Detalhe da pesquisa
1.
The Effect of ACTN3 Gene Doping on Skeletal Muscle Performance.
Am J Hum Genet
; 102(5): 845-857, 2018 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29706347
2.
Morpholino-induced exon skipping stimulates cell-mediated and humoral responses to dystrophin in mdx mice.
J Pathol
; 248(3): 339-351, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30883742
3.
Annexin A2 links poor myofiber repair with inflammation and adipogenic replacement of the injured muscle.
Hum Mol Genet
; 26(11): 1979-1991, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28334824
4.
Analysis of the ACTN3 heterozygous genotype suggests that α-actinin-3 controls sarcomeric composition and muscle function in a dose-dependent fashion.
Hum Mol Genet
; 25(5): 866-77, 2016 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26681802
5.
Single-cell transcriptomic analysis of the identity and function of fibro/adipogenic progenitors in healthy and dystrophic muscle.
iScience
; 26(8): 107479, 2023 Aug 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37599828
6.
Single-cell and spatial transcriptomics identify a macrophage population associated with skeletal muscle fibrosis.
Sci Adv
; 9(27): eadd9984, 2023 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37418531
7.
Single-cell and spatial transcriptomics identify a macrophage population associated with skeletal muscle fibrosis.
bioRxiv
; 2023 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37131694
8.
Pathogenic role and therapeutic potential of fibro-adipogenic progenitors in muscle disease.
Trends Mol Med
; 28(1): 8-11, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34750068
9.
Anoctamin 5 Knockout Mouse Model Recapitulates LGMD2L Muscle Pathology and Offers Insight Into in vivo Functional Deficits.
J Neuromuscul Dis
; 8(s2): S243-S255, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34633328
10.
TGF-ß-driven muscle degeneration and failed regeneration underlie disease onset in a DMD mouse model.
JCI Insight
; 5(6)2020 03 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32213706
11.
Fibroadipogenic progenitors are responsible for muscle loss in limb girdle muscular dystrophy 2B.
Nat Commun
; 10(1): 2430, 2019 06 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31160583
12.
Dysregulation of Mitochondrial Ca2+ Uptake and Sarcolemma Repair Underlie Muscle Weakness and Wasting in Patients and Mice Lacking MICU1.
Cell Rep
; 29(5): 1274-1286.e6, 2019 10 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-31665639
13.
Author Correction: Myoblasts and macrophages are required for therapeutic morpholino antisense oligonucleotide delivery to dystrophic muscle.
Nat Commun
; 9(1): 1256, 2018 03 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-29572439
14.
Author Correction: Myoblasts and macrophages are required for therapeutic morpholino antisense oligonucleotide delivery to dystrophic muscle.
Nat Commun
; 9(1): 208, 2018 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29335405
15.
Mitochondrial redox signaling enables repair of injured skeletal muscle cells.
Sci Signal
; 10(495)2017 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28874604
16.
Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy.
Nat Commun
; 8: 14143, 2017 01 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-28139640
17.
Effect of endurance exercise on microRNAs in myositis skeletal muscle-A randomized controlled study.
PLoS One
; 12(8): e0183292, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28829792
18.
Myoblasts and macrophages are required for therapeutic morpholino antisense oligonucleotide delivery to dystrophic muscle.
Nat Commun
; 8(1): 941, 2017 10 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29038471
19.
Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophy.
Cell Death Differ
; 24(2): 330-342, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27834955
20.
Elusive sources of variability of dystrophin rescue by exon skipping.
Skelet Muscle
; 5: 44, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26634117