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1. Full Text Early lineage restriction in temporally distinct populations of Mesp1 progenitors during mammalian heart development
by Lescroart, Fabienne and Chabab, Samira and Lin, Xionghui and Rulands, Steffen and Paulissen, Catherine and Rodolosse, Annie and Auer, Herbert and Achouri, Younes and Dubois, Christine and Bondue, Antoine and Simons, Benjamin D and Blanpain, Cédric
Nature Cell Biology, ISSN 1465-7392, 2014, Volume 16, Issue 9, pp. 829 - 840
Cardiac development arises from two sources of mesoderm progenitors, the first heart field (FHF) and the second (SHF). Mesp1 has been proposed to mark the most... 
Heart Ventricles - cytology | Basic Helix-Loop-Helix Transcription Factors - genetics | Heart Atria - cytology | Heart Atria - embryology | Transcriptome | Heart Ventricles - embryology | Mice, Transgenic | Organ Specificity | Heart Atria - metabolism | Cell Lineage | Fetal Heart - cytology | Animals | Basic Helix-Loop-Helix Transcription Factors - metabolism | Gene Expression Regulation, Developmental | Body Patterning | Female | Stem Cells - physiology | Cell Differentiation | Heart Ventricles - metabolism | Mice | Fetal Heart - metabolism | Physiological aspects | Genetic aspects | Endothelial growth factors | Mammals | Developmental biology | Analysis
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2. Full Text Identification of Myocardial and Vascular Precursor Cells in Human and Mouse Epicardium
by Limana, Federica and Zacheo, Antonella and Mocini, David and Mangoni, Antonella and Borsellino, Giovanna and Diamantini, Adamo and De Mori, Roberta and Battistini, Luca and Vigna, Elisa and Santini, Massimo and Loiaconi, Vincenzo and Pompilio, Giulio and Germani, Antonia and Capogrossi, Maurizio C
Circulation Research, ISSN 0009-7330, 12/2007, Volume 101, Issue 12, pp. 1255 - 1265
During cardiac development, the epicardium is the source of multipotent mesenchymal cells, which give rise to endothelial and smooth muscle cells in coronary... 
Epicardium | Infarction | Cardiovascular differentiation | Stem cells | PROGENITOR CELLS | stem cells | CARDIAC & CARDIOVASCULAR SYSTEMS | MULTIPOTENT | infarction | CARDIAC STEM-CELLS | INFARCTED MYOCARDIUM | HUMAN ADIPOSE-TISSUE | HEART REGENERATION | ENDOTHELIAL-CELLS | epicardium | PERIPHERAL VASCULAR DISEASE | GROWTH-FACTOR | DIFFERENTIATION | HEMATOLOGY | cardiovascular differentiation | HUMAN PERICARDIAL FLUID | Endothelium, Vascular - cytology | Fetal Heart - physiology | Myocytes, Cardiac - cytology | Humans | Mice, Inbred C57BL | Stem Cells - cytology | Cell Movement - physiology | Pericardium - cytology | Endothelium, Vascular - physiology | Myocardium - cytology | Fetal Heart - cytology | Animals | Pericardium - physiology | Myocytes, Cardiac - physiology | Pericardium - embryology | Female | Stem Cells - physiology | Mice | Endothelium, Vascular - embryology
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3. Full Text Lineage and morphogenetic analysis of the cardiac valves
by de Lange, Frederik J and Moorman, Antoon F. M and Anderson, Robert H and Männer, Jörg and Soufan, Alexane T and de Gier-de Vries, Corrie and Schneider, Michael D and Webb, Sana and van den Hoff, Maurice J. B and Christoffels, Vincent M
Circulation research, ISSN 0009-7330, 2004, Volume 95, Issue 6, pp. 645 - 654
We used a genetic lineage-labeling system to establish the material contributions of the progeny of 3 specific cell types to the cardiac valves. Thus, we... 
