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These alterations were likewise confirmed at molecular level by analysing gene expression profiles in both liver and kidney, exhibiting altered expression patterns, which are typical of dysfunctional mitochondrialas pathologies, such as fibrosis, necrosis, and ischemia (El-Shenawy, 2009)

Furthermore, the interaction between the unliganded -CT and the FnIII-1 domain, together with the disulfide bonds between the two -CTs, restricts the conformational change of unliganded -CT, which is required for the binding of a second IGF1 molecule (Fig

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