Detalhe da pesquisa
1.
Treatment with a triazole inhibitor of the mitochondrial permeability transition pore fully corrects the pathology of sapje zebrafish lacking dystrophin.
Pharmacol Res;
165: 105421, 2021 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33429034
2.
Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype.
Int J Mol Sci;
22(14)2021 Jul 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34298968
3.
De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy.
Hum Mutat;
39(9): 1161-1172, 2018 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29858533
4.
A fluorescent reporter detects details of aromatic ligand interference in drug-binding sites of human serum albumin.
Biochem Biophys Res Commun;
478(1): 462-466, 2016 09 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27318089
5.
Adsorbed plasma proteins modulate the effects of single-walled carbon nanotubes on neutrophils in blood.
Nanomedicine;
12(6): 1615-25, 2016 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27015767
6.
Various lamin A/C mutations alter expression profile of mesenchymal stem cells in mutation specific manner.
Mol Genet Metab;
115(2-3): 118-27, 2015.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25982065
7.
Diagnostic challenge in desmin cardiomyopathy with transformation of clinical phenotypes.
Pediatr Cardiol;
34(2): 467-70, 2013 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22484823
8.
Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness.
Methods Mol Biol;
2644: 3-14, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37142912
9.
RBM20-Associated Ventricular Arrhythmias in a Patient with Structurally Normal Heart.
Genes (Basel);
12(1)2021 01 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33450993
10.
Case Reports: Emery-Dreifuss Muscular Dystrophy Presenting as a Heart Rhythm Disorders in Children.
Front Cardiovasc Med;
8: 668231, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34026875
11.
Hydrodynamic properties of cyclodextrin molecules in dilute solutions.
Eur Biophys J;
39(3): 371-9, 2010 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19159925
12.
Sodium current abnormalities and deregulation of Wnt/ß-catenin signaling in iPSC-derived cardiomyocytes generated from patient with arrhythmogenic cardiomyopathy harboring compound genetic variants in plakophilin 2 gene.
Biochim Biophys Acta Mol Basis Dis;
1866(11): 165915, 2020 11 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32768677
13.
Desmin mutations result in mitochondrial dysfunction regardless of their aggregation properties.
Biochim Biophys Acta Mol Basis Dis;
1866(6): 165745, 2020 06 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32105824
14.
Neutrophil activation by Escherichia coli isolates from human intestine: effects of bacterial hydroperoxidase activity and surface hydrophobicity.
FEBS Open Bio;
10(3): 414-426, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31961067
15.
Infantile restrictive cardiomyopathy: cTnI-R170G/W impair the interplay of sarcomeric proteins and the integrity of thin filaments.
PLoS One;
15(3): e0229227, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32182250
16.
Truncating Variant in Myof Gene Is Associated With Limb-Girdle Type Muscular Dystrophy and Cardiomyopathy.
Front Genet;
10: 608, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31297131
17.
Influence of Antipsychotic Drug Risperidone on Human Serum Albumin Affinity to Organic Anions.
Curr Drug Discov Technol;
15(3): 263-269, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29110619
18.
Time- and Ventricular-Specific Expression Profiles of Genes Encoding Z-Disk Proteins in Pressure Overload Model of Left Ventricular Hypertrophy.
Front Genet;
9: 684, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30666270
19.
Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness.
Methods Mol Biol;
1601: 79-87, 2017.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28470519
20.
Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing.
PLoS One;
11(9): e0163362, 2016.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27662471