Tyrosine impairs enzymes of energy metabolism in cerebral cortex of rats

Author:

de Andrade Rodrigo Binkowski,Gemelli Tanise,Rojas Denise Bertin,Funchal Cláudia,Dutra-Filho Carlos Severo,Wannmacher Clovis Milton Duval

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,General Medicine

Reference50 articles.

1. Natt E, Westphal EM, Toth-Fejel SE, Magenis RE, Buist NR, Rettenmeier R, Scherer G (1987) Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1–q22.3 in a patient with tyrosinemia type II. Hum Genet 77:352–358

2. Scott CR (2006) The genetic tyrosinemias. Am J Med Genet Part C 142C:121–126

3. Buist NR, Kennaway NG, Fellman JH (1995) Tyrosinaemia type II. In: Bickel H, Wachtel V (eds) Inherited diseases of aminoacid metabolism, 1st edn. Georg Thieme Verlag, Stuttgart, pp 203–235

4. Rice DN, Houston IB, Lyon IC, Macarthur BA, Mullins PR, Veale AM, Guthrie R (1989) Transient neonatal tyrosinaemia. Inherit Metab Dis 12:13–22

5. Shasi VK, Pratap RMP, Rao SL (1997) Inhibition of tyrosine aminotransferase by beta-N-oxalyl-l-alpha, beta-diaminopropionic acid, the Lathyrus sativus neurotoxin. J Neurochem 68:2477–2484

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