Cellular Mechanisms of the System Regulating the Aggregate State of Blood PDF Download
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Author: S. V. Andreev
Publisher: CRC Press
ISBN: 9783718649617
Category : Medical
Languages : en
Pages : 90
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Book Description
Author: S. V. Andreev
Publisher: CRC Press
ISBN: 9783718649617
Category : Medical
Languages : en
Pages : 90
Get Book Here
Book Description
Author: S. V. Andreev
Publisher: CRC Press
ISBN: 9783718649631
Category : Medical
Languages : en
Pages : 142
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Book Description
The series, Hematology reviews, focuses on key developments in Soviet fundamental and applied research, making recent medical advances in the USSR available to the researcher who does not read Russian. Topics reviewed in this volume include the biochemical and physiological mechanisms of blood clotting, the molecular and biological bases of hemostasis and the role played by prostaglandins in the regulation of blood clotting and fibrinolysis. Book club price, $31. Annotation copyrighted by Book News, Inc., Portland, OR
Author: M. Kh Aliev
Publisher: CRC Press
ISBN: 9783718649600
Category : Medical
Languages : en
Pages : 128
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Book Description
Author: O. K. Gavrilov
Publisher: CRC Press
ISBN: 9783718652426
Category : Medical
Languages : en
Pages : 156
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Book Description
Hemopoiesis Regulation Mechanisms under Stress by Goldberg and Dygai describes recent results concerning the role of the neuroendocrine system and inter-cellular interactions in the regulation of hemopoiesis under stress. The authors also detail the role of the nervous and opioid systems, glucocorticoids, T-lymphocytes, phagocytic mononuclear cells and stromal mechanocytes in the regulation of the proliferation and differentiation of the various types of hemopoietic cells while the organism is under stress. Other articles discuss the hemostatic potential in various blood circulation departments, thrombohemorrhagic syndrome as a fundamental basis of general pathology, and effects of the gravisurgical correction of the aggregate state of blood on the functions of some organs and systems in case of ischemic heart disease. Among the five papers in this volume, RASB System and Hemopoiesis by O.K. Gavrilov characterizes the main types of RASB (Regulation of the Aggregate State of Blood
Author: Daniel Laskowitz
Publisher: CRC Press
ISBN: 1498766579
Category : Medical
Languages : en
Pages : 388
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Book Description
Traumatic brain injury (TBI) remains a significant source of death and permanent disability, contributing to nearly one-third of all injury related deaths in the United States and exacting a profound personal and economic toll. Despite the increased resources that have recently been brought to bear to improve our understanding of TBI, the developme
Author: Robert Fitridge
Publisher: University of Adelaide Press
ISBN: 1922064009
Category : Medical
Languages : en
Pages : 589
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Book Description
New updated edition first published with Cambridge University Press. This new edition includes 29 chapters on topics as diverse as pathophysiology of atherosclerosis, vascular haemodynamics, haemostasis, thrombophilia and post-amputation pain syndromes.
Author: Oguz Baskurt
Publisher: CRC Press
ISBN: 1439841802
Category : Medical
Languages : en
Pages : 326
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Book Description
Red blood cells in humans—and most other mammals—have a tendency to form aggregates with a characteristic face-to-face morphology, similar to a stack of coins. Known as rouleaux, these aggregates are a normally occurring phenomenon and have a major impact on blood rheology. What is the underlying mechanism that produces this pattern? Does this really happen in blood circulation? And do these rouleaux formations have a useful function? The first book to offer a comprehensive review of the subject, Red Blood Cell Aggregation tackles these and other questions related to red blood cell (RBC) aggregates. The book covers basic, clinical, and physiological aspects of this important biophysical phenomenon and integrates these areas with concepts in bioengineering. It brings together state-of-the-art research on the determinants, mechanisms, and measurement and effects of RBC aggregation as well as on variations and comparative aspects. After an introductory overview, the book outlines factors and conditions that affect RBC aggregation. It presents the two hypotheses—the bridging model and the depletion model—that provide potential mechanisms for the adhesive forces that lead to the regular packing of the cells in rouleaux formations. The book also reviews the methods used to quantify RBC aggregation in vitro, focusing on their importance in clinical practice. Chapters discuss the effect of RBC aggregation on the in vitro rheology of blood as well as on tube flow. The book also looks at what happens in the circulation when red blood cells aggregate and examines variations due to physiological and pathophysiological challenges. The concluding chapter explores the formation of red blood cell aggregates in other mammals. Written by leading researchers in the field, this is an invaluable resource for basic science, medical, and clinical researchers; graduate students; and clinicians interested in mammalian red blood cells.
Author: Michael S. Wolfe
Publisher: Academic Press
ISBN: 0128113057
Category : Medical
Languages : en
Pages : 561
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Book Description
The Molecular and Cellular Basis of Neurodegenerative Diseases: Underlying Mechanisms presents the pathology, genetics, biochemistry and cell biology of the major human neurodegenerative diseases, including Alzheimer's, Parkinson's, frontotemporal dementia, ALS, Huntington's, and prion diseases. Edited and authored by internationally recognized leaders in the field, the book's chapters explore their pathogenic commonalities and differences, also including discussions of animal models and prospects for therapeutics. Diseases are presented first, with common mechanisms later. Individual chapters discuss each major neurodegenerative disease, integrating this information to offer multiple molecular and cellular mechanisms that diseases may have in common. This book provides readers with a timely update on this rapidly advancing area of investigation, presenting an invaluable resource for researchers in the field. - Covers the spectrum of neurodegenerative diseases and their complex genetic, pathological, biochemical and cellular features - Focuses on leading hypotheses regarding the biochemical and cellular dysfunctions that cause neurodegeneration - Details features, advantages and limitations of animal models, as well as prospects for therapeutic development - Authored by internationally recognized leaders in the field - Includes illustrations that help clarify and consolidate complex concepts
Author: Mikhail G. Kolonin
Publisher: Humana Press
ISBN: 9781617799426
Category : Science
Languages : en
Pages : 0
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Book Description
Stem cell mobilization represents a transient increase in the levels of circulating stem and progenitor cells. In Stem Cell Mobilization: Methods in Protocols, expert researchers in the field detail cell mobilization methodology and recent developments in the field for basic and biomedical research community. Specifically clinical hematopoietic progenitor cell mobilization protocols, frontiers in mobilization and analysis of non-hematopoietic progenitors, mesenchymal progenitor cells, monocyte-derived fibroblast progenitors, and very small embryonic like cells. Written in the highly successful Methods in Molecular BiologyTM series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and key tips on troubleshooting and avoiding known pitfalls. Authoritative and practical, Stem Cell Mobilization: Methods and Protocols seeks to aid scientists in the further study of this important stem cell research.
Author: Fernando Ferreira Costa
Publisher: Springer
ISBN: 3319067133
Category : Medical
Languages : en
Pages : 439
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Book Description
Although sickle cell anemia was the first molecular disease to be identified, its complex and fascinating pathophysiology is still not fully understood. A single mutation in the beta-globin gene incurs numerous molecular and cellular mechanisms that contribute to the plethora of symptoms associated with the disease. Our knowledge regarding sickle cell disease mechanisms, while still not complete, has broadened considerably over the last decades. Sickle Cell Anemia: From Basic Science to Clinical Practice aims to provide an update on our current understanding of the disease’s pathophysiology and use this information as a basis to discuss its manifestations in childhood and adulthood. Current therapies and prospects for the development of new approaches for the management of the disease are also covered.
