-
1
-
-
28744436103
-
Hypodontia: Genetics and future perspectives
-
Pemberton, T.J., Das, P., Patel, P.I. Hypodontia: genetics and future perspectives. Braz. J. Oral Sci., 2005, 4: 695-706.
-
(2005)
Braz. J. Oral Sci.
, vol.4
, pp. 695-706
-
-
Pemberton, T.J.1
Das, P.2
Patel, P.I.3
-
2
-
-
0027865406
-
Anomalies associated with hypodontia of the permanent lateral incisor and second premolar
-
Symons, A.I., Stritzel, F., Stamation, J. Anomalies associated with hypodontia of the permanent lateral incisor and second premolar. J. Clin. Pediatr. Dent., 1993, 17: 109-111.
-
(1993)
J. Clin. Pediatr. Dent.
, vol.17
, pp. 109-111
-
-
Symons, A.I.1
Stritzel, F.2
Stamation, J.3
-
3
-
-
3242692389
-
Agenesis of third molar germs depends on sagittal maxillary jaw dimensions in orthodontic patients in Japan
-
Kajii, T.S., Sato, Y., Kajii, S., Sugawara, Y., Iida, J. Agenesis of third molar germs depends on sagittal maxillary jaw dimensions in orthodontic patients in Japan. Angle. Orthod., 2004, 74: 337-342.
-
(2004)
Angle. Orthod.
, vol.74
, pp. 337-342
-
-
Kajii, T.S.1
Sato, Y.2
Kajii, S.3
Sugawara, Y.4
Iida, J.5
-
4
-
-
0036549520
-
Relationship between congenitally missing lower third molars and late formation of tooth germs
-
Baba-Kawano, S., Toyoshima, Y., Regalado, L., Sa'do, B., Nakasima, A. Relationship between congenitally missing lower third molars and late formation of tooth germs. Angle. Orthod., 2002, 72: 112-117.
-
(2002)
Angle. Orthod.
, vol.72
, pp. 112-117
-
-
Baba-Kawano, S.1
Toyoshima, Y.2
Regalado, L.3
Sa'do, B.4
Nakasima, A.5
-
5
-
-
0033278240
-
Molecular genetics of tooth morphogenesis and patterning: The right shape in the right place
-
Tucker, A.S., Sharpe, P.T. Molecular genetics of tooth morphogenesis and patterning: the right shape in the right place. J. Dent. Res., 1999, 78: 826-834.
-
(1999)
J. Dent. Res.
, vol.78
, pp. 826-834
-
-
Tucker, A.S.1
Sharpe, P.T.2
-
6
-
-
0033998420
-
Reiterative signaling and patterning during mammalian tooth morphogenesis
-
Jernvall, J., Thesleff, I. Reiterative signaling and patterning during mammalian tooth morphogenesis. Mech. Dev., 2000, 92: 19-29.
-
(2000)
Mech. Dev.
, vol.92
, pp. 19-29
-
-
Jernvall, J.1
Thesleff, I.2
-
7
-
-
0027363024
-
Identification of BMP-4 as a signal mediating secondary induction between epithelial and mesenchymal tissues during early tooth development
-
Vainio, S., Karavanova, I., Jowett, A., Thesleff, I. Identification of BMP-4 as a signal mediating secondary induction between epithelial and mesenchymal tissues during early tooth development. Cell., 1993, 75: 45-58.
-
(1993)
Cell.
, vol.75
, pp. 45-58
-
-
Vainio, S.1
Karavanova, I.2
Jowett, A.3
Thesleff, I.4
-
8
-
-
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(27): 35-2747.
-
(1998)
Genes Dev.
, vol.12
, Issue.27
, pp. 35-2747
-
-
Peters, H.1
Neubuser, A.2
Kratochwil, K.3
Balling, R.4
-
9
-
-
0033082377
-
Teeth. Where and how to make them
-
Peters, H., Balling, R. Teeth. Where and how to make them. Trends Genet., 1999, 15: 59-65.
-
(1999)
Trends Genet.
