| 1 | EOMES, FOXH1
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| Nodal-dependent mesendoderm specification requires the combinatorial activities of FoxH1 and Eomesodermin.
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| Slagle CE, Aoki T, Burdine RD.
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| PLoS Genet 7(5):e1002072. Epub 2011 May 26.
2011
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| 2 | NODAL, GDF1, TDGF1, FOXH1
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| Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
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| Roessler E, Ouspenskaia MV, Karkera JD, VŽlez JI, Kantipong A, Lacbawan F, Bowers P, Belmont JW, Towbin JA, Goldmuntz E, Feldman B, Muenke M.
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| Am J Hum Genet 83(1):18-29. Epub 2008 Jun 5. 2008
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| 3 | FOXH1, SESN1
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| Sesn1 is a novel gene for left-right asymmetry and mediating nodal signaling.
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| Peeters H, Voz ML, Verschueren K, De Cat B, Pendeville H, Thienpont B, Schellens A, Belmont JW, David G, Van De Ven WJ, Fryns JP, Gewillig M, Huylebroeck D, Peers B, Devriendt K.
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| Hum Mol Genet 15(22):3369-77. Epub 2006 Oct 12.
2006
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| 4 | FOXH1
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| Foxh1 is essential for development of the anterior heart field.
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| von Both I, Silvestri C, Erdemir T, Lickert H, Walls JR, Henkelman RM, Rossant J, Harvey RP, Attisano L, Wrana JL.
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| Dev Cell 7(3):331-45. 2004
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| 5 | FOXH1
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| Characterization of human FAST-1, a TGF beta and activin signal transducer.
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| Zhou S, Zawel L, Lengauer C, Kinzler KW, Vogelstein B.
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| Mol Cell 2(1):121-7 1998
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