-
1
-
-
33750454039
-
Arteries define the position of the thyroid gland during its developmental relocalisation
-
Alt B., Elsalini O.A., Schrumpf P., Haufs N., Lawson N.D., Schwabe G.C., Mundlos S., Gruters A., Krude H., and Rohr K.B. Arteries define the position of the thyroid gland during its developmental relocalisation. Development 133 (2006) 3797-3804
-
(2006)
Development
, vol.133
, pp. 3797-3804
-
-
Alt, B.1
Elsalini, O.A.2
Schrumpf, P.3
Haufs, N.4
Lawson, N.D.5
Schwabe, G.C.6
Mundlos, S.7
Gruters, A.8
Krude, H.9
Rohr, K.B.10
-
2
-
-
19444371444
-
Dissecting contiguous gene defects: TBX1
-
Baldini A. Dissecting contiguous gene defects: TBX1. Curr. Opin. Genet. Dev. 15 (2005) 279-284
-
(2005)
Curr. Opin. Genet. Dev.
, vol.15
, pp. 279-284
-
-
Baldini, A.1
-
4
-
-
0032536823
-
Soluble dominant-negative receptor uncovers essential roles for fibroblast growth factors in multi-organ induction and patterning
-
Celli G., LaRochelle W.J., Mackem S., Sharp R., and Merlino G. Soluble dominant-negative receptor uncovers essential roles for fibroblast growth factors in multi-organ induction and patterning. Embo. J. 17 (1998) 1642-1655
-
(1998)
Embo. J.
, vol.17
, pp. 1642-1655
-
-
Celli, G.1
LaRochelle, W.J.2
Mackem, S.3
Sharp, R.4
Merlino, G.5
-
5
-
-
5444271023
-
Thyroid development and its disorders: genetics and molecular mechanisms
-
De Felice D.L. Thyroid development and its disorders: genetics and molecular mechanisms. Endocr. Rev. 25 (2004) 722-746
-
(2004)
Endocr. Rev.
, vol.25
, pp. 722-746
-
-
De Felice, D.L.1
-
6
-
-
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., Scholer H., Macchia V., and Di Lauro R. A mouse model for hereditary thyroid dysgenesis and cleft palate. Nat. Genet. 19 (1998) 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
Scholer, H.10
Macchia, V.11
Di Lauro, R.12
-
7
-
-
30744475470
-
The developing mouse thyroid: embryonic vessel contacts and parenchymal growth pattern during specification, budding, migration, and lobulation
-
Fagman H., Andersson L., and Nilsson M. The developing mouse thyroid: embryonic vessel contacts and parenchymal growth pattern during specification, budding, migration, and lobulation. Dev. Dyn. 235 (2006) 444-455
-
(2006)
Dev. Dyn.
, vol.235
, pp. 444-455
-
-
Fagman, H.1
Andersson, L.2
Nilsson, M.3
-
8
-
-
0041314035
-
Expression of classical cadherins in thyroid development: maintenance of an epithelial phenotype throughout organogenesis
-
Fagman H., Grande M., Edsbagge J., Semb H., and Nilsson M. Expression of classical cadherins in thyroid development: maintenance of an epithelial phenotype throughout organogenesis. Endocrinology 144 (2003) 3618-3624
-
(2003)
Endocrinology
, vol.144
, pp. 3618-3624
-
-
Fagman, H.1
Grande, M.2
Edsbagge, J.3
Semb, H.4
Nilsson, M.5
-
9
-
-
1942533388
-
Genetic deletion of sonic hedgehog causes hemiagenesis and ectopic development of the thyroid in mouse
-
Fagman H., Grande M., Gritli-Linde A., and Nilsson M. Genetic deletion of sonic hedgehog causes hemiagenesis and ectopic development of the thyroid in mouse. Am. J. Pathol. 164 (2004) 1865-1872
-
(2004)
Am. J. Pathol.
