-
1
-
-
78650384005
-
Disruption of long-distance highly conserved noncoding elements in neurocristopathies
-
Amiel J, Benko S, Gordon CT, Lyonnet S. 2010. Disruption of long-distance highly conserved noncoding elements in neurocristopathies. Ann N Y Acad Sci 1214: 34-46.
-
(2010)
Ann N Y Acad Sci
, vol.1214
, pp. 34-46
-
-
Amiel, J.1
Benko, S.2
Gordon, C.T.3
Lyonnet, S.4
-
2
-
-
0038046074
-
Sox10 regulates the development of the neural crest-derived melanocytes in Xenopus
-
Aoki Y, Saint-Germain N, Gyda M, Magner-Fink EK, Lee Y-H, Credidio C, Saint-Jeannet J-P. 2003. Sox10 regulates the development of the neural crest-derived melanocytes in Xenopus. Dev Biol 259: 19-33.
-
(2003)
Dev Biol
, vol.259
, pp. 19-33
-
-
Aoki, Y.1
Saint-Germain, N.2
Gyda, M.3
Magner-Fink, E.K.4
Lee, Y.-H.5
Credidio, C.6
Saint-Jeannet, J.-P.7
-
3
-
-
33644989691
-
Long-range upstream and downstream enhancers control distinct subsets of the complex spatiotemporal Sox9 expression pattern
-
Bagheri-Fam S, Barrionuevo F, Dohrmann U, Gunther T, Schule R, Kemler R, Mallo M, Kanzler B, Scherer G. 2006. Long-range upstream and downstream enhancers control distinct subsets of the complex spatiotemporal Sox9 expression pattern. Dev Biol 291: 382-397.
-
(2006)
Dev Biol
, vol.291
, pp. 382-397
-
-
Bagheri-Fam, S.1
Barrionuevo, F.2
Dohrmann, U.3
Gunther, T.4
Schule, R.5
Kemler, R.6
Mallo, M.7
Kanzler, B.8
Scherer, G.9
-
4
-
-
61349104285
-
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence
-
Benko S, Fantes JA, Amiel J, Kleinjan DJ, Thomas S, Ramsay J, Jamshidi N, Essafi A, Heaney S, Gordon CT, McBride D, Golzio C, Fisher M, Perry P, Abadie V, Ayuso C, Holder-Espinasse M, Kilpatrick N, Lees MM, Picard A, Temple IK, Thomas P, Vazquez MP, Vekemans M, Crollius HR, Hastie ND, Munnich A, Etchevers HC, Pelet A, Farlie PG, Fitzpatrick DR, Lyonnet S. 2009. Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence. Nat Genet 41: 359-364.
-
(2009)
Nat Genet
, vol.41
, pp. 359-364
-
-
Benko, S.1
Fantes, J.A.2
Amiel, J.3
Kleinjan, D.J.4
Thomas, S.5
Ramsay, J.6
Jamshidi, N.7
Essafi, A.8
Heaney, S.9
Gordon, C.T.10
McBride, D.11
Golzio, C.12
Fisher, M.13
Perry, P.14
Abadie, V.15
Ayuso, C.16
Holder-Espinasse, M.17
Kilpatrick, N.18
Lees, M.M.19
Picard, A.20
Temple, I.K.21
Thomas, P.22
Vazquez, M.P.23
Vekemans, M.24
Crollius, H.R.25
Hastie, N.D.26
Munnich, A.27
Etchevers, H.C.28
Pelet, A.29
Farlie, P.G.30
Fitzpatrick, D.R.31
Lyonnet, S.32
more..
-
5
-
-
0042703900
-
Dimerization of SOX9 is required for chondrogenesis, but not for sex determination
-
Bernard P, Tang P, Liu S, Dewing P, Harley VR, Vilain E. 2003. Dimerization of SOX9 is required for chondrogenesis, but not for sex determination. Hum Mol Genet 12: 1755-1765.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1755-1765
-
-
Bernard, P.1
Tang, P.2
Liu, S.3
Dewing, P.4
Harley, V.R.5
Vilain, E.6
-
6
-
-
0345711458
-
Sox9 is required for cartilage formation
-
Bi W, Deng JM, Zhang Z, Behringer RR, de Crombrugghe B. 1999. Sox9 is required for cartilage formation. Nat Genet 22: 85-89.
