What is the translation of " VITRO STUDY " in Swedish?

• in vitro-studie
• in vitro studie

Examples of using Vitro study in English and their translations into Swedish

In an in vitro study MAO contributed to the metabolism of the active metabolite of dronedarone.
I en in vitro studie bidrog monoaminoxidas(MAO) till metabolismen av den aktiva metaboliten av dronedaron.

was evaluated in an in vitro study.
genom kontinuerlig venovenös hemofiltration(CVVH) utvärderades i en in vitro-studie.

In an in vitro study, dibotermin alfa was shown to bind to fibrin-based haemostatic agents or sealants.
I en in vitro-studie visades det att dibotermin alfa binds till fibrinbaserade hemostasmedel eller vävnadslim.

C21 has a strong impact on several markers in an in vitro study for pulmonary fibrosis- Vicore Pharma Holding AB.
C21 visar goda egenskaper på viktiga markörer i en in vitro-undersökning av lungfibros- Vicore Pharma Holding AB.

Secondly, in this in vitro study, Forskolin was able to raise testosterone levels by almost 200% in isolated rat Leydig cells.
För det andra, i denna studie in vitro, var Forskolin kunna höja testosteronnivåerna med nästan 200% i isolerad rått Leydigceller.

Interactions with drugs that are P-glycoprotein substrates In an in vitro study, temsirolimus inhibited the transport of P-glycoprotein substrates with an IC50 value of 2 µM.
Interaktioner med läkemedel som är P- glykoprotein substrat Temsirolimus hämmade tranporten av P- glykoprotein substrat i en in vitro studie med ett IC50 värde på 2 µM.

In an in vitro study with human hepatocytes, lenalidomide, at various concentrations
I en in vitro-studie med humana hepatocyter inducerades inte CYP1A2,

An increased chromosome fragility has been observed in one in vitro study on lymphocytes taken from patients after long term treatment with somatropin and following the addition of the radiomimetic drug bleomycin.
Ökad kromosomfragilitet har observerats i en in vitro-studie på lymfocyter från patienter som under lång tid behandlats med somatropin och efter tillägg av det radiomimetiska läkemedlet bleomycin.

In an in vitro study, zoledronic acid showed low affinity for the cellular components of human blood,
I en in vitro-studie uppvisade zoledronsyra låg affinitet till de cellulära komponenterna i humant blod,

In an in vitro study, temsirolimus inhibited the transport of P-glycoprotein(P-gp)
Temsirolimus hämmade tranporten av P-glykoprotein(P-gp) substrat i en in vitro studie med ett IC50 värde på 2_µM. Effekten av P-gp

In in vitro studies, daptomycin was not metabolised by human liver microsomes.
I studier in vitro metaboliserades daptomycin ej av humana levermikrosomer.

The specificity of eculizumab for C5 in human serum was evaluated in two in vitro studies.
Eculizumabs specificitet för C5 i humant serum bedömdes i två in vitro-studier.

Vorapaxar inhibits thrombin-induced platelet aggregation in in vitro studies.
Vorapaxar hämmar trombininducerad trombocytaggregation i in vitro-studier.

Desloratadine has demonstrated antiallergic properties from in vitro studies.
Desloratadin har visat sig ha antiallergiska egenskaper i in vitro studier.

Moreover, insulin release is potentiated with increasing glucose concentration in in vitro studies.
Dessutom potentieras insulinfrisättningen med ökande glukoskoncentration i in vitro-försök.

In in vitro studies, laropiprant did not inhibit CYP1A2,
I in vitro studier hämmade inte laropiprant CYP1A2-,

In in vitro studies, nicotinic acid
I in vitro studier hämmade inte nikotinsyra

Dapagliflozin: In in vitro studies, dapagliflozin neither inhibited cytochrome P450(CYP)
Dapagliflozin: I in vitro-studier hämmade dapagliflozin varken cytokrom P450(CYP)

In addition, in vitro studies demonstrated no induction of the CYP1A2,
In vitro-studierna visade dessutom

In in vitro studies, no antagonism has been observed between tigecycline and other commonly used antibiotic classes.
I studier in vitro har ingen antagonism mellan tigecyklin och andra frekvent använda klasser av antibiotika observerats.

In in vitro studies in human hepatic microsomes, minor inhibition of CYP1A2 and CYP2B6 was observed.
I in vitro-studier på humana levermikrosomer observerades en mindre hämning av CYP1A2 och CYP2B6.

In in vitro studies in human liver microsomes, avanafil showed a negligible potential
I in vitro-studier i humana levermikrosomer visade avanafil en försumbar risk för interaktioner via CYP1A1/2,

In in vitro studies the activity of telithromycin was reduced against organisms that express the erythromycin erm(B)
I in vitro studier var aktiviteten hos telitromycin reducerad mot organismer som ger uttryck för erm(B)

In in vitro studies with human hepatocytes, plerixafor does not induce CYP1A2,
I in vitro-studier med humana hepatocyter inducerar plerixafor inte CYP1A2-,

In in vitro studies, bosutinib inhibits proliferation
I in vitro-studier hämmar bosutinib proliferation

In in vitro studies, lixisenatide did not affect the activity of cytochrome P450 isozymes or human transporters tested.
I in vitro-studier påverkade inte lixisenatid aktiviteten hos cytokrom P450-enzymer eller humana transportpoteiner som testades.

In in vitro studies, nicotinic acid
I in vitro studier hämmade inte nikotinsyra

In these in vitro studies, a complete disappearance of glycerol phenylbutyrate did not produce molar equivalent PBA, suggesting the formation of mono- or bis-ester metabolites.
I dessa in vitro-studier gav en fullständig eliminering av glycerolfenylbutyrat inte molarekvivalent PBA, vilket tyder på en bildning av mono- eller bis-estermetaboliter.

In vitro studies have determined that doripenem does not inhibit or induce the activities of CYP isoforms 1A2,
I in vitro-studier har fastställts att doripenem inte hämmar eller inducerar aktivitet hos CYP-isoformerna 1A2, 2A6, 2C9, 2C19,

In clinical Phase I and in vitro studies no metabolic pharmacokinetic interactions with other drugs undergoing Phase I biotransformation involving cytochrome P450 enzymes were observed.
I in vitro studier och kliniska fas I studier observerades inga metaboliska farmakokinetiska interaktioner med andra läkemedel som genomgår Fas I- biotransformation med cytokrom P- 450- enzymer.