The liver pharmacological and xenobiotic gene response repertoire.
about
Beyond modules and hubs: the potential of gene coexpression networks for investigating molecular mechanisms of complex brain disordersExploiting dependencies of pairwise comparison outcomes to predict patterns of gene responsePrediction of pharmacological and xenobiotic responses to drugs based on time course gene expression profilesPredictive Power Estimation Algorithm (PPEA)--a new algorithm to reduce overfitting for genomic biomarker discoveryCharacterization of chemically induced liver injuries using gene co-expression modulesMeta-Analysis of Large-Scale Toxicogenomic Data Finds Neuronal Regeneration Related Protein and Cathepsin D to Be Novel Biomarkers of Drug-Induced ToxicityMining kidney toxicogenomic data by using gene co-expression modulesFunctional analysis of multiple genomic signatures demonstrates that classification algorithms choose phenotype-related genes.A transcriptomics data-driven gene space accurately predicts liver cytopathology and drug-induced liver injuryData-driven methods to discover molecular determinants of serious adverse drug events.Maximizing biomarker discovery by minimizing gene signatures.Tissue-level modeling of xenobiotic metabolism in liver: An emerging tool for enabling clinical translational researchToxicogenomic biomarkers for liver toxicityCharacterization of Conserved Toxicogenomic Responses in Chemically Exposed Hepatocytes across Species and Platforms.Characterization of drug-induced transcriptional modules: towards drug repositioning and functional understanding.Using molecular features of xenobiotics to predict hepatic gene expression responseBiomarkers for drug-induced liver injury.Integrative genomics strategies to elucidate the complexity of drug response.In silico models for drug-induced liver injury--current status.Transcriptional profiling of reactive metabolites for elucidating toxicological mechanisms: a case study of quinoneimine-forming agents.Temporal endogenous gene expression profiles in response to lipid-mediated transfection.Prediction of the number of activated genes in multiple independent Cd(+2)- and As(+3)-induced malignant transformations of human urothelial cells (UROtsa).Integrative chemical-biological read-across approach for chemical hazard classification.Temporal endogenous gene expression profiles in response to polymer-mediated transfection and profile comparison to lipid-mediated transfection.
P2860
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P2860
The liver pharmacological and xenobiotic gene response repertoire.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
The liver pharmacological and xenobiotic gene response repertoire.
@ast
The liver pharmacological and xenobiotic gene response repertoire.
@en
type
label
The liver pharmacological and xenobiotic gene response repertoire.
@ast
The liver pharmacological and xenobiotic gene response repertoire.
@en
prefLabel
The liver pharmacological and xenobiotic gene response repertoire.
@ast
The liver pharmacological and xenobiotic gene response repertoire.
@en
P2093
P2860
P356
P1476
The liver pharmacological and xenobiotic gene response repertoire.
@en
P2093
Alan H Roter
Barrett P Eynon
Cecelia I Pearson
Georges Natsoulis
Jeremy Gollub
Kurt Jarnagin
Mark R Fielden
Radha Idury
P2860
P356
10.1038/MSB.2008.9
P577
2008-03-25T00:00:00Z