Cre-lox | Tendinous chord | Atrioventricular valve | Lineage analysis | Mitral | Tricuspid | Valvular | lineage analysis | CARDIAC & CARDIOVASCULAR SYSTEMS | tendinous chord | MOUSE EMBRYOS | IN-SITU HYBRIDIZATION | CRE RECOMBINASE | ENDOCARDIAL CUSHION | atrioventricular valve | SMOOTH-MUSCLE | valvular | CONGENITAL HEART-DISEASE | tricuspid | ATRIOVENTRICULAR VALVES | CHICK-EMBRYO | PERIPHERAL VASCULAR DISEASE | mitral | NEURAL CREST | HEMATOLOGY | EXPRESSION | Wnt1 Protein | Sequence Deletion | Wnt Proteins | Mesoderm - cytology | Chordae Tendineae - cytology | Tricuspid Valve - embryology | Morphogenesis | Chimera - embryology | Coturnix - embryology | Heart Valves - embryology | Endocardium - cytology | Imaging, Three-Dimensional | Genes, Reporter | Neural Crest - cytology | Mitral Valve - cytology | Intercellular Signaling Peptides and Proteins - genetics | Viral Proteins - genetics | Mice, Transgenic | Chick Embryo | Gestational Age | Myocardium - cytology | Receptor, TIE-2 - genetics | Tricuspid Valve - cytology | Cell Lineage | Fetal Heart - cytology | Animals | Chordae Tendineae - embryology | Mitral Valve - embryology | Mice | Heart Valves - cytology | Integrases - genetics | Apoptosis | Cell Movement
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4. Full Text Life and death of cardiac stem cells: A paradigm shift in cardiac biology
by Anversa, Piero and Kajstura, Jan and Leri, Annarosa and Bolli, Roberto
Circulation, ISSN 0009-7322, 03/2006, Volume 113, Issue 11, pp. 1451 - 1463
Heart failure | Regeneration | Stem cells | PROGENITOR CELLS | heart failure | stem cells | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIOMYOCYTE DNA-SYNTHESIS | regeneration | FAILING HUMAN HEART | PROLIFERATION | THERAPEUTIC ANGIOGENESIS | FAILURE | REGENERATE INFARCTED MYOCARDIUM | MYOCYTE DEATH | ISCHEMIC DISEASE | PERIPHERAL VASCULAR DISEASE | DIFFERENTIATION | HEMATOLOGY | Myocytes, Cardiac - cytology | Heart - growth & development | Humans | Biomarkers - analysis | Homeostasis | Rats | Antigens, Ly - analysis | Proto-Oncogene Proteins c-kit - analysis | Myocardium - cytology | Cell Lineage | Fetal Heart - cytology | Multipotent Stem Cells - chemistry | Animals | Aging - physiology | Cellular Senescence | Multipotent Stem Cells - cytology | Cell Division | Myocardial Infarction - pathology | Dogs | Mice | Apoptosis
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5. Full Text Expression and localisation of thymosin beta-4 in the developing human early fetal heart
by Saunders, Vinay and Dewing, Jennifer M and Sanchez-Elsner, Tilman and Wilson, David I
PLoS ONE, ISSN 1932-6203, 11/2018, Volume 13, Issue 11, p. e0207248
Background The objective of this study was to investigate the expression and localisation of thymosin beta 4 (T beta 4) in the developing human heart. T beta 4... 
CORNEAL | MIGRATION | APOPTOSIS | CELLS | IN-VITRO | VIVO | MULTIDISCIPLINARY SCIENCES | ALKALI INJURY | Immunohistochemistry | Heart Ventricles - cytology | Thymosin - genetics | Myocytes, Cardiac - cytology | Endothelial Cells - metabolism | Fetal Heart - embryology | Humans | RNA, Messenger - genetics | Heart Ventricles - embryology | Coronary Vessels - embryology | RNA, Messenger - metabolism | Coronary Vessels - metabolism | Pregnancy | Fetal Heart - cytology | Coronary Vessels - cytology | Endothelial Cells - cytology | Gene Expression Regulation, Developmental | Myocytes, Cardiac - metabolism | Thymosin - metabolism | Female | Heart Ventricles - metabolism | Fetal Heart - metabolism | Heart | Usage | Messenger RNA | Thymosin | Research | Gene expression | Health aspects | Endothelium | RNA | Myosin | Fluorescence | Muscle proteins | Cornea | Smooth muscle | mRNA | Cell adhesion & migration | Proteins | Localization | Atria | Vascular endothelial growth factor | Congenital diseases | Fetuses | Septum | Epicardium | Blood vessels | Cardiomyocytes | Endothelial cells | Medicine | Studies | Coronary vessels | Stem cells | Myocardium | Microvasculature | Ventricle | Position (location) | Apoptosis
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6. Full Text Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes: Insights Into Molecular, Cellular, and Functional Phenotypes
by Karakikes, Ioannis and Ameen, Mohamed and Termglinchan, Vittavat and Wu, Joseph C
Circulation Research, ISSN 0009-7330, 06/2015, Volume 117, Issue 1, pp. 80 - 88
Disease models are essential for understanding cardiovascular disease pathogenesis and developing new therapeutics. The human induced pluripotent stem cell... 
cardiovascular disease modeling | myocytes, cardiac | precision medicine | induced pluripotent stem cells | cardiovascular diseases | CARDIAC & CARDIOVASCULAR SYSTEMS | HEART-FAILURE | CARDIOMYOPATHY | LONG-QT SYNDROME | MATURATION | CULTURE | myocytes | IN-VITRO | DISEASE | PURIFICATION | ANIMAL-MODELS | PERIPHERAL VASCULAR DISEASE | CARDIAC DIFFERENTIATION | HEMATOLOGY | cardiac | Excitation Contraction Coupling | Cations - metabolism | Humans | Electrophysiology | Gene Expression Profiling | Cardiovascular Diseases - pathology | Bioengineering - methods | Action Potentials | Cell Differentiation | Cell Culture Techniques | Induced Pluripotent Stem Cells - cytology | Calcium Signaling | Induced Pluripotent Stem Cells - metabolism | Myocardial Contraction | Drug Evaluation, Preclinical - methods | Induced Pluripotent Stem Cells - drug effects | Myocytes, Cardiac - cytology | Cell Lineage | Fetal Heart - cytology | Phenotype | Energy Metabolism | Ion Channels - metabolism | Myocytes, Cardiac - metabolism | Myocytes, Cardiac - classification | Myocytes, Cardiac - ultrastructure | Index Medicus | cardiomyocytes
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7. Full Text Human fetal cardiac progenitors: The role of stem cells and progenitors in the fetal and adult heart
by Bulatovic, Ivana, MD and Månsson-Broberg, Agneta, MD, PhD and Sylvén, Christer, MD, PhD and Grinnemo, Karl-Henrik, MD, PhD
Best Practice & Research: Clinical Obstetrics & Gynaecology, ISSN 1521-6934, 2015, Volume 31, pp. 58 - 68
The human fetal heart is formed early during embryogenesis as a result of cell migrations, differentiation, and formative blood flow. It begins to beat around... 
Obstetrics and Gynecology | congenital heart disease | stem cells | embryonic | transcription factors | human | heart | MULTIPOTENT | GENE NKX2-5 | REGENERATION | OUTFLOW TRACT | OBSTETRICS & GYNECOLOGY | MAMMALIAN HEART | SMOOTH-MUSCLE | DISEASE | CARDIOMYOCYTE DIFFERENTIATION | NEURAL CREST | TRANSCRIPTION FACTOR | Neural Crest - cytology | Fetal Stem Cells - cytology | Heart Defects, Congenital - embryology | Endocardium - embryology | Fetal Heart - embryology | Humans | Coronary Vessels - embryology | Mesoderm - cytology | Pericardium - cytology | Myocardium - cytology | Fetal Heart - cytology | Coronary Vessels - cytology | Pericardium - embryology | Cell Differentiation | Endocardium - cytology | Cell Movement | Heart | Genetic disorders | Cardiology | Cell differentiation | Heart diseases | Stem cells
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8. Full Text Intracardiac septation requires hedgehog-dependent cellular contributions from outside the heart
by Matthew M. Goddeeris and Silvia Rho and Alexandra Petiet and Chandra L. Davenport and G. Allan Johnson and Erik N. Meyers and John Klingensmith
Development, ISSN 0950-1991, 05/2008, Volume 135, Issue 10, pp. 1887 - 1895
Septation of the mammalian heart into four chambers requires the orchestration of multiple tissue progenitors. Abnormalities in this process can result in... 
