Browsing by Author "8dc38d12-e79c-4733-bb6f-119226ec1245"

Now showing items 1-3 of 3

    • First genetic record of a strap-toothed beaked whale (mesoplodon layardii) stranding in Chile 
      Español Jiménez, Sonia; Abaud, Constanza; Aceituno, Camila; Alvarado Rybak, Mario; Borroni, Cintya; Chiang, Gustavo; Diaz, Javier; Espejo, Winfred; Estay, María Luisa; García Cegarra, Ana; González, Carlos; Gutiérrez, Belén; Gutiérrez, Josefina; Henríquez, Daniel; Hirmas, Andrea; Mejías, Pamela; Merino, Constanza; Molina, Charity; Naretto, Camilo; Olivares, Florencia; Pereira, Patricia; Peñaloza, Diego; Pincheira, Betsy; Pinto, Nicolás; Rojas, Omar; Alemán Sánchez, Carolina María; Toro, Bárbara; Toro, Frederick; Undurraga, Raimundo (European Assoc. Aquatic Mammals, 2020)
    • Genome-wide circulating microRNA expression profiling reveals potential biomarkers for amyotrophic lateral ... 
      Matamala, José Manuel; Arias Carrasco, Raul; Sánchez, Carolina; Uhrig, Markus; Bargsted, Leslie; Matus, Soledad; Maracaja Coutinho, Vinicius; Abarzua, Sebastián; Van Zundert, Brigitte; Verdugo Latorre, Renato; Manque, Patricio; Hetz Flores, Claudio (Elsevier, 2018)
      The occurrence of mutations of TDP-43, FUS, and C9ORF72 in amyotrophic lateral sclerosis (ALS) suggests pathogenic alterations to RNA metabolism and specifically to microRNA (miRNA) biology. Moreover, several ALS-related ...
    • NOTCH3 gene mutation in a chilean cerebral autosomal dominant arteriopathy with subcortical infarcts and ... 
      Gallardo Vera, Andrés; Latapiat, Verónica; Rivera, Alejandra; Fonseca, Beatriz; Roldán, Andrés; Sandoval, Patricio; Sánchez, Carolina; Matamala Capponi, José (Elsevier, 2020)
      Introduction: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare hereditary stroke disorder caused by mutations in the NOTCH3 gene. We report the first Chilean ...