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Volumn 84, Issue 5, 2013, Pages 429-440

Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis

Author keywords

Association; Nucleotide variant; Tooth agenesis; Wnt pathway; WNT10A

Indexed keywords

APC PROTEIN; CTNNB1 PROTEIN; DISHEVELLED 2; NUCLEOTIDE; PROTEIN; TRANSCRIPTION FACTOR MSX1; TRANSCRIPTION FACTOR PAX9; UNCLASSIFIED DRUG; WNT10A PROTEIN; WNT11 PROTEIN;

EID: 84885870052     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/cge.12061     Document Type: Article
Times cited : (65)

References (48)
  • 4
    • 84862907088 scopus 로고    scopus 로고
    • Genetic basis of non-syndromic anomalies of human tooth number
    • Galluccio G, Castellano M, La Monaca C. Genetic basis of non-syndromic anomalies of human tooth number. Arch Oral Biol 2012: 57 (7): 918-930.
    • (2012) Arch Oral Biol , vol.57 , Issue.7 , pp. 918-930
    • Galluccio, G.1    Castellano, M.2    La Monaca, C.3
  • 5
    • 33845340816 scopus 로고    scopus 로고
    • The genetic basis of tooth development and dental defects
    • Thesleff I. The genetic basis of tooth development and dental defects. Am J Med Genet A 2006: 140 (23): 2530-2535.
    • (2006) Am J Med Genet A , vol.140 , Issue.23 , pp. 2530-2535
    • Thesleff, I.1
  • 6
    • 47749109092 scopus 로고    scopus 로고
    • The genetic basis of inherited anomalies of the teeth. Part 1: clinical and molecular aspects of non-syndromic dental disorders
    • Bailleul-Forestier I, Molla M, Verloes A, Berdal A. The genetic basis of inherited anomalies of the teeth. Part 1: clinical and molecular aspects of non-syndromic dental disorders. Eur J Med Genet 2008: 51 (4): 273-291.
    • (2008) Eur J Med Genet , vol.51 , Issue.4 , pp. 273-291
    • Bailleul-Forestier, I.1    Molla, M.2    Verloes, A.3    Berdal, A.4
  • 8
    • 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. A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nat Genet 1996: 13 (4): 417-421.
    • (1996) Nat Genet , vol.13 , Issue.4 , pp. 417-421
    • Vastardis, H.1    Karimbux, N.2    Guthua, S.W.3    Seidman, J.G.4    Seidman, C.E.5
  • 10
    • 2342613578 scopus 로고    scopus 로고
    • Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer
    • Lammi L, Arte S, Somer M et al. Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. Am J Hum Genet 2004: 74 (5): 1043-1050.
    • (2004) Am J Hum Genet , vol.74 , Issue.5 , pp. 1043-1050
    • Lammi, L.1    Arte, S.2    Somer, M.3
  • 11
    • 33744990403 scopus 로고    scopus 로고
    • A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia
    • Tao R, Jin B, Guo SZ et al. A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia. J Hum Genet 2006: 51 (5): 498-502.
    • (2006) J Hum Genet , vol.51 , Issue.5 , pp. 498-502
    • Tao, R.1    Jin, B.2    Guo, S.Z.3
  • 12
    • 79955003002 scopus 로고    scopus 로고
    • WNT10A and isolated hypodontia
    • Kantaputra P, Sripathomsawat W. WNT10A and isolated hypodontia. Am J Med Genet A 2011: 155A (5): 1119-1122.
    • (2011) Am J Med Genet A , vol.155 A , Issue.5 , pp. 1119-1122
    • Kantaputra, P.1    Sripathomsawat, W.2
  • 13
    • 84864094899 scopus 로고    scopus 로고
    • Mutations in WNT10A are present in more than half of isolated hypodontia cases
    • van den Boogaard MJ, Créton M, Bronkhorst Y et al. Mutations in WNT10A are present in more than half of isolated hypodontia cases. J Med Genet 2012: 49 (5): 327-331.
    • (2012) J Med Genet , vol.49 , Issue.5 , pp. 327-331
    • van den Boogaard, M.J.1    Créton, M.2    Bronkhorst, Y.3
  • 14
    • 77949612030 scopus 로고    scopus 로고
    • Wnt/beta-catenin signaling in oral tissue development and disease
    • Liu F, Millar SE. Wnt/beta-catenin signaling in oral tissue development and disease. J Dent Res 2010: 89 (4): 318-330.
