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Hepatic tyrosine aminotransferase in tyrosinaemia type II. 1982

K Kida, and M Takahashi, and Y Fujisawa, and H Matsuda, and H Machino, and Y Miki

UI MeSH Term Description Entries
D008099 Liver A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. Livers
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000592 Amino Acid Metabolism, Inborn Errors Disorders affecting amino acid metabolism. The majority of these disorders are inherited and present in the neonatal period with metabolic disturbances (e.g., ACIDOSIS) and neurologic manifestations. They are present at birth, although they may not become symptomatic until later in life. Amino Acidopathies, Congenital,Amino Acid Metabolism Disorders, Inborn,Amino Acid Metabolism, Inborn Error,Amino Acid Metabolism, Inherited Disorders,Amino Acidopathies, Inborn,Congenital Amino Acidopathies,Inborn Errors, Amino Acid Metabolism,Inherited Errors of Amino Acid Metabolism,Amino Acidopathy, Congenital,Amino Acidopathy, Inborn,Congenital Amino Acidopathy,Inborn Amino Acidopathies,Inborn Amino Acidopathy
D014443 Tyrosine A non-essential amino acid. In animals it is synthesized from PHENYLALANINE. It is also the precursor of EPINEPHRINE; THYROID HORMONES; and melanin. L-Tyrosine,Tyrosine, L-isomer,para-Tyrosine,L Tyrosine,Tyrosine, L isomer,para Tyrosine
D014444 Tyrosine Transaminase An enzyme that catalyzes the conversion of L-TYROSINE and 2-oxoglutarate to 4-hydroxyphenylpyruvate and L-GLUTAMATE. It is a pyridoxal-phosphate protein. L-PHENYLALANINE is hydroxylated to L-tyrosine. The mitochondrial enzyme may be identical with ASPARTATE AMINOTRANSFERASES (EC 2.6.1.1.). Deficiency of this enzyme may cause type II Tyrosinemia (see TYROSINEMIAS). EC 2.6.1.5. Tyrosine Aminotransferase,Aminotransferase, Tyrosine,Transaminase, Tyrosine
D015111 4-Hydroxyphenylpyruvate Dioxygenase An enzyme that catalyzes the conversion of 4-hydroxyphenylpyruvate plus oxygen to homogentisic acid and carbon dioxide. EC 1.13.11.27. P-Hydroxyphenylpyruvate Hydroxylase,P-Hydroxyphenylpyruvate Oxidase,para-Hydroxyphenylpyruvate Hydroxylase,para-Hydroxyphenylpyruvate Oxidase,Dioxygenase, 4-Hydroxyphenylpyruvate,Hydroxylase, P-Hydroxyphenylpyruvate,Hydroxylase, para-Hydroxyphenylpyruvate,Oxidase, P-Hydroxyphenylpyruvate,Oxidase, para-Hydroxyphenylpyruvate,P Hydroxyphenylpyruvate Hydroxylase,P Hydroxyphenylpyruvate Oxidase,para Hydroxyphenylpyruvate Hydroxylase,para Hydroxyphenylpyruvate Oxidase

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