168 related articles for article (PubMed ID: 23613216)
1. Development of the human aortic arch system captured in an interactive three-dimensional reference model.
Rana MS; Sizarov A; Christoffels VM; Moorman AF
Am J Med Genet A; 2014 Jun; 164A(6):1372-83. PubMed ID: 23613216
[TBL] [Abstract][Full Text] [Related]
2. Inactivation of Bmp4 from the Tbx1 expression domain causes abnormal pharyngeal arch artery and cardiac outflow tract remodeling.
Nie X; Brown CB; Wang Q; Jiao K
Cells Tissues Organs; 2011; 193(6):393-403. PubMed ID: 21123999
[TBL] [Abstract][Full Text] [Related]
3.
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]
4. Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome.
Ryckebüsch L; Bertrand N; Mesbah K; Bajolle F; Niederreither K; Kelly RG; Zaffran S
Circ Res; 2010 Mar; 106(4):686-94. PubMed ID: 20110535
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Prdm1 functions in the mesoderm of the second heart field, where it interacts genetically with Tbx1, during outflow tract morphogenesis in the mouse embryo.
Vincent SD; Mayeuf-Louchart A; Watanabe Y; Brzezinski JA; Miyagawa-Tomita S; Kelly RG; Buckingham M
Hum Mol Genet; 2014 Oct; 23(19):5087-101. PubMed ID: 24821700
[TBL] [Abstract][Full Text] [Related]
7. Clarification of the identity of the mammalian fifth pharyngeal arch artery.
Bamforth SD; Chaudhry B; Bennett M; Wilson R; Mohun TJ; Van Mierop LH; Henderson DJ; Anderson RH
Clin Anat; 2013 Mar; 26(2):173-82. PubMed ID: 22623372
[TBL] [Abstract][Full Text] [Related]
8. The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis.
Kelly RG; Jerome-Majewska LA; Papaioannou VE
Hum Mol Genet; 2004 Nov; 13(22):2829-40. PubMed ID: 15385444
[TBL] [Abstract][Full Text] [Related]
9. Tbx1 genetically interacts with the transforming growth factor-β/bone morphogenetic protein inhibitor Smad7 during great vessel remodeling.
Papangeli I; Scambler PJ
Circ Res; 2013 Jan; 112(1):90-102. PubMed ID: 23011393
[TBL] [Abstract][Full Text] [Related]
10. Identification of a Tbx1/Tbx2/Tbx3 genetic pathway governing pharyngeal and arterial pole morphogenesis.
Mesbah K; Rana MS; Francou A; van Duijvenboden K; Papaioannou VE; Moorman AF; Kelly RG; Christoffels VM
Hum Mol Genet; 2012 Mar; 21(6):1217-29. PubMed ID: 22116936
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways.
Vitelli F; Morishima M; Taddei I; Lindsay EA; Baldini A
Hum Mol Genet; 2002 Apr; 11(8):915-22. PubMed ID: 11971873
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis.
Morishima M; Yanagisawa H; Yanagisawa M; Baldini A
Dev Dyn; 2003 Sep; 228(1):95-104. PubMed ID: 12950083
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Abnormal patterning of the aortic arch arteries does not evoke cardiac malformations.
Kirby ML; Hunt P; Wallis K; Thorogood P
Dev Dyn; 1997 Jan; 208(1):34-47. PubMed ID: 8989519
[TBL] [Abstract][Full Text] [Related]
17. 22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development.
Scambler PJ
Pediatr Cardiol; 2010 Apr; 31(3):378-90. PubMed ID: 20054531
[TBL] [Abstract][Full Text] [Related]
18. Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
Lindsay EA; Vitelli F; Su H; Morishima M; Huynh T; Pramparo T; Jurecic V; Ogunrinu G; Sutherland HF; Scambler PJ; Bradley A; Baldini A
Nature; 2001 Mar; 410(6824):97-101. PubMed ID: 11242049
[TBL] [Abstract][Full Text] [Related]
19. Loss of CXCL12/CXCR4 signalling impacts several aspects of cardiovascular development but does not exacerbate Tbx1 haploinsufficiency.
Page M; Ridge L; Gold Diaz D; Tsogbayar T; Scambler PJ; Ivins S
PLoS One; 2018; 13(11):e0207251. PubMed ID: 30408103
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]