| scholarly article | Q13442814 |
| P2093 | author name string | M L Kirby | |
| K T Wallis | |||
| H A Stadt | |||
| D H Kumiski | |||
| D H Platt | |||
| K L Waldo | |||
| M R Hutson | |||
| P433 | issue | 16 | |
| P1104 | number of pages | 10 | |
| P304 | page(s) | 3179-3188 | |
| P577 | publication date | 2001-08-01 | |
| P1433 | published in | Development | Q3025404 |
| P1476 | title | Conotruncal myocardium arises from a secondary heart field | |
| P478 | volume | 128 |
| Q64095805 | 4-D Computational Modeling of Cardiac Outflow Tract Hemodynamics over Looping Developmental Stages in Chicken Embryos |
| Q28589314 | A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis |
| Q41881568 | A caudal proliferating growth center contributes to both poles of the forming heart tube |
| Q27008549 | A new heart for a new head in vertebrate cardiopharyngeal evolution |
| Q33755344 | A purified population of multipotent cardiovascular progenitors derived from primate pluripotent stem cells engrafts in postmyocardial infarcted nonhuman primates. |
| Q33939495 | ACE2 improves right ventricular function in a pressure overload model |
| Q37407385 | An FGF autocrine loop initiated in second heart field mesoderm regulates morphogenesis at the arterial pole of the heart |
| Q27863351 | An Nkx2-5/Bmp2/Smad1 negative feedback loop controls heart progenitor specification and proliferation |
| Q38356744 | Aortopathy associated with congenital heart disease: A current literature review |
| Q34295833 | Apelin enhances directed cardiac differentiation of mouse and human embryonic stem cells |
| Q42504346 | Arterial pole progenitors interpret opposing FGF/BMP signals to proliferate or differentiate. |
| Q85215749 | Association of growth/differentiation factor 1 gene polymorphisms with the risk of congenital heart disease in the Chinese Han population |
| Q36780615 | Autophagy is involved in ethanol-induced cardia bifida during chick cardiogenesis |
| Q27311429 | Autophagy is involved in high glucose-induced heart tube malformation |
| Q28586500 | BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium |
| Q37850773 | BMP signaling in congenital heart disease: new developments and future directions |
| Q34316234 | BMP signaling modulates hedgehog-induced secondary heart field proliferation |
| Q28594976 | BMP4 is required in the anterior heart field and its derivatives for endocardial cushion remodeling, outflow tract septation, and semilunar valve development |
| Q58720436 | Bicuspid aortic valve formation: mutation leads to abnormal lineage patterning of neural crest cells and the second heart field |
| Q35758029 | Bidirectional fusion of the heart-forming fields in the developing chick embryo |
| Q27333800 | Biomechanics of the chick embryonic heart outflow tract at HH18 using 4D optical coherence tomography imaging and computational modeling |
| Q40252804 | Blocking hedgehog signaling after ablation of the dorsal neural tube allows regeneration of the cardiac neural crest and rescue of outflow tract septation |
| Q42027007 | Bmp signaling exerts opposite effects on cardiac differentiation |
| Q28507815 | Bmp4 signaling is required for outflow-tract septation and branchial-arch artery remodeling |
| Q26765120 | Building and re-building the heart by cardiomyocyte proliferation |
| Q28588651 | Canonical Wnt signaling functions in second heart field to promote right ventricular growth |
| Q35865003 | Canonical Wnt signaling is a positive regulator of mammalian cardiac progenitors |
| Q59938199 | Cardiac Transcription Factors Driven Lineage-Specification of Adult Stem Cells |
| Q34588417 | Cardiac muscle regeneration: lessons from development |
| Q34855977 | Cardiac neural crest is dispensable for outflow tract septation in Xenopus |
| Q42183159 | Cardiac origin of smooth muscle cells in the inflow tract |
| Q38135363 | Cardiac outflow tract anomalies |
| Q36915882 | Cardiac progenitors and the embryonic cell cycle |
| Q36417290 | Cardiac teratogenicity in mouse maternal phenylketonuria: defining phenotype parameters and genetic background influences |
| Q37766199 | Cardiogenesis: an embryological perspective. |
| Q36360713 | Changes in fetal cardiac geometry with gestation: implications for 3- and 4-dimensional fetal echocardiography |
| Q37083019 | Characterization of human bone morphogenetic protein gene variants for possible roles in congenital heart disease |
| Q46357737 | Chondrichthyans have a bulbus arteriosus at the arterial pole of the heart: morphological and evolutionary implications |
| Q37530115 | Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms |
| Q36856002 | Common arterial trunk and ventricular non-compaction in Lrp2 knockout mice indicate a crucial role of LRP2 in cardiac development |
