-
1
-
-
0000003824
-
De l'acrocephalosyndactylie
-
Apert E (1906) De l'acrocephalosyndactylie. Bull Mem Soc Med Hop Paris 23:1310
-
(1906)
Bull Mem Soc Med Hop Paris
, vol.23
, pp. 1310
-
-
Apert, E.1
-
2
-
-
0027176543
-
An updated pediatric perspective on the Apert syndrome
-
8362820
-
Cohen MM Jr, Kreiborg S (1993) An updated pediatric perspective on the Apert syndrome. Am J Dis Child 147:989-993
-
(1993)
Am J Dis Child
, vol.147
, pp. 989-993
-
-
Cohen, Jr.M.M.1
Kreiborg, S.2
-
3
-
-
0026568156
-
Birth prevalence study of the Apert syndrome
-
1303629 10.1002/ajmg.1320420505
-
Cohen MM Jr, Kreiborg S, Lammer EJ, Cordero JF, Mastroiacovo P, Erickson JD, Roeper P, Martinez-Frias ML (1992) Birth prevalence study of the Apert syndrome. Am J Med Genet 42:655-659
-
(1992)
Am J Med Genet
, vol.42
, pp. 655-659
-
-
Cohen, Jr.M.M.1
Kreiborg, S.2
Lammer, E.J.3
Cordero, J.F.4
Mastroiacovo, P.5
Erickson, J.D.6
Roeper, P.7
Martinez-Frias, M.L.8
-
4
-
-
0032966331
-
Clinical variability in patients with Apert's syndrome
-
10067911 10.3171/jns.1999.90.3.0443 1:STN:280:DyaK1M7msFagtg%3D%3D
-
Lajeunie E, Cameron R, El Ghouzzi V, de Parseval N, Journeau P, Gonzales M, Delezoide AL, Bonaventure J, Le Merrer M, Renier D (1999) Clinical variability in patients with Apert's syndrome. J Neurosurg 90:443-447
-
(1999)
J Neurosurg
, vol.90
, pp. 443-447
-
-
Lajeunie, E.1
Cameron, R.2
El Ghouzzi, V.3
De Parseval, N.4
Journeau, P.5
Gonzales, M.6
Delezoide, A.L.7
Bonaventure, J.8
Le Merrer, M.9
Renier, D.10
-
5
-
-
0029059280
-
Analysis of phenotypic features and FGFR2 mutations in Apert syndrome
-
7668257 1:CAS:528:DyaK2MXotFOjtrs%3D
-
Park WJ, Theda C, Maestri NE, Meyers GA, Fryburg JS, Dufresne C, Cohen MM Jr, Jabs EW (1995) Analysis of phenotypic features and FGFR2 mutations in Apert syndrome. Am J Hum Genet 57:321-328
-
(1995)
Am J Hum Genet
, vol.57
, pp. 321-328
-
-
Park, W.J.1
Theda, C.2
Maestri, N.E.3
Meyers, G.A.4
Fryburg, J.S.5
Dufresne, C.6
Cohen, Jr.M.M.7
Jabs, E.W.8
-
6
-
-
0028798546
-
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
-
7719344 10.1038/ng0295-165 1:CAS:528:DyaK2MXjsFOmsb4%3D
-
Wilkie AO, Slaney SF, Oldridge M, Poole MD, Ashworth GJ, Hockley AD, Hayward RD, David DJ, Pulleyn LJ, Rutland P et al (1995) Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nat Genet 9:165-172
-
(1995)
Nat Genet
, vol.9
, pp. 165-172
-
-
Wilkie, A.O.1
Slaney, S.F.2
Oldridge, M.3
Poole, M.D.4
Ashworth, G.J.5
Hockley, A.D.6
Hayward, R.D.7
David, D.J.8
Pulleyn, L.J.9
Rutland, P.10
-
7
-
-
0035957378
-
Uncoupling fibroblast growth factor receptor 2 ligand binding specificity leads to Apert syndrome-like phenotypes
-
11274381 10.1073/pnas.081082498 1:CAS:528:DC%2BD3MXis1Kitbo%3D
-
Yu K, Ornitz DM (2001) Uncoupling fibroblast growth factor receptor 2 ligand binding specificity leads to Apert syndrome-like phenotypes. Proc Natl Acad Sci USA 98:3641-3643
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 3641-3643
-
-
Yu, K.1
Ornitz, D.M.2
-
8
-
-
17844393110
-
Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogonia
-
15840724 10.1073/pnas.0500267102 1:CAS:528:DC%2BD2MXkt1Cmu7c%3D
