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30. Evidence that Shh cooperates with a retinoic acid inducible co-factor to establish ZPA-like activity. 
Ogura, T., Alvarez, S., Vogel, A., Rodriguez, C., Evans, R. and Izpisua Belmonte, J.C.
Development (1996) 122:537-542. [link]

31. Teleost HoxD and HoxA  genes:  comparison with tetrapods and functional evolution of the HOXD complex.
Van der Hoeven, F., Sordino, P., Fraudeau, N., Izpisua Belmonte, J.C. and Duboule, D.
Mech. Dev. (1996) 54:9-21. [link]

32. Involvement of FGF-8 in initiation, outgrowth, and patterning of the vertebrate limb.
Vogel, A., Rodriguez, C. and Izpisua Belmonte, J. C.
Development (1996) 122:1737-1750. [link]

33. The limb field mesoderm determines initial limb bud anteroposterior asymmetry and budding independent of sonic hedgehog or apical ectodermal gene expressions.
Ros, M., Lopez Martinez, A., Simandl, B. K., Rodriguez, C., Izpisua Belmonte, J. C., Dahn, R. and Fallon, J.
Development (1996) 122:2319-2330. [link]

34. Shh, HoxD, Bmp-2, and Fgf-4 gene expression during development of the polydactylous talpid2, diplopodia1, and diplopodia4 mutant chick limb buds.
Rodriguez, C., Kos, R., Macias, D., Abbott, U. K. and Izpisua Belmonte, J. C.
Dev. Genetics (1996) 19:26-32. [link]