Phenylalanine

phenylalanine hydroxylase ; Homo sapiens







246 Article(s)
Download
PMID
Title
Pub. Year
#Total Relationships
201 9860305 Molecular characterization of phenylketonuria in Japanese patients. 1998 Nov 1
202 9204951 Pteridines in the control of pigmentation. 1997 Jul 1
203 9380432 Analysis of phenylalanine hydroxylase genotypes and hyperphenylalaninemia phenotypes using L-[1-13C]phenylalanine oxidation rates in vivo: a pilot study. 1997 Oct 1
204 8573072 Phosphorylation of recombinant human phenylalanine hydroxylase: effect on catalytic activity, substrate activation and protection against non-specific cleavage of the fusion protein by restriction protease. 1996 Jan 15 3
205 8632937 Molecular basis of phenylketonuria and a correlation between genotype and phenotype in a heterogeneous southeastern US population. 1996 Apr 1
206 8828600 The influence of mutations of enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiency. 1996 Jul 1
207 8892014 In vivo disposal of phenylalanine in phenylketonuria: a study of two siblings. 1996 1
208 8921003 Recombinant human phenylalanine hydroxylase is a substrate for the ubiquitin-conjugating enzyme system. 1996 Nov 1 2
209 8946176 Phenylalanine hydroxylase gene mutation R408W is present on 84% of Estonian phenylketonuria chromosomes. 1996 2
210 9022714 Structure/function relationships in human phenylalanine hydroxylase. Effect of terminal deletions on the oligomerization, activation and cooperativity of substrate binding to the enzyme. 1996 Dec 15 14
211 7547912 Tryptophan fluorescence of human phenylalanine hydroxylase produced in Escherichia coli. 1995 Sep 19 1
212 7762520 Phenylalanine hydroxylase activity in preterm infants: is tyrosine a conditionally essential amino acid? 1995 Jun 3
213 7766948 Gene therapy for phenylketonuria. 1994 Dec 2
214 7967476 Severity of mutation in the phenylalanine hydroxylase gene influences phenylalanine metabolism in phenylketonuria and hyperphenylalaninaemia heterozygotes. 1994 5
215 8132651 Functional characterization of a unique liver gene promoter. 1994 Mar 25 2
216 8352282 Mutation in the 4a-carbinolamine dehydratase gene leads to mild hyperphenylalaninemia with defective cofactor metabolism. 1993 Sep 1
217 8444221 Relation between genotype and phenotype in Swedish phenylketonuria and hyperphenylalaninemia patients. 1993 Feb 2
218 1288453 [Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene]. 1992 Oct 1
219 1326329 Structural characterization of the 5' regions of the human phenylalanine hydroxylase gene. 1992 Sep 8 1
220 1355046 7-substituted pterins in humans with suspected pterin-4a-carbinolamine dehydratase deficiency. Mechanism of formation via non-enzymatic transformation from 6-substituted pterins. 1992 Aug 15 1
221 1671881 Two distinct mutations at a single BamHI site in phenylketonuria. 1991 Jan 1
222 1709636 A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuria. 1991 May 25 1
223 1867197 Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: the contribution of mutations for classical phenylketonuria. 1991 Aug 1
224 1944771 Studies on the partially uncoupled oxidation of tetrahydropterins by phenylalanine hydroxylase. 1991 Jul 1
225 2014036 Molecular basis of phenotypic heterogeneity in phenylketonuria. 1991 May 2 2
226 2069475 [High-dose methotrexate and hyperphenylalaninemia]. 1991 Apr 1
227 2220810 DNA haplotype analyses of patients with hyperphenylalaninemia. 1990 Oct 3
228 3186165 [Phenylalanine hydroxylase of human embryos: its homology with the enzyme from the liver of adults]. 1988 Jul-Aug 1
229 3326734 Enzymology of the phenylalanine-hydroxylating system. 1987 2
230 3019383 Characterization of phenylalanine hydroxylase. 1986 Jul 29 1
231 3751555 Children with inborn errors of phenylalanine metabolism: prognosis and phenylalanine tolerance. 1986 Jul 1
232 3930837 Hyperphenylalaninaemia caused by defects in biopterin metabolism. 1985 1
233 3994703 Effects of phenylalanine on phenylalanine hydroxylase separation and stability. 1985 Feb 1
234 6489353 Some aspects of the phosphorylation of phenylalanine 4-monooxygenase by a calcium-dependent and calmodulin-dependent protein kinase. 1984 Nov 15 1
235 6495818 Studies on the possible mechanism of inactivation of phenylalanine hydroxylase by destructive oxygen species. 1984 Jul-Aug 2
236 6530447 Determination of quinonoid dihydrobiopterin by liquid chromatography and electrochemical detection. 1984 Dec 28 1
237 6698976 Ligand effects on the phosphorylation state of hepatic phenylalanine hydroxylase. 1984 Feb 25 1
238 6282659 The mechanism of phenylalanine hydroxylase. 1982 Jul 1
239 7132735 The conversion of phenylalanine to tyrosine in man. Direct measurement by continuous intravenous tracer infusions of L-[ring-2H5]phenylalanine and L-[1-13C] tyrosine in the postabsorptive state. 1982 Oct 2
240 6803767 Comparative studies of four monoclonal antibodies to phenylalanine hydroxylase exhibiting different properties with respect to substrate-dependence, species-specificity and a range of effects on enzyme activity. 1981 Dec 1 1
241 221463 The activity of 2,4,5-triamino-6-hydroxypyrimidine in the phenylalanine hydroxylase system. 1979 Jun 25 1
242 511154 Genetics and biochemistry of the phenylketonuria-present state. 1979 Oct 2 1
243 624182 Loads versus tracers for assessing phenylalanine hydroxylase activity using plasma phenylalanine decay curves. 1978 Feb 15 1
244 8429 Isolation and characterization of dihydropteridine reductase from Pseudomonas species. 1976 Sep 1
245 1160969 Phenylketonuria due to a deficiency of dihydropteridine reductase. 1975 Oct 16 1
246 5686299 Phenylalanine hydroxylase activity towards two substrates simultaneously: enhancement of inhibition by phenylalanine, tryptophan and their derivatives. 1968 Aug 27 1