-
(1999)
Nat Genet
, vol.22
, pp. 85-89
-
-
Bi, W.1
Deng, J.M.2
Zhang, Z.3
Behringer, R.R.4
de Crombrugghe, B.5
-
7
-
-
0035810951
-
Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization
-
Bi W, Huang W, Whitworth DJ, Deng JM, Zhang Z, Behringer RR, de Crombrugghe B. 2001. Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization. Proc Natl Acad Sci USA 98: 6698-6703.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 6698-6703
-
-
Bi, W.1
Huang, W.2
Whitworth, D.J.3
Deng, J.M.4
Zhang, Z.5
Behringer, R.R.6
de Crombrugghe, B.7
-
8
-
-
0034669139
-
Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators
-
Bowles J, Schepers G, Koopman P. 2000. Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators. Dev Biol 227: 239-255.
-
(2000)
Dev Biol
, vol.227
, pp. 239-255
-
-
Bowles, J.1
Schepers, G.2
Koopman, P.3
-
9
-
-
13344259902
-
The transcriptional control of trunk neural crest induction, survival, and delamination
-
Cheung M, Chaboissier MC, Mynett A, Hirst E, Schedl A, Briscoe J. 2005. The transcriptional control of trunk neural crest induction, survival, and delamination. Dev Cell 8: 179-192.
-
(2005)
Dev Cell
, vol.8
, pp. 179-192
-
-
Cheung, M.1
Chaboissier, M.C.2
Mynett, A.3
Hirst, E.4
Schedl, A.5
Briscoe, J.6
-
10
-
-
0035281835
-
Two sox9 genes on duplicated zebrafish chromosomes: Expression of similar transcription activators in distinct sites
-
Chiang EF, Pai CI, Wyatt M, Yan YL, Postlethwait J, Chung B. 2001. Two sox9 genes on duplicated zebrafish chromosomes: Expression of similar transcription activators in distinct sites. Dev Biol 231: 149-163.
-
(2001)
Dev Biol
, vol.231
, pp. 149-163
-
-
Chiang, E.F.1
Pai, C.I.2
Wyatt, M.3
Yan, Y.L.4
Postlethwait, J.5
Chung, B.6
-
11
-
-
0028135336
-
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
-
Foster JW, Dominguez-Steglich MA, Guioli S, Kowk G, Weller PA, Stevanovic M, Weissenbach J, Mansour S, Young ID, Goodfellow PN, Brook JD, Schafer AJ. 1994. Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene. Nature 372: 525-530.
-
(1994)
Nature
, vol.372
, pp. 525-530
-
-
Foster, J.W.1
Dominguez-Steglich, M.A.2
Guioli, S.3
Kowk, G.4
Weller, P.A.5
Stevanovic, M.6
Weissenbach, J.7
Mansour, S.8
Young, I.D.9
Goodfellow, P.N.10
Brook, J.D.11
Schafer, A.J.12
-
12
-
-
70349705754
-
Long-range regulation of the SOX9 locus in development and disease
-
Gordon CT, Tan TY, Benko S, Fitzatrick D, Lyonnet S, Farlie PG. 2009. Long-range regulation of the SOX9 locus in development and disease. J Med Genet 46: 649-656.
-
(2009)
J Med Genet
, vol.46
, pp. 649-656
-
-
Gordon, C.T.1
Tan, T.Y.2
Benko, S.3
Fitzatrick, D.4
Lyonnet, S.5
Farlie, P.G.6
-
13
-
-
57349122369
-
Segmentation of the vertebrate skull: Neural-crest derivation of adult cartilages in the clawed frog, Xenopus laevis
-
Gross JB, Hanken J. 2008. Segmentation of the vertebrate skull: Neural-crest derivation of adult cartilages in the clawed frog, Xenopus laevis. Int Comp Biol 48: 681-696.