| Q50027290 | Competent for commitment: you've got to have heart! |
| Q33984704 | Congenital heart malformations induced by hemodynamic altering surgical interventions |
| Q28587943 | Cooperative interaction of Nkx2.5 and Mef2c transcription factors during heart development |
| Q24642861 | Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly |
| Q45982609 | Deletion of Cdc42 in embryonic cardiomyocytes results in right ventricle hypoplasia. |
| Q24674182 | Development of the heart: (1) formation of the cardiac chambers and arterial trunks |
| Q35201256 | Development of the heart: (3) formation of the ventricular outflow tracts, arterial valves, and intrapericardial arterial trunks |
| Q88723294 | Developmental Origin of the Cardiac Conduction System: Insight from Lineage Tracing |
| Q51944236 | Developmental signaling in myocardial progenitor cells: a comprehensive view of Bmp- and Wnt/beta-catenin signaling. |
| Q42322638 | Disheveled mediated planar cell polarity signaling is required in the second heart field lineage for outflow tract morphogenesis |
| Q30487250 | Distinct phases of cardiomyocyte differentiation regulate growth of the zebrafish heart |
| Q36276867 | Distinct roles of Wnt/beta-catenin and Bmp signaling during early cardiogenesis |
| Q51829029 | Dual role for neural crest cells during outflow tract septation in the neural crest-deficient mutant Splotch(2H). |
| Q36029873 | Dynamic expression patterns of leucine-rich repeat containing protein 10 in the heart |
| Q35771443 | Embryonic and foetal Islet-1 positive cells in human hearts are also positive to c-Kit. |
| 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 |
| Q38027106 | Embryonic template-based generation and purification of pluripotent stem cell-derived cardiomyocytes for heart repair |
| Q36831801 | Endothelial Notch1 Is Required for Proper Development of the Semilunar Valves and Cardiac Outflow Tract |
| Q50212997 | Endothelium in the pharyngeal arches 3, 4 and 6 is derived from the second heart field |
| Q37878713 | Epigenetic factors and cardiac development |
| Q36545329 | Evolutionary conservation of Nkx2.5 autoregulation in the second heart field |
| Q48156775 | Expansion and patterning of cardiovascular progenitors derived from human pluripotent stem cells. |
| Q35534912 | Expression and function of Ccbe1 in the chick early cardiogenic regions are required for correct heart development. |
| Q34525856 | Fate mapping identifies the origin of SHF/AHF progenitors in the chick primitive streak. |
| Q42395539 | Fibulin-1 is required for morphogenesis of neural crest-derived structures |
| Q90192495 | Follow Me! A Tale of Avian Heart Development with Comparisons to Mammal Heart Development |
| Q39219136 | GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient. |
| Q37871427 | Genetic counseling in the adult with congenital heart disease: what is the role? |
| Q33938401 | Genetic interaction between Bmp2 and Bmp4 reveals shared functions during multiple aspects of mouse organogenesis |
| Q37219657 | Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndrome |
| Q35916112 | Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome |
| Q33572905 | Genome-wide association study of maternal and inherited loci for conotruncal heart defects |
| Q47713543 | Growth and Morphogenesis during Early Heart Development in Amniotes. |
| Q42334882 | HCN4 charges up the first heart field |
| Q39450582 | HEART DEVELOPMENT. Integration of Bmp and Wnt signaling by Hopx specifies commitment of cardiomyoblasts |
| Q48210816 | Highly restricted BMP10 expression in the trabeculating myocardium of the chick embryo |
| Q54977880 | Hippo signaling determines the number of venous pole cells that originate from the anterior lateral plate mesoderm in zebrafish. |
| Q36283869 | Histone Deacetylase 3 Coordinates Deacetylase-independent Epigenetic Silencing of Transforming Growth Factor-β1 (TGF-β1) to Orchestrate Second Heart Field Development |
| Q35046633 | Hox genes define distinct progenitor sub-domains within the second heart field. |
| Q36092734 | ISL1 common variant rs1017 is not associated with susceptibility to congenital heart disease in a Chinese population |
| Q30470799 | ISL1 directly regulates FGF10 transcription during human cardiac outflow formation |
| Q30477207 | Imaging cellular signals in the heart in vivo: Cardiac expression of the high-signal Ca2+ indicator GCaMP2. |
| Q36141384 | Impaired development of left anterior heart field by ectopic retinoic acid causes transposition of the great arteries. |
| Q88716757 | Influence of blood flow on cardiac development |
