Gene Review:
MEOX1 - mesenchyme homeobox 1
Homo sapiens
Synonyms:
Homeobox protein MOX-1, KFS2, MOX1, Mesenchyme homeobox 1
- Isolation of a diverged homeobox gene, MOX1, from the BRCA1 region on 17q21 by solution hybrid capture. Futreal, P.A., Cochran, C., Rosenthal, J., Miki, Y., Swenson, J., Hobbs, M., Bennett, L.M., Haugen-Strano, A., Marks, J., Barrett, J.C. Hum. Mol. Genet. (1994)
- A 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch population. Staehling-Hampton, K., Proll, S., Paeper, B.W., Zhao, L., Charmley, P., Brown, A., Gardner, J.C., Galas, D., Schatzman, R.C., Beighton, P., Papapoulos, S., Hamersma, H., Brunkow, M.E. Am. J. Med. Genet. (2002)
- The human homeobox genes MSX-1, MSX-2, and MOX-1 are differentially expressed in the dermis and epidermis in fetal and adult skin. Stelnicki, E.J., Kömüves, L.G., Holmes, D., Clavin, W., Harrison, M.R., Adzick, N.S., Largman, C. Differentiation (1997)