Protein-bound uremic toxins: putative modulators of calcineurin inhibitor exposure
Author:
Affiliation:
1. Department of Nephrology, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon , Pierre-Bénite , France
2. CarMeN laboratory, Université Claude Bernard , Villeurbanne , France
Funder
Hospices Civils de Lyon
University of Lyon
Publisher
Oxford University Press (OUP)
Subject
Transplantation,Nephrology
Link
https://academic.oup.com/ndt/advance-article-pdf/doi/10.1093/ndt/gfac229/45600678/gfac229.pdf
Reference36 articles.
1. A randomized controlled trial comparing the efficacy of cyp3a5 genotype-based with body-weight-based tacrolimus dosing after living donor kidney transplantation;Shuker;Am J Transplant,2016
2. Estimation of drug exposure by machine learning based on simulations from published pharmacokinetic models: the example of tacrolimus;Woillard;Pharmacol Res,2021
3. Potential interactions between uremic toxins and drugs: an application in kidney transplant recipients treated with calcineurin inhibitors;André;Nephrol Dial Transplant,2021
4. Spontaneous variability of pre-dialysis concentrations of uremic toxins over time in stable hemodialysis patients;Eloot;PLoS One,2017
5. Indoxyl sulfate upregulates liver P-glycoprotein expression and activity through aryl hydrocarbon receptor signaling;Santana Machado;J Am Soc Nephrol,2018
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