Aberrant early growth of individual trigeminal sensory and motor axons in a series of mouse genetic models of 22q11.2 deletion syndrome

We identified divergent modes of initial axon growth that prefigure disrupted differentiation of the trigeminal nerve (CN V), a cranial nerve essential for suckling, feeding and swallowing (S/F/S), a key innate behavior compromised in multiple genetic developmental disorders including DiGeorge/22q11...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Hum Mol Genet
Päätekijät: Motahari, Zahra, Maynard, Thomas M, Popratiloff, Anastas, Moody, Sally A, LaMantia, Anthony-S
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2020
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General Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7645708/
https://ncbi.nlm.nih.gov/pubmed/32901287
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddaa199
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