Detalhe da pesquisa
1.
Mutation-independent Proteomic Signatures of Pathological Progression in Murine Models of Duchenne Muscular Dystrophy.
Mol Cell Proteomics
; 19(12): 2047-2068, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32994316
2.
Light modulation ameliorates expression of circadian genes and disease progression in spinal muscular atrophy mice.
Hum Mol Genet
; 27(20): 3582-3597, 2018 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29982483
3.
Seasonal induction of GABAergic excitation in the central mammalian clock.
Proc Natl Acad Sci U S A
; 111(26): 9627-32, 2014 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24979761
4.
Current understanding of molecular pathology and treatment of cardiomyopathy in duchenne muscular dystrophy.
Molecules
; 20(5): 8823-55, 2015 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25988613
5.
Uniform sarcolemmal dystrophin expression is required to prevent extracellular microRNA release and improve dystrophic pathology.
J Cachexia Sarcopenia Muscle
; 11(2): 578-593, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31849191
6.
Interventions Targeting Glucocorticoid-Krüppel-like Factor 15-Branched-Chain Amino Acid Signaling Improve Disease Phenotypes in Spinal Muscular Atrophy Mice.
EBioMedicine
; 31: 226-242, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29735415