| First Author | Kraus P | Year | 1999 |
| Journal | J Cell Biochem | Volume | Suppl 32-33 |
| Pages | 133-40 | PubMed ID | 10629112 |
| Mgi Jnum | J:60128 | Mgi Id | MGI:1352794 |
| Doi | 10.1002/(sici)1097-4644(1999)75:32+<133::aid-jcb16>3.0.co;2-e | Citation | Kraus P, et al. (1999) Mammalian Dlx homeobox gene control of craniofacial and inner ear morphogenesis. J Cell Biochem Suppl 32-33:133-40 |
| abstractText | The Dlx homeobox gene family is of ancient origin, with apparent ancestral developmental functions in both nervous system regionalization and appendage (limb) outgrowth. Additional roles in inner ear and craniofacial development were likely acquired by the Dlx gene family during the course of animal evolution. Loss-of-function genetic mutations generated in the mouse have revealed a striking role for Dlx genes in patterning of the mammalian central nervous system, craniofacial structures and inner ear. Interestingly, none of the individual murine Dlx gene mutations to date have resulted in limb defects, suggesting a potentially significant developmental overlap of Dlx activity in this embryonic structure. J. Cell. Biochem. Suppls. 32/33:133-140, 1999. Copyright 1999 Wiley-Liss, Inc. |
