-
1
-
-
17144464108
-
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome
-
Clement-Jones, M., Schiller, S., Rao, E., Blaschke, R.J., Zuniga, A., Zeller, R., Robson, S.C., Binder, G., Glass, I., Strachan, T. et al. (2000) The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome. Hum. Mol. Genet., 9, 695-702.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 695-702
-
-
Clement-Jones, M.1
Schiller, S.2
Rao, E.3
Blaschke, R.J.4
Zuniga, A.5
Zeller, R.6
Robson, S.C.7
Binder, G.8
Glass, I.9
Strachan, T.10
-
2
-
-
33748967708
-
Expression of the short stature homeobox gene Shox is restricted by proximal and distal signals in chick limb buds and affects the length of skeletal elements
-
Tiecke, E., Bangs, F., Blaschke, R., Farrell, E.R., Rappold, G. and Tickle, C. (2006) Expression of the short stature homeobox gene Shox is restricted by proximal and distal signals in chick limb buds and affects the length of skeletal elements. Dev. Biol., 298, 585-596.
-
(2006)
Dev. Biol.
, vol.298
, pp. 585-596
-
-
Tiecke, E.1
Bangs, F.2
Blaschke, R.3
Farrell, E.R.4
Rappold, G.5
Tickle, C.6
-
3
-
-
4043066666
-
Expression of SHOX in human fetal and childhood growth plate
-
Munns, C.J., Haase, H.R., Crowther, L.M., Hayes, M.T., Blaschke, R., Rappold, G., Glass, I.A. and Batch, J.A. (2004) Expression of SHOX in human fetal and childhood growth plate. J. Clin. Endocrinol. Metab., 89, 4130-4135.
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 4130-4135
-
-
Munns, C.J.1
Haase, H.R.2
Crowther, L.M.3
Hayes, M.T.4
Blaschke, R.5
Rappold, G.6
Glass, I.A.7
Batch, J.A.8
-
4
-
-
36248998258
-
BNP is a transcriptional target of the short stature homeobox gene SHOX
-
Marchini, A., Hacker, B., Marttila, T., Hesse, V., Emons, J., Weiss, B., Karperien, M. and Rappold, G. (2007) BNP is a transcriptional target of the short stature homeobox gene SHOX. Hum. Mol. Genet., 16, 3081-3087.
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 3081-3087
-
-
Marchini, A.1
Hacker, B.2
Marttila, T.3
Hesse, V.4
Emons, J.5
Weiss, B.6
Karperien, M.7
Rappold, G.8
-
5
-
-
4344560627
-
The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes
-
Marchini, A., Marttila, T., Winter, A., Caldeira, S., Malanchi, I., Blaschke, R.J., Hacker, B., Rao, E., Karperien, M., Wit, J.M. et al. (2004) The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes. J. Biol. Chem., 279, 37103-37114.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 37103-37114
-
-
Marchini, A.1
Marttila, T.2
Winter, A.3
Caldeira, S.4
Malanchi, I.5
Blaschke, R.J.6
Hacker, B.7
Rao, E.8
Karperien, M.9
Wit, J.M.10
-
6
-
-
0030940217
-
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
-
Rao, E., Weiss, B., Fukami, M., Rump, A., Niesler, B., Mertz, A., Muroya, K., Binder, G., Kirsch, S., Winkelmann, M. et al. (1997) Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nat. Genet., 16, 54-63.
-
(1997)
Nat. Genet.
, vol.16
, pp. 54-63
-
-
Rao, E.1
Weiss, B.2
Fukami, M.3
Rump, A.4
Niesler, B.5
Mertz, A.6
Muroya, K.7
Binder, G.8
Kirsch, S.9
Winkelmann, M.10
-
7
-
-
0030877094
-
PHOG, a candidate gene for involvement in the short stature of Turner syndrome
-
Ellison, J.W., Wardak, Z., Young, M.F., Gehron Robey, P., Laig-Webster, M. and Chiong, W. (1997) PHOG, a candidate gene for involvement in the short stature of Turner syndrome. Hum. Mol. Genet., 6, 1341-1347.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1341-1347
-
-
Ellison, J.W.1
Wardak, Z.2
Young, M.F.3
Gehron Robey, P.4
Laig-Webster, M.5
Chiong, W.6
-
8
-
-
17344363774
-
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)
-
Belin, V., Cusin, V., Viot, G., Girlich, D., Toutain, A., Moncla, A., Vekemans, M., Le Merrer, M., Munnich, A. and Cormier-Daire, V. (1998) SHOX mutations in dyschondrosteosis (Leri-Weill syndrome). Nat. Genet., 19, 67-69.
