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320 Possible Causes for L phenylalanine,, N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)

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  • Phenylalanine Increased

    Name L-Phenylalanine (phenylethylamine, phenethylamine) L-Phenylalanine and Cognitive Function L-Phenylalanine confers a number of positive effects on cognitive function,[naturalstacks.com] My Personal Experience With DLPA and L-Phenylalanine I have taken l-tyrosine, DLPA, and l-phenylalanine. I personally react better to l-phenylalanine.[dominatedepression.com] , from l-tyrosine from l-phenylalanine occur at all?[bluelight.org]

    Missing: N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)
  • Melphalan

    4-(Bis(2-chloroethyl)amino)-L-phenylalanine p-N,N-bis(2-chloroethyl)amino-L-phenylalanine P-N-Bis(2-chloroethyl)amino-L-phenylalanine P-Di-(2-chloroethyl)amino-L-phenylalanine[wikidata.org] […] mustard p-N-Bis(2-chloroethyl)amino-L-phenylalanine Phenylalanine mustard p-L-Sarcolysin p-Bis(beta-chloroethyl)aminophenylalanine p-Di-(2-chloroethyl)amino-L-phenylalanine[wikidata.org] From Wikidata Jump to navigation Jump to search chemical compound Alkeran CB-3025 L-phenylalanine mustard (L-PAM) L-sarcolysine melfalan Sarcolysin Phenylalanine nitrogen[wikidata.org]

    Missing: N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)
  • Hyperphenylalaninemia

    This case report concerns a female infant born in 1976 with a presumptive positive PKU screening test on the third day of life of 240 mumol/L phenylalanine.[ncbi.nlm.nih.gov] Transient expression of mutant full-length cDNAs in human HEK293 cells yielded PAH variants whose l-phenylalanine hydroxylase activity was between 40% and 70% that of the[ncbi.nlm.nih.gov] […] concentrations 360 μmol/L or all patients with phenylalanine concentrations 600 μmol/L require treatment.[ncbi.nlm.nih.gov]

    Missing: N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)
  • Dianhydrogalactitol

    Abstract The incidence of hyponatremia in 34 patients following administration of high-dose L-phenylalanine mustard (L-PAM) and dianhydrogalactitol (DAG) was determined.[ncbi.nlm.nih.gov] Only a combination of L-phenylalanine mustard and dianhydrogalactitol produced a limited response in both the patient and the mice.[ncbi.nlm.nih.gov]

    Missing: N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)
  • Phenylketonuria

    Differential pulse voltammetry were used for the quantitative l-Phenylalanine detection.[ncbi.nlm.nih.gov] If blood phenylalanine exceeded the target range, the CGMP-AA dose was reduced and replaced with Phe-free L-amino acids. The control group remained on Phe-free L-AAs.[ncbi.nlm.nih.gov] Before hospitalization, all but 1 of the patients had blood phenylalanine levels above 1,000 mumol/L; in 1 patient the blood phenylalanine level was 703 mumol/L.[ncbi.nlm.nih.gov]

    Missing: N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)
  • Classical Phenylketonuria

    Abstract Phenylketonuria (PKU) is a metabolic disorder due primarily to mutations in the PAH gene that impair both phenylalanine hydroxylase activity and disposal of l-phenylalanine[ncbi.nlm.nih.gov] Abstract Treatment of phenylketonuria (PKU, OMIM 261600) means a diet restricted in natural protein and supplemented with phenylalanine (Phe)-free L-amino acid mixtures.[ncbi.nlm.nih.gov] It seems essential to initiate diet early, and to keep blood phenylalanine levels 600 mumol/L and well controlled to at least age 10 to ensure satisfactory long-term development[ncbi.nlm.nih.gov]

    Missing: N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)
  • Atypical Phenylketonuria

    Lehman WD, Heinrich HC (1985) Oral versus intravenous l -phenylalanine loading compared by simultaneous application of l -[-2H5] and l -[-15N]phenylalanine.[link.springer.com] The patients with the classical or typical form of PKU have phenylalanine levels above 1200 μ mol/L due to hepatic phenylalanine hydroxylase residual activity μ mol/L and[jn.nutrition.org] #2913796 exam.step1 - 07/16/13 18:50 treatment: restrict phenylalanin, give L-Dopa and 5-hydroxytryptophan thanks :) Report Abuse Page 1 of 1 [ [ ... Message ...[usmleforum.com]

    Missing: N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)
  • Levodopa

    3,4-Dihydroxy-L-phenylalanine, 98 % MDL MFCD00002598 EINECS 200-445-2 Chemische Eigenschaften Formel C 9 H 1 1 NO 4 Molmasse 197.19 Schmelzpunkt ca 295 dec.[alfa.com] Levodopum β-(3,4-dihydroxyphenyl)alanine L-beta-(3,4-Dihydroxyphenyl)alanine 3,4-Dihydroxy-L-phenylalanine ( )-3-(3,4-dihydroxyphenyl)-L-alanine ( )-dopa Dihydroxy-L-phenylalanine[wikidata.org] , 3-hydroxy-; Alanine, 3-(3,4-dihydroxyphenyl)-, L-; β-(3,4-Dihydroxyphenyl)-L-alanine; β-(3,4-Dihydroxyphenyl)alanine; (-)-(3,4-Dihydroxyphenyl)alanine; (-)-Dopa; Dihydroxy-L-phenylalanine[webbook.nist.gov]

    Missing: N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)
  • Disorder of Catecholamine Synthesis

    ) 7-Tetrahydropterin 4-Chloro-DL-phenylalanine ( C6506 ) 4-Chloro-L-phenylalanine ( C8655 ) L-Tyrosine ( T2006 ) –––––––––––– Tyrosine-3-hydroxylase Oxygen Tetrahydrobiopterin[sigmaaldrich.com] Enzyme or Protein Biochemistry Syndromes Phenylalanine hydroxylase L-phenylalanine to L-tyrosine Phenylketonuria Tyrosine hydroxylase L-tyrosine to L-DOPA L-DOPA responsive[neuromuscular.wustl.edu] Chem. 332, 1963 McGilvery, R.W., Cohen, P.P.; ''The decarboxylation of L-phenylalanine by Streptococcus faecalis R.''; J. Biol.[wikipathways.org]

    Missing: N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)
  • 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency

    Initial diagnostic work-up showed elevated blood phenylalanine of 1100 mmol/L and low tyrosine. Limited protein diet and phenylalanine-free formula were prescribed.[ncbi.nlm.nih.gov] Tetrahydrobipterin plays a role as a cofactor in Phenylalanine, L-Dopa and Serotonin metabolism.[treatable-id.org] The BH4 can be administered to normalize phenylalanine (PHE) levels easily, but, owing to severe side effects, the neurotransmitters, L-DOPA and 5-hydroxytryptophan, should[ncbi.nlm.nih.gov]

    Missing: N (N(2) (N (N (N (N L tyrosylglycyl)glycyl) L phenylalanyl) l methionyl) L arginyl)

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