Ablation of the Chaperone Protein ERdj5 Results in a Sjögren's Syndrome-Like Phenotype in Mice, Consistent With an Upregulated Unfolded Protein Response in Human Patients

Samankaltaisia teoksia

• Ablation of the Chaperone Protein ERdj5 Results in a Sjögren's Syndrome-Like Phenotype in Mice, Consistent With an Upregulated Unfolded Protein Response in Human Patients
  Tekijä: Eirini Apostolou, et al.
  Julkaistu: (2019-03-01)
• Deregulation of the Kallikrein Protease Family in the Salivary Glands of the Sjögren’s Syndrome ERdj5 Knockout Mouse Model
  Tekijä: Moustardas, Petros, et al.
  Julkaistu: (2021)
• The co-chaperone and reductase ERdj5 facilitates rod opsin biogenesis and quality control
  Tekijä: Athanasiou, Dimitra, et al.
  Julkaistu: (2014)
• Corrigendum to: The co-chaperone and reductase ERdj5 facilitates rod opsin biogenesis and quality control
  Tekijä: Athanasiou, Dimitra, et al.
  Julkaistu: (2020)
• Regulated release of ERdj3 from unfolded proteins by BiP
  Tekijä: Jin, Yi, et al.
  Julkaistu: (2008)