Primary carnitine deficiency (PCD) is an autosomal recessive disorder characterized by a lack of plasma membrane carnitine transport owing to a shortcoming in the OCTN2 carnitine transporter
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It does not cause the irritation, photosensitivity, or barrier disruption associated with retinoids
Lactylation and tumors of the nervous system Glioblastoma Gliomas comprise a major fraction of primary brain tumors, with glioblastoma representing the most common malignant subtype in adults and remaining highly lethal despite multimodal therapy [257, 258]
Genome-wide identification, characterization, and expression analysis related to autotoxicity of the GST gene family in Cucumis melo L
Lipid peroxidation pathway The process by which PUFA-rich membrane structures are damaged by ROS and affect membrane function is known as lipid peroxidation