Book Synopsis The Nature and Origin of Amyloid Fibrils by : Gregory R. Bock

Download or read book The Nature and Origin of Amyloid Fibrils written by Gregory R. Bock and published by John Wiley & Sons. This book was released on 2008-04-30 with total page 266 pages. Available in PDF, EPUB and Kindle. Book excerpt: Amyloid fibrils are associated with a range of pathological disorders including Alzheimer's Disease, Down's syndrome, diabetes, cardiomyopathies, and transmissible spongiform encephalopathies. This volume is a comprehensive account of recent developments in the understanding of the process of amyloid fibrils. Contains up-to-date data on all of the clinical problems which, despite their pathological significance, are still largely unsolved.