-
(2008)
Int Comp Biol
, vol.48
, pp. 681-696
-
-
Gross, J.B.1
Hanken, J.2
-
14
-
-
76549094979
-
SoxE factors as multifunctional neural crest regulatory factors
-
Haldin CE, Labonne C. 2010. SoxE factors as multifunctional neural crest regulatory factors. Int J Bioch Cell Biol 42: 441-444.
-
(2010)
Int J Bioch Cell Biol
, vol.42
, pp. 441-444
-
-
Haldin, C.E.1
Labonne, C.2
-
16
-
-
0020615253
-
The campomelic syndrome: Review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux in 1971
-
Houston CS, Opitz JM, Spranger JW, Macpherson RI, Reed MH, Gilbert EF, Herrmann J, Schinzel A. 1983. The campomelic syndrome: Review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al. in 1971. Am J Med Genet 15: 3-28.
-
(1983)
Am J Med Genet
, vol.15
, pp. 3-28
-
-
Houston, C.S.1
Opitz, J.M.2
Spranger, J.W.3
Macpherson, R.I.4
Reed, M.H.5
Gilbert, E.F.6
Herrmann, J.7
Schinzel, A.8
-
17
-
-
34250765325
-
Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2
-
Jakobsen LP, Ullmann R, Christensen SB, Jensen KE, Molsted K, Henriksen KF, Hansen C, Knudsen MA, Larsen LA, Tommerup N, Tumer Z. 2007. Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2. J Med Genet 44: 381-386.
-
(2007)
J Med Genet
, vol.44
, pp. 381-386
-
-
Jakobsen, L.P.1
Ullmann, R.2
Christensen, S.B.3
Jensen, K.E.4
Molsted, K.5
Henriksen, K.F.6
Hansen, C.7
Knudsen, M.A.8
Larsen, L.A.9
Tommerup, N.10
Tumer, Z.11
-
18
-
-
0034175998
-
Pairing SOX off: With partners in the regulation of embryonic development
-
Kamachi Y, Uchikawa M, Kondoh H. 2000. Pairing SOX off: With partners in the regulation of embryonic development. Trends Genet 16: 182-187.
-
(2000)
Trends Genet
, vol.16
, pp. 182-187
-
-
Kamachi, Y.1
Uchikawa, M.2
Kondoh, H.3
-
19
-
-
34250641817
-
Runx2 is essential for larval hyobranchial cartilage formation in Xenopus laevis
-
Kerney R, Gross JB, Hanken J. 2007. Runx2 is essential for larval hyobranchial cartilage formation in Xenopus laevis. Dev Dyn 236: 1650-1662.
-
(2007)
Dev Dyn
, vol.236
, pp. 1650-1662
-
-
Kerney, R.1
Gross, J.B.2
Hanken, J.3
-
20
-
-
0028882260
-
Mutations in SOX9, the gene responsible for campomelic dysplasia and autosomal sex reversal
-
Kwok C, Weller PA, Guioli S, Foster JW, Mansour S, Zuffardi O, Punnett HH, Dominguez-Steglich MA, Brook JD, Young ID, Goodfellow PN, Schafer AJ. 1995. Mutations in SOX9, the gene responsible for campomelic dysplasia and autosomal sex reversal. Am J Hum Genet 57: 1028-1036.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1028-1036
-
-
Kwok, C.1
Weller, P.A.2
Guioli, S.3
Foster, J.W.4
Mansour, S.5
Zuffardi, O.6
Punnett, H.H.7
Dominguez-Steglich, M.A.8
Brook, J.D.9
Young, I.D.10
Goodfellow, P.N.11
Schafer, A.J.12
-
22
-
-
4644291070
-
Early requirement of the transcriptional activator Sox9 for neural crest specification in Xenopus
-
Lee YH, Aoki Y, Hong CS, Saint-Germain N, Credidio C, Saint-Jeannet JP. 2004. Early requirement of the transcriptional activator Sox9 for neural crest specification in Xenopus. Dev Biol 275: 93-103.
