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Volumn 81, Issue 4, 2002, Pages 274-278

The role of MSX1 in human tooth agenesis

Author keywords

Dental patterning; Homeobox; MSX1; Odontogenesis

Indexed keywords

HOMEODOMAIN PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR MSX1;

EID: 0036528341     PISSN: 00220345     EISSN: None     Source Type: Journal    
DOI: 10.1177/154405910208100410     Document Type: Article
Times cited : (156)

References (30)
  • 2
    • 0035058579 scopus 로고    scopus 로고
    • Evidence of a sex-dependent association between the MSX1 locus and nonsyndromic cleft lip with or without cleft palate in the Chilean population
    • Blanco R, Chakraborty R, Barton SA, Carreno H, Paredes M, Jara L, et al, (2001). Evidence of a sex-dependent association between the MSX1 locus and nonsyndromic cleft lip with or without cleft palate in the Chilean population. Hum Biol 73(1):81-89.
    • (2001) Hum Biol , vol.73 , Issue.1 , pp. 81-89
    • Blanco, R.1    Chakraborty, R.2    Barton, S.A.3    Carreno, H.4    Paredes, M.5    Jara, L.6
  • 4
    • 0029924238 scopus 로고    scopus 로고
    • Comparison of MSX-1 and MSX-2 suggests a molecular basis for functional redundancy
    • Catron KM, Wang H, Hu G, Shen MM, Abate-Shen C (1996). Comparison of MSX-1 and MSX-2 suggests a molecular basis for functional redundancy. Mech Dev 55:185-199.
    • (1996) Mech Dev , vol.55 , pp. 185-199
    • Catron, K.M.1    Wang, H.2    Hu, G.3    Shen, M.M.4    Abate-Shen, C.5
  • 5
    • 0030883003 scopus 로고    scopus 로고
    • Relationships among msx gene structure and function in zebrafish and other vertebrates
    • Ekker M, Akimenko M, Allende M, Smith R, Drouin G, Langille R, et al. (1997). Relationships among msx gene structure and function in zebrafish and other vertebrates. Mol Biol Evol 14:1008-1022.
    • (1997) Mol Biol Evol , vol.14 , pp. 1008-1022
    • Ekker, M.1    Akimenko, M.2    Allende, M.3    Smith, R.4    Drouin, G.5    Langille, R.6
  • 6
    • 0028365905 scopus 로고
    • Craniofacial malformations: Towards a molecular understanding
    • Ferguson MWJ (1994). Craniofacial malformations: towards a molecular understanding. Nat Genet 6:329-330.
    • (1994) Nat Genet , vol.6 , pp. 329-330
    • Ferguson, M.W.J.1
  • 8
    • 0026043763 scopus 로고
    • Structure and sequence of the human homeobox gene HOX7
    • Hewitt JE, Clark LN, Ivens A, Williamson R (1991). Structure and sequence of the human homeobox gene HOX7. Genomics 11:670-678.
    • (1991) Genomics , vol.11 , pp. 670-678
    • Hewitt, J.E.1    Clark, L.N.2    Ivens, A.3    Williamson, R.4
  • 9
    • 0345471389 scopus 로고    scopus 로고
    • A conserved motif in goosecoid mediates groucho-dependent repression in Drosophila embryos
    • Jimenez G, Verrijzer CP, Ish-Horowicz D (1999). A conserved motif in goosecoid mediates groucho-dependent repression in Drosophila embryos. Mol Cell Biol 19:2080-2087.
    • (1999) Mol Cell Biol , vol.19 , pp. 2080-2087
    • Jimenez, G.1    Verrijzer, C.P.2    Ish-Horowicz, D.3
  • 11
    • 0029886532 scopus 로고    scopus 로고
    • Parametric and nonparametric linkage analysis: A unified multipoint approach
    • Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES (1996). Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 58:1347-1363.
    • (1996) Am J Hum Genet , vol.58 , pp. 1347-1363
    • Kruglyak, L.1    Daly, M.J.2    Reeve-Daly, M.P.3    Lander, E.S.4
  • 13
    • 0025979545 scopus 로고
    • The homeobox gene Hox 7.1 has specific regional and temporal expression patterns during early murine craniofacial embryogenesis, especially tooth development in vivo and in vitro
    • MacKenzie A, Leeming GL, Jowett AK, Ferguson MWJ, Sharpe PT (1991). The homeobox gene Hox 7.1 has specific regional and temporal expression patterns during early murine craniofacial embryogenesis, especially tooth development in vivo and in vitro. Development 111:269-285.
    • (1991) Development , vol.111 , pp. 269-285
    • MacKenzie, A.1    Leeming, G.L.2    Jowett, A.K.3    Ferguson, M.W.J.4    Sharpe, P.T.5
  • 14
    • 0029083386 scopus 로고
    • Gene defect in hypodontia: Exclusion of MSX1 and MSX2 as candidate genes
    • Nieminen P, Arte S, Pirinen S, Peltonen L, Thesleff I (1995). Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes. Human Genet 96:305-308.
    • (1995) Human Genet , vol.96 , pp. 305-308
    • Nieminen, P.1    Arte, S.2    Pirinen, S.3    Peltonen, L.4    Thesleff, I.5
  • 16
    • 0030955889 scopus 로고    scopus 로고
    • Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: Mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches
    • Qiu M, Bulfone A, Ghattas I, Meneses JJ, Christensen L, Sharpe PT, et al. (1997). Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches. Dev Biol 185:165-184.
