-
1
-
-
35348987509
-
Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: The odonto-onycho-dermal dysplasia
-
L. Adaimy, E. Chouery, H. Megarbane, S. Mroueh, V. Delague, and E. Nicolas et al. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia Am J Hum Genet 81 2007 821 828
-
(2007)
Am J Hum Genet
, vol.81
, pp. 821-828
-
-
Adaimy, L.1
Chouery, E.2
Megarbane, H.3
Mroueh, S.4
Delague, V.5
Nicolas, E.6
-
2
-
-
84876542725
-
Full mouth implant rehabilitation of a patient with ectodermal dysplasia after orthognathic surgery, sinus and ridge augmentation: A clinical report
-
M. Bayat, M.M. Khobyari, M. Dalband, and F. Momen-Heravi Full mouth implant rehabilitation of a patient with ectodermal dysplasia after orthognathic surgery, sinus and ridge augmentation: a clinical report J Adv Prosthodont 3 2011 96 100
-
(2011)
J Adv Prosthodont
, vol.3
, pp. 96-100
-
-
Bayat, M.1
Khobyari, M.M.2
Dalband, M.3
Momen-Heravi, F.4
-
3
-
-
47249128542
-
Implant failure in young children with ectodermal dysplasia: A retrospective evaluation of use and outcome of dental implant treatment in children in Sweden
-
B. Bergendal, A. Ekman, and P. Nilsson Implant failure in young children with ectodermal dysplasia: a retrospective evaluation of use and outcome of dental implant treatment in children in Sweden Int J Oral Maxillofac Implants 23 2008 520 524
-
(2008)
Int J Oral Maxillofac Implants
, vol.23
, pp. 520-524
-
-
Bergendal, B.1
Ekman, A.2
Nilsson, P.3
-
5
-
-
67649880580
-
WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes
-
A. Bohring, T. Stamm, C. Spaich, C. Haase, K. Spree, and U. Hehr 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 85 2009 97 105
-
(2009)
Am J Hum Genet
, vol.85
, pp. 97-105
-
-
Bohring, A.1
Stamm, T.2
Spaich, C.3
Haase, C.4
Spree, K.5
Hehr, U.6
-
6
-
-
56749144138
-
Schöpf-Schulz-Passarge syndrome: Further delineation of the phenotype and genetic considerations
-
M. Castori, S. Ruggieri, L. Giannetti, G. Annessi, and G. Zambruno Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations Acta Derm Venereol 88 2008 607 612
-
(2008)
Acta Derm Venereol
, vol.88
, pp. 607-612
-
-
Castori, M.1
Ruggieri, S.2
Giannetti, L.3
Annessi, G.4
Zambruno, G.5
-
7
-
-
78649987736
-
Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum
-
M. Castori, D. Castiglia, F. Brancati, M. Foglio, S. Heath, and G. Floriddia et al. Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum Clin Genet 79 2011 92 95
-
(2011)
Clin Genet
, vol.79
, pp. 92-95
-
-
Castori, M.1
Castiglia, D.2
Brancati, F.3
Foglio, M.4
Heath, S.5
Floriddia, G.6
-
8
-
-
77951219194
-
Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia cases
-
N. Chassaing, C. Cluzeau, E. Bal, P. Guigue, M.C. Vincent, and G. Viot et al. Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia cases Br J Dermatol 162 2010 1044 1048
-
(2010)
Br J Dermatol
, vol.162
, pp. 1044-1048
-
-
Chassaing, N.1
Cluzeau, C.2
Bal, E.3
Guigue, P.4
Vincent, M.C.5
Viot, G.6
-
9
-
-
79955411359
-