    • (2010) J Dent Res , vol.89 , Issue.4 , pp. 318-330
    • Liu, F.1    Millar, S.E.2
  • 16
    • 80052775652 scopus 로고    scopus 로고
    • Wnt5a plays a crucial role in determining tooth size during murine tooth development
    • Cai J, Mutoh N, Shin JO et al. Wnt5a plays a crucial role in determining tooth size during murine tooth development. Cell Tissue Res 2011: 345 (3): 367-377.
    • (2011) Cell Tissue Res , vol.345 , Issue.3 , pp. 367-377
    • Cai, J.1    Mutoh, N.2    Shin, J.O.3
  • 17
    • 0033167366 scopus 로고    scopus 로고
    • Expression of Wnt signalling pathway genes during tooth development
    • Sarkar L, Sharpe PT. Expression of Wnt signalling pathway genes during tooth development. Mech Dev 1999: 85 (1-2): 197-200.
    • (1999) Mech Dev , vol.85 , Issue.1-2 , pp. 197-200
    • Sarkar, L.1    Sharpe, P.T.2
  • 18
    • 67650230896 scopus 로고    scopus 로고
    • Wnt/beta-catenin signaling: components, mechanisms, and diseases
    • MacDonald BT, Tamai K, He X. Wnt/beta-catenin signaling: components, mechanisms, and diseases. Dev Cell 2009: 17 (1): 9-26.
    • (2009) Dev Cell , vol.17 , Issue.1 , pp. 9-26
    • MacDonald, B.T.1    Tamai, K.2    He, X.3
  • 19
    • 42449110795 scopus 로고    scopus 로고
    • Regulation of cell-cell adhesion by the cadherin-catenin complex
    • Nelson WJ. Regulation of cell-cell adhesion by the cadherin-catenin complex. Biochem Soc Trans 2008: 36 (Pt 2): 149-155.
    • (2008) Biochem Soc Trans , vol.36 , Issue.2 PART , pp. 149-155
    • Nelson, W.J.1
  • 20
    • 0036113510 scopus 로고    scopus 로고
    • WNT signals are required for the initiation of hair follicle development
    • Andl T, Reddy ST, Gaddapara T, Millar SE. WNT signals are required for the initiation of hair follicle development. Dev Cell 2002: 2 (5): 643-653.
    • (2002) Dev Cell , vol.2 , Issue.5 , pp. 643-653
    • Andl, T.1    Reddy, S.T.2    Gaddapara, T.3    Millar, S.E.4
  • 21
    • 11844273322 scopus 로고    scopus 로고
    • LEF1 is a critical epithelial survival factor during tooth morphogenesis
    • Sasaki T, Ito Y, Xu X et al. LEF1 is a critical epithelial survival factor during tooth morphogenesis. Dev Biol 2005: 278 (1): 130-143.
    • (2005) Dev Biol , vol.278 , Issue.1 , pp. 130-143
    • Sasaki, T.1    Ito, Y.2    Xu, X.3
  • 22
    • 37349092090 scopus 로고    scopus 로고
    • Wnt/beta-catenin signaling directs multiple stages of tooth morphogenesis
    • Liu F, Chu EY, Watt B et al. Wnt/beta-catenin signaling directs multiple stages of tooth morphogenesis. Dev Biol 2008: 313 (1): 210-224.
    • (2008) Dev Biol , vol.313 , Issue.1 , pp. 210-224
    • Liu, F.1    Chu, E.Y.2    Watt, B.3
  • 24
    • 69549134095 scopus 로고    scopus 로고
    • Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood
    • Wang XP, O'Connell DJ, Lund JJ et al. Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood. Development 2009: 136 (11): 1939-1949.
    • (2009) Development , vol.136 , Issue.11 , pp. 1939-1949
    • Wang, X.P.1    O'Connell, D.J.2    Lund, J.J.3
  • 25
    • 84864395840 scopus 로고    scopus 로고
    • WNT secretion and signalling in human disease
    • Herr P, Hausmann G, Basler K. WNT secretion and signalling in human disease. Trends Mol Med 2012: 18 (8): 483-493.
    • (2012) Trends Mol Med , vol.18 , Issue.8 , pp. 483-493
    • Herr, P.1    Hausmann, G.2    Basler, K.3
  • 26
    • 46349108966 scopus 로고    scopus 로고
    • Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate
    • Chiquet BT, Blanton SH, Burt A et al. Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate. Hum Mol Genet 2008: 17 (14): 2212-2218.
    • (2008) Hum Mol Genet , vol.17 , Issue.14 , pp. 2212-2218
