Gene Review:
Cfdp1 - craniofacial development protein 1
Mus musculus
Synonyms:
27 kDa craniofacial protein, AA408409, Bcnt, Bucentaur, Cfdp, ...
- Contribution of mGluR and Fmr1 functional pathways to neurite morphogenesis, craniofacial development and fragile X syndrome. Tucker, B., Richards, R.I., Lardelli, M. Hum. Mol. Genet. (2006)
- Role of cyclic AMP, prostaglandins, and catecholamines during normal palate development. Greene, R.M., Garbarino, M.P. Curr. Top. Dev. Biol. (1984)
- Msx1/Bmp4 genetic pathway regulates mammalian alveolar bone formation via induction of Dlx5 and Cbfa1. Zhang, Z., Song, Y., Zhang, X., Tang, J., Chen, J., Chen, Y. Mech. Dev. (2003)
- Genomewide analysis of gene expression associated with Tcof1 in mouse neuroblastoma. Mogass, M., York, T.P., Li, L., Rujirabanjerd, S., Shiang, R. Biochem. Biophys. Res. Commun. (2004)
- Phenytoin-induced alterations in craniofacial gene expression. Gelineau-van Waes, J., Bennett, G.D., Finnell, R.H. Teratology (1999)
- Epidermal growth factor receptor function is necessary for normal craniofacial development and palate closure. Miettinen, P.J., Chin, J.R., Shum, L., Slavkin, H.C., Shuler, C.F., Derynck, R., Werb, Z. Nat. Genet. (1999)
- Deficiency of the beta 3 subunit of the type A gamma-aminobutyric acid receptor causes cleft palate in mice. Culiat, C.T., Stubbs, L.J., Woychik, R.P., Russell, L.B., Johnson, D.K., Rinchik, E.M. Nat. Genet. (1995)
- Smad2 role in mesoderm formation, left-right patterning and craniofacial development. Nomura, M., Li, E. Nature (1998)
- Role of Dlx6 in regulation of an endothelin-1-dependent, dHAND branchial arch enhancer. Charité, J., McFadden, D.G., Merlo, G., Levi, G., Clouthier, D.E., Yanagisawa, M., Richardson, J.A., Olson, E.N. Genes Dev. (2001)
- Connexin43 deficiency causes delayed ossification, craniofacial abnormalities, and osteoblast dysfunction. Lecanda, F., Warlow, P.M., Sheikh, S., Furlan, F., Steinberg, T.H., Civitelli, R. J. Cell Biol. (2000)
- Regulation of gene expression in cultured embryonic mouse mandibular mesenchyme by serotonin antagonists. Moiseiwitsch, J.R., Lauder, J.M. Anat. Embryol. (1997)
- Cloning, gene expression, and characterization of CP27, a novel gene in mouse embryogenesis. Diekwisch, T.G., Marches, F., Williams, A., Luan, X. Gene (1999)
- Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients. Braybrook, C., Lisgo, S., Doudney, K., Henderson, D., Marçano, A.C., Strachan, T., Patton, M.A., Villard, L., Moore, G.E., Stanier, P., Lindsay, S. Hum. Mol. Genet. (2002)
- Differential recognition of response elements determines target gene specificity for p53 and p63. Osada, M., Park, H.L., Nagakawa, Y., Yamashita, K., Fomenkov, A., Kim, M.S., Wu, G., Nomoto, S., Trink, B., Sidransky, D. Mol. Cell. Biol. (2005)
- Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis. Chai, Y., Jiang, X., Ito, Y., Bringas, P., Han, J., Rowitch, D.H., Soriano, P., McMahon, A.P., Sucov, H.M. Development (2000)
- The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis. Kelly, R.G., Jerome-Majewska, L.A., Papaioannou, V.E. Hum. Mol. Genet. (2004)
- Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse. Abu-Issa, R., Smyth, G., Smoak, I., Yamamura, K., Meyers, E.N. Development (2002)
- AP2-dependent signals from the ectoderm regulate craniofacial development in the zebrafish embryo. Knight, R.D., Javidan, Y., Zhang, T., Nelson, S., Schilling, T.F. Development (2005)
- Expression of a Xenopus Distal-less homeobox gene involved in forebrain and cranio-facial development. Dirksen, M.L., Mathers, P., Jamrich, M. Mech. Dev. (1993)
- Mammalian Dlx homeobox gene control of craniofacial and inner ear morphogenesis. Kraus, P., Lufkin, T. J. Cell. Biochem. (1999)
- Serotonin regulates mouse cranial neural crest migration. Moiseiwitsch, J.R., Lauder, J.M. Proc. Natl. Acad. Sci. U.S.A. (1995)
- TGIF inhibits retinoid signaling. Bartholin, L., Powers, S.E., Melhuish, T.A., Lasse, S., Weinstein, M., Wotton, D. Mol. Cell. Biol. (2006)
- Teratogenic effects of dosage levels and time of administration of carbamazepine, sodium valproate, and diphenylhydantoin on craniofacial development in the CD-1 mouse fetus. Eluma, F.O., Sucheston, M.E., Hayes, T.G., Paulson, R.B. J. Craniofac. Genet. Dev. Biol. (1984)
- Effects of retinoic acid on embryonic development of mice in culture. Watanabe, T., Pratt, R.M. Experientia (1991)
- Expression of Dlx and Lhx family homeobox genes in fetal thymus and thymocytes. Woodside, K.J., Shen, H., Muntzel, C., Daller, J.A., Sommers, C.L., Love, P.E. Gene Expr. Patterns (2004)
- Revelations of the RYK receptor. Halford, M.M., Stacker, S.A. Bioessays (2001)
- Correlation of Hsp110 expression with caspase-3 and -9 during apoptosis induced by in vivo embryonic exposition to retinoic acid or irradiation in early mouse craniofacial development. Gashegu, J., Vanmuylder, N., Philippson, C., Choa-Duterre, M., Rooze, M., Louryan, S. Orthodontics & craniofacial research. (2006)
- Sox9 is required for determination of the chondrogenic cell lineage in the cranial neural crest. Mori-Akiyama, Y., Akiyama, H., Rowitch, D.H., de Crombrugghe, B. Proc. Natl. Acad. Sci. U.S.A. (2003)
- Goosecoid-like (Gscl), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development. Saint-Jore, B., Puech, A., Heyer, J., Lin, Q., Raine, C., Kucherlapati, R., Skoultchi, A.I. Hum. Mol. Genet. (1998)
- Dkk1, -2, and -3 expression in mouse craniofacial development. Nie, X. Journal of molecular histology. (2005)
- Targeted deletion of a branchial arch-specific enhancer reveals a role of dHAND in craniofacial development. Yanagisawa, H., Clouthier, D.E., Richardson, J.A., Charité, J., Olson, E.N. Development (2003)
- Distribution of C-CAM in developing oral tissues. Rass, A., Lüning, C., Wroblewski, J., Obrink, B. Anat. Embryol. (1994)
- Expression of E-cadherin during craniofacial development. Lüning, C., Rass, A., Rozell, B., Wroblewski, J., Obrink, B. J. Craniofac. Genet. Dev. Biol. (1994)
- Identification and developmental expression analysis of a novel homeobox gene closely linked to the mouse Twirler mutation. Liu, H., Liu, W., Maltby, K.M., Lan, Y., Jiang, R. Gene Expr. Patterns (2006)