Detalhe da pesquisa
1.
ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis.
Hum Mol Genet
; 27(8): 1311-1331, 2018 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29409023
2.
Protein Disulfide Isomerase Endoplasmic Reticulum Protein 57 (ERp57) is Protective Against ALS-Associated Mutant TDP-43 in Neuronal Cells.
Neuromolecular Med
; 26(1): 23, 2024 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38861223
3.
Correction to: the Cysteine (Cys) Residues Cys-6 and Cys-111 in Mutant Superoxide Dismutase 1 (SOD1) A4V Are Required for Induction of Endoplasmic Reticulum Stress in Amyotrophic Lateral Sclerosis.
J Mol Neurosci
; 70(9): 1369, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32529537
4.
The Cysteine (Cys) Residues Cys-6 and Cys-111 in Mutant Superoxide Dismutase 1 (SOD1) A4V Are Required for Induction of Endoplasmic Reticulum Stress in Amyotrophic Lateral Sclerosis.
J Mol Neurosci
; 70(9): 1357-1368, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32445072
5.
The Redox Activity of Protein Disulfide Isomerase Inhibits ALS Phenotypes in Cellular and Zebrafish Models.
iScience
; 23(5): 101097, 2020 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32446203
6.
Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations.
Mol Neurodegener
; 15(1): 51, 2020 09 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32907630
7.
Protein Disulphide Isomerases: emerging roles of PDI and ERp57 in the nervous system and as therapeutic targets for ALS.
Expert Opin Ther Targets
; 21(1): 37-49, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27786579
8.
Protein Quality Control and the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia Continuum.
Front Mol Neurosci
; 10: 119, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28539871
9.
The Unfolded Protein Response and the Role of Protein Disulfide Isomerase in Neurodegeneration.
Front Cell Dev Biol
; 3: 80, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26779479