-
1
-
-
0036387193
-
Forkhead transcription factors: key players in development and metabolism
-
Carlsson, P. and Mahlapuu, M. (2002) Forkhead transcription factors: key players in development and metabolism. Dev. Biol., 250, 1-23.
-
(2002)
Dev. Biol.
, vol.250
, pp. 1-23
-
-
Carlsson, P.1
Mahlapuu, M.2
-
2
-
-
22144486551
-
Chromosome-wide mapping of estrogen receptor binding reveals long-range regulation requiring the forkhead protein FoxA1
-
Carroll, J.S., Liu, X.S., Brodsky, A.S., Li, W., Meyer, C.A., Szary, A.J., Eeckhoute, J., Shao, W., Hestermann, E.V., Geistlinger, T.R. et al. (2005) Chromosome-wide mapping of estrogen receptor binding reveals long-range regulation requiring the forkhead protein FoxA1. Cell, 122, 33-43.
-
(2005)
Cell
, vol.122
, pp. 33-43
-
-
Carroll, J.S.1
Liu, X.S.2
Brodsky, A.S.3
Li, W.4
Meyer, C.A.5
Szary, A.J.6
Eeckhoute, J.7
Shao, W.8
Hestermann, E.V.9
Geistlinger, T.R.10
-
3
-
-
16644382513
-
Human FOX gene family
-
Katoh, M. (2004) Human FOX gene family. Int. J. Oncol., 25, 1495-1500.
-
(2004)
Int. J. Oncol.
, vol.25
, pp. 1495-1500
-
-
Katoh, M.1
-
4
-
-
20544473735
-
The initiation of liver development is dependent on Foxa transcription factors
-
Lee, C.S., Friedman, J.R., Fulmer, J.T. and Kaestner, K.H. (2005) The initiation of liver development is dependent on Foxa transcription factors. Nature, 435, 944-947.
-
(2005)
Nature
, vol.435
, pp. 944-947
-
-
Lee, C.S.1
Friedman, J.R.2
Fulmer, J.T.3
Kaestner, K.H.4
-
5
-
-
0037866671
-
Fox's in development and disease
-
Lehmann, O.J., Sowden, J.C., Carlsson, P., Jordan, T. and Bhattacharya, S.S. (2003) Fox's in development and disease. Trends Genet., 19, 339-344.
-
(2003)
Trends Genet.
, vol.19
, pp. 339-344
-
-
Lehmann, O.J.1
Sowden, J.C.2
Carlsson, P.3
Jordan, T.4
Bhattacharya, S.S.5
-
6
-
-
0031149301
-
FKHL15, a new human member of the forkhead gene family located on chromosome 9q22
-
Chadwick, B.P., Obermayr, F. and Frischauf, A.M. (1997) FKHL15, a new human member of the forkhead gene family located on chromosome 9q22. Genomics, 41, 390-396.
-
(1997)
Genomics
, vol.41
, pp. 390-396
-
-
Chadwick, B.P.1
Obermayr, F.2
Frischauf, A.M.3
-
7
-
-
18344404449
-
TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of the differentiation
-
Zannini, M., Avantaggiato, V., Biffali, E., Arnone, M.I., Sato, K., Pischetola, M., Taylor, B.A., Phillips, S.J., Simeone, A. and Di Lauro, R. (1997) TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of the differentiation. EMBO J., 16, 3185-3197.
-
(1997)
EMBO J.
, vol.16
, pp. 3185-3197
-
-
Zannini, M.1
Avantaggiato, V.2
Biffali, E.3
Arnone, M.I.4
Sato, K.5
Pischetola, M.6
Taylor, B.A.7
Phillips, S.J.8
Simeone, A.9
Di Lauro, R.10
-
8
-
-
0036022315
-
Distribution of the titf2/foxe1 gene product is consistent with an important role in development of foregut endoderm, palate, and hair
-
Dathan, N., Parlato, R., Rosica, A., De Felice, M. and Di Lauro, R. (2002) Distribution of the titf2/foxe1 gene product is consistent with an important role in development of foregut endoderm, palate, and hair. Dev. Dyn., 224, 450-456.
