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Phenylalanine
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31	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
32	Prooxidative effects of aspartame on antioxidant defense status in erythrocytes of rats MARKO D PROKIĆ1 , MILICA G PAUNOVIĆ2 , MILOŠ M MATIĆ2 , NATAŠA Z DJORDJEVIĆ3 , BRANKA I OGNJANOVIĆ2,* , ANDRAŠ Š ŠTAJN2 an Add to Reading List Source URL: www.ias.ac.in Language: English - Date: 2014-11-12 00:51:10 Superoxide dismutase Oxidative stress Reactive oxygen species Red blood cell Glutathione Neurotoxicity Aspartame Phenylalanine Sugar substitute Chemistry Biology Antioxidants
33	AR1113[removed]ARKANSAS INDIVIDUAL INCOME TAX CLICK HERE TO CLEAR FORM Add to Reading List Source URL: www.dfa.arkansas.gov Language: English - Date: 2014-12-11 12:27:55 Tax credits Organic chemistry Income tax in the United States Galactosemia PKU Phenylalanine Health Chemistry Mental retardation Phenylketonuria
34	file:///C:/Users/jhook/AppData/Local/Temp/RELMA_2_41_DEVELOPER_ Add to Reading List Source URL: loinc.org Language: English - Date: 2013-07-01 14:33:23 Hematology Pediatrics Analytical chemistry Transfusion medicine Dried blood spot Newborn screening Hemoglobin Phenylalanine Blood transfusion Chemistry Medicine Health
35	Phenylketonuria (PKU) What is Phenylketonuria? Phenylketonuria (also known as PKU) is an inherited condition that affects the way a person’s body uses protein. A person with PKU cannot use a component of protein called Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:48:27 Mental retardation Phenylketonuria PKU Phenylalanine Dominance Hyperphenylalanemia Medical genetics Newborn screening Tetrahydrobiopterin deficiency Medicine Health Biology
36	Microsoft Word - Amino_Acidemias.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:35:52 Medical genetics Maple syrup urine disease Glycine encephalopathy Newborn screening Phenylketonuria Amino acid Phenylalanine Organic acidemia Propionic acidemia Health Rare diseases Genetic genealogy
37	Phenylketonuria (PKU) Jewell C. Ward, MD, Ph D, Chief, Division of Medical Genetics Department of Pediatrics University of Tennessee-Memphis 711 Jefferson, CDD, Room 522 Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2006-10-30 12:01:41 Mental retardation Phenylketonuria Aromatic amino acids Glucogenic amino acids Ketogenic amino acids Proteinogenic amino acids Hyperphenylalanemia Phenylalanine racemase Medicine Health Chemistry
38	For more information about the Organization of Teratology Information Specialists Add to Reading List Source URL: www.mothertobaby.org Language: English - Date: 2014-09-16 15:48:58 Coenzymes Pteridines Mental retardation Phenylketonuria Hyperphenylalanemia Infant feeding Tetrahydrobiopterin PKU Phenylalanine Health Chemistry Medicine
39	Postharvest Biology and Technology[removed] /193 www.elsevier.com/locate/postharvbio Relationship between browning and the activities of polyphenol oxidase and phenylalanine ammonia lyase in banana peel during low Add to Reading List Source URL: kukr.lib.ku.ac.th Language: English - Date: 2008-06-25 23:16:31 Chemistry Polyphenol oxidase Gros Michel banana Polyphenol Browning Banana Cavendish banana Phenylalanine ammonia-lyase Musa Banana cultivars Food and drink Agriculture
40	http://www.greenfacts.org/ Copyright © GreenFacts Scientific Facts on Add to Reading List Source URL: www.greenfacts.org Language: English - Date: 2014-11-26 05:40:26 Food and drink Aspartame Sugar substitute Phenylalanine GreenFacts Diet soda Canderel Sweetness Acceptable daily intake Chemistry Sweeteners Organic chemistry