, vol.164
, pp. 1865-1872
-
-
Fagman, H.1
Grande, M.2
Gritli-Linde, A.3
Nilsson, M.4
-
10
-
-
33847296702
-
The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning
-
Fagman H., Liao J., Westerlund J., Andersson L., Morrow B.E., and Nilsson M. The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning. Hum. Mol. Genet. 16 (2007) 276-285
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 276-285
-
-
Fagman, H.1
Liao, J.2
Westerlund, J.3
Andersson, L.4
Morrow, B.E.5
Nilsson, M.6
-
11
-
-
9444265974
-
Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors
-
Hu T., Yamagishi H., Maeda J., McAnally J., Yamagishi C., and Srivastava D. Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors. Development 131 (2004) 5491-5502
-
(2004)
Development
, vol.131
, pp. 5491-5502
-
-
Hu, T.1
Yamagishi, H.2
Maeda, J.3
McAnally, J.4
Yamagishi, C.5
Srivastava, D.6
-
12
-
-
34547664865
-
A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field
-
Huynh T., Chen L., Terrell P., and Baldini A. A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field. Genesis 45 (2007) 470-475
-
(2007)
Genesis
, vol.45
, pp. 470-475
-
-
Huynh, T.1
Chen, L.2
Terrell, P.3
Baldini, A.4
-
13
-
-
0035865048
-
Tie2-Cre transgenic mice: a new model for endothelial cell-lineage analysis in vivo
-
Kisanuki Y.Y., Hammer R.E., Miyazaki J., Williams S.C., Richardson J.A., and Yanagisawa M. Tie2-Cre transgenic mice: a new model for endothelial cell-lineage analysis in vivo. Dev. Biol. 230 (2001) 230-242
-
(2001)
Dev. Biol.
, vol.230
, pp. 230-242
-
-
Kisanuki, Y.Y.1
Hammer, R.E.2
Miyazaki, J.3
Williams, S.C.4
Richardson, J.A.5
Yanagisawa, M.6
-
14
-
-
4344645793
-
Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage
-
Liao J., Kochilas L., Nowotschin S., Arnold J.S., Aggarwal V.S., Epstein J.A., Brown M.C., Adams J., and Morrow B.E. Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage. Hum. Mol. Genet. 13 (2004) 1577-1585
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 1577-1585
-
-
Liao, J.1
Kochilas, L.2
Nowotschin, S.3
Arnold, J.S.4
Aggarwal, V.S.5
Epstein, J.A.6
Brown, M.C.7
Adams, J.8
Morrow, B.E.9
-
15
-
-
0035263599
-
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice
-
Lindsay E.A., Vitelli F., Su H., Morishima M., Huynh T., Pramparo T., Jurecic V., Ogunrinu G., Sutherland H.F., Scambler P.J., Bradley A., and Baldini A. Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. Nature 410 (2001) 97-101
-
(2001)
Nature
, vol.410
, pp. 97-101
-
-
Lindsay, E.A.1
Vitelli, F.2
Su, H.3
Morishima, M.4
Huynh, T.5
Pramparo, T.6
Jurecic, V.7
Ogunrinu, G.8
Sutherland, H.F.9
Scambler, P.J.10
Bradley, A.11
Baldini, A.12
-
16
-
-
0029030722
-
The role of Hoxa-3 in mouse thymus and thyroid development
-
Manley N.R., and Capecchi M.R. The role of Hoxa-3 in mouse thymus and thyroid development. Development 121 (1995) 1989-2003
-
(1995)
Development
, vol.121
, pp. 1989-2003
-
-
Manley, N.R.1
Capecchi, M.R.2
-
17
-
-
0031777309
-
Follicular cells of the thyroid gland require Pax8 gene function
-
Mansouri A., Chowdhury K., and Gruss P. Follicular cells of the thyroid gland require Pax8 gene function. Nat. Genet. 19 (1998) 87-90
-
(1998)
Nat. Genet.
, vol.19
, pp. 87-90
-
-
Mansouri, A.1
Chowdhury, K.2
Gruss, P.3
-
18
-
-
0038678572
-
Perturbed thyroid morphology and transient hypothyroidism symptoms in Hoxa5 mutant mice
-
Meunier D., Aubin J., and Jeannotte L. Perturbed thyroid morphology and transient hypothyroidism symptoms in Hoxa5 mutant mice. Dev. Dyn. 227 (2003) 367-378
-
(2003)
Dev. Dyn.
