Cargando…
Histone deacetylase inhibition reduces cardiac connexin43 expression and gap junction communication
Histone deacetylase inhibitors (HDACIs) are being investigated as novel therapies for cancer, inflammation, neurodegeneration, and heart failure. The effects of HDACIs on the functional expression of cardiac gap junctions (GJs) are essentially unknown. The purpose of this study was to determine the...
Autores principales: | Xu, Qin, Lin, Xianming, Andrews, Laura, Patel, Dakshesh, Lampe, Paul D., Veenstra, Richard D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625725/ https://www.ncbi.nlm.nih.gov/pubmed/23596417 http://dx.doi.org/10.3389/fphar.2013.00044 |
Ejemplares similares
-
Differences in Functional Expression of Connexin43 and Na(V)1.5 by Pan- and Class-Selective Histone Deacetylase Inhibition in Heart
por: Zhang, Xian, et al.
Publicado: (2018) -
Monovalent Ion Selectivity Sequences of the Rat Connexin43 Gap Junction Channel
por: Wang, Hong-Zhan, et al.
Publicado: (1997) -
Phosphorylation of Connexin43 on Serine368 by Protein Kinase C Regulates Gap Junctional Communication
por: Lampe, Paul D., et al.
Publicado: (2000) -
The effects of the histone deacetylase inhibitor 4-phenylbutyrate on gap junction conductance and permeability
por: Kaufman, Joshua, et al.
Publicado: (2013) -
Ser364 of connexin43 and the upregulation of gap junction assembly by cAMP
por: TenBroek, Erica M., et al.
Publicado: (2001)