, vol.15
, pp. 59-65
-
-
Peters, H.1
Balling, R.2
-
10
-
-
33645478323
-
Genes and tooth development: Reviewing the structure and function of some key players
-
Scarel-Caminaga, R.M., Silva, E.R., Peres, R.C.R. Genes and tooth development: reviewing the structure and function of some key players. Braz. J. Oral. Sci., 2003, 7: 339-347.
-
(2003)
Braz. J. Oral. Sci.
, vol.7
, pp. 339-347
-
-
Scarel-Caminaga, R.M.1
Silva, E.R.2
Peres, R.C.R.3
-
11
-
-
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
-
12
-
-
0033986083
-
Mutation of PAX9 is associated with oligodontia
-
Stockton, D.W., Das, P., Goldenberg, M., D'Souza, R.N., Patel, P.I. 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
-
13
-
-
0034748051
-
Identification of a nonsense mutation in the PAX9 gene in molar oligodontia
-
Nieminen, P., Arte, S., Tanner, D., Paulin, L., Alaluusua, S., Thesleff, I., Pirinen, S. Identification of a nonsense mutation in the PAX9 gene in molar oligodontia. Eur. J. Hum. Genet., 2001, 9: 743-746.
-
(2001)
Eur. J. Hum. Genet.
, vol.9
, pp. 743-746
-
-
Nieminen, P.1
Arte, S.2
Tanner, D.3
Paulin, L.4
Alaluusua, S.5
Thesleff, I.6
Pirinen, S.7
-
14
-
-
0036479444
-
A novel mutation in human PAX9 causes molar oligodontia
-
Frazier-Bowers, S.A., Guo, D.C., Cavender, A., Xue, L., Evans, B., King, T., Milewicz, D., D'Souza, R.N. A novel mutation in human PAX9 causes molar oligodontia. J. Dent. Res., 2002, 81: 129-133.
-
(2002)
J. Dent. Res.
, vol.81
, pp. 129-133
-
-
Frazier-Bowers, S.A.1
Guo, D.C.2
Cavender, A.3
Xue, L.4
Evans, B.5
King, T.6
Milewicz, D.7
D'Souza, R.N.8
-
15
-
-
0036556243
-
Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia
-
Das, P., Stockton, D.W., Bauer, C., Shaffer, L.G., D'Souza, R.N., Wright, T., Patel, P.I. Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia. Hum. Genet., 2002, 110: 371-376.
-
(2002)
Hum. Genet.
, vol.110
, pp. 371-376
-
-
Das, P.1
Stockton, D.W.2
Bauer, C.3
Shaffer, L.G.4
D'Souza, R.N.5
Wright, T.6
Patel, P.I.7
-
16
-
-
0042822121
-
Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia
-
Das, P., Hai, M., Elcock, C., Leal, S.M., Brown, D.T., Brook, A.H., Patel, P.I. Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia. Am. J. Med. Genet. A., 2003, 118: 35-42.
-
(2003)
Am. J. Med. Genet. A.
, vol.118
, pp. 35-42
-
-
Das, P.1
Hai, M.2
Elcock, C.3
Leal, S.M.4
Brown, D.T.5
Brook, A.H.6
Patel, P.I.7
-
17
-
-
0242609823
-
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
-
Lammi, L., Halonen, K., Pirinen, S., Thesleff, I., Arte, S., Nieminen, P. A missense mutation in PAX9 in a family with distinct phenotype of oligodontia. Eur. J. Hum. Genet., 2003, 11: 866-871.
-
(2003)
Eur. J. Hum. Genet.
, vol.11
, pp. 866-871
-
-
Lammi, L.1
Halonen, K.2
Pirinen, S.3
Thesleff, I.4
Arte, S.5
Nieminen, P.6
-
18
-
-
0043014474
-
Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia
-
Mostowska, A., Kobielak, A., Biedziak, B., Trzeciak, W.H. Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia. Eur. J. Oral. Sci., 2003, 111: 272-276.
-
(2003)
Eur. J. Oral. Sci.
, vol.111
, pp. 272-276
-
-
Mostowska, A.1
Kobielak, A.2
Biedziak, B.3
Trzeciak, W.H.4
-
19
-
-
1142299588
-
A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia
-
Jumlongras, D., Lin, J.Y., Chapra, A., Seidman, C.E., Seidman, J.G., Maas, R.L., Olsen, B.R. A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia. Hum. Genet., 2004, 114: 242-249.
