-
1
-
-
77955276209
-
Differential activation of canonical Wnt signaling determines cranial sutures fate: a novel mechanism for sagittal suture craniosynostosis
-
Behr, B., Longaker, M. T., and Quarto, N. (2010). Differential activation of canonical Wnt signaling determines cranial sutures fate: a novel mechanism for sagittal suture craniosynostosis. Dev. Biol. 344, 922-940.
-
(2010)
Dev. Biol.
, vol.344
, pp. 922-940
-
-
Behr, B.1
Longaker, M.T.2
Quarto, N.3
-
2
-
-
0029798614
-
Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes
-
Bellus, G. A., Gaudenz, K., Zackai, E. H., Clarke, L. A., Szabo, J., Francomano, C. A., and Muenke, M. (1996). Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes. Nat. Genet. 14,174-176.
-
(1996)
Nat. Genet.
, vol.14
, pp. 174-176
-
-
Bellus, G.A.1
Gaudenz, K.2
Zackai, E.H.3
Clarke, L.A.4
Szabo, J.5
Francomano, C.A.6
Muenke, M.7
-
3
-
-
12144288066
-
A twist code determines the onset of osteoblast differentiation
-
Bialek, P., Kern, B., Yang, X., Schrock, M., Sosic, D., Hong, N., Wu, H., Yu, K., Ornitz, D. M., Olson, E. N., Justice, M. J., and Karsenty, G. (2004). A twist code determines the onset of osteoblast differentiation. Dev. Cell 6,423-435.
-
(2004)
Dev. Cell
, vol.6
, pp. 423-435
-
-
Bialek, P.1
Kern, B.2
Yang, X.3
Schrock, M.4
Sosic, D.5
Hong, N.6
Wu, H.7
Yu, K.8
Ornitz, D.M.9
Olson, E.N.10
Justice, M.J.11
Karsenty, G.12
-
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, F. (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, F.7
-
5
-
-
0036788297
-
Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome
-
Carver, E. A., Oram, K. F., and Gridley, T. (2002). Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome. Anat. Rec. 268, 90-92.
-
(2002)
Anat. Rec.
, vol.268
, pp. 90-92
-
-
Carver, E.A.1
Oram, K.F.2
Gridley, T.3
-
6
-
-
0141678494
-
A Ser250Trp substitution in mouse fibroblast growth factor receptor 2 (Fgfr2) results in craniosynostosis
-
Chen, L., Li, D., Li, C., Engel, A., and Deng, C. X. (2003). A Ser250Trp 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
-
7
-
-
0028933142
-
Twist is required in head mesenchyme for cranial neural tube morphogenesis
-
Chen, Z. F., and Behringer, R. R. (1995). Twist is required in head mesenchyme for cranial neural tube morphogenesis. Genes Dev. 9, 686-699.
-
(1995)
Genes Dev
, vol.9
, pp. 686-699
-
-
Chen, Z.F.1
Behringer, R.R.2
-
8
-
-
0001956946
-
Eine eigenartige familiaere Entwicklungsstoer ung (Akrocephalosyndaktylie Dysostosis craniofacialis und Hypertelorismus)
-
Chotzen, F. (1932). Eine eigenartige familiaere Entwicklungsstoer ung (Akrocephalosyndaktylie, Dysostosis craniofacialis und Hypertelorismus). Monatsschr. Kinderheilkd. 55, 97-122.
-
(1932)
Monatsschr. Kinderheilkd.
, vol.55
, pp. 97-122
-
-
Chotzen, F.1
-
9
-
-
0027383692
-
Sutural biology and the correlates of craniosynostosis
-
Cohen, M. M. Jr. (1993). Sutural biology and the correlates of craniosynostosis. Am. J. Med. Genet. 47, 581-616
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 581-616
-
-
Cohen Jr., M.M.1
-
10
-
-
44349160002
-
Twist1 homodimers enhance FGF responsiveness of the cranial sutures and promote suture closure
-
Connerney, J., Andreeva, V., Leshem, Y., Mercado, M. A., Dowell, K., Yang, X., Lindner, V., Friesel, R. E., and Spicer, D. B. (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
-
11
-
-
33744906742
-
Twist1 dimer selection regulates cranial suture patterning and fusion
-
Connerney, J., Andreeva, V., Leshem, Y., Muentener, C., Mercado, M. A., and Spicer, D. B. (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
-
12
-
-
34547133743
-
Syndromic craniosynostosis: from history to hydrogen bonds
-
Cunningham, M. L., Seto, M. L., Ratisoontorn, C., Heike, C. L., and Hing, A. V. (2007). Syndromic craniosynostosis: from history to hydrogen bonds. Orthod. Craniofac. Res. 10, 67-81.
