223 related articles for article (PubMed ID: 25249461)
21. Increased thymus- and decreased parathyroid-fated organ domains in Splotch mutant embryos.
Griffith AV; Cardenas K; Carter C; Gordon J; Iberg A; Engleka K; Epstein JA; Manley NR; Richie ER
Dev Biol; 2009 Mar; 327(1):216-27. PubMed ID: 19135046
[TBL] [Abstract][Full Text] [Related]
22. Modulation of Bmp4 signalling in the epithelial-mesenchymal interactions that take place in early thymus and parathyroid development in avian embryos.
Neves H; Dupin E; Parreira L; Le Douarin NM
Dev Biol; 2012 Jan; 361(2):208-19. PubMed ID: 22057081
[TBL] [Abstract][Full Text] [Related]
23. Hoxa3 regulates the proliferation and differentiation of the third pharyngeal arch mesenchyme in mice.
Chisaka O; Kameda Y
Cell Tissue Res; 2005 Apr; 320(1):77-89. PubMed ID: 15714286
[TBL] [Abstract][Full Text] [Related]
24. EZH2 is required for parathyroid and thymic development through differentiation of the third pharyngeal pouch endoderm.
Caprio C; Lania G; Bilio M; Ferrentino R; Chen L; Baldini A
Dis Model Mech; 2021 Mar; 14(3):. PubMed ID: 33608392
[TBL] [Abstract][Full Text] [Related]
25. Shh signalling restricts the expression of Gcm2 and controls the position of the developing parathyroids.
Grevellec A; Graham A; Tucker AS
Dev Biol; 2011 May; 353(2):194-205. PubMed ID: 21349263
[TBL] [Abstract][Full Text] [Related]
26. Gcm2 and Foxn1 mark early parathyroid- and thymus-specific domains in the developing third pharyngeal pouch.
Gordon J; Bennett AR; Blackburn CC; Manley NR
Mech Dev; 2001 May; 103(1-2):141-3. PubMed ID: 11335122
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Endoderm-specific deletion of Tbx1 reveals an FGF-independent role for Tbx1 in pharyngeal apparatus morphogenesis.
Jackson A; Kasah S; Mansour SL; Morrow B; Basson MA
Dev Dyn; 2014 Sep; 243(9):1143-51. PubMed ID: 24812002
[TBL] [Abstract][Full Text] [Related]
29. Distinct effects of Hoxa2 overexpression in cranial neural crest populations reveal that the mammalian hyomandibular-ceratohyal boundary maps within the styloid process.
Kitazawa T; Fujisawa K; Narboux-Nême N; Arima Y; Kawamura Y; Inoue T; Wada Y; Kohro T; Aburatani H; Kodama T; Kim KS; Sato T; Uchijima Y; Maeda K; Miyagawa-Tomita S; Minoux M; Rijli FM; Levi G; Kurihara Y; Kurihara H
Dev Biol; 2015 Jun; 402(2):162-74. PubMed ID: 25889273
[TBL] [Abstract][Full Text] [Related]
30. Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1.
Ivins S; Lammerts van Beuren K; Roberts C; James C; Lindsay E; Baldini A; Ataliotis P; Scambler PJ
Dev Biol; 2005 Sep; 285(2):554-69. PubMed ID: 16109395
[TBL] [Abstract][Full Text] [Related]
31. Expression of the semaphorins Sema 3D and Sema 3F in the developing parathyroid and thymus.
Takahashi K; Ishida M; Hirokawa K; Takahashi H
Dev Dyn; 2008 Jun; 237(6):1699-708. PubMed ID: 18489001
[TBL] [Abstract][Full Text] [Related]
32. HOXA3 functions as the on-off switch to regulate the development of hESC-derived third pharyngeal pouch endoderm through EPHB2-mediated Wnt pathway.
Fu Y; Zhang X; Wu H; Zhang P; Liu S; Guo T; Shan H; Liang Y; Chen H; Xie J; Duan Y
Front Immunol; 2023; 14():1258074. PubMed ID: 38259452
[TBL] [Abstract][Full Text] [Related]
33. Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development.
Zhang Z; Huynh T; Baldini A
Development; 2006 Sep; 133(18):3587-95. PubMed ID: 16914493
[TBL] [Abstract][Full Text] [Related]
34. Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome.
Hasten E; Morrow BE
PLoS Genet; 2019 Aug; 15(8):e1008301. PubMed ID: 31412026
[TBL] [Abstract][Full Text] [Related]
35. Hoxa3 and signaling molecules involved in aortic arch patterning and remodeling.
Kameda Y
Cell Tissue Res; 2009 May; 336(2):165-78. PubMed ID: 19290546
[TBL] [Abstract][Full Text] [Related]
36. Disruption of the Hoxa3 homeobox gene results in anomalies of the carotid artery system and the arterial baroreceptors.
Kameda Y; Watari-Goshima N; Nishimaki T; Chisaka O
Cell Tissue Res; 2003 Mar; 311(3):343-52. PubMed ID: 12658442
[TBL] [Abstract][Full Text] [Related]
37. Retinoic acid is required for endodermal pouch morphogenesis and not for pharyngeal endoderm specification.
Kopinke D; Sasine J; Swift J; Stephens WZ; Piotrowski T
Dev Dyn; 2006 Oct; 235(10):2695-709. PubMed ID: 16871626
[TBL] [Abstract][Full Text] [Related]
38. Notch and Hedgehog in the thymus/parathyroid common primordium: Crosstalk in organ formation.
Figueiredo M; Silva JC; Santos AS; Proa V; Alcobia I; Zilhão R; Cidadão A; Neves H
Dev Biol; 2016 Oct; 418(2):268-82. PubMed ID: 27544844
[TBL] [Abstract][Full Text] [Related]
39. The pharyngeal pouches and clefts: Development, evolution, structure and derivatives.
Grevellec A; Tucker AS
Semin Cell Dev Biol; 2010 May; 21(3):325-32. PubMed ID: 20144910
[TBL] [Abstract][Full Text] [Related]
40. The regional pattern of retinoic acid synthesis by RALDH2 is essential for the development of posterior pharyngeal arches and the enteric nervous system.
Niederreither K; Vermot J; Le Roux I; Schuhbaur B; Chambon P; Dollé P
Development; 2003 Jun; 130(11):2525-34. PubMed ID: 12702665
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]