Personalized Mapping of Drug Metabolism by the Human Gut Microbiome is a research paper published in Cell (2020). On theSindex it has a DataRank of 0. It has been cited 468 times.
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National Institutes of Health
Grant: 1DP2AI124441
National Science Foundation
Grant: 2017249408
National Institute of General Medical Sciences
Grant: T32GM007388
NIAID NIH HHS
Grant: DP2 AI124441
Princeton University
FWCI
17.22
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 1 of Gut microbiome modulates tacrolimus pharmacokinetics through the transcriptional regulation of ABCB1
Additional file 1 of Gut microbiome modulates tacrolimus pharmacokinetics through the transcriptional regulation of ABCB1
Additional file 2 of Gut microbiome modulates tacrolimus pharmacokinetics through the transcriptional regulation of ABCB1
Additional file 2 of Gut microbiome modulates tacrolimus pharmacokinetics through the transcriptional regulation of ABCB1
Additional file 1 of Analysis of metabolites in human gut: illuminating the design of gut-targeted drugs
Additional file 1 of Analysis of metabolites in human gut: illuminating the design of gut-targeted drugs
Additional file 2 of Understanding the âindividual drug reactionâ from the perspective of the interaction between probiotics and lovastatin in vitro and in vivo
Additional file 2 of Understanding the âindividual drug reactionâ from the perspective of the interaction between probiotics and lovastatin in vitro and in vivo
Additional file 1 of Understanding the âindividual drug reactionâ from the perspective of the interaction between probiotics and lovastatin in vitro and in vivo
Additional file 1 of Understanding the âindividual drug reactionâ from the perspective of the interaction between probiotics and lovastatin in vitro and in vivo
Additional file 1 of Bacteroides salyersiae is a potent chondroitin sulfate-degrading species in the human gut microbiota
Additional file 1 of Bacteroides salyersiae is a potent chondroitin sulfate-degrading species in the human gut microbiota