| scholarly article | Q13442814 |
| P50 | author | David M. Ornitz | Q37386214 |
| Andrew C White | Q61118786 | ||
| P2093 | author name string | Chi-chung Hui | |
| Kyunghee Choi | |||
| Fanxin Long | |||
| Kory J Lavine | |||
| Craig S Smith | |||
| Changwon Park | |||
| P2860 | cites work | YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis | Q22009123 |
| Proper coronary vascular development and heart morphogenesis depend on interaction of GATA-4 with FOG cofactors | Q24602111 | ||
| Essential function of p300 acetyltransferase activity in heart, lung and small intestine formation | Q24672302 | ||
| Generalized lacZ expression with the ROSA26 Cre reporter strain | Q27860837 | ||
| Flt-1 lacking the tyrosine kinase domain is sufficient for normal development and angiogenesis in mice | Q28504776 | ||
| FGF9 and SHH signaling coordinate lung growth and development through regulation of distinct mesenchymal domains | Q28505242 | ||
| Cell adhesion events mediated by alpha 4 integrins are essential in placental and cardiac development | Q28507437 | ||
| SOX7 and GATA-4 are competitive activators of Fgf-3 transcription | Q28508654 | ||
| FOG-2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium | Q28587401 | ||
| Hedgehog signaling is essential for endothelial tube formation during vasculogenesis | Q28587747 | ||
| Mice lacking the vascular endothelial growth factor-B gene (Vegfb) have smaller hearts, dysfunctional coronary vasculature, and impaired recovery from cardiac ischemia | Q28589545 | ||
| Defective development of the embryonic and extraembryonic circulatory systems in vascular cell adhesion molecule (VCAM-1) deficient mice | Q28590782 | ||
| Endocardial and epicardial derived FGF signals regulate myocardial proliferation and differentiation in vivo | Q28590848 | ||
| Failure of blood-island formation and vasculogenesis in Flk-1-deficient mice | Q28593600 | ||
| GATA4 is essential for formation of the proepicardium and regulates cardiogenesis | Q28594766 | ||
| Heterozygous embryonic lethality induced by targeted inactivation of the VEGF gene | Q29547732 | ||
| Molecular characterization of mouse gastric epithelial progenitor cells | Q31117042 | ||
| Tie-1-directed expression of Cre recombinase in endothelial cells of embryoid bodies and transgenic mice | Q31918898 | ||
| A PCR primer bank for quantitative gene expression analysis | Q33447710 | ||
| Multiple roles for the Wilms' tumor suppressor, WT1. | Q33590932 | ||
| Orchestration of angiogenesis and arteriovenous contribution by angiopoietins and vascular endothelial growth factor (VEGF). | Q34032032 | ||
| Epicardial retinoid X receptor alpha is required for myocardial growth and coronary artery formation | Q34234421 | ||
| Cardiac-specific overexpression of fibroblast growth factor-2 protects against myocardial dysfunction and infarction in a murine model of low-flow ischemia | Q34281173 | ||
| Intracoronary basic fibroblast growth factor enhances myocardial collateral perfusion in dogs | Q73453266 | ||
| The morphogen Sonic hedgehog is an indirect angiogenic agent upregulating two families of angiogenic growth factors | Q73954844 | ||
| Intracavernosal injections of vascular endothelial growth factor protects endothelial dependent corpora cavernosal smooth muscle relaxation in the hypercholesterolemic rabbit: a preliminary study | Q74058909 | ||
| Opposite effects of FGF and BMP-4 on embryonic blood formation: roles of PV.1 and GATA-2 | Q77222955 | ||
| Smooth muscle cells and fibroblasts of the coronary arteries derive from epithelial-mesenchymal transformation of the epicardium | Q77296275 | ||
| Phase 1/2 placebo-controlled, double-blind, dose-escalating trial of myocardial vascular endothelial growth factor 2 gene transfer by catheter delivery in patients with chronic myocardial ischemia | Q78019724 | ||
| Embryonic development of coronary vasculature in rats: corrosion casting studies | Q78782711 | ||