-
(2002)
Dev. Dyn.
, vol.224
, pp. 450-456
-
-
Dathan, N.1
Parlato, R.2
Rosica, A.3
De Felice, M.4
Di Lauro, R.5
-
9
-
-
12244250148
-
PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations
-
Trueba, S.S., Augé, J., Mattei, G., Etchevers, H., Martinovic, J., Czernichow, P., Vekemans, M., Polak, M. and Attié-Bitak, T. (2005) PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations. J. Clin. Endocrinol. Metab., 90, 455-462.
-
(2005)
J. Clin. Endocrinol. Metab.
, vol.90
, pp. 455-462
-
-
Trueba, S.S.1
Augé, J.2
Mattei, G.3
Etchevers, H.4
Martinovic, J.5
Czernichow, P.6
Vekemans, M.7
Polak, M.8
Attié-Bitak, T.9
-
10
-
-
17344366813
-
A mouse model for hereditary thyroid dysgenesis and cleft palate
-
De Felice, M., Ovitt, C., Biffali, E., Rodriguez-Mallon, A., Arra, C., Anastassiadis, K., Macchia, P.E., Mattei, M.G., Mariano, A., Schöler, H. et al. (1998) A mouse model for hereditary thyroid dysgenesis and cleft palate. Nat. Genet., 19, 395-398.
-
(1998)
Nat. Genet.
, vol.19
, pp. 395-398
-
-
De Felice, M.1
Ovitt, C.2
Biffali, E.3
Rodriguez-Mallon, A.4
Arra, C.5
Anastassiadis, K.6
Macchia, P.E.7
Mattei, M.G.8
Mariano, A.9
Schöler, H.10
-
11
-
-
0024555045
-
Congenital hypothyroidism, spiky hair, and cleft palate
-
Bamforth, J.S., Hughes, I.A., Lazarus, J.H., Weaver, C.M. and Harper, P.S. (1989) Congenital hypothyroidism, spiky hair, and cleft palate. J. Med. Genet., 26, 49-51.
-
(1989)
J. Med. Genet.
, vol.26
, pp. 49-51
-
-
Bamforth, J.S.1
Hughes, I.A.2
Lazarus, J.H.3
Weaver, C.M.4
Harper, P.S.5
-
12
-
-
77955390096
-
Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism
-
Castanet, M., Mallya, U., Agostini, M., Schoenmakers, E., Mitchell, C., Demuth, S., Raymond, F.L., Schwabe, J., Gurnell, M. and Chatterjee, V.K. (2010) Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism. J. Clin. Endocrinol. Metab., 95, 4031-4036.
-
(2010)
J. Clin. Endocrinol. Metab.
, vol.95
, pp. 4031-4036
-
-
Castanet, M.1
Mallya, U.2
Agostini, M.3
Schoenmakers, E.4
Mitchell, C.5
Demuth, S.6
Raymond, F.L.7
Schwabe, J.8
Gurnell, M.9
Chatterjee, V.K.10
-
13
-
-
33749549653
-
A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis
-
Baris, I., Arisoy, A.E., Smith, A., Agostini, M., Mitchell, C.S., Park, S.M., Halefoǧlu, A.M., Zengin, E., Chatterjee, V.K. and Battaloglu, E. (2006) A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis. J. Clin. Endocrinol. Metab., 91, 4183-4187.