-
Goriely A, McVean GA, van Pelt AM, O'Rourke AW, Wall SA, de Rooij DG, Wilkie AO (2005) Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogonia. Proc Natl Acad Sci USA 102:6051-6056
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 6051-6056
-
-
Goriely, A.1
McVean, G.A.2
Van Pelt, A.M.3
O'Rourke, A.W.4
Wall, S.A.5
De Rooij, D.G.6
Wilkie, A.O.7
-
9
-
-
8044233698
-
Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2
-
9002682 10.1093/hmg/6.1.137 1:CAS:528:DyaK2sXlslCksA%3D%3D
-
Oldridge M, Lunt PW, Zackai EH, McDonald-McGinn DM, Muenke M, Moloney DM, Twigg SR, Heath JK, Howard TD, Hoganson G, Gagnon DM, Jabs EW, Wilkie AO (1997) Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2. Hum Mol Genet 6:137-143
-
(1997)
Hum Mol Genet
, vol.6
, pp. 137-143
-
-
Oldridge, M.1
Lunt, P.W.2
Zackai, E.H.3
McDonald-Mcginn, D.M.4
Muenke, M.5
Moloney, D.M.6
Twigg, S.R.7
Heath, J.K.8
Howard, T.D.9
Hoganson, G.10
Gagnon, D.M.11
Jabs, E.W.12
Wilkie, A.O.13
-
10
-
-
0033073850
-
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome
-
9973282 10.1086/302245 1:CAS:528:DyaK1MXhslOltLw%3D
-
Oldridge M, Zackai EH, McDonald-McGinn DM, Iseki S, Morriss-Kay GM, Twigg SR, Johnson D, Wall SA, Jiang W, Theda C, Jabs EW, Wilkie AO (1999) De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome. Am J Hum Genet 64:446-461
-
(1999)
Am J Hum Genet
, vol.64
, pp. 446-461
-
-
Oldridge, M.1
Zackai, E.H.2
McDonald-Mcginn, D.M.3
Iseki, S.4
Morriss-Kay, G.M.5
Twigg, S.R.6
Johnson, D.7
Wall, S.A.8
Jiang, W.9
Theda, C.10
Jabs, E.W.11
Wilkie, A.O.12
-
11
-
-
80053176299
-
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
-
21943124 10.1186/1471-2350-12-122 1:CAS:528:DC%2BC3MXhtlWjsb7K
-
Fenwick AL, Bowdin SC, Klatt RE, Wilkie AO (2011) A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome. BMC Med Genet 12:122
-
(2011)
BMC Med Genet
, vol.12
, pp. 122
-
-
Fenwick, A.L.1
Bowdin, S.C.2
Klatt, R.E.3
Wilkie, A.O.4
-
12
-
-
0029983638
-
Exclusive paternal origin of new mutations in Apert syndrome
-
8673103 10.1038/ng0596-48 1:CAS:528:DyaK28XksVWgtbg%3D
-
Moloney DM, Slaney SF, Oldridge M, Wall SA, Sahlin P, Stenman G, Wilkie AO (1996) Exclusive paternal origin of new mutations in Apert syndrome. Nat Genet 13:48-53
-
(1996)
Nat Genet
, vol.13
, pp. 48-53
-
-
Moloney, D.M.1
Slaney, S.F.2
Oldridge, M.3
Wall, S.A.4
Sahlin, P.5
Stenman, G.6
Wilkie, A.O.7
-
13
-
-
59749092295
-
Rare mutations of FGFR2 causing Apert syndrome: Identification of the first partial gene deletion, and an Alu element insertion from a new subfamily
-
18726952 10.1002/humu.20825 1:CAS:528:DC%2BD1MXjtFKmsbg%3D
-
Bochukova EG, Roscioli T, Hedges DJ, Taylor IB, Johnson D, David DJ, Deininger PL, Wilkie AO (2009) Rare mutations of FGFR2 causing Apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily. Hum Mutat 30:204-211
-
(2009)
Hum Mutat
, vol.30
, pp. 204-211
-
-
Bochukova, E.G.1
Roscioli, T.2
Hedges, D.J.3
Taylor, I.B.4
Johnson, D.5
David, D.J.6
Deininger, P.L.7
Wilkie, A.O.8
-
14
-
-
84862180948
-
FGFs: Neurodevelopment's Jack-of-all-tradeshow do they do it?
