Detalhe da pesquisa
1.
Pharmacological activation of SERCA ameliorates dystrophic phenotypes in dystrophin-deficient mdx mice.
Hum Mol Genet
; 30(11): 1006-1019, 2021 05 31.
Artigo
Inglês
| MEDLINE | ID: mdl-33822956
2.
Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes.
Development
; 147(21)2020 09 02.
Artigo
Inglês
| MEDLINE | ID: mdl-32878913
3.
Formation of subcellular compartments by condensation-prone protein OsJAZ2 in Oryza sativa and Nicotiana benthamiana leaf cells.
Plant Cell Rep
; 42(2): 269-286, 2023 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-36449075
4.
Establishment of a Triple Quadrupole HPLC-MS Quantitation Method for Dystrophin Protein in Mouse and Human Skeletal Muscle.
Int J Mol Sci
; 25(1)2023 Dec 25.
Artigo
Inglês
| MEDLINE | ID: mdl-38203473
5.
Mutation-independent Proteomic Signatures of Pathological Progression in Murine Models of Duchenne Muscular Dystrophy.
Mol Cell Proteomics
; 19(12): 2047-2068, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-32994316
6.
Viral isolation analysis of SARS-CoV-2 from clinical specimens of COVID-19 patients.
J Infect Chemother
; 28(2): 347-351, 2022 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-34774431
7.
High-resolution spatiotemporal transcriptome analyses during cellularization of rice endosperm unveil the earliest gene regulation critical for aleurone and starchy endosperm cell fate specification.
J Plant Res
; 134(5): 1061-1081, 2021 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-34279738
8.
Periostin Is Required for the Maintenance of Muscle Fibers during Muscle Regeneration.
Int J Mol Sci
; 22(7)2021 Mar 31.
Artigo
Inglês
| MEDLINE | ID: mdl-33807264
9.
The nSMase2/Smpd3 gene modulates the severity of muscular dystrophy and the emotional stress response in mdx mice.
BMC Med
; 18(1): 343, 2020 11 19.
Artigo
Inglês
| MEDLINE | ID: mdl-33208172
10.
Glycerophospholipid profile alterations are associated with murine muscle-wasting phenotype.
Muscle Nerve
; 62(3): 413-418, 2020 09.
Artigo
Inglês
| MEDLINE | ID: mdl-32496590
11.
Efficacy of Multi-exon Skipping Treatment in Duchenne Muscular Dystrophy Dog Model Neonates.
Mol Ther
; 27(1): 76-86, 2019 01 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30448197
12.
Exons 45-55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD Gene.
Mol Ther
; 27(11): 2005-2017, 2019 11 06.
Artigo
Inglês
| MEDLINE | ID: mdl-31416775
13.
Phase II multi-institutional prospective trial of nab-paclitaxel as second-line chemotherapy for advanced gastric cancer refractory to fluoropyrimidine with modified dose reduction criteria (CCOG1303).
Int J Clin Oncol
; 25(10): 1793-1799, 2020 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-32567012
14.
iNOS is not responsible for RyR1 S-nitrosylation in mdx mice with truncated dystrophin.
BMC Musculoskelet Disord
; 21(1): 479, 2020 Jul 21.
Artigo
Inglês
| MEDLINE | ID: mdl-32693782
15.
Effects of systemic multiexon skipping with peptide-conjugated morpholinos in the heart of a dog model of Duchenne muscular dystrophy.
Proc Natl Acad Sci U S A
; 114(16): 4213-4218, 2017 04 18.
Artigo
Inglês
| MEDLINE | ID: mdl-28373570
16.
Amelioration of intracellular Ca2+ regulation by exon-45 skipping in Duchenne muscular dystrophy-induced pluripotent stem cell-derived cardiomyocytes.
Biochem Biophys Res Commun
; 520(1): 179-185, 2019 11 26.
Artigo
Inglês
| MEDLINE | ID: mdl-31585729
17.
Elliptic neutron-focusing supermirror for illuminating small samples in neutron reflectometry.
Opt Express
; 27(19): 26807-26820, 2019 Sep 16.
Artigo
Inglês
| MEDLINE | ID: mdl-31674555
18.
Synthesis of 2'-O-(N-methylcarbamoylethyl) 5-methyl-2-thiouridine and its application to splice-switching oligonucleotides.
Bioorg Med Chem Lett
; 29(2): 160-163, 2019 01 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30551900
19.
Reactive oxygen species upregulate expression of muscle atrophy-associated ubiquitin ligase Cbl-b in rat L6 skeletal muscle cells.
Am J Physiol Cell Physiol
; 314(6): C721-C731, 2018 06 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29513566
20.
Vascular abnormalities in the placenta of Chst14-/- fetuses: implications in the pathophysiology of perinatal lethality of the murine model and vascular lesions in human CHST14/D4ST1 deficiency.
Glycobiology
; 28(2): 80-89, 2018 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29206923