Detalhe da pesquisa
1.
Glycine receptor subunit-ß-deficiency in a mouse model of spasticity results in attenuated physical performance, growth, and muscle strength.
Am J Physiol Regul Integr Comp Physiol
; 322(5): R368-R388, 2022 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35108108
2.
Rescue of GSDIII Phenotype with Gene Transfer Requires Liver- and Muscle-Targeted GDE Expression.
Mol Ther
; 26(3): 890-901, 2018 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29396266
3.
Phosphatidylinositol 3-kinase inhibition restores Ca2+ release defects and prolongs survival in myotubularin-deficient mice.
Proc Natl Acad Sci U S A
; 113(50): 14432-14437, 2016 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-27911767
4.
Site-specific Mtm1 mutagenesis by an AAV-Cre vector reveals that myotubularin is essential in adult muscle.
Hum Mol Genet
; 22(9): 1856-66, 2013 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23390130
5.
Blockade of ActRIIB signaling triggers muscle fatigability and metabolic myopathy.
Mol Ther
; 22(8): 1423-1433, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24861054
6.
Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus.
PLoS Genet
; 8(11): e1003043, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23209425
7.
DHPR alpha1S subunit controls skeletal muscle mass and morphogenesis.
EMBO J
; 29(3): 643-54, 2010 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-20033060
8.
Myostatin is a key mediator between energy metabolism and endurance capacity of skeletal muscle.
Am J Physiol Regul Integr Comp Physiol
; 307(4): R444-54, 2014 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24965795
9.
Myocytic androgen receptor controls the strength but not the mass of limb muscles.
Proc Natl Acad Sci U S A
; 107(32): 14327-32, 2010 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-20660752
10.
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice.
Hum Mol Genet
; 19(24): 4820-36, 2010 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20858595
11.
Restoration of muscle functionality by genetic suppression of glycogen synthesis in a murine model of Pompe disease.
Hum Mol Genet
; 19(4): 684-96, 2010 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19959526
12.
Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres.
Hum Mol Genet
; 19(11): 2191-207, 2010 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20207626
13.
Effect of locomotor training on muscle performance in the context of nerve-muscle communication dysfunction.
Muscle Nerve
; 45(4): 567-77, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22431091
14.
A new model of experimental fibrosis in hindlimb skeletal muscle of adult mdx mouse mimicking muscular dystrophy.
Muscle Nerve
; 45(6): 803-14, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22581532
15.
Combination of myostatin pathway interference and dystrophin rescue enhances tetanic and specific force in dystrophic mdx mice.
Mol Ther
; 18(5): 881-7, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20104211
16.
Recombinant botulinum neurotoxin serotype A1 in vivo characterization.
Pharmacol Res Perspect
; 9(5): e00857, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34632725
17.
Evidence of a dosage effect and a physiological endplate acetylcholinesterase deficiency in the first mouse models mimicking Schwartz-Jampel syndrome neuromyotonia.
Hum Mol Genet
; 17(20): 3166-79, 2008 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18647752
18.
Skeletal muscle telomere length in healthy, experienced, endurance runners.
Eur J Appl Physiol
; 109(2): 323-30, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20101406
19.
Genetic ablation of acetylcholinesterase alters muscle function in mice.
Chem Biol Interact
; 175(1-3): 129-30, 2008 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-18550042
20.
Intravenous Administration of a MTMR2-Encoding AAV Vector Ameliorates the Phenotype of Myotubular Myopathy in Mice.
J Neuropathol Exp Neurol
; 77(4): 282-295, 2018 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29408998