| Origin of coronary endothelial cells from epicardial mesothelium in avian embryos | Q78810466 | ||
| Neural tissue in ascidian embryos is induced by FGF9/16/20, acting via a combination of maternal GATA and Ets transcription factors | Q79338933 | ||
| Conserved cardiogenic functions of the multitype zinc-finger proteins: U-shaped and FOG-2. | Q34399536 | ||
| The angiopoietins and Tie2/Tek: adding to the complexity of cardiovascular development. | Q34611010 | ||
| Mechanisms of embryonic coronary artery development | Q34641873 | ||
| Development of the coronary vessel system | Q34986182 | ||
| Biological activities of fibroblast growth factor-2 in the adult myocardium | Q35035307 | ||
| Regulation of vascular development by fibroblast growth factors. | Q35173667 | ||
| Coronary vessel development: a unique form of vasculogenesis | Q35549960 | ||
| Therapeutic angiogenesis: a biologic bypass | Q35677534 | ||
| Molecular profiling of angiogenesis markers. | Q35747435 | ||
| Sonic hedgehog-dependent activation of Gli2 is essential for embryonic hair follicle development | Q35963725 | ||
| The biology of vascular endothelial growth factors. | Q36017169 | ||
| Fibroblast Growth Factor-2 (FGF-2) Induces Vascular Endothelial Growth Factor (VEGF) Expression in the Endothelial Cells of Forming Capillaries: An Autocrine Mechanism Contributing to Angiogenesis | Q36256017 | ||
| Retroviral analysis of cardiac morphogenesis: discontinuous formation of coronary vessels | Q37242170 | ||
| Dose-dependent response of FGF-2 for lymphangiogenesis | Q37415307 | ||
| Pharmacological treatment of coronary artery disease with recombinant fibroblast growth factor-2: double-blind, randomized, controlled clinical trial | Q38523342 | ||
| Fibroblast growth factor-2-mediated capillary morphogenesis of endothelial cells requires signals via Flt-1/vascular endothelial growth factor receptor-1: possible involvement of c-Akt | Q40617929 | ||
| Sonic hedgehog induces capillary morphogenesis by endothelial cells through phosphoinositide 3-kinase | Q40679340 | ||
| Epicardial induction of fetal cardiomyocyte proliferation via a retinoic acid-inducible trophic factor | Q40701785 | ||
| The role of insulin-like and basic fibroblast growth factors on ischemic and infarcted myocardium: a mini review | Q40902941 | ||
| Temporally regulated and tissue-specific gene manipulations in the adult and embryonic heart using a tamoxifen-inducible Cre protein | Q43664631 | ||
| Localization of VEGF-B in the mouse embryo suggests a paracrine role of the growth factor in the developing vasculature | Q43826839 | ||
| Angiopoietin-2 is required for postnatal angiogenesis and lymphatic patterning, and only the latter role is rescued by Angiopoietin-1. | Q44166149 | ||
| Erythropoietin and retinoic acid, secreted from the epicardium, are required for cardiac myocyte proliferation | Q44369644 | ||
| A conserved enhancer element that drives FGF4 gene expression in the embryonic myotomes is synergistically activated by GATA and bHLH proteins | Q44926519 | ||
| Sonic hedgehog myocardial gene therapy: tissue repair through transient reconstitution of embryonic signaling | Q45887964 | ||
| Fgf8 signalling from the AER is essential for normal limb development. | Q45967231 | ||
| RXR alpha mutant mice establish a genetic basis for vitamin A signaling in heart morphogenesis. | Q46123728 | ||
| Common Epicardial Origin of Coronary Vascular Smooth Muscle, Perivascular Fibroblasts, and Intermyocardial Fibroblasts in the Avian Heart | Q46186694 | ||
| Evidence for novel fate of Flk1+ progenitor: contribution to muscle lineage | Q52107873 | ||
| Role of VEGF family members and receptors in coronary vessel formation | Q52112918 | ||
| Ptc1 and Ptc2 transcripts provide distinct readouts of Hedgehog signaling activity during chick embryogenesis. | Q52125407 | ||
| Interaction of the TEK and TIE receptor tyrosine kinases during cardiovascular development. | Q52174314 | ||