, vol.227
, pp. 367-378
-
-
Meunier, D.1
Aubin, J.2
Jeannotte, L.3
-
19
-
-
0031916557
-
An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination
-
Meyers E.N., Lewandoski M., and Martin G.R. An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination. Nat. Genet. 18 (1998) 136-141
-
(1998)
Nat. Genet.
, vol.18
, pp. 136-141
-
-
Meyers, E.N.1
Lewandoski, M.2
Martin, G.R.3
-
20
-
-
0033135419
-
Defects in tracheoesophageal and lung morphogenesis in Nkx2.1(-/-) mouse embryos
-
Minoo P., Su G., Drum H., Bringas P., and Kimura S. Defects in tracheoesophageal and lung morphogenesis in Nkx2.1(-/-) mouse embryos. Dev. Biol. 209 (1999) 60-71
-
(1999)
Dev. Biol.
, vol.209
, pp. 60-71
-
-
Minoo, P.1
Su, G.2
Drum, H.3
Bringas, P.4
Kimura, S.5
-
21
-
-
29744440528
-
Crkl deficiency disrupts fgf8 signaling in a mouse model of 22q11 deletion syndromes
-
Moon A.M., Guris D.L., Seo J.H., Li L., Hammond J., Talbot A., and Imamoto A. Crkl deficiency disrupts fgf8 signaling in a mouse model of 22q11 deletion syndromes. Dev. Cell. 10 (2006) 71-80
-
(2006)
Dev. Cell.
, vol.10
, pp. 71-80
-
-
Moon, A.M.1
Guris, D.L.2
Seo, J.H.3
Li, L.4
Hammond, J.5
Talbot, A.6
Imamoto, A.7
-
22
-
-
0034597752
-
FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development
-
Ohuchi H., Hori Y., Yamasaki M., Harada H., Sekine K., Kato S., and Itoh N. FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development. Biochem. Biophys. Res. Commun. 277 (2000) 643-649
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.277
, pp. 643-649
-
-
Ohuchi, H.1
Hori, Y.2
Yamasaki, M.3
Harada, H.4
Sekine, K.5
Kato, S.6
Itoh, N.7
-
23
-
-
18244368524
-
A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: data from the Italian Registry for Congenital Hypothyroidism (1991-1998)
-
Olivieri A., Stazi M.A., Mastroiacovo P., Fazzini C., Medda E., Spagnolo A., De Angelis S., Grandolfo M.E., Taruscio D., Cordeddu V., and Sorcini M. A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: data from the Italian Registry for Congenital Hypothyroidism (1991-1998). J. Clin. Endocrinol. Metab. 87 (2002) 557-562
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 557-562
-
-
Olivieri, A.1
Stazi, M.A.2
Mastroiacovo, P.3
Fazzini, C.4
Medda, E.5
Spagnolo, A.6
De Angelis, S.7
Grandolfo, M.E.8
Taruscio, D.9
Cordeddu, V.10
Sorcini, M.11
-
24
-
-
33745390405
-
Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling
-
Park E.J., Ogden L.A., Talbot A., Evans S., Cai C.L., Black B.L., Frank D.U., and Moon A.M. Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling. Development 133 (2006) 2419-2433
-
(2006)
Development
, vol.133
, pp. 2419-2433
-
-
Park, E.J.1
Ogden, L.A.2
Talbot, A.3
Evans, S.4
Cai, C.L.5
Black, B.L.6
Frank, D.U.7
Moon, A.M.8
-
25
-
-
39749130549
-
System for tamoxifen-inducible expression of cre-recombinase from the Foxa2 locus in mice
-
Park E.J., Sun X., Nichol P., Saijoh Y., Martin J.F., and Moon A.M. System for tamoxifen-inducible expression of cre-recombinase from the Foxa2 locus in mice. Dev. Dyn. 237 (2008) 447-453
-
(2008)
Dev. Dyn.
