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Journal Article
Journal Article
Reference
eBook
Cardiovascular Research, ISSN 0008-6363, 10/2018, Volume 114, Issue 12, pp. e87 - e88
Commentary on 'The dynamics of gene expression in vertebrate embryogenesis at single-cell resolution' by Briggs JA et al., Science, 2018;360:eaar5780.... 
HEART | GRAFTS | CARDIAC & CARDIOVASCULAR SYSTEMS | Index Medicus
Journal Article
Circulation, ISSN 0009-7322, 04/2007, Volume 115, Issue 14, pp. 1830 - 1838
Background - Identifying molecular pathways regulating the development of pacemaking and coordinated heartbeat is crucial for a comprehensive mechanistic... 
Heart rate | Immunohistochemistry | Arrhythmia | Genes | Heart defects, congenital | PATHWAYS | heart rate | CARDIAC & CARDIOVASCULAR SYSTEMS | genes | CARDIAC CONDUCTION SYSTEM | MODEL | HOMEOBOX GENES | SHORT-STATURE | arrhythmia | CONGENITAL HEART-DISEASE | GROWTH | heart defects, congenital | PERIPHERAL VASCULAR DISEASE | MICE | immunohistochemistry | NKX2-5 | Bradycardia - embryology | Bradycardia - genetics | Heart Defects, Congenital - embryology | Heart - embryology | Zebrafish - embryology | Mice - embryology | Genes, Lethal | Heart Conduction System - embryology | Heart Defects, Congenital - genetics | Gene Expression Regulation, Developmental | Heart Valves - embryology | Connexin 43 - analysis | Gene Targeting | Transcription Factors - physiology | Myocytes, Cardiac - cytology | Mice, Inbred C57BL | Embryonic Development - genetics | Myocardium - pathology | Sinoatrial Node - embryology | Transcription Factors - genetics | Homeodomain Proteins - genetics | Zebrafish Proteins - physiology | Fetal Heart - pathology | Mice, Knockout | Homeobox Protein Nkx-2.5 | Phenotype | Zebrafish Proteins - deficiency | Animals | Heart Conduction System - physiopathology | Homeodomain Proteins - analysis | Transcription Factors - analysis | Zebrafish Proteins - genetics | Homeodomain Proteins - physiology | Connexins - analysis | Care and treatment | Pacemaker, Artificial (Heart) | Research | DNA binding proteins | Health aspects | Index Medicus | Abridged Index Medicus
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 10/2017, Volume 37, Issue 10, pp. 1033 - 1039
Journal Article
Development, ISSN 0950-1991, 10/2002, Volume 129, Issue 19, pp. 4613 - 4625
We present here an analysis of cardiovascular and pharyngeal arch development in mouse embryos hypomorphic for Fgf8 . Previously, we have described the... 
Transposition | Arch artery | Fgf8 | Patterning | Mouse | Pharyngeal arch | Cardiovascular | Cell death | Double outlet right ventricle | 22q11 | DiGeaorge | Neural crest | MIGRATION | SIGNALING PATHWAYS | cell death | arch artery | SONIC HEDGEHOG | neural crest | FIRST BRANCHIAL ARCH | DEVELOPMENTAL BIOLOGY | cardiovascular | patterning | DiGeorge | DIGEORGE-SYNDROME REGION | transposition | mouse | double outlet right ventricle | GENE | pharyngeal arch | CHICK-EMBRYO | NEURAL CREST ABLATION | EXPRESSION | TRANSGENIC MICE | Heart Defects, Congenital - embryology | Cell Count | Heart - embryology | Fibroblast Growth Factors - genetics | Male | Helix-Loop-Helix Motifs | Transcription Factor AP-2 | Receptors, Retinoic Acid - genetics | Neural Crest - metabolism | Branchial Region - abnormalities | Cell Division | Body Patterning | Female | Cardiovascular Abnormalities - metabolism | Cardiovascular System - embryology | Basic Helix-Loop-Helix Transcription Factors | Fibroblast Growth Factors - physiology | Pulmonary Artery - embryology | Gene Expression | Neural Crest - cytology | Aorta, Thoracic - embryology | Zebrafish Proteins | Pulmonary Artery - abnormalities | Coronary Vessels - embryology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | T-Box Domain Proteins - genetics | Mice, Inbred ICR | Mice, Knockout | Animals | Neural Crest - embryology | Biomarkers | Heart Defects, Congenital - metabolism | Mice | Apoptosis | Branchial Region - embryology | Cell Movement | Fibroblast Growth Factor 8 | Index Medicus
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 10/2011, Volume 20, Issue 19, pp. 3725 - 3737
The primary cilium is emerging as a crucial regulator of signaling pathways central to vertebrate development and human disease. We identified atrioventricular... 