| Q38066128 | Insights from cardiac development relevant to congenital defects and adult clinical anatomy |
| Q42095294 | Intracardiac septation requires hedgehog-dependent cellular contributions from outside the heart |
| Q28190508 | Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart |
| Q42169259 | Isl1 is a direct transcriptional target of Forkhead transcription factors in second-heart-field-derived mesoderm. |
| Q43243916 | Islet 1 is expressed in distinct cardiovascular lineages, including pacemaker and coronary vascular cells |
| Q28261364 | Islet1 derivatives in the heart are of both neural crest and second heart field origin |
| Q38004839 | Islet1-expressing cardiac progenitor cells: a comparison across species. |
| Q38343279 | Jarid2 is among a set of genes differentially regulated by Nkx2.5 during outflow tract morphogenesis |
| Q35869406 | Latent TGF-β binding protein 3 identifies a second heart field in zebrafish |
| Q49257420 | Lineages of the Cardiac Conduction System |
| Q47106282 | Live imaging of heart tube development in mouse reveals alternating phases of cardiac differentiation and morphogenesis |
| Q55638745 | Location, Location, Location: Signals in Muscle Specification. |
| Q35239339 | Loss of Wnt5a disrupts second heart field cell deployment and may contribute to OFT malformations in DiGeorge syndrome |
| Q24657983 | Loss of both GATA4 and GATA6 blocks cardiac myocyte differentiation and results in acardia in mice |
| Q35709087 | Mesodermal Nkx2.5 is necessary and sufficient for early second heart field development |
| Q38320233 | Molecular regulation of cardiomyocyte differentiation |
| Q28509654 | Morphogenesis of the right ventricle requires myocardial expression of Gata4 |
| Q30481126 | Mouse ES cell-derived cardiac precursor cells are multipotent and facilitate identification of novel cardiac genes |
| Q28504710 | Murine Jagged1/Notch signaling in the second heart field orchestrates Fgf8 expression and tissue-tissue interactions during outflow tract development |
| Q37819523 | Myocardial lineage development |
| Q38920772 | Myocardial plasticity: cardiac development, regeneration and disease |
| Q38045804 | Myocardial regeneration of the failing heart |
| Q38193042 | Myocardial tissue engineering: in vitro models |
| Q42367522 | Myocardial wall stiffening in a mouse model of persistent truncus arteriosus |
| Q37222049 | Myocardin marks the earliest cardiac gene expression and plays an important role in heart development |
| Q41834366 | N-cadherin is required for neural crest remodeling of the cardiac outflow tract |
| Q38570387 | NOTCH1 missense alleles associated with left ventricular outflow tract defects exhibit impaired receptor processing and defective EMT. |
| Q34341676 | Nkx2-5 regulates cardiac growth through modulation of Wnt signaling by R-spondin3 |
| Q33591207 | Nkx2.5 marks angioblasts that contribute to hemogenic endothelium of the endocardium and dorsal aorta. |
| Q30597476 | Normal and abnormal development of the intrapericardial arterial trunks in humans and mice |
| Q49262687 | Notch1 haploinsufficiency causes ascending aortic aneurysms in mice |
| Q30561780 | Numb family proteins are essential for cardiac morphogenesis and progenitor differentiation |
| Q36108192 | Numb family proteins: novel players in cardiac morphogenesis and cardiac progenitor cell differentiation |
| Q36321793 | Oriented clonal cell growth in the developing mouse myocardium underlies cardiac morphogenesis |
| Q37766810 | Origin of cardiac progenitor cells in the developing and postnatal heart |
| Q33655265 | Outflow tract septation and the aortic arch system in reptiles: lessons for understanding the mammalian heart. |
| Q36178682 | Partitioning the heart: mechanisms of cardiac septation and valve development |
| Q30483203 | Patterning of the heart field in the chick |
| Q37865965 | Pharyngeal mesoderm development during embryogenesis: implications for both heart and head myogenesis |
| Q33971634 | Phenotypic and genetic characterization of a patient with a de novo interstitial 14q24.1q24.3 deletion |
| Q28586689 | Pitx2 regulates cardiac left-right asymmetry by patterning second cardiac lineage-derived myocardium |
| Q28578165 | Plakophilin-2 and the migration, differentiation and transformation of cells derived from the epicardium of neonatal rat hearts |
| Q36736933 | Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects. |
| Q43068955 | Pulmonary atresia or persistent truncus arteriosus: is it important to make the distinction and how do we do it? |
| Q36323777 | Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome. |
| Q42339225 | Regulation of Sema3c and the Interaction between Cardiac Neural Crest and Second Heart Field during Outflow Tract Development |