-
22164131 10.3389/fnins.2011.00133
-
Hebert JM (2011) FGFs: neurodevelopment's Jack-of-all-tradeshow do they do it? Front Neurosci 5:133
-
(2011)
Front Neurosci
, vol.5
, pp. 133
-
-
Hebert, J.M.1
-
15
-
-
67651121761
-
FGFR2 abnormalities underlie a spectrum of bone, skin, and cancer pathologies
-
19387476 10.1038/jid.2009.97 1:CAS:528:DC%2BD1MXosFSlurs%3D
-
Katoh M (2009) FGFR2 abnormalities underlie a spectrum of bone, skin, and cancer pathologies. J Invest Dermatol 129:1861-1867
-
(2009)
J Invest Dermatol
, vol.129
, pp. 1861-1867
-
-
Katoh, M.1
-
16
-
-
78249281919
-
Role of FGFR2-signaling in the pathogenesis of acne
-
20436882 10.4161/derm.1.3.8474 1:CAS:528:DC%2BD1MXhsVeit7zJ
-
Melnik BC (2009) Role of FGFR2-signaling in the pathogenesis of acne. Dermatoendocrinol 1:141-156
-
(2009)
Dermatoendocrinol
, vol.1
, pp. 141-156
-
-
Melnik, B.C.1
-
17
-
-
74049139927
-
Preparing for the first breath: Genetic and cellular mechanisms in lung development
-
20152174 10.1016/j.devcel.2009.12.010 1:CAS:528:DC%2BC3cXkvVWhs78%3D
-
Morrisey EE, Hogan BL (2010) Preparing for the first breath: genetic and cellular mechanisms in lung development. Dev Cell 18:8-23
-
(2010)
Dev Cell
, vol.18
, pp. 8-23
-
-
Morrisey, E.E.1
Hogan, B.L.2
-
18
-
-
0037097976
-
FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease
-
12080084 10.1101/gad.990702 1:CAS:528:DC%2BD38XltVGmtL8%3D
-
Ornitz DM, Marie PJ (2002) FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease. Genes Dev 16:1446-1465
-
(2002)
Genes Dev
, vol.16
, pp. 1446-1465
-
-
Ornitz, D.M.1
Marie, P.J.2
-
19
-
-
0042413846
-
Expression of FGF receptors 1, 2, 3 in the embryonic and postnatal mouse brain compared with Pdgfralpha, Olig2 and Plp/dm20: Implications for oligodendrocyte development
-
12966207 10.1159/000072258 1:CAS:528:DC%2BD3sXntFSlt7Y%3D
-
Bansal R, Lakhina V, Remedios R, Tole S (2003) Expression of FGF receptors 1, 2, 3 in the embryonic and postnatal mouse brain compared with Pdgfralpha, Olig2 and Plp/dm20: implications for oligodendrocyte development. Dev Neurosci 25:83-95
-
(2003)
Dev Neurosci
, vol.25
, pp. 83-95
-
-
Bansal, R.1
Lakhina, V.2
Remedios, R.3
Tole, S.4
-
20
-
-
0033373550
-
Fgfr1 and Fgfr2 have distinct differentiation- and proliferation-related roles in the developing mouse skull vault
-
10572038 1:CAS:528:DC%2BD3cXlt1SmsA%3D%3D
-
Iseki S, Wilkie AO, Morriss-Kay GM (1999) Fgfr1 and Fgfr2 have distinct differentiation- and proliferation-related roles in the developing mouse skull vault. Development 126:5611-5620
-
(1999)
Development
, vol.126
, pp. 5611-5620
-
-
Iseki, S.1
Wilkie, A.O.2
Morriss-Kay, G.M.3
-
21
-
-
0027199056
-
Developmental localization of the splicing alternatives of fibroblast growth factor receptor-2 (FGFR2)
-
8393815 10.1006/dbio.1993.1205 1:CAS:528:DyaK3sXltlWqsbY%3D
-
Orr-Urtreger A, Bedford MT, Burakova T, Arman E, Zimmer Y, Yayon A, Givol D, Lonai P (1993) Developmental localization of the splicing alternatives of fibroblast growth factor receptor-2 (FGFR2). Dev Biol 158:475-486
-
(1993)
Dev Biol
, vol.158
