-
1
-
-
85031177126
-
Death receptor signaling giving life to ectodermal organs
-
Thesleff I, Mikkola ML. Death receptor signaling giving life to ectodermal organs. Science's STKE (http://stke.sciencemag.org/cgi/content/full/oc-sigtrans;2002/131/pe22).
-
Science's STKE
-
-
Thesleff, I.1
Mikkola, M.L.2
-
2
-
-
9344250077
-
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
-
Kere J, Srivastava AK, Montonen O. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet 1996;13:409-16.
-
(1996)
Nat Genet
, vol.13
, pp. 409-416
-
-
Kere, J.1
Srivastava, A.K.2
Montonen, O.3
-
3
-
-
0028127041
-
Ectodermal dysplasias: A clinical classification and a causal review
-
Pinheiro M, Freire-Maia N. Ectodermal dysplasias: a clinical classification and a causal review. Am J Med Genet 1994;53:153-62.
-
(1994)
Am J Med Genet
, vol.53
, pp. 153-162
-
-
Pinheiro, M.1
Freire-Maia, N.2
-
5
-
-
0032811085
-
Mutations in the human homologue of mouse d1 cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia
-
Monreal AW, Ferguson BM, Headon DJ, Street SL, Overbeek PA, Zonana J. Mutations in the human homologue of mouse d1 cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nat Genet 1999;22:366-9.
-
(1999)
Nat Genet
, vol.22
, pp. 366-369
-
-
Monreal, A.W.1
Ferguson, B.M.2
Headon, D.J.3
Street, S.L.4
Overbeek, P.A.5
Zonana, J.6
-
6
-
-
0035924366
-
Gene defect in ectodermal dysplasia implicates a death domain adapter in development
-
Headon DJ, Emmal SA, Ferguson BM, et al. Gene defect in ectodermal dysplasia implicates a death domain adapter in development. Nature 2001;414:913-6.
-
(2001)
Nature
, vol.414
, pp. 913-916
-
-
Headon, D.J.1
Emmal, S.A.2
Ferguson, B.M.3
-
8
-
-
0014833344
-
Clinical spectrum of anhidrotic ectodermal dysplasia
-
Reed WB, Lopez DA, Landing B. Clinical spectrum of anhidrotic ectodermal dysplasia. Arch Dermatol 1970;102:134-43.
-
(1970)
Arch Dermatol
, vol.102
, pp. 134-143
-
-
Reed, W.B.1
Lopez, D.A.2
Landing, B.3
-
9
-
-
0001086726
-
A totally sex-linked gene in the house mouse
-
Falconer DS. A totally sex-linked gene in the house mouse. Nature 1952;169:664-5.
-
(1952)
Nature
, vol.169
, pp. 664-665
-
-
Falconer, D.S.1
-
10
-
-
0013806515
-
Genes and genotypes affecting the teeth of the mouse
-
Grüneberg H. Genes and genotypes affecting the teeth of the mouse. J Embryol Exp Morph 1965;14:137-59.
-
(1965)
J Embryol Exp Morph
, vol.14
, pp. 137-159
-
-
Grüneberg, H.1
-
11
-
-
0014566957
-
Aspects of the Tabby-crinkled-downless syndrome. I. The development of Tabby teeth
-
Sofaer JA. Aspects of the Tabby-crinkled-downless syndrome. I. The development of Tabby teeth. J Embryol Exp Morph 1969;22:181-205.
-
(1969)
J Embryol Exp Morph
, vol.22
, pp. 181-205
-
-
Sofaer, J.A.1
-
12
-
-
0036088977
-
The Mouse Genome Database (MGD): The model organism database for the laboratory mouse
-
And the mouse database group
-
Blake JA, Richardson JE, Bult CJ, Kadin JA, Eppig JT. And the mouse database group. The Mouse Genome Database (MGD): the model organism database for the laboratory mouse. Nucl Acids Res 2002;30:113-5.
-
(2002)
Nucl Acids Res
, vol.30
, pp. 113-115
-
-
Blake, J.A.1
Richardson, J.E.2
Bult, C.J.3
Kadin, J.A.4
Eppig, J.T.5
-
13
-
-
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 AK, Pispa J, Hartung AJ, et al. 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 Natl Acad Sci USA 1997;94:13069-74.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 13069-13074
-
-
Srivastava, A.K.1
Pispa, J.2
Hartung, A.J.3
-
14
-
-
0030833393
-
Cloning of Tabby, the murine homolog of the human Eda gene - Evidence for a membrane-associated protein with a short collagenous domain
-
Ferguson BM, Brockdorff N, Formstone E, Ngyuen T, Kronmiller JE, Zonana J. Cloning of Tabby, the murine homolog of the human Eda gene - evidence for a membrane-associated protein with a short collagenous domain. Hum Mol Genet 1997;6:1589-94.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1589-1594
-
-
Ferguson, B.M.1
Brockdorff, N.2
Formstone, E.3
Ngyuen, T.4
Kronmiller, J.E.5
Zonana, J.6
-
15
-
-
0032775933
-
Involvement of a novel TNF receptor homologue in hair follicle induction
-
Headon DJ, Overbeek PA. Involvement of a novel TNF receptor homologue in hair follicle induction. Nat Genet 1999;22:370-4.
