review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1002/CPT.1818 |
P698 | PubMed publication ID | 32119114 |
P50 | author | Sanjay K Nigam | Q111165276 |
P2093 | author name string | Kevin T Bush | |
Samuel M Poloyac | |||
Jeremiah D Momper | |||
Vibha Bhatnagar | |||
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Evolution of gene expression patterns in a model of branching morphogenesis | Q40923783 | ||
Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members | Q41905911 | ||
Prostaglandin E2 produced by microsomal prostaglandin E synthase-1 regulates the onset and the maintenance of wakefulness | Q42491994 | ||
Induction of influx and efflux transporters and cytochrome P450 3A4 in primary human hepatocytes by rifampin, rifabutin, and rifapentine | Q42872165 | ||
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Cytochrome P450 eicosanoids in hypertension and renal disease | Q28252210 | ||
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A novel transporter of SLC22 family specifically transports prostaglandins and co-localizes with 15-hydroxyprostaglandin dehydrogenase in renal proximal tubules | Q28593864 | ||
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Human organic anion transporters and human organic cation transporters mediate renal transport of prostaglandins. | Q34119825 | ||
Structure and function of the human breast cancer resistance protein (BCRP/ABCG2). | Q34176588 | ||
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The organic anion transporter family: from physiology to ontogeny and the clinic | Q34310328 | ||
Bile acid dysregulation, gut dysbiosis, and gastrointestinal cancer | Q34425909 | ||
Bile acids and the gut microbiome | Q34432618 | ||
Multiple organic anion transporters contribute to net renal excretion of uric acid | Q34470733 | ||
Overview: ABC transporters and human disease | Q34502433 | ||
Functional interactions between P-glycoprotein and CYP3A in drug metabolism | Q34550483 | ||
Multidrug resistance protein 4 (MRP4/ABCC4) regulates cAMP cellular levels and controls human leukemia cell proliferation and differentiation | Q34606100 | ||
Cytochrome P450 pathways of arachidonic acid metabolism. | Q34667725 | ||
Remote communication through solute carriers and ATP binding cassette drug transporter pathways: an update on the remote sensing and signaling hypothesis | Q34865706 | ||
Role of the breast cancer resistance protein (BCRP/ABCG2) in drug transport--an update | Q34871636 | ||
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Untargeted metabolomics identifies enterobiome metabolites and putative uremic toxins as substrates of organic anion transporter 1 (Oat1). | Q35446350 | ||
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Crosstalk between Bile Acids and Gut Microbiota and Its Impact on Farnesoid X Receptor Signalling | Q36294227 | ||
Shared Ligands Between Organic Anion Transporters (OAT1 and OAT6) and Odorant Receptors | Q36316477 | ||
Human cytochromes P450 in health and disease | Q36512912 | ||
What do drug transporters really do? | Q36571217 | ||
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cDNA cloning of three new forms of rat brain cytochrome P450 belonging to the CYP4F subfamily | Q36790347 | ||
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Growth hormone treatment of premature ovarian failure in a mouse model via stimulation of the Notch-1 signaling pathway | Q37001887 | ||
Bile acids: chemistry, pathochemistry, biology, pathobiology, and therapeutics | Q37167278 | ||
Multispecific drug transporter Slc22a8 (Oat3) regulates multiple metabolic and signaling pathways | Q37193094 | ||
Targeting bile-acid signalling for metabolic diseases | Q37231731 | ||
Toward a systems level understanding of organic anion and other multispecific drug transporters: a remote sensing and signaling hypothesis | Q37314370 | ||
Soluble epoxide hydrolase inhibitor trans-4-[4-(3-adamantan-1-yl-ureido)-cyclohexyloxy]-benzoic acid is neuroprotective in rat model of ischemic stroke. | Q37440238 | ||
Polymorphism of human cytochrome P450 2D6 and its clinical significance: Part I. | Q37611786 | ||
CYP2D6 variation, behaviour and psychopathology: implications for pharmacogenomics-guided clinical trials | Q37678050 | ||
In vitro and in vivo evidence of the importance of organic anion transporters (OATs) in drug therapy | Q37811961 | ||
Pharmacological mechanism-based drug safety assessment and prediction | Q37864922 | ||
Bile acid transporters and regulatory nuclear receptors in the liver and beyond | Q38033967 | ||
Pharmacogenetics in the evaluation of new drugs: a multiregional regulatory perspective | Q38078188 | ||
Role of ABC transporters in lipid transport and human disease | Q38082105 | ||
Physiological and molecular biochemical mechanisms of bile formation | Q38164702 | ||
Human bile salt export pump promoter is transactivated by the farnesoid X receptor/bile acid receptor. | Q38300264 | ||
Future Avenues to Decrease Uremic Toxin Concentration | Q38616213 | ||
The drug transporter OAT3 (SLC22A8) regulates endogenous metabolite flow through the gut-liver-kidney axis | Q38648038 | ||
Key Role for the Organic Anion Transporters, OAT1 and OAT3, in the in vivo Handling of Uremic Toxins and Solutes | Q38685365 | ||
Identification of Endogenous Biomarkers to Predict the Propensity of Drug Candidates to Cause Hepatic or Renal Transporter-Mediated Drug-Drug Interactions | Q38729347 | ||
Intestinal Crosstalk between Bile Acids and Microbiota and Its Impact on Host Metabolism | Q38869873 | ||
Effect of Cytochrome P450 Metabolites of Arachidonic Acid in Nephrology | Q39431317 | ||
P577 | publication date | 2020-03-02 | |
P1433 | published in | Clinical Pharmacology & Therapeutics | Q1101529 |
P1476 | title | The Systems Biology of Drug Metabolizing Enzymes and Transporters: Relevance to Quantitative Systems Pharmacology |
Q100564981 | The Role of the Microbiome in Central Nervous System Clinical Pharmacology: More Than a Gut Feeling | cites work | P2860 |
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