Interactions between Shh, Sostdc1 and Wnt signaling and a new feedback loop for spatial patterning of the teeth
-
S.W. Cho, S. Kwak, T.E. Woolley, M.J. Lee, E.J. Kim, and R.E. Baker et al. Interactions between Shh, Sostdc1 and Wnt signaling and a new feedback loop for spatial patterning of the teeth Development 138 2011 1807 1816
-
(2011)
Development
, vol.138
, pp. 1807-1816
-
-
Cho, S.W.1
Kwak, S.2
Woolley, T.E.3
Lee, M.J.4
Kim, E.J.5
Baker, R.E.6
-
10
-
-
77955835996
-
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: Genotypic-dental phenotypic findings
-
F. Clauss, N. Chassaing, A. Smahi, M.C. Vincent, P. Calvas, and M. Molla et al. X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings Clin Genet 78 2010 257 266
-
(2010)
Clin Genet
, vol.78
, pp. 257-266
-
-
Clauss, F.1
Chassaing, N.2
Smahi, A.3
Vincent, M.C.4
Calvas, P.5
Molla, M.6
-
11
-
-
0032941717
-
Regulation of LEF-1/TCF transcription factors by Wnt and other signals
-
Q. Eastman, and R. Grosschedl Regulation of LEF-1/TCF transcription factors by Wnt and other signals Curr Opin Cell Biol 11 1999 233 240
-
(1999)
Curr Opin Cell Biol
, vol.11
, pp. 233-240
-
-
Eastman, Q.1
Grosschedl, R.2
-
13
-
-
78650578135
-
Implant treatment in grafted and native bone in patients affected by ectodermal dysplasia
-
F. Grecchi, L. Pagliani, G.E. Mancini, I. Zollino, and F. Carinci Implant treatment in grafted and native bone in patients affected by ectodermal dysplasia J Craniofac Surg 21 2010 1776 1780
-
(2010)
J Craniofac Surg
, vol.21
, pp. 1776-1780
-
-
Grecchi, F.1
Pagliani, L.2
Mancini, G.E.3
Zollino, I.4
Carinci, F.5
-
14
-
-
84884208689
-
Leukocyte-platelet-rich plasma (L-PRP) impairs the osteoconductive capacity of the autograft associated to changes in the immunolocalization of TGF-β1 and its co-expression with Wnt10b and CD34
-
A. Giovanini, T. Deliberador, J. Nemeth, V. Crivellaro, G. Portela, and M. de Oliveira Filho et al. Leukocyte-platelet-rich plasma (L-PRP) impairs the osteoconductive capacity of the autograft associated to changes in the immunolocalization of TGF-β1 and its co-expression with Wnt10b and CD34 J Cranio-Maxillofacial Surg 41 2013 180 186
-
(2013)
J Cranio-Maxillofacial Surg
, vol.41
, pp. 180-186
-
-
Giovanini, A.1
Deliberador, T.2
Nemeth, J.3
Crivellaro, V.4
Portela, G.5
De Oliveira Filho, M.6
-
16
-
-
0002172340
-
Patient selection and preparation
-
P.I. Branemark, G.A. Zarb, T. Albrektsson, Quintessence
-
U. Lekholm, and G. Zarb Patient selection and preparation P.I. Branemark, G.A. Zarb, T. Albrektsson, Tissue integrated prostheses 1985 Quintessence 199 210
-
(1985)
Tissue Integrated Prostheses
, pp. 199-210
-
-
Lekholm, U.1
Zarb, G.2
-
17
-
-
77952989890
-
Wnt proteins promote bone regeneration
-
S. Minear, P. Leucht, J. Jiang, B. Liu, A. Zeng, and C. Fuerer et al. Wnt proteins promote bone regeneration Sci Transl Med 2 2010 29 30
-
(2010)
Sci Transl Med
, vol.2
, pp. 29-30
-
-
Minear, S.1
Leucht, P.2
Jiang, J.3
Liu, B.4
Zeng, A.5
Fuerer, C.6
-
19
-
-
77953132557
-
Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A
