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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
2016
Review
2016
Hedgehog receptor function during craniofacial development.
The Hedgehog signalling pathway plays a fundamental role in orchestrating normal craniofacial development in vertebrates. In… 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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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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