-
1
-
-
37349004829
-
Craniofacial and upper airway cephalometrics in hypohidrotic ectodermal dys-plasia
-
Arslan, S., Devecioglu Kama, J., Ozer, T., andYavuz, I. (2007). Craniofacial and upper airway cephalometrics in hypohidrotic ectodermal dys-plasia. Dentomaxittofac Radio!. 36, 478-483.
-
(2007)
Dentomaxittofac Radio!
, vol.36
, pp. 478-483
-
-
Arslan, S.1
Devecioglu Kama, J.2
Ozer, T.3
Yavuz, I.4
-
2
-
-
0023033040
-
Anhidrosis and absence of sweat glands in mice hemizygous for the tabby gene: supportive evidence for the hypothesis of homology between tabby and human anhidrotic (hypohidrotic) ectodermal dysplasia (Christ-Siemens-Touraine syndrome)
-
Blecher, S. R. (1986). Anhidrosis and absence of sweat glands in mice hemizygous for the tabby gene: supportive evidence for the hypothesis of homology between tabby and human anhidrotic (hypohidrotic) ectodermal dysplasia (Christ-Siemens-Touraine syndrome). J. Invest. Dermatol 87, 720-722.
-
(1986)
J. Invest. Dermatol
, vol.87
, pp. 720-722
-
-
Blecher, S.R.1
-
3
-
-
0036562458
-
Analysis of facial growth in subjects with syndromic ectodermal dysplasia: a longitudinal analysis
-
Bondarets, N., Jones, R.M., and McDonald, F. (2002). Analysis of facial growth in subjects with syndromic ectodermal dysplasia: a longitudinal analysis. Orthod. Craniofac Res. 5, 71-84.
-
(2002)
Orthod. Craniofac Res.
, vol.5
, pp. 71-84
-
-
Bondarets, N.1
Jones, R.M.2
McDonald, F.3
-
4
-
-
0031832127
-
The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome
-
Bourgeois, P., Bolcato-Bellemin, A. L., Danse, J. M., Bloch-Zupan, A., Yoshiba, K., Stoetzel, C, and Perrin-Schmitt, E (1998). The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome. Hum. Mol. Genet. 7, 945-957.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 945-957
-
-
Bourgeois, P.1
Bolcato-Bellemin, A.L.2
Danse, J.M.3
Bloch-Zupan, A.4
Yoshiba, K.5
Stoetzel, C.6
Perrin-Schmitt, E.7
-
5
-
-
0035437862
-
NF-kappaB mediates FGF signal regulation of msx-1 expression
-
Bushdid, P. B., Chen, C. L, Brantley, D. M., Yull, E, Raghow, R., Kerr, L. D., and Bamett J.V. (2001). NF-kappaB mediates FGF signal regulation of msx-1 expression. Dev. Biol. 237, 107-115.
-
(2001)
Dev. Biol.
, vol.237
, pp. 107-115
-
-
Bushdid, P.B.1
Chen, C.L.2
Brantley, D.M.3
Yull, E.4
Raghow, R.5
Kerr, L.D.6
Bamett, J.V.7
-
6
-
-
0033952715
-
Clinical findings in mosaic carriers of hypo-hidrotic ectodermal dysplasia
-
Cambiaghi, S., Restano, L., Paakkonen, K., Caputo, R., and Kere, J. (2000). Clinical findings in mosaic carriers of hypo-hidrotic ectodermal dysplasia. Arch. Dermatol. 136,217-224.
-
(2000)
Arch. Dermatol.
, vol.136
, pp. 217-224
-
-
Cambiaghi, S.1
Restano, L.2
Paakkonen, K.3
Caputo, R.4
Kere, J.5
-
7
-
-
59949097734
-
Effect of eda loss of function on upper jugal tooth morphology
-
Charles, C, Pantalacci, S., Perterkova, R., Tafforeau, P., Laudet, V., and Viriot, L. (2009). Effect of eda loss of function on upper jugal tooth morphology. Anat. Rec. 292,299-308.
-
(2009)
Anat. Rec.
