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Epilepsia 25(1):S14S22 Nezu J, Tamai I, Oku A, Ohashi R, Yabuuchi H, Hashimoto N, Nikaido H, Sai Y, Koizumi A, Shoji Y, Takada G, Matsuishi T, Yoshino M, Kato H, Ohura T, Tsujimoto G, Hayakawa J, Shimane M, Tsuji A (1999) Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion dependent carnitine transporter

Latres, E., Chiaur, D

Powerful tools for the invivo investigation of local E GSH were developed in the form of redoxsensitive fluorescent proteins, rxYFP (Ostergaard et al , 2001, 2004) and the redoxsensitive green fluorescent proteins (roGFPs

The PGD gene is located on chromosome 1p36.33 and is composed of 13 exons that generate three alternatively spliced mRNAs, each of which encode different sized protein isoforms

Possibly owing to the high density of NMDA receptors, lower KynA/QA ratios have been repeatedly associated with reduced hippocampal volume and functionality in MDD, BD, and concussed athletes with depressive symptoms [118]

Doza zilnic maxim este de 10ml