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Fundamentals of Neurodegeneration and Protein Misfolding Disorders

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This text introduces students and researchers to misfolded proteins, toxic oligomers, and amyloid assemblages, highlighting their connection to neurological diseases. Recent discoveries have reinforced the links between protein quality control failures and disorders such as prion diseases, Alzheimer’s, Parkinson’s, Huntington’s, amyotrophic lateral sclerosis, and frontotemporal lobar degeneration. Beginning with the basics of protein folding and quality control, the reader learns how misfolded proteins contribute to these diseases. The author presents the material in a clear, engaging style, addressing a leading area of science and medicine. Emphasis is placed on groundbreaking biophysical and biochemical methods that facilitate molecular-level exploration and conceptual breakthroughs. Each major disease class is covered in separate chapters, focusing on common factors such as failures in synaptic transmission, mitochondrial control, axonal transport, RNA processing breakdowns, environmental influences, and neuroinflammation effects. This book is suitable for advanced undergraduate and graduate teaching and serves as a comprehensive reference for students and researchers in neuroscience, molecular biology, biological physics, and biomedical engineering.

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Fundamentals of Neurodegeneration and Protein Misfolding Disorders, Martin Beckerman

Sprache
Erscheinungsdatum
2015
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(Hardcover)
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Titel
Fundamentals of Neurodegeneration and Protein Misfolding Disorders
Sprache
Englisch
Autor*innen
Martin Beckerman
Verlag
Springer
Erscheinungsdatum
2015
Einband
Hardcover
Seitenzahl
378
ISBN10
3319221167
ISBN13
9783319221168
Reihe
Bewertung
3 von 5 Sternen
Beschreibung
This text introduces students and researchers to misfolded proteins, toxic oligomers, and amyloid assemblages, highlighting their connection to neurological diseases. Recent discoveries have reinforced the links between protein quality control failures and disorders such as prion diseases, Alzheimer’s, Parkinson’s, Huntington’s, amyotrophic lateral sclerosis, and frontotemporal lobar degeneration. Beginning with the basics of protein folding and quality control, the reader learns how misfolded proteins contribute to these diseases. The author presents the material in a clear, engaging style, addressing a leading area of science and medicine. Emphasis is placed on groundbreaking biophysical and biochemical methods that facilitate molecular-level exploration and conceptual breakthroughs. Each major disease class is covered in separate chapters, focusing on common factors such as failures in synaptic transmission, mitochondrial control, axonal transport, RNA processing breakdowns, environmental influences, and neuroinflammation effects. This book is suitable for advanced undergraduate and graduate teaching and serves as a comprehensive reference for students and researchers in neuroscience, molecular biology, biological physics, and biomedical engineering.