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Additional nanoformulations including supramolecular self-assembled structures, proteins, peptides, metal-organic frameworks, and coordination polymers will then be described
[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
Biochem Biophys Res Commun 373(2):246252 You M et al (2015) Sirtuin 1 signaling and alcoholic fatty liver disease
Human stem cell models of neurodegeneration: from basic science of amyotrophic lateral sclerosis to clinical translation
[DOI] [PubMed] [Google Scholar] 16.Bandeira L, Silva BC, Bilezikian JP
Article 18
