Cardiovascular development: towards biomedical applicability
暂无分享,去创建一个
[1] Kazuko Koshiba-Takeuchi,et al. Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesis. , 2006, Developmental biology.
[2] L. Perrin,et al. Control of Cardiac Rhythm by ORK1, a Drosophila Two-Pore Domain Potassium Channel , 2006, Current Biology.
[3] H. Simon,et al. LMP4 regulates Tbx5 protein subcellular localization and activity , 2006, The Journal of cell biology.
[4] B. Bilican,et al. Cell cycle regulation of the T-box transcription factor tbx2. , 2006, Experimental cell research.
[5] F. Vitelli,et al. Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants. , 2006, Developmental biology.
[6] F. Conlon,et al. TBX5 is required for embryonic cardiac cell cycle progression , 2006, Development.
[7] D. Srivastava,et al. Potential of stem-cell-based therapies for heart disease , 2006, Nature.
[8] A. Moorman,et al. Formation of the Venous Pole of the Heart From an Nkx2–5–Negative Precursor Population Requires Tbx18 , 2006, Circulation research.
[9] Roger M. Ilagan,et al. Fgf8 is required for anterior heart field development , 2006, Development.
[10] A. Moon,et al. Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling , 2006, Development.
[11] B. Morrow,et al. Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field , 2006, Development.
[12] Christine L Mummery,et al. Isl1Cre reveals a common Bmp pathway in heart and limb development , 2006, Development.
[13] D. Srivastava,et al. Tbx1 is regulated by forkhead proteins in the secondary heart field † , 2006, Developmental dynamics : an official publication of the American Association of Anatomists.
[14] G. Merlo,et al. Novel TBX3 mutation data in families with ulnar-mammary syndrome indicate a genotype-phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects. , 2006, European journal of medical genetics.
[15] Deepak Srivastava,et al. Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart , 2006, Nature Genetics.
[16] R. Schwartz,et al. Bmp2 is essential for cardiac cushion epithelial-mesenchymal transition and myocardial patterning , 2005, Development.
[17] E. Olson,et al. A WW domain protein TAZ is a critical coactivator for TBX5, a transcription factor implicated in Holt-Oram syndrome. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[18] R. Harvey,et al. T-box transcription factors and their roles in regulatory hierarchies in the developing heart , 2005, Development.
[19] V. Papaioannou,et al. T-box genes in vertebrate development. , 2005, Annual review of genetics.
[20] M. Buckingham,et al. Building the mammalian heart from two sources of myocardial cells , 2005, Nature Reviews Genetics.
[21] I. Komuro,et al. Cardiac transcription factor Csx/Nkx2-5: Its role in cardiac development and diseases. , 2005, Pharmacology & therapeutics.
[22] A. Kispert,et al. Tbx20 is essential for cardiac chamber differentiation and repression of Tbx2 , 2005, Development.
[23] A. Baldini. Dissecting contiguous gene defects: TBX1. , 2005, Current opinion in genetics & development.
[24] M. Rosenfeld,et al. T-box genes coordinate regional rates of proliferation and regional specification during cardiogenesis , 2005, Development.
[25] B. Bruneau,et al. Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development , 2005, Development.
[26] Milena B. Furtado,et al. Murine T-box transcription factor Tbx20 acts as a repressor during heart development, and is essential for adult heart integrity, function and adaptation , 2005, Development.
[27] B. Bruneau,et al. Serum Response Factor, an Enriched Cardiac Mesoderm Obligatory Factor, Is a Downstream Gene Target for Tbx Genes* , 2005, Journal of Biological Chemistry.
[28] Keith W. Vance,et al. Tbx2 is overexpressed and plays an important role in maintaining proliferation and suppression of senescence in melanomas. , 2005, Cancer research.
[29] Satoru Takahashi,et al. Tbx3 expression is related to apoptosis and cell proliferation in rat bladder both hyperplastic epithelial cells and carcinoma cells. , 2005, Cancer letters.