, vol.237
, pp. 447-453
-
-
Park, E.J.1
Sun, X.2
Nichol, P.3
Saijoh, Y.4
Martin, J.F.5
Moon, A.M.6
-
26
-
-
9944248248
-
An integrated regulatory network controlling survival and migration in thyroid organogenesis
-
Parlato R., Rosica A., Rodriguez-Mallon A., Affuso A., Postiglione M.P., Arra C., Mansouri A., Kimura S., Di Lauro R., and De Felice M. An integrated regulatory network controlling survival and migration in thyroid organogenesis. Dev. Biol. 276 (2004) 464-475
-
(2004)
Dev. Biol.
, vol.276
, pp. 464-475
-
-
Parlato, R.1
Rosica, A.2
Rodriguez-Mallon, A.3
Affuso, A.4
Postiglione, M.P.5
Arra, C.6
Mansouri, A.7
Kimura, S.8
Di Lauro, R.9
De Felice, M.10
-
27
-
-
0032841613
-
MesP1 is expressed in the heart precursor cells and required for the formation of a single heart tube
-
Saga Y., Miyagawa-Tomita S., Takagi A., Kitajima S., Miyazaki J., and Inoue T. MesP1 is expressed in the heart precursor cells and required for the formation of a single heart tube. Development 126 (1999) 3437-3447
-
(1999)
Development
, vol.126
, pp. 3437-3447
-
-
Saga, Y.1
Miyagawa-Tomita, S.2
Takagi, A.3
Kitajima, S.4
Miyazaki, J.5
Inoue, T.6
-
28
-
-
0027228303
-
Deletions of human chromosome 22 and associated birth defects
-
Scambler P.J. Deletions of human chromosome 22 and associated birth defects. Curr. Opin. Genet. Dev. 3 (1993) 432-437
-
(1993)
Curr. Opin. Genet. Dev.
, vol.3
, pp. 432-437
-
-
Scambler, P.J.1
-
29
-
-
0031893397
-
Thyroid abnormalities as a feature of DiGeorge syndrome: a patient report and review of the literature
-
Scuccimarri R., and Rodd C. Thyroid abnormalities as a feature of DiGeorge syndrome: a patient report and review of the literature. J. Pediatr. Endocrinol. Metab. 11 (1998) 273-276
-
(1998)
J. Pediatr. Endocrinol. Metab.
, vol.11
, pp. 273-276
-
-
Scuccimarri, R.1
Rodd, C.2
-
30
-
-
13444310931
-
Different thresholds of fibroblast growth factors pattern the ventral foregut into liver and lung
-
Serls A.E., Doherty S., Parvatiyar P., Wells J.M., and Deutsch G.H. Different thresholds of fibroblast growth factors pattern the ventral foregut into liver and lung. Development 132 (2005) 35-47
-
(2005)
Development
, vol.132
, pp. 35-47
-
-
Serls, A.E.1
Doherty, S.2
Parvatiyar, P.3
Wells, J.M.4
Deutsch, G.H.5
-
31
-
-
28044450587
-
Velo-cardio-facial syndrome
-
Shprintzen R.J., Higgins A.M., Antshel K., Fremont W., Roizen N., and Kates W. Velo-cardio-facial syndrome. Curr. Opin. Pediatr. 17 (2005) 725-730
-
(2005)
Curr. Opin. Pediatr.
, vol.17
, pp. 725-730
-
-
Shprintzen, R.J.1
Higgins, A.M.2
Antshel, K.3
Fremont, W.4
Roizen, N.5
Kates, W.6
-
32
-
-
0032923739
-
Generalized lacZ expression with the ROSA26 Cre reporter strain [letter]
-
Soriano P. Generalized lacZ expression with the ROSA26 Cre reporter strain [letter]. Nat. Genet. 21 (1999) 70-71
-
(1999)
Nat. Genet.
, vol.21
, pp. 70-71
-
-
Soriano, P.1
-
33
-
-
33745239739
-
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants
-
Vitelli F., Zhang Z., Huynh T., Sobotka A., Mupo A., and Baldini A. Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants. Dev. Biol. 295 (2006) 559-570
-
(2006)
Dev. Biol.