, pp. 475-486
-
-
Orr-Urtreger, A.1
Bedford, M.T.2
Burakova, T.3
Arman, E.4
Zimmer, Y.5
Yayon, A.6
Givol, D.7
Lonai, P.8
-
22
-
-
33744937606
-
Receptor specificity of the fibroblast growth factor family. the complete mammalian FGF family
-
16597617 10.1074/jbc.M601252200 1:CAS:528:DC%2BD28Xlt1Cktrc%3D
-
Zhang X, Ibrahimi OA, Olsen SK, Umemori H, Mohammadi M, Ornitz DM (2006) Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family. J Biol Chem 281:15694-15700
-
(2006)
J Biol Chem
, vol.281
, pp. 15694-15700
-
-
Zhang, X.1
Ibrahimi, O.A.2
Olsen, S.K.3
Umemori, H.4
Mohammadi, M.5
Ornitz, D.M.6
-
23
-
-
0029883637
-
Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome
-
8651276 1:STN:280:DyaK283hs1WnsQ%3D%3D
-
Slaney SF, Oldridge M, Hurst JA, Moriss-Kay GM, Hall CM, Poole MD, Wilkie AO (1996) Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome. Am J Hum Genet 58:923-932
-
(1996)
Am J Hum Genet
, vol.58
, pp. 923-932
-
-
Slaney, S.F.1
Oldridge, M.2
Hurst, J.A.3
Moriss-Kay, G.M.4
Hall, C.M.5
Poole, M.D.6
Wilkie, A.O.7
-
24
-
-
0033998110
-
Genotype-phenotype analysis in Apert syndrome suggests opposite effects of the two recurrent mutations on syndactyly and outcome of craniofacial surgery
-
10.1034/j.1399-0004.2000.570208.x
-
von Gernet S, Golla A, Ehrenfels Y, Schuffenhauer S, Fairley JD (2000) Genotype-phenotype analysis in Apert syndrome suggests opposite effects of the two recurrent mutations on syndactyly and outcome of craniofacial surgery. Clin Genet 57:137-139
-
(2000)
Clin Genet
, vol.57
, pp. 137-139
-
-
Von Gernet, S.1
Golla, A.2
Ehrenfels, Y.3
Schuffenhauer, S.4
Fairley, J.D.5
-
25
-
-
0035912715
-
Structural basis for fibroblast growth factor receptor 2 activation in Apert syndrome
-
11390973 10.1073/pnas.121183798 1:CAS:528:DC%2BD3MXkslWmt7o%3D
-
Ibrahimi OA, Eliseenkova AV, Plotnikov AN, Yu K, Ornitz DM, Mohammadi M (2001) Structural basis for fibroblast growth factor receptor 2 activation in Apert syndrome. Proc Natl Acad Sci U S A 98:7182-7187
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 7182-7187
-
-
Ibrahimi, O.A.1
Eliseenkova, A.V.2
Plotnikov, A.N.3
Yu, K.4
Ornitz, D.M.5
Mohammadi, M.6
-
26
-
-
5444250989
-
Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities
-
15282208 10.1093/hmg/ddh235 1:CAS:528:DC%2BD2cXns1Onu78%3D
-
Ibrahimi OA, Zhang F, Eliseenkova AV, Itoh N, Linhardt RJ, Mohammadi M (2004) Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities. Hum Mol Genet 13:2313-2324
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2313-2324
-
-
Ibrahimi, O.A.1
Zhang, F.2
Eliseenkova, A.V.3
Itoh, N.4
Linhardt, R.J.5
Mohammadi, M.6
-
27
-
-
0035957343
-
A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes
-
11274405 10.1073/pnas.071586898 1:CAS:528:DC%2BD3MXis1Khs7w%3D
-
Hajihosseini MK, Wilson S, De Moerlooze L, Dickson C (2001) A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes. Proc Natl Acad Sci USA 98:3855-3860
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 3855-3860
-
-
Hajihosseini, M.K.1
Wilson, S.2
De Moerlooze, L.3
Dickson, C.4
