Biochemistry and Cell Biology of Ageing: Part III Biomedical Science
This book provides a state-of-the-art overview of key areas of subcellular aging research in human cells.
The reader is introduced to the historical development and progress in biomedical aging research and learns, for example, about the role of microRNAs, circRNAs, mitochondria and extracellular vesicles in cellular senescence. The reader will also learn more about how gap junctions, the nuclear pore complex and the proteasome are affecting the ageing processes. In addition, novel therapeutic opportunities through modulation of cellular senescence are discussed.
The book follows on from Parts I and II of Biochemistry and Cell Biology of Ageing (Volumes 90 and 91 of the Subcellular Biochemistry book series) by covering interesting and significant biomedical ageing topics not included in the earlier volumes. Comprehensive and cutting-edge, this book is a valuable resource for experienced researchers and early career scientist alike, who are interested in learning more about the fascinating and challenging question of why and how our cells age.
- Publisher: Springer
- Publish Date: Jan 7th, 2024
- Pages: 424
- Language: English
- Edition: 2023 -
- Dimensions: 9.21in - 6.14in - 0.89in - 1.34lb
- EAN: 9783031214127
- Categories: • Life Stages - Later Years• Life Sciences - Molecular Biology• Biochemistry
About the Author
Prof J. Robin Harris is an Honorary Professor of the University of Mainz, who specialized in macromolecular electron microscopy. He has been the Series Editor of the Subcellular Biochemistry Series for many years and his broad scientific interests are reflected in the diversity of content of the Series.Dr Viktor Korolchuk is Reader in Molecular Cell Biology at Newcastle University. His scientific interests lie in the area of intracellular protein trafficking and degradation pathways. The current focus of research in his laboratory is autophagy (literally self-eating) where portions of cytoplasm are recruited into intracellular vesicles called autophagosomes and transported for degradation by lysosomal hydrolases.