-
(2006)
J. Clin. Endocrinol. Metab.
, vol.91
, pp. 4183-4187
-
-
Baris, I.1
Arisoy, A.E.2
Smith, A.3
Agostini, M.4
Mitchell, C.S.5
Park, S.M.6
Halefoǧlu, A.M.7
Zengin, E.8
Chatterjee, V.K.9
Battaloglu, E.10
-
14
-
-
0037101847
-
A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate
-
Castanet, M., Park, S.M., Smith, A., Bost, M., Leger, J., Lyonnet, S., Pelet, A., Czernichow, P., Chatterjee, K. and Polak, M. (2002) A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate. Hum. Mol. Genet., 11, 2051-2059.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2051-2059
-
-
Castanet, M.1
Park, S.M.2
Smith, A.3
Bost, M.4
Leger, J.5
Lyonnet, S.6
Pelet, A.7
Czernichow, P.8
Chatterjee, K.9
Polak, M.10
-
15
-
-
0031820442
-
Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia
-
Clifton-Bligh, R.J., Wentworth, J.M., Heinz, P., Crisp, M.S., John, R., Lazarus, J.H., Ludgate, M. and Chatterjee, V.K. (1998) Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia. Nat. Genet., 19, 399-401.
-
(1998)
Nat. Genet.
, vol.19
, pp. 399-401
-
-
Clifton-Bligh, R.J.1
Wentworth, J.M.2
Heinz, P.3
Crisp, M.S.4
John, R.5
Lazarus, J.H.6
Ludgate, M.7
Chatterjee, V.K.8
-
16
-
-
0027507599
-
Identification of a cis-regulatory element and a thyroid-specific nuclear factor mediating the hormonal regulation of rat thyroid peroxidase promoter activity
-
Aza-Blanc, P., Di Lauro, R. and Santisteban, P. (1993) Identification of a cis-regulatory element and a thyroid-specific nuclear factor mediating the hormonal regulation of rat thyroid peroxidase promoter activity. Mol. Endocrinol., 7, 1297-1306.
-
(1993)
Mol. Endocrinol.
, vol.7
, pp. 1297-1306
-
-
Aza-Blanc, P.1
Di Lauro, R.2
Santisteban, P.3
-
17
-
-
0024425390
-
A thyroid-specific nuclear protein essential for tissue-specific expression of the thyroglobulin promoter
-
Civitareale, D., Lonigro, R., Sinclair, A.J. and Di Lauro, R. (1989) A thyroid-specific nuclear protein essential for tissue-specific expression of the thyroglobulin promoter. EMBO J., 8, 2537-2542.
-
(1989)
EMBO J.
, vol.8
, pp. 2537-2542
-
-
Civitareale, D.1
Lonigro, R.2
Sinclair, A.J.3
Di Lauro, R.4
-
18
-
-
5444271023
-
Thyroid development and its disorders: genetics and molecular mechanisms
-
De Felice, M. and Di Lauro, R. (2004) Thyroid development and its disorders: genetics and molecular mechanisms. Endocr. Rev., 25, 722-746.
-
(2004)
Endocr. Rev.
, vol.25
, pp. 722-746
-
-
De Felice, M.1
Di Lauro, R.2
-
19
-
-
0026593301
-
Cell-type-specific expression of the rat thyroperoxidase promoter indicates common mechanisms for thyroid-specific gene expression
-
Francis-Lang, H., Price, M., Polycarpou-Schwarz, M. and Di Lauro, R. (1992) Cell-type-specific expression of the rat thyroperoxidase promoter indicates common mechanisms for thyroid-specific gene expression. Mol. Cell. Biol., 12, 576-588.
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 576-588
-
-
Francis-Lang, H.1
Price, M.2
Polycarpou-Schwarz, M.3
Di Lauro, R.4
-
20
-
-
0026662799
-
Insulin and insulin-like growth factor I regulate a thyroid-specific nuclear protein that binds to the thyroglobulin promoter
-
Santisteban, P., Acebron, A., Polycarpou-Schwarz, M. and Di Lauro, R. (1992) Insulin and insulin-like growth factor I regulate a thyroid-specific nuclear protein that binds to the thyroglobulin promoter. Mol. Endocrinol., 6, 1310-1317.
-
(1992)
Mol. Endocrinol.