-
(1998)
Nat. Genet.
, vol.19
, pp. 67-69
-
-
Belin, V.1
Cusin, V.2
Viot, G.3
Girlich, D.4
Toutain, A.5
Moncla, A.6
Vekemans, M.7
Le Merrer, M.8
Munnich, A.9
Cormier-Daire, V.10
-
9
-
-
0031747158
-
Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis
-
Shears, D.J., Vassal, H.J., Goodman, F.R., Palmer, R.W., Reardon, W., Superti-Furga, A., Scambler, P.J. and Winter, R.M. (1998) Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis. Nat. Genet., 19, 70-73.
-
(1998)
Nat. Genet.
, vol.19
, pp. 70-73
-
-
Shears, D.J.1
Vassal, H.J.2
Goodman, F.R.3
Palmer, R.W.4
Reardon, W.5
Superti-Furga, A.6
Scambler, P.J.7
Winter, R.M.8
-
10
-
-
0033994671
-
Phenotypic variation and genetic heterogeneity in Leri-Weill syndrome
-
Schiller, S., Spranger, S., Schechinger, B., Fukami, M., Merker, S., Drop, S.L., Troger, J., Knoblauch, H., Kunze, J., Seidel, J. et al. (2000) Phenotypic variation and genetic heterogeneity in Leri-Weill syndrome. Eur. J. Hum. Genet., 8, 54-62.
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 54-62
-
-
Schiller, S.1
Spranger, S.2
Schechinger, B.3
Fukami, M.4
Merker, S.5
Drop, S.L.6
Troger, J.7
Knoblauch, H.8
Kunze, J.9
Seidel, J.10
-
11
-
-
25444470259
-
A novel class of pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis
-
Benito-Sanz, S., Thomas, N.S., Huber, C., Gorbenko del Blanco, D., Aza-Carmona, M., Crolla, J.A., Maloney, V., Rappold, G., Argente, J., Campos-Barros, A. et al. (2005) A novel class of pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis. Am. J. Hum. Genet., 77, 533-544.
-
(2005)
Am. J. Hum. Genet.
, vol.77
, pp. 533-544
-
-
Benito-Sanz, S.1
Thomas, N.S.2
Huber, C.3
Gorbenko del Blanco, D.4
Aza-Carmona, M.5
Crolla, J.A.6
Maloney, V.7
Rappold, G.8
Argente, J.9
Campos-Barros, A.10
-
12
-
-
72749122013
-
Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain
-
Chen, J., Wildhardt, G., Zhong, Z., Roth, R., Weiss, B., Steinberger, D., Decker, J., Blum, W.F. and Rappold, G. (2009) Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain. J. Med. Genet., 46, 834-839.
-
(2009)
J. Med. Genet.
, vol.46
, pp. 834-839
-
-
Chen, J.1
Wildhardt, G.2
Zhong, Z.3
Roth, R.4
Weiss, B.5
Steinberger, D.6
Decker, J.7
Blum, W.F.8
Rappold, G.9
-
13
-
-
33845662367
-
SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variability
-
Jorge, A.A., Souza, S.C., Nishi, M.Y., Billerbeck, A.E., Liborio, D.C., Kim, C.A., Arnhold, I.J. and Mendonca, B.B. (2007) SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variability. Clin. Endocrinol. (Oxf.), 66, 130-135.
-
(2007)
Clin. Endocrinol. (Oxf.)
, vol.66
, pp. 130-135
-
-
Jorge, A.A.1
Souza, S.C.2
Nishi, M.Y.3
Billerbeck, A.E.4
Liborio, D.C.5
Kim, C.A.6
Arnhold, I.J.7
Mendonca, B.B.8
-
14
-
-
34248379653
-
Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency
-
Rappold, G., Blum, W.F., Shavrikova, E.P., Crowe, B.J., Roeth, R., Quigley, C.A., Ross, J.L. and Niesler, B. (2007) Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency. J. Med. Genet., 44, 306-313.
