메뉴 건너뛰기




Volumn 83, Issue 8, 2004, Pages 608-612

Amelogenesis imperfecta in a new animal model - A mutation in chromosome 5 (human 4q21)

Author keywords

Amelogenesis imperfecta (AI); Collagen cross links; Hydroxyproline; Pyridinoline; Structure

Indexed keywords

ENAMEL PROTEIN; ETHYLNITROSOUREA; MUTAGENIC AGENT;

EID: 4444317320     PISSN: 00220345     EISSN: None     Source Type: Journal    
DOI: 10.1177/154405910408300805     Document Type: Article
Times cited : (8)

References (31)
  • 1
    • 0028349129 scopus 로고
    • A rapid method for the isolation of the mature collagen cross-links, hydroxylysylpyridinoline (HP) and lysylpyridinoline (LP)
    • Açil Y, Müller PK (1994). A rapid method for the isolation of the mature collagen cross-links, hydroxylysylpyridinoline (HP) and lysylpyridinoline (LP). J Chromatogr A 664:183-188.
    • (1994) J Chromatogr A , vol.664 , pp. 183-188
    • Açil, Y.1    Müller, P.K.2
  • 2
    • 0344211448 scopus 로고    scopus 로고
    • Concentration of collagen cross-links in human dentin bears no relation to the individual age
    • Açil Y, Springer ING, Prasse JG, Hedderich J, Jepsen S (2002). Concentration of collagen cross-links in human dentin bears no relation to the individual age. Int J Legal Med 116:340-343.
    • (2002) Int J Legal Med , vol.116 , pp. 340-343
    • Açil, Y.1    Springer, I.N.G.2    Prasse, J.G.3    Hedderich, J.4    Jepsen, S.5
  • 3
    • 0029262346 scopus 로고
    • Amelogenesis imperfecta - Towards a new classification
    • Aldred MJ, Crawford PJ (1995). Amelogenesis imperfecta - towards a new classification. Oral Dis 1:2-5.
    • (1995) Oral Dis , vol.1 , pp. 2-5
    • Aldred, M.J.1    Crawford, P.J.2
  • 4
    • 0030631977 scopus 로고    scopus 로고
    • Molecular biology of hereditary enamel defects
    • Aldred MJ, Crawford PJ (1997). Molecular biology of hereditary enamel defects. Ciba Found Symp 205:200-209.
    • (1997) Ciba Found Symp , vol.205 , pp. 200-209
    • Aldred, M.J.1    Crawford, P.J.2
  • 5
    • 0037281187 scopus 로고    scopus 로고
    • Amelogenesis imperfecta: A classification and catalogue for the 21st century
    • Aldred MJ, Savarirayan R, Crawford PJ (2003). Amelogenesis imperfecta: a classification and catalogue for the 21st century. Oral Dis 9:19-23.
    • (2003) Oral Dis , vol.9 , pp. 19-23
    • Aldred, M.J.1    Savarirayan, R.2    Crawford, P.J.3
  • 6
    • 0026288942 scopus 로고
    • The extent and distribution of intratubular collagen fibrils in human dentine
    • Dai XF, Ten Cate AR, Limeback H (1991). The extent and distribution of intratubular collagen fibrils in human dentine. Arch Oral Biol 36:775-778.
    • (1991) Arch Oral Biol , vol.36 , pp. 775-778
    • Dai, X.F.1    Ten Cate, A.R.2    Limeback, H.3
  • 7
    • 0019947037 scopus 로고
    • A method for the study of undecalcified bones and teeth with attached soft tissues. The Säge-Schliff (sawing and grinding) technique
    • Donath K, Breuner G (1982). A method for the study of undecalcified bones and teeth with attached soft tissues. The Säge-Schliff (sawing and grinding) technique. J Oral Pathol 11:318.
    • (1982) J Oral Pathol , vol.11 , pp. 318
    • Donath, K.1    Breuner, G.2
  • 8
    • 84995870935 scopus 로고
    • New biomarkers of bone resorption
    • Eyre D (1992). New biomarkers of bone resorption. J Clin Endocrinol Metab 74:470A-470C.