, vol.6
, pp. 1310-1317
-
-
Santisteban, P.1
Acebron, A.2
Polycarpou-Schwarz, M.3
Di Lauro, R.4
-
21
-
-
0025051411
-
The tissue-specific expression of the thyroglobulin gene requires interaction between thyroid specific and ubiquitous factors
-
Sinclair, A.J., Lonigro, R., Civitareale, D., Ghibelli, L. and Di Lauro, R. (1990) The tissue-specific expression of the thyroglobulin gene requires interaction between thyroid specific and ubiquitous factors. Eur. J. Biochem., 193, 311-318.
-
(1990)
Eur. J. Biochem.
, vol.193
, pp. 311-318
-
-
Sinclair, A.J.1
Lonigro, R.2
Civitareale, D.3
Ghibelli, L.4
Di Lauro, R.5
-
22
-
-
0036831913
-
Tgf-beta1, Tgf-beta2
-
Adab, K., Sayne, J.R., Carlson, D.S. and Opperman, L.A. (2002) Tgf-beta1, Tgf-beta2, Tgf-beta3 and Msx2 expression is elevated during frontonasal suture morphogenesis and during active postnatal facial growth. Orthod. Craniofac. Res., 5, 227-237.
-
(2002)
Tgf-beta3 and Msx2 expression is elevated during frontonasal suture morphogenesis and during active postnatal facial growth. Orthod. Craniofac. Res.
, vol.5
, pp. 227-237
-
-
Adab, K.1
Sayne, J.R.2
Carlson, D.S.3
Opperman, L.A.4
-
23
-
-
1842853098
-
Msx homeobox gene family and craniofacial development
-
Alappat, S., Zhang, Z.Y. and Chen, Y.P. (2003) Msx homeobox gene family and craniofacial development. Cell Res., 13, 429-442.
-
(2003)
Cell Res.
, vol.13
, pp. 429-442
-
-
Alappat, S.1
Zhang, Z.Y.2
Chen, Y.P.3
-
24
-
-
57449119326
-
Differential impact of MSX1 and MSX2 homeogenes on mouse maxillofacial skeleton
-
Berdal, A., Molla, M., Hotton, D., Aïoub, M., Lézot, F., Néfussi, J.R. and Goubin, G. (2009) Differential impact of MSX1 and MSX2 homeogenes on mouse maxillofacial skeleton. Cells Tissues Organs, 189, 126-132.
-
(2009)
Cells Tissues Organs
, vol.189
, pp. 126-132
-
-
Berdal, A.1
Molla, M.2
Hotton, D.3
Aïoub, M.4
Lézot, F.5
Néfussi, J.R.6
Goubin, G.7
-
25
-
-
0036714198
-
Rescue of cleft palate in MSX1-deficient mice by transgenic BMP4 reveals a network of BMP and Shh signalling in the regulation of mammalian palatogenesis
-
Zhang, Z., Song, Y., Zhao, X., Zhang, X., Fermin, C. and Chen, Y. (2002) Rescue of cleft palate in MSX1-deficient mice by transgenic BMP4 reveals a network of BMP and Shh signalling in the regulation of mammalian palatogenesis. Development, 129, 4135-4146.
-
(2002)
Development
, vol.129
, pp. 4135-4146
-
-
Zhang, Z.1
Song, Y.2
Zhao, X.3
Zhang, X.4
Fermin, C.5
Chen, Y.6
-
26
-
-
0025743150
-
The Msh-like homeobox genes define domains in the developing vertebrate eye
-
Monaghan, A.P., Davidson, D.R., Sime, C., Graham, E., Baldock, R., Bhattacharya, S.S. and Hill, R.E. (1991) The Msh-like homeobox genes define domains in the developing vertebrate eye. Development, 112, 1053-1061.
-
(1991)
Development
, vol.112
, pp. 1053-1061
-
-
Monaghan, A.P.1
Davidson, D.R.2
Sime, C.3
Graham, E.4
Baldock, R.5
Bhattacharya, S.S.6
Hill, R.E.7
-
27
-
-
0030899176
-
Disruption of Msx-1 and Msx-2 reveals roles for these genes in craniofacial, eye, and axial development
-
Foerst-Potts, L. and Sadler, T.W. (1997) Disruption of Msx-1 and Msx-2 reveals roles for these genes in craniofacial, eye, and axial development. Dev. Dyn., 209, 70-84.
