l-carnitine for autistic children Unique acyl-carnitine profiles are potential biomarkers acquired mitochondrial disease in autism spectrum disorder Biomarkers of mitochondrial dysfunction in

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The glutathione cycle can complement the glutamate-glutamine shuttle and influence excitatory neurotransmission under conditions of glutamine restriction The glutamate-glutamine shuttle (Fig

In basal-like breast tumors, LSD2 expression is higher compared with other breast cancer subtypes or normal breast tissue

Keywords: Urea cycle disorders, UCD, Hyperammonemia, N-acetylglutamate synthase, Carbamoylphosphate synthetase 1, Ornithine transcarbamylase, Ornithine carbamoyl transferase, Argininosuccinate synthetase, Argininosuccinate lyase, Arginase 1, Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Introduction Urea cycle disorders (UCDs) are inborn errors of nitrogen detoxification/arginine synthesis due to defects in the urea cycle enzymes (Figure 1), carbamoylphosphate synthetase 1 (CPS1), ornithine transcarbamylase (OTC), argininosuccinate synthetase (ASS), argininosuccinate lyase (ASL) and arginase 1 (ARG1), leading to respective deficiencies (abbreviated CPS1D, OTCD, ASSD, ASLD and ARG1D

Sci Rep 7(1):114

Zhu AK, Shan YQ, Zhang J, Liu XC, Ying RC, Kong WC (2021) Exosomal NNMT from peritoneum lavage fluid promotes peritoneal metastasis in gastric cancer