Now showing items 1-6 of 6

    • Silva-Pavez, Eduardo; Villar, Paulina; Trigo, César; Caamaño, Esteban; Niechi, Ignacio; Pérez, Pablo; Muñoz, Juan P.; Aguayo, Francisco; Burzio, Verónica A.; Varas Godoy, Manuel; Castro, Ariel F.; Colombo, María I.; Tapia, Julio C. (Nature Publishing Group, 2019)
      Protein kinase CK2 is a highly conserved and constitutively active Ser/Thr-kinase that phosphorylates a large number of substrates, resulting in increased cell proliferation and survival. A known target of CK2 is Akt, a ...
    • Fuentes Villalobos, Francisco; Farkas, Carlos; Riquelme Barrios, Sebastián; Armijo, Marisol E.; Soto Rifo, Ricardo; Pincheira, Roxana; Castro, Ariel F. (Elsevier B.V., 2019)
      Variation in Disrupted-in-Schizophrenia 1 (DISC1) increases the risk for neurodegenerative diseases, schizophrenia, and other mental disorders. However, the functions of DISC1 associated with the development of these ...
    • Campos, Tania; Ziehe, Javiera; Fuentes Villalobos, Francisco; Riquelme, Orlando; Peña, Daniela; Troncoso Cotal, Rodrigo; Lavandero González, Sergio; Morín, Violeta; Pincheira, Roxana; Castro, Ariel F. (Elsevier, 2016)
      Tuberous sclerosis complex (TSC) disease results from inactivation of the TSC1 or TSC2 gene, and is characterized by benign tumors in several organs. Because TSC tumorigenesis correlates with hyperactivation of mTORC1, ...
    • Hermosilla, Viviana; Salgado, Ginessa; Riffo, Elizabeth; Escobar, David; Hepp, Matias; Farkas, Carlos; Galindo, Mario; Morín, Violeta; García-Robles, María; Castro, Ariel; Pincheira, Roxana (Wiley, 2018-06)
      SALL2 is a poorly characterized transcription factor that belongs to the Spalt-like family involved in development. Mutations on SALL2 have been associated with ocular coloboma and cancer. In cancers, SALL2 is deregulated ...
    • Hermosilla, Viviana E.; Escobar, David E.; Hepp, Matias I.; Riffo, Elizabeth N.; Salgado, Ginessa; Morin, Violeta; Galindo, Mario A.; Castro, Ariel F.; Pincheira, Roxana (Amer Assoc. Cancer Research, 2018-05)
    • Pinto, Cristina; Medinas, Danilo B.; Fuentes Villalobos, Francisco; Maripillán, Jaime; Castro, Ariel F.; Martínez, Agustín D.; Osses, Nelson; Hetz Flores, Claudio; Henríquez, Juan P. (Academic Press Inc., 2019)
      Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by motor neuron death. A 20% of familial ALS cases are associated with mutations in the gene coding for superoxide dismutase 1 (SOD1). The ...