-
(1999)
Nat Genet
, vol.22
, pp. 370-374
-
-
Headon, D.J.1
Overbeek, P.A.2
-
16
-
-
0037022539
-
Identification of a novel death domain-containing adaptor molecule for ectodysplasin-A receptor that is mutated in crinkled mice
-
Yan MH, Zhang ZM, Brady JR, Schilbach S, Fairbrother WJ, Dixit VM. Identification of a novel death domain-containing adaptor molecule for ectodysplasin-A receptor that is mutated in crinkled mice. Curr Biol 2002;12:409-13.
-
(2002)
Curr Biol
, vol.12
, pp. 409-413
-
-
Yan, M.H.1
Zhang, Z.M.2
Brady, J.R.3
Schilbach, S.4
Fairbrother, W.J.5
Dixit, V.M.6
-
17
-
-
0033572260
-
Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF
-
Pispa J, Jung HS, Jernvall J, et al. Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF. Dev Biol 1999;216:521-34.
-
(1999)
Dev Biol
, vol.216
, pp. 521-534
-
-
Pispa, J.1
Jung, H.S.2
Jernvall, J.3
-
18
-
-
84971737311
-
The initiation and development of the hair follicle population in Tabby mice
-
Claxton JH. The initiation and development of the hair follicle population in Tabby mice. Genet Res 1967;10:161-71.
-
(1967)
Genet Res
, vol.10
, pp. 161-171
-
-
Claxton, J.H.1
-
19
-
-
0009950083
-
Some observations on the skin and hair of Tabby mice
-
Kindred B. Some observations on the skin and hair of Tabby mice. J Hered 1967;58:197-9.
-
(1967)
J Hered
, vol.58
, pp. 197-199
-
-
Kindred, B.1
-
20
-
-
0015016111
-
The glandular aspects of the Tabby syndrome in the mouse
-
Grüneberg H. The glandular aspects of the Tabby syndrome in the mouse. J Embryol Exp Morph 1971;25:1-19.
-
(1971)
J Embryol Exp Morph
, vol.25
, pp. 1-19
-
-
Grüneberg, H.1
-
21
-
-
0020507360
-
Pleiotropic effect of Tabby gene on epidermal growth factor-containing cells of mouse submandibular gland
-
Blecher SR, Debertin M, Murphy JS. Pleiotropic effect of Tabby gene on epidermal growth factor-containing cells of mouse submandibular gland. Anat Rec 1983;207:25-9.
-
(1983)
Anat Rec
, vol.207
, pp. 25-29
-
-
Blecher, S.R.1
Debertin, M.2
Murphy, J.S.3
-
22
-
-
0031716740
-
The anhidrotic ectodermal dysplasia gene (Eda) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats
-
Bayés M, Hartung AJ, Ezer S, et al. The anhidrotic ectodermal dysplasia gene (Eda) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats. Hum Mol Genet 1998;7:1661-9.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1661-1669
-
-
Bayés, M.1
Hartung, A.J.2
Ezer, S.3
-
23
-
-
0032850832
-
Ectodysplasin, a protein required for epithelial morphogenesis, is a novel TNF homologue and promotes cell-matrix adhesion
-
Mikkola ML, Pispa J, Pekkanen M, et al. Ectodysplasin, a protein required for epithelial morphogenesis, is a novel TNF homologue and promotes cell-matrix adhesion. Mech Dev 1999;88:133-46.
-
(1999)
Mech Dev
, vol.88
, pp. 133-146
-
-
Mikkola, M.L.1
Pispa, J.2
Pekkanen, M.3
-
24
-
-
0032852542
-
Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells
-
Ezer S, Bayés M, Elomaa O, Schlessinger D, Kere J. Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells. Hum Mol Genet 1999;8:2079-86.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 2079-2086
-
-
Ezer, S.1
Bayés, M.2
Elomaa, O.3
Schlessinger, D.4
Kere, J.5
-
25
-
-
0033005418
-
The gene for X-linked anhidrotic ectodermal dysplasia encodes a TNF-like domain
-
Copley RR. The gene for X-linked anhidrotic ectodermal dysplasia encodes a TNF-like domain. J Mol Med 1999;77:361-3.
-
(1999)
J Mol Med
, vol.77
, pp. 361-363
-
-
Copley, R.R.1
-
26
-
-
0033761628
-
Two-amino acid molecular switch in an epithelial morphogen that regulates binding to two distinct receptors
-
Yan MH, Wang LC, Hymowitz SG, et al. Two-amino acid molecular switch in an epithelial morphogen that regulates binding to two distinct receptors. Science 2000;290:523-7.
-
(2000)
Science
, vol.290
, pp. 523-527
-
-
Yan, M.H.1
Wang, L.C.2
Hymowitz, S.G.3
-
27
-
-
0035379554
-
Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A
-
Schneider P, Street SL, Gaide O, et al. Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A. J Biol Chem 2001;276:18819.
-
(2001)
J Biol Chem
, vol.276
, pp. 18819
-
-
Schneider, P.1
Street, S.L.2
Gaide, O.3
-
28
-
-
0033040906
-
Modular organization of proteins containing C1q-like gobular domain
-
Kishore U, Reid KB. Modular organization of proteins containing C1q-like gobular domain. Immunopharmacology 1999;42:15-21.
