| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1104304340 |
| P356 | DOI | 10.1007/S10967-018-5932-Z |
| P932 | PMC publication ID | 6061101 |
| P698 | PubMed publication ID | 30100649 |
| P50 | author | Małgorzata Pająk | Q86746047 |
| P2093 | author name string | Marianna Kańska | |
| Katarzyna Pałka | |||
| Elżbieta Winnicka | |||
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| L-Phenylalanine ammonia-lyase (maize, potato, and Rhodotorula glutinis). Studies of the prosthetic group with nitromethane | Q40315175 | ||
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| Stereochemical course of tryptophan dehydrogenation during biosynthesis of the calcium-dependent lipopeptide antibiotics. | Q42168117 | ||
| Determination of plasma Ntau-methylhistamine in vivo by isotope dilution using benchtop gas chromatography-mass spectrometry | Q42548491 | ||
| Effect of L-ascorbic acid on the monophenolase activity of tyrosinase | Q42815015 | ||
| Prospective study of p-[123I]iodo-L-phenylalanine and SPECT for the evaluation of newly diagnosed cerebral lesions: specific confirmation of glioma. | Q42949836 | ||
| Mechanistic deductions from multiple kinetic and solvent deuterium isotope effects and pH studies of pyridoxal phosphate dependent carbon-carbon lyases: Escherichia coli tryptophan indole-lyase | Q43977135 | ||
| Characterization of 3-[125I]iodo-alpha-methyl-L-tyrosine transport via human L-type amino acid transporter 1. | Q44257024 | ||
| Isotopic labelling of tryptophan and tryptophan residues in polypeptides. | Q44552950 | ||
| Stereochemistry and mechanism of reactions catalyzed by tyrosine phenol-lyase from Escherichia intermedia. | Q46659086 | ||
| Conversion of L-tyrosine to 3,4-dihydroxyphenylalanine by cell-free preparations of brain and sympathetically innervated tissues | Q46778622 | ||
| NMR confirmation that tryptophan dehydrogenation occurs with syn stereochemistry during the biosynthesis of CDA in Streptomyces coelicolor. | Q46955463 | ||
| Methylhistamine: evidence for selective deamination by MAO B in the rat brain in vivo | Q48254228 | ||
| Synthesis of no-carrier-added L- and D-[1-11C]-DOPA. | Q48710374 | ||
| Isotope effects in mechanistic studies of l-tyrosine halogen derivatives hydroxylation catalyzed by tyrosinase. | Q49163904 | ||
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| The Tyrosine Hydroxylase Activity of Mammalian Tyrosinase | Q71089062 | ||
| Selective Exchange of Nuclear Protons in Hydroxyindoles | Q71097776 | ||
| Studies of enzyme-mediated reactions. Part 12. Stereochemical course of the decarboxylation of (2S)-tyrosine to tyramine by microbial, mammalian, and plant systems | Q71494722 | ||
| Studies related to the chemistry of melanins. Part IX. Syntheses of specifically deuteriated 3,4-dihydroxyphenethylamines and (±)-3,4-dihydroxyphenylalanines | Q71555668 | ||
| Synthesis and separation of tritium-labeled intermediates of the shikimate pathway | Q71658950 | ||
| L-Phenylalanine ammonia-lyase. II. Mechanism and kinetic properties of the enzyme from potato tubers | Q72057157 | ||
| Studies of enzyme-mediated reactions. Part 13. Stereochemical course of the formation of histamine by decarboxylation of (2S)-histidine with enzymes from Clostridium welchii and Lactobacillus 30a | Q72845086 | ||
| Automatic synthesis of L-[beta-11C]amino acids using an immobilized enzyme column | Q73499743 | ||
| Development of an automated synthesis apparatus for L-[3-11C] labeled aromatic amino acids | Q73759083 | ||
| Enzymatic synthesis of isotopically labelled serine and tryptophan for application in peptide synthesis | Q73927693 | ||
| Synthesis of tritium-labelled N tau-methylhistamine for the improvement of extraction efficiency of N tau-methylhistamine from biological fluids | Q74001415 | ||
