Buscar
Mostrando ítems 31-40 de 111
Neuregulin-1/erbB activities with focus on the susceptibility of the heart to anthracyclines
(Baishideng Publishing Group, 2014-07)
Neuregulin-1 (NRG1) signaling through the tyrosine kinase receptors erbB2 and erbB4 is required for cardiac morphogenesis, and it plays an essential role in maintaining the myocardial architecture during adulthood. The ...
Frataxin deficiency in neonatal rat ventricular myocytes targets mitochondria and lipid metabolism
(Elsevier, 2014-08)
Friedreich ataxia (FRDA) is a hereditary disease caused by deficient frataxin expression. This mitochondrial protein has been related to iron homeostasis, energy metabolism, and oxidative stress. Patients with FRDA experience ...
Atrophic Cardiac Remodeling Induced by Taurine Deficiency in Wistar Rats
(Public Library Science, 2014)
Determinación de variantes genéticas en una muestra de población colombiana con miocardiopatías hereditarias: Un estudio piloto
(Universidad Nacional de ColombiaBogotá - Medicina - Maestría en Genética HumanaFacultad de MedicinaBogotáUniversidad Nacional de Colombia - Sede Bogotá, 2020)
La más importante manifestación de las canalopatías y miocardiopatías es la muerte súbita cardiaca; por ello la evaluación de estas patologías es de gran importancia. Las canalopatías cardíacas congénitas son causadas por ...
Pompe disease: Clinical perspectives
(Dove Medical, 2017)
Pompe disease (acid alpha-glucosidase deficiency, OMIM 232300) is a rare lysosomal storage disorder due to autosomal recessive mutations in the GAA gene. It has also been called acid maltase deficiency and glycogen storage ...