, vol.292
, pp. 299-308
-
-
Charles, C.1
Pantalacci, S.2
Perterkova, R.3
Tafforeau, P.4
Laudet, V.5
Viriot, L.6
-
8
-
-
58149383851
-
Dento-craniofacial phenotypes and underlying molecular mechanisms in hypohidrotic ectodermal dysplasia (HED): a review
-
Clauss, E, Maniere, M. C, Obry, E, Waltmann, E., Hadj-Rabia, S., Bodemer, C, Alembik, Y., Lesot, H., and Schmittbuhl, M. (2008). Dento-craniofacial phenotypes and underlying molecular mechanisms in hypohidrotic ectodermal dysplasia (HED): a review. J. Dent. Res. 87, 1089-1099.
-
(2008)
J. Dent. Res.
, vol.87
, pp. 1089-1099
-
-
Clauss, E.1
Maniere, M.C.2
Obry, E.3
Waltmann, E.4
Hadj-Rabia, S.5
Bodemer, C.6
Alembik, Y.7
Lesot, H.8
Schmittbuhl, M.9
-
9
-
-
77955504140
-
Craniofacial growth in ectodermal dysplasia An 8 year longitudinal evaluation of Italian subjects
-
Dellavia, C, Catti, E, Sforza, C, Tommasi, D. G., and Ferrario, V. E (2010). Craniofacial growth in ectodermal dysplasia. An 8 year longitudinal evaluation of Italian subjects. Angle Orthod. 80, 545-551.
-
(2010)
Angle Orthod
, vol.80
, pp. 545-551
-
-
Dellavia, C.1
Catti, E.2
Sforza, C.3
Tommasi, D.G.4
Ferrario, V.E.5
-
10
-
-
33750590319
-
Palatal size and shape in 6-year olds affected by hypohidrotic ectodermal dysplasia
-
Dellavia, C, Sforza, C, Malerba, A., Strohmenger, L., and Ferrario, V. F. (2006). Palatal size and shape in 6-year olds affected by hypohidrotic ectodermal dysplasia. Angle Orthod. 76, 978-983.
-
(2006)
Angle Orthod
, vol.76
, pp. 978-983
-
-
Dellavia, C.1
Sforza, C.2
Malerba, A.3
Strohmenger, L.4
Ferrario, V.F.5
-
11
-
-
69249083674
-
Approach towards a new classification for ectodermal dyspla-sias: integration of the clinical and molecular knowledge
-
DiGiovanna, J. J., Priolo, M., and Itin, P. (2009). Approach towards a new classification for ectodermal dyspla-sias: integration of the clinical and molecular knowledge. Am. J. Med. Genet. A 149, 2068-2070.
-
(2009)
Am. J. Med. Genet. A
, vol.149
, pp. 2068-2070
-
-
DiGiovanna, J.J.1
Priolo, M.2
Itin, P.3
-
12
-
-
85009088967
-
Prenatal development of the facial skeleton
-
eds A. D. Dixon, D. A. N Hoyte, and O. Ronning (Boca Raton: CRC Press)
-
Dixon, A. D. (1997). "Prenatal development of the facial skeleton," in Fundamentals of Craniofacial Growth, eds A. D. Dixon, D. A. N Hoyte, and O. Ronning (Boca Raton: CRC Press), 59-97.
-
(1997)
Fundamentals of Craniofacial Growth
, pp. 59-97
-
-
Dixon, A.D.1
-
14
-
-
0015016111
-
The glandular aspects of the tabby syndrome in the mouse
-
Griineberg, H. (1971). The glandular aspects of the tabby syndrome in the mouse. J. Embryol. Exp. Morphol. 25, 1-19.
-
(1971)
J. Embryol. Exp. Morphol.
, vol.25
, pp. 1-19
-
-
Griineberg, H.1
-
15
-
-
0018911140
-
Tissue interactions and the initiation of osteogenesis and chondrogenesis in the neural crest-derived mandibular skeleton of the embryonic mouse as seen in isolated murine tissues and in recombinations of murine and avian tissues
-
Hall, B. K. (1980). Tissue interactions and the initiation of osteogenesis and chondrogenesis in the neural crest-derived mandibular skeleton of the embryonic mouse as seen in isolated murine tissues and in recombinations of murine and avian tissues. J. Embryol. Exp. Morphol. 58, 251-264.
