l-carnitine for autistic children Unique acyl-carnitine profiles are potential biomarkers acquired mitochondrial disease in autism spectrum disorder Healthy - A review published

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

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

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

Nighot M, Liao P-L, Morris N et al (2022) Long term use of proton pump inhibitor disrupts intestinal tight junction barrier and exaggerates experimental colitis

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