PATTERNING GENES | SONIC HEDGEHOG | PATHWAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | MOUSE | GENETICS & HEREDITY | RECESSIVE INHERITANCE | MICE | IDENTIFICATION | ASSOCIATION | PRIMARY CILIUM | GLI2 | Limb Deformities, Congenital - genetics | Heart Defects, Congenital - embryology | Kidney - embryology | Humans | Spine - metabolism | Hedgehog Proteins - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | Limb Deformities, Congenital - embryology | Trachea - metabolism | Hydrocephalus - metabolism | Anal Canal - metabolism | Spine - abnormalities | Heart Defects, Congenital - genetics | Kidney - metabolism | Hedgehog Proteins - genetics | Tumor Suppressor Proteins - genetics | Spine - embryology | Hydrocephalus - genetics | Intracellular Signaling Peptides and Proteins - genetics | Disease Models, Animal | Trachea - abnormalities | Mice - genetics | Tumor Suppressor Proteins - metabolism | Mice, Inbred C57BL | Esophagus - metabolism | Limb Deformities, Congenital - metabolism | Signal Transduction - genetics | Esophagus - abnormalities | Trachea - embryology | Cilia - metabolism | Mice, Inbred C3H | Cilia - genetics | Protein Transport | Anal Canal - abnormalities | Anal Canal - embryology | Hydrocephalus - embryology | Animals | Kidney - abnormalities | Mutagenesis | Mice - metabolism | Alleles | Esophagus - embryology | Heart Defects, Congenital - metabolism | Mutation | Index Medicus | Signal transduction | Animal models | Axonemes | Hydrocephalus | Hedgehog protein | Canals | Embryo fibroblasts | Protein transport | Embryos | Cilia
Journal Article
Pediatric Research, ISSN 0031-3998, 12/2014, Volume 76, Issue 6, pp. 500 - 507
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 06/2014, Volume 164, Issue 6, pp. 1425 - 1430
Costello syndrome (CS) is a RASopathy characterized by a wide range of cardiac, musculoskeletal, dermatological, and developmental abnormalities. The... 
MAPK pathway | tooth development | craniofacial development | Ras | signal transduction | occlusion | RASopathy | Costello syndrome | malocclusion | gingival hyperplasia | enamel | receptor tyrosine kinase | Occlusion | Craniofacial development | Signal transduction | Tooth development | Enamel | Gingival hyperplasia | Malocclusion | Receptor tyrosine kinase | GENES | GENETICS & HEREDITY | GERMLINE MUTATIONS | HRAS | Heart Defects, Congenital - embryology | Proto-Oncogene Proteins p21(ras) - genetics | Humans | Craniofacial Abnormalities - embryology | Tooth Abnormalities - embryology | Male | Abnormalities, Multiple - embryology | Young Adult | Heart Defects, Congenital - genetics | MAP Kinase Signaling System - genetics | Tooth - embryology | Facies | Adult | Female | Gingival Hyperplasia - embryology | Child | Failure to Thrive - embryology | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Tooth Abnormalities - genetics | Failure to Thrive - genetics | Ectodermal Dysplasia - embryology | Gingival Hyperplasia - genetics | Malocclusion - genetics | Phosphatidylinositol 3-Kinases - genetics | Dental Enamel Hypoplasia - embryology | Costello Syndrome - genetics | Malocclusion - embryology | Adolescent | Mitogen-Activated Protein Kinases - genetics | Ectodermal Dysplasia - genetics | Mutation | Dental Enamel Hypoplasia - genetics | Index Medicus | CS
Journal Article