    • (1992) J Clin Endocrinol Metab , vol.74
    • Eyre, D.1
  • 11
    • 9144248989 scopus 로고    scopus 로고
    • Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
    • Hart TC, Hart PS, Gorry MC, Michalec MD, Ryu OH, Uygur C, et al. (2003). Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects. J Med Genet 40:900-906.
    • (2003) J Med Genet , vol.40 , pp. 900-906
    • Hart, T.C.1    Hart, P.S.2    Gorry, M.C.3    Michalec, M.D.4    Ryu, O.H.5    Uygur, C.6
  • 12
    • 0032565508 scopus 로고    scopus 로고
    • Large scale ENU screens in the mouse: Genetics meets genomics
    • Hrabe de Angelis M, Balling R (1998). Large scale ENU screens in the mouse: genetics meets genomics. Mutat Res 400:25-32.
    • (1998) Mutat Res , vol.400 , pp. 25-32
    • Hrabe De Angelis, M.1    Balling, R.2
  • 15
    • 0036827621 scopus 로고    scopus 로고
    • Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary
    • Kida M, Ariga T, Shirakawa T, Oguchi H, Sakiyama Y (2002). Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary. J Dent Res 81:738-742.
    • (2002) J Dent Res , vol.81 , pp. 738-742
    • Kida, M.1    Ariga, T.2    Shirakawa, T.3    Oguchi, H.4    Sakiyama, Y.5
  • 16
    • 0037590912 scopus 로고    scopus 로고
    • The structure of the rat ameloblastin gene and its expression in amelogenesis
    • Lee SK, Kim SM, Lee YJ, Yamada KM, Yamada Y, Chi JG (2003). The structure of the rat ameloblastin gene and its expression in amelogenesis. Mol Cells 15:216-225.
    • (2003) Mol Cells , vol.15 , pp. 216-225
    • Lee, S.K.1    Kim, S.M.2    Lee, Y.J.3    Yamada, K.M.4    Yamada, Y.5    Chi, J.G.6
  • 17
    • 17544404939 scopus 로고    scopus 로고
    • Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21
    • MacDougall M, DuPont BR, Simmons D, Reus B, Krebsbach P, Karrman C, et al. (1997). Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21. Genomics 41:115-118.
    • (1997) Genomics , vol.41 , pp. 115-118
    • MacDougall, M.1    DuPont, B.R.2    Simmons, D.3    Reus, B.4    Krebsbach, P.5    Karrman, C.6
  • 18
    • 0033278076 scopus 로고    scopus 로고
    • Genetic linkage of the dentinogenesis imperfecta type III locus to chromosome 4q
    • MacDougall M, Jeffords LG, Gu TT, Knight CB, Frei G, Reus BE, et al. (1999). Genetic linkage of the dentinogenesis imperfecta type III locus to chromosome 4q. J Dent Res 78:1277-1282.
    • (1999) J Dent Res , vol.78 , pp. 1277-1282
    • MacDougall, M.1    Jeffords, L.G.2    Gu, T.T.3    Knight, C.B.4    Frei, G.5    Reus, B.E.6
  • 19
    • 2542434141 scopus 로고    scopus 로고
    • Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II
    • Malmgren B, Lindskog S, Elgadi A, Norgren S (2004). Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II. Hum Genet 114:491-498.
    • (2004) Hum Genet , vol.114 , pp. 491-498
    • Malmgren, B.1    Lindskog, S.2    Elgadi, A.3    Norgren, S.4
  • 20
    • 0036566265 scopus 로고    scopus 로고
    • A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2)
    • Mardh CK, Backman B, Holmgren G, Hu JC, Simmer JP, Forsman-Semb K (2002). A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2). Hum Mol Genet 11:1069-1074.
    • (2002) Hum Mol Genet , vol.11 , pp. 1069-1074
    • Mardh, C.K.1    Backman, B.2    Holmgren, G.3    Hu, J.C.4    Simmer, J.P.5    Forsman-Semb, K.6
  • 21
    • 3142675387 scopus 로고    scopus 로고