-
(2007)
J. Med. Genet.
, vol.44
, pp. 306-313
-
-
Rappold, G.1
Blum, W.F.2
Shavrikova, E.P.3
Crowe, B.J.4
Roeth, R.5
Quigley, C.A.6
Ross, J.L.7
Niesler, B.8
-
15
-
-
33749245482
-
High incidence of SHOX anomalies in individuals with short stature
-
Huber, C., Rosilio, M., Munnich, A. and Cormier-Daire, V. (2006) High incidence of SHOX anomalies in individuals with short stature. J. Med. Genet., 43, 735-739.
-
(2006)
J. Med. Genet.
, vol.43
, pp. 735-739
-
-
Huber, C.1
Rosilio, M.2
Munnich, A.3
Cormier-Daire, V.4
-
16
-
-
0037097345
-
Complete SHOX deficiency causes Langer mesomelic dysplasia
-
Zinn, A.R., Wei, F., Zhang, L., Elder, F.F., Scott, C.I. Jr., Marttila, P. and Ross, J.L. (2002) Complete SHOX deficiency causes Langer mesomelic dysplasia. Am. J. Med. Genet., 110, 158-163.
-
(2002)
Am. J. Med. Genet.
, vol.110
, pp. 158-163
-
-
Zinn, A.R.1
Wei, F.2
Zhang, L.3
Elder, F.F.4
Scott Jr., C.I.5
Marttila, P.6
Ross, J.L.7
-
17
-
-
18044404490
-
Histopathological analysis of Leri-Weill dyschondrosteosis: disordered growth plate
-
Munns, C.F., Glass, I.A., LaBrom, R., Hayes, M., Flanagan, S., Berry, M., Hyland, V.J., Batch, J.A., Philips, G.E. and Vickers, D. (2001) Histopathological analysis of Leri-Weill dyschondrosteosis: disordered growth plate. Hand. Surg., 6, 13-23.
-
(2001)
Hand. Surg.
, vol.6
, pp. 13-23
-
-
Munns, C.F.1
Glass, I.A.2
LaBrom, R.3
Hayes, M.4
Flanagan, S.5
Berry, M.6
Hyland, V.J.7
Batch, J.A.8
Philips, G.E.9
Vickers, D.10
-
18
-
-
0024240142
-
Ultrasonographic prenatal diagnosis and fetal pathology of Langer mesomelic dwarfism
-
Evans, M.I., Zador, I.E., Qureshi, F., Budev, H., Quigg, M.H. and Nadler, H.L. (1988) Ultrasonographic prenatal diagnosis and fetal pathology of Langer mesomelic dwarfism. Am. J. Med. Genet., 31, 915-920.
-
(1988)
Am. J. Med. Genet.
, vol.31
, pp. 915-920
-
-
Evans, M.I.1
Zador, I.E.2
Qureshi, F.3
Budev, H.4
Quigg, M.H.5
Nadler, H.L.6
-
19
-
-
77951621736
-
Enhancer elements upstream of the SHOX gene are active in the developing limb
-
Durand, C., Bangs, F., Signolet, J., Decker, E., Tickle, C. and Rappold, G. (2010) Enhancer elements upstream of the SHOX gene are active in the developing limb. Eur. J. Hum. Genet., 18, 527-532.
-
(2010)
Eur. J. Hum. Genet.
, vol.18
, pp. 527-532
-
-
Durand, C.1
Bangs, F.2
Signolet, J.3
Decker, E.4
Tickle, C.5
Rappold, G.6
-
20
-
-
33846617772
-
Long-range conserved non-coding SHOX sequences regulate expression in developing chicken limb and are associated with short stature phenotypes in human patients
-
Sabherwal, N., Bangs, F., Roth, R., Weiss, B., Jantz, K., Tiecke, E., Hinkel, G.K., Spaich, C., Hauffa, B.P., van der Kamp, H. et al. (2007) Long-range conserved non-coding SHOX sequences regulate expression in developing chicken limb and are associated with short stature phenotypes in human patients. Hum. Mol. Genet., 16, 210-222.