-
(1980)
J. Embryol. Exp. Morphol.
, vol.58
, pp. 251-264
-
-
Hall, B.K.1
-
16
-
-
0024990350
-
Reciprocal interactions between epithelium, mesenchyme, and epidermal growth factor (EGF) in the regulation of mandibular mitotic activity in the embryonic chick
-
Hall, B. K., and Coffin-Collins, P. A. (1990). Reciprocal interactions between epithelium, mesenchyme, and epidermal growth factor (EGF) in the regulation of mandibular mitotic activity in the embryonic chick. J. Craniofac. Genet. Dev. Biol. 10, 241-261.
-
(1990)
J. Craniofac. Genet. Dev. Biol.
, vol.10
, pp. 241-261
-
-
Hall, B.K.1
Coffin-Collins, P.A.2
-
17
-
-
34748886657
-
PAST: paleontological statistics software package for education and data analysis
-
Hammer, O., Harper, D. A. T., and Ryan, P. D. (2001). PAST: paleontological statistics software package for education and data analysis. Paheontol. Electronica 4, 1-9.
-
(2001)
Paheontol. Electronica
, vol.4
, pp. 1-9
-
-
Hammer, O.1
Harper, D.A.T.2
Ryan, P.D.3
-
18
-
-
7244255985
-
Regionalisation of early head ectoderm is regulated by endoderm and prepatterns the orofacial epithelium
-
Haworth, K.E., Healy, C, Morgan, P., and Sharpe, P.T. (2004). Regionalisation of early head ectoderm is regulated by endoderm and prepatterns the orofacial epithelium. Development 131, 4797-4806.
-
(2004)
Development
, vol.131
, pp. 4797-4806
-
-
Haworth, K.E.1
Healy, C.2
Morgan, P.3
Sharpe, P.T.4
-
19
-
-
0036485796
-
Mutation of the ectodysplasin-A gene results in bone defects in mice
-
Hill, N. L, Laib, A., and Duncan, M. K. (2002). Mutation of the ectodysplasin-A gene results in bone defects in mice. J. Comp. Pathol. 126, 220-225.
-
(2002)
J. Comp. Pathol.
, vol.126
, pp. 220-225
-
-
Hill, N.L.1
Laib, A.2
Duncan, M.K.3
-
20
-
-
69249088571
-
Rationale and background as basis for a new classification of the ectodermal dysplasias
-
Itin, P. H. (2009). Rationale and background as basis for a new classification of the ectodermal dysplasias. Am.]. Med. Genet. A 149, 1973-1976.
-
(2009)
Am. ]. Med. Genet. A
, vol.149
, pp. 1973-1976
-
-
Itin, P.H.1
-
21
-
-
0036837684
-
Analysis of craniofacial development in children with hypohidrotic ectodermal dysplasia
-
Johnson, E. L., Roberts, M. W., Guckes, A. D., Bailey, L. J., Phillips, C. L, and Wright, J. T. (2002). Analysis of craniofacial development in children with hypohidrotic ectodermal dysplasia. Am.]. Med. Genet. 112, 327-334.
-
(2002)
Am. ]. Med. Genet.
, vol.112
, pp. 327-334
-
-
Johnson, E.L.1
Roberts, M.W.2
Guckes, A.D.3
Bailey, L.J.4
Phillips, C.L.5
Wright, J.T.6
-
22
-
-
0036831443
-
Different mor-photypes of functional dentition in the lower molar region of tabby (EDA) mice
-
Kristenova, P., Peterka, M., Lisi, S., Gendrault, J. L., Lesot, H., and Peterkova, R. (2002). Different mor-photypes of functional dentition in the lower molar region of tabby (EDA) mice. Orthod. Craniofac. Res. 5, 205-214.
-
(2002)
Orthod. Craniofac. Res.
, vol.5
, pp. 205-214
-
-
Kristenova, P.1
Peterka, M.2
Lisi, S.3
Gendrault, J.L.4
Lesot, H.5
Peterkova, R.6
-
24
-
-
0033005419
-
Hindlimb patterning and mandible development require the Ptxl gene
-
Lanctot, C, Moreau, A., Chamberland, M., Tremblay, M.L., and Drouin, J. (1999). Hindlimb patterning and mandible development require the Ptxl gene. Development 126, 1805-1810.
-
(1999)
Development
, vol.126
, pp. 1805-1810
-
-
Lanctot, C.1
Moreau, A.2
Chamberland, M.3
Tremblay, M.L.4
Drouin, J.5
-
25
-
-
77649198704
-
Consequences of X-linked hypohidrotic ectodermal dysplasia for the human jaw bone
-
Lesot, H., Clauss, E, Maniere, M. C, and Schmittbuhl.M. (2009). Consequences of X-linked hypohidrotic ectodermal dysplasia for the human jaw bone. Front. Oral Biol. 13, 93-99.