-
28
-
-
0141678494
-
A Ser252Trp [corrected] substitution in mouse fibroblast growth factor receptor 2 (Fgfr2) results in craniosynostosis
-
14499350 10.1016/S8756-3282(03)00222-9 1:CAS:528:DC%2BD3sXnt1Glsbg%3D
-
Chen L, Li D, Li C, Engel A, Deng CX (2003) A Ser252Trp [corrected] substitution in mouse fibroblast growth factor receptor 2 (Fgfr2) results in craniosynostosis. Bone 33:169-178
-
(2003)
Bone
, vol.33
, pp. 169-178
-
-
Chen, L.1
Li, D.2
Li, C.3
Engel, A.4
Deng, C.X.5
-
29
-
-
24344453489
-
Abnormalities in cartilage and bone development in the Apert syndrome FGFR2(+/S252W) mouse
-
15975938 10.1242/dev.01914 1:CAS:528:DC%2BD2MXpvFOis7s%3D
-
Wang Y, Xiao R, Yang F, Karim BO, Iacovelli AJ, Cai J, Lerner CP, Richtsmeier JT, Leszl JM, Hill CA, Yu K, Ornitz DM, Elisseeff J, Huso DL, Jabs EW (2005) Abnormalities in cartilage and bone development in the Apert syndrome FGFR2(+/S252W) mouse. Development 132:3537-3548
-
(2005)
Development
, vol.132
, pp. 3537-3548
-
-
Wang, Y.1
Xiao, R.2
Yang, F.3
Karim, B.O.4
Iacovelli, A.J.5
Cai, J.6
Lerner, C.P.7
Richtsmeier, J.T.8
Leszl, J.M.9
Hill, C.A.10
Yu, K.11
Ornitz, D.M.12
Elisseeff, J.13
Huso, D.L.14
Jabs, E.W.15
-
30
-
-
77649302376
-
Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice
-
20175913 10.1186/1471-213X-10-22
-
Wang Y, Sun M, Uhlhorn VL, Zhou X, Peter I, Martinez-Abadias N, Hill CA, Percival CJ, Richtsmeier JT, Huso DL, Jabs EW (2010) Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice. BMC Dev Biol 10:22
-
(2010)
BMC Dev Biol
, vol.10
, pp. 22
-
-
Wang, Y.1
Sun, M.2
Uhlhorn, V.L.3
Zhou, X.4
Peter, I.5
Martinez-Abadias, N.6
Hill, C.A.7
Percival, C.J.8
Richtsmeier, J.T.9
Huso, D.L.10
Jabs, E.W.11
-
31
-
-
40949140612
-
A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
-
18242159 10.1016/j.bone.2007.11.019 1:CAS:528:DC%2BD1cXjs1Whuro%3D
-
Yin L, Du X, Li C, Xu X, Chen Z, Su N, Zhao L, Qi H, Li F, Xue J (2008) A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis. Bone 42:631-643
-
(2008)
Bone
, vol.42
, pp. 631-643
-
-
Yin, L.1
Du, X.2
Li, C.3
Xu, X.4
Chen, Z.5
Su, N.6
Zhao, L.7
Qi, H.8
Li, F.9
Xue, J.10
-
32
-
-
0019508988
-
Suture pathology in craniosynostosis
-
7463140 10.3171/jns.1981.54.3.0384 1:STN:280:DyaL3M7hvFWqsQ%3D%3D
-
Albright AL, Byrd RP (1981) Suture pathology in craniosynostosis. J Neurosurg 54:384-387
-
(1981)
J Neurosurg
, vol.54
, pp. 384-387
-
-
Albright, A.L.1
Byrd, R.P.2
-
33
-
-
0030011334
-
The role of bone centers in the pathogenesis of craniosynostosis: An embryologic approach using CT measurements in isolated craniosynostosis and Apert and Crouzon syndromes
-
8657773 10.1097/00006534-199607000-00004 1:STN:280:DyaK283mt1SktA%3D%3D
-
Mathijssen IM, Vaandrager JM, van der Meulen JC, Pieterman H, Zonneveld FW, Kreiborg S, Vermeij-Keers C (1996) The role of bone centers in the pathogenesis of craniosynostosis: an embryologic approach using CT measurements in isolated craniosynostosis and Apert and Crouzon syndromes. Plast Reconstr Surg 98:17-26
-
(1996)
Plast Reconstr Surg
, vol.98
, pp. 17-26
-
-
