209 related articles for article (PubMed ID: 32466118)
1.
Stothard CA; Mazzotta S; Vyas A; Schneider JE; Mohun TJ; Henderson DJ; Phillips HM; Bamforth SD
J Cardiovasc Dev Dis; 2020 May; 7(2):. PubMed ID: 32466118
[TBL] [Abstract][Full Text] [Related]
2.
Phillips HM; Stothard CA; Shaikh Qureshi WM; Kousa AI; Briones-Leon JA; Khasawneh RR; O'Loughlin C; Sanders R; Mazzotta S; Dodds R; Seidel K; Bates T; Nakatomi M; Cockell SJ; Schneider JE; Mohun TJ; Maehr R; Kist R; Peters H; Bamforth SD
Development; 2019 Sep; 146(18):. PubMed ID: 31444215
[TBL] [Abstract][Full Text] [Related]
3. Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype.
Khasawneh RR; Kist R; Queen R; Hussain R; Coxhead J; Schneider JE; Mohun TJ; Zaffran S; Peters H; Phillips HM; Bamforth SD
BMC Dev Biol; 2021 Oct; 21(1):14. PubMed ID: 34615475
[TBL] [Abstract][Full Text] [Related]
4. Loss of Gbx2 results in neural crest cell patterning and pharyngeal arch artery defects in the mouse embryo.
Byrd NA; Meyers EN
Dev Biol; 2005 Aug; 284(1):233-45. PubMed ID: 15996652
[TBL] [Abstract][Full Text] [Related]
5. Pharyngeal epithelial deletion of Tbx1 causes caudal pharyngeal arch defect but not cardiac conotruncal anomaly.
Wei L; Wang W; Yang J; Huang X; Baldini A; Zhang Z
Biochem Biophys Res Commun; 2020 Dec; 533(4):1315-1322. PubMed ID: 33066956
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations.
Arnold JS; Werling U; Braunstein EM; Liao J; Nowotschin S; Edelmann W; Hebert JM; Morrow BE
Development; 2006 Mar; 133(5):977-87. PubMed ID: 16452092
[TBL] [Abstract][Full Text] [Related]
9. Ripply3, a Tbx1 repressor, is required for development of the pharyngeal apparatus and its derivatives in mice.
Okubo T; Kawamura A; Takahashi J; Yagi H; Morishima M; Matsuoka R; Takada S
Development; 2011 Jan; 138(2):339-48. PubMed ID: 21177346
[TBL] [Abstract][Full Text] [Related]
10. p53 Suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome.
Caprio C; Baldini A
Proc Natl Acad Sci U S A; 2014 Sep; 111(37):13385-90. PubMed ID: 25197075
[TBL] [Abstract][Full Text] [Related]
11. An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.
Frank DU; Fotheringham LK; Brewer JA; Muglia LJ; Tristani-Firouzi M; Capecchi MR; Moon AM
Development; 2002 Oct; 129(19):4591-603. PubMed ID: 12223415
[TBL] [Abstract][Full Text] [Related]
12. Ablation of specific expression domains reveals discrete functions of ectoderm- and endoderm-derived FGF8 during cardiovascular and pharyngeal development.
Macatee TL; Hammond BP; Arenkiel BR; Francis L; Frank DU; Moon AM
Development; 2003 Dec; 130(25):6361-74. PubMed ID: 14623825
[TBL] [Abstract][Full Text] [Related]
13. Retinoid signaling is essential for patterning the endoderm of the third and fourth pharyngeal arches.
Wendling O; Dennefeld C; Chambon P; Mark M
Development; 2000 Apr; 127(8):1553-62. PubMed ID: 10725232
[TBL] [Abstract][Full Text] [Related]
14. A genetic link between Tbx1 and fibroblast growth factor signaling.
Vitelli F; Taddei I; Morishima M; Meyers EN; Lindsay EA; Baldini A
Development; 2002 Oct; 129(19):4605-11. PubMed ID: 12223416
[TBL] [Abstract][Full Text] [Related]
15. Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development.
Zhang Z; Cerrato F; Xu H; Vitelli F; Morishima M; Vincentz J; Furuta Y; Ma L; Martin JF; Baldini A; Lindsay E
Development; 2005 Dec; 132(23):5307-15. PubMed ID: 16284121
[TBL] [Abstract][Full Text] [Related]
16. Pharyngeal arch artery defects and lethal malformations of the aortic arch and its branches in mice deficient for the Hrt1/Hey1 transcription factor.
Fujita M; Sakabe M; Ioka T; Watanabe Y; Kinugasa-Katayama Y; Tsuchihashi T; Utset MF; Yamagishi H; Nakagawa O
Mech Dev; 2016 Feb; 139():65-73. PubMed ID: 26577899
[TBL] [Abstract][Full Text] [Related]
17. Expression of avian Pax1 and Pax9 is intrinsically regulated in the pharyngeal endoderm, but depends on environmental influences in the paraxial mesoderm.
Müller TS; Ebensperger C; Neubüser A; Koseki H; Balling R; Christ B; Wilting J
Dev Biol; 1996 Sep; 178(2):403-17. PubMed ID: 8812138
[TBL] [Abstract][Full Text] [Related]
18. Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm.
Calmont A; Ivins S; Van Bueren KL; Papangeli I; Kyriakopoulou V; Andrews WD; Martin JF; Moon AM; Illingworth EA; Basson MA; Scambler PJ
Development; 2009 Sep; 136(18):3173-83. PubMed ID: 19700621
[TBL] [Abstract][Full Text] [Related]
19. Morphogenesis of the Mammalian Aortic Arch Arteries.
Anderson RH; Bamforth SD
Front Cell Dev Biol; 2022; 10():892900. PubMed ID: 35620058
[TBL] [Abstract][Full Text] [Related]
20. Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome.
van Bueren KL; Papangeli I; Rochais F; Pearce K; Roberts C; Calmont A; Szumska D; Kelly RG; Bhattacharya S; Scambler PJ
Dev Biol; 2010 Apr; 340(2):369-80. PubMed ID: 20122914
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
