Peer review Peer review information Nature Reviews Endocrinology thanks Michael Pollak and the other, anonymous, reviewer(s) for their contribution to the peer review of this work
[3] In humans, defects in GSS are inherited in an autosomal recessive way and are the cause of severe metabolic acidosis, 5-oxoprolinuria, increased rate of haemolysis, and defective function of the central nervous system
References NASA Exoplanet Archive
We also discuss science-based tools to preserve cognitive function, reduce dementia risk, and offset loss of memory after a concussion or other brain injury
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MOTS-c is a mitochondrial-derived peptide with AMPK-linked signaling, and AOD-9604 is a GH-fragment-derived lipolysis compound