-
(2004)
Hum. Genet.
, vol.114
, pp. 242-249
-
-
Jumlongras, D.1
Lin, J.Y.2
Chapra, A.3
Seidman, C.E.4
Seidman, J.G.5
Maas, R.L.6
Olsen, B.R.7
-
20
-
-
16644366228
-
Novel mutation of the initiation codon of PAX9 causes oligodontia
-
Klein, M.L., Nieminen, P., Lammi, L., Niebuhr, E., Kreiborg, S. Novel mutation of the initiation codon of PAX9 causes oligodontia. J. Dent. Res., 2005, 84: 43-47.
-
(2005)
J. Dent. Res.
, vol.84
, pp. 43-47
-
-
Klein, M.L.1
Nieminen, P.2
Lammi, L.3
Niebuhr, E.4
Kreiborg, S.5
-
21
-
-
0030017452
-
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
-
Vastardis, H., Karimbux, N., Guthua, S.W., Seidman, J.G., Seidman, C.E. 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
-
22
-
-
0034028899
-
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
-
Van Den Boogaard, M.J., Dorland, M., Beemer, F.A., Van Amstel, H.K. MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat. Genet., 2000, 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
-
23
-
-
0034969492
-
A nonsense mutation in MSX1 causes Witkop syndrome
-
Jumlongras, D., Bei, M., Stimson, J.M., Wang, W.F., DePalma, S.R., Seidman, C.E., Felbor, U., Maas, R., Seidman, J.G., Olsen, B.R. 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
-
24
-
-
0036528341
-
The role of MSX1 in human tooth agenesis
-
Lidral, A.C., Reising, B.C. The role of MSX1 in human tooth agenesis. J. Dent. Res., 2002, 81: 274-278.
-
(2002)
J. Dent. Res.
, vol.81
, pp. 274-278
-
-
Lidral, A.C.1
Reising, B.C.2
-
25
-
-
3343015549
-
A novel MSX1 mutation in hypodontia
-
De Muynck, S., Schollen, E., Matthijs, G., Verdonck, A., Devriendt, K., Carels, C. A novel MSX1 mutation in hypodontia. Am. J. Med. Genet. A., 2004, 128: 401-403.
-
(2004)
Am. J. Med. Genet. A.
, vol.128
, pp. 401-403
-
-
De Muynck, S.1
Schollen, E.2
Matthijs, G.3
Verdonck, A.4
Devriendt, K.5
Carels, C.6
-
26
-
-
0032477776
-
Association between homeobox-containing gene MSX1 and the occurrence of limb deficiency
-
Hwang, S.J., Beaty, T.H., Mcintosh, I., Hefferon, T., Panny, S.R. Association between homeobox-containing gene MSX1 and the occurrence of limb deficiency. Am. J. Med. Genet., 1998, 75: 419-423.
-
(1998)
Am. J. Med. Genet.
, vol.75
, pp. 419-423
-
-
Hwang, S.J.1
Beaty, T.H.2
McIntosh, I.3
Hefferon, T.4
Panny, S.R.5
-
27
-
-
4644312296
-
MSX1, PAX9, and TGFA contribute to tooth agenesis in humans
-
Vieira, A.R., Meira, R., Modesto, A., Murray, J.C. MSX1, PAX9, and TGFA contribute to tooth agenesis in humans. J. Dent. Res., 2004, 83: 723-727.
-
(2004)
J. Dent. Res.
, vol.83
, pp. 723-727
-
-
Vieira, A.R.1
Meira, R.2
Modesto, A.3
Murray, J.C.4
-
28
-
-
24044433565
-
Association between PAX-9 promoter polymorphisms and hypodontia in humans
-
Peres, R.C.R., Scarel-Caminaga, R.M., Do Espirito Santo, A.R., Line, S.R.P. Association between PAX-9 promoter polymorphisms and hypodontia in humans. Arch. Oral. Biol., 2005, 50: 861-871.
-
(2005)
Arch. Oral. Biol.
