A simple, rapid, and economical method is reported for the determination of 3,4-dihydroxyphenylalanine, tyrosine, 4-hydroxyphenyllactic acid, 4-hydroxyphenylacetic acid, 4-hydroxyphenethylamine, and 3-(4-hydroxyphenyl)propionic acid in human serum by ultra-performance liquid chromatography coupled with fluorescence detection. Separation was achieved on a C-18 column with isocratic elution using 95:5 (v/v) 50mM ammonium formate buffer at pH 5.8 and acetonitrile. Fluorescence detection was performed with excitation and emission wavelengths of 277 and 316nm, respectively. Under the optimized conditions, all compounds were eluted within 10min. The effectiveness of various protein precipitants was investigated for the pretreatment of serum sampl...
We describe a method for determining those urinary total phenolic compounds that are tyrosine analog...
For screening early-stage gastric malignancies, the existing serum biomarkers have limited sensitivi...
Tyrosine plays a key role in mammalian biochemistry and defects in its metabolism (e.g., tyrosinemia...
In this paper, a fast and reliable method was developed for simultaneous quantification of tyrosine,...
Human serum contains resolved materials of protein and these resolution shows one section of protein...
A new enzymatic method for rapid direct measurement of serum tyrosine is described, based on the amp...
The protein-like materials of gastric juice consists of many kinds of non-heat precipitated mucous m...
Stable 3-nitro tyrosine (3-NO2-Tyr), o-, m-, and p-tyrosine isomers induced by oxidation of tyrosine...
We have developed a reversed-phase liquid-chromatograph-ic procedurefor simultaneouslydetermining ph...
A paper chromatographic method for the determination of serum phenylalanine and tyrosine has been de...
Gas-liquid chromatographic methods have been developed for the analysis of: urinary phenylalanine me...
of l-tyrosine in urine have been Millon’s reaction, microbiologic technics, paper chromatography, en...
Introduction: Inborn errors of metabolism (IEM) are a collective group of rare genetic disorders tha...
Alkaptonuria (AKU) is a rare debilitating autosomal recessive disorder of tyrosine (TYR) metabolism ...
Práce na téma fenylalanin a tyrosin se zaměřením na jejich simultánní stanovení v suchých krevních s...
We describe a method for determining those urinary total phenolic compounds that are tyrosine analog...
For screening early-stage gastric malignancies, the existing serum biomarkers have limited sensitivi...
Tyrosine plays a key role in mammalian biochemistry and defects in its metabolism (e.g., tyrosinemia...
In this paper, a fast and reliable method was developed for simultaneous quantification of tyrosine,...
Human serum contains resolved materials of protein and these resolution shows one section of protein...
A new enzymatic method for rapid direct measurement of serum tyrosine is described, based on the amp...
The protein-like materials of gastric juice consists of many kinds of non-heat precipitated mucous m...
Stable 3-nitro tyrosine (3-NO2-Tyr), o-, m-, and p-tyrosine isomers induced by oxidation of tyrosine...
We have developed a reversed-phase liquid-chromatograph-ic procedurefor simultaneouslydetermining ph...
A paper chromatographic method for the determination of serum phenylalanine and tyrosine has been de...
Gas-liquid chromatographic methods have been developed for the analysis of: urinary phenylalanine me...
of l-tyrosine in urine have been Millon’s reaction, microbiologic technics, paper chromatography, en...
Introduction: Inborn errors of metabolism (IEM) are a collective group of rare genetic disorders tha...
Alkaptonuria (AKU) is a rare debilitating autosomal recessive disorder of tyrosine (TYR) metabolism ...
Práce na téma fenylalanin a tyrosin se zaměřením na jejich simultánní stanovení v suchých krevních s...
We describe a method for determining those urinary total phenolic compounds that are tyrosine analog...
For screening early-stage gastric malignancies, the existing serum biomarkers have limited sensitivi...
Tyrosine plays a key role in mammalian biochemistry and defects in its metabolism (e.g., tyrosinemia...