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Volumn 212, Issue 8, 2012, Pages 377-379

Amelogenesis imperfecta: An introduction

Author keywords

[No Author keywords available]

Indexed keywords

ENAMEL PROTEIN;

EID: 84860438371     PISSN: 00070610     EISSN: 17417503     Source Type: Journal    
DOI: 10.1038/sj.bdj.2012.314     Document Type: Review
Times cited : (100)

References (18)
  • 1
    • 34047127502 scopus 로고    scopus 로고
    • Prevalence and distribution of dental anomalies in orthodontic patients
    • Altug-Atac A T, Erdem D. Prevalence and distribution of dental anomalies in orthodontic patients. Am J Orthod Dentofacial Orthop 2007; 131: 510-514.
    • (2007) Am J Orthod Dentofacial Orthop , vol.131 , pp. 510-514
    • Altug-Atac, A.T.1    Erdem, D.2
  • 2
    • 0022670545 scopus 로고
    • Amelogenesis imperfecta: Prevalence and incidence in a northern Swedish county
    • Bäckman B, Holm A K. Amelogenesis imperfecta: prevalence and incidence in a northern Swedish county. Community Dent Oral Epidemiol 1986; 14: 43-47.
    • (1986) Community Dent Oral Epidemiol , vol.14 , pp. 43-47
    • Bäckman, B.1    Holm, A.K.2
  • 3
    • 0016611181 scopus 로고
    • Congenital oral anomalies in Argentinian children
    • Sedano H O. Congenital oral anomalies in Argentinian children. Community Dent Oral Epidemiol 1975; 3: 61-63.
    • (1975) Community Dent Oral Epidemiol , vol.3 , pp. 61-63
    • Sedano, H.O.1
  • 4
    • 0018409771 scopus 로고
    • Amelogenesis imperfecta among Israeli Jews and the description of a new type of local hypoplastic autosomal recessive amelogenesis imperfecta
    • Chosack A, Eidelman E, Wisotski I, Cohen T. Amelogenesis imperfecta among Israeli Jews and the description of a new type of local hypoplastic autosomal recessive amelogenesis imperfecta. Oral Surg Oral Med Oral Pathol 1979; 47: 148-156.
    • (1979) Oral Surg Oral Med Oral Pathol , vol.47 , pp. 148-156
    • Chosack, A.1    Eidelman, E.2    Wisotski, I.3    Cohen, T.4
  • 5
    • 0037281187 scopus 로고    scopus 로고
    • Amelogenesis imperfecta: A classification and catalogue for the 21st century
    • Aldred M J, Savarirayan R, Crawford P J. Amelogenesis imperfecta: a classification and catalogue for the 21st century. Oral Dis 2003; 9: 19-23.
    • (2003) Oral Dis , vol.9 , pp. 19-23
    • Aldred, M.J.1    Savarirayan, R.2    Crawford, P.J.3
  • 6
    • 57449090278 scopus 로고    scopus 로고
    • Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4
    • Wright J T, Hart T C, Hart P S et al. Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4. Cells Tissues Organs 2009; 189: 224-229.
    • (2009) Cells Tissues Organs , vol.189 , pp. 224-229
    • Wright, J.T.1    Hart, T.C.2    Hart, P.S.3
  • 7
    • 0036566265 scopus 로고    scopus 로고
    • 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. A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2). Hum Mol Genet 2002; 11: 1069-1074.
    • (2002) Hum Mol Genet , vol.11 , pp. 1069-1074
    • Mardh, C.K.1    Bäckman, B.2    Holmgren, G.3    Hu, J.C.4    Simmer, J.P.5    Forsman-Semb, K.6
  • 8
    • 44849142485 scopus 로고    scopus 로고
    • Enamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in mice
    • Hu J C, Hu Y, Smith C E et al. Enamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in mice. J Biol Chem 2008; 283: 10858-10871.
    • (2008) J Biol Chem , vol.283 , pp. 10858-10871
    • Hu, J.C.1    Hu, Y.2    Smith, C.E.3
  • 9
    • 0035943668 scopus 로고    scopus 로고
