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To confirm that the nemp-1(zu501) mutation was responsible for the nLD phenotype, we used Crispr-Cas9 to engineer identical ( zu522 ) and similar ( zu523 ) mutations, and found that both mutations resulted in apparently identical nLD phenotypes

Gilliland, Claudia Leonardi, Tekeda F

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Conducting comprehensive clinical research on cancer patients poses several challenges, but further studies in this direction are anticipated in the future (Chung and Park 2017

Since several genes within the -oxidation pathway were downregulated in SKM following clenbuterol treatment (Fig

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