Morphogenesis | Sonic hedgehog | Atrioventricular septal defect | Intracardiac septation | Mouse | Heart development | MYOCARDIUM | CELLS | heart development | MOUSE HEART | FIELD | OUTFLOW TRACT | intracardiac septation | DEVELOPMENTAL BIOLOGY | MICROSCOPY | CARDIAC DEVELOPMENT | atrioventricular septal defect | mouse | morphogenesis | sonic hedgehog | EXPRESSION | SONIC-HEDGEHOG | REVEALS | Heart Septal Defects, Ventricular - embryology | Heart Atria - cytology | Signal Transduction | Fetal Heart - embryology | Heart Atria - embryology | Hedgehog Proteins - metabolism | Mesoderm - cytology | Fetal Heart - cytology | Animals | Hedgehog Proteins - genetics | Mice, Mutant Strains | Mice | Mutation
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9. Full Text Myocyte enlargement, differentiation, and proliferation kinetics in the fetal sheep heart
by Sonnet S. Jonker and Lubo Zhang and Samantha Louey and George D. Giraud and Kent L. Thornburg and J. Job Faber
Journal of Applied Physiology, ISSN 8750-7587, 03/2007, Volume 102, Issue 3, pp. 1130 - 1142
The generation of new myocytes is an essential process of in utero heart growth. Most, or all, cardiac myocytes lose their capacity for proliferation during... 
Terminal differentiation | Hyperplasia | Apoptosis | Hypertrophy | Pregnancy | Fetal Heart - cytology | Animals | Cell Proliferation | Myocytes, Cardiac - cytology | Fetal Heart - embryology | Myocytes, Cardiac - physiology | Fetal Development | Female | Sheep | Cell Enlargement | Kinetics
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10. Full Text RNA Sequencing of Mouse Sinoatrial Node Reveals an Upstream Regulatory Role for Islet-1 in Cardiac Pacemaker Cells
by Vedantham, Vasanth and Galang, Giselle and Evangelista, Melissa and Deo, Rahul C and Srivastava, Deepak
Circulation Research, ISSN 0009-7330, 02/2015, Volume 116, Issue 5, pp. 797 - 803
RATIONALE:Treatment of sinus node disease with regenerative or cell-based therapies will require a detailed understanding of gene regulatory networks in... 
Isl1 protein, mouse | Laser capture microdissection | Transcription factors | Hcn4 protein, mouse | Sinoatrial node | High-throughput RNA sequencing | Isl1 protein | CARDIAC & CARDIOVASCULAR SYSTEMS | transcription factors | CONVERSION | sinoatrial node | high-throughput RNA sequencing | laser capture microdissection | mouse | Hcn4 protein | PERIPHERAL VASCULAR DISEASE | DIFFERENTIATION | HEMATOLOGY | EXPRESSION | RNA, Messenger - isolation & purification | Heart Atria - embryology | Transcription Factors - deficiency | Transcriptome | Laser Capture Microdissection | Molecular Sequence Data | Male | Gene Expression Profiling | Gene Regulatory Networks | Subtraction Technique | RNA, Messenger - biosynthesis | LIM-Homeodomain Proteins - deficiency | Gene Expression Regulation, Developmental | Female | Transcription, Genetic | Genes, Reporter | Myocardial Contraction | Transcription Factors - physiology | Heart Atria - cytology | RNA, Messenger - genetics | Sinoatrial Node - cytology | Sinoatrial Node - embryology | Transcription Factors - genetics | Heart Atria - metabolism | Fetal Heart - cytology | LIM-Homeodomain Proteins - genetics | Animals | Myocytes, Cardiac - metabolism | Sinoatrial Node - metabolism | High-Throughput Nucleotide Sequencing | Mice | LIM-Homeodomain Proteins - physiology | Hcn4 | RNA-Seq | mouse heart development | Isl1
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11. Full Text Fetal Mammalian Heart Generates a Robust Compensatory Response to Cell Loss
by Sturzu, Anthony C and Rajarajan, Kuppusamy and Passer, Derek and Plonowska, Karolina and Riley, Alyssa and Tan, Timothy C and Sharma, Arun and Xu, Adele F and Engels, Marc C and Feistritzer, Rebecca and Li, Guang and Selig, Martin K and Geissler, Richard and Robertson, Keston D and Scherrer-Crosbie, Marielle and Domian, Ibrahim J and Wu, Sean M
Circulation, ISSN 0009-7322, 07/2015, Volume 132, Issue 2, pp. 109 - 121
Background-Heart development is tightly regulated by signaling events acting on a defined number of progenitor and differentiated cardiac cells. Although loss... 
