Etonogestrel Administration Reduces the Expression of PHOX2B and Its Target Genes in the Solitary Tract Nucleus

Heterozygous mutations of the transcription factor PHOX2B are responsible for Congenital Central Hypoventilation Syndrome, a neurological disorder characterized by inadequate respiratory response to hypercapnia and life-threatening hypoventilation during sleep. Although no cure is currently availabl...

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Detalles Bibliográficos
Autores principales: Cardani, Silvia, Janes, Tara A., Saini, Jasmeen K., Di Lascio, Simona, Benfante, Roberta, Fornasari, Diego, Pagliardini, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101578/
https://www.ncbi.nlm.nih.gov/pubmed/35563209
http://dx.doi.org/10.3390/ijms23094816

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101578/
https://www.ncbi.nlm.nih.gov/pubmed/35563209
http://dx.doi.org/10.3390/ijms23094816

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