Mathijssen, I.M.1
Vaandrager, J.M.2
Van Der Meulen, J.C.3
Pieterman, H.4
Zonneveld, F.W.5
Kreiborg, S.6
Vermeij-Keers, C.7
-
34
-
-
63349106487
-
Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology
-
19389359 10.1016/j.ydbio.2009.01.026 1:CAS:528:DC%2BD1MXktFahtr8%3D
-
Holmes G, Rothschild G, Roy UB, Deng CX, Mansukhani A, Basilico C (2009) Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology. Dev Biol 328:273-284
-
(2009)
Dev Biol
, vol.328
, pp. 273-284
-
-
Holmes, G.1
Rothschild, G.2
Roy, U.B.3
Deng, C.X.4
Mansukhani, A.5
Basilico, C.6
-
35
-
-
0036149534
-
Tissue origins and interactions in the mammalian skull vault
-
11784098 10.1006/dbio.2001.0487 1:CAS:528:DC%2BD3MXptVWiuro%3D
-
Jiang X, Iseki S, Maxson RE, Sucov HM, Morriss-Kay GM (2002) Tissue origins and interactions in the mammalian skull vault. Dev Biol 241:106-116
-
(2002)
Dev Biol
, vol.241
, pp. 106-116
-
-
Jiang, X.1
Iseki, S.2
Maxson, R.E.3
Sucov, H.M.4
Morriss-Kay, G.M.5
-
36
-
-
50849122961
-
Cell lineage in mammalian craniofacial mesenchyme
-
18617001 10.1016/j.mod.2008.06.007 1:CAS:528:DC%2BD1cXhtVyltr7E
-
Yoshida T, Vivatbutsiri P, Morriss-Kay G, Saga Y, Iseki S (2008) Cell lineage in mammalian craniofacial mesenchyme. Mech Dev 125:797-808
-
(2008)
Mech Dev
, vol.125
, pp. 797-808
-
-
Yoshida, T.1
Vivatbutsiri, P.2
Morriss-Kay, G.3
Saga, Y.4
Iseki, S.5
-
37
-
-
33645810601
-
Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis
-
16540516 10.1093/hmg/ddl052 1:CAS:528:DC%2BD28XjtV2gtbs%3D
-
Merrill AE, Bochukova EG, Brugger SM, Ishii M, Pilz DT, Wall SA, Lyons KM, Wilkie AO, Maxson RE (2006) Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis. Hum Mol Genet 15:1319-1328
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1319-1328
-
-
Merrill, A.E.1
Bochukova, E.G.2
Brugger, S.M.3
Ishii, M.4
Pilz, D.T.5
Wall, S.A.6
Lyons, K.M.7
Wilkie, A.O.8
Maxson, R.E.9
-
38
-
-
44349160002
-
Twist1 homodimers enhance FGF responsiveness of the cranial sutures and promote suture closure
-
18471809 10.1016/j.ydbio.2008.03.037 1:CAS:528:DC%2BD1cXmsFKrt7s%3D
-
Connerney J, Andreeva V, Leshem Y, Mercado MA, Dowell K, Yang X, Lindner V, Friesel RE, Spicer DB (2008) Twist1 homodimers enhance FGF responsiveness of the cranial sutures and promote suture closure. Dev Biol 318:323-334
-
(2008)
Dev Biol
, vol.318
, pp. 323-334
-
-
Connerney, J.1
Andreeva, V.2
Leshem, Y.3
Mercado, M.A.4
Dowell, K.5
Yang, X.6
Lindner, V.7
Friesel, R.E.8
Spicer, D.B.9
-
39
-
-
33744906742
-
Twist1 dimer selection regulates cranial suture patterning and fusion
-
16502419 10.1002/dvdy.20717 1:CAS:528:DC%2BD28XlvVygtL4%3D
-
Connerney J, Andreeva V, Leshem Y, Muentener C, Mercado MA, Spicer DB (2006) Twist1 dimer selection regulates cranial suture patterning and fusion. Dev Dyn 235:1345-1357
-
(2006)
Dev Dyn
, vol.235
, pp. 1345-1357
-
-
Connerney, J.1
Andreeva, V.2
Leshem, Y.3
Muentener, C.4
Mercado, M.A.5
Spicer, D.B.6
-
40
-
-
0034106166
-
Integration of FGF and TWIST in calvarial bone and suture development
-
10751173 1:CAS:528:DC%2BD3cXjslentbg%3D
-