stem cells | myocytes cardiac | regeneration | mice | heart | myocytes, cardiac | CARDIAC & CARDIOVASCULAR SYSTEMS | ZEBRAFISH | HIPPO PATHWAY | PROLIFERATION | CARDIAC PROGENITOR CELLS | CARDIOMYOCYTES | EMBRYONIC STEM-CELLS | IN-VIVO | PERIPHERAL VASCULAR DISEASE | DIFFERENTIATION | EXPRESSION | Fetal Heart - growth & development | Fetal Heart - cytology | Animals | Cell Count - methods | Myocytes, Cardiac - physiology | Cell Proliferation - physiology | Mice, Transgenic | Mice | Embryonic Stem Cells - physiology | Gene Knock-In Techniques | stem cell plasticity | cardiac progenitor cells | cardiac development | cardiomyocyte
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12. Full Text Endocardium Contributes to Cardiac Fat
by Zhang, Hui and Pu, Wenjuan and Liu, Qiaozhen and He, Lingjuan and Huang, Xiuzhen and Tian, Xueying and Zhang, Libo and Nie, Yu and Hu, Shengshou and Lui, Kathy O and Zhou, Bin
Circulation Research, ISSN 0009-7330, 01/2016, Volume 118, Issue 2, pp. 254 - 265
RATIONALE:Unraveling the developmental origin of cardiac fat could offer important implications for the treatment of cardiovascular disease. The recent... 
homeostasis | endothelial cells | pericardium | adipocytes | endocardium | HEART FIELD | CELLS | CARDIAC & CARDIOVASCULAR SYSTEMS | MYOCARDIAL-INFARCTION | ANGIOGENESIS | FORM | MESENCHYMAL TRANSITION | CORONARY-ARTERIES | CRE | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | LINEAGE | ADIPOSE-TISSUE | Biomarkers - metabolism | Mice, Inbred C57BL | NFATC Transcription Factors - metabolism | Homeostasis | Adipocytes - cytology | Mice, Transgenic | Myocardial Infarction - metabolism | Gestational Age | Mice, Inbred ICR | Endocardium - metabolism | Cell Lineage | Fetal Heart - cytology | Phenotype | Animals | Gene Expression Regulation, Developmental | Adipocytes - metabolism | Myocardial Infarction - pathology | Endocardium - cytology | Adipogenesis | Disease Models, Animal | NFATC Transcription Factors - genetics
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13. Full Text Dishevelled-associated activator of morphogenesis 1 (Daam1) is required for heart morphogenesis
by Li, Deqiang and Hallett, Mark A and Zhu, Wuqiang and Rubart, Michael and Liu, Ying and Yang, Zhenyun and Chen, Hanying and Haneline, Laura S and Chan, Rebecca J and Schwartz, Robert J and Field, Loren J and Atkinson, Simon J and Shou, Weinian
Development, ISSN 0950-1991, 01/2011, Volume 138, Issue 2, pp. 303 - 315
Dishevelled-associated activator of morphogenesis 1 (Daam1), a member of the formin protein family, plays an important role in regulating the actin... 
