Detalhe da pesquisa
1.
A Ca2+-Dependent Mechanism Boosting Glycolysis and OXPHOS by Activating Aralar-Malate-Aspartate Shuttle, upon Neuronal Stimulation.
J Neurosci
; 42(19): 3879-3895, 2022 05 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35387872
2.
Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations.
Int J Mol Sci
; 20(18)2019 Sep 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31540302
3.
Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity.
iScience
; 27(6): 109930, 2024 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38832025
4.
Targeting the Ubiquitin-Proteasome System in Limb-Girdle Muscular Dystrophy With CAPN3 Mutations.
Front Cell Dev Biol
; 10: 822563, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35309930
5.
A genotyping method combining primer competition PCR with HRM analysis to identify point mutations in Duchenne animal models.
Sci Rep
; 10(1): 17224, 2020 10 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057138