-
(2004)
Dev Biol
, vol.275
, pp. 93-103
-
-
Lee, Y.H.1
Aoki, Y.2
Hong, C.S.3
Saint-Germain, N.4
Credidio, C.5
Saint-Jeannet, J.P.6
-
23
-
-
0000958271
-
Towards understanding Sox9 function in chondrocyte differentiation
-
Lefebvre V, de Crombrugghe B. 1998. Towards understanding Sox9 function in chondrocyte differentiation. Matrix Biol 16: 529-540.
-
(1998)
Matrix Biol
, vol.16
, pp. 529-540
-
-
Lefebvre, V.1
de Crombrugghe, B.2
-
24
-
-
26844502418
-
Transcriptional control of chondrocyte fate and differentiation
-
Lefebvre V, Smits P. 2005. Transcriptional control of chondrocyte fate and differentiation. Birth Defects Res 75: 200-212.
-
(2005)
Birth Defects Res
, vol.75
, pp. 200-212
-
-
Lefebvre, V.1
Smits, P.2
-
25
-
-
33845528754
-
Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia
-
Leipoldt M, Erdel M, Bien-Willner G, Smyk M, Theurl M, Yatsenko S, Lupski J, Lane A, Shanske A, Stankiewicz P, Scherer G. 2007. Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia. Clin Genet 71: 67-75.
-
(2007)
Clin Genet
, vol.71
, pp. 67-75
-
-
Leipoldt, M.1
Erdel, M.2
Bien-Willner, G.3
Smyk, M.4
Theurl, M.5
Yatsenko, S.6
Lupski, J.7
Lane, A.8
Shanske, A.9
Stankiewicz, P.10
Scherer, G.11
-
26
-
-
0036943587
-
Zebrafish sox9b is an early neural crest marker
-
Li M, Zhao C, Wang Y, Zhao Z, Meng A. 2002. Zebrafish sox9b is an early neural crest marker. Dev Genes Evol 212: 203-206.
-
(2002)
Dev Genes Evol
, vol.212
, pp. 203-206
-
-
Li, M.1
Zhao, C.2
Wang, Y.3
Zhao, Z.4
Meng, A.5
-
27
-
-
76549089509
-
The early history of the Sox genes
-
Lovell-Badge R. 2010. The early history of the Sox genes. Int J Bioch Cell Biol 42: 378-380.
-
(2010)
Int J Bioch Cell Biol
, vol.42
, pp. 378-380
-
-
Lovell-Badge, R.1
-
29
-
-
0036344516
-
The phenotype of survivors of campomelic dysplasia
-
Mansour S, Offiah AC, McDowall S, Sim P, Tolmie J, Hall C. 2002. The phenotype of survivors of campomelic dysplasia. J Med Genet 39: 597-602.
-
(2002)
J Med Genet
, vol.39
, pp. 597-602
-
-
Mansour, S.1
Offiah, A.C.2
McDowall, S.3
Sim, P.4
Tolmie, J.5
Hall, C.6
-
30
-
-
0015236288
-
Le syndrome campomelique
-
Maroteaux P, Spranger J, Opitz JM, Kucera J, Lowry RB, Schimke RN, Kagan SM. 1971. Le syndrome campomelique. Presse Med 79: 1157-1162.
-
(1971)
Presse Med
, vol.79
, pp. 1157-1162
-
-
Maroteaux, P.1
Spranger, J.2
Opitz, J.M.3
Kucera, J.4
Lowry, R.B.5
Schimke, R.N.6
Kagan, S.M.7
-
31
-
-
0033588337
-
Functional and structural studies of wild type SOX9 and mutations causing campomelic dysplasia
-
McDowall S, Argentaro A, Ranganathan S, Weller P, Mertin S, Mansour S, Tolmie J, Harley V. 1999. Functional and structural studies of wild type SOX9 and mutations causing campomelic dysplasia. J Biol Chem 274: 24023-24030.
