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Published in 2018 at "Journal of Cellular Physiology"
DOI: 10.1002/jcp.26177
Abstract: Mitochondrial 3‐hydroxy‐3‐methylglutaryl‐CoA (HMG‐CoA) synthase (HMGCS2) catalyses the first step of ketogenesis and is critical in various metabolic conditions. Several nutrient molecules were able to differentially modulate HMGCS2 expression levels. Docosahexaenoic acid (DHA, C22:6, n‐3), eicosapentaenoic…
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Keywords:
mitochondrial hydroxy;
hydroxy methylglutaryl;
expression;
coa ... See more keywords
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Published in 2022 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2021.816779
Abstract: Background: Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency (HMGCS2D) is a rare autosomal recessive metabolic disorder caused by mutations of the HMGCS2 gene. To date, no more than 60 patients have been reported throughout the world. Purpose: To…
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Keywords:
synthase deficiency;
methylglutaryl coa;
mitochondrial hydroxy;
chinese patients ... See more keywords