| Multiple developmental roles of VEGF suggested by a LacZ-tagged allele | Q52175349 | ||
| Pericardial mesoderm generates a population of coronary smooth muscle cells migrating into the heart along with ingrowth of the epicardial organ | Q53678848 | ||
| Intrapericardial basic fibroblast growth factor induces myocardial angiogenesis in a rabbit model of chronic ischemia | Q58976540 | ||
| Functional inhibition of secreted angiopoietin: a novel role for angiopoietin 1 in coronary vessel patterning | Q61204087 | ||
| Histone acetyltransferase p300 promotes the activation of human WT1 promoter and intronic enhancer | Q64378886 | ||
| Endothelial growth factor receptors in human fetal heart. | Q64948158 | ||
| Angiogenic therapy of acute myocardial infarction by intrapericardial injection of basic fibroblast growth factor and heparin sulfate: an experimental study | Q71550675 | ||
| Epicardial outgrowth inhibition leads to compensatory mesothelial outflow tract collar and abnormal cardiac septation and coronary formation | Q73221474 | ||
| P433 | issue | 12 | |
| P921 | main subject | Sonic hedgehog | Q14860215 |
| Fibroblast growth factor receptor 2 | Q14911646 | ||
| Fibroblast growth factor receptor 1 | Q14914262 | ||
| Angiopoietin 2 | Q21981189 | ||
| Fibroblast growth factor 9 | Q21985353 | ||
| Vascular endothelial growth factor A | Q21992409 | ||
| P304 | page(s) | 1651-1666 | |
| P577 | publication date | 2006-06-01 | |
| P1433 | published in | Genes & Development | Q1524533 |
| P1476 | title | Fibroblast growth factor signals regulate a wave of Hedgehog activation that is essential for coronary vascular development | |
| P478 | volume | 20 |
| Q39478832 | A Method for Labeling Vasculature in Embryonic Mice |
| Q43626717 | A glimpse of Cre-mediated controversies in epicardial signalling. |
| Q37032939 | A novel ex vivo culture method for the embryonic mouse heart |
| Q34875955 | Adult mouse epicardium modulates myocardial injury by secreting paracrine factors |
| Q28586566 | Angiogenic factors stimulate tubular branching morphogenesis of sonic hedgehog-deficient lungs |
| Q42001387 | Approaches to augment vascularisation and regeneration of the adult heart via the reactivated epicardium |
| Q33954831 | BMPER-induced BMP signaling promotes coronary artery remodeling |
| Q36354005 | Cardiac gene activation analysis in mammalian non-myoblasic cells by Nkx2-5, Tbx5, Gata4 and Myocd |
| Q36176132 | Cell-based therapy for prevention and reversal of myocardial remodeling |
| Q38337373 | Cellular origin and developmental program of coronary angiogenesis. |
| Q54506625 | Chapter 9. Development of coronary vessels. |
| Q38711945 | Congenital coronary artery anomalies: a bridge from embryology to anatomy and pathophysiology--a position statement of the development, anatomy, and pathology ESC Working Group. |
| Q35541471 | Connecting the coronaries: how the coronary plexus develops and is functionalized |
| Q33909846 | Coronary Artery Development: Progenitor Cells and Differentiation Pathways |
| Q60951774 | Coronary Vasculature in Cardiac Development and Regeneration |
| Q42530831 | Coronary arteries form by developmental reprogramming of venous cells |
| Q45901128 | Coronary development is regulated by ATP-dependent SWI/SNF chromatin remodeling component BAF180. |
| Q38825014 | Coronary endothelial proliferation and morphogenesis are regulated by a VEGF-mediated pathway. |
| Q64905070 | Covering and Re-Covering the Heart: Development and Regeneration of the Epicardium. |
| Q27004417 | Cutaneous wound healing: recruiting developmental pathways for regeneration |
| Q27316236 | Directed differentiation of embryonic stem cells using a bead-based combinatorial screening method |
| Q33699799 | Dissection of zebrafish shha function using site-specific targeting with a Cre-dependent genetic switch |