-
(1999)
J Biol Chem
, vol.274
, pp. 24023-24030
-
-
McDowall, S.1
Argentaro, A.2
Ranganathan, S.3
Weller, P.4
Mertin, S.5
Mansour, S.6
Tolmie, J.7
Harley, V.8
-
32
-
-
8044219672
-
Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: Lack of genotype/phenotype correlations
-
Meyer J, Sudbeck P, Held M, Wagner T, Schmitz ML, Bricarelli FD, Eggermont E, Friedrich U, Haas OA, Kobelt A, Leroy JG, Van Maldergem L, Michel E, Mitulla B, Pfeiffer RA, Schinzel A, Schmidt H, Scherer G. 1997. Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: Lack of genotype/phenotype correlations. Hum Mol Genet 6: 91-98.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 91-98
-
-
Meyer, J.1
Sudbeck, P.2
Held, M.3
Wagner, T.4
Schmitz, M.L.5
Bricarelli, F.D.6
Eggermont, E.7
Friedrich, U.8
Haas, O.A.9
Kobelt, A.10
Leroy, J.G.11
Van Maldergem, L.12
Michel, E.13
Mitulla, B.14
Pfeiffer, R.A.15
Schinzel, A.16
Schmidt, H.17
Scherer, G.18
-
33
-
-
77955747295
-
Molecular mechanisms of cranial neural crest cell migration and patterning in craniofacial development
-
Minoux M, Rijli FM. 2010. Molecular mechanisms of cranial neural crest cell migration and patterning in craniofacial development. Development 137: 2605-2621.
-
(2010)
Development
, vol.137
, pp. 2605-2621
-
-
Minoux, M.1
Rijli, F.M.2
-
35
-
-
0041923688
-
Sox9 is required for determination of the chondrogenic cell lineage in the cranial neural crest
-
Mori-Akiyama Y, Akiyama H, Rowitch DH, de Crombrugghe B. 2003. Sox9 is required for determination of the chondrogenic cell lineage in the cranial neural crest. Proc Natl Acad Sci USA 100: 9360- 9365.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 9360-9365
-
-
Mori-Akiyama, Y.1
Akiyama, H.2
Rowitch, D.H.3
de Crombrugghe, B.4
-
36
-
-
0031104994
-
SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse
-
Ng LJ, Wheatley S, Muscat GE, Conway-Campbell J, Bowles J, Wright E, Bell DM, Tam PP, Cheah KS, Koopman P. 1997. SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse. Dev Biol 183: 108-121.
-
(1997)
Dev Biol
, vol.183
, pp. 108-121
-
-
Ng, L.J.1
Wheatley, S.2
Muscat, G.E.3
Conway-Campbell, J.4
Bowles, J.5
Wright, E.6
Bell, D.M.7
Tam, P.P.8
Cheah, K.S.9
Koopman, P.10
-
37
-
-
33645145093
-
Sox9 mRNA expression in the developing palate and craniofacial muscles and skeletons
-
Nie X. 2006. Sox9 mRNA expression in the developing palate and craniofacial muscles and skeletons. Acta Odontol Scand 64: 97-103.
-
(2006)
Acta Odontol Scand
, vol.64
, pp. 97-103
-
-
Nie, X.1
-
39
-
-
84934443137
-
Neural crest cells and the community of plan for craniofacial development: Historical debates and current perspectives
-
Noden DM, Schneider RA. 2006. Neural crest cells and the community of plan for craniofacial development: Historical debates and current perspectives. Adv Exp Med Biol 589: 1-23.