    • Relative levels of mRNA encoding enamel proteins in enamel organ epithelia and odontoblasts
    • Nagano T, Oida S, Ando H, Gomi K, Arai T, Fukae M (2003). Relative levels of mRNA encoding enamel proteins in enamel organ epithelia and odontoblasts. J Dent Res 82:982-986.
    • (2003) J Dent Res , vol.82 , pp. 982-986
    • Nagano, T.1    Oida, S.2    Ando, H.3    Gomi, K.4    Arai, T.5    Fukae, M.6
  • 23
    • 0035422249 scopus 로고    scopus 로고
    • Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta
    • Rajpar MH, Harley K, Laing C, Davies RM, Dixon MJ (2001). Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta. Hum Mol Genet 10:1673-1677.
    • (2001) Hum Mol Genet , vol.10 , pp. 1673-1677
    • Rajpar, M.H.1    Harley, K.2    Laing, C.3    Davies, R.M.4    Dixon, M.J.5
  • 24
    • 0004102213 scopus 로고
    • Berlin: Springer Verlag
    • Sachs L (1992). Angewandte Statistik. Berlin: Springer Verlag, pp. 510-515.
    • (1992) Angewandte Statistik , pp. 510-515
    • Sachs, L.1
  • 25
    • 0035996556 scopus 로고    scopus 로고
    • Inheritance pattern and elemental composition of enamel affected by hypomaturation amelogenesis imperfecta
    • Shore RC, Backman B, Brookes SJ, Kirkham J, Wood SR, Robinson C (2002). Inheritance pattern and elemental composition of enamel affected by hypomaturation amelogenesis imperfecta. Connect Tissue Res 43:466-471.
    • (2002) Connect Tissue Res , vol.43 , pp. 466-471
    • Shore, R.C.1    Backman, B.2    Brookes, S.J.3    Kirkham, J.4    Wood, S.R.5    Robinson, C.6
  • 26
    • 0036313496 scopus 로고    scopus 로고
    • Adaptive adjustment of the adolescent porcine mandibular condyle
    • Springer ING, Suhr M, Fleiner B (2002). Adaptive adjustment of the adolescent porcine mandibular condyle. Bone 31:1190-1195.
    • (2002) Bone , vol.31 , pp. 1190-1195
    • Springer, I.N.G.1    Suhr, M.2    Fleiner, B.3
  • 28
    • 0022763634 scopus 로고
    • Hereditary aspects and classification of hereditary amelogenesis imperfecta
    • Sundell S, Valentin J (1986). Hereditary aspects and classification of hereditary amelogenesis imperfecta. Community Dent Oral Epidemiol 14:211-216.
    • (1986) Community Dent Oral Epidemiol , vol.14 , pp. 211-216
    • Sundell, S.1    Valentin, J.2
  • 29
    • 0016742662 scopus 로고
    • Enamel hypoplasia and anomalies of the enamel
    • Winter GB, Brook AH (1975). Enamel hypoplasia and anomalies of the enamel. Dent Clin North Am 19:3-24.
    • (1975) Dent Clin North Am , vol.19 , pp. 3-24
    • Winter, G.B.1    Brook, A.H.2
  • 30
    • 0026353528 scopus 로고
    • Characterization of the enamel ultrastructure and mineral content in hypoplastic amelogenesis imperfecta
    • Wright JT, Robinson C, Shore R (1991). Characterization of the enamel ultrastructure and mineral content in hypoplastic amelogenesis imperfecta. Oral Surg Oral Med Oral Pathol 72:594-601.
    • (1991) Oral Surg Oral Med Oral Pathol , vol.72 , pp. 594-601
    • Wright, J.T.1    Robinson, C.2    Shore, R.3
  • 31
    • 0035136682 scopus 로고    scopus 로고
    • Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
    • Xiao S, Yu C, Chou X, Yuan W, Wang Y, Bu L, et al. (2001). Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP. Nat Genet 27:201-204.
    • (2001) Nat Genet , vol.27 , pp. 201-204
    • Xiao, S.1    Yu, C.2    Chou, X.3    Yuan, W.4    Wang, Y.5    Bu, L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.