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 210-222
-
-
Sabherwal, N.1
Bangs, F.2
Roth, R.3
Weiss, B.4
Jantz, K.5
Tiecke, E.6
Hinkel, G.K.7
Spaich, C.8
Hauffa, B.P.9
van der Kamp, H.10
-
21
-
-
77951758776
-
Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy
-
Ottesen, A.M., Aksglaede, L., Garn, I., Tartaglia, N., Tassone, F., Gravholt, C.H., Bojesen, A., Sorensen, K., Jorgensen, N., Rajpert-De Meyts, E. et al. (2010) Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy. Am. J. Med. Genet. A, 152A, 1206-1212.
-
(2010)
Am. J. Med. Genet. A
, vol.152 A
, pp. 1206-1212
-
-
Ottesen, A.M.1
Aksglaede, L.2
Garn, I.3
Tartaglia, N.4
Tassone, F.5
Gravholt, C.H.6
Bojesen, A.7
Sorensen, K.8
Jorgensen, N.9
Rajpert-De Meyts, E.10
-
22
-
-
0034456564
-
Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature
-
Ogata, T., Kosho, T., Wakui, K., Fukushima, Y., Yoshimoto, M. and Miharu, N. (2000) Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature. J. Clin. Endocrinol. Metab., 85, 2927-2930.
-
(2000)
J. Clin. Endocrinol. Metab.
, vol.85
, pp. 2927-2930
-
-
Ogata, T.1
Kosho, T.2
Wakui, K.3
Fukushima, Y.4
Yoshimoto, M.5
Miharu, N.6
-
23
-
-
0033051415
-
High density micromass cultures of embryonic limb bud mesenchymal cells: an in vitro model of endochondral skeletal development
-
Mello, M.A. and Tuan, R.S. (1999) High density micromass cultures of embryonic limb bud mesenchymal cells: an in vitro model of endochondral skeletal development. In Vitro Cell. Dev. Biol. Anim., 35, 262-269.
-
(1999)
Vitro Cell. Dev. Biol. Anim.
, vol.35
, pp. 262-269
-
-
Mello, M.A.1
Tuan, R.S.2
-
24
-
-
0017739437
-
Stage-related capacity for limb chondrogenesis in cell culture
-
Ahrens, P.B., Solursh, M. and Reiter, R.S. (1977) Stage-related capacity for limb chondrogenesis in cell culture. Dev. Biol., 60, 69-82.
-
(1977)
Dev. Biol.
, vol.60
, pp. 69-82
-
-
Ahrens, P.B.1
Solursh, M.2
Reiter, R.S.3
-
25
-
-
22144457621
-
Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri-Weill dyschondrosteosis
-
Schneider, K.U., Marchini, A., Sabherwal, N., Roth, R., Niesler, B., Marttila, T., Blaschke, R.J., Lawson, M., Dumic, M. and Rappold, G. (2005) Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri-Weill dyschondrosteosis. Hum. Mutat., 26, 44-52.
-
(2005)
Hum. Mutat.
, vol.26
, pp. 44-52
-
-
Schneider, K.U.1
Marchini, A.2
Sabherwal, N.3
Roth, R.4
Niesler, B.5
Marttila, T.6
Blaschke, R.J.7
Lawson, M.8
Dumic, M.9
Rappold, G.10
-
26
-
-
0032478120
-
SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb development
-
Blaschke, R.J., Monaghan, A.P., Schiller, S., Schechinger, B., Rao, E., Padilla-Nash, H., Ried, T. and Rappold, G.A. (1998) SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb development. Proc. Natl Acad. Sci. USA, 95, 2406-2411.
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 2406-2411
-
-
Blaschke, R.J.1
Monaghan, A.P.2
Schiller, S.3
Schechinger, B.4
Rao, E.5
Padilla-Nash, H.6
Ried, T.7
Rappold, G.A.8
-
27
-
-
0035894660
-
The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator
-
Rao, E., Blaschke, R.J., Marchini, A., Niesler, B., Burnett, M. and Rappold, G.A. (2001) The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator. Hum. Mol. Genet., 10, 3083-3091.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 3083-3091
-
-
Rao, E.1
Blaschke, R.J.2
Marchini, A.3
Niesler, B.4
Burnett, M.5
Rappold, G.A.6
-
28
-
-
63849103182
-
The RCAS retroviral expression system in the study of skeletal development
-
Gordon, C.T., Rodda, F.A. and Farlie, P.G. (2009) The RCAS retroviral expression system in the study of skeletal development. Dev. Dyn., 238, 797-811.
