| Literature DB >> 12547018 |
Andreas Russ1, Gabriele Stumm, Martin Augustin, Reinhard Sedlmeier, Sigrid Wattler, Michael Nehls.
Abstract
The flood of raw information generated by large-scale data acquisition technologies in genomics, microarrays and proteomics is changing the early stages of the drug discovery process. Although many more potential drug targets are now available compared with the pre-genomics era, knowledge about the physiological context in which these targets act--information crucial to both discovery and development--is scarce. Random mutagenesis strategies in the mouse provide scalable approaches for both the gene-driven validation of candidate targets in vivo and the discovery of new physiological pathways by phenotype-driven screens.Entities:
Mesh:
Year: 2002 PMID: 12547018 DOI: 10.1016/s1359-6446(02)02515-1
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851