Detalhe da pesquisa
1.
Microutrophin expression in dystrophic mice displays myofiber type differences in therapeutic effects.
PLoS Genet
; 16(11): e1009179, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33175853
2.
Fnip1 regulates skeletal muscle fiber type specification, fatigue resistance, and susceptibility to muscular dystrophy.
Proc Natl Acad Sci U S A
; 112(2): 424-9, 2015 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25548157
3.
Muscle structure influences utrophin expression in mdx mice.
PLoS Genet
; 10(6): e1004431, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24922526
4.
Microtubule binding distinguishes dystrophin from utrophin.
Proc Natl Acad Sci U S A
; 111(15): 5723-8, 2014 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24706788
5.
Expression of the dystrophin isoform Dp116 preserves functional muscle mass and extends lifespan without preventing dystrophy in severely dystrophic mice.
Hum Mol Genet
; 20(24): 4978-90, 2011 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21949353
6.
Successful regional delivery and long-term expression of a dystrophin gene in canine muscular dystrophy: a preclinical model for human therapies.
Mol Ther
; 20(8): 1501-7, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22692496
7.
The polyproline site in hinge 2 influences the functional capacity of truncated dystrophins.
PLoS Genet
; 6(5): e1000958, 2010 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-20502633
8.
Molecular and cellular adaptations to chronic myotendinous strain injury in mdx mice expressing a truncated dystrophin.
Hum Mol Genet
; 17(24): 3975-86, 2008 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18799475
9.
Sequencing protocols to genotype mdx, mdx(4cv), and mdx(5cv) mice.
Muscle Nerve
; 42(2): 268-70, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20544945
10.
Truncated dystrophins can influence neuromuscular synapse structure.
Mol Cell Neurosci
; 40(4): 433-41, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19171194
11.
Dramatic elevation in urinary amino terminal titin fragment excretion quantified by immunoassay in Duchenne muscular dystrophy patients and in dystrophin deficient rodents.
Neuromuscul Disord
; 27(7): 635-645, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28554556
12.
Glycinergic and GABAergic synaptic activity differentially regulate motoneuron survival and skeletal muscle innervation.
J Neurosci
; 25(5): 1249-59, 2005 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-15689563
13.
Loss of niche-satellite cell interactions in syndecan-3 null mice alters muscle progenitor cell homeostasis improving muscle regeneration.
Skelet Muscle
; 6: 34, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27757223
14.
Elucidating the molecular mechanisms that underlie the target control of motoneuron death.
Int J Dev Biol
; 46(4): 551-8, 2002.
Artigo
em Inglês
| MEDLINE | ID: mdl-12141443
15.
Genetic disruption of the growth hormone receptor does not influence motoneuron survival in the developing mouse.
Int J Dev Biol
; 47(1): 41-9, 2003 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-12653250
16.
Myofiber branching rather than myofiber hyperplasia contributes to muscle hypertrophy in mdx mice.
Skelet Muscle
; 4: 10, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24910770
17.
Animal models of muscular dystrophy.
Prog Mol Biol Transl Sci
; 105: 83-111, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22137430
18.
Prevention of muscle aging by myofiber-associated satellite cell transplantation.
Sci Transl Med
; 2(57): 57ra83, 2010 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21068442
19.
Preclinical studies for gene therapy of Duchenne muscular dystrophy.
J Child Neurol
; 25(9): 1149-57, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20498332
20.
The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategies.
Curr Top Dev Biol
; 84: 431-53, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-19186250