-
(2006)
Adv Exp Med Biol
, vol.589
, pp. 1-23
-
-
Noden, D.M.1
Schneider, R.A.2
-
40
-
-
0033531956
-
Campomelic syndrome and deletion of Sox9
-
Olney PN, Kean LS, Graham D, Elsas LJ, May KM. 1999. Campomelic syndrome and deletion of Sox9. Am J Med Genet 84: 20-24.
-
(1999)
Am J Med Genet
, vol.84
, pp. 20-24
-
-
Olney, P.N.1
Kean, L.S.2
Graham, D.3
Elsas, L.J.4
May, K.M.5
-
41
-
-
0033358653
-
Campomelic dysplasia translocation breakpoints are scattered over 1Mb proximal to SOX9: Evidence for an extended control region
-
Pfeifer D, Kist R, Dewar K, Devon K, Lander ES, Birren B, Korniszewsky L, Back E, Scherer G. 1999. Campomelic dysplasia translocation breakpoints are scattered over 1Mb proximal to SOX9: Evidence for an extended control region. Am J Hum Genet 65: 111-124.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 111-124
-
-
Pfeifer, D.1
Kist, R.2
Dewar, K.3
Devon, K.4
Lander, E.S.5
Birren, B.6
Korniszewsky, L.7
Back, E.8
Scherer, G.9
-
42
-
-
0035958975
-
Compound effects of point mutations causing campomelic dysplasia/autosmal sex reversal upon SOX9 structure, nuclear transport, DNA binding, and transcriptional activation
-
Preiss S, Argentaro A, Clayton A, John A, Jans DA, Ogata T, Nagai T, Barroso I, Schafer AJ, Harley VR. 2001. Compound effects of point mutations causing campomelic dysplasia/autosmal sex reversal upon SOX9 structure, nuclear transport, DNA binding, and transcriptional activation. J Biol Chem 276: 27864-27872.
-
(2001)
J Biol Chem
, vol.276
, pp. 27864-27872
-
-
Preiss, S.1
Argentaro, A.2
Clayton, A.3
John, A.4
Jans, D.A.5
Ogata, T.6
Nagai, T.7
Barroso, I.8
Schafer, A.J.9
Harley, V.R.10
-
43
-
-
0023445262
-
Neural crest development in the Xenopus laevis embryo, studied by interspecific transplantation and scanning electron microscopy
-
Sadaghiani B, Thiebaud CH. 1987. Neural crest development in the Xenopus laevis embryo, studied by interspecific transplantation and scanning electron microscopy. Dev Biol 124: 91-110.
-
(1987)
Dev Biol
, vol.124
, pp. 91-110
-
-
Sadaghiani, B.1
Thiebaud, C.H.2
-
44
-
-
18844403626
-
Sox9 neural crest determinant gene controls patterning and closure of the posterior frontal cranial suture
-
Sahar DE, Longaker MT, Quarto N. 2005. Sox9 neural crest determinant gene controls patterning and closure of the posterior frontal cranial suture. Dev Biol 280: 244-261.
-
(2005)
Dev Biol
, vol.280
, pp. 244-261
-
-
Sahar, D.E.1
Longaker, M.T.2
Quarto, N.3
-
45
-
-
0037220387
-
Variable expression of campomelic dysplasia in a father and his 46, XY daughter
-
Savarirayan R, Robertson SP, Bankier A, Rogers JG. 2003. Variable expression of campomelic dysplasia in a father and his 46, XY daughter. Ped Path Mol Med 22: 37-46.
-
(2003)
Ped Path Mol Med
, vol.22
, pp. 37-46
-
-
Savarirayan, R.1
Robertson, S.P.2
Bankier, A.3
Rogers, J.G.4
-
46
-
-
0036696817
-
Twenty pairs of sox: Extent, homology, and nomenclature of the mouse and human sox transcription factor gene families
-
Schepers GE, Teasdale RD, Koopman P. 2002. Twenty pairs of sox: Extent, homology, and nomenclature of the mouse and human sox transcription factor gene families. Dev Cell 3: 167-170.
