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liver, increases plasma amino acids levels, and causes alpha-cell proliferation and hypersecretion of glucagon ( 5 ). It is a matter of debate which amino acids are responsible for signaling to alpha cells to increase glucagon secretion. Alanine and
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adipocyte proliferation and differentiation, it furthermore positively affects insulin-stimulated but not basal glucose uptake in 3T3-derived adipocytes ( 38 , 39 , 40 ). Accordingly, an increase of glucose uptake after activation of CB 1 was demonstrated
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ulcers ( 8 ). Inadequate secretion of ECM proteins ( 9 ), dysregulation of macrophage activity ( 10 , 11 ), proliferation and increased apoptosis of cutaneous fibroblasts, impaired angiogenesis, and re-epithelialization ( 12 , 13 ) have all been
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series of experiments to explore the mechanism in it ( 6 ). The current study explored the mechanism further from other aspect. THs play a crucial role in fetal brain development and are involved in the proliferation, differentiation, maturation and
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–30%) ( 1 ). In about 25% of cases, MTC is caused by inherited germline-activating mutations of the ‘rearranged during transfection’ (RET) proto-oncogene, which constitutively activates cellular signalling, resulting in persistent cell proliferation and MTC
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positively charged aliphatic amines. As biological routers, polyamines interact with different macromolecules such as DNA, RNA and proteins and have the ability to regulate their biochemical activities. Polyamines direct cell proliferation by regulating
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the proliferation marker Ki67. The system that was recently proposed for GEP-NETs by the European Neuroendocrine Tumor Society (ENETS) and recommended by WHO uses either mitotic rate or the Ki67 labelling index ( 2 ). Except for neuroendocrine
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some GH-secreting tumor cells responsive to an AMPK activator. These factors may include proliferation rate, activation of mTOR pathway downstream of cell surface growth factor receptors, basal AMPK activity and differences in cellular bioenergetics
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, this complex recognition is not capable itself of stimulating the naive T lymphocyte for proliferation and differentiation into an active T lymphocyte, but costimulatory molecules are necessary. Such molecules are the B7.1 (CD80) and B7.2 (CD86
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(23, 24) . Vasostatins have been linked to vasculogenesis and remodeling (12) . In contrast to catestatin, vasostatin inhibits VEGF-induced endothelial cell proliferation and migration and the formation of capillary-like structures (25) . However