Crosstalk between the UPR and autophagy pathway contributes to handling cellular stress in neurodegenerative disease

Por Vidal, René L., Hetz, Claudio
Publicado em 2012

Unspliced XBP1 controls autophagy through FoxO1

Por Vidal, Rene L, Hetz, Claudio
Publicado em 2013

Cellular and subcellular localization of Marlin-1 in the brain

Por Vidal, René L, Valenzuela, José I, Luján, Rafael, Couve, Andrés
Publicado em 2009

Dendritic Assembly of Heteromeric γ-Aminobutyric Acid Type B Receptor Subunits in Hippocampal Neurons

Por Ramírez, Omar A., Vidal, René L., Tello, Judith A., Vargas, Karina J., Kindler, Stefan, Härtel, Steffen, Couve, Andrés
Publicado em 2009

Control of dopaminergic neuron survival by the unfolded protein response transcription factor XBP1

Por Valdés, Pamela, Mercado, Gabriela, Vidal, Rene L., Molina, Claudia, Parsons, Geoffrey, Court, Felipe A., Martinez, Alexis, Galleguillos, Danny, Armentano, Donna, Schneider, Bernard L., Hetz, Claudio
Publicado em 2014

Functional Role of the Disulfide Isomerase ERp57 in Axonal Regeneration

Por Castillo, Valentina, Oñate, Maritza, Woehlbier, Ute, Rozas, Pablo, Andreu, Catherine, Medinas, Danilo, Valdés, Pamela, Osorio, Fabiola, Mercado, Gabriela, Vidal, René L., Kerr, Bredford, Court, Felipe A., Hetz, Claudio
Publicado no PLoS One (2015)

Correction: Functional Role of the Disulfide Isomerase ERp57 in Axonal Regeneration

Por Castillo, Valentina, Oñate, Maritza, Woehlbier, Ute, Rozas, Pablo, Andreu, Catherine, Medinas, Danilo, Valdés, Pamela, Osorio, Fabiola, Mercado, Gabriela, Vidal, René L., Kerr, Bredford, Court, Felipe A., Hetz, Claudio
Publicado no PLoS One (2015)

Targeting the UPR transcription factor XBP1 protects against Huntington's disease through the regulation of FoxO1 and autophagy

Por Vidal, Rene L., Figueroa, Alicia, Court, Felipe A., Thielen, Peter, Molina, Claudia, Wirth, Craig, Caballero, Benjamin, Kiffin, Roberta, Segura-Aguilar, Juan, Cuervo, Ana Maria, Glimcher, Laurie H., Hetz, Claudio
Publicado em 2012

A failure in energy metabolism and antioxidant uptake precede symptoms of Huntington’s disease in mice

Por Acuña, Aníbal I., Esparza, Magdalena, Kramm, Carlos, Beltrán, Felipe A., Parra, Alejandra V., Cepeda, Carlos, Toro, Carlos A., Vidal, René L., Hetz, Claudio, Concha, Ilona I., Brauchi, Sebastián, Levine, Michael S., Castro, Maite A.
Publicado em 2013

ALS‐linked protein disulfide isomerase variants cause motor dysfunction

Por Woehlbier, Ute, Colombo, Alicia, Saaranen, Mirva J, Pérez, Viviana, Ojeda, Jorge, Bustos, Fernando J, Andreu, Catherine I, Torres, Mauricio, Valenzuela, Vicente, Medinas, Danilo B, Rozas, Pablo, Vidal, Rene L, Lopez‐Gonzalez, Rodrigo, Salameh, Johnny, Fernandez‐Collemann, Sara, Muñoz, Natalia, Matus, Soledad, Armisen, Ricardo, Sagredo, Alfredo, Palma, Karina, Irrazabal, Thergiory, Almeida, Sandra, Gonzalez‐Perez, Paloma, Campero, Mario, Gao, Fen‐Biao, Henny, Pablo, van Zundert, Brigitte, Ruddock, Lloyd W, Concha, Miguel L, Henriquez, Juan P, Brown, Robert H, Hetz, Claudio
Publicado no EMBO J (2016)