Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 152

Similar articles for PubMed (Select 16720879)


Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling.

Park EJ, Ogden LA, Talbot A, Evans S, Cai CL, Black BL, Frank DU, Moon AM.

Development. 2006 Jun;133(12):2419-33.


FGF8 coordinates tissue elongation and cell epithelialization during early kidney tubulogenesis.

Atsuta Y, Takahashi Y.

Development. 2015 Jul 1;142(13):2329-37. doi: 10.1242/dev.122408.


Impaired development of left anterior heart field by ectopic retinoic acid causes transposition of the great arteries.

Narematsu M, Kamimura T, Yamagishi T, Fukui M, Nakajima Y.

J Am Heart Assoc. 2015 Apr 30;4(5). pii: e001889. doi: 10.1161/JAHA.115.001889.


Numb family proteins: novel players in cardiac morphogenesis and cardiac progenitor cell differentiation.

Wu M, Li J.

Biomol Concepts. 2015 Apr;6(2):137-48. doi: 10.1515/bmc-2015-0003.


Dual developmental role of transcriptional regulator Ets1 in Xenopus cardiac neural crest vs. heart mesoderm.

Nie S, Bronner ME.

Cardiovasc Res. 2015 Apr 1;106(1):67-75. doi: 10.1093/cvr/cvv043. Epub 2015 Feb 17.


Galnt1 is required for normal heart valve development and cardiac function.

Tian E, Stevens SR, Guan Y, Springer DA, Anderson SA, Starost MF, Patel V, Ten Hagen KG, Tabak LA.

PLoS One. 2015 Jan 23;10(1):e0115861. doi: 10.1371/journal.pone.0115861. eCollection 2015.


Vangl2-regulated polarisation of second heart field-derived cells is required for outflow tract lengthening during cardiac development.

Ramsbottom SA, Sharma V, Rhee HJ, Eley L, Phillips HM, Rigby HF, Dean C, Chaudhry B, Henderson DJ.

PLoS Genet. 2014 Dec 18;10(12):e1004871. doi: 10.1371/journal.pgen.1004871. eCollection 2014 Dec.


TBX1 regulates epithelial polarity and dynamic basal filopodia in the second heart field.

Francou A, Saint-Michel E, Mesbah K, Kelly RG.

Development. 2014 Nov;141(22):4320-31. doi: 10.1242/dev.115022.


Arid3b is essential for second heart field cell deployment and heart patterning.

Uribe V, Badía-Careaga C, Casanova JC, Domínguez JN, de la Pompa JL, Sanz-Ezquerro JJ.

Development. 2014 Nov;141(21):4168-81. doi: 10.1242/dev.109918.


Multiple roles for HOXA3 in regulating thymus and parathyroid differentiation and morphogenesis in mouse.

Chojnowski JL, Masuda K, Trau HA, Thomas K, Capecchi M, Manley NR.

Development. 2014 Oct;141(19):3697-708. doi: 10.1242/dev.110833. Epub 2014 Sep 5.


Simulating tissue morphogenesis and signaling.

Iber D, Tanaka S, Fried P, Germann P, Menshykau D.

Methods Mol Biol. 2015;1189:323-38. doi: 10.1007/978-1-4939-1164-6_21.


Tbx1 controls the morphogenesis of pharyngeal pouch epithelia through mesodermal Wnt11r and Fgf8a.

Choe CP, Crump JG.

Development. 2014 Sep;141(18):3583-93. doi: 10.1242/dev.111740. Epub 2014 Aug 19.


Islet is a key determinant of ascidian palp morphogenesis.

Wagner E, Stolfi A, Gi Choi Y, Levine M.

Development. 2014 Aug;141(15):3084-92. doi: 10.1242/dev.110684. Epub 2014 Jul 3.


The impact of flow-induced forces on the morphogenesis of the outflow tract.

Biechler SV, Junor L, Evans AN, Eberth JF, Price RL, Potts JD, Yost MJ, Goodwin RL.

Front Physiol. 2014 Jun 17;5:225. doi: 10.3389/fphys.2014.00225. eCollection 2014.


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 4th, Miyagawa-Tomita S, Kelly RG, Buckingham M.

Hum Mol Genet. 2014 Oct 1;23(19):5087-101. doi: 10.1093/hmg/ddu232. Epub 2014 May 12.


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. doi: 10.1002/dvdy.24147. Epub 2014 Jun 12.


Pulmonary endoderm, second heart field and the morphogenesis of distal outflow tract in mouse embryonic heart.

Liang S, Li HC, Wang YX, Wu SS, Cai YJ, Cui HL, Yang YP, Ya J.

Dev Growth Differ. 2014 May;56(4):276-92. doi: 10.1111/dgd.12129. Epub 2014 Apr 3.


AcvR1-mediated BMP signaling in second heart field is required for arterial pole development: implications for myocardial differentiation and regional identity.

Thomas PS, Rajderkar S, Lane J, Mishina Y, Kaartinen V.

Dev Biol. 2014 Jun 15;390(2):191-207. doi: 10.1016/j.ydbio.2014.03.008. Epub 2014 Mar 27.


Mesodermal Nkx2.5 is necessary and sufficient for early second heart field development.

Zhang L, Nomura-Kitabayashi A, Sultana N, Cai W, Cai X, Moon AM, Cai CL.

Dev Biol. 2014 Jun 1;390(1):68-79. doi: 10.1016/j.ydbio.2014.02.023. Epub 2014 Mar 5.


Endocytosis of Fgf8 is a double-stage process and regulates spreading and signaling.

Rengarajan C, Matzke A, Reiner L, Orian-Rousseau V, Scholpp S.

PLoS One. 2014 Jan 20;9(1):e86373. doi: 10.1371/journal.pone.0086373. eCollection 2014.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk