Tyrosine aminotransferase isoenzyme deficiency
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference4 articles.
1. Molecular biology and molecular pathology of a newly described molecular disease—tyrosinemia type II (The Richner-Hanhart syndrome);Goldsmith;Exp Cell Biol,1978
2. Soluble and mitochondrial forms of tyrosine aminotransferase. Relationship to human tyrosinemia;Fellman;Biochemistry,1969
3. Metabolic studies in a patient with hepatic cytosol tyrosine aminotransferase deficiency;Kennaway;Pediatr Res,1971
4. Assay of tyrosine transaminase activity by conversion of P-hydroxyphenylpyruvate to P-hydroxybenzaldehyde;Diamondstone;Anal Biochem,1966
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1. Role of antioxidant treatment on DNA and lipid damage in the brain of rats subjected to a chemically induced chronic model of tyrosinemia type II;Molecular and Cellular Biochemistry;2017-05-25
2. Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects with a novel founder mutation;Clinical Genetics;2017-05-18
3. The characterization of neuroenergetic effects of chronic L-tyrosine administration in young rats: evidence for striatal susceptibility;Metabolic Brain Disease;2014-09-25
4. An Evaluation of the Effects of Acute and Chronic l-Tyrosine Administration on BDNF Levels and bdnf mRNA Expression in the Rat Brain;Molecular Neurobiology;2013-10-04
5. Acute administration of l ‐tyrosine alters energetic metabolism of hippocampus and striatum of infant rats;International Journal of Developmental Neuroscience;2013-04-16
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