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Description

The concentrations of Sp and L-DOPA were kept similar for all experiments unless otherwise mentioned

Primary carnitine deficiency (PCD) is an autosomal recessive disorder characterized by a lack of plasma membrane carnitine transport owing to a shortcoming in the OCTN2 carnitine transporter

A multimag that has more than one magnesium

Foulkes, Karlsruhe Institute of Technology, Germany Received: August 13, 2012

The results have also illustrated that the protein expression of ACSL4 NOX4 and COX2 was markedly reduced, while the level of GPX4 and FTH was notably elevated in KTC-1-shFTO in comparison with that of the vector group ( Figure 7D )