Browsing by Author "Valladares, Denisse"
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Henríquez Olguín, Carlos; Altamirano, Francisco; Valladares, Denisse; López, José; Allen, Paul; Jaimovich Pérez, Enrique (Elsevier, 2015)Duchenne muscular dystrophy is a fatal X-linked genetic disease, caused by mutations in the dystrophin gene, which cause functional loss of this protein. This pathology is associated with an increased production of reactive ...
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Henríquez Olguín, Carlos; Altamirano, Francisco; Valladares, Denisse; López, José R.; Allen, Paul D.; Jaimovich Pérez, Enrique (Elsevier, 2015)Duchenne muscular dystrophy is a fatal X-linked genetic disease, caused by mutations in the dystrophin gene, which cause functional loss of this protein. This pathology is associated with an increased production of reactive ...
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Valladares, Denisse; Almarza, Gonzalo; Contreras, Ariel; Pavez, Mario; Buvinic Radic, Sonja; Jaimovich Pérez, Enrique; Casas Atala, Mariana (2013-11)ATP signaling has been shown to regulate gene expression in skeletal muscle and to be altered in models of muscular dystrophy. We have previously shown that in normal muscle fibers, ATP released through Pannexin1 (Panx1) ...
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Valladares, Denisse; Utreras Mendoza, Yildy; Campos, Cristian; Morales, Camilo; Díaz Vegas, Alexis; Contreras Ferrat, Ariel Eduardo; Westermeier, Francisco; Jaimovich Pérez, Enrique; Marchi, Saverio; Pinton, Paolo; Lavandero González, Sergio (Elsevier B.V., 2018)© 2018 Duchenne muscular dystrophy (DMD) is characterized by a severe and progressive destruction of muscle fibers associated with altered Ca2+ homeostasis. We have previously shown that the IP3 receptor (IP3R) plays a ...