[30] Arnold Munnich,et al. Mutation in myosin heavy chain 6 causes atrial septal defect , 2005, Nature Genetics.
[31] R. Kelly. Molecular inroads into the anterior heart field. , 2005, Trends in cardiovascular medicine.
[32] F. Conlon,et al. Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis , 2005, Development.
[33] K. Yutzey,et al. T‐box genes and heart development: Putting the “T” in heart , 2005, Developmental dynamics : an official publication of the American Association of Anatomists.
[34] Robert H. Anderson,et al. Reconstruction of the Patterns of Gene Expression in the Developing Mouse Heart Reveals an Architectural Arrangement That Facilitates the Understanding of Atrial Malformations and Arrhythmias , 2004, Circulation research.
[35] R. Bodmer,et al. Insulin regulation of heart function in aging fruit flies , 2004, Nature Genetics.
[36] Jeffrey L. Wrana,et al. Baf60c is essential for function of BAF chromatin remodelling complexes in heart development , 2004, Nature.
[37] D. Srivastava,et al. Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors , 2004, Development.
[38] A. Moorman,et al. Architectural plan for the heart: early patterning and delineation of the chambers and the nodes. , 2004, Trends in cardiovascular medicine.
[39] L. Silver,et al. Tbx2 is essential for patterning the atrioventricular canal and for morphogenesis of the outflow tract during heart development , 2004, Development.
[40] H. Simon,et al. Tbx5 and Tbx4 transcription factors interact with a new chicken PDZ-LIM protein in limb and heart development. , 2004, Developmental biology.
[41] J. Seidman,et al. The T-Box transcription factor Tbx5 is required for the patterning and maturation of the murine cardiac conduction system , 2004, Development.
[42] Joe C. Adams,et al. Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage. , 2004, Human molecular genetics.
[43] B. Bruneau,et al. Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract , 2004, Development.
[44] A. Moorman,et al. The transcriptional repressor Tbx3 delineates the developing central conduction system of the heart. , 2004, Cardiovascular research.
[45] A. Kispert,et al. The T-box transcription factor Tbx18 maintains the separation of anterior and posterior somite compartments. , 2004, Genes & development.
[46] B. Bruneau,et al. TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed , 2004, Current opinion in cardiology.
[47] K. Yutzey,et al. Differential Expression and Function of Tbx5 and Tbx20 in Cardiac Development* , 2004, Journal of Biological Chemistry.
[48] W. Giles,et al. Nkx2-5 Pathways and Congenital Heart Disease Loss of Ventricular Myocyte Lineage Specification Leads to Progressive Cardiomyopathy and Complete Heart Block , 2004, Cell.
[49] D. Roden,et al. Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system. , 2004, The Journal of clinical investigation.
[50] A. Moorman,et al. T‐box transcription factor Tbx2 represses differentiation and formation of the cardiac chambers , 2004, Developmental dynamics : an official publication of the American Association of Anatomists.
[51] F. Couch,et al. The Role of Tbx2 and Tbx3 in Mammary Development and Tumorigenesis , 2004, Journal of Mammary Gland Biology and Neoplasia.
[52] J. Epstein,et al. Cre-mediated excision of Fgf8 in the Tbx1 expression domain reveals a critical role for Fgf8 in cardiovascular development in the mouse. , 2004, Developmental biology.
[53] Keith W. Vance,et al. Tbx2 Directly Represses the Expression of the p21WAF1 Cyclin-Dependent Kinase Inhibitor , 2004, Cancer Research.
[54] Jonathan A. Epstein,et al. Development Gone Awry: Congenital Heart Disease , 2004, Circulation research.
[55] M. Kerszberg,et al. Oriented clonal cell growth in the developing mouse myocardium underlies cardiac morphogenesis , 2004, The Journal of cell biology.