-
(2007)
Orthod. Craniofac. Res.
, vol.10
, pp. 67-81
-
-
Cunningham, M.L.1
Seto, M.L.2
Ratisoontorn, C.3
Heike, C.L.4
Hing, A.V.5
-
13
-
-
85026151671
-
Postnatal onset of craniosynostosis in a case of Saethre-Chotzen syndrome
-
de Heer, I. M., Hoogeboom, J., Vermeij-Keers, C., de Klein, A., and Vaandrager, J. M. (2004). Postnatal onset of craniosynostosis in a case of Saethre-Chotzen syndrome. J. Craniofac. Surg. 15, 1048-1052.
-
(2004)
J. Craniofac. Surg.
, vol.15
, pp. 1048-1052
-
-
de Heer, I.M.1
Hoogeboom, J.2
Vermeij-Keers, C.3
de Klein, A.4
Vaandrager, J.M.5
-
14
-
-
0031012353
-
Mutations of the TWIST gene in the Saethre-Chotzen syndrome
-
el Ghouzzi, V., Le Merrer, M., Perrin-Schmitt, F., Lajeunie, E., Benit, P., Renier, D., Bourgeois, P., Bolcato-Bellemin, A. L., Munnich, A., and Bonaventure, J. (1997). Mutations of the TWIST gene in the Saethre-Chotzen syndrome. Nat. Genet. 15, 42-46.
-
(1997)
Nat. Genet.
, vol.15
, pp. 42-46
-
-
el Ghouzzi, V.1
Le Merrer, M.2
Perrin-Schmitt, F.3
Lajeunie, E.4
Benit, P.5
Renier, D.6
Bourgeois, P.7
Bolcato-Bellemin, A.L.8
Munnich, A.9
Bonaventure, J.10
-
15
-
-
33845475612
-
Attenuation of signaling pathways stimulated by pathologically activated FGF-receptor 2 mutants prevents craniosynostosis
-
Eswarakumar, V. P., Ozcan, F., Law, E. D., Bae, J. H., Tome, F., Booth, C. J., Adams, D. J., Lax, I., and Schlessinger, J. (2006). Attenuation of signaling pathways stimulated by pathologically activated FGF-receptor 2 mutants prevents craniosynostosis. PNAS 103, 18603-18608.
-
(2006)
PNAS
, vol.103
, pp. 18603-18608
-
-
Eswarakumar, V.P.1
Ozcan, F.2
Law, E.D.3
Bae, J.H.4
Tome, F.5
Booth, C.J.6
Adams, D.J.7
Lax, I.8
Schlessinger, J.9
-
16
-
-
0035957343
-
A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes
-
Hajihosseini, M. K., Wilson, S., De Moerlooze, L., and 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. U.S.A. 98, 3855-3860.
-
(2001)
Proc. Natl. Acad. Sci. U. S. A.
, vol.98
, pp. 3855-3860
-
-
Hajihosseini, M.K.1
Wilson, S.2
De Moerlooze, L.3
Dickson, C.4
-
17
-
-
63349106487
-
Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology
-
Holmes, G., Rothschild, G., Roy, U. B., Deng, C. X., Mansukhani, A., and 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
-
18
-
-
0031021336
-
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome
-
Howard, T. D., Paznekas, W. A., Green, E. D., Chiang, L. C., Ma, N., Ortiz de Luna, R. I., Garcia Delgado, C., Gonzalez-Ramos, M., Kline, A. D., and Jabs, E. W. (1997). Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome. Nat. Genet. 15, 36-41.
-
(1997)
Nat. Genet.
, vol.15
, pp. 36-41
-
-
Howard, T.D.1
Paznekas, W.A.2
Green, E.D.3
Chiang, L.C.4
Ma, N.5
Ortiz de Luna, R.I.6
Garcia Delgado, C.7
Gonzalez-Ramos, M.8
Kline, A.D.9
Jabs, E.W.10
-
19
-
-
0345700653
-
Twist is up-regulated in response to Wnt1 and inhibits mouse mammary cell differentiation
-
Howe, L. R., Watanabe, O., Leonard, J., and Brown, A. M. (2003). Twist is up-regulated in response to Wnt1 and inhibits mouse mammary cell differentiation. Cancer Res. 63, 1906-1913.
-
(2003)
Cancer Res
, vol.63
, pp. 1906-1913
-
-
Howe, L.R.1
Watanabe, O.2
Leonard, J.3
Brown, A.M.4
-
20
-
-
0028113931
-
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2
-
Jabs, E. W., Li, X., Scott, A. F., Meyers, G., Chen, W., Eccles, M., Mao, J. I., Charnas, L. R., Jackson, C. E., and Jaye, M. (1994). Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nat. Genet. 8,275-279.