Planar cell polarity (PCP) | Daam1 | Mouse | Actin | Heart development | Cytoskeletal architecture | Sarcomere organization | Congenital heart defects | Formin protein | POLARITY | MECHANISM | CYTOSKELETON | CONVERGENT EXTENSION | ACTIN DYNAMICS | DEVELOPMENTAL BIOLOGY | FORMIN PROTEINS | DISRUPTION | GROWTH | CELL | rho GTP-Binding Proteins - deficiency | Cell Proliferation | Heart Defects, Congenital - embryology | Actins - metabolism | Microfilament Proteins - physiology | DNA Primers - genetics | Heart Defects, Congenital - genetics | Gene Expression Regulation, Developmental | Base Sequence | Female | Cell Differentiation | Fetal Heart - abnormalities | Microfilament Proteins - genetics | Fetal Heart - metabolism | Microfilament Proteins - deficiency | Morphogenesis - genetics | Myocytes, Cardiac - cytology | Fetal Heart - embryology | rho GTP-Binding Proteins - genetics | Cells, Cultured | Mice, Transgenic | rho GTP-Binding Proteins - physiology | Cell Adhesion | Mice, Knockout | Pregnancy | Fetal Heart - cytology | Phenotype | Animals | Monomeric GTP-Binding Proteins - metabolism | Myocytes, Cardiac - metabolism | Heart Defects, Congenital - metabolism | Mice | Morphogenesis - physiology | Apoptosis
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14. Full Text Developmental changes in the balance of glycolytic ATP production and oxidative phosphorylation in ventricular cells: A simulation study
by Sano, Hitomi I and Toki, Tamami and Naito, Yasuhiro and Tomita, Masaru
Journal of Theoretical Biology, ISSN 0022-5193, 04/2017, Volume 419, pp. 269 - 277
The developmental program of the heart requires accurate regulation to ensure continuous circulation and simultaneous cardiac morphogenesis, because any... 
Mitochondria | Anoxia | Oxidative phosphorylation | Creatine | Glycogen | MYOCYTES | NEONATAL MAMMALIAN HEART | ULTRASTRUCTURAL DIFFERENTIATION | SARCOPLASMIC-RETICULUM | CARDIOMYOCYTES | HYPOXIA | FETAL GUINEA-PIG | IONIC CURRENT SYSTEMS | SKELETAL-MUSCLE | CARDIAC-MUSCLE-CELLS | BIOLOGY | MATHEMATICAL & COMPUTATIONAL BIOLOGY | Fetal Heart - physiology | Heart Ventricles - cytology | Guinea Pigs | Myocytes, Cardiac - cytology | Models, Cardiovascular | Sarcomeres - metabolism | Oxidative Phosphorylation | Heart Ventricles - embryology | Adenosine Triphosphate - biosynthesis | Action Potentials | Fetal Heart - cytology | Animals | Glycogen - metabolism | Energy Metabolism | Myocytes, Cardiac - physiology | Computer Simulation | Glycolysis | Myocytes, Cardiac - metabolism | Heart Ventricles - metabolism | Fetal Hypoxia | Hexokinase - metabolism | Fetal Heart - metabolism | Heart | Genetic disorders | Analysis | Stem cells | Congenital heart disease
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15. Full Text Hox genes define distinct progenitor sub-domains within the second heart field
by Bertrand, Nicolas and Roux, Marine and Ryckebüsch, Lucile and Niederreither, Karen and Dollé, Pascal and Moon, Anne and Capecchi, Mario and Zaffran, Stéphane
Developmental Biology, ISSN 0012-1606, 05/2011, Volume 353, Issue 2, pp. 266 - 274
Much of the heart, including the atria, right ventricle and outflow tract (OFT) is derived from a progenitor cell population termed the second heart field... 
Mouse | Hox genes | Cardiac progenitor cells | Retinoic acid | Heart development | MYOCARDIUM DERIVES | INNER-EAR |