    • Chiquet, B.T.1    Blanton, S.H.2    Burt, A.3
  • 27
    • 78649562450 scopus 로고    scopus 로고
    • Studies with Wnt genes and nonsyndromic cleft lip and palate
    • Menezes R, Letra A, Kim AH et al. Studies with Wnt genes and nonsyndromic cleft lip and palate. Birth Defects Res A Clin Mol Teratol 2010: 88 (11): 995-1000.
    • (2010) Birth Defects Res A Clin Mol Teratol , vol.88 , Issue.11 , pp. 995-1000
    • Menezes, R.1    Letra, A.2    Kim, A.H.3
  • 28
    • 84856495235 scopus 로고    scopus 로고
    • Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate
    • Mostowska A, Hozyasz KK, Biedziak B, Wojcicki P, Lianeri M, Jagodzinski PP. Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate. Eur J Oral Sci 2012: 120 (1): 1-8.
    • (2012) Eur J Oral Sci , vol.120 , Issue.1 , pp. 1-8
    • Mostowska, A.1    Hozyasz, K.K.2    Biedziak, B.3    Wojcicki, P.4    Lianeri, M.5    Jagodzinski, P.P.6
  • 29
    • 33645234495 scopus 로고    scopus 로고
    • Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis
    • Mostowska A, Biedziak B, Jagodzinski PP. Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis. J Hum Genet 2006: 51 (3): 262-266.
    • (2006) J Hum Genet , vol.51 , Issue.3 , pp. 262-266
    • Mostowska, A.1    Biedziak, B.2    Jagodzinski, P.P.3
  • 31
    • 67649880580 scopus 로고    scopus 로고
    • WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes
    • Bohring A, Stamm T, Spaich C et al. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. Am J Hum Genet 2009: 85 (1): 97-105.
    • (2009) Am J Hum Genet , vol.85 , Issue.1 , pp. 97-105
    • Bohring, A.1    Stamm, T.2    Spaich, C.3
  • 32
    • 78649987736 scopus 로고    scopus 로고
    • Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum
    • Castori M, Castiglia D, Brancati F et al. Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum. Clin Genet 2011: 79 (1): 92-95.
    • (2011) Clin Genet , vol.79 , Issue.1 , pp. 92-95
    • Castori, M.1    Castiglia, D.2    Brancati, F.3
  • 33
  • 34
    • 0032531880 scopus 로고    scopus 로고
    • Analysis of epithelial-mesenchymal interactions in the initial morphogenesis of the mammalian tooth
    • Dassule HR, McMahon AP. Analysis of epithelial-mesenchymal interactions in the initial morphogenesis of the mammalian tooth. Dev Biol 1998: 202 (2): 215-227.
    • (1998) Dev Biol , vol.202 , Issue.2 , pp. 215-227
    • Dassule, H.R.1    McMahon, A.P.2
  • 35
    • 34249012740 scopus 로고    scopus 로고
    • Wnt10a regulates dentin sialophosphoprotein mRNA expression and possibly links odontoblast differentiation and tooth morphogenesis
    • Yamashiro T, Zheng L, Shitaku Y et al. Wnt10a regulates dentin sialophosphoprotein mRNA expression and possibly links odontoblast differentiation and tooth morphogenesis. Differentiation 2007: 75 (5): 452-462.
    • (2007) Differentiation , vol.75 , Issue.5 , pp. 452-462
    • Yamashiro, T.1    Zheng, L.2    Shitaku, Y.3
  • 36
    • 0029839141 scopus 로고    scopus 로고
    • Murine Wnt10a and Wnt10b: cloning and expression in developing limbs, face and skin of embryos and in adults
    • Wang J, Shackleford GM. Murine Wnt10a and Wnt10b: cloning and expression in developing limbs, face and skin of embryos and in adults. Oncogene 1996: 13 (7): 1537-1544.
    • (1996) Oncogene , vol.13 , Issue.7 , pp. 1537-1544
    • Wang, J.1    Shackleford, G.M.2
  • 37
    • 0034880422 scopus 로고    scopus 로고
    • Characterization of Wnt gene expression in developing and postnatal hair follicles and identification of Wnt5a as a target of Sonic hedgehog in hair follicle morphogenesis
    • Reddy S, Andl T, Bagasra A et al. Characterization of Wnt gene expression in developing and postnatal hair follicles and identification of Wnt5a as a target of Sonic hedgehog in hair follicle morphogenesis. Mech Dev 2001: 107 (1-2): 69-82.