-
(1994)
Nat. Genet.
, vol.8
, pp. 275-279
-
-
Jabs, E.W.1
Li, X.2
Scott, A.F.3
Meyers, G.4
Chen, W.5
Eccles, M.6
Mao, J.I.7
Charnas, L.R.8
Jackson, C.E.9
Jaye, M.10
-
21
-
-
0027431005
-
A mutation in the home-odomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
-
Jabs, E. W., Muller, U., Li, X., Ma, L., Luo, W., Haworth, I. S., Klisak, I., Sparkes, R., Warman, M. L., and Mulliken, J. B. (1993). A mutation in the home-odomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell 75, 443-450.
-
(1993)
Cell
, vol.75
, pp. 443-450
-
-
Jabs, E.W.1
Muller, U.2
Li, X.3
Ma, L.4
Luo, W.5
Haworth, I.S.6
Klisak, I.7
Sparkes, R.8
Warman, M.L.9
Mulliken, J.B.10
-
22
-
-
0036149534
-
Tissue origins and interactions in the mammalian skull vault
-
Jiang, X., Iseki, S., Maxson, R. E., Sucov, H. M., and Morriss-Kay, G. M. (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
-
23
-
-
33845625248
-
Craniosynostosis caused by Axin2 deficiency is mediated through distinct functions of beta-catenin in proliferation and differentiation
-
Liu, B., Yu, H. M., and Hsu, W. (2007). Craniosynostosis caused by Axin2 deficiency is mediated through distinct functions of beta-catenin in proliferation and differentiation. Dev. Biol. 301,298-308.
-
(2007)
Dev. Biol.
, vol.301
, pp. 298-308
-
-
Liu, B.1
Yu, H.M.2
Hsu, W.3
-
24
-
-
33645810601
-
Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis
-
Merrill, A. E., Bochukova, E. G., Brugger, S. M., Ishii, M., Pilz, D. T., Wall, S. A., Lyons, K. M., Wilkie, A. O., and Maxson, R. E. Jr. (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 Jr., R.E.9
-
25
-
-
28444453646
-
Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies
-
Morriss-Kay, G. M., and Wilkie, A. O. (2005). Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies. J. Anat. 207, 637-653.
-
(2005)
J. Anat.
, vol.207
, pp. 637-653
-
-
Morriss-Kay, G.M.1
Wilkie, A.O.2
-
26
-
-
0033662265
-
Cranial sutures as intramembranous bone growth sites
-
Opperman, L. A. (2000). Cranial sutures as intramembranous bone growth sites. Dev. Dyn. 219, 472-485.
-
(2000)
Dev. Dyn.
, vol.219
, pp. 472-485
-
-
Opperman, L.A.1
-
27
-
-
23844558626
-
Gene profiling of cells expressing different FGF-2 forms
-
Quarto, N., Fong, K. D., and Longaker, M. T. (2005). Gene profiling of cells expressing different FGF-2 forms. Gene 356,49-68.
-
(2005)
Gene
, vol.356
, pp. 49-68
-
-
Quarto, N.1
Fong, K.D.2
Longaker, M.T.3
-
28
-
-
33644934734
-
The zebrafish (Danio rerio): a model system for cranial suture patterning
-
Quarto, N., and Longaker, M. T. (2005). The zebrafish (Danio rerio): a model system for cranial suture patterning. Cells Tissues Organs (Print) 181, 109-118.
-
(2005)
Cells Tissues Organs (Print)
, vol.181
, pp. 109-118
-
-
Quarto, N.1
Longaker, M.T.2
-
29
-
-
43449083485
-
Molecular mechanisms of FGF-2 inhibitory activity in the osteogenic context of mouse adipose -derived stem cells (mASCs)
-
Quarto, N., Wan, D. C., and Longaker, M.T. (2008). Molecular mechanisms of FGF-2 inhibitory activity in the osteogenic context of mouse adipose - derived stem cells (mASCs). Bone 42, 1040-1052.
