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Posters
- Adaptation of microdialysis techniques to study brain penetration of drugs and substrate-inhibitor interactions of ABC transporters at the BBB in mice
- Seliciclib(R-Roscovitine) is a selective ABCB1 substrate
- Multidrug resistance testing with in vitro ABC transporter assay
- Development of High-throughput Human OCT2 Expressing Uptake Assay System
- Mouse Bsep ATPase assay - a non-radioactive tool for assessment of the cholestatic potential of drug
- MRP2-mediated E217βG transport potentiation: in vitro - in vivo correlation and species specificity
- Kinetic characterization of sulfasalazine transport by ABCG2
- Passive permeability is a crucial parameter in choosing the right assay to detect the interaction of compounds with ABCB1 (Pgp) and ABCG2 (BCRP)
- Comparison of cell based and membrane based high throughput assays for the detection of drugs interacting with the BCRP transporter
- Comparative Analysis of Human Multidrug Resistance-Associated Protein 2 (MRP2) and Rat Mrp2
- Characterization of the interactions between BCRP (ABCG2/MXR) transporter and DMARDs; sulfasalazine, leflunomide and methotrexate
- Excipients may modulate the pathways in ADME/Tox via ABC-transporters
- Carry and Cramp - Cyclodextrins with dual function
- Interaction of quercetin and its metabolites with the transporter ABCC2 (cMOAT, MRP2)
- Chloroacetanilide herbicides and their metabolites interact with human Efflux Transporters and modulate drug absorption
- Interaction of Pesticides with human Efflux Transporters
- Multidrog transzporter fehérjék aktivitása krónikus limfoid leukémiában
- Laboratory validation and multicenter performance evaluation of the Solvo MDQ-Kit
- Multicenter performance evaluation of the MultiDrugQuant assay kit
- Membrane transporters as determinants ofADMETox (AbsorptionMetabolism-Excretion-Toxicity) properties ofdrugs and environmental toxicants
- Interactions of cytostatics with MDR Proteins
- Chlorothiazide is an OAT1, OAT3 and BCRP substrate - implications in renal secretion of chlorothiazide
- Effect of PSC-833 (Valspodar) on the intestinal absorption of digoxin in mouse and rat, using different in vivo and ex vivo methods
- Revised approach in assessing Bsep-Cyclosporin A interactions in bile duct cannulated rats
- Seeking the Optimal BCRP (ABCG2) Probe
- Optimization of cellular uptake assays for the determination of test compound interactions with OAT1 (SLC22A6)
- Chlorothiazide is a substrate for the human uptake transporters OAT1 and OAT3
