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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
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Disease relevance of Amelogenesis


Psychiatry related information on Amelogenesis


High impact information on Amelogenesis


Biological context of Amelogenesis


Anatomical context of Amelogenesis


Associations of Amelogenesis with chemical compounds


Gene context of Amelogenesis


Analytical, diagnostic and therapeutic context of Amelogenesis


  1. Tuftelin--aspects of protein and gene structure. Deutsch, D., Palmon, A., Dafni, L., Mao, Z., Leytin, V., Young, M., Fisher, L.W. Eur. J. Oral Sci. (1998) [Pubmed]
  2. Open bite deformity in amelogenesis imperfecta. Part 1: An analysis of contributory factors and implications for treatment. Hoppenreijs, T.J., Voorsmit, R.A., Freihofer, H.P. Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery. (1998) [Pubmed]
  3. Hypocalcification type amelogenesis imperfecta in permanent dentition in association with heavily worn primary teeth, gingival hyperplasia, hypodontia and impacted teeth. Atasu, M., Biren, S., Mumcu, G. The Journal of clinical pediatric dentistry. (1999) [Pubmed]
  4. "Risk periods" associated with the development of dental fluorosis in maxillary permanent central incisors: a meta-analysis. Bårdsen, A. Acta Odontol. Scand. (1999) [Pubmed]
  5. A syndrome of epilepsy, dementia, and amelogenesis imperfecta: genetic and clinical features. Christodoulou, J., Hall, R.K., Menahem, S., Hopkins, I.J., Rogers, J.G. J. Med. Genet. (1988) [Pubmed]
  6. Ameloblastin is a cell adhesion molecule required for maintaining the differentiation state of ameloblasts. Fukumoto, S., Kiba, T., Hall, B., Iehara, N., Nakamura, T., Longenecker, G., Krebsbach, P.H., Nanci, A., Kulkarni, A.B., Yamada, Y. J. Cell Biol. (2004) [Pubmed]
  7. The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes. Salido, E.C., Yen, P.H., Koprivnikar, K., Yu, L.C., Shapiro, L.J. Am. J. Hum. Genet. (1992) [Pubmed]
  8. Mapping of the gene for X-linked amelogenesis imperfecta by linkage analysis. Lagerström, M., Dahl, N., Iselius, L., Bäckman, B., Pettersson, U. Am. J. Hum. Genet. (1990) [Pubmed]
  9. Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI). Masuya, H., Shimizu, K., Sezutsu, H., Sakuraba, Y., Nagano, J., Shimizu, A., Fujimoto, N., Kawai, A., Miura, I., Kaneda, H., Kobayashi, K., Ishijima, J., Maeda, T., Gondo, Y., Noda, T., Wakana, S., Shiroishi, T. Hum. Mol. Genet. (2005) [Pubmed]
  10. A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2). Mårdh, C.K., Bäckman, B., Holmgren, G., Hu, J.C., Simmer, J.P., Forsman-Semb, K. Hum. Mol. Genet. (2002) [Pubmed]
  11. SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1). Lench, N.J., Brook, A.H., Winter, G.B. Hum. Mol. Genet. (1994) [Pubmed]
  12. Enamelysin (matrix metalloproteinase 20)-deficient mice display an amelogenesis imperfecta phenotype. Caterina, J.J., Skobe, Z., Shi, J., Ding, Y., Simmer, J.P., Birkedal-Hansen, H., Bartlett, J.D. J. Biol. Chem. (2002) [Pubmed]
  13. The enamel protein amelogenin binds to the N-acetyl-D-glucosamine-mimicking peptide motif of cytokeratins. Ravindranath, R.M., Tam, W.Y., Nguyen, P., Fincham, A.G. J. Biol. Chem. (2000) [Pubmed]
  14. Investigation of osteocalcin, osteonectin, and dentin sialophosphoprotein in developing human teeth. Papagerakis, P., Berdal, A., Mesbah, M., Peuchmaur, M., Malaval, L., Nydegger, J., Simmer, J., Macdougall, M. Bone (2002) [Pubmed]
  15. Mapping of the locus for autosomal dominant amelogenesis imperfecta (AIH2) to a 4-Mb YAC contig on chromosome 4q11-q21. Kärrman, C., Bäckman, B., Dixon, M., Holmgren, G., Forsman, K. Genomics (1997) [Pubmed]
  16. Molecular cloning, chromosomal mapping, and characteristic expression in tooth organ of rat and mouse Krox-25. Lee, S.K., Kim, Y.S., Lee, S.S., Lee, Y.J., Song, I.S., Park, S.C., Kozak, C., Yamada, Y. Genomics (2004) [Pubmed]
