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SHANK3 mutations are likely to cause mitochondrial dysfunction in PMS because six mitochondrial genes, including NADH dehydrogenase 1 alpha subcomplex subunit 6 (NDUFA6 ), cytochrome c oxidase assembly ( SCO2 ), tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase ( TRMU ), thymidine phosphorylase ( TYMP ), carnitine palmitoyltransferase 1B ( CPT1B ), and aconitase 2 ( ACO2 ), are adjacent to SHANK3 in the 22q13.3 region [339]

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parent compound to identify the bioactivity reason of HTY

Superoxide release and cellular gluthatione peroxidase activity in leukocytes from children with persistent asthma

Astrocytes phagocytose adult hippocampal synapses for circuit homeostasis

Current research does not justify a guaranteed human hair-regrowth claim for a cosmetic copper peptide product