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Its documented interaction with over 4,000 human genes as suggested by some genomic profiling research makes it a versatile tool for exploratory and hypothesis-driven studies alike

The association between LC supplementation and the regulation of metabolic pathways involved in muscle protein balance have been shown in several animal studies (Fig

Homozygous and mutated SLC19A3 gene can cause various conditions such as biotin-thiamine responsive basal ganglia disease (BTBGD), lactic acidosis combined with encephalopathy, infantile epileptic spasms, and early childhood encephalopathy induced by disease or trauma

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Comparing initial CMR imaging to 24 months demonstrated improvement in LVEF and RVEF from 40% to 66% and 41% to 64%, respectively, with normalized ventricular volumes and mass