-
(1997)
Dev. Dyn.
, vol.209
, pp. 70-84
-
-
Foerst-Potts, L.1
Sadler, T.W.2
-
28
-
-
0028292605
-
MSX1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
-
Satokata, I. and Maas, R. (1994) MSX1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat. Genet., 6, 348-356.
-
(1994)
Nat. Genet.
, vol.6
, pp. 348-356
-
-
Satokata, I.1
Maas, R.2
-
29
-
-
0032128807
-
Genetic variation of MSX1 has a sexual dimorphism in non-syndromic cleft palate in the Chilean population
-
Blanco, R., Jara, L., Villaseca, C., Palomino, H. and Careno, H. (1998) Genetic variation of MSX1 has a sexual dimorphism in non-syndromic cleft palate in the Chilean population. Rev. Med. Chil., 126, 781-787.
-
(1998)
Rev. Med. Chil.
, vol.126
, pp. 781-787
-
-
Blanco, R.1
Jara, L.2
Villaseca, C.3
Palomino, H.4
Careno, H.5
-
30
-
-
0032231873
-
Association of MSX1 and TGF-β3 with nonsyndromic clefting in humans
-
Lidral, A.C., Romitti, P.A., Basart, A.M., Doetschman, T., Leysens, N.J., Daack-Hirsch, S., Semin, E.V., Johnson, L.R., Machida, J., Burds, A. et al. (1998) Association of MSX1 and TGF-β3 with nonsyndromic clefting in humans. Am. J. Hum. Genet., 63, 557-568.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 557-568
-
-
Lidral, A.C.1
Romitti, P.A.2
Basart, A.M.3
Doetschman, T.4
Leysens, N.J.5
Daack-Hirsch, S.6
Semin, E.V.7
Johnson, L.R.8
Machida, J.9
Burds, A.10
-
31
-
-
0034028899
-
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
-
Van den Boogaard, M.J., Dorland, M., Beemer, F.A. and van Amstel, H.K. (2000) MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat. Genet., 24, 342-343.
-
(2000)
Nat. Genet.
, vol.24
, pp. 342-343
-
-
Van den Boogaard, M.J.1
Dorland, M.2
Beemer, F.A.3
van Amstel, H.K.4
-
32
-
-
0030017452
-
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
-
Vastardis, H., Karimbux, N., Guthua, S.W., Seidman, J.G. and Seidman, C.E. (1996) A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nat. Genet., 13, 417-421.
-
(1996)
Nat. Genet.
, vol.13
, pp. 417-421
-
-
Vastardis, H.1
Karimbux, N.2
Guthua, S.W.3
Seidman, J.G.4
Seidman, C.E.5
-
33
-
-
0025287681
-
Differential expression of TGF-β isoforms in murine palatogenesis
-
Fitzpatrick, D.R., Denhez, F., Kondaiah, P. and Akhurst, R. (1990) Differential expression of TGF-β isoforms in murine palatogenesis. Development, 109, 585-595.
-
(1990)
Development
, vol.109
, pp. 585-595
-
-
Fitzpatrick, D.R.1
Denhez, F.2
Kondaiah, P.3
Akhurst, R.4
-
34
-
-
0026032366
-
Immunodetection of the transforming growth factors β1 and β2 in the developing murine palate
-
Gehris, A., D'Angelo, M. and Greene, R.M. (1991) Immunodetection of the transforming growth factors β1 and β2 in the developing murine palate. Int. J. Dev. Biol., 35, 17-24.
-
(1991)
Int. J. Dev. Biol.
