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1
المؤلفون: Sankar Surendran, Reuben Matalon, Stephen K. Tyring
المصدر: Neurochemistry International. 46:595-599
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Phenylalanine hydroxylase, Sialoglycoproteins, Central nervous system, Vesicular Transport Proteins, Down-Regulation, Gene Expression, Nerve Tissue Proteins, Phenylalanine, Biology, Mice, Cellular and Molecular Neuroscience, Phenylketonurias, Internal medicine, Gene expression, medicine, Animals, RNA, Messenger, Phenylketonuria (PKU), Oligonucleotide Array Sequence Analysis, Calpastatin, Gene Expression Profiling, Calcium-Binding Proteins, Wild type, Brain, Membrane Proteins, Proteins, nutritional and metabolic diseases, Cell Biology, medicine.disease, Mice, Mutant Strains, Up-Regulation, Disease Models, Animal, Endocrinology, medicine.anatomical_structure, biology.protein, Intercellular Signaling Peptides and Proteins, Osteopontin, Neuronatin, Cognition Disorders
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2
المؤلفون: Kimberlee Michals-Matalon, Lisbeth Birk Møller, Sankar Surendran, Reuben Matalon, Heidi Erlandsen, Anne Romstad, Alejandra Gámez, Raymond C. Stevens, Stephen K. Tyring, Kathryn Moseley, Richard Koch, Flemming Güttler
المصدر: Genetics in Medicine. 6:27-32
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Phenylalanine hydroxylase, Phenylketonurias, Phenylalanine, DNA Mutational Analysis, Administration, Oral, Biopterin, chemistry.chemical_compound, Internal medicine, medicine, Humans, Tyrosine, Child, Gene, Genetics (clinical), chemistry.chemical_classification, biology, business.industry, Infant, Tetrahydrobiopterin, Endocrinology, Enzyme, Biochemistry, chemistry, Child, Preschool, biology.protein, Female, business, medicine.drug
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3
المؤلفون: Reuben Matalon, Sankar Surendran, Michael J. Quast, Kimberlee Michals Matalon, Stephen K. Tyring, Sylvia Szucs, Edward L. Ezell, Wei Jinga
المصدر: Pediatrics. 112:1570-1574
مصطلحات موضوعية: chemistry.chemical_classification, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Normal diet, Dose, business.industry, Ratón, Central nervous system, nutritional and metabolic diseases, Phenylalanine, Cerebro, Blood–brain barrier, Amino acid, medicine.anatomical_structure, Endocrinology, chemistry, Internal medicine, Pediatrics, Perinatology and Child Health, Medicine, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c5cccc4b23568e1696027a0e1a7e2688
https://doi.org/10.1542/peds.112.s4.1570 -
4
المؤلفون: Gopalrao V.N. Velagaleti, Reuben Matalon, Dena Matalon, Sankar Surendran, Stephen K. Tyring, Peter L. Rady
المصدر: Neuroscience letters. 382(3)
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Phenylalanine hydroxylase, Microarray, Phenylketonurias, Blotting, Western, Gene Expression, Phenylalanine, Mice, Internal medicine, Gene expression, medicine, Animals, Phenylketonuria (PKU), RNA, Messenger, Eye Proteins, Myocilin, Glycoproteins, Oligonucleotide Array Sequence Analysis, biology, Microarray analysis techniques, Reverse Transcriptase Polymerase Chain Reaction, General Neuroscience, nutritional and metabolic diseases, Brain, Phenylalanine Hydroxylase, medicine.disease, Cytoskeletal Proteins, Disease Models, Animal, Endocrinology, Gene Expression Regulation, biology.protein
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5
المؤلفون: Raymond C. Stevens, Stephen K. Tyring, Sankar Surendran, Heidi Erlandsen, Woomi Kim, Reuben Matalon, Alejandra Gámez, Kimberlee Michols-Matalon
المصدر: Molecular therapy : the journal of the American Society of Gene Therapy. 10(2)
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Phenylalanine hydroxylase, Phenylalanine, Capsules, Phenylalanine ammonia-lyase, Bioinformatics, Polyethylene Glycols, Drug Therapy, Internal medicine, Phenylketonurias, Drug Discovery, Genetics, medicine, Enzyme therapy, Humans, Amino acid metabolism, Molecular Biology, Phenylalanine Ammonia-Lyase, Pharmacology, biology, business.industry, nutritional and metabolic diseases, Phenylalanine Hydroxylase, Enzyme replacement therapy, Biopterin, Endocrinology, Dietary treatment, biology.protein, Molecular Medicine, business
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6
المؤلفون: Peter L. Rady, Stephen K. Tyring, Kimberlee Michals-Matalon, Sankar Surendran, Reuben Matalon, Sylvia Szucs
المصدر: Biochemical and biophysical research communications. 317(2)
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Lateral hypothalamus, Phenylalanine, Biophysics, Neuropeptide, Glutamic Acid, Biology, Biochemistry, Orexin-A, Mice, Internal medicine, Phenylketonurias, mental disorders, medicine, Animals, Molecular Biology, gamma-Aminobutyric Acid, Oligonucleotide Array Sequence Analysis, Messenger RNA, Orexins, Microarray analysis techniques, Gene Expression Profiling, Neuropeptides, Glutamate receptor, Intracellular Signaling Peptides and Proteins, nutritional and metabolic diseases, Brain, Cell Biology, Orexin, Endocrinology, nervous system, Gene Expression Regulation, Carrier Proteins, hormones, hormone substitutes, and hormone antagonists, Signal Transduction
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7
المؤلفون: Reuben, Matalon, Sankar, Surendran, Kimberlee Michals, Matalon, Stephen, Tyring, Michael, Quast, Wei, Jinga, Edward, Ezell, Sylvia, Szucs
المصدر: Pediatrics. 112(6 Pt 2)
مصطلحات موضوعية: Disease Models, Animal, Mice, Amino Acids, Neutral, Blood-Brain Barrier, Phenylalanine, Phenylketonurias, Animals, Brain, Biological Transport, Energy Metabolism, Mice, Mutant Strains
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::292d764f009215d32e7a41a362e87031
https://pubmed.ncbi.nlm.nih.gov/14654667