-
(2009)
Front. Oral Biol.
, vol.13
, pp. 93-99
-
-
Lesot, H.1
Clauss, E.2
Maniere, M.C.3
Schmittbuhl, M.4
-
26
-
-
7144223296
-
Gene action in the X-chromosome of the mouse (Mus musculusL)
-
Lyon, M. (1961). Gene action in the X-chromosome of the mouse (Mus musculusL.). Nature 190, 372-373.
-
(1961)
Nature
, vol.190
, pp. 372-373
-
-
Lyon, M.1
-
27
-
-
0034798059
-
Regulation of mandibular growth and morphogenesis
-
Mina, M. (2001).Regulation of mandibular growth and morphogenesis. Crit. Rev. Oral Biol. Med. 12, 276-300.
-
(2001)
Crit. Rev. Oral Biol. Med.
, vol.12
, pp. 276-300
-
-
Mina, M.1
-
28
-
-
0032231350
-
Identification of anew splice form of theEDAl gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations
-
Monreal, A. W., Zonana, J., and Ferguson, B. (1998).Identification of anew splice form of theEDAl gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations. Am. J. Hum. Genet. 63, 380-389.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 380-389
-
-
Monreal, A.W.1
Zonana, J.2
Ferguson, B.3
-
29
-
-
14444283147
-
The gene defective in anhid-rotic ectodermal dysplasia is expressed in the developing epithelium, neu-roectoderm, thymus, and bone
-
Montonen, O., Ezer, S., Saarialho-Kere, U. K., Herva, R., Karjalainen-Lindsberg, M. L., Kaitila, I., Schlessinger, D., Srivastava, A. K., Thesleff, I., and Kere, J. (1998). The gene defective in anhid-rotic ectodermal dysplasia is expressed in the developing epithelium, neu-roectoderm, thymus, and bone. J. Histochem. Cytochem. 46, 281-289.
-
(1998)
J. Histochem. Cytochem.
, vol.46
, pp. 281-289
-
-
Montonen, O.1
Ezer, S.2
Saarialho-Kere, U.K.3
Herva, R.4
Karjalainen-Lindsberg, M.L.5
Kaitila, I.6
Schlessinger, D.7
Srivastava, A.K.8
Thesleff, I.9
Kere, J.10
-
30
-
-
0036831065
-
Different mor-photypes of the tabby (EDA) dentition in the mouse mandible result from a defect in the mesio-distal segmentation of dental epithelium
-
Peterkova, R., Kristenova, P., Lesot, H., Lisi, S., Vonesch, J. L., Gendrault, J. L., and Peterka, M. (2002). Different mor-photypes of the tabby (EDA) dentition in the mouse mandible result from a defect in the mesio-distal segmentation of dental epithelium. Orthod. Craniofac. Res. 5, 215-226.
-
(2002)
Orthod. Craniofac. Res.
, vol.5
, pp. 215-226
-
-
Peterkova, R.1
Kristenova, P.2
Lesot, H.3
Lisi, S.4
Vonesch, J.L.5
Gendrault, J.L.6
Peterka, M.7
-
31
-
-
0028127041
-
Ectodermal dysplasias: a clinical classification and a causal review
-
Pinheiro, M., and Freire-Maia, N. (1994). Ectodermal dysplasias: a clinical classification and a causal review. Am. J. Med. Genet. 53, 153-162.
-
(1994)
Am. J. Med. Genet.
, vol.53
, pp. 153-162
-
-
Pinheiro, M.1
Freire-Maia, N.2
-
32
-
-
0036948659
-
XIST RNA and the mechanism of X chromosome inactivation
-
Plath, K., Mlynarczyk-Evans, S., Nusinow, D., and Panning, B. (2002). XIST RNA and the mechanism of X chromosome inactivation. Annu. Rev. Genet. 36, 233-278.
-
(2002)
Annu. Rev. Genet.