[56] Y. Saijoh,et al. Tbx5 specifies the left/right ventricles and ventricular septum position during cardiogenesis , 2003, Development.
[57] Yunqing Shi,et al. Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart. , 2003, Developmental cell.
[58] Mauro W. Costa,et al. Cardiac T-box factor Tbx20 directly interacts with Nkx2-5, GATA4, and GATA5 in regulation of gene expression in the developing heart. , 2003, Developmental biology.
[59] A. Moorman,et al. Cardiac chamber formation: development, genes, and evolution. , 2003, Physiological reviews.
[60] Jonathan C. Cohen,et al. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5 , 2003, Nature.
[61] T. Ogura,et al. Tbx5 and Tbx4 trigger limb initiation through activation of the Wnt/Fgf signaling cascade , 2003, Development.
[62] Thomas Brand,et al. Heart development: molecular insights into cardiac specification and early morphogenesis. , 2003, Developmental biology.
[63] A. Moorman,et al. Regulatory modules in the developing heart. , 2003, Cardiovascular research.
[64] Mugen Liu,et al. Functional Analysis of TBX5 Missense Mutations Associated with Holt-Oram Syndrome* , 2003, The Journal of Biological Chemistry.
[65] D. Srivastava,et al. Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer. , 2003, Genes & development.
[66] M. Capecchi,et al. An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome. , 2002, Development.
[67] K. Yamamura,et al. Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse. , 2002, Development.
[68] F. Vitelli,et al. A genetic link between Tbx1 and fibroblast growth factor signaling. , 2002, Development.
[69] M. van Lohuizen,et al. The T-box Repressors TBX2 and TBX3Specifically Regulate the Tumor Suppressor Genep14 ARF via a Variant T-site in the Initiator* , 2002, The Journal of Biological Chemistry.
[70] R. Harvey. Organogenesis: Patterning the vertebrate heart , 2002, Nature Reviews Genetics.
[71] A. Meyer,et al. Cloning of zebrafish T-box genes tbx15 and tbx18 and their expression during embryonic development , 2002, Mechanisms of Development.
[72] P. Hurlin,et al. Tbx3 impinges on the p53 pathway to suppress apoptosis, facilitate cell transformation and block myogenic differentiation , 2002, Oncogene.
[73] 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.
[74] M. Buckingham,et al. The anterior heart-forming field: voyage to the arterial pole of the heart. , 2002, Trends in genetics : TIG.
[75] B. Bruneau. Transcriptional Regulation of Vertebrate Cardiac Morphogenesis , 2002, Circulation research.
[76] M. MacDonald,et al. TBX-3, the Gene Mutated in Ulnar-Mammary Syndrome, Is a Negative Regulator of p19 ARF and Inhibits Senescence* , 2002, The Journal of Biological Chemistry.
[77] C. Basson,et al. Getting the T-box dose right , 2001, Nature Medicine.
[78] P. Hurlin,et al. A dominant repression domain in Tbx3 mediates transcriptional repression and cell immortalization: relevance to mutations in Tbx3 that cause ulnar-mammary syndrome. , 2001, Human molecular genetics.
[79] 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.
[80] D. Srivastava,et al. Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development. , 2001, Developmental biology.
[81] Ryozo Nagai,et al. Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation , 2001, Nature Genetics.
[82] P. Chambon,et al. Embryonic retinoic acid synthesis is essential for heart morphogenesis in the mouse. , 2001, Development.
[83] V. Papaioannou,et al. DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1 , 2001, Nature Genetics.
[84] Birgit Funke,et al. TBX1 Is Responsible for Cardiovascular Defects in Velo-Cardio-Facial/DiGeorge Syndrome , 2001, Cell.
[85] T. Mikawa,et al. TBX5 transcription factor regulates cell proliferation during cardiogenesis. , 2001, Developmental biology.
[86] A. Kispert,et al. Cloning and expression analysis of the mouse T-box gene Tbx18 , 2001, Mechanisms of Development.
