Ashkenazi, A. and Dixit, V. M (1998). Death receptors: signaling and modulation. Science 281, 1305-1308.[Abstract/Free Full Text]
Bayes, M., Hartung, A. J., Ezer, S., Pispa, J., Thesleff, I., Srivastava, A. K. and Kere, J (1998). The anhidrotic ectodermal dsyplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats. Hum. Mol. Genet 7, 1661-1669.[Abstract/Free Full Text]
Butler, P. M (1956). The ontogeny of molar pattern. Biol. Rev 31, 30-70.
Chen, T. C., Hinton, D. R., Sippy, B. D. and Hofman, F. M (1997). Soluble TNF-alpha receptors are constitutively shed and downregulate adhesion molecule expression in malignant gliomas. J. Neuropathol. Exp. Neurol 56, 541-550.[Medline]
Crawford, P. J. M., Aldred, M. J. and Clarke, A (1991). Clinical and radiographic dental findings in X-linked hypohidrotic ectodermal dysplasia. J. Med. Genet 28, 181-185.[Abstract/Free Full Text]
Dassule, H. R. and McMahon, A. P (1998). Analysis of epithelial-mesenchmal interactions in the initial morphogenesis of the mammalian tooth. Dev. Biol 202, 215-227.[Medline]
Ezer, S., Sclessinger, D., Srivastava, A. K. and Kere, J (1997). Anhidotic ectodermal dysplasia (EDA) protein expressed in MCF-7 cells associates with cell membrane and induces rounding. Hum. Mol. Genet 6, 1581-1587.[Abstract/Free Full Text]
Falconer, D. S (1952). A totally sex-linked gene in the house mouse. Nature 169, 664-.[Medline]
Feinstein, E., Kimchi, A., Wallach, D., Boldin, M. and Varfolomeev, E (1995). The death domain: a module shared by proteins with diverse cellular functions. Trends Biochem. Sci 20, 342-344.[Medline]
Ferguson, B. M., Brockdorff, N., Formstone, E., Ngyuen, T., Kronmiller, J. E. and Zonana, J (1997). Cloning of Tabby , the murine homologue of the human EDA gene: evidence for a membrane associated protein with a short collagenous domain. Hum. Mol. Genet 6, 1589-1594.[Abstract/Free Full Text]
Ferguson, B. M., Monreal, A., Headon, D., Overbeek, P. and Zonana, J (1998). An apparent new member of the TNF superfamily is encoded for by the EDA1 gene: evidence from mutation and two-hybrid analysis. Am. J. Hum. Genet 63, 52-.[Medline]
Giese, K., Cox, K. and Grosschedl, R (1992). The HMG domain of lymphoid enhancer factor 1 bends DNA and facilitates assembly of functional nucleoprotein structures. Cell 69, 185-195.[Medline]
Gruneberg, H (1965). Genes and genotypes affecting the teeth of the mouse. J.Embryol. Exp. Morphol 14, 137-159.[Medline]
Gruneberg, H (1966). The molars of the tabby mouse, and a test of the \324single activated X-chromosome' hypothesis. J. Embryol. Exp. Morphol 15, 223-244.[Medline]
Gruneberg, H (1971). The glandular aspect of the tabby syndrome in the mouse. J. Embryol. Exp. Morphol 25, 1-19.[Medline]
Headon, D. J. and Overbeek, P. A (1999). Involvement of a novel TNF receptor homolog in hair follicle development. Nat. Genet 22, 370-374.[Medline]
Hoschuetzky, H., Aberle, H. and Kemler, R (1994). \247-catenin mediates the interaction of the cadherin-catenin complex with epidermal growth factor receptor. J. Cell Biol 127, 1375-1380.[Abstract/Free Full Text]
Jernvall, J., Kettunen, P., Karavanova, I., Martin, L. B. and Thesleff, I (1994). Evidence for the role of the enamel knot as a control centre in mammalian tooth cusp formation: non dividing cells express growth factor Fgf-4 gene. Int. J. Dev. Biol 38, 463-469.[Medline]
Jernvall, J., \201berg, T., Kettunen, P., Ker\212nen, S. and Thesleff, I (1998). The life history of an embryonic signalling center: BMP4 induces p21 and is associated with apoptosis in the mouse tooth enamel knot. Development 125, 161-169.[Abstract]
Kere, J., Srivasta, A. K., Montonen, O., Zonana, J., Thomas, N., Ferguson, B., Munoz, F., Morgan, D., Clarke, A., Baybayan, P., Chen, E. Y., Ezer, S., Saarialho-Kere, U., de la Chapelle, A. and Schlessinger, D (1996). X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by a mutation in a novel transmembrane protein. Nat. Genet 13, 409-416.[Medline]
Kratochwil, K., Dull, M., Farinas, I., Galceran, J. and Grosschedl, R (1996). Lef-1 expression is activated by BMP-4 and regulates inductive tissue interactions in tooth and hair development. Genes Dev 10, 1382-1394.[Abstract/Free Full Text]
Mayer, T. C., Miller, C. K. and Green, M. C (1977). Site of action of the crinkled (cr) locus in the mouse. Dev. Biol 55, 397-401.[Medline]
Miard, S., Peterkova, R., Vonesch, J-L., Peterka., M., Ruch., J-V. and Lesot, H (1999). Alterations in the incisor development in the Tabby mouse. Int. J. Dev. Biol 43, 517-529.[Medline]
Micheau, O., Solary, E., Hammann, A. and Dimanche-Boitrel, M. T (1999). FasL independent, FADD-mediated activation of the Fas death pathway by anti-cancer drugs. J. Biol. Chem 274, 7987-7992.[Abstract/Free Full Text]
Mikkola, M. L., Pista, J., Pekkanen, M., Kere, J. and Thesleff, I (1998). Characterisation of the mouse Tabby protein, mutation of which causes ectodermal dysplasia. Mol. Biol. Cell 9, 1789-.