, vol.35
, pp. 17-24
-
-
Gehris, A.1
D'Angelo, M.2
Greene, R.M.3
-
35
-
-
0025018368
-
Differential expression of the genes encoding TGFs β1, β2, and β3 during murine palate formation
-
Pelton, R.W., Hogan, B.L., Miller, D.A. and Moses, H.L. (1990) Differential expression of the genes encoding TGFs β1, β2, and β3 during murine palate formation. Dev. Biol., 141, 456-460.
-
(1990)
Dev. Biol.
, vol.141
, pp. 456-460
-
-
Pelton, R.W.1
Hogan, B.L.2
Miller, D.A.3
Moses, H.L.4
-
36
-
-
0028989842
-
Inhibition of TGF-β3 (but not TGF-β1 or TGF-β2) activity prevents normal mouse embryonic palate fusion
-
Brunet, C.L., Sharpe, P.M. and Ferguson, M.W.J. (1995) Inhibition of TGF-β3 (but not TGF-β1 or TGF-β2) activity prevents normal mouse embryonic palate fusion. Int. J. Dev. Biol., 39, 345-355.
-
(1995)
Int. J. Dev. Biol.
, vol.39
, pp. 345-355
-
-
Brunet, C.L.1
Sharpe, P.M.2
Ferguson, M.W.J.3
-
37
-
-
0028806184
-
Abnormal lung development and cleft palate in mice lacking TGF-β3 indicates defects of epithelial-mesenchymal interaction
-
Kaartinen, V., Voncken, J.W., Shuler, C., Warburton, D., Bu, D., Heisterkamp, N. and Groffen, J. (1995) Abnormal lung development and cleft palate in mice lacking TGF-β3 indicates defects of epithelial-mesenchymal interaction. Nat. Genet., 11, 415-421.
-
(1995)
Nat. Genet.
, vol.11
, pp. 415-421
-
-
Kaartinen, V.1
Voncken, J.W.2
Shuler, C.3
Warburton, D.4
Bu, D.5
Heisterkamp, N.6
Groffen, J.7
-
38
-
-
0028972869
-
Transforming growth factor-β3 is required for secondary palate fusion
-
Proetzel, G., Pawlowski, S.A., Wiles, M.V., Yin, M., Bolvin, G.P., Howles, P.N., Ding, J., Ferguson, M.W. and Doetschman, T. (1995) Transforming growth factor-β3 is required for secondary palate fusion. Nat. Genet., 11, 409-414.
-
(1995)
Nat. Genet.
, vol.11
, pp. 409-414
-
-
Proetzel, G.1
Pawlowski, S.A.2
Wiles, M.V.3
Yin, M.4
Bolvin, G.P.5
Howles, P.N.6
Ding, J.7
Ferguson, M.W.8
Doetschman, T.9
-
39
-
-
0942268094
-
Transforming growth factor-beta3 gene SfaN1 polymorphism in Korean nonsyndromic cleft lip and palate patients
-
Kim, M.H., Kim, H.J., Choi, J.Y. and Nahm, D.S. (2003) Transforming growth factor-beta3 gene SfaN1 polymorphism in Korean nonsyndromic cleft lip and palate patients. J. Biochem. Mol. Biol., 36, 533-537.
-
(2003)
J. Biochem. Mol. Biol.
, vol.36
, pp. 533-537
-
-
Kim, M.H.1
Kim, H.J.2
Choi, J.Y.3
Nahm, D.S.4
-
40
-
-
33747874536
-
TGFβ3 expression in non-syndromic orofacial clefts
-
Rullo, R., Gombos, F., Ferraraccio, F., Farina, A., Morano, D., Festa, V.M., Guida, L., Martinelli, M., Scapoli, L., Pezzetti, F. and Carinci, F. (2006) TGFβ3 expression in non-syndromic orofacial clefts. Int. J. Pediatr. Otorhinolaryngol., 70, 1759-1764.
-
(2006)
Int. J. Pediatr. Otorhinolaryngol.
