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5-Oxoprolinase deficiency Disease name 5-Oxoprolinase deficiency (OMIM 260005) Definition and diagnostic criteria 5-Oxoprolinase deficiency is a very rare autosomal recessive disease characterized by 5-oxoprolinuria and very heterogeneous clinical presentation (renal stone formation, enterocolitis, mental retardation, neonatal hypoglycemia, microcytic anemia and microcephaly)

is supported by NIH P01 CA244118 and Melanoma Research Alliance 691165

Performance and endurance related cellular markers examined in laboratory energy regulation research

In Vitro vs In Vivo Applications IGF-1 LR3 is particularly well suited for cell culture work