-
(2009)
Dev. Dyn.
, vol.238
, pp. 797-811
-
-
Gordon, C.T.1
Rodda, F.A.2
Farlie, P.G.3
-
29
-
-
0036569779
-
Role of Runx genes in chondrocyte differentiation
-
Stricker, S., Fundele, R., Vortkamp, A. and Mundlos, S. (2002) Role of Runx genes in chondrocyte differentiation. Dev. Biol., 245, 95-108.
-
(2002)
Dev. Biol.
, vol.245
, pp. 95-108
-
-
Stricker, S.1
Fundele, R.2
Vortkamp, A.3
Mundlos, S.4
-
30
-
-
77953191249
-
Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation
-
Villavicencio-Lorini, P., Kuss, P., Friedrich, J., Haupt, J., Farooq, M., Turkmen, S., Duboule, D., Hecht, J. and Mundlos, S. (2010) Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation. J. Clin. Invest., 120, 1994-2004.
-
(2010)
J. Clin. Invest.
, vol.120
, pp. 1994-2004
-
-
Villavicencio-Lorini, P.1
Kuss, P.2
Friedrich, J.3
Haupt, J.4
Farooq, M.5
Turkmen, S.6
Duboule, D.7
Hecht, J.8
Mundlos, S.9
-
31
-
-
77951874066
-
Homotypic clusters of transcription factor binding sites are a key component of human promoters and enhancers
-
Gotea, V., Visel, A., Westlund, J.M., Nobrega, M.A., Pennacchio, L.A. and Ovcharenko, I. (2010) Homotypic clusters of transcription factor binding sites are a key component of human promoters and enhancers. Genome Res., 20, 565-577.
-
(2010)
Genome Res.
, vol.20
, pp. 565-577
-
-
Gotea, V.1
Visel, A.2
Westlund, J.M.3
Nobrega, M.A.4
Pennacchio, L.A.5
Ovcharenko, I.6
-
32
-
-
0033767384
-
Cell signaling switches HOX-PBX complexes from repressors to activators of transcription mediated by histone deacetylases and histone acetyltransferases
-
Saleh, M., Rambaldi, I., Yang, X.J. and Featherstone, M.S. (2000) Cell signaling switches HOX-PBX complexes from repressors to activators of transcription mediated by histone deacetylases and histone acetyltransferases. Mol. Cell. Biol., 20, 8623-8633.
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 8623-8633
-
-
Saleh, M.1
Rambaldi, I.2
Yang, X.J.3
Featherstone, M.S.4
-
33
-
-
33748416500
-
Hox transcription factors and their elusive mammalian gene targets
-
Svingen, T. and Tonissen, K.F. (2006) Hox transcription factors and their elusive mammalian gene targets. Heredity, 97, 88-96.
-
(2006)
Heredity
, vol.97
, pp. 88-96
-
-
Svingen, T.1
Tonissen, K.F.2
-
34
-
-
77958540480
-
Cell-type-specific activation and repression of PU.1 by a complex of discrete, functionally specialized cis-regulatory elements
-
Zarnegar, M.A., Chen, J. and Rothenberg, E.V. (2010) Cell-type-specific activation and repression of PU.1 by a complex of discrete, functionally specialized cis-regulatory elements. Mol. Cell. Biol., 30, 4922-4939.
-
(2010)
Mol. Cell. Biol.
, vol.30
, pp. 4922-4939
-
-
Zarnegar, M.A.1
Chen, J.2
Rothenberg, E.V.3
-
35
-
-
28844502841
-
PU.1/Spi-1 binds to the human TAL-1 silencer to mediate its activity
-
Le Clech, M., Chalhoub, E., Dohet, C., Roure, V., Fichelson, S., Moreau-Gachelin, F. and Mathieu, D. (2006) PU.1/Spi-1 binds to the human TAL-1 silencer to mediate its activity. J. Mol. Biol., 355, 9-19.
