Escot, Sophie <br/><br/>
Disruption of CXCR4 signaling in pharyngeal neural crest cells causes DiGeorge syndrome-like malformations.  [electronic resource] 

 -  Development (Cambridge, England)  Feb 2016 
 - 582-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1477-9129 
<br/><br/><label>Standard No.: </label>10.1242/dev.126573  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Branchial Region--pathology<br/>Cell Movement<br/>Chemokine CXCL12--metabolism<br/>Craniofacial Abnormalities--pathology<br/>DiGeorge Syndrome--metabolism<br/>Mice, Mutant Strains<br/>Neural Crest--metabolism<br/>Neurons--pathology<br/>Receptors, CXCR4--metabolism<br/>Signal Transduction<br/>T-Box Domain Proteins--metabolism