-
(1999)
Immunopharmacology
, vol.42
, pp. 15-21
-
-
Kishore, U.1
Reid, K.B.2
-
29
-
-
0032510463
-
The crystal structure of a complement-1q family protein suggests an evolutionary link to tumor necrosis factor
-
Shapiro L, Scherer PE. The crystal structure of a complement-1q family protein suggests an evolutionary link to tumor necrosis factor. Curr Biol 1998;8:335-8.
-
(1998)
Curr Biol
, vol.8
, pp. 335-338
-
-
Shapiro, L.1
Scherer, P.E.2
-
30
-
-
0031980020
-
Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: Diagnostic implications
-
Ferguson BM, Thomas NS, Munoz F, Morgan D, Clarke A, Zonana J. Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications. J Med Genet 1998;35:112-5.
-
(1998)
J Med Genet
, vol.35
, pp. 112-115
-
-
Ferguson, B.M.1
Thomas, N.S.2
Munoz, F.3
Morgan, D.4
Clarke, A.5
Zonana, J.6
-
31
-
-
0032231350
-
Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations
-
Monreal AW, Zonana J, Ferguson B. Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations. Am J Hum Genet 1998;63:380-9.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 380-389
-
-
Monreal, A.W.1
Zonana, J.2
Ferguson, B.3
-
32
-
-
0031892339
-
A novel missense mutation (402C → T) in exon 1 in the Eda gene in a family with X-linked hypohidrotic ectodermal dysplasia
-
Hertz JM, Norgaard HK, Juncker I, Kjeldsen M, Gregersen N. A novel missense mutation (402C → T) in exon 1 in the Eda gene in a family with X-linked hypohidrotic ectodermal dysplasia. Clin Genet 1998;53:205-9.
-
(1998)
Clin Genet
, vol.53
, pp. 205-209
-
-
Hertz, J.M.1
Norgaard, H.K.2
Juncker, I.3
Kjeldsen, M.4
Gregersen, N.5
-
33
-
-
0033506530
-
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia caused by a novel mutation in EDA1 gene: 406T → G (Leu55Arg)
-
Martinez F, Millan JM, Orellana C, Prieto F. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia caused by a novel mutation in EDA1 gene: 406T → G (Leu55Arg). J Invest Dermatol 1999;113:285-6.
-
(1999)
J Invest Dermatol
, vol.113
, pp. 285-286
-
-
Martinez, F.1
Millan, J.M.2
Orellana, C.3
Prieto, F.4
-
34
-
-
0032457229
-
A novel point mutation of the Eda gene in a Japanese family with anhidrotic ectodermal dysplasia
-
Yotsumoto S, Fukumaru S, Matsushita S, et al. A novel point mutation of the Eda gene in a Japanese family with anhidrotic ectodermal dysplasia. J Invest Dermatol 1998;111:1246-7.
-
(1998)
J Invest Dermatol
, vol.111
, pp. 1246-1247
-
-
Yotsumoto, S.1
Fukumaru, S.2
Matsushita, S.3
-
35
-
-
0033624559
-
A novel arginine → Serine mutation in EDA1 in a Japanese family with X-linked anhidrotic ectodermal dysplasia
-
Aoki N, Ito K, Tachibana T, Ito M. A novel arginine → Serine mutation in EDA1 in a Japanese family with X-linked anhidrotic ectodermal dysplasia. J Invest Dermatol 2000;115:329-30.
-
(2000)
J Invest Dermatol
, vol.115
, pp. 329-330
-
-
Aoki, N.1
Ito, K.2
Tachibana, T.3
Ito, M.4
-
36
-
-
0035912849
-
Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia
-
Chen Y, Molloy SS, Thomas L. Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia. Proc Natl Acad Sci USA 2001;98:7218-23.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 7218-7223
-
-
Chen, Y.1
Molloy, S.S.2
Thomas, L.3
-
37
-
-
0035341488
-
Mutations in the Eda gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia
-
Kobielak K, Kobielak A, Roszkiewicz J, Wierzba J, Limon J, Trzeciak WH. Mutations in the Eda gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia. Am J Med Genet 2001;100:191-7.
-
(2001)
Am J Med Genet
, vol.100
, pp. 191-197
-
-
Kobielak, K.1
Kobielak, A.2
Roszkiewicz, J.3
Wierzba, J.4
Limon, J.5
Trzeciak, W.H.6
-
38
-
-
0035320883
-
The mutation spectrum of the Eda gene in X-linked anhidrotic ectodermal dysplasia
-
Pääkkönen K, Cambiaghi S, Novelli G, et al. The mutation spectrum of the Eda gene in X-linked anhidrotic ectodermal dysplasia. Hum Mutat 2001;17:349.
-
(2001)
Hum Mutat
, vol.17
, pp. 349
-
-
Pääkkönen, K.1
Cambiaghi, S.2
Novelli, G.3
-
39
-
-
0034981134
-
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia
-
Vincent MC, Biancalana V, Ginisty D, Mandel JL, Calvas P. Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia. Eur J Hum Genet 2001;9:355-63.
