-
1
-
-
0026828661
-
Distribution of missing teeth and tooth morphology in patients with oligodontia
-
Schalk-Van Der WY, Steen WH, Bosman F. Distribution of missing teeth and tooth morphology in patients with oligodontia. ASDC J Dent Child 1992; 59: 133-140.
-
(1992)
ASDC J Dent Child
, vol.59
, pp. 133-140
-
-
Schalk-Van Der, W.Y.1
Steen, W.H.2
Bosman, F.3
-
2
-
-
0020526490
-
Classification and genetics of numeric anomalies of dentition
-
Burzynski NJ, Escobar VH. Classification and genetics of numeric anomalies of dentition. Birth Defects Orig Artic Ser 1983; 19: 95-106.
-
(1983)
Birth Defects Orig Artic Ser
, vol.19
, pp. 95-106
-
-
Burzynski, N.J.1
Escobar, V.H.2
-
3
-
-
0030017452
-
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: 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
-
4
-
-
0033986083
-
Mutation of PAX9 is associated with oligodontia
-
Stockton DW, Das P, Goldenberg M, D'Souza RN, Patel PI. Mutation of PAX9 is associated with oligodontia. Nat Genet 2000; 24: 18-19.
-
(2000)
Nat Genet
, vol.24
, pp. 18-19
-
-
Stockton, D.W.1
Das, P.2
Goldenberg, M.3
D'Souza, R.N.4
Patel, P.I.5
-
5
-
-
33749064639
-
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families
-
Chishti MS, Muhammad D, Haider M, Ahmad W. A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families. J Hum Genet 2006; 51: 872-878.
-
(2006)
J Hum Genet
, vol.51
, pp. 872-878
-
-
Chishti, M.S.1
Muhammad, D.2
Haider, M.3
Ahmad, W.4
-
6
-
-
33744990403
-
A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia
-
Tao R, Jin B, Guo SZ, Qing W, Feng GY, Brooks DG, Liu L, Xu J, Li T, Yan Y, He L. A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia. J Hum Genet 2006; 51: 498-502.
-
(2006)
J Hum Genet
, vol.51
, pp. 498-502
-
-
Tao, R.1
Jin, B.2
Guo, S.Z.3
Qing, W.4
Feng, G.Y.5
Brooks, D.G.6
Liu, L.7
Xu, J.8
Li, T.9
Yan, Y.10
He, L.11
-
8
-
-
26644460427
-
Hypodontia in orthodontically treated children
-
Fekonja A. Hypodontia in orthodontically treated children. Eur J Orthod 2005; 27: 457-460.
-
(2005)
Eur J Orthod
, vol.27
, pp. 457-460
-
-
Fekonja, A.1
-
9
-
-
31544469545
-
A survey of hypodontia in Japanese orthodontic patients
-
Endo T, Ozoe R, Kubota M, Akiyama M, Shimooka S. A survey of hypodontia in Japanese orthodontic patients. Am J Orthod Dentofacial Orthop 2006; 129: 29-35.
-
(2006)
Am J Orthod Dentofacial Orthop
, vol.129
, pp. 29-35
-
-
Endo, T.1
Ozoe, R.2
Kubota, M.3
Akiyama, M.4
Shimooka, S.5
-
10
-
-
0004208199
-
Oligodontia. A clinical, radiographic and genetic evaluation
-
Chapter 10.
-
Schalk-Van Der WY. Oligodontia. A clinical, radiographic and genetic evaluation. Chapter 10. Utrecht Acad Thesis 1992.
-
(1992)
Utrecht Acad Thesis
-
-
Schalk-Van Der, W.Y.1
-
11
-
-
0039738462
-
Oligodontia in Danish schoolchildren
-
Rolling S, Poulsen S. Oligodontia in Danish schoolchildren. Acta Odontol Scand 2001; 59: 111-112.
