Your browser doesn't support javascript.
loading
ALS-FTLD associated mutations of SQSTM1 impact on Keap1-Nrf2 signalling.
Goode, Alice; Rea, Sarah; Sultana, Melanie; Shaw, Barry; Searle, Mark S; Layfield, Robert.
  • Goode A; School of Life Sciences, University of Nottingham, UK. Electronic address: alice.goode@nottingham.ac.uk.
  • Rea S; Harry Perkins Institute of Medical Research, University of Western Australia, Australia; Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Sultana M; Harry Perkins Institute of Medical Research, University of Western Australia, Australia; Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Shaw B; School of Life Sciences, University of Nottingham, UK.
  • Searle MS; Centre for Biomolecular Sciences, School of Chemistry, University of Nottingham, Nottingham, UK.
  • Layfield R; School of Life Sciences, University of Nottingham, UK.
Mol Cell Neurosci ; 76: 52-58, 2016 10.
Article en En | MEDLINE | ID: mdl-27554286

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Mutación Missense / Factor 2 Relacionado con NF-E2 / Degeneración Lobar Frontotemporal / Proteína 1 Asociada A ECH Tipo Kelch / Proteína Sequestosoma-1 / Esclerosis Amiotrófica Lateral Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Mutación Missense / Factor 2 Relacionado con NF-E2 / Degeneración Lobar Frontotemporal / Proteína 1 Asociada A ECH Tipo Kelch / Proteína Sequestosoma-1 / Esclerosis Amiotrófica Lateral Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2016 Tipo del documento: Article