Mikkola, M. L., Pista, J., Pekkanen, M., Paulin, L., Nieminen, P., Kere, J. and Thesleff, I (1999). Ectodysplasin, a protein required for epithelial morphogensis, is a novel TNF homologue and promotes cell-matrix adhesion. Mech Dev 88, 133-146.[Medline]
Montonen, O., Ezer, S., Saarialho-Kere, U. K., Herva, R., Karjalainen-Linsberg, M., Kaitila, I., Sclessinger, D., Srivastava, A. K., Thesleff, I. and Kere, J (1998). The gene defective in anhidrotic ectodermal dysplasia is expressed in developing epithelium, neuroectoderm, thymus and bone. J. Histochem. Cytochem 46, 281-289.[Abstract/Free Full Text]
Monreal, A. W., Zonana, J. and Ferguson, B (1998). Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations. Am. J. Hum. Genet 63, 380-389.[Medline]
Monreal, A. W., Ferguson, B. M., Headon, D. J., Street, S. L., Overbeek, P. A. and Zonana, J (1999). Mutations in the human homolog of the mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nat. Genet 22, 366-369.[Medline]
Newton, K., Harris, A. W., Bath, M. L., Smith, K. G. C. and Strasser, A (1998). A dominant interfering mutant of FADD/MORT1 enhances deletion of autoreactive thymocytes and inhibits proliferation of mature T lymphocytes. EMBO J 17, 706-718.[Medline]
Pispa, J., Jung, H-S., Jernvall, J., Kettunen, P., Mustonen, T., Tabata, M. J., Kere, J. and Thesleff, I (1999). Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF. Dev. Biol 216, 521-534.[Medline]
Sarkar, L. and Sharpe, P. T (1999). Expression of Wnt signalling pathway genes during tooth development. Mech. Dev 85, 197-200.[Medline]
Saxen, L (1966). The effect of Tetracyclin on osteogenesis in vitro. J. Exp. Zool 162, 269-294.
Schneider, P., MacKay, F., Steiner,V., Hofmann, K., Bodmer, J. L., Holler,N., Ambrose, C., Lawton, P., Bixler, S., AchaOrbea, H. et al (1999). BAFF, a novel ligand of the TNF family stimulates B cell growth. J. Exp. Med 189, 1747-1756.[Abstract/Free Full Text]
Schneider, P (2000). Production of recombinant TRAIL and TRAIL receptors: Fc chimeric proteins. Meth. Enzymol 322, 325-345.[Medline]
Sofaer, J. A (1969). Aspects of the tabby-crinkled-downless syndrome I. The development of tabby teeth. J. Embryol. Exp. Morphol 22, 181-205.[Medline]
Sofaer, J. A (1969). Aspects of the tabby-crinkled-downless syndrome II. Observations on the reaction to changes of genetic background. J. Embryol. Exp. Morphol 22, 207-227.[Medline]
Sofaer, J. A (1977). Short communication: The teeth of the \324Sleek' mouse. Arch. Oral Biol 22, 299-301.[Medline]
Srivastava, A. K., Pispa, J., Hartung, A. J., Du, Y., Ezer, S., Jenks, T., Shimada, T., Pekkanen, M., Mikkola, M. L., Ko, M. S. H. et al (1997). The Tabby phenotype is caused by mutations in a mouse homoloue of the EDA gene that reveals novel mouse and human exons and encodes a proetin (ectodysplasin-A) with collagenous domains. Proc. Natl. Acad. Sci. USA 94, 13069-13074.[Abstract/Free Full Text]
Trowel, O. A (1959). The culture of mature organs in a synthetic medium. Exp. Cell Res 16, 118-147.[Medline]
Tucker, A. S., Al Khamis, A., Ferguson, C. A., Bach, I., Rosenfeld, M. G. and Sharpe, P. T (1999). Conserved regulation of mesenchymal gene expression by Fgf-8 in face and limb development. Development 126, 221-228.[Abstract]
Tucker, A. S. and Sharpe, P. T (1999). Molecular genetics of tooth morphogenesis and patterning: the right shape in the right place. J. Dental Res 78, 826-834.[Abstract/Free Full Text]
Vaahtokari, A., \201berg., T. and Thesleff. I (1996). Apoptosis in the developing tooth: association with an embryonic signalling centre and suppression by EGF and FGF-4. Development 122, 121-129.[Abstract]
Vaahtokari, A., \201berg., T., Jernvall, J., Ker\212nen, S. and Thesleff. I (1996). The enamel knot as a signalling centre in the developing mouse tooth. Mech. Dev 54, 39-43.[Medline]
van Genderen, C., Okamura, R. M., Farinas, I., Quo, R., Parslow, T. G., Bruhn, L. and Grosschedl, R (1994). Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1 deficient mice. Genes Dev 8, 2691-2703.[Abstract/Free Full Text]
Zhou, P., Byrne, C., Jacobs, J. and Fuchs, E (1995). Lymphoid enhancer factor 1 directs hair follicle patterning and epithelial cell fate. Genes Dev 9, 700-713.[Abstract/Free Full Text]
