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Titlebook: Heat Shock Proteins and the Cardiovascular System; A. A. Knowlton Book 1997 Springer Science+Business Media New York 1997 atherosclerosis.

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Heat Shock Proteins and Antioxidative Enzymes in Myocardial Protection,tion of cell loss after metabolic injury, such as brief ischemia, is paramount to myocardial functional recovery. While various pharmacological treatments have been shown to be of some benefit, interest has also developed on endogenous cellular mechanisms which can increase cellular protection and f
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Changes in Heat Shock Proteins in Cardiac Hypertrophy,ck proteins (HSPs) and many other genes. For example, the induction of HSPs is observed after an episode of ischemia or hypoxia to which the heart does not usually respond with myocyte hypertrophy, and after pressure- or volume-overload to which the heart responds with hypertrophy, later. In additio
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Heat Shock Protein Expression in the Aging Cardiovascular System, when faced with conditions of stress (Shock et al., 1984; Martin et al., 1993). The cardiovascular system is no exception as aging constitutes a major risk factor for the development of cardiovascular disease, with the incidence of hypertension, atherosclerosis, stroke and myocardial infarction all
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,Tumor Necrosis Factor-α and the Myocardial Stress Response,ia/infarction, ultimately determines whether the heart will decompensate and fail, or whether instead it will maintain preserved function. As shown in Figure 1, the adult heart adapts to a superimposed environmental stress by at least three interrelated and integrated mechanisms: cardiac hypertrophy
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Role of Small Heat Shock Proteins in the Cardiovascular System,idered important for the cardiovascular system. The properties of the three structurally related sHSPs, . and ., and their location in developing and differentiated heart tissues, in particular in cardiomyocytes, support their participation in heart muscle contraction, in which way, however, is in d
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Role of Small HSP Gene Expression in Myocardial Ischemia and Reperfusion,ess-inducible proteins. Among them, heat shock proteins (HSPs) are ubiquitously present in almost all organisms including mammalian tissues. Most of the mammalian systems studied so far respond to stresses by inducing genes for highly conserved proteins encoding HSP 70 and HSP 90. mRNAs for these HS
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Ischemia, Infarction and HSP70,ardium following an infarction is a highly desirable aim. Recent evidence indicates that endogenous protective mechanisms are readily activated in cardiomyocytes during an ischemic event, thus a better understanding of these endogenous protective mechanisms will most likely lead to additional myocar
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