Essential roles of the winged helix transcription factor MFH-1 in aortic arch patterning and skeletogenesis

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				H. Hayashi, H. Sano, S. Seo, and T. Kume The Foxc2 Transcription Factor Regulates Angiogenesis via Induction of Integrin {beta}3 Expression J. Biol. Chem., August 29, 2008; 283(35): 23791 - 23800. [Abstract] [Full Text] [PDF]

				V. Sachdev, L. A. Matura, S. Sidenko, V. B. Ho, A. E. Arai, D. R. Rosing, and C. A. Bondy Aortic Valve Disease in Turner Syndrome J. Am. Coll. Cardiol., May 13, 2008; 51(19): 1904 - 1909. [Abstract] [Full Text] [PDF]

				K. N. Papanicolaou, Y. Izumiya, and K. Walsh Forkhead Transcription Factors and Cardiovascular Biology Circ. Res., January 4, 2008; 102(1): 16 - 31. [Abstract] [Full Text] [PDF]

				Z. Zhang, F. Cerrato, H. Xu, F. Vitelli, M. Morishima, J. Vincentz, Y. Furuta, L. Ma, J. F. Martin, A. Baldini, et al. Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development Development, December 1, 2005; 132(23): 5307 - 5315. [Abstract] [Full Text] [PDF]

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				M. L. Loscalzo, P. L. Van, V. B. Ho, V. K. Bakalov, D. R. Rosing, C. A. Malone, H. C. Dietz, and C. A. Bondy Association Between Fetal Lymphedema and Congenital Cardiovascular Defects in Turner Syndrome Pediatrics, March 1, 2005; 115(3): 732 - 735. [Abstract] [Full Text] [PDF]

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				D. G.M. Molin, R. E. Poelmann, M. C. DeRuiter, M. Azhar, T. Doetschman, and A. C. Gittenberger-de Groot Transforming Growth Factor {beta}-SMAD2 Signaling Regulates Aortic Arch Innervation and Development Circ. Res., November 26, 2004; 95(11): 1109 - 1117. [Abstract] [Full Text] [PDF]

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				J. Jeong, J. Mao, T. Tenzen, A. H. Kottmann, and A. P. McMahon Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia Genes & Dev., April 15, 2004; 18(8): 937 - 951. [Abstract] [Full Text] [PDF]

				B. M. T. Burgering and R. H. Medema Decisions on life and death: FOXO Forkhead transcription factors are in command when PKB/Akt is off duty J. Leukoc. Biol., June 1, 2003; 73(6): 689 - 701. [Abstract] [Full Text] [PDF]

				B. M. Kriederman, T. L. Myloyde, M. H. Witte, S. L. Dagenais, C. L. Witte, M. Rennels, M. J. Bernas, M. T. Lynch, R. P. Erickson, M. S. Caulder, et al. FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome Hum. Mol. Genet., May 15, 2003; 12(10): 1179 - 1185. [Abstract] [Full Text] [PDF]

				H. Yamagishi, J. Maeda, T. Hu, J. McAnally, S. J. Conway, T. Kume, E. N. Meyers, C. Yamagishi, and D. Srivastava Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer Genes & Dev., January 15, 2003; 17(2): 269 - 281. [Abstract] [Full Text] [PDF]

				M. Ridderstrale, E. Carlsson, M. Klannemark, A. Cederberg, C. Kosters, H. Tornqvist, H. Storgaard, A. Vaag, S. Enerback, and L. Groop FOXC2 mRNA Expression and a 5' Untranslated Region Polymorphism of the Gene Are Associated With Insulin Resistance Diabetes, December 1, 2002; 51(12): 3554 - 3560. [Abstract] [Full Text] [PDF]

				D. G.M Molin, M. C DeRuiter, L. J Wisse, M. Azhar, T. Doetschman, R. E Poelmann, and A. C Gittenberger-de Groot Altered apoptosis pattern during pharyngeal arch artery remodelling is associated with aortic arch malformations in Tgf{beta}2 knock-out mice Cardiovasc Res, November 1, 2002; 56(2): 312 - 322. [Abstract] [Full Text] [PDF]

