Cellular Senescence in Disease

Forfatter: info mangler
Bog
  • Format
  • Bog, paperback
  • Engelsk

Beskrivelse

Winner of the 2023 PROSE award in Biomedicine and Neuroscience! Research in the field of senescence has boomed recently due to the gradual realization that senescent cells are associated with a significant number of diseases. The genetic or pharmacological elimination of senescent cells can cause widespread benefits and improves outcomes for most of those diseases. Cellular Senescence in Diseases presents an updated review of the role of cellular senescence in multiple pathologies. Focus is given to those diseases where the implication of senescence has been more extensively documented, such as (cancer, lung and liver diseases, diabetes, Neurodegenerative diseases and others). The Editors recruited a group of worldwide experts in each individual pathology to review the role of cellular senescence in each one of them, aiming at identifying potential therapeutic pathways. The first two chapters provide an overview of the cellular senescence principles. Next, the chapters are divided into specific diseases. Cancer, including premalignant lesions (OIS), Advanced disease (TIS), and Metastasis are covered. The following condition covered is Lung diseases, including IPF, COPD, and Pulmonary Hypertension. Next Liver Diseases are covered, including Fibrosis and Cirrhosis, and Fatty liver disease. Next there is coverage for Kidney implications, including fibrosis and transplantation. Vascular diseases are covered next including infarction and hear fibrosis, and atherosclerosis. Both diabetes types 1 and 2 are covered next. Following chapters cover Obesity, Sarcopenia, and Bone and Cartilage disorders, respectively. Neurodegenerative diseases are covered next, focusing on Alzheimer's and Parkinson's. The next chapter discusses accumulation of senescent cell in tissues during aging. The two final chapters cover current developments and conclusions. Cellular Senescence in Diseases is designed for researchers and clinicians with a focus on the cellular mechanisms of diseases. All chapters cover current experimental therapeutic approaches to eliminate or cancel the pathological effects of senescent cells. Pharmaceutical scientists may also benefit from the contents of the book in the exploration of novel therapeutic opportunities.

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Detaljer
  • SprogEngelsk
  • Sidetal472
  • Udgivelsesdato02-12-2021
  • ISBN139780128225141
  • Forlag Academic Press Inc
  • FormatPaperback
Størrelse og vægt
  • Vægt970 g
  • coffee cup img
    10 cm
    book img
    19,1 cm
    23,5 cm

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    Diabetes Pap Obesity Regeneration Aging Inflammation Osteoarthritis. Fractures Pulmonary hypertension Osteoporosis Carcinogenesis Atherosclerosis Fibrosis Adipose Tissue Telomere Extracellular matrix Cartilage Kidney Transplantation Pancreatic beta cells PH Emphysema Frailty Cellular Senescence Ischemia/reperfusion injury PEC Chronic kidney disease Nash Senescence Oncogene Hypoxia Type 1 diabetes Chondrogenesis Liver disease NAFLD Biomaterials Chondrocyte TGF-beta Tumor suppression Senescence-Associated Secretory Phenotype SYNOVITIS Bone loss COPD ECM Degenerative diseases Ageing PAH Tissue repair DNA damage response Chronic bronchitis Liver failure Oncogene-Induced Senescence Senolytics Synovium Acute Rejection Alzheimer disease (AD)Immune clearance BMPR2Bone morphogenic protein receptor 2DDR Cell Cycle Arrest Donor age Donor tissue quality interstitial lung Maladaptive repair Navitoclax osteopontin PASMC p16p21p53SASP IL-17IL-4IL-6Immunity Pulmonary vascular endothelial cells Senomorphics Interleukin 17Interleukin 4Interleukin 6IPFP Pulmonary Artery Smooth Muscle Cells Senolytic SASP senotherapy Transplant-related injuries Transient versus chronic senescence Senolytic therapy UBX0101 Tubular atrophy Tubulointerstitial fibrosis Mitotic versus postmitotic senescence Tubular cell senescence osteophyte precancerous OPN Premalignant Preneoplastic Pulmonary artery hypertension Pulmonary artery pressure Parkinson disease (PD)Senescence-associated secretory phenotype (SASP)Senescent glia Senolysis

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