Rice DP, Aberg T, Chan Y, Tang Z, Kettunen PJ, Pakarinen L, Maxson RE, Thesleff I (2000) Integration of FGF and TWIST in calvarial bone and suture development. Development 127:1845-1855
-
(2000)
Development
, vol.127
, pp. 1845-1855
-
-
Rice, D.P.1
Aberg, T.2
Chan, Y.3
Tang, Z.4
Kettunen, P.J.5
Pakarinen, L.6
Maxson, R.E.7
Thesleff, I.8
-
41
-
-
84864027660
-
Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome
-
Holmes G, Basilico C (2012) Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome. Dev Biol 368:283-293
-
(2012)
Dev Biol
, vol.368
, pp. 283-293
-
-
Holmes, G.1
Basilico, C.2
-
42
-
-
70350441830
-
Fibroblast growth factor 10 plays a causative role in the tracheal cartilage defects in a mouse model of Apert syndrome
-
19581825 10.1203/PDR.0b013e3181b45580 1:CAS:528:DC%2BD1MXhtFamsrbJ
-
Tiozzo C, De Langhe S, Carraro G, Alam DA, Nagy A, Wigfall C, Hajihosseini MK, Warburton D, Minoo P, Bellusci S (2009) Fibroblast growth factor 10 plays a causative role in the tracheal cartilage defects in a mouse model of Apert syndrome. Pediatr Res 66:386-390
-
(2009)
Pediatr Res
, vol.66
, pp. 386-390
-
-
Tiozzo, C.1
De Langhe, S.2
Carraro, G.3
Alam, D.A.4
Nagy, A.5
Wigfall, C.6
Hajihosseini, M.K.7
Warburton, D.8
Minoo, P.9
Bellusci, S.10
-
43
-
-
0025159354
-
The central nervous system in the Apert syndrome
-
2405668 10.1002/ajmg.1320350108
-
Cohen MM Jr, Kreiborg S (1990) The central nervous system in the Apert syndrome. Am J Med Genet 35:36-45
-
(1990)
Am J Med Genet
, vol.35
, pp. 36-45
-
-
Cohen, Jr.M.M.1
Kreiborg, S.2
-
44
-
-
0029911270
-
Comparative endocranial vascular changes due to craniosynostosis and artificial cranial deformation
-
8922183 10.1002/(SICI)1096-8644(199611)101:3<369: AID-AJPA6>3.0. CO;2-U
-
O'Loughlin VD (1996) Comparative endocranial vascular changes due to craniosynostosis and artificial cranial deformation. Am J Phys Anthropol 101:369-385
-
(1996)
Am J Phys Anthropol
, vol.101
, pp. 369-385
-
-
O'Loughlin, V.D.1
-
45
-
-
85026140920
-
Aberrant bony vasculature associated with activating fibroblast growth factor receptor mutations accompanying Crouzon syndrome
-
15111803 10.1097/00001665-200405000-00016
-
Tholpady SS, Abdelaal MM, Dufresne CR, Gampper TJ, Lin KY, Jane JA Sr, Morgan RF, Ogle RC (2004) Aberrant bony vasculature associated with activating fibroblast growth factor receptor mutations accompanying Crouzon syndrome. J Craniofac Surg 15:431-435
-
(2004)
J Craniofac Surg
, vol.15
, pp. 431-435
-
-
Tholpady, S.S.1
Abdelaal, M.M.2
Dufresne, C.R.3
Gampper, T.J.4
Lin, K.Y.5
Jane, Sr.J.A.6
Morgan, R.F.7
Ogle, R.C.8
-
46
-
-
36349033602
-
Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: A review
-
17882438 10.1007/s00381-007-0474-7
-
Raybaud C, Di Rocco C (2007) Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review. Childs Nerv Syst 23:1379-1388
-
(2007)
Childs Nerv Syst
, vol.23
, pp. 1379-1388
-
-
Raybaud, C.1
Di Rocco, C.2
-
47
-
-
77149127680
-
Brain phenotypes in two FGFR2 mouse models for Apert syndrome
-
20077479 10.1002/dvdy.22218 1:CAS:528:DC%2BC3cXkslSmtL4%3D