  17. The cadherin-catenin complex is expressed alternately with the adenomatous polyposis coli protein during rat incisor amelogenesis. Sorkin, B.C., Wang, M.Y., Dobeck, J.M., Albergo, K.L., Skobe, Z. J. Histochem. Cytochem. (2000) [Pubmed]
  18. Disturbances of the secretory stage of amelogenesis in fluorosed deer teeth: a scanning electron-microscopic study. Kierdorf, H., Kierdorf, U. Cell Tissue Res. (1997) [Pubmed]
  19. Analysis of developmental processes possibly related to human dental sexual dimorphism in permanent and deciduous canines. Moss, M.L., Moss-Salentijn, L. Am. J. Phys. Anthropol. (1977) [Pubmed]
  20. Evidence by signal peptide trap technology for the expression of carbonic anhydrase 6 in rat incisor enamel organs. Smith, C.E., Nanci, A., Moffatt, P. Eur. J. Oral Sci. (2006) [Pubmed]
  21. Amelogenin interacts with cytokeratin-5 in ameloblasts during enamel growth. Ravindranath, R.M., Basilrose, R.M., Ravindranath, N.H., Vaitheesvaran, B. J. Biol. Chem. (2003) [Pubmed]
  22. Amelogenin-cytokeratin 14 interaction in ameloblasts during enamel formation. Ravindranath, R.M., Tam, W.Y., Bringas, P., Santos, V., Fincham, A.G. J. Biol. Chem. (2001) [Pubmed]
  23. Possible function of matrix proteins in fluoride incorporation into enamel mineral during porcine amelogenesis. Aoba, T., Collins, J., Moreno, E.C. J. Dent. Res. (1989) [Pubmed]
  24. Reversible structural changes of octacalcium phosphate and labile acid phosphate. Suzuki, O., Yagishita, H., Amano, T., Aoba, T. J. Dent. Res. (1995) [Pubmed]
  25. Subunit structures in hydroxyapatite crystal development in enamel: implications for amelogenesis imperfecta. Robinson, C., Shore, R.C., Wood, S.R., Brookes, S.J., Smith, D.A., Wright, J.T., Connell, S., Kirkham, J. Connect. Tissue Res. (2003) [Pubmed]
  26. Gene expression patterns of murine dentin matrix protein 1 (Dmp1) and dentin sialophosphoprotein (DSPP) suggest distinct developmental functions in vivo. D'Souza, R.N., Cavender, A., Sunavala, G., Alvarez, J., Ohshima, T., Kulkarni, A.B., MacDougall, M. J. Bone Miner. Res. (1997) [Pubmed]
  27. Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta. Lagerström-Fermér, M., Nilsson, M., Bäckman, B., Salido, E., Shapiro, L., Pettersson, U., Landegren, U. Genomics (1995) [Pubmed]
  28. MMP20 active-site mutation in hypomaturation amelogenesis imperfecta. Ozdemir, D., Hart, P.S., Ryu, O.H., Choi, S.J., Ozdemir-Karatas, M., Firatli, E., Piesco, N., Hart, T.C. J. Dent. Res. (2005) [Pubmed]
  29. Msx2 controls ameloblast terminal differentiation. Bei, M., Stowell, S., Maas, R. Dev. Dyn. (2004) [Pubmed]
  30. Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients. Mårdh, C.K., Bäckman, B., Simmons, D., Golovleva, I., Gu, T.T., Holmgren, G., MacDougall, M., Forsman-Semb, K. Eur. J. Oral Sci. (2001) [Pubmed]
  31. Fluoride enhances intracellular degradation of amelogenins during secretory phase of amelogenesis of hamster teeth in organ culture. Bronckers, A.L., Lyaruu, D.M., Bervoets, T.J., Wöltgens, J.H. Connect. Tissue Res. (2002) [Pubmed]
  32. Histogenetic aspects of the composition and structure of human ectopic enamel, studied by scanning electron microscopy. Gaspersic, D. Arch. Oral Biol. (1992) [Pubmed]
  33. X-linked (recessive) hypomaturation amelogenesis imperfecta: a prosthodontic, genetic, and histopathologic report. Patel, R.R., Hovijitra, S., Kafrawy, A.H., Bixler, D. The Journal of prosthetic dentistry. (1991) [Pubmed]
  34. PCR detection of the human amelogenin gene and its application to the diagnosis of amelogenesis imperfecta. Sekiguchi, H., Minaguchi, K., Machida, Y., Yakushiji, M. Bull. Tokyo Dent. Coll. (1998) [Pubmed]
  35. Open bite deformity in amelogenesis imperfecta. Part 2: Le Fort I osteotomies and treatment results. Hoppenreijs, T.J., Voorsmit, R.A., Freihofer, H.P., van 't Hof, M.A. Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery. (1998) [Pubmed]
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