Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome

22q11.2 Deletion Syndrome (22q11DS) is a neurodevelopmental disorder associated with cranial nerve anomalies and disordered oropharyngeal function, including pediatric dysphagia. Using the LgDel 22q11DS mouse model, we investigated whether sensory neuron differentiation in the trigeminal ganglion (C...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Dis Model Mech
Main Authors: Karpinski, Beverly A., Maynard, Thomas M., Bryan, Corey A., Yitsege, Gelila, Horvath, Anelia, Lee, Norman H., Moody, Sally A., LaMantia, Anthony-Samuel
Format: Artigo
Jezik:Inglês
Izdano: The Company of Biologists Ltd 2021
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8126478/
https://ncbi.nlm.nih.gov/pubmed/33722956
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.047357
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