Detalhe da pesquisa
1.
CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.
Brain
; 143(3): 783-799, 2020 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32185393
2.
Amyotrophic lateral sclerosis-linked UBQLN2 mutants inhibit endoplasmic reticulum to Golgi transport, leading to Golgi fragmentation and ER stress.
Cell Mol Life Sci
; 77(19): 3859-3873, 2020 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-31802140
3.
ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis.
Hum Mol Genet
; 27(8): 1311-1331, 2018 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-29409023
4.
C9orf72-Associated Dipeptide Repeat Expansions Perturb ER-Golgi Vesicular Trafficking, Inducing Golgi Fragmentation and ER Stress, in ALS/FTD.
Mol Neurobiol
; 2024 May 09.
Artigo
Inglês
| MEDLINE | ID: mdl-38722513
5.
ALS/FTD-associated mutation in cyclin F inhibits ER-Golgi trafficking, inducing ER stress, ERAD and Golgi fragmentation.
Sci Rep
; 13(1): 20467, 2023 11 22.
Artigo
Inglês
| MEDLINE | ID: mdl-37993492
6.
The Redox Activity of Protein Disulfide Isomerase Inhibits ALS Phenotypes in Cellular and Zebrafish Models.
iScience
; 23(5): 101097, 2020 May 22.
Artigo
Inglês
| MEDLINE | ID: mdl-32446203
7.
Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations.
Mol Neurodegener
; 15(1): 51, 2020 09 09.
Artigo
Inglês
| MEDLINE | ID: mdl-32907630
8.
Motor Neuron Susceptibility in ALS/FTD.
Front Neurosci
; 13: 532, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31316328