, vol.50
, pp. 861-871
-
-
Peres, R.C.R.1
Scarel-Caminaga, R.M.2
Do Espirito Santo, A.R.3
Line, S.R.P.4
-
29
-
-
0034046926
-
Use of buccal epithelial cells for PCR amplification of large DNA fragments
-
Trevilatto, P.C., Line, S.R. Use of buccal epithelial cells for PCR amplification of large DNA fragments. J. Forensic. Odontostomatol., 2000, 18: 6-9.
-
(2000)
J. Forensic. Odontostomatol.
, vol.18
, pp. 6-9
-
-
Trevilatto, P.C.1
Line, S.R.2
-
30
-
-
0031978284
-
Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocols
-
Markoff, A., Sormbroen, H., Bogdanova, N., Preisler-Adams, S., Ganev, V., Dworniczak, B., Horst, J. Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocols. Eur. J. Hum. Genet., 1998, 6: 145-150.
-
(1998)
Eur. J. Hum. Genet.
, vol.6
, pp. 145-150
-
-
Markoff, A.1
Sormbroen, H.2
Bogdanova, N.3
Preisler-Adams, S.4
Ganev, V.5
Dworniczak, B.6
Horst, J.7
-
31
-
-
0028116158
-
Rapid silver staining and recovery of PCR products separated on polyacrylamide gels
-
Sanguinetti, C.J., Dias Neto, E., Simpson, A.J. Rapid silver staining and recovery of PCR products separated on polyacrylamide gels. Biotechniques, 1994, 17: 914-921.
-
(1994)
Biotechniques
, vol.17
, pp. 914-921
-
-
Sanguinetti, C.J.1
Dias Neto, E.2
Simpson, A.J.3
-
32
-
-
0034686587
-
Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia
-
Scarel, R.M., Trevilatto, P.C., Di Hipólito, O. Jr., Camargo, L., Line, S.R.P. Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia. Am. J. Med. Genet., 2000, 92: 346-349.
-
(2000)
Am. J. Med. Genet.
, vol.92
, pp. 346-349
-
-
Scarel, R.M.1
Trevilatto, P.C.2
Di Hipólito Jr., O.3
Camargo, L.4
Line, S.R.P.5
-
33
-
-
25444525458
-
3(TG/CA)n repeats in human gene families: Abundance and selective patterns of distribution according to function and gene length
-
Sharma, V.K., Brahmachari, S.K., Ramachandran, S. 3(TG/CA)n repeats in human gene families: abundance and selective patterns of distribution according to function and gene length. BMC Genomics., 2005, 6: 83.
-
(2005)
BMC Genomics.
, vol.6
, pp. 83
-
-
Sharma, V.K.1
Brahmachari, S.K.2
Ramachandran, S.3
-
34
-
-
21344437571
-
Sp1-like transcription factors are regulators of embryonic development in vertebrates
-
Zhao, C., Meng, A. Sp1-like transcription factors are regulators of embryonic development in vertebrates. Dev. Growth Differ., 2005, 47: 201-211.
-
(2005)
Dev. Growth Differ.
, vol.47
, pp. 201-211
-
-
Zhao, C.1
Meng, A.2
-
35
-
-
1242294402
-
Functional analysis of a mutation in PAX9 associated with familial tooth agenesis in humans
-
Mensah, J.K., Ogawa, T., Kapadia, H., Cavender, A.C., D'Souza, R.N. Functional analysis of a mutation in PAX9 associated with familial tooth agenesis in humans. J. Biol. Chem., 2004, 279: 5924-5933.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 5924-5933
-
-
Mensah, J.K.1
Ogawa, T.2
Kapadia, H.3
Cavender, A.C.4
D'Souza, R.N.5
-
36
-
-
0036523997
-
Proposed guidelines for paper describing DNA polymorphisms-disease associations
-
Cooper, D.N., Nussbaum, R.L., Krawczak, M. Proposed guidelines for paper describing DNA polymorphisms-disease associations. Hum. Genet., 2002, 110: 207-208
-
(2002)
Hum. Genet.
, vol.110
, pp. 207-208
-
-
Cooper, D.N.1
Nussbaum, R.L.2
Krawczak, M.3
|