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searching for Phenylalanine hydroxylase 18 found (169 total)

alternate case: phenylalanine hydroxylase

PCBD1 (1,069 words) [view diff] exact match in snippet view article find links to article

B, Neuheiser F, Curtius HC, Hunziker P, et al. (March 1993). "Phenylalanine hydroxylase-stimulating protein/pterin-4 alpha-carbinolamine dehydratase from
6,7-dihydropteridine reductase (512 words) [view diff] exact match in snippet view article find links to article
1093/oxfordjournals.jbchem.a131432. PMID 191436. Kaufman S (1962). "Phenylalanine hydroxylase". Methods Enzymol. 5: 809–816. doi:10.1016/s0076-6879(62)05317-3
Outline of biochemistry (703 words) [view diff] exact match in snippet view article find links to article
disorder in which the individual is missing an enzyme called phenylalanine hydroxylase. Absence of this enzyme allows the buildup of phenylalanine, which
List of medical abbreviations: P (66 words) [view diff] exact match in snippet view article find links to article
(meaning intermittent AF) PAH pulmonary arterial hypertension phenylalanine hydroxylase PAI-1 plasminogen activator inhibitor-1 PAL posterior axillary
Tyrosine hydroxylase deficiency (727 words) [view diff] exact match in snippet view article find links to article
3-methoxy-4-hydroxyphenylethylene glycol; NMN, normetanephrine; PAH, phenylalanine hydroxylase; PLP, pyridoxal phosphate; PNMT, phenylethanolamine N-methyltransferase;
4a-hydroxytetrahydrobiopterin dehydratase (136 words) [view diff] exact match in snippet view article find links to article
1DCO, 1DCP, and 1RU0. Blau N, Ghisla S, Heizmann CW (1993). "Phenylalanine hydroxylase-stimulating protein/pterin-4 alpha-carbinolamine dehydratase from
Pterin (1,075 words) [view diff] exact match in snippet view article find links to article
effect hydroxylation. The aromatic amino acid hydroxylases include phenylalanine hydroxylase, tyrosine hydroxylase, and tryptophan hydroxylases. They are involved
Richard Cotton (geneticist) (2,041 words) [view diff] exact match in snippet view article
executing myeloma studies, conceiving affinity adsorbents for PAH (phenylalanine hydroxylase, the enzyme deficient in PKU) & DHPR (di-hydro-folate reductase
Compound heterozygosity (1,243 words) [view diff] exact match in snippet view article find links to article
1966). "Atypical phenylketonuric heterozygote. Deficiency in phenylalanine hydroxylase and transaminase activity". Journal of Pediatrics. 68 (3): 351–360
6-Pyruvoyltetrahydropterin synthase deficiency (1,336 words) [view diff] case mismatch in snippet view article find links to article
PMID 21949628. Regier, Debra S; Greene, Carol L (January 5, 2017). "Phenylalanine Hydroxylase Deficiency". University of Washington, Seattle. PMID 20301677
ASCL1 (1,566 words) [view diff] exact match in snippet view article find links to article
"Localization of the human achaete-scute homolog gene (ASCL1) distal to phenylalanine hydroxylase (PAH) and proximal to tumor rejection antigen (TRA1) on chromosome
List of diseases (P) (1,908 words) [view diff] exact match in snippet view article
sulfotransferase deficiency Phenothiazine antenatal infection Phenylalanine hydroxylase deficiency Phenylalaninemia Phenylketonuria type II Phenylketonuria
Newborn Screening Saves Lives Reauthorization Act of 2013 (1,505 words) [view diff] exact match in snippet view article find links to article
S2CID 19949842. Mitchell, J. J.; Trakadis, Y. J.; Scriver, C. R. (2011). "Phenylalanine hydroxylase deficiency". Genetics in Medicine. 13 (8): 697–707. doi:10.1097/GIM
4-hydroxyphenylpyruvate dioxygenase inhibitor (3,373 words) [view diff] exact match in snippet view article find links to article
, Ohno, M., Takeuchi,T. and Umezawa,H. (1982). Inhibition of phenylalanine hydroxylase, a pterin-requiring monooxygenase, by ouudenone and its derivatives
Mescaline (4,803 words) [view diff] exact match in snippet view article find links to article
tyrosine which, in turn, is derived from phenylalanine by the enzyme phenylalanine hydroxylase. In Lophophora williamsii (Peyote), dopamine converts into mescaline
Andrea Superti-Furga (2,272 words) [view diff] exact match in snippet view article find links to article
unrecognized phenylketonuria in their mothers homozygous for the phenylalanine hydroxylase Arg-261-Gln mutation". European Journal of Pediatrics. 150 (7):
Rhesus macaque (9,078 words) [view diff] exact match in snippet view article find links to article
profound disease in humans. For example, the normal sequence of phenylalanine hydroxylase in macaques and chimpanzees is the mutated sequence responsible
Newborn screening (7,686 words) [view diff] exact match in snippet view article find links to article
PMID 21689452. Mitchell JJ, Trakadis YJ, Scriver CR (2011). "Phenylalanine hydroxylase deficiency". Genetics in Medicine. 13 (8): 697–707. doi:10.1097/GIM