-
(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
-
40
-
-
0035871196
-
Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein
-
Elomaa O, Pulkkinen K, Hannelius U, Mikkola M, Saarialho-Kere U, Kere J. Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein. Hum Mol Genet 2001;10:953-62.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 953-962
-
-
Elomaa, O.1
Pulkkinen, K.2
Hannelius, U.3
Mikkola, M.4
Saarialho-Kere, U.5
Kere, J.6
-
41
-
-
0035862916
-
TNF signaling via the ligand-receptor pair ectodysplasin and Edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis
-
Laurikkala J, Mikkola M, Mustonen T, et al. TNF signaling via the ligand-receptor pair ectodysplasin and Edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis. Dev Biol 2001;229:443-55.
-
(2001)
Dev Biol
, vol.229
, pp. 443-455
-
-
Laurikkala, J.1
Mikkola, M.2
Mustonen, T.3
-
42
-
-
0036333966
-
Regulation of hair follicle development by the TNF signal ectodysplasin and its receptor Edar
-
Laurikkala J, Pispa J, Jung HS, et al. Regulation of hair follicle development by the TNF signal ectodysplasin and its receptor Edar. Development 2002;129:2541-53.
-
(2002)
Development
, vol.129
, pp. 2541-2553
-
-
Laurikkala, J.1
Pispa, J.2
Jung, H.S.3
-
43
-
-
0033693832
-
Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis
-
Tucker AS, Headon DJ, Schneider P, et al. Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis. Development 2000;127:4691-700.
-
(2000)
Development
, vol.127
, pp. 4691-4700
-
-
Tucker, A.S.1
Headon, D.J.2
Schneider, P.3
-
44
-
-
0035951783
-
Ectodermal dysplasia receptor activates the nuclear factor κB, c-Jun N-terminal kinase and cell death pathways and binds to ectodysplasin-A
-
Kumar A, Eby MT, Sinha S, Jasmin A, Chaudhary PM. Ectodermal dysplasia receptor activates the nuclear factor κB, c-Jun N-terminal kinase and cell death pathways and binds to ectodysplasin-A. J Biol Chem 2001;276:2668-77.
-
(2001)
J Biol Chem
, vol.276
, pp. 2668-2677
-
-
Kumar, A.1
Eby, M.T.2
Sinha, S.3
Jasmin, A.4
Chaudhary, P.M.5
-
45
-
-
0032734626
-
Characterization of TNFRSF19, a novel member of the tumor necrosis factor receptor superfamily
-
Hu S, Tamada K, Ni J, Vincenz C, Chen L. Characterization of TNFRSF19, a novel member of the tumor necrosis factor receptor superfamily. Genomics 1999;62:103-7.
-
(1999)
Genomics
, vol.62
, pp. 103-107
-
-
Hu, S.1
Tamada, K.2
Ni, J.3
Vincenz, C.4
Chen, L.5
-
46
-
-
0034686080
-
TAJ, a novel member of the tumor necrosis factor receptor family, activates the c-Jun N-terminal kinase pathway and mediates caspase-independent cell death
-
Eby MT, Jasmin A, Kumar A, Sharma K, Chaudhary PM. TAJ, a novel member of the tumor necrosis factor receptor family, activates the c-Jun N-terminal kinase pathway and mediates caspase-independent cell death. J Biol Chem 2000;275:15336-42.
-
(2000)
J Biol Chem
, vol.275
, pp. 15336-15342
-
-
Eby, M.T.1
Jasmin, A.2
Kumar, A.3
Sharma, K.4
Chaudhary, P.M.5
-
47
-
-
0034617087
-
TROY, a newly identified member of the tumor necrosis factor receptor superfamily, exhibits a homology with Edar and is expressed in embryonic skin and hair follicles
-
Kojima T, Morikawa Y, Copeland NG, et al. TROY, a newly identified member of the tumor necrosis factor receptor superfamily, exhibits a homology with Edar and is expressed in embryonic skin and hair follicles. J Biol Chem 2000;275:20742-7.
-
(2000)
J Biol Chem
, vol.275
, pp. 20742-20747
-
-
Kojima, T.1
Morikawa, Y.2
Copeland, N.G.3
-
48
-
-
0026744103
-
Tumor necrosis factor receptor signaling. A dominant negative mutation suppresses the activation of the 55 kDa tumor necrosis factor receptor
-
Tartaglia LA, Goeddel DV. Tumor necrosis factor receptor signaling. A dominant negative mutation suppresses the activation of the 55 kDa tumor necrosis factor receptor. J Biol Chem 1992;267:4304-7.
-
(1992)
J Biol Chem
, vol.267
, pp. 4304-4307
-
-
Tartaglia, L.A.1
Goeddel, D.V.2
-
49
-
-
0029025441
-
Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome
-
Fisher GH, Rosenberg FJ, Straus SE, et al. Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. Cell 1995;81:935-46.