-
(2006)
J. Mol. Biol.
, vol.355
, pp. 9-19
-
-
Le Clech, M.1
Chalhoub, E.2
Dohet, C.3
Roure, V.4
Fichelson, S.5
Moreau-Gachelin, F.6
Mathieu, D.7
-
36
-
-
0032570693
-
Regulation of the fibroblast growth factor receptor 3 promoter and intron I enhancer by Sp1 family transcription factors
-
McEwen, D.G. and Ornitz, D.M. (1998) Regulation of the fibroblast growth factor receptor 3 promoter and intron I enhancer by Sp1 family transcription factors. J. Biol. Chem., 273, 5349-5357.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 5349-5357
-
-
McEwen, D.G.1
Ornitz, D.M.2
-
37
-
-
31944443701
-
Prox1 promotes lineage-specific expression of fibroblast growth factor (FGF) receptor-3 in lymphatic endothelium: a role for FGF signaling in lymphangiogenesis
-
Shin, J.W., Min, M., Larrieu-Lahargue, F., Canron, X., Kunstfeld, R., Nguyen, L., Henderson, J.E., Bikfalvi, A., Detmar, M. and Hong, Y.K. (2006) Prox1 promotes lineage-specific expression of fibroblast growth factor (FGF) receptor-3 in lymphatic endothelium: a role for FGF signaling in lymphangiogenesis. Mol. Biol. Cell, 17, 576-584.
-
(2006)
Mol. Biol. Cell
, vol.17
, pp. 576-584
-
-
Shin, J.W.1
Min, M.2
Larrieu-Lahargue, F.3
Canron, X.4
Kunstfeld, R.5
Nguyen, L.6
Henderson, J.E.7
Bikfalvi, A.8
Detmar, M.9
Hong, Y.K.10
-
38
-
-
67651151314
-
Remodeling of chromatin structure within the promoter is important for bmp-2-induced fgfr3 expression
-
Sun, F., Chen, Q., Yang, S., Pan, Q., Ma, J., Wan, Y., Chang, C.H. and Hong, A. (2009) Remodeling of chromatin structure within the promoter is important for bmp-2-induced fgfr3 expression. Nucleic Acids Res., 37, 3897-3911.
-
(2009)
Nucleic Acids Res.
, vol.37
, pp. 3897-3911
-
-
Sun, F.1
Chen, Q.2
Yang, S.3
Pan, Q.4
Ma, J.5
Wan, Y.6
Chang, C.H.7
Hong, A.8
-
39
-
-
77949538773
-
Fgfr3 is a transcriptional target of Ap2delta and Ash2l-containing histone methyltransferase complexes
-
Tan, C.C., Walsh, M.J. and Gelb, B.D. (2009) Fgfr3 is a transcriptional target of Ap2delta and Ash2l-containing histone methyltransferase complexes. PLoS One, 4, e8535.
-
(2009)
PLoS One
, vol.4
-
-
Tan, C.C.1
Walsh, M.J.2
Gelb, B.D.3
-
40
-
-
77950469694
-
p73 and p63 regulate the expression of fibroblast growth factor receptor 3
-
Sayan, A.E., D'Angelo, B., Sayan, B.S., Tucci, P., Cimini, A., Ceru, M.P., Knight, R.A. and Melino, G. (2010) p73 and p63 regulate the expression of fibroblast growth factor receptor 3. Biochem. Biophys. Res. Commun., 394, 824-828.
-
(2010)
Biochem. Biophys. Res. Commun.
, vol.394
, pp. 824-828
-
-
Sayan, A.E.1
D'Angelo, B.2
Sayan, B.S.3
Tucci, P.4
Cimini, A.5
Ceru, M.P.6
Knight, R.A.7
Melino, G.8
-
41
-
-
58149178539
-
FGFR3-related dwarfism and cell signaling
-
Harada, D., Yamanaka, Y., Ueda, K., Tanaka, H. and Seino, Y. (2009) FGFR3-related dwarfism and cell signaling. J. Bone Miner. Metab., 27, 9-15.
-
(2009)
J. Bone Miner. Metab.
, vol.27
, pp. 9-15
-
-
Harada, D.1
Yamanaka, Y.2
Ueda, K.3
Tanaka, H.4
Seino, Y.5
-
42
-
-
0034142212
-
Ectopic expression of fibroblast growth factor receptor 3 promotes myeloma cell proliferation and prevents apoptosis
-
Plowright, E.E., Li, Z., Bergsagel, P.L., Chesi, M., Barber, D.L., Branch, D.R., Hawley, R.G. and Stewart, A.K. (2000) Ectopic expression of fibroblast growth factor receptor 3 promotes myeloma cell proliferation and prevents apoptosis. Blood, 95, 992-998.
