253 related articles for article (PubMed ID: 12203737)
21. Anterior endoderm is sufficient to rescue foregut apoptosis and heart tube morphogenesis in an embryo lacking retinoic acid.
Ghatpande S; Ghatpande A; Zile M; Evans T
Dev Biol; 2000 Mar; 219(1):59-70. PubMed ID: 10677255
[TBL] [Abstract][Full Text] [Related]
22. A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate.
Castanet M; Park SM; Smith A; Bost M; Léger J; Lyonnet S; Pelet A; Czernichow P; Chatterjee K; Polak M
Hum Mol Genet; 2002 Aug; 11(17):2051-9. PubMed ID: 12165566
[TBL] [Abstract][Full Text] [Related]
23. Glucocorticoid receptor gene expression during rat embryogenesis. An in situ hybridization study.
Kitraki E; Kittas C; Stylianopoulou F
Differentiation; 1997 Oct; 62(1):21-31. PubMed ID: 9373944
[TBL] [Abstract][Full Text] [Related]
24. Zebrafish gcm2 is required for gill filament budding from pharyngeal ectoderm.
Hogan BM; Hunter MP; Oates AC; Crowhurst MO; Hall NE; Heath JK; Prince VE; Lieschke GJ
Dev Biol; 2004 Dec; 276(2):508-22. PubMed ID: 15581882
[TBL] [Abstract][Full Text] [Related]
25. Differential expression of Sonic hedgehog along the anterior-posterior axis regulates patterning of pharyngeal pouch endoderm and pharyngeal endoderm-derived organs.
Moore-Scott BA; Manley NR
Dev Biol; 2005 Feb; 278(2):323-35. PubMed ID: 15680353
[TBL] [Abstract][Full Text] [Related]
26. Spectrum of Human Foxe1/TTF2 Mutations.
Castanet M; Polak M
Horm Res Paediatr; 2010; 73(6):423-9. PubMed ID: 20453517
[TBL] [Abstract][Full Text] [Related]
27. Regional specification of the endoderm in the early chick embryo.
Kimura W; Yasugi S; Fukuda K
Dev Growth Differ; 2007 Jun; 49(5):365-72. PubMed ID: 17428263
[TBL] [Abstract][Full Text] [Related]
28. Altered binding of MYF-5 to FOXE1 promoter in non-syndromic and CHARGE-associated cleft palate.
Venza M; Visalli M; Venza I; Torino C; Tripodo B; Melita R; Teti D
J Oral Pathol Med; 2009 Jan; 38(1):18-23. PubMed ID: 19192046
[TBL] [Abstract][Full Text] [Related]
29. Isolation and developmental expression analysis of Tbx22, the mouse homolog of the human X-linked cleft palate gene.
Bush JO; Lan Y; Maltby KM; Jiang R
Dev Dyn; 2002 Nov; 225(3):322-6. PubMed ID: 12412015
[TBL] [Abstract][Full Text] [Related]
30. Nasal and pharyngeal abnormalities caused by the mouse goosecoid gene mutation.
Yamada G; Ueno K; Nakamura S; Hanamure Y; Yasui K; Uemura M; Eizuru Y; Mansouri A; Blum M; Sugimura K
Biochem Biophys Res Commun; 1997 Apr; 233(1):161-5. PubMed ID: 9144415
[TBL] [Abstract][Full Text] [Related]
31. Ectoderm, endoderm, and the evolution of heterodont dentitions.
Ohazama A; Haworth KE; Ota MS; Khonsari RH; Sharpe PT
Genesis; 2010 Jun; 48(6):382-9. PubMed ID: 20533405
[TBL] [Abstract][Full Text] [Related]
32. CNBP regulates forebrain formation at organogenesis stage in chick embryos.
Abe Y; Chen W; Huang W; Nishino M; Li YP
Dev Biol; 2006 Jul; 295(1):116-27. PubMed ID: 16626683
[TBL] [Abstract][Full Text] [Related]
33. The role of the endoderm in the development and evolution of the pharyngeal arches.
Graham A; Okabe M; Quinlan R
J Anat; 2005 Nov; 207(5):479-87. PubMed ID: 16313389
[TBL] [Abstract][Full Text] [Related]
34. FRS2alpha is required for the separation, migration, and survival of pharyngeal-endoderm derived organs including thyroid, ultimobranchial body, parathyroid, and thymus.
Kameda Y; Ito M; Nishimaki T; Gotoh N
Dev Dyn; 2009 Mar; 238(3):503-13. PubMed ID: 19235715
[TBL] [Abstract][Full Text] [Related]
35. An integrated regulatory network controlling survival and migration in thyroid organogenesis.
Parlato R; Rosica A; Rodriguez-Mallon A; Affuso A; Postiglione MP; Arra C; Mansouri A; Kimura S; Di Lauro R; De Felice M
Dev Biol; 2004 Dec; 276(2):464-75. PubMed ID: 15581879
[TBL] [Abstract][Full Text] [Related]
36. PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations.
Trueba SS; Augé J; Mattei G; Etchevers H; Martinovic J; Czernichow P; Vekemans M; Polak M; Attié-Bitach T
J Clin Endocrinol Metab; 2005 Jan; 90(1):455-62. PubMed ID: 15494458
[TBL] [Abstract][Full Text] [Related]
37. Loss of the extraembryonic ectoderm in Elf5 mutants leads to defects in embryonic patterning.
Donnison M; Beaton A; Davey HW; Broadhurst R; L'Huillier P; Pfeffer PL
Development; 2005 May; 132(10):2299-308. PubMed ID: 15829518
[TBL] [Abstract][Full Text] [Related]
38. A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis.
Baris I; Arisoy AE; Smith A; Agostini M; Mitchell CS; Park SM; Halefoglu AM; Zengin E; Chatterjee VK; Battaloglu E
J Clin Endocrinol Metab; 2006 Oct; 91(10):4183-7. PubMed ID: 16882747
[TBL] [Abstract][Full Text] [Related]
39. Spatio-temporal expression of Pbx3 during mouse organogenesis.
Di Giacomo G; Koss M; Capellini TD; Brendolan A; Pöpperl H; Selleri L
Gene Expr Patterns; 2006 Oct; 6(7):747-57. PubMed ID: 16434237
[TBL] [Abstract][Full Text] [Related]
40. MSX1 and TGF-beta3 are novel target genes functionally regulated by FOXE1.
Venza I; Visalli M; Parrillo L; De Felice M; Teti D; Venza M
Hum Mol Genet; 2011 Mar; 20(5):1016-25. PubMed ID: 21177256
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