-
(1995)
Cell
, vol.81
, pp. 935-946
-
-
Fisher, G.H.1
Rosenberg, F.J.2
Straus, S.E.3
-
50
-
-
0037160061
-
Role of Traf3 and -6 in the activation of the NF-κB and JNK pathways by X-linked ectodermal dysplasia receptor
-
Sinha SK, Zachariah S, Quiñones HI, Shindo M, Chaudhary PM. Role of Traf3 and -6 in the activation of the NF-κB and JNK pathways by X-linked ectodermal dysplasia receptor. J Biol Chem 2002;277:44953-61.
-
(2002)
J Biol Chem
, vol.277
, pp. 44953-44961
-
-
Sinha, S.K.1
Zachariah, S.2
Quiñones, H.I.3
Shindo, M.4
Chaudhary, P.M.5
-
51
-
-
0035478074
-
Signalling and subcellular localization of the TNF receptor Edar
-
Koppinen P, Pispa J, Laurikkala J, Thesleff I, Mikkola ML. Signalling and subcellular localization of the TNF receptor Edar. Exp Cell Res 2001;269:180-92.
-
(2001)
Exp Cell Res
, vol.269
, pp. 180-192
-
-
Koppinen, P.1
Pispa, J.2
Laurikkala, J.3
Thesleff, I.4
Mikkola, M.L.5
-
52
-
-
0037098958
-
Eda targets revealed by skin gene expression profiles of wild-type, Tabby and Tabby Eda-A1 transgenic mice
-
Cui CY, Durmowicz M, Tanaka TS, et al. Eda targets revealed by skin gene expression profiles of wild-type, Tabby and Tabby Eda-A1 transgenic mice. Hum Mol Genet 2002;11:1763-73.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1763-1773
-
-
Cui, C.Y.1
Durmowicz, M.2
Tanaka, T.S.3
-
53
-
-
0037173095
-
Traf6-deficient mice display hypohidrotic ectodermal dysplasia
-
Naito A, Yoshida H, Nishioka E, et al. Traf6-deficient mice display hypohidrotic ectodermal dysplasia. Proc Natl Acad Sci USA 2002;99:8766-71.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 8766-8771
-
-
Naito, A.1
Yoshida, H.2
Nishioka, E.3
-
54
-
-
0036234459
-
Missing pieces in the NF-κB puzzle
-
Ghosh S, Karin M. Missing pieces in the NF-κB puzzle. Cell 2002;109:S81-96.
-
(2002)
Cell
, vol.109
-
-
Ghosh, S.1
Karin, M.2
-
55
-
-
0033658369
-
A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKKγ (NEMO)
-
Zonana J, Elder ME, Schneider LC, et al. A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKKγ (NEMO). Am J Hum Genet 2000;67:1555-62.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1555-1562
-
-
Zonana, J.1
Elder, M.E.2
Schneider, L.C.3
-
56
-
-
0035093630
-
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling
-
Döffinger R, Smahi A, Bessia C, et al. X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling. Nat Genet 2001;27:277-85.
-
(2001)
Nat Genet
, vol.27
, pp. 277-285
-
-
Döffinger, R.1
Smahi, A.2
Bessia, C.3
-
57
-
-
0034771886
-
A recurrent deletion in the ubiquitously expressed NEMO (IKKγ) gene accounts for the vast majority of incontinentia pigmenti mutations
-
Aradhya S, Woffendin H, Jakins T, et al. A recurrent deletion in the ubiquitously expressed NEMO (IKKγ) gene accounts for the vast majority of incontinentia pigmenti mutations. Hum Mol Genet 2001;10:2171-9.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2171-2179
-
-
Aradhya, S.1
Woffendin, H.2
Jakins, T.3
-
58
-
-
0035286726
-
Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia
-
Jain A, Ma CA, Liu S, Brown M, Cohen J, Strober W. Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia. Nat Immunol 2001;2:223-8.
-
(2001)
Nat Immunol
, vol.2
, pp. 223-228
-
-
Jain, A.1
Ma, C.A.2
Liu, S.3
Brown, M.4
Cohen, J.5
Strober, W.6
-
59
-
-
0036599324
-
Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother
-
Dupuis-Girod S, Corradini N, Hadj-Rabia S, et al. Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother. Pediatrics 2002;109:e97.
-
(2002)
Pediatrics
, vol.109
-
-
Dupuis-Girod, S.1
Corradini, N.2
Hadj-Rabia, S.3
-
60
-
-
0035281865
-
Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection
-
Mansour S, Woffendin H, Mitton S, et al. Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection. Am J Med Genet 2001;99:172-7.
-
(2001)
Am J Med Genet
, vol.99
, pp. 172-177
-
-
Mansour, S.1
Woffendin, H.2
Mitton, S.3
-
61
-
-
0036771830
-
The NF-κB signalling pathway in human disease: From incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes
-
Smahi A, Courtois G, Rabia SH, et al. The NF-κB signalling pathway in human disease: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes. Hum Mol Genet 2002;11:2371-5.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2371-2375
-
-
Smahi, A.1
Courtois, G.2
Rabia, S.H.3
-
62
-
-
0034740688
-
Requirement of NF-κB/Rel for the development of hair follicles and other epidermal appendices
-
Schmidt-Ullrich R, Aebischer T, Hulsken J, Birchmeier W, Klemm U, Scheidereit C. Requirement of NF-κB/Rel for the development of hair follicles and other epidermal appendices. Development 2001;128:3843-53.
