Browsing by Author "cff476ab-c980-44d2-9280-bdf7c7d113d9"
Now showing items 1-6 of 6
-
Connexin-based hemichannels are key factors in the pathological mechanism underlying dysferlinopathy Fernandez, G.; Bevilacqua, Jorge; Cárdenas, A.; Saez, J.; Caviedes Fernández, Pablo; Cea Pisani, Luis Andrés (Elsevier, 2017)
-
Cea Pisani, Luis; Balboa, Elisa; Puebla, Carlos; Vargas, Aníbal; Cisterna, Bruno; Escamilla, Rosalba; Regueira, Tomás; Sáez, Juan C. (Elsevier, 2016)Long-term treatment with high glucocorticoid doses induces skeletal muscle atrophy. However, the molecular mechanism of such atrophy remains unclear. We evaluated the possible involvement of connexin-based hemichannels (Cx ...
-
Cárdenas, Ana María; González Jamett, Arlek M.; Cea Pisani, Luis Andrés; Bevilacqua, Jorge; Caviedes Fernández, Pablo (2016)Mutations in the dysferlin gene are linked to a group of muscular dystrophies known as dysferlinopathies. These myopathies are characterized by progressive atrophy. Studies in muscle tissue from dysferlinopathy patients ...
-
Cea Pisani, Luis Andrés; Puebla, Carlos; Cisterna, Bruno A.; Escamilla, Rosalba; Vargas, Anibal A.; Frank, Marina; Martinez Montero, Paloma; Prior, Carmen; Molano, Jesus; Esteban Rodríguez, Isabel; Pascual, Ignacio; Gallano, Pía; Lorenzo, Gustavo; Pian, Héctor; Barrio, Luis C.; Willecke, Kla; Saez, Juan C. (Springer, 2016)Skeletal muscles of patients with Duchenne muscular dystrophy (DMD) show numerous alterations including inflammation, apoptosis, and necrosis of myofibers. However, the molecular mechanism that explains these changes remains ...
-
Balboa, Elisa; Saavedra Leiva, Fujiko; Cea Pisani, Luis Andrés; Vargas, Anibal A.; Ramírez, Valeria; Escamilla, Rosalba; Saez, Juan C.; Regueira, Tomás (Lippincott Williams & Wilkins, 2018)Skeletal muscles (similar to 50% of the body weight) are affected during acute and late sepsis and represent one sepsis associate organ dysfunction. Cell membrane changes have been proposed to result from a channelopathy ...
-
Cea Pisani, Luis Andrés; Bevilacqua, Jorge; Arriagada Abarzúa, Christian; Cárdenas, Ana María; Bigot, Anne; Mouly, Vincent; Sáez, Juan C.; Caviedes Fernández, Pablo (2016)Background: Mutations in the gene encoding for dysferlin cause recessive autosomal muscular dystrophies called dysferlinopathies. These mutations induce several alterations in skeletal muscles, including, inflammation, ...