    • (2001) Mech Dev , vol.107 , Issue.1-2 , pp. 69-82
    • Reddy, S.1    Andl, T.2    Bagasra, A.3
  • 38
    • 35348987509 scopus 로고    scopus 로고
    • Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia
    • Adaimy L, Chouery E, Megarbane H et al. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. Am J Hum Genet 2007: 81 (4): 821-828.
    • (2007) Am J Hum Genet , vol.81 , Issue.4 , pp. 821-828
    • Adaimy, L.1    Chouery, E.2    Megarbane, H.3
  • 39
    • 70450233732 scopus 로고    scopus 로고
    • WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome
    • Nawaz S, Klar J, Wajid M et al. WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome. Eur J Hum Genet 2009: 17 (12): 1600-1605.
    • (2009) Eur J Hum Genet , vol.17 , Issue.12 , pp. 1600-1605
    • Nawaz, S.1    Klar, J.2    Wajid, M.3
  • 40
    • 79959505447 scopus 로고    scopus 로고
    • Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes
    • Bergendal B, Klar J, Stecksén-Blicks C, Norderyd J, Dahl N. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes. Am J Med Genet A 2011: 155A (7): 1616-1622.
    • (2011) Am J Med Genet A , vol.155 A , Issue.7 , pp. 1616-1622
    • Bergendal, B.1    Klar, J.2    Stecksén-Blicks, C.3    Norderyd, J.4    Dahl, N.5
  • 41
    • 47649105553 scopus 로고    scopus 로고
    • Tooth agenesis: from molecular genetics to molecular dentistry
    • Matalova E, Fleischmannova J, Sharpe PT, Tucker AS. Tooth agenesis: from molecular genetics to molecular dentistry. J Dent Res 2008: 87 (7): 617-623.
    • (2008) J Dent Res , vol.87 , Issue.7 , pp. 617-623
    • Matalova, E.1    Fleischmannova, J.2    Sharpe, P.T.3    Tucker, A.S.4
  • 42
    • 0037229938 scopus 로고    scopus 로고
    • Runnin' with the Dvl: proteins that associate with Dsh/Dvl and their significance to Wnt signal transduction
    • Wharton KA Jr. Runnin' with the Dvl: proteins that associate with Dsh/Dvl and their significance to Wnt signal transduction. Dev Biol 2003: 253: 1-17.
    • (2003) Dev Biol , vol.253 , pp. 1-17
    • Wharton Jr, K.A.1
  • 43
    • 34547750005 scopus 로고    scopus 로고
    • Dynamic recruitment of axin by Dishevelled protein assemblies
    • Schwarz-Romond T, Metcalfe C, Bienz M. Dynamic recruitment of axin by Dishevelled protein assemblies. J Cell Sci 2007: 120 (Pt 14): 2402-2412.
    • (2007) J Cell Sci , vol.120 , Issue.14 PART , pp. 2402-2412
    • Schwarz-Romond, T.1    Metcalfe, C.2    Bienz, M.3
  • 45
    • 35348870990 scopus 로고    scopus 로고
    • Defining subphenotypes for oral clefts based on dental development
    • Letra A, Menezes R, Granjeiro JM, Vieira AR. Defining subphenotypes for oral clefts based on dental development. J Dent Res 2007: 86 (10): 986-991.
    • (2007) J Dent Res , vol.86 , Issue.10 , pp. 986-991
    • Letra, A.1    Menezes, R.2    Granjeiro, J.M.3    Vieira, A.R.4
  • 47
    • 0029587042 scopus 로고
    • A tale of four syndromes: familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome
    • Foulkes WD. A tale of four syndromes: familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome. QJM 1995: 88 (12): 853-863.
    • (1995) QJM , vol.88 , Issue.12 , pp. 853-863
    • Foulkes, W.D.1
  • 48
    • 77955735139 scopus 로고    scopus 로고
    • Dvl2 promotes intestinal length and neoplasia in the ApcMin mouse model for colorectal cancer
    • Metcalfe C, Ibrahim AE, Graeb M et al. Dvl2 promotes intestinal length and neoplasia in the ApcMin mouse model for colorectal cancer. Cancer Res 2010: 70 (16): 6629-6638.
    • (2010) Cancer Res , vol.70 , Issue.16 , pp. 6629-6638
    • Metcalfe, C.1    Ibrahim, A.E.2    Graeb, M.3


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