-
Aldridge K, Hill CA, Austin JR, Percival C, Martinez-Abadias N, Neuberger T, Wang Y, Jabs EW, Richtsmeier JT (2010) Brain phenotypes in two FGFR2 mouse models for Apert syndrome. Dev Dyn 239:987-997
-
(2010)
Dev Dyn
, vol.239
, pp. 987-997
-
-
Aldridge, K.1
Hill, C.A.2
Austin, J.R.3
Percival, C.4
Martinez-Abadias, N.5
Neuberger, T.6
Wang, Y.7
Jabs, E.W.8
Richtsmeier, J.T.9
-
48
-
-
77958594664
-
Beyond the closed suture in Apert syndrome mouse models: Evidence of primary effects of FGFR2 signaling on facial shape at birth
-
20842696 10.1002/dvdy.22414
-
Martinez-Abadias N, Percival C, Aldridge K, Hill CA, Ryan T, Sirivunnabood S, Wang Y, Jabs EW, Richtsmeier JT (2010) Beyond the closed suture in Apert syndrome mouse models: evidence of primary effects of FGFR2 signaling on facial shape at birth. Dev Dyn 239:3058-3071
-
(2010)
Dev Dyn
, vol.239
, pp. 3058-3071
-
-
Martinez-Abadias, N.1
Percival, C.2
Aldridge, K.3
Hill, C.A.4
Ryan, T.5
Sirivunnabood, S.6
Wang, Y.7
Jabs, E.W.8
Richtsmeier, J.T.9
-
49
-
-
59649102280
-
Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse model
-
18773495 10.1002/dvdy.21648 1:CAS:528:DC%2BD1MXjtlyhs7k%3D
-
Hajihosseini MK, Duarte R, Pegrum J, Donjacour A, Lana-Elola E, Rice DP, Sharpe J, Dickson C (2009) Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse model. Dev Dyn 238:376-385
-
(2009)
Dev Dyn
, vol.238
, pp. 376-385
-
-
Hajihosseini, M.K.1
Duarte, R.2
Pegrum, J.3
Donjacour, A.4
Lana-Elola, E.5
Rice, D.P.6
Sharpe, J.7
Dickson, C.8
-
50
-
-
34548371795
-
RNA interference and inhibition of MEK-ERK signaling prevent abnormal skeletal phenotypes in a mouse model of craniosynostosis
-
17694057 10.1038/ng2096 1:CAS:528:DC%2BD2sXps12gtLk%3D
-
Shukla V, Coumoul X, Wang R, Kim H, Deng CX (2007) RNA interference and inhibition of MEK-ERK signaling prevent abnormal skeletal phenotypes in a mouse model of craniosynostosis. Nat Genet 39:1145-1150
-
(2007)
Nat Genet
, vol.39
, pp. 1145-1150
-
-
Shukla, V.1
Coumoul, X.2
Wang, R.3
Kim, H.4
Deng, C.X.5
-
51
-
-
70350344035
-
Medical treatment of craniosynostosis: Recombinant Noggin inhibits coronal suture closure in the rat craniosynostosis model
-
19627528 10.1111/j.1601-6343.2009.01460.x 1:STN:280: DC%2BD1Mrht1CnsA%3D%3D
-
Shen K, Krakora SM, Cunningham M, Singh M, Wang X, Hu FZ, Post JC, Ehrlich GD (2009) Medical treatment of craniosynostosis: recombinant Noggin inhibits coronal suture closure in the rat craniosynostosis model. Orthod Craniofac Res 12:254-262
-
(2009)
Orthod Craniofac Res
, vol.12
, pp. 254-262
-
-
Shen, K.1
Krakora, S.M.2
Cunningham, M.3
Singh, M.4
Wang, X.5
Hu, F.Z.6
Post, J.C.7
Ehrlich, G.D.8
-
52
-
-
0242668281
-
The BMP antagonist noggin regulates cranial suture fusion
-
12687003 10.1038/nature01545 1:CAS:528:DC%2BD3sXislCgtLY%3D
-
Warren SM, Brunet LJ, Harland RM, Economides AN, Longaker MT (2003) The BMP antagonist noggin regulates cranial suture fusion. Nature 422:625-629
-
(2003)
Nature
, vol.422
, pp. 625-629
-
-
Warren, S.M.1
Brunet, L.J.2
Harland, R.M.3
Economides, A.N.4
Longaker, M.T.5
|