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craniofacial development

 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
MicroRNA Profiling during Craniofacial Development: Potential Roles for Mir23b and Mir133b
Defects in mid-facial development, including cleft lip/palate, account for a large number of human birth defects annually. In… Expand
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2016
2016
IFT46 plays crucial roles in craniofacial and cilia development.
The intraflagellar transport (IFT) system is essential for bidirectional movement of ciliary components from the basal body to… Expand
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2016
2016
Expression of forkhead box transcription factor genes Foxp1 and Foxp2 during jaw development.
Development of the face is regulated by a large number of genes that are expressed in temporally and spatially specific patterns… Expand
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2016
2016
Association between Genes Involved in Craniofacial Development and Nonsyndromic Cleft Lip and/or Palate in the Brazilian Population
Objective To determine the association of single-nucleotide polymorphisms (SNPs) in genes related to craniofacial development… Expand
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Review
2015
Review
2015
Signaling Pathways in Craniofacial Development: Insights from Rare Skeletal Disorders.
In the developing embryo, signaling pathways define how the mesenchymal precursors of bone form individual skeletal elements with… Expand
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2015
2015
Three‐Dimensional Visualization of Developing Neurovascular Architecture in the Craniofacial Region of Embryonic Mice
Recent studies have highlighted the mechanism of vascular and axonal guidance to ensure proper morphogenesis and organogenesis… Expand
2014
2014
Defective Craniofacial Development and Brain Function in a Mouse Model for Depletion of Intracellular Inositol Synthesis*
Background: Lithium exerts a mood-stabilizing effect and inhibits myo-inositol monophosphatase (IMPase). Results: IMPase mutant… Expand
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2014
2014
CNBP modulates the transcription of Wnt signaling pathway components.
BACKGROUND Cellular nucleic acid binding protein (CNBP) is a small and highly conserved protein with nucleic acid chaperone… Expand
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2014
2014
Identification of a Face Enhancer Reveals Direct Regulation of LIM Homeobox 8 (Lhx8) by Wingless-Int (WNT)/β-Catenin Signaling*♦
Background: Lhx8 is an important gene for craniofacial development, but its regulation had been poorly understood. Results: We… Expand
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Review
2013
Review
2013
Understanding the basis of auriculocondylar syndrome: Insights from human, mouse and zebrafish genetic studies
Among human birth defect syndromes, malformations affecting the face are perhaps the most striking due to cultural and… Expand
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