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These findings further support ASTs capacity to protect neural tissue under severe inflammatory and oxidative conditions

The Cell: Organelles Reduced amount of CPG III oxidase Oxidase Neisseria leads to hereditary coproporphyria Hereditary coproporphyria An autosomal dominant porphyria that is due to a deficiency of coproporphyrinogen oxidase in the liver, the sixth enzyme in the 8-enzyme biosynthetic pathway of heme

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113,114 Early stages of CAN may be asymptomatic and detectable only through reduced heart rate variability (HRV) during deep breathing

[DOI] [PMC free article] [PubMed] [Google Scholar] ElDesoky, N

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