The development of strategies which allow the inactivation of specific muri
ne genes by homologous recombination in embryonic cells has revolutionized
biological science in the last 10 years. A large number of mice carrying ge
netic lesions, generated by gene targeting technology, has tremendously inc
reased our knowledge in many areas of biology, culminating in the identific
ation of mouse models for human genetic disorders. These findings have been
recently complemented by "conditional" gene targeting technology, allowing
gene inactivation in a defined tissue and at a specific time point during
development or adulthood, thereby extending the sophistication and potentia
l of this technology.