Cargando…
miRNA and mRNA Profiling Links Connexin Deficiency to Deafness via Early Oxidative Damage in the Mouse Stria Vascularis
Pathogenic mutations in the non-syndromic hearing loss and deafness 1 (DFNB1) locus are the primary cause of monogenic inheritance for prelingual hearing loss. To unravel molecular pathways involved in etiopathology and look for early degeneration biomarkers, we used a system biology approach to ana...
Autores principales: | Gentile, Giulia, Paciello, Fabiola, Zorzi, Veronica, Spampinato, Antonio Gianmaria, Guarnaccia, Maria, Crispino, Giulia, Tettey-Matey, Abraham, Scavizzi, Ferdinando, Raspa, Marcello, Fetoni, Anna Rita, Cavallaro, Sebastiano, Mammano, Fabio |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868390/ https://www.ncbi.nlm.nih.gov/pubmed/33569381 http://dx.doi.org/10.3389/fcell.2020.616878 |
Ejemplares similares
-
Connexin 30 deletion exacerbates cochlear senescence and age-related hearing loss
por: Paciello, Fabiola, et al.
Publicado: (2022) -
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway
por: Fetoni, Anna Rita, et al.
Publicado: (2018) -
Tissue-Resident Macrophages in the Stria Vascularis
por: Ito, Taku, et al.
Publicado: (2022) -
Organ of Corti and Stria Vascularis: Is there an Interdependence for Survival?
por: Liu, Huizhan, et al.
Publicado: (2016) -
Transcript Profiles of Stria Vascularis in Models of Waardenburg Syndrome
por: Chen, Linjun, et al.
Publicado: (2020)