-
(2008)
Bone
, vol.42
, pp. 1040-1052
-
-
Quarto, N.1
Wan, D.C.2
Longaker, M.T.3
-
30
-
-
33644982685
-
The Wnt-inducible transcription factor Twist1 inhibits chondrogenesis
-
Reinhold, M. I., Kapadia, R. M., Liao, Z., and Naski, M. C. (2006). The Wnt-inducible transcription factor Twist1 inhibits chondrogenesis. J. Biol. Chem. 281, 1381-1388.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 1381-1388
-
-
Reinhold, M.I.1
Kapadia, R.M.2
Liao, Z.3
Naski, M.C.4
-
31
-
-
0034106166
-
Integration of FGF and TWIST in calvarial bone and suture development
-
Rice, D. P., Aberg, T., Chan, Y., Tang, Z., Kettunen, P. J., Pakarinen, L., Maxson, R. E., and 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
-
32
-
-
0001636485
-
Ein Beitrag zum Turmschaedelproblem (Pathogenese Erblichkeit und Symptomatologie)
-
Saethre, M. (1931). Ein Beitrag zum Turmschaedelproblem (Pathogenese, Erblichkeit und Symptomatologie). Dtsch. Z. Nervenheilkd. 119,533-555.
-
(1931)
Dtsch. Z. Nervenheilkd.
, vol.119
, pp. 533-555
-
-
Saethre, M.1
-
33
-
-
18844403626
-
Sox9 neural crest determinant gene controls patterning and closure of the posterior frontal cranial suture
-
Sahar, D. E., Longaker, M. T., and Quarto, N. (2005). Sox9 neural crest determinant gene controls patterning and closure of the posterior frontal cranial suture. Dev. Biol. 280, 344-361.
-
(2005)
Dev. Biol.
, vol.280
, pp. 344-361
-
-
Sahar, D.E.1
Longaker, M.T.2
Quarto, N.3
-
34
-
-
2942560339
-
Mutations of ephrin-B1 (EFNB1),amarker of tissue boundary formation, cause craniofrontonasal syndrome
-
Twigg, S. R., Kan, R., Babbs, C., Bochukova, E. G., Robertson, S. P., Wall, S. A., Morriss-Kay, G. M., and Wilkie, A. O. (2004). Mutations of ephrin-B1 (EFNB1),amarker of tissue boundary formation, cause craniofrontonasal syndrome. Proc. Natl. Acad. Sci. U.S.A. 101,8652-8657.
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, pp. 8652-8657
-
-
Twigg, S.R.1
Kan, R.2
Babbs, C.3
Bochukova, E.G.4
Robertson, S.P.5
Wall, S.A.6
Morriss-Kay, G.M.7
Wilkie, A.O.8
-
35
-
-
2442661362
-
Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome
-
Wieland, I., Jakubiczka, S., Muschke, P., Cohen, M., Thiele, H., Gerlach, K. L., Adams, R. H., and Wieacker, P. (2004). Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome. Am. J. Hum. Genet. 74, 1209-1215.
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 1209-1215
-
-
Wieland, I.1
Jakubiczka, S.2
Muschke, P.3
Cohen, M.4
Thiele, H.5
Gerlach, K.L.6
Adams, R.H.7
Wieacker, P.8
-
36
-
-
0030769180
-
Craniosynostosis: genes and mechanisms
-
Wilkie, A. O. (1997). Craniosynostosis: genes and mechanisms. Hum. Mol. Genet. 6, 1647-1656.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1647-1656
-
-
Wilkie, A.O.1
-
37
-
-
40949140612
-
A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
-
Yin, L., Du, X., Li, C., Xu, X., Chen, Z., Su, N., Zhao, L., Qi, H., Li, F., Xue, J., Yang, J., Jin, M., Deng, C., and Chen, L. (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
Yang, J.11
Jin, M.12
Deng, C.13
Chen, L.14
-
38
-
-
19044393472
-
Twist is required for establishment of the mouse coronal suture
-
Yoshida, T., Phylactou, L. A., Uney, J. B., Ishikawa, I., Eto, K., and Iseki, S. (2005). Twist is required for establishment of the mouse coronal suture. J. Anat. 206,437-444.
-
(2005)
J. Anat.
, vol.206
, pp. 437-444
-
-
Yoshida, T.1
Phylactou, L.A.2
Uney, J.B.3
Ishikawa, I.4
Eto, K.5
Iseki, S.6
-
39
-
-
18844362603
-
The role of Axin2 in calvarial morphogenesis and craniosynostosis
-
Yu, H. M., Jerchow, B., Sheu, T. J., Liu, B., Costantini, F., Puzas, J. E., Birchmeier, W., and Hsu, W. (2005). The role of Axin2 in calvarial morphogenesis and craniosynostosis. Development 132,1995-2005.
-
(2005)
Development
, vol.132
, pp. 1995-2005
-
-
Yu, H.M.1
Jerchow, B.2
Sheu, T.J.3
Liu, B.4
Costantini, F.5
Puzas, J.E.6
Birchmeier, W.7
Hsu, W.8
|