spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Summary Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tucker, A. S.
Right arrow Articles by Sharpe, P. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tucker, A. S.
Right arrow Articles by Sharpe, P. T.
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]





This Article
Right arrow Summary Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tucker, A. S.
Right arrow Articles by Sharpe, P. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tucker, A. S.
Right arrow Articles by Sharpe, P. T.