-
(2001)
Acta Odontol Scand
, vol.59
, pp. 111-112
-
-
Rolling, S.1
Poulsen, S.2
-
13
-
-
0034969492
-
A nonsense mutation in MSX1 causes Witkop syndrome
-
Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR. A nonsense mutation in MSX1 causes Witkop syndrome. Am J Hum Genet 2001; 69: 67-74.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 67-74
-
-
Jumlongras, D.1
Bei, M.2
Stimson, J.M.3
Wang, W.F.4
DePalma, S.R.5
Seidman, C.E.6
Felbor, U.7
Maas, R.8
Seidman, J.G.9
Olsen, B.R.10
-
14
-
-
2342613578
-
Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer
-
Lammi L, Arte S, Somer M, Jarvinen H, Lahermo P, Thesleff I, Pirinen S, Nieminen P. Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. Am J Hum Genet 2004; 74: 1043-1050.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1043-1050
-
-
Lammi, L.1
Arte, S.2
Somer, M.3
Jarvinen, H.4
Lahermo, P.5
Thesleff, I.6
Pirinen, S.7
Nieminen, P.8
-
15
-
-
0028292605
-
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
-
Satokata I, Maas R. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat Genet 1994; 6: 348-356.
-
(1994)
Nat Genet
, vol.6
, pp. 348-356
-
-
Satokata, I.1
Maas, R.2
-
16
-
-
0032169255
-
Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities
-
Peters H, Neubuser A, Kratochwil K, Balling R. Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities. Genes Dev 1998; 12: 2735-2747.
-
(1998)
Genes Dev
, vol.12
, pp. 2735-2747
-
-
Peters, H.1
Neubuser, A.2
Kratochwil, K.3
Balling, R.4
-
17
-
-
0029802695
-
Msx1 controls inductive signaling in mammalian tooth morphogenesis
-
Chen Y, Bei M, Woo I, Satokata I, Maas R. Msx1 controls inductive signaling in mammalian tooth morphogenesis. Development 1996; 122: 3035-3044.
-
(1996)
Development
, vol.122
, pp. 3035-3044
-
-
Chen, Y.1
Bei, M.2
Woo, I.3
Satokata, I.4
Maas, R.5
-
18
-
-
33645234495
-
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: 262-266.
-
(2006)
J Hum Genet
, vol.51
, pp. 262-266
-
-
Mostowska, A.1
Biedziak, B.2
Jagodzinski, P.P.3
-
19
-
-
0029944653
-
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. 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 U S A 1996; 93: 1764-1769.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 1764-1769
-
-
Zhang, H.1
Catron, K.M.2
Abate-Shen, C.3
-
20
-
-
0030962036
-
Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism
-
Zhang H, Hu G, Wang H, Sciavolino P, Iler N, Shen MM, Abate-Shen C. Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism. Mol Cell Biol 1997; 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.M.6
Abate-Shen, C.7
-
21
-
-
80052693035
-
The Msx1 homeoprotein recruits polycomb to the nuclear periphery during development
-
Wang J, Kumar RM, Biggs VJ, Lee H, Chen Y, Kagey MH, Young RA, Abate-Shen C. The Msx1 homeoprotein recruits polycomb to the nuclear periphery during development. Dev Cell 2011; 21: 575-588.
-
(2011)
Dev Cell
, vol.21
, pp. 575-588
-
-
Wang, J.1
Kumar, R.M.2
Biggs, V.J.3
Lee, H.4
Chen, Y.5
Kagey, M.H.6
Young, R.A.7
Abate-Shen, C.8
-
22
-
-
84864070073
-
Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family
-
Liang J, Zhu L, Meng L, Chen D, Bian Z. Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family. Eur J Oral Sci 2012; 120: 278-282.
