Find link

language:

Find link is a tool written by Edward Betts.

searching for Phenylalanine hydroxylase 22 found (198 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

Cyromazine (484 words) [view diff] exact match in snippet view article find links to article

target mechanisms of the growth inhibitor cyromazine: Studies of phenylalanine hydroxylase, puparial amino acids, and dihydrofolate reductase in dipteran

6,7-dihydropteridine reductase (528 words) [view diff] exact match in snippet view article find links to article

1093/oxfordjournals.jbchem.a131432. PMID 191436. Kaufman S (1962). "Phenylalanine hydroxylase: TPNH + H+ + phenylalanine + O2 → TPN+ + H2O + tyrosine". Methods

Our Fragile Intellect (2,116 words) [view diff] exact match in snippet view article find links to article

genes may not even be expressed in the brain. For example, the phenylalanine hydroxylase gene is expressed only in the liver, yet its mutation leads to

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

Chromosome 12 (1,843 words) [view diff] exact match in snippet view article find links to article

enzyme Diphosphoinositol polyphosphate phosphohydrolase 2 PAH: phenylalanine hydroxylase PIP4K2C: encoding protein Phosphatidylinositol-5-phosphate 4-kinase

4a-hydroxytetrahydrobiopterin dehydratase (144 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

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

Pterin (1,076 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

Pterin (1,076 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

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

Tyrosine hydroxylase deficiency (748 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;

Compound heterozygosity (1,252 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

ASCL1 (1,570 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 (1,500 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 (3,403 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 (6,055 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 (2,269 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 (8,557 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 (7,844 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