Cargando…
Impact of a NDUFC2 Variant on the Occurrence of Acute Coronary Syndromes
BACKGROUND: Among several potential mechanisms, mitochondrial dysfunction has been proposed to be involved in the pathogenesis of coronary artery disease (CAD). A mitochondrial complex I deficiency severely impairs cardiovascular health and contributes to CAD development. Previous evidence highlight...
Autores principales: | Gallo, Giovanna, Migliarino, Serena, Cotugno, Maria, Stanzione, Rosita, Burocchi, Simone, Bianchi, Franca, Marchitti, Simona, Autore, Camillo, Volpe, Massimo, Rubattu, Speranza |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197441/ https://www.ncbi.nlm.nih.gov/pubmed/35711349 http://dx.doi.org/10.3389/fcvm.2022.921244 |
Ejemplares similares
-
Polymorphic variants at NDUFC2, encoding a mitochondrial complex I subunit, associate with cardiac hypertrophy in human hypertension
por: Gallo, Giovanna, et al.
Publicado: (2023) -
Functional Role of Natriuretic Peptides in Risk Assessment and Prognosis of Patients with Mitral Regurgitation
por: Gallo, Giovanna, et al.
Publicado: (2020) -
Pathogenesis of Ischemic Stroke: Role of Epigenetic Mechanisms
por: Stanzione, Rosita, et al.
Publicado: (2020) -
The C2238/αANP Variant Is a Negative Modulator of Both Viability and Function of Coronary Artery Smooth Muscle Cells
por: Rubattu, Speranza, et al.
Publicado: (2014) -
Ndufc2 Gene Inhibition Is Associated With Mitochondrial Dysfunction and Increased Stroke Susceptibility in an Animal Model of Complex Human Disease
por: Rubattu, Speranza, et al.
Publicado: (2016)