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Volumn 50, Issue 2 SPEC. ISS., 2005, Pages 181-184

Distribution and structure of dental enamel in incisors of Tabby mice

Author keywords

Enamel; Incisor; Mouse; Scanning electron microscopy; Tabby

Indexed keywords


EID: 13844254353     PISSN: 00039969     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.archoralbio.2004.11.003     Document Type: Conference Paper
Times cited : (13)

References (10)
  • 1
    • 0021032858 scopus 로고
    • Evidence from thiol histochemistry for homology between the Tabby-crinkled syndrome in mice and human ectodermal dysplasia
    • N.L. Weeks, and S.R. Blecher Evidence from thiol histochemistry for homology between the Tabby-crinkled syndrome in mice and human ectodermal dysplasia J Histochem Cytochem 31 1983 1407 1411
    • (1983) J Histochem Cytochem , vol.31 , pp. 1407-1411
    • Weeks, N.L.1    Blecher, S.R.2
  • 2
    • 0013806515 scopus 로고
    • Genes and genotypes affecting the teeth of the mouse
    • H. Grüneberg Genes and genotypes affecting the teeth of the mouse J Embryol Exp Morphol 14 1965 137 159
    • (1965) J Embryol Exp Morphol , vol.14 , pp. 137-159
    • Grüneberg, H.1
  • 5
    • 10244229122 scopus 로고    scopus 로고
    • Morphological characteristics of mouse incisor enamel
    • C.B. Møinichen, S.P. Lyngstadaas, and S. Risnes Morphological characteristics of mouse incisor enamel J Anat 189 1996 325 333
    • (1996) J Anat , vol.189 , pp. 325-333
    • Møinichen, C.B.1    Lyngstadaas, S.P.2    Risnes, S.3
  • 6
    • 0014566957 scopus 로고
    • Aspects of the tabby-crinkled-downless syndrome. Part I. The development of tabby teeth
    • J.A. Sofaer Aspects of the tabby-crinkled-downless syndrome. Part I. The development of tabby teeth J Embryol Exp Morphol 22 1969 181 205
    • (1969) J Embryol Exp Morphol , vol.22 , pp. 181-205
    • Sofaer, J.A.1
  • 7
    • 12644310324 scopus 로고    scopus 로고
    • The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains
    • A. Srivastava, J. Pispa, A.J. Hartung, Y. Du, S. Ezer, and T. Jenks The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains Proc Natl Acad Sci USA 94 1997 13069 13074
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 13069-13074
    • Srivastava, A.1    Pispa, J.2    Hartung, A.J.3    Du, Y.4    Ezer, S.5    Jenks, T.6
  • 8
    • 0035862916 scopus 로고    scopus 로고
    • TNF signaling via the ligand-receptor pair ectodysplasin and Edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis
    • J. Laurikkala, M. Mikkola, T. Mustonen, T. Åberg, P. Koppinen, and J. Pispa TNF signaling via the ligand-receptor pair ectodysplasin and Edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis Dev Biol 229 2001 443 455
    • (2001) Dev Biol , vol.229 , pp. 443-455
    • Laurikkala, J.1    Mikkola, M.2    Mustonen, T.3    Åberg, T.4    Koppinen, P.5    Pispa, J.6
  • 10
    • 0035924366 scopus 로고    scopus 로고
    • Gene defect in ectodermal dysplasia implicates a death domain adapter in development
    • D.J. Headon, S.A. Emmal, B.M. Ferguson, A.S. Tucker, M.J. Justice, and P.T. Sharpe Gene defect in ectodermal dysplasia implicates a death domain adapter in development Nature 414 2001 913 916
    • (2001) Nature , vol.414 , pp. 913-916
    • Headon, D.J.1    Emmal, S.A.2    Ferguson, B.M.3    Tucker, A.S.4    Justice, M.J.5    Sharpe, P.T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.