-
N. Nagy, E. Wedgeworth, T. Hamada, J.M. White, T. Hashimoto, and J.A. McGrath Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A J Dermatol 58 2010 220 222
-
(2010)
J Dermatol
, vol.58
, pp. 220-222
-
-
Nagy, N.1
Wedgeworth, E.2
Hamada, T.3
White, J.M.4
Hashimoto, T.5
McGrath, J.A.6
-
20
-
-
70450233732
-
WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome
-
S. Nawaz, J. Klar, M. Wajid, M. Aslam, M. Tariq, and J. Schuster et al. WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome Eur J Hum Genet 17 2009 1600 1605
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 1600-1605
-
-
Nawaz, S.1
Klar, J.2
Wajid, M.3
Aslam, M.4
Tariq, M.5
Schuster, J.6
-
21
-
-
80054839269
-
High-bone-mass-producing mutations in the Wnt signaling pathway result in distinct skeletal phenotypes
-
P.J. Niziolek, T.L. Farmer, Y. Cui, C.H. Turner, M.L. Warman, and A.G. Robling High-bone-mass-producing mutations in the Wnt signaling pathway result in distinct skeletal phenotypes Bone 49 2011 1010 1019
-
(2011)
Bone
, vol.49
, pp. 1010-1019
-
-
Niziolek, P.J.1
Farmer, T.L.2
Cui, Y.3
Turner, C.H.4
Warman, M.L.5
Robling, A.G.6
-
22
-
-
80051801625
-
Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A
-
G. Petrof, K. Fong, J.E. Lai-Cheong, S.E. Cockayne, and J.A. McGrath Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A Australas J Dermatol 52 2011 224 226
-
(2011)
Australas J Dermatol
, vol.52
, pp. 224-226
-
-
Petrof, G.1
Fong, K.2
Lai-Cheong, J.E.3
Cockayne, S.E.4
McGrath, J.A.5
-
23
-
-
0034880422
-
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
-
S. Reddy, T. Andl, A. Bagasra, M.M. Lu, D.J. Epstein, and E.E. Morrisey 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 107 2001 69 82
-
(2001)
Mech Dev
, vol.107
, pp. 69-82
-
-
Reddy, S.1
Andl, T.2
Bagasra, A.3
Lu, M.M.4
Epstein, D.J.5
Morrisey, E.E.6
-
24
-
-
79953026459
-
Simultaneous maxillary sinus lifting and implant placement with autogenous parietal bone graft: Outcome of 17 cases
-
S. Sakka, and C. Krenkel Simultaneous maxillary sinus lifting and implant placement with autogenous parietal bone graft: outcome of 17 cases J Cranio-Maxillofacial Surg 39 2011 187 191
-
(2011)
J Cranio-Maxillofacial Surg
, vol.39
, pp. 187-191
-
-
Sakka, S.1
Krenkel, C.2
-
25
-
-
60849091616
-
Bone morphogenetic protein-2 enhances Wnt/beta-catenin signaling-induced osteoprotegerin expression
-
M.M. Sato, A. Nakashima, M. Nashimoto, Y. Yawaka, and M. Tamura Bone morphogenetic protein-2 enhances Wnt/beta-catenin signaling-induced osteoprotegerin expression Genes Cells 14 2009 141 153
-
(2009)
Genes Cells
, vol.14
, pp. 141-153
-
-
Sato, M.M.1
Nakashima, A.2
Nashimoto, M.3
Yawaka, Y.4
Tamura, M.5
-
26
-
-
84884211522
-
Volume changes of autogenous bone after sinus lifting and grafting procedures: A 6-year computerized tomographic follow-up
-
C. Sbordone, P. Toti, F. Guidetti, L. Califano, P. Bufo, and L. Sbordone Volume changes of autogenous bone after sinus lifting and grafting procedures: a 6-year computerized tomographic follow-up J Cranio-Maxillofacial Surg 41 2013 235 241
