407 related articles for article (PubMed ID: 16352730)
1. Epicardial retinoid X receptor alpha is required for myocardial growth and coronary artery formation.
Merki E; Zamora M; Raya A; Kawakami Y; Wang J; Zhang X; Burch J; Kubalak SW; Kaliman P; Izpisua Belmonte JC; Chien KR; Ruiz-Lozano P
Proc Natl Acad Sci U S A; 2005 Dec; 102(51):18455-60. PubMed ID: 16352730
[TBL] [Abstract][Full Text] [Related]
2. Analysis of the proepicardium-epicardium transition during the malformation of the RXRalpha-/- epicardium.
Jenkins SJ; Hutson DR; Kubalak SW
Dev Dyn; 2005 Jul; 233(3):1091-101. PubMed ID: 15861408
[TBL] [Abstract][Full Text] [Related]
3. An FGF autocrine loop initiated in second heart field mesoderm regulates morphogenesis at the arterial pole of the heart.
Park EJ; Watanabe Y; Smyth G; Miyagawa-Tomita S; Meyers E; Klingensmith J; Camenisch T; Buckingham M; Moon AM
Development; 2008 Nov; 135(21):3599-610. PubMed ID: 18832392
[TBL] [Abstract][Full Text] [Related]
4. BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium.
Stottmann RW; Choi M; Mishina Y; Meyers EN; Klingensmith J
Development; 2004 May; 131(9):2205-18. PubMed ID: 15073157
[TBL] [Abstract][Full Text] [Related]
5. In vivo and in vitro analysis of the vasculogenic potential of avian proepicardial and epicardial cells.
Guadix JA; Carmona R; Muñoz-Chápuli R; Pérez-Pomares JM
Dev Dyn; 2006 Apr; 235(4):1014-26. PubMed ID: 16456846
[TBL] [Abstract][Full Text] [Related]
6. Frs2alpha-deficiency in cardiac progenitors disrupts a subset of FGF signals required for outflow tract morphogenesis.
Zhang J; Lin Y; Zhang Y; Lan Y; Lin C; Moon AM; Schwartz RJ; Martin JF; Wang F
Development; 2008 Nov; 135(21):3611-22. PubMed ID: 18832393
[TBL] [Abstract][Full Text] [Related]
7. Platelet-derived growth factors in the developing avian heart and maturating coronary vasculature.
Van Den Akker NM; Lie-Venema H; Maas S; Eralp I; DeRuiter MC; Poelmann RE; Gittenberger-De Groot AC
Dev Dyn; 2005 Aug; 233(4):1579-88. PubMed ID: 15973731
[TBL] [Abstract][Full Text] [Related]
8. Common epicardial origin of coronary vascular smooth muscle, perivascular fibroblasts, and intermyocardial fibroblasts in the avian heart.
Dettman RW; Denetclaw W; Ordahl CP; Bristow J
Dev Biol; 1998 Jan; 193(2):169-81. PubMed ID: 9473322
[TBL] [Abstract][Full Text] [Related]
9. FGFR-1 is required by epicardium-derived cells for myocardial invasion and correct coronary vascular lineage differentiation.
Pennisi DJ; Mikawa T
Dev Biol; 2009 Apr; 328(1):148-59. PubMed ID: 19389363
[TBL] [Abstract][Full Text] [Related]
10. The bone morphogenetic protein antagonist noggin regulates mammalian cardiac morphogenesis.
Choi M; Stottmann RW; Yang YP; Meyers EN; Klingensmith J
Circ Res; 2007 Feb; 100(2):220-8. PubMed ID: 17218603
[TBL] [Abstract][Full Text] [Related]
11. Retroviral targeting of FGF and FGFR in cardiomyocytes and coronary vascular cells during heart development.
Mikawa T
Ann N Y Acad Sci; 1995 Mar; 752():506-16. PubMed ID: 7755295
[No Abstract] [Full Text] [Related]
12. Fibroblast growth factors and Hedgehogs: at the heart of the epicardial signaling center.
Lavine KJ; Ornitz DM
Trends Genet; 2008 Jan; 24(1):33-40. PubMed ID: 18054407
[TBL] [Abstract][Full Text] [Related]
13. FOG-2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium.
Tevosian SG; Deconinck AE; Tanaka M; Schinke M; Litovsky SH; Izumo S; Fujiwara Y; Orkin SH
Cell; 2000 Jun; 101(7):729-39. PubMed ID: 10892744
[TBL] [Abstract][Full Text] [Related]
14. Novel tool to suppress cell proliferation in vivo demonstrates that myocardial and coronary vascular growth represent distinct developmental programs.
Lavine KJ; Schmid GJ; Smith CS; Ornitz DM
Dev Dyn; 2008 Mar; 237(3):713-24. PubMed ID: 18297725
[TBL] [Abstract][Full Text] [Related]
15. Fibulin-2 expression marks transformed mesenchymal cells in developing cardiac valves, aortic arch vessels, and coronary vessels.
Tsuda T; Wang H; Timpl R; Chu ML
Dev Dyn; 2001 Sep; 222(1):89-100. PubMed ID: 11507771
[TBL] [Abstract][Full Text] [Related]
16. Epicardial-myocardial signaling directing coronary vasculogenesis.
Olivey HE; Svensson EC
Circ Res; 2010 Mar; 106(5):818-32. PubMed ID: 20299672
[TBL] [Abstract][Full Text] [Related]
17. Tbx5 is required for avian and Mammalian epicardial formation and coronary vasculogenesis.
Diman NY; Brooks G; Kruithof BP; Elemento O; Seidman JG; Seidman CE; Basson CT; Hatcher CJ
Circ Res; 2014 Oct; 115(10):834-44. PubMed ID: 25245104
[TBL] [Abstract][Full Text] [Related]
18. Myocardial heterogeneity in permissiveness for epicardium-derived cells and endothelial precursor cells along the developing heart tube at the onset of coronary vascularization.
Lie-Venema H; Eralp I; Maas S; Gittenberger-De Groot AC; Poelmann RE; DeRuiter MC
Anat Rec A Discov Mol Cell Evol Biol; 2005 Feb; 282(2):120-9. PubMed ID: 15627984
[TBL] [Abstract][Full Text] [Related]
19. Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis.
Feng Y; Chen MH; Moskowitz IP; Mendonza AM; Vidali L; Nakamura F; Kwiatkowski DJ; Walsh CA
Proc Natl Acad Sci U S A; 2006 Dec; 103(52):19836-41. PubMed ID: 17172441
[TBL] [Abstract][Full Text] [Related]
20. Tbx18 function in epicardial development.
Greulich F; Farin HF; Schuster-Gossler K; Kispert A
Cardiovasc Res; 2012 Dec; 96(3):476-83. PubMed ID: 22926762
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
