Detalhe da pesquisa
1.
Neuromuscular junction denervation and terminal Schwann cell loss in the hTDP-43 overexpression mouse model of amyotrophic lateral sclerosis.
Neuropathol Appl Neurobiol
; 49(4): e12925, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37465879
2.
Temporal and tissue-specific variability of SMN protein levels in mouse models of spinal muscular atrophy.
Hum Mol Genet
; 27(16): 2851-2862, 2018 08 15.
Artigo
Inglês
| MEDLINE | ID: mdl-29790918
3.
UBA1/GARS-dependent pathways drive sensory-motor connectivity defects in spinal muscular atrophy.
Brain
; 141(10): 2878-2894, 2018 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30239612
4.
Long-term muscle-specific overexpression of DOK7 in mice using AAV9-tMCK-DOK7.
Mol Ther Nucleic Acids
; 33: 617-628, 2023 Sep 12.
Artigo
Inglês
| MEDLINE | ID: mdl-37637210
5.
SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in disease.
Nat Commun
; 14(1): 5466, 2023 09 25.
Artigo
Inglês
| MEDLINE | ID: mdl-37749075
6.
Targeting phosphoglycerate kinase 1 with terazosin improves motor neuron phenotypes in multiple models of amyotrophic lateral sclerosis.
EBioMedicine
; 83: 104202, 2022 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-35963713
7.
The mitochondrial protein Sideroflexin 3 (SFXN3) influences neurodegeneration pathways in vivo.
FEBS J
; 289(13): 3894-3914, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35092170
8.
Robust Comparison of Protein Levels Across Tissues and Throughout Development Using Standardized Quantitative Western Blotting.
J Vis Exp
; (146)2019 04 09.
Artigo
Inglês
| MEDLINE | ID: mdl-31033956