| Q34348632 | Embryonic coronary vasculogenesis and angiogenesis are regulated by interactions between multiple FGFs and VEGF and are influenced by mesenchymal stem cells. |
| Q38148527 | Embryonic heart progenitors and cardiogenesis |
| Q33927331 | Endogenous retinoic acid regulates cardiac progenitor differentiation. |
| Q26767045 | Epicardial Epithelial-to-Mesenchymal Transition in Heart Development and Disease |
| Q37656165 | Epicardial GATA factors regulate early coronary vascular plexus formation |
| Q38015278 | Epicardial Progenitor Cells in Cardiac Development and Regeneration |
| Q33163160 | Epicardial calcineurin-NFAT signals through Smad2 to direct coronary smooth muscle cell and arterial wall development |
| Q37412452 | Epicardial control of myocardial proliferation and morphogenesis |
| Q39468700 | Epicardial epithelial-to-mesenchymal transition in injured heart |
| Q46355504 | Epicardial function of canonical Wnt-, Hedgehog-, Fgfr1/2-, and Pdgfra-signalling |
| Q24303956 | Epicardial-myocardial signaling directing coronary vasculogenesis |
| Q36767594 | Epicardium-derived cells in cardiogenesis and cardiac regeneration |
| Q36156815 | Epicardium-derived progenitor cells require beta-catenin for coronary artery formation |
| Q42975318 | Epicardium-to-fat transition in injured heart. |
| Q34603067 | Estrogen-induced CCN1 is critical for establishment of endometriosis-like lesions in mice |
| Q40002264 | Ets1 is required for proper migration and differentiation of the cardiac neural crest. |
| Q38423857 | Extracellular matrix communication and turnover in cardiac physiology and pathology |
| Q37578056 | FGF-16 is released from neonatal cardiac myocytes and alters growth-related signaling: a possible role in postnatal development |
| Q37583647 | FGF-16 is required for embryonic heart development |
| Q35530095 | FGF10 Signaling Enhances Epicardial Cell Expansion during Neonatal Mouse Heart Repair |
| Q59804731 | FGF10 Signaling in Heart Development, Homeostasis, Disease and Repair |
| Q30502384 | FGF10/FGFR2b signaling is essential for cardiac fibroblast development and growth of the myocardium |
| Q37488450 | FGF16 promotes invasive behavior of SKOV-3 ovarian cancer cells through activation of mitogen-activated protein kinase (MAPK) signaling pathway. |
| Q28505595 | FGF18 is required for early chondrocyte proliferation, hypertrophy and vascular invasion of the growth plate |
| Q40807184 | FGF9 and SHH regulate mesenchymal Vegfa expression and development of the pulmonary capillary network |
| Q28592971 | FGF9 regulates early hypertrophic chondrocyte differentiation and skeletal vascularization in the developing stylopod |
| Q42008716 | FGFR-1 is required by epicardium-derived cells for myocardial invasion and correct coronary vascular lineage differentiation |
| Q34946895 | FUBP3 interacts with FGF9 3′ microsatellite and positively regulates FGF9 translation |
| Q27312628 | Fibroblast Growth Factor 9 Imparts Hierarchy and Vasoreactivity to the Microcirculation of Renal Tumors and Suppresses Metastases |
| Q31005484 | Fibroblast growth factor 9 delivery during angiogenesis produces durable, vasoresponsive microvessels wrapped by smooth muscle cells |
| Q47338066 | Fibroblast growth factor 9 subfamily and the heart. |
| Q28507340 | Fibroblast growth factor receptor signaling is essential for lens fiber cell differentiation |
| Q37129668 | Fibroblast growth factor regulation of neovascularization |
| Q47951267 | Fibroblasts in an endocardial fibroelastosis disease model mainly originate from mesenchymal derivatives of epicardium |
| Q36408032 | Fluid pressure is a magnitude-dependent modulator of early endothelial tubulogenic activity: implications related to a potential tissue-engineering control parameter |
| Q33840082 | Gi proteins mediate activation of the canonical hedgehog pathway in the myocardium |
| Q92521035 | HHIPL1, a Gene at the 14q32 Coronary Artery Disease Locus, Positively Regulates Hedgehog Signaling and Promotes Atherosclerosis |
