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 Übersetzung für 'tryptophan deficiency' von Englisch nach Deutsch
biochem.med.
tryptophan deficiency
Tryptophanmangel {m}
Teiltreffer
biochem.
tryptophan residue
Tryptophanrest {m}
biochem.
tryptophan metabolism
Tryptophan-Stoffwechsel {m}
biochem.
tryptophan metabolism
Tryptophanstoffwechsel {m}
med.
purine nucleoside phosphorylase deficiency <PNPD, PNP-deficiency>
Purinnukleosidphosphorylasemangel {m} <PNP-Mangel>
biochem.
tryptophan <Trp, W> [C11H12N2O2]
Tryptophan {n} <Trp, W>
375
deficiencyFehlbestand {m}
11
deficiencyFehlbetrag {m}
16
deficiencyFehlen {n}
45
deficiencyGebrechen {n}
17
med.
deficiency
Defizienz {f}
17
deficiencyMangelhaftigkeit {f}
28
deficiencySchwäche {f}
123
deficiencyDefizit {n}
959
deficiencyFehler {m}
32
deficiencyAusfallbetrag {m}
14
deficiencyAusfall {m}
83
deficiencyUnzulänglichkeit {f}
102
deficiencyMangel {m}
1461
deficiencyManko {n}
19
deficiencyMissstand {m}
156
21 Übersetzungen
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Anwendungsbeispiele Englisch
  • Amino acids are reabsorbed by sodium dependent transporters in the proximal tubule. Hartnup disease is a deficiency of the tryptophan amino acid transporter, which results in pellagra.
  • His research led to the first understanding of nicotinic acid deficiency and the discovery of the tryptophan-nicotinic acid relationship.
  • Moderate or heavy clinical infection of fish with whirling disease can be presumptively diagnosed on the basis of changes in behavior and appearance about 35 to 80 days after initial infection, though "injury or deficiency in dietary tryptophan and ascorbic acid can evoke similar signs", so conclusive diagnosis may require finding myxospores in the fish's cartilage.
  • Specifically, maternal alleles for codon 234 exhibit this mutation which changes a tryptophan to a glycine.
  • The Tryptophan operon leader is an RNA element found at the 5′ of some bacterial tryptophan operons.

  • Tetrahydrobiopterin is a cofactor in the production of L-DOPA from tyrosine and 5-hydroxy-L-tryptophan from tryptophan, which must be supplemented as treatment in addition to the supplements for classical PKU.
  • It was not until 1937 that Conrad Elvehjem discovered that pellagra is caused by a dietary lack of the B vitamin niacin, along with reduced levels of the essential amino acid tryptophan.
  • The most prominent of the lesions is due to impaired tryptophan–niacin conversion.
  • Biosynthesis of niacin occurs by metabolism of tryptophan via the kynurenine pathway to quinolinic acid, the niacin precursor.
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Enthält Übersetzungen von der TU Chemnitz sowie aus Mr Honey's Business Dictionary (nur Englisch/Deutsch).
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