Transgenic gene knock-outs: functional genomics and therapeutic target selection
- 1 November 2000
- journal article
- review article
- Published by Taylor & Francis in Pharmacogenomics
- Vol. 1 (4) , 433-443
- https://doi.org/10.1517/14622416.1.4.433
Abstract
The completion of the first draft of the human genome presents both a tremendous opportunity and enormous challenge to the pharmaceutical industry since the whole community, with few exceptions, will soon have access to the same pool of candidate gene sequences from which to select future therapeutic targets. The commercial imperative to select and pursue therapeutically relevant genes from within the overall content of the genome will be particularly intense for those gene families that currently represent the chemically tractable or ‘drugable’ gene targets. As a consequence the emphasis within exploratory research has shifted towards the evaluation and adoption of technology platforms that can add additional value to the gene selection process, either through functional studies or direct/indirect measures of disease alignment e.g., genetics, differential gene expression, proteomics, tissue distribution, comparative species data etc. The selection of biological targets for the development of potential ne...Keywords
This publication has 55 references indexed in Scilit:
- The Biology of Chemokines and their ReceptorsAnnual Review of Immunology, 2000
- Mouse mutants from chemically mutagenized embryonic stem cellsNature Genetics, 2000
- Genotype-based screen for ENU-induced mutations in mouse embryonic stem cellsNature Genetics, 2000
- Review: Somatic Cell Nuclear Transfer in Mammals: Progress and ApplicationsCloning, 1999
- Genomics and intellectual property rightsDrug Discovery Today, 1999
- Genomics: the race is onDrug Discovery Today, 1999
- Conditional genome alteration in miceBioEssays, 1998
- Mouse models of human disease. Part II: recent progress and future directions.Genes & Development, 1997
- A candidate gene for the mouse mutation tubbyNature, 1996
- Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activityNature Genetics, 1995