-
(2013)
J Cranio-Maxillofacial Surg
, vol.41
, pp. 235-241
-
-
Sbordone, C.1
Toti, P.2
Guidetti, F.3
Califano, L.4
Bufo, P.5
Sbordone, L.6
-
28
-
-
69249108859
-
Classifying functional manifestations of ectodermal dysplasias
-
R.J. Simeonsson Classifying functional manifestations of ectodermal dysplasias Am J Med Genet A 149 2009 2014 2019
-
(2009)
Am J Med Genet A
, vol.149
, pp. 2014-2019
-
-
Simeonsson, R.J.1
-
29
-
-
77957329671
-
Role of the Wnt signaling pathway in bone and tooth
-
M. Tamura, E. Nemoto, M.M. Sato, A. Nakashima, and H. Shimauchi Role of the Wnt signaling pathway in bone and tooth Front Biosci 2 2010 1405 1413
-
(2010)
Front Biosci
, vol.2
, pp. 1405-1413
-
-
Tamura, M.1
Nemoto, E.2
Sato, M.M.3
Nakashima, A.4
Shimauchi, H.5
-
31
-
-
44449142932
-
Mutation screening of the ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia
-
A.H. Van der Hout, G.G. Oudesluijs, A. Venema, J.B. Verheij, B.G. Mol, and P. Rump et al. Mutation screening of the ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia Eur J Hum Genet 16 2008 673 679
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 673-679
-
-
Van Der Hout, A.H.1
Oudesluijs, G.G.2
Venema, A.3
Verheij, J.B.4
Mol, B.G.5
Rump, P.6
-
32
-
-
77952713260
-
Phenotypic variability associated with WNT10A nonsense mutations
-
M. Van Geel, M. Gattas, Y. Kesler, P. Tong, H. Yan, and K. Tran et al. Phenotypic variability associated with WNT10A nonsense mutations Br J Dermatol 162 2010 1403 1406
-
(2010)
Br J Dermatol
, vol.162
, pp. 1403-1406
-
-
Van Geel, M.1
Gattas, M.2
Kesler, Y.3
Tong, P.4
Yan, H.5
Tran, K.6
-
33
-
-
84867647501
-
Bone quality and quantity of the anterior maxillary trabecular bone in dental implant sites
-
M. Wakimoto, T. Matsumura, T. Ueno, N. Mizukawa, Y. Yanagi, and S. Lida Bone quality and quantity of the anterior maxillary trabecular bone in dental implant sites Clin Oral Implants Res 23 2012 1314 1319
-
(2012)
Clin Oral Implants Res
, vol.23
, pp. 1314-1319
-
-
Wakimoto, M.1
Matsumura, T.2
Ueno, T.3
Mizukawa, N.4
Yanagi, Y.5
Lida, S.6
-
34
-
-
79955719427
-
Intra-familial variability of ectodermal defects associated with WNT10A mutations
-
E.K. Wedgeworth, N. Nagy, J.M. White, A.C. Pembroke, and J.A. McGrath Intra-familial variability of ectodermal defects associated with WNT10A mutations Acta Derm Venereol 91 2011 346 347
-
(2011)
Acta Derm Venereol
, vol.91
, pp. 346-347
-
-
Wedgeworth, E.K.1
Nagy, N.2
White, J.M.3
Pembroke, A.C.4
McGrath, J.A.5
-
35
-
-
67650230898
-
Reciprocal requirements for EDA/EDAR/NF-kappaB and Wnt/beta-catenin signaling pathways in hair follicle induction
-
Y. Zhang, P. Tomann, T. Andl, N.M. Gallant, J. Huelsken, and B. Jerchow et al. Reciprocal requirements for EDA/EDAR/NF-kappaB and Wnt/beta-catenin signaling pathways in hair follicle induction Dev Cell 17 2009 49 61
-
(2009)
Dev Cell
, vol.17
, pp. 49-61
-
-
Zhang, Y.1
Tomann, P.2
Andl, T.3
Gallant, N.M.4
Huelsken, J.5
Jerchow, B.6
|