[87] A. Kispert,et al. Cloning and expression analysis of the mouse T-box gene Tbx20 , 2001, Mechanisms of Development.
[88] N. Rosenthal,et al. From the bottom of the heart: anteroposterior decisions in cardiac muscle differentiation. , 2000, Current opinion in cell biology.
[89] G. Eichele,et al. Expression of chick Tbx-2, Tbx-3, and Tbx-5 genes during early heart development: evidence for BMP2 induction of Tbx2. , 2000, Developmental biology.
[90] R. Gronostajski,et al. Differential DNA binding and transcription modulation by three T-box proteins, T, TBX1 and TBX2. , 2000, Gene.
[91] Marc J. van de Vijver,et al. Senescence bypass screen identifies TBX2, which represses Cdkn2a (p19ARF) and is amplified in a subset of human breast cancers , 2000, Nature Genetics.
[92] P. Scambler. The 22q11 deletion syndromes. , 2000, Human molecular genetics.
[93] A. Moorman,et al. Chamber formation and morphogenesis in the developing mammalian heart. , 2000, Developmental biology.
[94] K. Yutzey,et al. Ventricular expression of tbx5 inhibits normal heart chamber development. , 2000, Developmental biology.
[95] Y. Rao,et al. Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[96] J. Seidman,et al. Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome. , 1999, Developmental biology.
[97] Concepción Rodríguez-Esteban,et al. The T-box genes Tbx4 and Tbx5 regulate limb outgrowth and identity , 1999, Nature.
[98] J. Seidman,et al. Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[99] S. Izumo,et al. The cardiac homeobox gene Csx/Nkx2.5 lies genetically upstream of multiple genes essential for heart development. , 1999, Development.
[100] C. R. Goding,et al. Brachyury-Related Transcription Factor Tbx2 and Repression of the Melanocyte-Specific TRP-1 Promoter , 1998, Molecular and Cellular Biology.
[101] J. Seidman,et al. Congenital heart disease caused by mutations in the transcription factor NKX2-5. , 1998, Science.
[102] C. Müller,et al. Crystallographic structure of the T domain–DNA complex of the Brachyury transcription factor , 1997, Nature.
[103] J. Seidman,et al. Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome , 1997, Nature Genetics.
[104] L. Silver,et al. Expression of the T‐box family genes, Tbx1–Tbx5, during early mouse development , 1996, Developmental dynamics : an official publication of the American Association of Anatomists.
[105] L. Silver,et al. Identification, characterization, and localization to Chromosome 17q21-22 of the human TBX2 homolog, member of a conserved developmental gene family , 1995, Mammalian Genome.
[106] B. Beatty,et al. Cloning and mapping of a human gene (TBX2) sharing a highly conserved protein motif with the Drosophila omb gene. , 1995, Genomics.
[107] Ruili Li,et al. Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5. , 1995, Genes & development.
[108] J. Rossant,et al. Defects in heart and lung development in compound heterozygotes for two different targeted mutations at the N-myc locus. , 1993, Development.
[109] R. Bodmer. The gene tinman is required for specification of the heart and visceral muscles in Drosophila. , 1993, Development.
[110] V. Stewart,et al. Embryonic lethality in mice homozygous for a targeted disruption of the N-myc gene. , 1992, Genes & development.
[111] A. Poustka,et al. Cloning of the T gene required in mesoderm formation in the mouse , 1990, Nature.
[112] T. Ogura,et al. Tbx Genes Specify Posterior Digit Identity through Shh and BMP Signaling. , 2004, Developmental cell.
[113] A. Moorman,et al. TBX5 overexpression stimulates differentiation of chamber myocardium in P19Cl6 embryonic carcinoma cells , 2004, Journal of Muscle Research & Cell Motility.
[114] R. Kucherlapati,et al. Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome , 1997, Nature Genetics.
[115] David I. Wilson,et al. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family , 1997, Nature Genetics.