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1 that of the core of the regulatory domain of phenylalanine hydroxylase.
2 tor of the tetrahydropterin-dependent enzyme phenylalanine hydroxylase.
3 ss-react with either tyrosine hydroxylase or phenylalanine hydroxylase.
4 ormality in the function of the liver enzyme phenylalanine hydroxylase.
5 ading to competitive inhibition of epidermal phenylalanine hydroxylase.
6 h(enu2) mice have a mutation in the gene for phenylalanine hydroxylase.
7 ving, in most cases, a deficient activity of phenylalanine hydroxylase.
8 droxylase and the 122 N-terminal residues of phenylalanine hydroxylase.
10 th high levels of 6BH4, and the induction of phenylalanine hydroxylase activities during the telogen/
11 phenylalanine concentrations and we measured phenylalanine hydroxylase activity and phenylalanine int
13 kinetic properties of pure recombinant human phenylalanine hydroxylase and on estimates of the in viv
14 mutations were incorporated into full-length phenylalanine hydroxylase and the complementary mutation
16 1 containing the C-terminal 331 residues of phenylalanine hydroxylase and the N-terminal 168 residue
17 ytic domains of the pterin-dependent enzymes phenylalanine hydroxylase and tyrosine hydroxylase are h
18 ordinates of two highly homologous proteins, phenylalanine hydroxylase and tyrosine hydroxylase, were
19 id hydroxylase family--tyrosine hydroxylase, phenylalanine hydroxylase, and tryptophan hydroxylase--r
20 tyrosine hydroxylase and of tyrosine 325 of phenylalanine hydroxylase are 5 and 4.5 A, respectively,
21 romatic amino acid hydroxylases tyrosine and phenylalanine hydroxylase both contain non-heme iron, ut
24 very pronounced asymmetry is observed in the phenylalanine hydroxylase, caused by the occurrence of t
25 hydroxylase locus using a full-length human phenylalanine hydroxylase cDNA clone as a hybridization
26 e site-specific genome integration of murine phenylalanine hydroxylase cDNA in the livers of phenylke
27 phage integration system, we delivered mouse phenylalanine hydroxylase cDNA to the livers of PKU mice
30 e of the divergent Chromobacterium violaceum phenylalanine hydroxylase (CvPheOH) ( approximately 24%
32 H, the C-terminal 336 amino acid residues of phenylalanine hydroxylase; Delta155TYH, the C-terminal 3
33 induced by the inclusion of an inhibitor of phenylalanine hydroxylase, DL-p-chlorophenylalanine, and
43 ne such interaction involves Tyr325 in human phenylalanine hydroxylase (hPAH), which forms a hydrogen
44 utations on the isolated catalytic domain of phenylalanine hydroxylase identified three residues that
46 he position corresponding to position 379 of phenylalanine hydroxylase is critical for dihydroxypheny
48 restriction site polymorphisms at the human phenylalanine hydroxylase locus among Caucasians are suc
49 ymorphisms have been identified at the human phenylalanine hydroxylase locus using a full-length huma
51 cture, dynamics, and function for the enzyme phenylalanine hydroxylase (PAH) can lead to needed new t
54 ave previously shown that the Fe(II) site in phenylalanine hydroxylase (PAH) converts from six-coordi
56 enylketonuria patients harboring a subset of phenylalanine hydroxylase (PAH) mutations have recently
57 -chain amino-acid transaminase 1 (BCAT1) and phenylalanine hydroxylase (PAH) with development of IFG.
58 th HPA harbor mutations in the gene encoding phenylalanine hydroxylase (PAH), and a small proportion
59 , inducible nitric oxide synthase (iNOS) and phenylalanine hydroxylase (PAH), and competition for BH4
60 Activated phenylalanine 4-monooxygenase, phenylalanine hydroxylase (PAH), is known to be involved
61 umans that arises from deficient activity of phenylalanine hydroxylase (PAH), which catalyzes the con
66 enase, the neural cell adhesion molecule L1, phenylalanine hydroxylase, paired box 6, the X-linked re
72 tyrosine hydroxylase (TyrH) whose homolog in phenylalanine hydroxylase (PheH) takes on a different co
75 ry dehydratase, together with genes encoding phenylalanine hydroxylase (PhhA) and aromatic aminotrans
76 i and is hypothesized to be the cofactor for phenylalanine hydroxylase (PhhA) in Pseudomonas aerugino
77 ssess a cluster of structural genes encoding phenylalanine hydroxylase (PhhA), carbinolamine dehydrat
82 rited disease caused by impaired activity of phenylalanine hydroxylase, the enzyme that converts phen
83 mutation of the corresponding valine 379 of phenylalanine hydroxylase to aspartate was not sufficien
84 ase to aspartate was not sufficient to allow phenylalanine hydroxylase to form dihydroxyphenylalanine
87 the family of pterin-dependent hydroxylases, phenylalanine hydroxylase, tyrosine hydroxylase, and try
88 uncated and chimeric mutants of tyrosine and phenylalanine hydroxylase were constructed: Delta117PAH,
89 proteins containing the catalytic domain of phenylalanine hydroxylase were unable to hydroxylate tyr
90 ficity, seven residues in the active site of phenylalanine hydroxylase whose side chains are dissimil
91 f a recombinant adeno-associated virus-mouse phenylalanine hydroxylase-woodchuck hepatitis virus post
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