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First, in gain-of-function experiments, we examined whether overexpression of secreted, catalytically active LOXL2 increases BHZ incorporation in vascular smooth muscle cells (VSMCs)

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Wilson Disease levels help separate Wilson disease Wilson disease Wilson disease (hepatolenticular degeneration) is an autosomal recessive disorder caused by various mutations in the ATP7B gene, which regulates copper transport within hepatocytes

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In vitro antitumor activity of Latcripin-15 regulator of chromosome condensation 1 domain protein