Results for isoforms translation from English to Danish

inhibition of cyp isoforms
hæmning af cyp-isoformer

cyp isoforms selective substrates:
cyp- isoformselektive substrater:

two isoforms, cox-1 and cox-2 have been identified.
der er identificeret to isoformer, cox- 1 og cox- 2.

two isoforms, cox-1 and cox-2, have been identified.
der er identificeret 2 iso-former, cox- 1 og cox-2.

there are two isoforms of cox, cox-1, and cox-2.
der findes to cox isoformer, cox-1 og cox-2.

rivaroxaban neither inhibits nor induces any major cyp isoforms like cyp3a4.
rivaroxaban hverken hæmmer eller inducerer væsentlige cyp-isoformer såsom cyp3a4.

it binds with high affinity to the vegf-a isoforms (e.g.
det binder sig med høj affinitet til isoformer af vegf- a (f.eks.

the cyclo-oxygenase enzyme (cox) is present in two isoforms.
cyclo-oxygenaseenzymet (cox) er til stede i to isoformer.

production of the primary metabolite, ucb l057, is not supported by liver cytochrome p450 isoforms.
dannelse af den primære metabolit, ucb l057 er ikke afhængig af lever cytochrom p450 isoformer.

based on in vitro studies, empagliflozin does not inhibit, inactivate, or induce cyp450 isoforms.
empagliflozin hverken hæmmer, inaktiverer eller inducerer cyp-isoformer.

from the recombinant cyp isoforms investigated in vitro cyp1a1 catalysed formation of riociguat’s main metabolite most effectively.
fra de rekombinante cyp-isoformer, der blev undersøgt, katalyserede in vitro-cyp1a1 dannelsen af riociguats primære metabolit mest effektivt.

it is unlikely that atosiban inhibits hepatic cytochrome p450 isoforms in humans (see section 4.5).
det er usandsynligt at atosiban hæmmer hepatisk cytochrom p450 isoformer i mennesker (se afsnit 4.5).

biotransformation tadalafil is predominantly metabolised by the cytochrome p450 (cyp) 3a4 isoform.
biotransformation tadalafil metaboliseres overvejende af cytokrom p450 (cyp) 3a4 isoformen.