-
(2001)
Development
, vol.128
, pp. 3843-3853
-
-
Schmidt-Ullrich, R.1
Aebischer, T.2
Hulsken, J.3
Birchmeier, W.4
Klemm, U.5
Scheidereit, C.6
-
63
-
-
0033393957
-
TRANCE, a TNF family member, activates Akt/PKB through a signaling complex involving Traf6 and c-Src
-
Wong BR, Besser D, Kim N, et al. TRANCE, a TNF family member, activates Akt/PKB through a signaling complex involving Traf6 and c-Src. Mol Cell 1999;4:1041-9.
-
(1999)
Mol Cell
, vol.4
, pp. 1041-1049
-
-
Wong, B.R.1
Besser, D.2
Kim, N.3
-
64
-
-
0033561039
-
Traf6 deficiency results in osteopetrosis and defective interleukin-1, CD40, and LPS signaling
-
Lomaga MA, Yeh WC, Sarosi I, et al. Traf6 deficiency results in osteopetrosis and defective interleukin-1, CD40, and LPS signaling. Genes Dev 1999;13:1015-24.
-
(1999)
Genes Dev
, vol.13
, pp. 1015-1024
-
-
Lomaga, M.A.1
Yeh, W.C.2
Sarosi, I.3
-
65
-
-
6544270833
-
Severe osteopetrosis, defective interleukin-1 signalling and lymph node organogenesis in Traf6-deficient mice
-
Naito A, Azuma S, Tanaka S, et al. Severe osteopetrosis, defective interleukin-1 signalling and lymph node organogenesis in Traf6-deficient mice. Genes Cells 1999;4:353-62.
-
(1999)
Genes Cells
, vol.4
, pp. 353-362
-
-
Naito, A.1
Azuma, S.2
Tanaka, S.3
-
66
-
-
0030050748
-
Apoptosis in the developing tooth: Association with an embryonic signaling center and suppression by EGF and FGF-4
-
Vaahtokari A, Åberg T, Thesleff I. Apoptosis in the developing tooth: association with an embryonic signaling center and suppression by EGF and FGF-4. Development 1996;122:121-9.
-
(1996)
Development
, vol.122
, pp. 121-129
-
-
Vaahtokari, A.1
Åberg, T.2
Thesleff, I.3
-
67
-
-
0031883625
-
The life history of an embryonic signaling center: BMP-4 induces p21 and is associated with apoptosis in the mouse tooth enamel knot
-
Jernvall J, Åberg T, Kettunen P, Keränen S, Thesleff I. The life history of an embryonic signaling center: BMP-4 induces p21 and is associated with apoptosis in the mouse tooth enamel knot. Development 1998;125:161-9.
-
(1998)
Development
, vol.125
, pp. 161-169
-
-
Jernvall, J.1
Åberg, T.2
Kettunen, P.3
Keränen, S.4
Thesleff, I.5
-
68
-
-
0033161898
-
Noggin is a mesenchymally derived stimulator of hair-follicle induction
-
Botchkarev VA, Botchkareva NV, Roth W, et al. Noggin is a mesenchymally derived stimulator of hair-follicle induction. Nat Cell Biol 1999;1:158-64.
-
(1999)
Nat Cell Biol
, vol.1
, pp. 158-164
-
-
Botchkarev, V.A.1
Botchkareva, N.V.2
Roth, W.3
-
69
-
-
0034985116
-
Patterns of proliferation and apoptosis during murine hair follicle morphogenesis
-
Magerl M, Tobin DJ, Muller-Rover S, et al. Patterns of proliferation and apoptosis during murine hair follicle morphogenesis. J Invest Dermatol 2001;116:947-55.
-
(2001)
J Invest Dermatol
, vol.116
, pp. 947-955
-
-
Magerl, M.1
Tobin, D.J.2
Muller-Rover, S.3
-
70
-
-
0036264391
-
The role of growth factors in tooth development
-
Thesleff I, Mikkola M. The role of growth factors in tooth development. Int Rev Cytol 2002;217:93-135.
-
(2002)
Int Rev Cytol
, vol.217
, pp. 93-135
-
-
Thesleff, I.1
Mikkola, M.2
-
71
-
-
0036178229
-
Molecular mechanisms regulating hair follicle development
-
Millar SE. Molecular mechanisms regulating hair follicle development. J Invest Dermatol 2002;118:216-25.
-
(2002)
J Invest Dermatol
, vol.118
, pp. 216-225
-
-
Millar, S.E.1
-
73
-
-
0035134022
-
Controls of hair follicle cycling
-
Stenn KS, Paus R. Controls of hair follicle cycling. Physiol Rev 2001;81:449-94.
-
(2001)
Physiol Rev
, vol.81
, pp. 449-494
-
-
Stenn, K.S.1
Paus, R.2
-
74
-
-
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
-
75
-
-
14444283147
-
The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and bone
-
Montonen O, Ezer S, Saarialho-Kere UK, et al. The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and bone. J Histochem Cytochem 1998;46:281-9.
