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PLoS ONE, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, p. e63218
The regulation of gene expression is accomplished by both genetic and epigenetic means and is required for the precise control of the development of the neural... 
II COLLAGEN | DORSAL-ROOT | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | NORADRENERGIC NEURONS | SOX9 | DIFFERENTIATION | SPECIFICATION | HISTONE DEACETYLASE INHIBITORS | TRANSCRIPTION FACTOR HAND2 | MOLECULAR-MECHANISMS | Peripheral Nervous System - embryology | Embryo, Nonmammalian - drug effects | Neural Crest - metabolism | Mandible - embryology | Time Factors | Skull - pathology | Mandible - drug effects | Hyoid Bone - abnormalities | Skull - abnormalities | Craniofacial Abnormalities - pathology | Neurons - metabolism | Sympathetic Nervous System - pathology | Mandible - abnormalities | Hyoid Bone - embryology | Embryo, Nonmammalian - pathology | Face - pathology | Hyoid Bone - pathology | Mutation - genetics | Phenotype | Neural Crest - embryology | Stem Cells - pathology | Face - embryology | Zebrafish Proteins - genetics | Branchial Region - embryology | Peripheral Nervous System - drug effects | Neurons - pathology | Sympathetic Nervous System - drug effects | Face - abnormalities | Mandible - pathology | Neural Crest - pathology | Craniofacial Abnormalities - embryology | Embryo, Nonmammalian - metabolism | Stem Cells - metabolism | Zebrafish - embryology | Sympathetic Nervous System - metabolism | Peripheral Nervous System - pathology | Branchial Region - abnormalities | Neurons - drug effects | Histone Deacetylase 1 - genetics | Hydroxamic Acids - pharmacology | Zebrafish Proteins - metabolism | Neural Crest - drug effects | Skull - embryology | Animals | Cell Differentiation - drug effects | Zebrafish - metabolism | Stem Cells - drug effects | Hyoid Bone - drug effects | Branchial Region - pathology | Histone Deacetylase 1 - metabolism | Gene expression | Epigenetic inheritance | Neurons | Histone deacetylase | Neurosciences | Chromatin | Transcription factors | Enzyme activity | Nervous system | Defects | Cartilage | Enteric nervous system | Enzymatic activity | Deoxyribonucleic acid--DNA | Peripheral nervous system | Enzymes | Mandible | Developmental biology | Zebrafish | Embryos | Neural crest | Mutants | Craniofacial growth | Collagen | Neural stem cells | Norepinephrine | Differentiation | Apoptosis | Deoxyribonucleic acid | DNA
Journal Article
Developmental Biology, ISSN 0012-1606, 2011, Volume 352, Issue 1, pp. 1 - 13
R-spondins are a recently characterized family of secreted proteins that activate Wnt/β-catenin signaling. Herein, we determine ( ) function in craniofacial... 
β-catenin | Craniofacial development | Cleft palate | Wnt | R-spondin2 ( Rspo2) | Branchial arch | R-spondin2 (Rspo2) | beta-catenin | ODONTOGENIC MESENCHYME | CASCADE INVOLVING ENDOTHELIN-1 | DEVELOPMENTAL BIOLOGY | MOUSE EMBRYO | NEURAL CREST CELLS | NONSYNDROMIC CLEFT-LIP | R-SPONDIN | CRANIAL PARAXIAL MESODERM | PIERRE-ROBIN-SEQUENCE | GENE-EXPRESSION | MOLECULAR-MECHANISMS | Ectoderm - embryology | LDL-Receptor Related Proteins - metabolism | Thrombospondins - genetics | Wnt Proteins - metabolism | LDL-Receptor Related Proteins - genetics | Embryo, Mammalian - metabolism | Organ Specificity - genetics | Ectoderm - metabolism | Gene Expression Regulation, Developmental | Skull - pathology | Skull - metabolism | Embryo, Mammalian - pathology | Low Density Lipoprotein Receptor-Related Protein-6 | Mesoderm - embryology | Signal Transduction | Branchial Region - metabolism | Face - pathology | Cleft Palate - embryology | beta Catenin - metabolism | Embryo, Mammalian - abnormalities | Skull - embryology | Animals | Thrombospondins - deficiency | Models, Biological | Cleft Palate - pathology | Cleft Palate - metabolism | Face - embryology | Mesoderm - metabolism | Mice | Bone Development - genetics | Body Patterning - genetics | Mesoderm - pathology | Thrombospondins - metabolism | Branchial Region - pathology | Apoptosis | Branchial Region - embryology | Gene expression | Fibroblast growth factors | Stem cells | branchial arch | cleft palate | craniofacial development
Journal Article
DMM Disease Models and Mechanisms, ISSN 1754-8403, 11/2011, Volume 4, Issue 6, pp. 763 - 776
Craniofacial and skeletal dysmorphologies account for the majority of birth defects. A number of the disease phenotypes have been attributed to abnormal... 