-
(2012)
Eur J Oral Sci
, vol.120
, pp. 278-282
-
-
Liang, J.1
Zhu, L.2
Meng, L.3
Chen, D.4
Bian, Z.5
-
23
-
-
0038545785
-
Complete sequencing shows a role for MSX1 in nonsyndromic cleft lip and palate
-
Jezewski PA, Vieira AR, Nishimura C, Ludwig B, Johnson M, O'Brien SE, Daack-Hirsch S, Schultz RE, Weber A, Nepomucena B, Romitti PA, Christensen K, Orioli IM, Castilla EE, Machida J, Natsume N, Murray JC. Complete sequencing shows a role for MSX1 in nonsyndromic cleft lip and palate. J Med Genet 2003; 40: 399-407.
-
(2003)
J Med Genet
, vol.40
, pp. 399-407
-
-
Jezewski, P.A.1
Vieira, A.R.2
Nishimura, C.3
Ludwig, B.4
Johnson, M.5
O'Brien, S.E.6
Daack-Hirsch, S.7
Schultz, R.E.8
Weber, A.9
Nepomucena, B.10
Romitti, P.A.11
Christensen, K.12
Orioli, I.M.13
Castilla, E.E.14
Machida, J.15
Natsume, N.16
Murray, J.C.17
-
24
-
-
79960618944
-
Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia
-
Kamamoto M, Machida J, Yamaguchi S, Kimura M, Ono T, Jezewski PA, Higashi Y, Nakayama A, Shimozato K, Tokita Y. Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia. Eur J Hum Genet 2011; 19: 844-850.
-
(2011)
Eur J Hum Genet
, vol.19
, pp. 844-850
-
-
Kamamoto, M.1
Machida, J.2
Yamaguchi, S.3
Kimura, M.4
Ono, T.5
Jezewski, P.A.6
Higashi, Y.7
Nakayama, A.8
Shimozato, K.9
Tokita, Y.10
-
25
-
-
0032231873
-
Association of MSX1 and TGFB3 with nonsyndromic clefting in humans
-
Lidral AC, Romitti PA, Basart AM, Doetschman T, Leysens NJ, Daack-Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, Parnell TJ, Rubenstein JL, Murray JC. Association of MSX1 and TGFB3 with nonsyndromic clefting in humans. Am J Hum Genet 1998; 63: 557-568.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 557-568
-
-
Lidral, A.C.1
Romitti, P.A.2
Basart, A.M.3
Doetschman, T.4
Leysens, N.J.5
Daack-Hirsch, S.6
Semina, E.V.7
Johnson, L.R.8
Machida, J.9
Burds, A.10
Parnell, T.J.11
Rubenstein, J.L.12
Murray, J.C.13
-
26
-
-
0037395472
-
MSX1 and TGFB3 contribute to clefting in South America
-
Vieira AR, Orioli IM, Castilla EE, Cooper ME, Marazita ML, Murray JC. MSX1 and TGFB3 contribute to clefting in South America. J Dent Res 2003; 82: 289-292.
-
(2003)
J Dent Res
, vol.82
, pp. 289-292
-
-
Vieira, A.R.1
Orioli, I.M.2
Castilla, E.E.3
Cooper, M.E.4
Marazita, M.L.5
Murray, J.C.6
-
27
-
-
2642522952
-
In a Vietnamese population, MSX1 variants contribute to cleft lip and palate
-
Suzuki Y, Jezewski PA, Machida J, Watanabe Y, Shi M, Cooper ME, le Viet T, Nguyen TD, Hai H, Natsume N, Shimozato K, Marazita ML, Murray JC. In a Vietnamese population, MSX1 variants contribute to cleft lip and palate. Genet Med 2004; 6: 117-125.
-
(2004)
Genet Med
, vol.6
, pp. 117-125
-
-
Suzuki, Y.1
Jezewski, P.A.2
Machida, J.3
Watanabe, Y.4
Shi, M.5
Cooper, M.E.6
le Viet, T.7
Nguyen, T.D.8
Hai, H.9
Natsume, N.10
Shimozato, K.11
Marazita, M.L.12
Murray, J.C.13
-
28
-
-
0035866071
-
Regulation of neuregulin expression in the injured rat brain and cultured astrocytes
-
Tokita Y, Keino H, Matsui F, Aono S, Ishiguro H, Higashiyama S, Oohira A. Regulation of neuregulin expression in the injured rat brain and cultured astrocytes. J Neurosci 2001; 21: 1257-1264.