-
(1998)
J Histochem Cytochem
, vol.46
, pp. 281-289
-
-
Montonen, O.1
Ezer, S.2
Saarialho-Kere, U.K.3
-
76
-
-
0031709530
-
Expression of the anhidrotic ectodermal dysplasia gene is reduced in skin cancer coinciding with reduced E-cadherin
-
Montonen O, Ezer S, Laurikkala J, et al. Expression of the anhidrotic ectodermal dysplasia gene is reduced in skin cancer coinciding with reduced E-cadherin. Exp Dermatol 1998;7:168-74.
-
(1998)
Exp Dermatol
, vol.7
, pp. 168-174
-
-
Montonen, O.1
Ezer, S.2
Laurikkala, J.3
-
77
-
-
0018117182
-
Epidermis is the site of action of Tabby (Ta) in the mouse
-
Mayer TC, Green MC. Epidermis is the site of action of Tabby (Ta) in the mouse. Genetics 1978;90:125-31.
-
(1978)
Genetics
, vol.90
, pp. 125-131
-
-
Mayer, T.C.1
Green, M.C.2
-
78
-
-
0021739715
-
The angora locus (go) in the mouse: Hair morphology, duration of growth cycle and site of action
-
Pennycuik PR, Raphael KA. The angora locus (go) in the mouse: hair morphology, duration of growth cycle and site of action. Genet Res 1984;44:283-91.
-
(1984)
Genet Res
, vol.44
, pp. 283-291
-
-
Pennycuik, P.R.1
Raphael, K.A.2
-
79
-
-
0037138353
-
The Eda gene is a target of, but does not regulate Wnt signaling
-
Durmowicz MC, Cui CY, Schlessinger D. The Eda gene is a target of, but does not regulate Wnt signaling. Gene 2002;285:203-11.
-
(2002)
Gene
, vol.285
, pp. 203-211
-
-
Durmowicz, M.C.1
Cui, C.Y.2
Schlessinger, D.3
-
80
-
-
0027945654
-
Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in Lef1-deficient mice
-
van Genderen C, Okamura RM, Farinas I, et al. Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in Lef1-deficient mice. Genes Dev 1994;8:2691-26703.
-
(1994)
Genes Dev
, vol.8
, pp. 2691-26703
-
-
Van Genderen, C.1
Okamura, R.M.2
Farinas, I.3
-
81
-
-
0032567078
-
De novo hair follicle morphogenesis and hair tumors in mice expressing a truncated β-catenin in skin
-
Gat U, DasGupta R, Degenstein L, Fuchs E. De novo hair follicle morphogenesis and hair tumors in mice expressing a truncated β-catenin in skin. Cell 1998;95:605-14.
-
(1998)
Cell
, vol.95
, pp. 605-614
-
-
Gat, U.1
DasGupta, R.2
Degenstein, L.3
Fuchs, E.4
-
82
-
-
0032871665
-
β-catenin signaling can initiate feather bud development
-
Noramly S, Freeman A, Morgan BA. β-Catenin signaling can initiate feather bud development. Development 1999;126:3509-21.
-
(1999)
Development
, vol.126
, pp. 3509-3521
-
-
Noramly, S.1
Freeman, A.2
Morgan, B.A.3
-
83
-
-
0035395874
-
Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
-
Merrill BJ, Gat U, DasGupta R, Fuchs E. Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin. Genes Dev 2001;15:1688-16705.
-
(2001)
Genes Dev
, vol.15
, pp. 1688-16705
-
-
Merrill, B.J.1
Gat, U.2
DasGupta, R.3
Fuchs, E.4
-
84
-
-
0036023356
-
Expression of ΔNLef1 in mouse epidermis results in differentiation of hair follicles into squamous epidermal cysts and formation of skin tumours
-
Niemann C, Owens DM, Hulsken J, Birchmeier W, Watt FM. Expression of ΔNLef1 in mouse epidermis results in differentiation of hair follicles into squamous epidermal cysts and formation of skin tumours. Development 2002;129:95-109.
-
(2002)
Development
, vol.129
, pp. 95-109
-
-
Niemann, C.1
Owens, D.M.2
Hulsken, J.3
Birchmeier, W.4
Watt, F.M.5
-
85
-
-
0035141830
-
Dorsal dermis development depends on a signal from the dorsal neural tube, which can be substituted by Wnt-1
-
Olivera-Martinez I, Thelu J, Teillet MA, Dhouailly D. Dorsal dermis development depends on a signal from the dorsal neural tube, which can be substituted by Wnt-1. Mech Dev 2001;100:233-44.
-
(2001)
Mech Dev
, vol.100
, pp. 233-244
-
-
Olivera-Martinez, I.1
Thelu, J.2
Teillet, M.A.3
Dhouailly, D.4
-
86
-
-
0028929863
-
Functional analysis of activins during mammalian development
-
Matzuk MM, Kumar TR, Vassalli A, et al. Functional analysis of activins during mammalian development. Nature 1995;374:354-6.
-
(1995)
Nature
, vol.374
, pp. 354-356
-
-
Matzuk, M.M.1
Kumar, T.R.2
Vassalli, A.3
-
87
-
-
0032567083
-
Splitting hairs: Dissecting roles of signaling systems in epidermal development
-
Oro AE, Scott MP. Splitting hairs: dissecting roles of signaling systems in epidermal development. Cell 1998;95:575-8.
