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Mutations of ABC lipid transporters are responsible for several human diseases, such as neonatal surfactant deficiency (ABCA3 mutation) or Tangier disease (ABCA1 mutation), characterized by decreased removal of cholesterol from peripheral tissues (103)

doi: 10.3389/fimmu.2023.1279846 Received 18 August 2023 Accepted 25 October 2023 Published 15 November 2023 Volume 14 - 2023 Edited by Qingqing Jiao, The First Affiliated Hospital of Soochow University, China Reviewed by Ma Lei, Shihezi University, China

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Growth Hormone Receptor cDNA microarray analysis identified GHR as abundantly upregulated following BPC-157 treatment, with dose-dependent increases reaching up to 7-fold elevation in both mRNA and protein levels (Chang et al., Molecules, 2014)

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Phytochemical study of polyphenols in Perilla Frutescens as an antioxidant