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发表于 2025-3-25 04:11:02 | 显示全部楼层
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https://doi.org/10.1007/978-3-030-06118-0nly in development but also in injury and disease [1]. One of these cytokines, transforming growth factor-ß (TGF-ß), a dimeric, multifunctional peptide [2], is expressed at high levels in the heart during both embryonic and adult life [3,4]. In this brief review, we will discuss the results of inves
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Anju Patel,Puja Khare,D. D. Patrae, by analogy and incrimination: proof for the paramount role of growth factors in the skeletal muscle lineage as regulators of myogenesis [1, 2] and differentiation [3–7], and evidence that growth factor-like activity accumulates in myocardium after experimental aortic constriction, promoting amino
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https://doi.org/10.1007/978-981-97-0672-3imals as well as in humans during ischemic heart disease, slowly developing occlusion of a large epicardial coronary artery leads to the formation of a collateral circulation [1,3,4]. This compensatory growth (collateralization) is able to prevent myocardial infarction and these alternate routes of
发表于 2025-3-26 01:05:13 | 显示全部楼层
Trevor A. Thorpe,Indra S. Harryoccurred over the last 5 years. Widespread use of recombinant DNA technology has led to the identification of new peptide growth factors (and in many cases their receptors) which are capable of stimulating angiogenesis. For example, the family of Heparin Binding Growth Factors (HBGF’s), which includ
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Parenchyma, Collenchyma, and Sclerenchymaluminal pressure such as occurs in arteriovenous fistulas and in pulmonary hypertension. The intimai smooth muscle accumulation in atherosclerosis, restenosis after angioplasty and in vein grafts is arguably a consequence of these same repair and haemodynamic adaptation mechanisms [1]. Intimai VSMC
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