| The behavior of substrate analogues and secondary deuterium isotope effects in the phenylalanine ammonia-lyase reaction | Q77502060 | ||
| Enzymatic N-methylation of histamine | Q78564203 | ||
| Syntheses of halogen derivatives of L-tryptophan, L-tyrosine and L-phenylalanine labeled with hydrogen isotopes | Q86746049 | ||
| Mechanistic deductions from kinetic isotope effects and pH studies of pyridoxal phosphate dependent carbon-carbon lyases: Erwinia herbicola and Citrobacter freundii tyrosine phenol-lyase. | Q51185711 | ||
| Improved synthetic methods for the selective deuteration of aromatic amino acids: applications of selective protonation towards the identification of protein folding intermediates through nuclear magnetic resonance. | Q54655748 | ||
| Preliminary X-ray crystallographic analysis of tryptophanase from Escherichia coli. | Q54695495 | ||
| Tyrosine hydroxylation catalyzed by mammalian tyrosinase: An improved method of assay | Q55062096 | ||
| Nomenclature and symbolism for amino acids and peptides (Recommendations 1983) | Q55868658 | ||
| Tritium Secondary Kinetic Isotope Effect on Phenylalanine Ammonia-Lyase-Catalyzed Reaction | Q61455932 | ||
| Studies on tyrosine phenol lyase. Modification of essential histidyl residues by diethylpyrocarbonate | Q66892136 | ||
| Preparation of L-tyrosine-ring- 14 C, L-DOPA-ring- 14 C and related metabolites | Q67247313 | ||
| Synthesis of L-Tyrosine-Related Amino Acids by β-Tyrosinase | Q67335614 | ||
| Studies of enzyme-mediated reactions. Part VII. Stereospecific syntheses of tritium-labelled (2R)- and (2S)-dopamines: stereochemical course of hydroxylation of dopamine by dopamine beta-hydroxylase (E.C. 1.14.17.1) | Q67769099 | ||
| Preparation of selectively deuterated aromatic amino acids for use in 1H NMR studies of proteins | Q67861827 | ||
| Routine synthesis of carbon-11-carboxyl-labeled L-dopa | Q69402270 | ||
| Studies of enzyme-mediated reactions. I. Syntheses of deuterium- or tritium-labelled (3S)-and (3R)-phenylalanines: stereochemical course of the elimination catalysed by L-phenylalanine ammonia-lyase | Q69454719 | ||
| Studies of enzyme-mediated reactions. II. Stereochemistry of the elimination of ammonia from L-tyrosine catalysed by the enzyme from maize | Q69454722 | ||
| Stereochemical probes of bovine plasma amine oxidase: evidence for mirror image processing and a syn abstraction of hydrogens from C-1 and C-2 of dopamine | Q69685088 | ||
| Stereospecific deuterium substitution at the alpha-carbon position of dopamine and its effect on oxidative deamination catalyzed by MAO-A and MAO-B from different tissues | Q70026154 | ||
| Biosynthetic production of 13C-labeled amino acids with site-specific enrichment | Q70214206 | ||
| Optimization of hydroxylation of tyrosine and tyrosine-containing peptides by mushroom tyrosinase | Q70297956 | ||
| Aromatic-L-amino acid decarboxylase | Q70345797 | ||
| , '- and , '-deuterium-labeled dopamine. Synthesis and pharmacologic actions | Q70418939 | ||
| Mechanism of dopamine-beta-hydroxylation. Semidehydroascorbate as the enzyme oxidation product of ascorbate | Q70541570 | ||
| The Shikimate pathway. Part III. The stereochemical course of the L-phenylalanine ammonia lyase reaction | Q70733981 | ||
| Syntheses of l‐Tyrosine‐Related Amino Acids by Tyrosine Phenol‐lyase of Citrobacter intermedius | Q70870602 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 2 | |
| P304 | page(s) | 643-666 | |
| P577 | publication date | 2018-05-30 | |
| P1433 | published in | Journal of Radioanalytical and Nuclear Chemistry | Q3186940 |
| P1476 | title | The chemo- enzymatic synthesis of labeled l-amino acids and some of their derivatives | |
| P478 | volume | 317 |
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