-
(2000)
Blood
, vol.95
, pp. 992-998
-
-
Plowright, E.E.1
Li, Z.2
Bergsagel, P.L.3
Chesi, M.4
Barber, D.L.5
Branch, D.R.6
Hawley, R.G.7
Stewart, A.K.8
-
43
-
-
70350646899
-
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors
-
Goriely, A., Hansen, R.M., Taylor, I.B., Olesen, I.A., Jacobsen, G.K., McGowan, S.J., Pfeifer, S.P., McVean, G.A., Meyts, E.R. and Wilkie, A.O. (2009) Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors. Nat. Genet., 41, 1247-1252.
-
(2009)
Nat. Genet.
, vol.41
, pp. 1247-1252
-
-
Goriely, A.1
Hansen, R.M.2
Taylor, I.B.3
Olesen, I.A.4
Jacobsen, G.K.5
McGowan, S.J.6
Pfeifer, S.P.7
McVean, G.A.8
Meyts, E.R.9
Wilkie, A.O.10
-
44
-
-
34548407864
-
FGFR3 protein expression and its relationship to mutation status and prognostic variables in bladder cancer
-
Tomlinson, D.C., Baldo, O., Harnden, P. and Knowles, M.A. (2007) FGFR3 protein expression and its relationship to mutation status and prognostic variables in bladder cancer. J. Pathol., 213, 91-98.
-
(2007)
J. Pathol.
, vol.213
, pp. 91-98
-
-
Tomlinson, D.C.1
Baldo, O.2
Harnden, P.3
Knowles, M.A.4
-
45
-
-
0034234569
-
A neonatal lethal mutation in FGFR3 uncouples proliferation and differentiation of growth plate chondrocytes in embryos
-
Iwata, T., Chen, L., Li, C., Ovchinnikov, D.A., Behringer, R.R., Francomano, C.A. and Deng, C.X. (2000) A neonatal lethal mutation in FGFR3 uncouples proliferation and differentiation of growth plate chondrocytes in embryos. Hum. Mol. Genet., 9, 1603-1613.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1603-1613
-
-
Iwata, T.1
Chen, L.2
Li, C.3
Ovchinnikov, D.A.4
Behringer, R.R.5
Francomano, C.A.6
Deng, C.X.7
-
46
-
-
34447288267
-
Achondroplasia
-
Horton, W.A., Hall, J.G. and Hecht, J.T. (2007) Achondroplasia. Lancet, 370, 162-172.
-
(2007)
Lancet
, vol.370
, pp. 162-172
-
-
Horton, W.A.1
Hall, J.G.2
Hecht, J.T.3
-
47
-
-
0032774475
-
Clinical spectrum of fibroblast growth factor receptor mutations
-
Passos-Bueno, M.R., Wilcox, W.R., Jabs, E.W., Sertie, A.L., Alonso, L.G. and Kitoh, H. (1999) Clinical spectrum of fibroblast growth factor receptor mutations. Hum. Mutat., 14, 115-125.
-
(1999)
Hum. Mutat.
, vol.14
, pp. 115-125
-
-
Passos-Bueno, M.R.1
Wilcox, W.R.2
Jabs, E.W.3
Sertie, A.L.4
Alonso, L.G.5
Kitoh, H.6
-
48
-
-
0029935895
-
Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia
-
Naski, M.C., Wang, Q., Xu, J. and Ornitz, D.M. (1996) Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia. Nat. Genet., 13, 233-237.
-
(1996)
Nat. Genet.
, vol.13
, pp. 233-237
-
-
Naski, M.C.1
Wang, Q.2
Xu, J.3
Ornitz, D.M.4
-
49
-
-
33751082112
-
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome
-
Toydemir, R.M., Brassington, A.E., Bayrak-Toydemir, P., Krakowiak, P.A., Jorde, L.B., Whitby, F.G., Longo, N., Viskochil, D.H., Carey, J.C. and Bamshad, M.J. (2006) A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome. Am. J. Hum. Genet., 79, 935-941.
-
(2006)
Am. J. Hum. Genet.