-
(2001)
J Neurosci
, vol.21
, pp. 1257-1264
-
-
Tokita, Y.1
Keino, H.2
Matsui, F.3
Aono, S.4
Ishiguro, H.5
Higashiyama, S.6
Oohira, A.7
-
29
-
-
0035834053
-
Crystal structure of the Msx-1 homeodomain/DNA complex
-
Hovde S, Abate-Shen C, Geiger JH. Crystal structure of the Msx-1 homeodomain/DNA complex. Biochemistry 2001; 40: 12013-12021.
-
(2001)
Biochemistry
, vol.40
, pp. 12013-12021
-
-
Hovde, S.1
Abate-Shen, C.2
Geiger, J.H.3
-
30
-
-
24744459873
-
The Groucho-related gene family regulates the gonadotropin-releasing hormone gene through interaction with the homeodomain proteins MSX1 and OCT1
-
Rave-Harel N, Miller NL, Givens ML, Mellon PL. The Groucho-related gene family regulates the gonadotropin-releasing hormone gene through interaction with the homeodomain proteins MSX1 and OCT1. J Biol Chem 2005; 280: 30975-30983.
-
(2005)
J Biol Chem
, vol.280
, pp. 30975-30983
-
-
Rave-Harel, N.1
Miller, N.L.2
Givens, M.L.3
Mellon, P.L.4
-
31
-
-
0030955889
-
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, Presley R, Pedersen RA, Rubenstein JL. 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 1997; 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
Presley, R.7
Pedersen, R.A.8
Rubenstein, J.L.9
-
32
-
-
79952050683
-
Msx1 mutations: how do they cause tooth agenesis?
-
Wang Y, Kong H, Mues G, D'Souza R. Msx1 mutations: how do they cause tooth agenesis? J Dent Res 2011; 90: 311-316.
-
(2011)
J Dent Res
, vol.90
, pp. 311-316
-
-
Wang, Y.1
Kong, H.2
Mues, G.3
D'Souza, R.4
-
33
-
-
33645516944
-
PIAS1 confers DNA-binding specificity on the Msx1 homeoprotein
-
Lee H, Quinn JC, Prasanth KV, Swiss VA, Economides KD, Camacho MM, Spector DL, Abate-Shen C. PIAS1 confers DNA-binding specificity on the Msx1 homeoprotein. Genes Dev 2006; 20: 784-794.
-
(2006)
Genes Dev
, vol.20
, pp. 784-794
-
-
Lee, H.1
Quinn, J.C.2
Prasanth, K.V.3
Swiss, V.A.4
Economides, K.D.5
Camacho, M.M.6
Spector, D.L.7
Abate-Shen, C.8
-
34
-
-
79959505447
-
Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes
-
Bergendal B, Klar J, Stecksen-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: 1616-1622.
-
(2011)
Am J Med Genet A
, vol.155 A
, pp. 1616-1622
-
-
Bergendal, B.1
Klar, J.2
Stecksen-Blicks, C.3
Norderyd, J.4
Dahl, N.5
-
35
-
-
84864094899
-
Mutations in WNT10A are present in more than half of isolated hypodontia cases
-
van den Boogaard MJ, Creton M, Bronkhorst Y, van der Hout A, Hennekam E, Lindhout D, Cune M, Ploos van Amstel HK. Mutations in WNT10A are present in more than half of isolated hypodontia cases. J Med Genet 2012; 49: 327-331.
-
(2012)
J Med Genet
, vol.49
, pp. 327-331
-
-
van den Boogaard, M.J.1
Creton, M.2
Bronkhorst, Y.3
van der Hout, A.4
Hennekam, E.5
Lindhout, D.6
Cune, M.7
Ploos van Amstel, H.K.8
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