, vol.295
, pp. 559-570
-
-
Vitelli, F.1
Zhang, Z.2
Huynh, T.3
Sobotka, A.4
Mupo, A.5
Baldini, A.6
-
34
-
-
0031924716
-
Growth hormone deficiency in patients with 22q11.2 deletion: expanding the phenotype
-
Weinzimer S.A., McDonald-McGinn D.M., Driscoll D.A., Emanuel B.S., Zackai E.H., and Moshang Jr. T. Growth hormone deficiency in patients with 22q11.2 deletion: expanding the phenotype. Pediatrics 101 (1998) 929-932
-
(1998)
Pediatrics
, vol.101
, pp. 929-932
-
-
Weinzimer, S.A.1
McDonald-McGinn, D.M.2
Driscoll, D.A.3
Emanuel, B.S.4
Zackai, E.H.5
Moshang Jr., T.6
-
35
-
-
34547483655
-
Early developmental specification of the thyroid gland depends on han-expressing surrounding tissue and on FGF signals
-
Wendl T., Adzic D., Schoenebeck J.J., Scholpp S., Brand M., Yelon D., and Rohr K.B. Early developmental specification of the thyroid gland depends on han-expressing surrounding tissue and on FGF signals. Development 134 (2007) 2871-2879
-
(2007)
Development
, vol.134
, pp. 2871-2879
-
-
Wendl, T.1
Adzic, D.2
Schoenebeck, J.J.3
Scholpp, S.4
Brand, M.5
Yelon, D.6
Rohr, K.B.7
-
36
-
-
0141481952
-
Expression of mouse fibroblast growth factor and fibroblast growth factor receptor genes during early inner ear development
-
Wright T.J., Hatch E.P., Karabagli H., Karabagli P., Schoenwolf G.C., and Mansour S.L. Expression of mouse fibroblast growth factor and fibroblast growth factor receptor genes during early inner ear development. Dev. Dyn. 228 (2003) 267-272
-
(2003)
Dev. Dyn.
, vol.228
, pp. 267-272
-
-
Wright, T.J.1
Hatch, E.P.2
Karabagli, H.3
Karabagli, P.4
Schoenwolf, G.C.5
Mansour, S.L.6
-
37
-
-
4043094751
-
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract
-
Xu H., Morishima M., Wylie J.N., Schwartz R.J., Bruneau B.G., Lindsay E.A., and Baldini A. Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. Development 131 (2004) 3217-3227
-
(2004)
Development
, vol.131
, pp. 3217-3227
-
-
Xu, H.1
Morishima, M.2
Wylie, J.N.3
Schwartz, R.J.4
Bruneau, B.G.5
Lindsay, E.A.6
Baldini, A.7
-
38
-
-
0036333792
-
Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid
-
Xu P.X., Zheng W., Laclef C., Maire P., Maas R.L., Peters H., and Xu X. Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid. Development 129 (2002) 3033-3044
-
(2002)
Development
, vol.129
, pp. 3033-3044
-
-
Xu, P.X.1
Zheng, W.2
Laclef, C.3
Maire, P.4
Maas, R.L.5
Peters, H.6
Xu, X.7
-
39
-
-
0038782306
-
Conditional inactivation of FGF receptor 2 reveals an essential role for FGF signaling in the regulation of osteoblast function and bone growth
-
Yu K., Xu J., Liu Z., Sosic D., Shao J., Olson E.N., Towler D.A., and Ornitz D.M. Conditional inactivation of FGF receptor 2 reveals an essential role for FGF signaling in the regulation of osteoblast function and bone growth. Development 130 (2003) 3063-3074
-
(2003)
Development
, vol.130
, pp. 3063-3074
-
-
Yu, K.1
Xu, J.2
Liu, Z.3
Sosic, D.4
Shao, J.5
Olson, E.N.6
Towler, D.A.7
Ornitz, D.M.8
-
40
-
-
33750282189
-
Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development
-
Zhang Z., Huynh T., and Baldini A. Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development. Development 133 (2006) 3587-3595
-
(2006)
Development
, vol.133
, pp. 3587-3595
-
-
Zhang, Z.1
Huynh, T.2
Baldini, A.3
|