-
(2002)
Dev Cell
, vol.3
, pp. 167-170
-
-
Schepers, G.E.1
Teasdale, R.D.2
Koopman, P.3
-
47
-
-
0038039240
-
Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia
-
Sock E, Pagon RA, Keymolen K, Lissens W, Wegner M, Scherer G. 2003. Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia. Hum Mol Genet 12: 1439-1447.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1439-1447
-
-
Sock, E.1
Pagon, R.A.2
Keymolen, K.3
Lissens, W.4
Wegner, M.5
Scherer, G.6
-
48
-
-
0036337980
-
The transcription factor Sox9 is required for cranial neural crest development in Xenopus
-
Spokony RF, Aoki Y, Saint-Germain N, Magner-Fink EK, Saint-Jeannet J-P. 2002. The transcription factor Sox9 is required for cranial neural crest development in Xenopus. Development 129: 421-432.
-
(2002)
Development
, vol.129
, pp. 421-432
-
-
Spokony, R.F.1
Aoki, Y.2
Saint-Germain, N.3
Magner-Fink, E.K.4
Saint-Jeannet, J.-P.5
-
49
-
-
76549123335
-
SoxE function in vertebrate nervous system development
-
Stolt CC, Wegner M. 2010. SoxE function in vertebrate nervous system development. Int J Biochem Cell Biol 42: 441-444.
-
(2010)
Int J Biochem Cell Biol
, vol.42
, pp. 441-444
-
-
Stolt, C.C.1
Wegner, M.2
-
50
-
-
0027324549
-
Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1
-
Tommerup N, Schempp W, Meinecke P, Pedersen S, Bolund L, Brandt C, Goodpasture C, Guldberg P, Held KR, Reinwein H, Saugstad OD, Scherer G, Skjeldal O, Toder R, Westvik J, van der Hagen CB, Wolf U. 1993. Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1. Nat Genet 4: 170-174.
-
(1993)
Nat Genet
, vol.4
, pp. 170-174
-
-
Tommerup, N.1
Schempp, W.2
Meinecke, P.3
Pedersen, S.4
Bolund, L.5
Brandt, C.6
Goodpasture, C.7
Guldberg, P.8
Held, K.R.9
Reinwein, H.10
Saugstad, O.D.11
Scherer, G.12
Skjeldal, O.13
Toder, R.14
Westvik, J.15
van der Hagen, C.B.16
Wolf, U.17
-
51
-
-
0028589588
-
Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9
-
Wagner T, Wirth J, Meyer J, Zabel B, Held M, Zimmer J, Pasantes J, Bricarelli FD, Keutel J, Hustert E, Wolf U, Tommerup N, Schempp W, Scherer G. 1994. Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell 79: 1111-1120.
-
(1994)
Cell
, vol.79
, pp. 1111-1120
-
-
Wagner, T.1
Wirth, J.2
Meyer, J.3
Zabel, B.4
Held, M.5
Zimmer, J.6
Pasantes, J.7
Bricarelli, F.D.8
Keutel, J.9
Hustert, E.10
Wolf, U.11
Tommerup, N.12
Schempp, W.13
Scherer, G.14
-
52
-
-
45949083140
-
A matter of identity: Transcriptional control in oligodendrocytes
-
Wegner M. 2008. A matter of identity: Transcriptional control in oligodendrocytes. J Mol Neurosci 35: 3-12.
-
(2008)
J Mol Neurosci
, vol.35
, pp. 3-12
-
-
Wegner, M.1
-
53
-
-
0036668285
-
Matching SOX: Partner proteins and co-factors of the SOX family of transcriptional regulators
-
Wilson M, Koopman P. 2002. Matching SOX: Partner proteins and co-factors of the SOX family of transcriptional regulators. Curr Opin Genet Dev 12: 441-446.
-
(2002)
Curr Opin Genet Dev
, vol.12
, pp. 441-446
-
-
Wilson, M.1
Koopman, P.2
-
54
-
-
0028830855
-
The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos
-
Wright E, Hargrave MR, Christiansen J, Cooper L, Kun J, Evans T, Gangadharan U, Greenfield A, Koopman P. 1995. The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos. Nat Genet 9: 15-20.
