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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Detalles Bibliográficos
Autores principales: Karpinski, Beverly A., Maynard, Thomas M., Bryan, Corey A., Yitsege, Gelila, Horvath, Anelia, Lee, Norman H., Moody, Sally A., LaMantia, Anthony-Samuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8126478/
https://www.ncbi.nlm.nih.gov/pubmed/33722956
http://dx.doi.org/10.1242/dmm.047357

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8126478/
https://www.ncbi.nlm.nih.gov/pubmed/33722956
http://dx.doi.org/10.1242/dmm.047357

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