| Q28511868 | Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling |
| Q35363873 | Requirement of DLG1 for cardiovascular development and tissue elongation during cochlear, enteric, and skeletal development: possible role in convergent extension |
| Q37038354 | Retinoic acid controls heart anteroposterior patterning by down-regulating Isl1 through the Fgf8 pathway |
| Q37360869 | Retinoid signaling in control of progenitor cell differentiation during mouse development |
| Q51835357 | Role for p21-activated kinase PAK4 in development of the mammalian heart. |
| Q28087290 | Signaling Pathways and Gene Regulatory Networks in Cardiomyocyte Differentiation |
| Q42107846 | Smad signaling in the neural crest regulates cardiac outflow tract remodeling through cell autonomous and non-cell autonomous effects |
| Q42931718 | Sonic hedgehog maintains proliferation in secondary heart field progenitors and is required for normal arterial pole formation |
| Q36746514 | Spatial regulation of cell cohesion by Wnt5a during second heart field progenitor deployment |
| Q46062119 | Specification and Diversification of Pericytes and Smooth Muscle Cells from Mesenchymoangioblasts. |
| Q42012136 | Stem cell populations in the heart and the role of Isl1 positive cells |
| Q34985684 | Stem cells and the formation of the myocardium in the vertebrate embryo |
| Q44352824 | Studies on morphogenesis and visualization of the early embryonic heart with regard to the development of conotruncal heart defects |
| Q35862809 | Tbx1 is regulated by forkhead proteins in the secondary heart field |
| Q35963888 | Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer |
| Q28511103 | Tbx1 regulates proliferation and differentiation of multipotent heart progenitors |
| Q28590164 | Tbx3 is required for outflow tract development |
| Q51169248 | Temporally Distinct Six2-Positive Second Heart Field Progenitors Regulate Mammalian Heart Development and Disease. |
| Q49296498 | The "Dead-End Tract" and Its Role in Arrhythmogenesis |
| Q36497257 | The AP-1 transcription factor component Fosl2 potentiates the rate of myocardial differentiation from the zebrafish second heart field. |
| Q48621270 | The Early Stages of Heart Development: Insights from Chicken Embryos |
| Q36899388 | The LIM protein Ajuba restricts the second heart field progenitor pool by regulating Isl1 activity |
| Q55363953 | The Role of Hedgehog Signalling in the Formation of the Ventricular Septum. |
| Q55082769 | The contribution of Islet1-expressing splanchnic mesoderm cells to distinct branchiomeric muscles reveals significant heterogeneity in head muscle development. |
| Q37395874 | The development and structure of the ventricles in the human heart. |
| Q51951890 | The expanding role for retinoid signaling in heart development. |
| Q36854392 | The heart-forming fields: one or multiple? |
| Q36838251 | The heart-placenta axis in the first month of pregnancy: induction and prevention of cardiovascular birth defects |
| Q38019645 | The pathogenesis of atrial and atrioventricular septal defects with special emphasis on the role of the dorsal mesenchymal protrusion |
| Q60924957 | The proximal segment of the embryonic outflow (conus) does not participate in aortic vestibule development |
| Q37616278 | The role of secondary heart field in cardiac development |
| Q39397719 | The trabecula septomarginalis (Leonardo's cord) in abnormal ventriculo-arterial connections: anatomic and morphogenetic implications |
| Q38322176 | Tissue engineering approaches to heart repair |
| Q64096155 | Tissue specific human fibroblast differential expression based on RNAsequencing analysis |
| Q37124590 | Tmem88a mediates GATA-dependent specification of cardiomyocyte progenitors by restricting WNT signaling |
| Q36727615 | Transcriptional pathways in second heart field development |
| Q90644144 | Transcriptional regulation of cell shape during organ morphogenesis |
| Q42079947 | Versican proteolysis mediates myocardial regression during outflow tract development |
| Q43095435 | Vessel and blood specification override cardiac potential in anterior mesoderm |
| Q40020289 | Wnt/beta-catenin signaling acts at multiple developmental stages to promote mammalian cardiogenesis |
| Q28511693 | Wnt/β-catenin and Bmp signals control distinct sets of transcription factors in cardiac progenitor cells |
| Q35075360 | Xenopus: An emerging model for studying congenital heart disease |
| Q41962292 | Zebrafish Mef2ca and Mef2cb are essential for both first and second heart field cardiomyocyte differentiation. |
| Q34966448 | Zebrafish cardiac development requires a conserved secondary heart field |
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