-
(1995)
Nat Genet
, vol.9
, pp. 15-20
-
-
Wright, E.1
Hargrave, M.R.2
Christiansen, J.3
Cooper, L.4
Kun, J.5
Evans, T.6
Gangadharan, U.7
Greenfield, A.8
Koopman, P.9
-
55
-
-
20244387602
-
Possible roles of Runx1 and Sox9 in incipient intramembranous ossification
-
Yamashiro T, Wang XP, Li Z, Oya S, Aberg T, Fukunaga T, Kamioka H, Speck NA, Takano-Yamamoto T, Thesleff I. 2004. Possible roles of Runx1 and Sox9 in incipient intramembranous ossification. J Bone Miner Res 19: 1671-1677.
-
(2004)
J Bone Miner Res
, vol.19
, pp. 1671-1677
-
-
Yamashiro, T.1
Wang, X.P.2
Li, Z.3
Oya, S.4
Aberg, T.5
Fukunaga, T.6
Kamioka, H.7
Speck, N.A.8
Takano-Yamamoto, T.9
Thesleff, I.10
-
56
-
-
0036848704
-
A zebrafish sox9 gene required for cartilage morphogenesis
-
Yan YL, Miller CT, Nissen RM, Singer A, Liu D, Kirn A, Draper B, Willoughby J, Morcos PA, Amsterdam A, Chung BC, Westerfield M, Haffter P, Hopkins N, Kimmel C, Postlethwait JH. 2002. A zebrafish sox9 gene required for cartilage morphogenesis. Development 129: 5065-5079.
-
(2002)
Development
, vol.129
, pp. 5065-5079
-
-
Yan, Y.L.1
Miller, C.T.2
Nissen, R.M.3
Singer, A.4
Liu, D.5
Kirn, A.6
Draper, B.7
Willoughby, J.8
Morcos, P.A.9
Amsterdam, A.10
Chung, B.C.11
Westerfield, M.12
Haffter, P.13
Hopkins, N.14
Kimmel, C.15
Postlethwait, J.H.16
-
57
-
-
20144388760
-
A pair of Sox: Distinct and overlapping functions of zebrafish sox9 co-orthologs in craniofacial and pectoral fin development
-
Yan YL, Willoughby J, Liu D, Crump JG, Wilson C, Miller CT, Singer A, Kimmel C, Westerfield M, Postlethwait JH. 2005. A pair of Sox: Distinct and overlapping functions of zebrafish sox9 co-orthologs in craniofacial and pectoral fin development. Development 132: 1069-1083.
-
(2005)
Development
, vol.132
, pp. 1069-1083
-
-
Yan, Y.L.1
Willoughby, J.2
Liu, D.3
Crump, J.G.4
Wilson, C.5
Miller, C.T.6
Singer, A.7
Kimmel, C.8
Westerfield, M.9
Postlethwait, J.H.10
-
58
-
-
0026528250
-
Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation
-
Young ID, Zuccollo JM, Maltby EL, Broderick NJ. 1992. Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation. J Med Genet 29: 251-252.
-
(1992)
J Med Genet
, vol.29
, pp. 251-252
-
-
Young, I.D.1
Zuccollo, J.M.2
Maltby, E.L.3
Broderick, N.J.4
-
59
-
-
0030855005
-
Parallel expression of Sox9 and Col2a1 in cells undergoing chondrogenesis
-
Zhao Q, Eberspaecher H, Lefebvre V, De Crombrugghe B. 1997. Parallel expression of Sox9 and Col2a1 in cells undergoing chondrogenesis. Dev Dyn 209: 377-386.
-
(1997)
Dev Dyn
, vol.209
, pp. 377-386
-
-
Zhao, Q.1
Eberspaecher, H.2
Lefebvre, V.3
De Crombrugghe, B.4
|