| Q35608420 | Hedgehog Signaling Pathway Database: a repository of current annotation efforts and resources for the Hh research community. |
| Q38769078 | Hedgehog signaling induces arterial endothelial cell formation by repressing venous cell fate. |
| Q30482359 | Hedgehog signaling is critical for maintenance of the adult coronary vasculature in mice |
| Q43119202 | Hedgehog signaling to distinct cell types differentially regulates coronary artery and vein development |
| Q36021595 | Hematopoietic progenitors are required for proper development of coronary vasculature |
| Q37410613 | Heparan sulfate deficiency disrupts developmental angiogenesis and causes congenital diaphragmatic hernia |
| Q39317210 | Hh signaling in regeneration of the ischemic heart |
| Q27646372 | Homodimerization Controls the Fibroblast Growth Factor 9 Subfamily's Receptor Binding and Heparan Sulfate-Dependent Diffusion in the Extracellular Matrix |
| Q34781425 | IGF signaling directs ventricular cardiomyocyte proliferation during embryonic heart development |
| Q37998444 | Importance of Myocyte-Nonmyocyte Interactions in Cardiac Development and Disease |
| Q28593518 | Indian hedgehog signaling from endothelial cells is required for sclera and retinal pigment epithelium development in the mouse eye |
| Q24338659 | Inhibition of tumor angiogenesis and growth by a small-molecule multi-FGF receptor blocker with allosteric properties |
| Q37579922 | KDR identifies a conserved human and murine hepatic progenitor and instructs early liver development. |
| Q28587262 | Loss of glypican-3 function causes growth factor-dependent defects in cardiac and coronary vascular development |
| Q37175769 | Mechanisms of cardioprotection resulting from Brown Norway chromosome 16 substitution in the salt-sensitive Dahl rat |
| Q30496686 | Mtmr8 is essential for vasculature development in zebrafish embryos. |
| Q37081778 | Muscle development and obesity: Is there a relationship? |
| Q33999797 | Mutation of the HEXIM1 gene results in defects during heart and vascular development partly through downregulation of vascular endothelial growth factor. |
| Q63487611 | Myocardial-specific R-spondin3 drives proliferation of the coronary stems primarily through the Leucine Rich Repeat G Protein coupled receptor LGR4 |
| Q38085110 | New Insights into the Developmental Mechanisms of Coronary Vessels and Epicardium |
| Q47164146 | Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development |
| Q51963495 | Novel tool to suppress cell proliferation in vivo demonstrates that myocardial and coronary vascular growth represent distinct developmental programs |
| Q37562047 | Overexpressing sonic hedgehog peptide restores periosteal bone formation in a murine bone allograft transplantation model |
| Q40009186 | PDGF-A as an epicardial mitogen during heart development |
| Q41493808 | Primitive Embryonic Macrophages are Required for Coronary Development and Maturation |
| Q39012408 | Prospects for improving neovascularization of the ischemic heart: Lessons from development |
| Q38226659 | Protein kinases and associated pathways in pluripotent state and lineage differentiation. |
| Q36328527 | Proteomic characterization of epicardial-myocardial signaling reveals novel regulatory networks including a role for NF-κB in epicardial EMT. |
| Q36785331 | Rebuilding the coronary vasculature: hedgehog as a new candidate for pharmacologic revascularization. |
| Q91843151 | Recent insights on the role and regulation of retinoic acid signaling during epicardial development |
| Q82691481 | Regulation of the expression balance of angiopoietin-1 and angiopoietin-2 by Shh and FGF-2 |
| Q34700297 | Regulator of G-Protein Signaling – 5 (RGS5) Is a Novel Repressor of Hedgehog Signaling |
| Q90297521 | Retinoic acid signaling in heart development |
| Q91886011 | Retinoic acid signaling in vascular development |
