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of neurodegenerative diseases of dramatic impact. Protein Misfolding in Neurodegenerative Diseases: Mechanisms and Therapeutic Strategies addresses key;
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of neurodegenerative diseases of dramatic impact. Protein Misfolding in Neurodegenerative Diseases: Mechanisms and Therapeutic Strategies addresses key;
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Research indicates that most neurodegenerative diseases, systemic amyloidoses and many others, arise from the misfolding and aggregation;
Vergelijkbare producten zoals Protein Misfolding, Aggregation and Conformational Diseases. Part A
Protein Misfolding, Volume 118, covers the wide spectrum of diseases and disorders that are attributed to protein misfolding, including;
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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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This book is a neurochemistry-based companion for Protein Misfolding and Neurodegenerative Diseases: Molecular Targets, an Elsevier;
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Bio-Nanoimaging: Protein Misfolding & Aggregation provides a unique introduction to both novel and established nanoimaging techniques;
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Aimed at "drug discoverers" - i.e. any scientist who is interested in neurodegenerative diseases in general, and in finding disease;
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fatally damaging protein misfolding disorders. This book represents an up-to-date review of different protein-misfolding diseases, serving as an;
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This book reviews current research on the important processes involved in neurodegenerative diseases (e.g. Alzheimer's disease) and the;
Vergelijkbare producten zoals Biophysics And Biochemistry Of Protein Aggregation: Experimental And Theoretical Studies On Folding, Misfolding, And Self-assembly Of Amyloidogenic Peptides
pathogenesis of neurodegenerative diseases. Substantial evidence has accumulated indicating that diverse neurodegenerative disorders might share a;
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Aggregates of the TAR DNA binding protein 43 (TDP-43), are hallmark features of the neurodegenerative diseases Amyotrophic Lateral;
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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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has a wider relevance due to similarities in the processes of protein misfolding and aggregation between prion disorders and other;
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leads to several diseases, such as Huntington's disease, Parkinson's disease, amyotrophic lateral sclerosis and Alzheimer's disease. These;
Vergelijkbare producten zoals Current Progress in Neurodegeneration
cells from toxic aggregated or misfolded protein states responsible for such diseases as Huntington's and Parkinson's diseases. Addressing the;
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amyotrophic lateral sclerosis. Despite the diversity in the amino acid sequence of the different proteins involved in these neurological diseases;
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Dementia and neurodegenerative diseases such as Parkinson's and Alzheimer's are becoming an increasingly important cause of medical and;
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Human Caspases and Neuronal Apoptosis in Neurodegenerative Diseases elucidates elaborately the role of caspase enzymes implicated in the;
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emerging group of diseases collectively known as 'Protein Folding Disorders.' This complex and diverse group of chronic and progressive entities;
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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;
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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;
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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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Proteostasis is central to the development of various human diseases caused due to excessive protein misfolding and the disregulation;
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