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Research indicates that most neurodegenerative diseases, systemic amyloidoses and many others, arise from the misfolding and aggregation;
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issues concerning protein misfolding and aggregation in neurodegenerative diseases. Building on recent developments, including the recognition;
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issues concerning protein misfolding and aggregation in neurodegenerative diseases. Building on recent developments, including the recognition;
Vergelijkbare producten zoals Protein Misfolding in Neurodegenerative Diseases
Bio-Nanoimaging: Protein Misfolding & Aggregation provides a unique introduction to both novel and established nanoimaging techniques;
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An increasingly aging population will add to the number of individuals suffering from amyloid. Protein Misfolding Diseases provides a;
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, protein structure, results of computer simulations of aggregation, and computational simulations focused on specific diseases such as Alzheimer's;
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. Integrates methods for studying protein misfolding, factors that trigger this process and its role in a wide spectrum of diseases;
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a fundamental understanding of the underlying oligomerization and aggregation processes of these diseases from both computational and;
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Proteins occasionally exhibit the potential to adopt alternate folds under natural or artificial conditions. These conformational changes;
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The most fascinating and unique feature of prion diseases is that they are caused almost exclusively by a proteinaceous and infectious;
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Early Stage Protein Misfolding and Amyloid Aggregation, Volume 329, the latest in the International Review of Cell and Molecular;
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understanding of (a) the folding process, (b) the binding of ligands to receptor molecules, and (c) peptide self-aggregation. In this context, different;
Vergelijkbare producten zoals Protein and Peptide Folding, Misfolding, and Non-Folding
has a wider relevance due to similarities in the processes of protein misfolding and aggregation between prion disorders and other;
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has a wider relevance due to similarities in the processes of protein misfolding and aggregation between prion disorders and other;
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It was twenty ?ve years ago this year that for the ?rst time a protein under- ing a form of human cerebral amyloidosis, the Icelandic-type;
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common pathological mechanism: the misfolding, aggregation and accumulation of proteins (termed amyloid ) in the brain. Metal ions have long;
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needs of the cell. Stress and aging can challenge the proteostasis network, resulting in the aggregation of misfolded proteins-a feature;
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neurodegenerative diseases associated with protein aggregation/fibrillization focusing on the nature of the pathogenic species and the cellular pathways;
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This book is a neurochemistry-based companion for Protein Misfolding and Neurodegenerative Diseases: Molecular Targets, an Elsevier;
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diseases of the brain that result. During the past few years the connections between failures in protein quality control and neurological disorders;
Vergelijkbare producten zoals Fundamentals of Neurodegeneration and Protein Misfolding Disorders
diseases of the brain that result. During the past few years the connections between failures in protein quality control and neurological disorders;
Vergelijkbare producten zoals Fundamentals of Neurodegeneration and Protein Misfolding Disorders
Proteostasis is central to the development of various human diseases caused due to excessive protein misfolding and the disregulation;
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the therapeutic intervention of neurodegenerative diseases and other metabolic disorders caused by protein aggregation or proteostasis failure;
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: Functional and Structural Properties of Inclusion Bodies in Bacterial Cells provides a large overview of protein folding and aggregation, including;
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diseases Presents a systems and precision biology perspective of TDP-43 Discusses therapeutics of TDP-43 proteinopathies
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-modifying treatments in particular - the first edition of Molecular Targets in Protein Misfolding and Neurodegenerative Disease will contain both a;
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