{"_id":"ycNa8553WdCfZhvQW","bibbaseid":"nicholson-connelly-lindon-holmes-metabonomicsaplatformforstudyingdrugtoxicityandgenefunction-2002","authorIDs":[],"author_short":["Nicholson, J. K","Connelly, J.","Lindon, J. C","Holmes, E."],"bibdata":{"bibtype":"article","type":"article","author":[{"firstnames":["Jeremy","K"],"propositions":[],"lastnames":["Nicholson"],"suffixes":[]},{"firstnames":["John"],"propositions":[],"lastnames":["Connelly"],"suffixes":[]},{"firstnames":["John","C"],"propositions":[],"lastnames":["Lindon"],"suffixes":[]},{"firstnames":["Elaine"],"propositions":[],"lastnames":["Holmes"],"suffixes":[]}],"title":"Metabonomics: A platform for studying drug toxicity and gene function.","journal":"Nat Rev Drug Discov","year":"2002","volume":"1","number":"2","pages":"153–161","abstract":"The later that a molecule or molecular class is lost from the drug development pipeline, the higher the financial cost. Minimizing attrition is therefore one of the most important aims of a pharmaceutical discovery programme. Novel technologies that increase the probability of making the right choice early save resources, and promote safety, efficacy and profitability. Metabonomics is a systems approach for studying in vivo metabolic profiles, which promises to provide information on drug toxicity, disease processes and gene function at several stages in the discovery-and-development process.","doi":"10.1038/nrd728","keywords":"Animals; Drug Design; Drug Industry; Genes; Genomics; Humans; Kidney, drug effects; Liver, drug effects; Magnetic Resonance Spectroscopy; Toxicology","optmonth":"February","owner":"fhufsky","pmid":"12120097","timestamp":"2011.06.28","bibtex":"@Article{nicholson02metabonomics,\n author = {Jeremy K Nicholson and John Connelly and John C Lindon and Elaine Holmes},\n title = {Metabonomics: A platform for studying drug toxicity and gene function.},\n journal = {Nat Rev Drug Discov},\n year = {2002},\n volume = {1},\n number = {2},\n pages = {153--161},\n abstract = {The later that a molecule or molecular class is lost from the drug development pipeline, the higher the financial cost. Minimizing attrition is therefore one of the most important aims of a pharmaceutical discovery programme. Novel technologies that increase the probability of making the right choice early save resources, and promote safety, efficacy and profitability. Metabonomics is a systems approach for studying in vivo metabolic profiles, which promises to provide information on drug toxicity, disease processes and gene function at several stages in the discovery-and-development process.},\n doi = {10.1038/nrd728},\n keywords = {Animals; Drug Design; Drug Industry; Genes; Genomics; Humans; Kidney, drug effects; Liver, drug effects; Magnetic Resonance Spectroscopy; Toxicology},\n optmonth = feb,\n owner = {fhufsky},\n pmid = {12120097},\n timestamp = {2011.06.28},\n}\n\n","author_short":["Nicholson, J. K","Connelly, J.","Lindon, J. C","Holmes, E."],"key":"nicholson02metabonomics","id":"nicholson02metabonomics","bibbaseid":"nicholson-connelly-lindon-holmes-metabonomicsaplatformforstudyingdrugtoxicityandgenefunction-2002","role":"author","urls":{},"keyword":["Animals; Drug Design; Drug Industry; Genes; Genomics; Humans; Kidney","drug effects; Liver","drug effects; Magnetic Resonance Spectroscopy; Toxicology"],"metadata":{"authorlinks":{}}},"bibtype":"article","biburl":"https://git.bio.informatik.uni-jena.de/fleisch/literature/raw/master/group-literature.bib","creationDate":"2019-11-19T16:50:42.450Z","downloads":0,"keywords":["animals; drug design; drug industry; genes; genomics; humans; kidney","drug effects; liver","drug effects; magnetic resonance spectroscopy; toxicology"],"search_terms":["metabonomics","platform","studying","drug","toxicity","gene","function","nicholson","connelly","lindon","holmes"],"title":"Metabonomics: A platform for studying drug toxicity and gene function.","year":2002,"dataSources":["C5FtkvWWggFfMJTFX"]}