Browsing by Author "de83c8f1-9019-433a-b00e-5177e6a1c243"
Now showing items 1-3 of 3
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Rojas, Cecilia V.; Santa María, Lorena; Santos, José Luis; Cortés, Fanny; Alliende, María Angélica (2002)Complete achromatopsia is genetically heterogeneous and segregates with mutations in CNGA3 or CNGB3 genes, which respectively encode for α- and β-subunits of the cyclic-nucleotide-gated (CNG) cation channel expressed in ...
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Rojas, Cecilia V.; Neely, Alan; Velasco-Loyden, Gabriela; Palma, Veronica; Kukuljan Padilla, Manuel (1999)Mutations in the human skeletal muscle Na+ channel underlie the autosomal dominant disease hyperkalemic periodic paralysis (HPP). Muscle fibers from affected individuals exhibit sustained Na+ currents thought to depolarize ...
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Medina Fuentes, Paula; Acuña, María José; Cifuentes, Mariana; Rojas, Cecilia V. (2010)Despite the importance of adipocyte formation for adipose tissue physiology, current knowledge about the mechanisms that regulate the recruitment of progenitor cells to undergo adipogenic differentiation is limited. A role ...