-
(1998)
Cell
, vol.95
, pp. 575-578
-
-
Oro, A.E.1
Scott, M.P.2
-
88
-
-
0035907041
-
β-catenin controls hair follicle morphogenesis and stem cell differentiation in the skin
-
Huelsken J, Vogel R, Erdmann B, Cotsarelis G, Birchmeier W. β-Catenin controls hair follicle morphogenesis and stem cell differentiation in the skin. Cell 2001;105:533-45.
-
(2001)
Cell
, vol.105
, pp. 533-545
-
-
Huelsken, J.1
Vogel, R.2
Erdmann, B.3
Cotsarelis, G.4
Birchmeier, W.5
-
89
-
-
18544379341
-
Mucosal addressin cell adhesion molecule 1 plays an unexpected role in the development of mouse guard hair
-
Nishioka E, Tanaka T, Yoshida H, et al. Mucosal addressin cell adhesion molecule 1 plays an unexpected role in the development of mouse guard hair. J Invest Dermatol 2002;119:632-8.
-
(2002)
J Invest Dermatol
, vol.119
, pp. 632-638
-
-
Nishioka, E.1
Tanaka, T.2
Yoshida, H.3
-
90
-
-
0028963360
-
Induction of the gene encoding mucosal vascular addressin cell adhesion molecule 1 by tumor necrosis factor α is mediated by NF-κB proteins
-
Takeuchi M, Baichwal VR. Induction of the gene encoding mucosal vascular addressin cell adhesion molecule 1 by tumor necrosis factor α is mediated by NF-κB proteins. Proc Natl Acad Sci USA 1995;92:3561-5.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3561-3565
-
-
Takeuchi, M.1
Baichwal, V.R.2
-
91
-
-
0032534231
-
Lymphotoxin α3 induces chemokines and adhesion molecules: Insight into the role of LTα in inflammation and lymphoid organ development
-
Cuff CA, Schwartz J, Bergman CM, Russell KS, Bender JR, Ruddle NH. Lymphotoxin α3 induces chemokines and adhesion molecules: insight into the role of LTα in inflammation and lymphoid organ development. J Immunol 1998;161:6853-60.
-
(1998)
J Immunol
, vol.161
, pp. 6853-6860
-
-
Cuff, C.A.1
Schwartz, J.2
Bergman, C.M.3
Russell, K.S.4
Bender, J.R.5
Ruddle, N.H.6
-
92
-
-
0031767259
-
BMPs mediate lateral inhibition at successive stages in feather tract development
-
Noramly S, Morgan BA. BMPs mediate lateral inhibition at successive stages in feather tract development. Development 1998;125:3775-87.
-
(1998)
Development
, vol.125
, pp. 3775-3787
-
-
Noramly, S.1
Morgan, B.A.2
-
93
-
-
0038467389
-
Stimulation of ectodermal organ development by ectodysplasin-A1
-
in press
-
Mustonen T, Pispa J, Mikkola ML, et al. Stimulation of ectodermal organ development by ectodysplasin-A1. Dev Biol 2003 (in press).
-
(2003)
Dev Biol
-
-
Mustonen, T.1
Pispa, J.2
Mikkola, M.L.3
-
94
-
-
0035489712
-
Signaling pathways in mammary gland development
-
Hennighausen L, Robinson GW. Signaling pathways in mammary gland development. Dev Cell 2001;1:467-75.
-
(2001)
Dev Cell
, vol.1
, pp. 467-475
-
-
Hennighausen, L.1
Robinson, G.W.2
-
95
-
-
0036113510
-
Wnt signals are required for the initiation of hair follicle development
-
Andl T, Reddy ST, Gaddapara T, Millar SE. Wnt signals are required for the initiation of hair follicle development. Dev Cell 2002;2:643-53.
-
(2002)
Dev Cell
, vol.2
, pp. 643-653
-
-
Andl, T.1
Reddy, S.T.2
Gaddapara, T.3
Millar, S.E.4
-
96
-
-
0035894745
-
Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in Tabby mice
-
Srivastava AK, Durmowicz MC, Hartung AJ, et al. Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in Tabby mice. Hum Mol Genet 2001;10:2973-81.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2973-2981
-
-
Srivastava, A.K.1
Durmowicz, M.C.2
Hartung, A.J.3
-
97
-
-
0037573629
-
Permanent correction of an inherited ectodermal dysplasia with recombinant EDA
-
in press
-
Gaide O, Schneider P. Permanent correction of an inherited ectodermal dysplasia with recombinant EDA. Nat Med 2003 (in press).
-
(2003)
Nat Med
-
-
Gaide, O.1
Schneider, P.2
-
98
-
-
0035822640
-
The medaka rs-3 locus required for scale development encodes ectodysplasin-A receptor
-
Kondo S, Kuwahara Y, Kondo M, et al. The medaka rs-3 locus required for scale development encodes ectodysplasin-A receptor. Curr Biol 2001;11:1202-6.
-
(2001)
Curr Biol
, vol.11
, pp. 1202-1206
-
-
Kondo, S.1
Kuwahara, Y.2
Kondo, M.3
|