SEC23A | MELANOSOME | GENE | MEMBRANE | TRAFFIC JAMS | DIFFERENTIATION | OSTEOARTHRITIS | PATHOLOGY | EXPRESSION | BINDING | CARTILAGE | CELL BIOLOGY | Bone and Bones - pathology | Transcription Factors - chemistry | Branchial Region - growth & development | Cartilage - pathology | Genetic Loci - genetics | Endoplasmic Reticulum - metabolism | Molecular Sequence Data | Endoplasmic Reticulum - ultrastructure | Gene Knockdown Techniques | Collagen Type II - metabolism | Morphogenesis | Extracellular Matrix Proteins - secretion | Notochord - metabolism | Base Sequence | Bone and Bones - metabolism | Craniofacial Abnormalities - pathology | Melanosomes - pathology | Craniofacial Abnormalities - metabolism | Chondrocytes - metabolism | Amino Acid Sequence | Chondrocytes - pathology | Zebrafish Proteins - chemistry | Branchial Region - metabolism | Zebrafish Proteins - metabolism | COP-Coated Vesicles - metabolism | Glycosaminoglycans - secretion | Transcription Factors - genetics | Cartilage - metabolism | Mutation - genetics | Zebrafish - genetics | Protein Transport | Transcription Factors - metabolism | Animals | Chondrocytes - ultrastructure | Endoplasmic Reticulum Stress | Zebrafish - metabolism | Notochord - pathology | Zebrafish Proteins - genetics | Bone and Bones - embryology | Melanosomes - metabolism | Branchial Region - pathology
Journal Article
Developmental Cell, ISSN 1534-5807, 2006, Volume 10, Issue 1, pp. 81 - 92
22q11 deletion ( ) syndrome is characterized genetically by heterozygous deletions within chromosome 22q11 and clinically by a constellation of congenital... 
HUMDISEASE | DEVBIO | Devbio | Hum disease | DIGEORGE-SYNDROME PHENOTYPE | PHARYNGEAL REGION | RETINOIC ACID SYNTHESIS | ENDODERM | DEVELOPMENTAL BIOLOGY | NEURAL CREST | CARDIOVASCULAR DEFECTS | EXPRESSION | DELETION SYNDROME | MOUSE EMBRYO | MICE LACKING | CELL BIOLOGY | Embryo, Mammalian | Gene Expression - genetics | Homeodomain Proteins - metabolism | Humans | Cytochrome P-450 Enzyme System - metabolism | Gene Expression Regulation, Developmental - genetics | Aorta - metabolism | Tretinoin - metabolism | Gene Deletion | Nuclear Proteins - deficiency | Thymus Gland - pathology | Chromosomes, Human, Pair 22 | Thymus Gland - metabolism | In Situ Hybridization - methods | Disease Models, Animal | Retinoic Acid 4-Hydroxylase | T-Box Domain Proteins - deficiency | Branchial Region - metabolism | Mice, Inbred C57BL | Aorta - embryology | Genotype | Nuclear Proteins - metabolism | Homeodomain Proteins - genetics | T-Box Domain Proteins - metabolism | Mice, Knockout | Aorta - pathology | Animals | DiGeorge Syndrome - metabolism | Adaptor Proteins, Signal Transducing - deficiency | Cytochrome P-450 Enzyme System - genetics | Signal Transduction - physiology | Mice | Thymus Gland - embryology | Adaptor Proteins, Signal Transducing - metabolism | Branchial Region - pathology | Branchial Region - embryology | Birth defects | Research | Developmental biology | Oncology, Experimental | Cancer | Tretinoin
Journal Article
Developmental Biology, ISSN 0012-1606, 07/2016, Volume 415, Issue 2, pp. 371 - 382
Mandibulofacial dysostosis (MFD) is a human developmental disorder characterized by defects of the facial bones. It is the second most frequent craniofacial... 
Xenopus | Sf3b4 | BMP | Nager syndrome | Craniofacial | Neural crest | Splicing factor | AUTOSOMAL RECESSIVE INHERITANCE | TREACHER-COLLINS-SYNDROME | DEVELOPMENTAL BIOLOGY | INDUCTION | GENE | CRANIAL NEURAL CREST | BMPR-IA | FACIAL DYSOSTOSES | RETINITIS-PIGMENTOSA | ACROFACIAL DYSOSTOSIS | Frameshift Mutation | Mandibulofacial Dysostosis - embryology | Xenopus Proteins - genetics | Cartilage - pathology | Humans | Gene Expression Regulation, Developmental - genetics | Molecular Sequence Data | Genetic Complementation Test | Gene Knockdown Techniques | Neural Crest - metabolism | Mandibulofacial Dysostosis - genetics | RNA Splicing - genetics | Skull - abnormalities | RNA Precursors - metabolism | Xenopus Proteins - biosynthesis | Xenopus laevis - genetics | Xenopus laevis - growth & development | Neural Plate - pathology | Maxillofacial Development - genetics | Disease Models, Animal | Amino Acid Sequence | Cartilage - growth & development | Neural Crest - cytology | Xenopus laevis - embryology | Branchial Region - metabolism | Mandibulofacial Dysostosis - physiopathology | RNA Precursors - genetics | Codon, Nonsense | RNA Splicing Factors - genetics | Cartilage - metabolism | Sequence Homology, Amino Acid | Skull - embryology | Phenotype | Sequence Alignment | Animals | Xenopus Proteins - deficiency | Neural Crest - embryology | Neural Plate - embryology | Morpholinos - pharmacology | Xenopus Proteins - physiology | Branchial Region - pathology | Skull - growth & development | Branchial Region - embryology | Medicine, Experimental | Medical research | Embryonic development | RNA | Gene expression
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 04/2013, Volume 123, Issue 4, pp. 1638 - 1646
Journal Article