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Results: 1 to 20 of 39

Cited In for PubMed (Select 1996351)

1.

The zebrafish model system in cardiovascular research: A tiny fish with mighty prospects.

Poon KL, Brand T.

Glob Cardiol Sci Pract. 2013 Nov 1;2013(1):9-28. doi: 10.5339/gcsp.2013.4. eCollection 2013. Review. No abstract available.

2.

The chick embryo as an expanding experimental model for cancer and cardiovascular research.

Kain KH, Miller JW, Jones-Paris CR, Thomason RT, Lewis JD, Bader DM, Barnett JV, Zijlstra A.

Dev Dyn. 2014 Feb;243(2):216-28. doi: 10.1002/dvdy.24093. Epub 2013 Dec 19. Review.

3.

Cilia and coordination of signaling networks during heart development.

Koefoed K, Veland IR, Pedersen LB, Larsen LA, Christensen ST.

Organogenesis. 2014 Jan 1;10(1):108-25. doi: 10.4161/org.27483. Epub 2013 Dec 17. Review.

4.

Loss of muscleblind-like 1 promotes invasive mesenchyme formation in endocardial cushions by stimulating autocrine TGFβ3.

LeMasters KE, Blech-Hermoni Y, Stillwagon SJ, Vajda NA, Ladd AN.

BMC Dev Biol. 2012 Aug 6;12:22. doi: 10.1186/1471-213X-12-22.

5.

Nf1 limits epicardial derivative expansion by regulating epithelial to mesenchymal transition and proliferation.

Baek ST, Tallquist MD.

Development. 2012 Jun;139(11):2040-9. doi: 10.1242/dev.074054. Epub 2012 Apr 25.

6.

Importance of myocyte-nonmyocyte interactions in cardiac development and disease.

Tian Y, Morrisey EE.

Circ Res. 2012 Mar 30;110(7):1023-34. doi: 10.1161/CIRCRESAHA.111.243899. Review.

7.

Roles of TGF-β signals in endothelial-mesenchymal transition during cardiac fibrosis.

Yoshimatsu Y, Watabe T.

Int J Inflam. 2011;2011:724080. doi: 10.4061/2011/724080. Epub 2011 Nov 30.

8.

The Sphingosine-1-phospate receptor 1 mediates S1P action during cardiac development.

Poulsen RR, McClaskey CM, Rivkees SA, Wendler CC.

BMC Dev Biol. 2011 Jun 13;11:37. doi: 10.1186/1471-213X-11-37.

9.

Arsenic exposure perturbs epithelial-mesenchymal cell transition and gene expression in a collagen gel assay.

Lencinas A, Broka DM, Konieczka JH, Klewer SE, Antin PB, Camenisch TD, Runyan RB.

Toxicol Sci. 2010 Jul;116(1):273-85. doi: 10.1093/toxsci/kfq086. Epub 2010 Mar 22.

10.

Effect of vascular cadherin knockdown on zebrafish vasculature during development.

Mitchell IC, Brown TS, Terada LS, Amatruda JF, Nwariaku FE.

PLoS One. 2010 Jan 20;5(1):e8807. doi: 10.1371/journal.pone.0008807.

11.
12.

Matrix metalloproteinase 2-integrin alpha(v)beta3 binding is required for mesenchymal cell invasive activity but not epithelial locomotion: a computational time-lapse study.

Rupp PA, Visconti RP, Czirók A, Cheresh DA, Little CD.

Mol Biol Cell. 2008 Dec;19(12):5529-40. doi: 10.1091/mbc.E07-05-0480. Epub 2008 Oct 15.

13.

Signaling via the Tgf-beta type I receptor Alk5 in heart development.

Sridurongrit S, Larsson J, Schwartz R, Ruiz-Lozano P, Kaartinen V.

Dev Biol. 2008 Oct 1;322(1):208-18. doi: 10.1016/j.ydbio.2008.07.038. Epub 2008 Aug 7.

14.

Palatal seam disintegration: to die or not to die? that is no longer the question.

Nawshad A.

Dev Dyn. 2008 Oct;237(10):2643-56. doi: 10.1002/dvdy.21599. Review.

15.
16.

Signals from both sides: Control of cardiac development by the endocardium and epicardium.

Smith TK, Bader DM.

Semin Cell Dev Biol. 2007 Feb;18(1):84-9. Epub 2006 Dec 29. Review.

17.

Atrioventricular cushion transformation is mediated by ALK2 in the developing mouse heart.

Wang J, Sridurongrit S, Dudas M, Thomas P, Nagy A, Schneider MD, Epstein JA, Kaartinen V.

Dev Biol. 2005 Oct 1;286(1):299-310.

18.

Beta-catenin is required for endothelial-mesenchymal transformation during heart cushion development in the mouse.

Liebner S, Cattelino A, Gallini R, Rudini N, Iurlaro M, Piccolo S, Dejana E.

J Cell Biol. 2004 Aug 2;166(3):359-67.

19.
20.

Endocardial cushion and myocardial defects after cardiac myocyte-specific conditional deletion of the bone morphogenetic protein receptor ALK3.

Gaussin V, Van de Putte T, Mishina Y, Hanks MC, Zwijsen A, Huylebroeck D, Behringer RR, Schneider MD.

Proc Natl Acad Sci U S A. 2002 Mar 5;99(5):2878-83. Epub 2002 Feb 19.

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