Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart
暂无分享,去创建一个
Deepak Srivastava | Kazuko Koshiba-Takeuchi | B. Bruneau | D. Srivastava | I. S. Kathiriya | C. Hui | J. Takeuchi | K. Koshiba-Takeuchi | R. Mo | Benoit G Bruneau | Chi-chung Hui | Rong Mo | Jun K Takeuchi | Eric P Arruda | Irfan S Kathiriya | Eric P. Arruda | Kazuko Koshiba-Takeuchi
[1] A. Moorman,et al. Cooperative action of Tbx2 and Nkx2.5 inhibits ANF expression in the atrioventricular canal: implications for cardiac chamber formation. , 2002, Genes & development.
[2] M. Logan. Finger or toe: the molecular basis of limb identity , 2003, Development.
[3] J. Seidman,et al. Connexin 40, a Target of Transcription Factor Tbx5, Patterns Wrist, Digits, and Sternum , 2005, Molecular and Cellular Biology.
[4] C. Minguillon,et al. Tbx5 and Tbx4 are not sufficient to determine limb-specific morphologies but have common roles in initiating limb outgrowth. , 2005, Developmental cell.
[5] C. Tickle,et al. Patterning systems--from one end of the limb to the other. , 2003, Developmental cell.
[6] R. Hennekam,et al. Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum , 2004, Journal of Medical Genetics.
[7] A. Poznanski,et al. Skeletal manifestations of the Holt-Oram syndrome. , 1970, Radiology.
[8] Denis Duboule,et al. A Global Control Region Defines a Chromosomal Regulatory Landscape Containing the HoxD Cluster , 2003, Cell.
[9] Jeffrey L. Wrana,et al. Baf60c is essential for function of BAF chromatin remodelling complexes in heart development , 2004, Nature.
[10] C. St. Hilaire,et al. Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family. , 2002, American journal of human genetics.
[11] Megan F. Cole,et al. Core Transcriptional Regulatory Circuitry in Human Embryonic Stem Cells , 2005, Cell.
[12] Matthew H. Kaufman,et al. The Atlas of Mouse Development , 1992 .
[13] J. Seidman,et al. Transcription factor haploinsufficiency: when half a loaf is not enough. , 2002, The Journal of clinical investigation.
[14] D. Durocher,et al. The cardiac transcription factors Nkx2‐5 and GATA‐4 are mutual cofactors , 1997, The EMBO journal.
[15] C. Tickle,et al. A model for anteroposterior patterning of the vertebrate limb based on sequential long- and short-range Shh signalling and Bmp signalling. , 2000, Development.
[16] Nobuyuki Itoh,et al. Fgf10 is essential for limb and lung formation , 1999, Nature Genetics.
[17] Mugen Liu,et al. Functional Analysis of TBX5 Missense Mutations Associated with Holt-Oram Syndrome* , 2003, The Journal of Biological Chemistry.
[18] A. Joyner,et al. Dynamic Changes in the Response of Cells to Positive Hedgehog Signaling during Mouse Limb Patterning , 2004, Cell.
[19] V. Papaioannou,et al. Loss of Tbx4 blocks hindlimb development and affects vascularization and fusion of the allantois , 2003, Development.
[20] A. Moorman,et al. The transcriptional repressor Tbx3 delineates the developing central conduction system of the heart. , 2004, Cardiovascular research.
[21] W. Reardon,et al. Cloning and expression analysis of SALL4, the murine homologue of the gene mutated in Okihiro syndrome. , 2002, Cytogenetic and genome research.
[22] E. A. Packham,et al. Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome. , 2001, Human molecular genetics.
[23] C. Lanctôt,et al. Hindlimb patterning and mandible development require the Ptx1 gene. , 1999, Development.
[24] T. Ogura,et al. Tbx Genes Specify Posterior Digit Identity through Shh and BMP Signaling. , 2004, Developmental cell.
[25] C. Tabin,et al. Role of Pitx1 upstream of Tbx4 in specification of hindlimb identity. , 1999, Science.
[26] R. Dahn,et al. Interdigital regulation of digit identity and homeotic transformation by modulated BMP signaling. , 2000, Science.
[27] J. Seidman,et al. Tbx5 is required for forelimb bud formation and continued outgrowth , 2003, Development.
[28] S. Shen-Orr,et al. Network motifs in the transcriptional regulation network of Escherichia coli , 2002, Nature Genetics.
[29] P. Beachy,et al. Manifestation of the limb prepattern: limb development in the absence of sonic hedgehog function. , 2001, Developmental biology.
[30] B. Bruneau,et al. TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed , 2004, Current opinion in cardiology.
[31] Yina Li,et al. Shh and Gli3 are dispensable for limb skeleton formation but regulate digit number and identity , 2002, Nature.
[32] J. Schmitt,et al. A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease , 2001, Cell.
[33] W. Reardon,et al. Okihiro syndrome is caused by SALL4 mutations. , 2002, Human molecular genetics.
[34] Rolf Zeller,et al. Progression of Vertebrate Limb Development Through SHH-Mediated Counteraction of GLI3 , 2002, Science.
[35] M. Bamshad,et al. Expressivity of Holt-Oram syndrome is not predicted by TBX5 genotype. , 2003, American journal of human genetics.
[36] Ryozo Nagai,et al. Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation , 2001, Nature Genetics.
[37] Concepción Rodríguez-Esteban,et al. Role of the Bicoid-related homeodomain factor Pitx1 in specifying hindlimb morphogenesis and pituitary development. , 1999, Genes & development.
[38] V. Papaioannou,et al. Evidence of a role for T-☐ genes in the evolution of limb morphogenesis and the specification of forelimb/hindlimb identity , 1996, Mechanisms of Development.
[39] S. Mangan,et al. Structure and function of the feed-forward loop network motif , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[40] R. Newbury-Ecob,et al. Holt-Oram syndrome: a clinical genetic study. , 1996, Journal of medical genetics.
[41] Virginia E. Papaioannou,et al. Mammary gland, limb and yolk sac defects in mice lacking Tbx3, the gene mutated in human ulnar mammary syndrome , 2003, Development.
[42] Rudolf Grosschedl,et al. Tbx5 is essential for forelimb bud initiation following patterning of the limb field in the mouse embryo , 2003, Development.
[43] S. Solomon,et al. The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome) , 1994, The New England journal of medicine.
[44] B. Bruneau. Transcriptional Regulation of Vertebrate Cardiac Morphogenesis , 2002, Circulation research.
[45] W. Reardon,et al. Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy , 2003, Journal of medical genetics.
[46] Jonathan C. Cohen,et al. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5 , 2003, Nature.
[47] C. Tabin,et al. Evidence for an Expansion-Based Temporal Shh Gradient in Specifying Vertebrate Digit Identities , 2004, Cell.