메뉴 건너뛰기




Volumn 78, Issue 6, 1999, Pages 1277-1282

Genetic Linkage of the Dentinogenesis Imperf ecta Type III Locus to Chromosome 4q

Author keywords

Chromosome 4q; Dentin dysplasia; Dentin matrix protein 1; Dentinogenesis imperfecta; Linkage

Indexed keywords

DMP1 PROTEIN, HUMAN; DNA; PHOSPHOPROTEIN; SCLEROPROTEIN;

EID: 0033278076     PISSN: 00220345     EISSN: None     Source Type: Journal    
DOI: 10.1177/00220345990780061301     Document Type: Article
Times cited : (27)

References (24)
  • 1
    • 0028844750 scopus 로고
    • Mapping of the human dentin matrix acidic phosphoprotein gene (DMP1) to the dentinogenesis imperfecta type II critical region at chromosome 4q21
    • Aplin HM, Hirst KL, Crosby AH, Dixon MJ (1995). Mapping of the human dentin matrix acidic phosphoprotein gene (DMP1) to the dentinogenesis imperfecta type II critical region at chromosome 4q21. Genomics 30:347-349.
    • (1995) Genomics , vol.30 , pp. 347-349
    • Aplin, H.M.1    Hirst, K.L.2    Crosby, A.H.3    Dixon, M.J.4
  • 3
    • 0345128844 scopus 로고
    • Polymorphic DNA region adjacent to the 5' end of the human insulin gene
    • Bell GI, Karam JH, Rutter WJ (1981). Polymorphic DNA region adjacent to the 5' end of the human insulin gene. Proc Nail Acad Sei USA 78:5759-5763.
    • (1981) Proc Nail Acad Sei USA , vol.78 , pp. 5759-5763
    • Bell, G.I.1    Karam, J.H.2    Rutter, W.J.3
  • 4
    • 0022989096 scopus 로고
    • An autosomal-dominant form of juvenile periodontitis: Its localization to chromosome 4 and linkage to dentinogenesis imperfecta
    • Boughman JA, Halloran SL, Roulston D, Schwartz S, Suzuki JB, Weitkamp LR, et al. (1986). An autosomal-dominant form of juvenile periodontitis: its localization to chromosome 4 and linkage to dentinogenesis imperfecta. J Craniofac Genet Dev Biol 6:341-350.
    • (1986) J Craniofac Genet Dev Biol , vol.6 , pp. 341-350
    • Boughman, J.A.1    Halloran, S.L.2    Roulston, D.3    Schwartz, S.4    Suzuki, J.B.5    Weitkamp, L.R.6
  • 10
    • 0029030406 scopus 로고
    • Genomic organization of the human osteopontin gene: Exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II
    • Crosby AH, Edwards SJ, Murray JC, Dixon MJ (1995b). Genomic organization of the human osteopontin gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II. Genomics 27:155-160.
    • (1995) Genomics , vol.27 , pp. 155-160
    • Crosby, A.H.1    Edwards, S.J.2    Murray, J.C.3    Dixon, M.J.4
  • 13
    • 13344259999 scopus 로고    scopus 로고
    • A comprehensive genetic map of the human genome based on 5,264 microsatellites
    • Dib C, Faure S, Fizames C, Samsom D, Drouot N, Vignal A, et al. (1996). A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154.
    • (1996) Nature , vol.380 , pp. 152-154
    • Dib, C.1    Faure, S.2    Fizames, C.3    Samsom, D.4    Drouot, N.5    Vignal, A.6
  • 14
    • 0028059583 scopus 로고
    • Localization of a gene form autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q
    • Forsman K, Lind L, Backman B, Westemark E, Holmgren G (1994). Localization of a gene form autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q. Hum Mol Genet 3:1621-1625.
    • (1994) Hum Mol Genet , vol.3 , pp. 1621-1625
    • Forsman, K.1    Lind, L.2    Backman, B.3    Westemark, E.4    Holmgren, G.5
  • 15
    • 0002408984 scopus 로고    scopus 로고
    • Elucidation of the sequence and the genomic organization of the human dentin matrix acidic phosphoprotein gene: Exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II
    • Hirst K, Simmons D, Feng J, Aplin H, Dixon MJ, MacDougall M (1997). Elucidation of the sequence and the genomic organization of the human dentin matrix acidic phosphoprotein gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II. Genomics 42:3845.
    • (1997) Genomics , vol.42 , pp. 3845
    • Hirst, K.1    Simmons, D.2    Feng, J.3    Aplin, H.4    Dixon, M.J.5    MacDougall, M.6
  • 18
    • 0020828116 scopus 로고
    • Dentinogenesis imperfecta in the Brandywine isolate (DGI type III): Clinical, radiologie and scanning electron scopic studies of the dentition
    • Levin LS, Leaf SH, Jelmini RJ, Rose JJ, Rosenbaum KN (1983). Dentinogenesis imperfecta in the Brandywine isolate (DGI type III): clinical, radiologie and scanning electron scopic studies of the dentition. Oral Surg Oral Med Oral Pathol 56:267-274.
    • (1983) Oral Surg Oral Med Oral Pathol , vol.56 , pp. 267-274
    • Levin, L.S.1    Leaf, S.H.2    Jelmini, R.J.3    Rose, J.J.4    Rosenbaum, K.N.5
  • 19
    • 0031601168 scopus 로고    scopus 로고
    • Refined mapping of the human dentin sialophosphoprotein (DSPP) gene within the critical dentinogenesis imperfecta type II and dentin dysplasia type II loci
    • MacDougall M (1998). Refined mapping of the human dentin sialophosphoprotein (DSPP) gene within the critical dentinogenesis imperfecta type II and dentin dysplasia type II loci. EurJOral Sei 106(Suppl l):227-233.
    • (1998) EurJOral Sei , vol.106 , Issue.50 SUPPL. , pp. 227-233
    • MacDougall, M.1
  • 20
    • 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
  • 21
    • 0015612856 scopus 로고
    • A proposed classification for heritable human dentin defects with a description of a new entity
    • Shields ED, Bixler D, El-Kafrawy AM (1973). A proposed classification for heritable human dentin defects with a description of a new entity. Arch Oral Biol 18:543-553.
    • (1973) Arch Oral Biol , vol.18 , pp. 543-553
    • Shields, E.D.1    Bixler, D.2    El-Kafrawy, A.M.3
  • 22
    • 84941021107 scopus 로고
    • Hereditary defects in enamel and dentin
    • Witkop CJ (1957). Hereditary defects in enamel and dentin. Acta Genet 7:236-239.
    • (1957) Acta Genet , vol.7 , pp. 236-239
    • Witkop, C.J.1
  • 23
    • 0015109963 scopus 로고
    • Manifestations of genetic disease in the human pulp
    • Witkop CJ Jr (1971). Manifestations of genetic disease in the human pulp. Oral Surg Oral Med Oral Patliol 32:278-316.
    • (1971) Oral Surg Oral Med Oral Patliol , vol.32 , pp. 278-316
    • Witkop Jr., C.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.