, vol.36
, pp. 233-278
-
-
Plath, K.1
Mlynarczyk-Evans, S.2
Nusinow, D.3
Panning, B.4
-
33
-
-
33846486935
-
Ectodysplasin has a dual role in ectodermal organogenesis: inhibition of Bmp activity and induction of Shh expression
-
Pummila, M., Fliniaux, I., Jaatinen, R., James, M. J., Laurikkala, J., Schneider, P., Thesleff, I., and Mikkola, M. L. (2007). Ectodysplasin has a dual role in ectodermal organogenesis: inhibition of Bmp activity and induction of Shh expression. Development 134, 117-125.
-
(2007)
Development
, vol.134
, pp. 117-125
-
-
Pummila, M.1
Fliniaux, I.2
Jaatinen, R.3
James, M.J.4
Laurikkala, J.5
Schneider, P.6
Thesleff, I.7
Mikkola, M.L.8
-
34
-
-
0036467052
-
Craniofacial phenotypes in segmen-tally trisomic mouse models for Down syndrome
-
Richtsmeier, J., Zumwalt, A., Carlson, E., Epstein, C, and Reeves, R. (2002). Craniofacial phenotypes in segmen-tally trisomic mouse models for Down syndrome. Am. J. Med. Genet. 107, 317-324.
-
(2002)
Am. J. Med. Genet.
, vol.107
, pp. 317-324
-
-
Richtsmeier, J.1
Zumwalt, A.2
Carlson, E.3
Epstein, C.4
Reeves, R.5
-
35
-
-
4344676383
-
Elliptical descriptors: some simplified morpho-metric parameters for the quantification of complex outlines
-
Schmittbuhl, M., Allenbach, B., Le Minor, J. M., and Schaaf, A. (2003). Elliptical descriptors: some simplified morpho-metric parameters for the quantification of complex outlines. Math. Geol. 35, 853-872.
-
(2003)
Math. Geol.
, vol.35
, pp. 853-872
-
-
Schmittbuhl, M.1
Allenbach, B.2
Le Minor, J.M.3
Schaaf, A.4
-
36
-
-
0014566957
-
Aspects of the tabby-crinkled and downless syndrome I. The development of tabby teeth.
-
Sofaer, J. A. (1969). Aspects of the tabby-crinkled and downless syndrome. I. The development of tabby teeth. J. Embryol. Exp. Morphol. 22, 181-205.
-
(1969)
J. Embryol. Exp. Morphol.
, vol.22
, pp. 181-205
-
-
Sofaer, J.A.1
-
37
-
-
12644310324
-
The tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains
-
Srivastava, A. K., Pispa, J., Hartung, A. J., Du, Y, Ezer, S., Jenks, T., Shimada, T., Pekkanen, M., Mikkola, M. L., Ko, M. S., Thesleff, I., Kere, J., and Schlessinger, D. (1997). The tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains. Proc. Nail. Acad. Sci. U.S.A. 94, 13069-13074.
-
(1997)
Proc. Nail. Acad. Sci. U. S. A.
, vol.94
, pp. 13069-13074
-
-
Srivastava, A.K.1
Pispa, J.2
Hartung, A.J.3
Du, Y.4
Ezer, S.5
Jenks, T.6
Shimada, T.7
Pekkanen, M.8
Mikkola, M.L.9
Ko, M.S.10
Thesleff, I.11
Kere, J.12
Schlessinger, D.13
-
38
-
-
0033693832
-
Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis
-
Tucker, A. S., Headon, D. J., Schneider, P., Ferguson, B. M., Overbeek, P., Tschopp, J., and Sharpe, P. T. (2000). Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis. Development 127, 4691-4700.
-
(2000)
Development
, vol.127
, pp. 4691-4700
-
-
Tucker, A.S.1
Headon, D.J.2
Schneider, P.3
Ferguson, B.M.4
Overbeek, P.5
Tschopp, J.6
Sharpe, P.T.7
-
39
-
-
0034981134
-
Mutational spectrum of the EDI gene in X-linked hypohidrotic ectodermal dysplasia
-
Vincent, M. C, Biancalana, V., Ginisty, D., Mandel, J. L., and Calvas, P. (2001). Mutational spectrum of the EDI gene in X-linked hypohidrotic ectodermal dysplasia. Eur. J. Hum. Genet. 9, 355-363.
-
(2001)
Eur. J. Hum. Genet.
, vol.9
, pp. 355-363
-
-
Vincent, M.C.1
Biancalana, V.2
Ginisty, D.3
Mandel, J.L.4
Calvas, P.5
|