, vol.70
, pp. 1759-1764
-
-
Rullo, R.1
Gombos, F.2
Ferraraccio, F.3
Farina, A.4
Morano, D.5
Festa, V.M.6
Guida, L.7
Martinelli, M.8
Scapoli, L.9
Pezzetti, F.10
Carinci, F.11
-
41
-
-
33645067959
-
Compound developmental eye disorders following inactivation of TGFβ signalling in neural-crest stem cells
-
Ittner, L.M., Wurdak, H., Schwerdtfeger, K., Kunz, T., Ille, F., Leveen, P., Hjalt, T.A., Suter, U., Karlsson, S., Hafezi, F., Born, W. and Sommer, L. (2005) Compound developmental eye disorders following inactivation of TGFβ signalling in neural-crest stem cells. J. Biol., 4, 11.
-
(2005)
J. Biol.
, vol.4
, pp. 11
-
-
Ittner, L.M.1
Wurdak, H.2
Schwerdtfeger, K.3
Kunz, T.4
Ille, F.5
Leveen, P.6
Hjalt, T.A.7
Suter, U.8
Karlsson, S.9
Hafezi, F.10
Born, W.11
Sommer, L.12
-
42
-
-
3042656861
-
TTF-2 stimulates expression of 17 genes, including one novel thyroid-specific gene which might be involved in thyroid development
-
Hishinuma, A., Ohmika, N., Namatame, T. and Ieiri, T. (2004) TTF-2 stimulates expression of 17 genes, including one novel thyroid-specific gene which might be involved in thyroid development. Mol. Cell. Endocrinol., 221, 33-46.
-
(2004)
Mol. Cell. Endocrinol.
, vol.221
, pp. 33-46
-
-
Hishinuma, A.1
Ohmika, N.2
Namatame, T.3
Ieiri, T.4
-
43
-
-
67649515610
-
Transcriptional mechanisms of WNT5A based on NF-kappaB, Hedgehog, TGFbeta, and Notch signaling cascades
-
Katoh, M. and Katoh, M. (2009) Transcriptional mechanisms of WNT5A based on NF-kappaB, Hedgehog, TGFbeta, and Notch signaling cascades. Int. J. Mol. Med., 23, 763-769.
-
(2009)
Int. J. Mol. Med.
, vol.23
, pp. 763-769
-
-
Katoh, M.1
Katoh, M.2
-
44
-
-
0030770823
-
Transcriptional control of the forkhead thyroid transcription factor TTF-2 by thyrotropin, insulin, and insulin-like growth factor I
-
Ortiz, L., Zannini, M., Di Lauro, R. and Santisteban, P. (1997) Transcriptional control of the forkhead thyroid transcription factor TTF-2 by thyrotropin, insulin, and insulin-like growth factor I. J. Biol. Chem., 272, 23334-23339.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 23334-23339
-
-
Ortiz, L.1
Zannini, M.2
Di Lauro, R.3
Santisteban, P.4
-
45
-
-
0034804293
-
Polymorphism of the polyalanine tract of thyroid transcription factor-2 gene in patients with thyroid dysgenesis
-
Hishinuma, A., Ohyama, Y., Kuribayashi, T., Nagakubo, N., Namatame, T., Shibayama, K., Arisaka, O., Matsuura, N. and Ieri, T. (2001) Polymorphism of the polyalanine tract of thyroid transcription factor-2 gene in patients with thyroid dysgenesis. Eur. J. Endocrinol., 145, 385-389.
-
(2001)
Eur. J. Endocrinol.
, vol.145
, pp. 385-389
-
-
Hishinuma, A.1
Ohyama, Y.2
Kuribayashi, T.3
Nagakubo, N.4
Namatame, T.5
Shibayama, K.6
Arisaka, O.7
Matsuura, N.8
Ieri, T.9
-
46
-
-
33846048399
-
Molecular control of secondary palate development
-
Gritli-Linde, A. (2007) Molecular control of secondary palate development. Dev. Biol., 301, 309-326.
-
(2007)
Dev. Biol.
, vol.301
, pp. 309-326
-
-
Gritli-Linde, A.1
|