    • Amelogenin-deficient mice display an amelogenesis imperfecta phenotype
    • Gibson C W, Yuan Z A, Hall B et al. Amelogenin-deficient mice display an amelogenesis imperfecta phenotype. J Biol Chem 2001; 276: 31871-31875.
    • (2001) J Biol Chem , vol.276 , pp. 31871-31875
    • Gibson, C.W.1    Yuan, Z.A.2    Hall, B.3
  • 10
    • 12244272406 scopus 로고    scopus 로고
    • Relationship of phenotype and genotype in X-linked amelogenesis imperfecta
    • Wright J T, Hart P S, Aldred M J et al. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta. Connect Tissue Res 2003; 1: 72-78.
    • (2003) Connect Tissue Res , vol.1 , pp. 72-78
    • Wright, J.T.1    Hart, P.S.2    Aldred, M.J.3
  • 11
    • 3142773337 scopus 로고    scopus 로고
    • Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
    • Hart P S, Hart T C, Michalec M D et al. Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta. J Med Genet 2004; 41: 545-549.
    • (2004) J Med Genet , vol.41 , pp. 545-549
    • Hart, P.S.1    Hart, T.C.2    Michalec, M.D.3
  • 12
    • 15044355868 scopus 로고    scopus 로고
    • MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta
    • Kim J W, Simmer J P, Hart T C et al. MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta. J Med Genet 2005; 42: 271-275.
    • (2005) J Med Genet , vol.42 , pp. 271-275
    • Kim, J.W.1    Simmer, J.P.2    Hart, T.C.3
  • 13
    • 67650529834 scopus 로고    scopus 로고
    • Hypomaturation enamel defects in Klk4 knockout/lacz knockin mice
    • Simmer J P, Hu Y, Lertlam R, Yamakoshi Y, Hu J C. Hypomaturation enamel defects in Klk4 knockout/lacz knockin mice. J Biol Chem 2009; 284: 19110-19121.
    • (2009) J Biol Chem , vol.284 , pp. 19110-19121
    • Simmer, J.P.1    Hu, Y.2    Lertlam, R.3    Yamakoshi, Y.4    Hu, J.C.5
  • 14
    • 34247857785 scopus 로고    scopus 로고
    • Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta
    • Santos M C, Hart P S, Ramaswami M, Kanno C M, Hart T C, Line S R. Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta. Head Face Med 2007; 3: 8.
    • (2007) Head Face Med , vol.3 , pp. 8
    • Santos, M.C.1    Hart, P.S.2    Ramaswami, M.3    Kanno, C.M.4    Hart, T.C.5    Line, S.R.6
  • 15
    • 65249169172 scopus 로고    scopus 로고
    • Mutational spectrum of FAM83H: The C-terminal portion is required for tooth enamel calcification
    • Lee S K, Hu J C, Bartlett J D et al. Mutational spectrum of FAM83H: the C-terminal portion is required for tooth enamel calcification. Hum Mutat 2008; 8: E95-E99.
    • (2008) Hum Mutat , vol.8
    • Lee, S.K.1    Hu, J.C.2    Bartlett, J.D.3
  • 16
    • 66149136519 scopus 로고    scopus 로고
    • Phenotypic variation in FAM83H-associated amelogenesis imperfecta
    • Wright J T, Frazier-Bowers S, Simmons D et al. Phenotypic variation in FAM83H-associated amelogenesis imperfecta. J Dent Res 2009; 88: 356-360.
    • (2009) J Dent Res , vol.88 , pp. 356-360
    • Wright, J.T.1    Frazier-Bowers, S.2    Simmons, D.3
  • 18
    • 47349127113 scopus 로고    scopus 로고
    • Amelogenesis imperfecta - A systematic literature review of associated dental and oro-facial abnormalities and their impact on patients
    • Poulsen S, Gjørup H, Haubek D et al. Amelogenesis imperfecta - A systematic literature review of associated dental and oro-facial abnormalities and their impact on patients. Acta Odontol Scand 2008; 66: 193-199.
    • (2008) Acta Odontol Scand , vol.66 , pp. 193-199
    • Poulsen, S.1    Gjørup, H.2    Haubek, D.3


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