Detalhe da pesquisa
1.
Receptor clustering and pathogenic complement activation in myasthenia gravis depend on synergy between antibodies with multiple subunit specificities.
Acta Neuropathol
; 144(5): 1005-1025, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36074148
2.
Identification of Small Molecules Which Induce Skeletal Muscle Differentiation in Embryonic Stem Cells via Activation of the Wnt and Inhibition of Smad2/3 and Sonic Hedgehog Pathways.
Stem Cells
; 34(2): 299-310, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26577380
3.
Engineering circuits of human iPSC-derived neurons and rat primary glia.
Front Neurosci
; 17: 1103437, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37250404
4.
Transmission-selective muscle pathology induced by the active propagation of mutant huntingtin across the human neuromuscular synapse.
Front Mol Neurosci
; 16: 1287510, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38235149
5.
Topologically controlled circuits of human iPSC-derived neurons for electrophysiology recordings.
Lab Chip
; 22(7): 1386-1403, 2022 03 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35253810
6.
Long-term blinded placebo-controlled study of SNT-MC17/idebenone in the dystrophin deficient mdx mouse: cardiac protection and improved exercise performance.
Eur Heart J
; 30(1): 116-24, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18784063
7.
Omigapil ameliorates the pathology of muscle dystrophy caused by laminin-alpha2 deficiency.
J Pharmacol Exp Ther
; 331(3): 787-95, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19759319
8.
Effect of calpain and proteasome inhibition on Ca2+-dependent proteolysis and muscle histopathology in the mdx mouse.
FASEB J
; 22(12): 4190-200, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18728218
9.
Modulation of Microglia by Voluntary Exercise or CSF1R Inhibition Prevents Age-Related Loss of Functional Motor Units.
Cell Rep
; 29(6): 1539-1554.e7, 2019 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31693894
10.
Preferential amplification of a human mitochondrial DNA deletion in vitro and in vivo.
Sci Rep
; 8(1): 1799, 2018 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-29379065
11.
CLK2 inhibition ameliorates autistic features associated with SHANK3 deficiency.
Science
; 351(6278): 1199-203, 2016 Mar 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26847545
12.
CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations.
Stem Cell Reports
; 7(6): 1059-1071, 2016 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-27840045
13.
High-Throughput Screening Using iPSC-Derived Neuronal Progenitors to Identify Compounds Counteracting Epigenetic Gene Silencing in Fragile X Syndrome.
J Biomol Screen
; 20(9): 1101-11, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26024946
14.
Detection of glucocorticoid-like activity in traditional Chinese medicine used for the treatment of Duchenne muscular dystrophy.
Neuromuscul Disord
; 13(9): 699-704, 2003 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-14561491
15.
Glucocorticoid-mediated regulation of utrophin levels in human muscle fibers.
Neuromuscul Disord
; 12 Suppl 1: S95-104, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12206803
16.
Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse.
Neuromuscul Disord
; 14(10): 675-82, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15351425
17.
NQO1-dependent redox cycling of idebenone: effects on cellular redox potential and energy levels.
PLoS One
; 6(3): e17963, 2011 Mar 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-21483849
18.
Orally available selective melanocortin-4 receptor antagonists stimulate food intake and reduce cancer-induced cachexia in mice.
PLoS One
; 4(3): e4774, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19295909
19.
Utrophin is a calpain substrate in muscle cells.
Muscle Nerve
; 33(6): 753-9, 2006 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-16598790
20.
Novel cell-penetrating alpha-keto-amide calpain inhibitors as potential treatment for muscular dystrophy.
Bioorg Med Chem Lett
; 15(23): 5176-81, 2005 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-16185867