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Titlebook: Biochemical Regulation of Myocardium; Roland Vetter,Ernst-Georg Krause Book 1996 Kluwer Academic Publishers 1996 ATP.Calcium.Glycogen.Lipi

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https://doi.org/10.1007/978-94-007-5137-8-regulated phosphoproteins e.g. troponin I and phospholamban were investigated in the ventricular tissue of 1, 7, 30 days old rats. Quantitative immunodetection revealed a 5.7-fold decrease in G. at 30th postnatal day compared with the postnatal day 1 and up to 15-fold at 4 months. The amounts of G.
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https://doi.org/10.1007/978-94-007-5137-8 α1, α2 and α3 isoforms of the Na,K-ATPase were studied in rat myocardium..The α1-subunit was identified predominantly on sarcolemma of cultured myocytes, neonatal, as well as adult cardiocytes. The α2 signal was localized around nuclei of cultured cardiocytes, very weak signals were seen in neonata
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https://doi.org/10.1007/978-94-007-5137-8lopment. In contrast, cardiomyocyte maturation, as evidenced by cellular hypertrophy, is a long-term process that can occupy the bulk of the life-span of the mature organism. As the newborn myocyte undergoes a ‘transition’ from proliferative to hypertrophic growth, ventricular remodeling of the non-
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https://doi.org/10.1007/978-3-030-53644-2alapril maleate. This reduced rate of growth is reflected . by reduced rates of ribosome formation and protein synthesis, and may be due to decreased availability of angiotensin II (AII), a potentially hypertrophic agent; decreased numbers of AII receptors; increased availability of bradykinin, a po
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https://doi.org/10.1007/978-3-030-53644-2ic receptor and the M2 muscarinic receptor. All sera of mice (4/4) in the acute phase recognized the β.-adrenergic receptor and the M2 muscarinic receptor peptides but not the β2-adrenergic receptor peptide. The same peptides were recognized during the chronic phase in half of the mice (6/12). The i
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