    • (1997) Dev Biol , vol.185 , pp. 165-184
    • Qiu, M.1    Bulfone, A.2    Ghattas, I.3    Meneses, J.J.4    Christensen, L.5    Sharpe, P.T.6
  • 18
    • 0028292605 scopus 로고
    • Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
    • Satokata I, Maas R (1994). Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat Genet 6:348-356.
    • (1994) Nat Genet , vol.6 , pp. 348-356
    • Satokata, I.1    Maas, R.2
  • 19
    • 0034029571 scopus 로고    scopus 로고
    • Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
    • Satokata I, Ma L, Ohshima H, Bei M, Woo I, Nishizawa K, et al. (2000). Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation. Nat Genet 24:391-395.
    • (2000) Nat Genet , vol.24 , pp. 391-395
    • Satokata, I.1    Ma, L.2    Ohshima, H.3    Bei, M.4    Woo, I.5    Nishizawa, K.6
  • 21
    • 0029188387 scopus 로고
    • Homeobox genes and orofacial development
    • Sharpe PT (1995). Homeobox genes and orofacial development. Connect Tissue Res 32(1-4):17-25.
    • (1995) Connect Tissue Res , vol.32 , Issue.1-4 , pp. 17-25
    • Sharpe, P.T.1
  • 22
    • 0029846335 scopus 로고    scopus 로고
    • A conserved region of engrailed, shared among all en-, gsc-, Nk1-, Nk2- and msh-class homeoproteins, mediates active transcriptional repression in vivo
    • Smith S, Jaynes J (1996). A conserved region of engrailed, shared among all en-, gsc-, Nk1-, Nk2- and msh-class homeoproteins, mediates active transcriptional repression in vivo. Development 122:3141-3150.
    • (1996) Development , vol.122 , pp. 3141-3150
    • Smith, S.1    Jaynes, J.2
  • 24
    • 0031602169 scopus 로고    scopus 로고
    • Patterning of the murine dentition by homeobox genes
    • Thomas BL, Sharpe PT (1998). Patterning of the murine dentition by homeobox genes. Eur J Oral Sci 106(Suppl 1):48-54.
    • (1998) Eur J Oral Sci , vol.106 , Issue.1 SUPPL. , pp. 48-54
    • Thomas, B.L.1    Sharpe, P.T.2
  • 25
    • 0034028899 scopus 로고    scopus 로고
    • MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
    • published erratum appears in Nat Genet 2000 May;25(1):125
    • van den Boogaard MJ, Dorland M, Beemer FA, van Amstel HK (2000). MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans [published erratum appears in Nat Genet 2000 May;25(1):125]. Nat Genet 24:342-343.
    • (2000) Nat Genet , vol.24 , pp. 342-343
    • Van Den Boogaard, M.J.1    Dorland, M.2    Beemer, F.A.3    Van Amstel, H.K.4
  • 26
    • 0034199841 scopus 로고    scopus 로고
    • The genetics of human tooth agenesis: New discoveries for understanding dental anomalies
    • Vastardis H (2000). The genetics of human tooth agenesis: new discoveries for understanding dental anomalies. Am J Orthod Dentofac Orthop 117:650-656.
    • (2000) Am J Orthod Dentofac Orthop , vol.117 , pp. 650-656
    • Vastardis, H.1
  • 27
    • 0030017452 scopus 로고    scopus 로고
    • A human MSX1 homeodomain missense mutation causes selective tooth agenesis
    • Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE (1996). A human MSX1 homeodomain missense mutation causes selective tooth agenesis [see comments]. Nat Genet 13:417-421.
    • (1996) Nat Genet , vol.13 , pp. 417-421
    • Vastardis, H.1    Karimbux, N.2    Guthua, S.W.3    Seidman, J.G.4    Seidman, C.E.5
  • 28
    • 8044228418 scopus 로고    scopus 로고
    • Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice
    • Winograd J, Reilly MP, Roe R, Lutz J, Laughner E, Xu X, et al. (1997). Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice. Hum Mol Genet 6:369-379.
    • (1997) Hum Mol Genet , vol.6 , pp. 369-379
    • Winograd, J.1    Reilly, M.P.2    Roe, R.3    Lutz, J.4    Laughner, E.5    Xu, X.6
  • 29
    • 0029944653 scopus 로고    scopus 로고
    • A role for the Msx-1 homeodomain in transcriptional regulation: Residues in the N-terminal arm mediate TATA binding protein interaction and transcriptional repression
    • Zhang H, Catron KM, Abate-Shen C (1996). A role for the Msx-1 homeodomain in transcriptional regulation: residues in the N-terminal arm mediate TATA binding protein interaction and transcriptional repression. Proc Natl Acad Sci USA 93:1764-1769.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 1764-1769
    • Zhang, H.1    Catron, K.M.2    Abate-Shen, C.3
  • 30
    • 0030962036 scopus 로고    scopus 로고
    • Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism
    • Zhang H, Hu G, Wang H, Sciavolino P, Iler N, Shen M, et al. (1997). Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism. Mol Cell Biol 17:2920-2932.
    • (1997) Mol Cell Biol , vol.17 , pp. 2920-2932
    • Zhang, H.1    Hu, G.2    Wang, H.3    Sciavolino, P.4    Iler, N.5    Shen, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.