-
1
-
-
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
-
2
-
-
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
-
3
-
-
0141617374
-
Developmental biology and building a tooth
-
Thesleff I: Developmental biology and building a tooth. Quintessence Int 2003; 34: 613-620.
-
(2003)
Quintessence Int
, vol.34
, pp. 613-620
-
-
Thesleff, I.1
-
4
-
-
0024741302
-
Hypodontia in the permanent dentition: A study of its prevalence in Malaysian children
-
Nik-Hussein NN: Hypodontia in theApermanent dentition: a study of its prevalence in Malaysian children. Aust Orthod J 1989; 11: 93-95.
-
(1989)
Aust Orthod J
, vol.11
, pp. 93-95
-
-
Nik-Hussein, N.N.1
-
5
-
-
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
-
6
-
-
0345014859
-
Molecular basis of non-syndromic tooth agenesis: Mutations of MSX1 and PAX9 reflect their role in patterning human dentition
-
Mostowska A, Kobielak A, Trzeciak WH: Molecular basis of non-syndromic tooth agenesis: Mutations of MSX1 and PAX9 reflect their role in patterning human dentition. Eur J Oral Sci 2003; 111: 365-370.
-
(2003)
Eur J Oral Sci
, vol.111
, pp. 365-370
-
-
Mostowska, A.1
Kobielak, A.2
Trzeciak, W.H.3
-
7
-
-
1242294402
-
Functional analysis of a mutation in PAX9 associated with familial tooth agenesis in humans
-
Mensah JK, Ogawa T, Kapadia H, Cavender AC, D'Souza RN: 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
-
8
-
-
0042822121
-
Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia
-
Das P, Hai M, Elcock C et al: Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia. Am J Med Genet 2003; 118A: 35-42.
-
(2003)
Am J Med Genet
, vol.118 A
, pp. 35-42
-
-
Das, P.1
Hai, M.2
Elcock, C.3
-
9
-
-
0036479444
-
A novel mutation in human PAX9 causes molar oligodontia
-
Frazier-Bowers SA, Guo DC, Cavender A et al: 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
-
10
-
-
0034748051
-
Identification of a nonsense mutation in the PAX9 gene in molar oligodontia
-
Nieminen P, Arte S, Tanner D et al: Identification of a nonsense mutation in the PAX9 gene in molar oligodontia. Eur J Hum Genet 2001; 10: 743-746.
-
(2001)
Eur J Hum Genet
, vol.10
, pp. 743-746
-
-
Nieminen, P.1
Arte, S.2
Tanner, D.3
-
11
-
-
16644366228
-
Novel mutation of the initiation codon of PAX9 causes oligodontia
-
Klein ML, 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
-
12
-
-
0036556243
-
Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia
-
Das P, Stockton DW, Bauer C et al: 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
-
13
-
-
1142299588
-
A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia
-
Jumlongras D, Lin JY, Chapra A et al: 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
-
14
-
-
0027426925
-
DNA sequence recognition by Pax proteins: Bipartite structure of the paired domain and its binding site
-
Czerny T, Schaffner G, Busslinger M: DNA sequence recognition by Pax proteins: Bipartite structure of the paired domain and its binding site. Genes Dev 1993; 7: 2048-2061.
-
(1993)
Genes Dev
, vol.7
, pp. 2048-2061
-
-
Czerny, T.1
Schaffner, G.2
Busslinger, M.3
-
15
-
-
0025875226
-
Pax3, a novel murine DNA binding protein expressed during early neurogenesis
-
Goulding MD, Chalepakis G, Deutsch U, Erselius JR, Gruss P: Pax3, a novel murine DNA binding protein expressed during early neurogenesis. EMBO J 1991; 10: 1135-1147.
-
(1991)
EMBO J
, vol.10
, pp. 1135-1147
-
-
Goulding, M.D.1
Chalepakis, G.2
Deutsch, U.3
Erselius, J.R.4
Gruss, P.5
-
16
-
-
0029153727
-
Characterization and developmental expression of Pax9, a paired-box-containing gene related to Pax1
-
Neubüser A, Koseki H, Balling R: Characterization and developmental expression of Pax9, a paired-box-containing gene related to Pax1. Dev Biol 1995; 170: 701-716.
-
(1995)
Dev Biol
, vol.170
, pp. 701-716
-
-
Neubüser, A.1
Koseki, H.2
Balling, R.3
-
17
-
-
0028919759
-
Crystal structure of a paired domain-DNA complex at a 2.5 Å resolution reveals a structural basis for Pax developmental mutations
-
Xu W, Rould M, Jun S, Desplan C, Pabo C: Crystal structure of a paired domain-DNA complex at a 2.5 Å resolution reveals a structural basis for Pax developmental mutations. Cell 1995; 80: 639-650.
-
(1995)
Cell
, vol.80
, pp. 639-650
-
-
Xu, W.1
Rould, M.2
Jun, S.3
Desplan, C.4
Pabo, C.5
-
18
-
-
0344731080
-
Crystal structure of the human Pax6 paired domain-DNA complex reveals specific roles for the linker region and carboxy-terminal subdomain in DNA binding
-
Xu E, Rould M, Xu W, Epstein J, Maas R, Pabo C: Crystal structure of the human Pax6 paired domain-DNA complex reveals specific roles for the linker region and carboxy-terminal subdomain in DNA binding. Genes Dev 1999; 13: 1263-1275.
-
(1999)
Genes Dev
, vol.13
, pp. 1263-1275
-
-
Xu, E.1
Rould, M.2
Xu, W.3
Epstein, J.4
Maas, R.5
Pabo, C.6
-
19
-
-
0030724892
-
The C-terminal subdomain makes an important contribution to the DNA binding activity of the Pax3 paired domain
-
Vogan KJ, Gros P: The C-terminal subdomain makes an important contribution to the DNA binding activity of the Pax3 paired domain. J Biol Chem 1997; 272: 28289-28295.
-
(1997)
J Biol Chem
, vol.272
, pp. 28289-28295
-
-
Vogan, K.J.1
Gros, P.2
-
20
-
-
0031059181
-
Functional analysis of paired box missense mutations in the PAX6 gene
-
Tang HK, Chao LY, Saunders GF: Functional analysis of paired box missense mutations in the PAX6 gene. Hum Mol Genet 1997; 6: 381-386.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 381-386
-
-
Tang, H.K.1
Chao, L.Y.2
Saunders, G.F.3
-
21
-
-
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
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