, vol.79
, pp. 935-941
-
-
Toydemir, R.M.1
Brassington, A.E.2
Bayrak-Toydemir, P.3
Krakowiak, P.A.4
Jorde, L.B.5
Whitby, F.G.6
Longo, N.7
Viskochil, D.H.8
Carey, J.C.9
Bamshad, M.J.10
-
50
-
-
0029917507
-
Fibroblast growth factor receptor 3 is a negative regulator of bone growth
-
Deng, C., Wynshaw-Boris, A., Zhou, F., Kuo, A. and Leder, P. (1996) Fibroblast growth factor receptor 3 is a negative regulator of bone growth. Cell, 84, 911-921.
-
(1996)
Cell
, vol.84
, pp. 911-921
-
-
Deng, C.1
Wynshaw-Boris, A.2
Zhou, F.3
Kuo, A.4
Leder, P.5
-
51
-
-
34247261472
-
Skeletal overgrowth is mediated by deficiency in a specific isoform of fibroblast growth factor receptor 3
-
Eswarakumar, V.P. and Schlessinger, J. (2007) Skeletal overgrowth is mediated by deficiency in a specific isoform of fibroblast growth factor receptor 3. Proc. Natl Acad. Sci. USA, 104, 3937-3942.
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 3937-3942
-
-
Eswarakumar, V.P.1
Schlessinger, J.2
-
52
-
-
18044379322
-
Phenotypes associated with SHOX deficiency
-
Ross, J.L., Scott, C. Jr, Marttila, P., Kowal, K., Nass, A., Papenhausen, P., Abboudi, J., Osterman, L., Kushner, H., Carter, P. et al. (2001) Phenotypes associated with SHOX deficiency. J. Clin. Endocrinol. Metab., 86, 5674-5680.
-
(2001)
J. Clin. Endocrinol. Metab.
, vol.86
, pp. 5674-5680
-
-
Ross, J.L.1
Scott Jr., C.2
Marttila, P.3
Kowal, K.4
Nass, A.5
Papenhausen, P.6
Abboudi, J.7
Osterman, L.8
Kushner, H.9
Carter, P.10
-
53
-
-
17344392308
-
A new mathematical model for relative quantification in real-time RT-PCR
-
Pfaffl, M.W. (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res., 29, e45.
-
(2001)
Nucleic Acids Res.
, vol.29
-
-
Pfaffl, M.W.1
-
54
-
-
67649834440
-
ChIP-seq: using high-throughput sequencing to discover protein-DNA interactions
-
Schmidt, D., Wilson, M.D., Spyrou, C., Brown, G.D., Hadfield, J. and Odom, D.T. (2009) ChIP-seq: using high-throughput sequencing to discover protein-DNA interactions. Methods, 48, 240-248.
-
(2009)
Methods
, vol.48
, pp. 240-248
-
-
Schmidt, D.1
Wilson, M.D.2
Spyrou, C.3
Brown, G.D.4
Hadfield, J.5
Odom, D.T.6
-
55
-
-
33845925394
-
Chromatin immunoprecipitation and microarray-based analysis of protein location
-
Lee, T.I., Johnstone, S.E. and Young, R.A. (2006) Chromatin immunoprecipitation and microarray-based analysis of protein location. Nat. Protoc., 1, 729-748.
-
(2006)
Nat. Protoc.
, vol.1
, pp. 729-748
-
-
Lee, T.I.1
Johnstone, S.E.2
Young, R.A.3
-
56
-
-
62349130698
-
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
-
Langmead, B., Trapnell, C., Pop, M. and Salzberg, S.L. (2009) Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol., 10, R25.
-
(2009)
Genome Biol.
, vol.10
-
-
Langmead, B.1
Trapnell, C.2
Pop, M.3
Salzberg, S.L.4
-
57
-
-
53849146020
-
Model-based analysis of ChIP-Seq (MACS)
-
Zhang, Y., Liu, T., Meyer, C.A., Eeckhoute, J., Johnson, D.S., Bernstein, B.E., Nusbaum, C., Myers, R.M., Brown, M., Li, W. et al. (2008) Model-based analysis of ChIP-Seq (MACS). Genome Biol., 9, R137.
-
(2008)
Genome Biol.
, vol.9
-
-
Zhang, Y.1
Liu, T.2
Meyer, C.A.3
Eeckhoute, J.4
Johnson, D.S.5
Bernstein, B.E.6
Nusbaum, C.7
Myers, R.M.8
Brown, M.9
Li, W.10
|