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Tyrosine hydroxylase
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#	Item
11	Exercise-induced Pgc-1α Expression does not Lower mtDNA Point Mutation Levels but Downregulates Tyrosine hydroxylase Expression in the Striatum Zera Ong Raffles Institution (Junior College), Singapore, Singapore Under t Add to Reading List Source URL: www.cee.org Language: English - Date: 2012-12-20 11:28:38 Mitochondrial DNA Mitochondrial biogenesis POLG Mitochondrion Mutation Senescence FGF21 Human mitochondrial genetics Biology DNA Aging
12	Phenylketonuria (PKU) Phenylketonuria is a genetic disorder that is characterized by a person’s inability to utilize the essential amino acid, phenylalanine. A person with PKU lacks the enzyme phenylalanine hydroxylase Add to Reading List Source URL: www.sde.idaho.gov Language: English - Date: 2009-03-18 18:56:23 Glucogenic amino acids Ketogenic amino acids Proteinogenic amino acids Mental retardation Phenylketonuria Phenylalanine Aspartame Tyrosine Protein Chemistry Organic chemistry Aromatic amino acids
13	Insciences J. 2013, 3(1), 1-23; doi: [removed]insc[removed]ISSN 1664-171X Review Paper Add to Reading List Source URL: journal.insciences.org Language: English - Date: 2013-04-25 10:42:14 Glucogenic amino acids Ketogenic amino acids Proteinogenic amino acids Electroanalytical methods Tyrosinase Biosensor Tyrosine L-DOPA Phenylalanine hydroxylase Chemistry Organic chemistry Aromatic amino acids
14	NIH Public Access Author Manuscript J Nutr. Author manuscript; available in PMC 2008 March 17. Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Aromatic amino acids Ketogenic amino acids Proteinogenic amino acids Phenols Phenylalanine hydroxylase Phenylketonuria Tyrosine Phenylalanine Protein Chemistry Organic chemistry Glucogenic amino acids
15	Review Article 1 Add to Reading List Source URL: memo.cgu.edu.tw Language: English - Date: 2009-09-14 05:13:58 Chemistry Dystonia Movement disorder Torsion dystonia GTP cyclohydrolase I Tyrosine hydroxylase Tetrahydrobiopterin Chromosome 14 L-DOPA Neurological disorders Medicine Health

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