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Protein Misfolding in Neurodegenerative Diseases: Mechanisms and Therapeutic Strategies [Mīkstie vāki]

  • Formāts: Paperback / softback, 596 pages, height x width: 234x156 mm, weight: 453 g
  • Izdošanas datums: 18-Oct-2019
  • Izdevniecība: CRC Press
  • ISBN-10: 036738812X
  • ISBN-13: 9780367388126
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  • Cena: 85,92 €
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  • Bibliotēkām
  • Formāts: Paperback / softback, 596 pages, height x width: 234x156 mm, weight: 453 g
  • Izdošanas datums: 18-Oct-2019
  • Izdevniecība: CRC Press
  • ISBN-10: 036738812X
  • ISBN-13: 9780367388126
Citas grāmatas par šo tēmu:
Research focused on protein folding, misfolding, and aggregation is leading to major advances across biochemistry and medicine. The elucidation of a folding code is proving to be of extreme importance in the postgenomic era, where a number of orphan genes have been identified for which no clear function has yet been established. This research is starting to shed light on the molecular and biochemical basis of a number of neurodegenerative diseases of dramatic impact.

Protein Misfolding in Neurodegenerative Diseases: Mechanisms and Therapeutic Strategies addresses key issues concerning protein misfolding and aggregation in neurodegenerative diseases. Building on recent developments, including the recognition of protein misfolding as both a marker and a causal agent, the text presents the work of those who are actively pursuing more effective treatments, as well as preventative measures, and a possible cure. These include the use of molecular chaperones to control misfolding and novel pharmaceuticals, as well as the potential role of various inhibitors and NSAIDS.

A Comprehensive Multifaceted Examination of the Complex Causal Agents Implicated in Protein Misfolding

Divided into five sections, this groundbreaking text provides up-to-date accounts for Alzheimer’s, Parkinson’s, Huntington’s, Amyotrophic Lateral Sclerosis and Transmissible Spongiform Encephalitis. It also explores the highly likelihood that multiple factors, including oxidative stress, play a role in these complex diseases.



Current research suggests that neurodegenerative diseases such as Alzheimer’s, Parkinson’s, Huntington’s, and Creutzfeldt-Jacob may be linked to disorders in protein shape referred to as protein misfolding. Continued study in this area could lead to promising advances in future treatment of these diseases. This groundbreaking text describes the latest findings regarding protein misfolding in the context of it being a marker, and perhaps a cause, in neurodegenerative diseases. Comprehensive coverage includes the diverse biochemical targets/markers for each disease, the currently limited success of drug therapies, and the cutting-edge research that could lead to more promising treatments.

Series Preface ix
Preface xi
Editors xiii
Contributors xv
Abbreviations xix
Chapter 1 Protein Folding and Misfolding, Relevance to Disease, and Biological Function
1(68)
Massimo Stefani
PART I ALZHEIMER'S DISEASE
Chapter 2 Alzheimer's Disease
69(26)
Charlotte E. Teunissen
Tischa J.M. van der Cammen
Chapter 3 Improving Cholinergic Transmission
95(50)
3.1 Cholinergic Transmission and Acetylcholine Release Enhancers
96(7)
Pierre Francotte
Pascal de Tullio
Bernard Pirotte
3.2 AChE and Its Inhibition
103(11)
Jure Stojan
3.3 AChE Inhibitors and Their Clinical Assessment
114(31)
Pierre Francotte
Pascal de Tullio
Bernard Pirotte
Chapter 4 Reduction in Plaque Formation
145(120)
4.1 Secretase and APP Processing
147(9)
Christian Czech
Helmut Jacobsen
Celine Adessi
4.2 Mechanism of Plaque Formation and A(3 Aggregation Inhibitors
156(7)
Christian Czech
Helmut Jacobsen
Celine Adessi
4.3 Nonsteroidal Anti-Inflammatory Drugs
163(29)
Bruno P. Imbimbo
Francesco Speroni
4.4 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Inhibitors
192(17)
Dario Cattaneo
4.5 Aβ Polymerization Reduction
209(56)
Harry LeVine
Corinne E. Augelli-Szafran
Chapter 5 Carbonic Anhydrase Activators as Potential Anti-Alzheimer's Disease Agents
265(24)
Claudiu T. Supuran
Andrea Scozzafava
Chapter 6 Detection and Reduction of Neurofibrillary Lesions
289(38)
Jeff Kuret
Chapter 7 Protein Misfolding in Alzheimer's Disease: Pathogenic or Protective?
327(10)
Rudy J. Castellani
Hyoung-Gon Lee
Akihiko Nunomura
Xiongwei Zhu
George Perry
Mark A. Smith
Chapter 8 Enhancement of Brain Retinoic Acid Levels
337(44)
Ann B. Goodman
Peter McCaffery
Joana A. Palha
Claire Simons
Arthur B. Pardee
PART II PARKINSONS DISEASE
Chapter 9 Parkinson's Disease: What Is It? What Causes It? And How Can It Be Cured?
381(34)
Tom Foltynie
Andrew W. Michell
Roger A. Barker
Chapter 10 Restoring Dopamine Levels
415(34)
P. Nuno Palma
Maria Joao Bonifacio
Luis Almeida
Patricio Soares-da-Silva
PART III HUNTINGTON'S DISEASE
Chapter 11 Huntington's Disease
449(30)
Claire-Anne Gutekunst
Fran Norflus
PART IV AMYOTROPHIC LATERAL SCLEROSIS
Chapter 12 Amyotrophic Lateral Sclerosis (Motor Neuron Disease)
479(38)
Teresa Sanelli
Janice Robertson
Avi Chakabartty
Michael J. Strong
PART V TRANSMISSIBLE SPONGIFORM ENCEPHALOPA THIES
Chapter 13 Transmissible Spongiform Encephalopathies
517(30)
Michael D. Geschwind
Giuseppe Legname
PART VI OVERVIEW
Chapter 14 Overview
547(10)
H. John Smith
Robert D.E. Sewell
Claire Simons
Index 557
H. John Smith, Claire Simons, Robert D. E. Sewell