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Additionally, we provide guidelines for data interpretation, quantification, and statistical analysis to ensure robust and reliable results

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

doi: 10.1089/thy.2005.15.210 91 MetereAFrezzottiFGravesCEVergineMDe LucaAPietraforteDet al

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Nanoemulsions delivering melittin and NO donors can reverse the activation of cancer-associated fibroblasts (CAFs), reduce the dense collagen that shields the tumor, and normalize blood vessels, thereby facilitating CTL infiltration