| Q93017658 | Role of Hedgehog Signaling in Vasculature Development, Differentiation, and Maintenance |
| Q55403478 | Role of Resident Stem Cells in Vessel Formation and Arteriosclerosis. |
| Q34079075 | Role of VEGF and tissue hypoxia in patterning of neural and vascular cells recruited to the embryonic heart |
| Q45815042 | Role of fibroblast growth factor signaling during proepicardium formation in the chick embryo |
| Q54487345 | Role of fibroblast growth factor signaling in vascular formation and maintenance: orchestrating signaling networks as an integrated system |
| Q37380465 | Shared circuitry: developmental signaling cascades regulate both embryonic and adult coronary vasculature |
| Q39752032 | Signaling required for blood vessel maintenance: molecular basis and pathological manifestations |
| Q36724285 | Signals from both sides: Control of cardiac development by the endocardium and epicardium |
| Q41266029 | Snai1 is important for avian epicardial cell transformation and motility |
| Q37990696 | Sonic Hedgehog on Microparticles and Neovascularization |
| Q92689430 | Sonic Hedgehog upregulation does not enhance the survival and engraftment of stem cell-derived cardiomyocytes in infarcted hearts |
| Q37463897 | Sonic hedgehog is a potent chemoattractant for human monocytes: diabetes mellitus inhibits Sonic hedgehog-induced monocyte chemotaxis. |
| Q57786980 | Sonic hedgehog signaling regulates hypoxia/reoxygenation-induced H9C2 myocardial cell apoptosis |
| Q39846766 | Sonic hedgehog: its expression in a healing cornea and its role in neovascularization |
| Q39017616 | Targeting the hedgehog signaling pathway for cardiac repair and regeneration |
| Q41903030 | Tbx18 regulates development of the epicardium and coronary vessels. |
| Q42561804 | Temporally expressed PDGF and FGF-2 regulate embryonic coronary artery formation and growth |
| Q35206661 | The Colorectal Tumor Microenvironment: The Next Decade |
| Q36861249 | The FGF system has a key role in regulating vascular integrity |
| Q42658620 | The Gli2 transcriptional activator is a crucial effector for Ihh signaling in osteoblast development and cartilage vascularization |
| Q26770132 | The Role of miR-378a in Metabolism, Angiogenesis, and Muscle Biology |
| Q35243583 | The cytoplasmic domain of TGFβR3 through its interaction with the scaffolding protein, GIPC, directs epicardial cell behavior |
| Q59755253 | The deployment of cell lineages that form the mammalian heart |
| Q37687321 | The epicardium as a candidate for heart regeneration. |
| Q37799410 | The epicardium in cardiac repair: From the stem cell view |
| Q37807765 | The role of Hedgehog signaling in fibrogenic liver repair |
| Q34999372 | The sinus venosus contributes to coronary vasculature through VEGFC-stimulated angiogenesis |
| Q37659191 | The zebrafish model system in cardiovascular research: A tiny fish with mighty prospects |
| Q33810438 | Three-dimensional micro-MRI analysis of cerebral artery development in mouse embryos |
| Q41055793 | Thymosin beta 4 treatment after myocardial infarction does not reprogram epicardial cells into cardiomyocytes |
| Q35209578 | Up-regulation of fibroblast growth factor (FGF) 9 expression and FGF-WNT/β-catenin signaling in laser-induced wound healing |
| Q43068971 | VEGF and IHH rescue definitive hematopoiesis in Gata-4 and Gata-6-deficient murine embryoid bodies |
| Q34216642 | VEGF signaling has distinct spatiotemporal roles during heart valve development |
| Q35140087 | VEGF-C and aortic cardiomyocytes guide coronary artery stem development |
| Q42100794 | WT1 regulates epicardial epithelial to mesenchymal transition through β-catenin and retinoic acid signaling pathways. |
| Q35774940 | Wnt and Hedgehog Gene Pathway Expression in Serous Ovarian Cancer |
| Q52656929 | Zinc and Zinc Transporters: Novel Regulators of Ventricular Myocardial Development. |
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