Cargando…
Loss of Elp1 disrupts trigeminal ganglion neurodevelopment in a model of familial dysautonomia
Familial dysautonomia (FD) is a sensory and autonomic neuropathy caused by mutations in elongator complex protein 1 (ELP1). FD patients have small trigeminal nerves and impaired facial pain and temperature perception. These signals are relayed by nociceptive neurons in the trigeminal ganglion, a str...
Autores principales: | Leonard, Carrie E, Quiros, Jolie, Lefcort, Frances, Taneyhill, Lisa A |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273214/ https://www.ncbi.nlm.nih.gov/pubmed/35713404 http://dx.doi.org/10.7554/eLife.71455 |
Ejemplares similares
-
Retina-specific loss of Ikbkap/Elp1 causes mitochondrial dysfunction that leads to selective retinal ganglion cell degeneration in a mouse model of familial dysautonomia
por: Ueki, Yumi, et al.
Publicado: (2018) -
Loss of Ikbkap Causes Slow, Progressive Retinal Degeneration in a Mouse Model of Familial Dysautonomia
por: Ueki, Yumi, et al.
Publicado: (2016) -
IKBKAP/ELP1 gene mutations: mechanisms of familial dysautonomia and gene-targeting therapies
por: Rubin, Berish Y, et al.
Publicado: (2017) -
Elp1 is required for development of visceral sensory peripheral and central circuitry
por: Tolman, Zariah, et al.
Publicado: (2022) -
Effects of IKAP/hELP1 Deficiency on Gene Expression in Differentiating Neuroblastoma Cells: Implications for Familial Dysautonomia
por: Cohen-Kupiec, Rachel, et al.
Publicado: (2011)