				M. K. Dahle, L. M. Gronning, A. Cederberg, H. K. Blomhoff, N. Miura, S. Enerback, K. A. Tasken, and K. Tasken Mechanisms of FOXC2- and FOXD1-mediated Regulation of the RIalpha Subunit of cAMP-dependent Protein Kinase Include Release of Transcriptional Repression and Activation by Protein Kinase Balpha and cAMP J. Biol. Chem., June 14, 2002; 277(25): 22902 - 22908. [Abstract] [Full Text] [PDF]

				P. Valet, G. Tavernier, I. Castan-Laurell, J. S. Saulnier-Blache, and D. Langin Understanding adipose tissue development from transgenic animal models J. Lipid Res., June 1, 2002; 43(6): 835 - 860. [Abstract] [Full Text] [PDF]

				M. Ormestad, A. Blixt, A. Churchill, T. Martinsson, S. Enerback, and P. Carlsson Foxe3 Haploinsufficiency in Mice: A Model for Peters' Anomaly Invest. Ophthalmol. Vis. Sci., May 1, 2002; 43(5): 1350 - 1357. [Abstract] [Full Text] [PDF]

				C. Liu, W. Liu, J. Palie, M. F. Lu, N. A. Brown, and J. F. Martin Pitx2c patterns anterior myocardium and aortic arch vessels and is required for local cell movement into atrioventricular cushions Development, January 11, 2002; 129(21): 5081 - 5091. [Abstract] [Full Text] [PDF]

				D. U. Frank, L. K. Fotheringham, J. A. Brewer, L. J. Muglia, M. Tristani-Firouzi, M. R. Capecchi, and A. M. Moon An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome Development, January 10, 2002; 129(19): 4591 - 4603. [Abstract] [Full Text] [PDF]

				J. Dupont, J. Khan, B.-H. Qu, P. Metzler, L. Helman, and D. LeRoith Insulin and IGF-1 Induce Different Patterns of Gene Expression in Mouse Fibroblast NIH-3T3 Cells: Identification by cDNA Microarray Analysis Endocrinology, November 1, 2001; 142(11): 4969 - 4975. [Abstract] [Full Text] [PDF]

				R. P Erickson, S. L Dagenais, M. S Caulder, C. A Downs, G. Herman, M. C Jones, W. S Kerstjens-Frederikse, A. C Lidral, M. McDonald, C. C Nelson, et al. Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations J. Med. Genet., November 1, 2001; 38(11): 761 - 766. [Abstract] [Full Text] [PDF]

				T. Kume, H. Jiang, J. M. Topczewska, and B. L.M. Hogan The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis Genes & Dev., September 15, 2001; 15(18): 2470 - 2482. [Abstract] [Full Text] [PDF]

				C. B. Brown, L. Feiner, M.-M. Lu, J. Li, X. Ma, A. L. Webber, L. Jia, J. A. Raper, and J. A. Epstein PlexinA2 and semaphorin signaling during cardiac neural crest development Development, August 15, 2001; 128(16): 3071 - 3080. [Abstract] [Full Text] [PDF]

				S. Ausoni and S. Sartore Cell Lineages and Tissue Boundaries in Cardiac Arterial and Venous Poles : Developmental Patterns, Animal Models, and Implications for Congenital Vascular Diseases Arterioscler Thromb Vasc Biol, March 1, 2001; 21(3): 312 - 320. [Abstract] [Full Text] [PDF]

				A. Calmont, K. Reichwald, P. Ronco, and J. Rossert Identification of a Short cis-Acting Element in the Human Vasopressin Type 2 Receptor Gene Which Confers High-Level Expression of a Reporter Gene Specifically in Collecting Duct Cells Mol. Endocrinol., October 1, 2000; 14(10): 1682 - 1695. [Abstract] [Full Text]

				C. Perez-Sanchez, M. A. Gomez-Ferreria, C. A. de la Fuente, B. Granadino, G. Velasco, A. Esteban-Gamboa, and J. Rey-Campos FHX, a Novel Fork Head Factor with a Dual DNA Binding Specificity J. Biol. Chem., April 21, 2000; 275(17): 12909 - 12916. [Abstract] [Full Text] [PDF]

				R. S. Smith, A. Zabaleta, T. Kume, O. V. Savinova, S. H. Kidson, J. E. Martin, D. Y. Nishimura, W. L. M. Alward, B. L. M. Hogan, and S. W. M. John Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development Hum. Mol. Genet., April 12, 2000; 9(7): 1021 - 1032. [Abstract] [Full Text] [PDF]