Detalhe da pesquisa
1.
Modulation of Notch Signaling at Early Stages of Differentiation of Human Induced Pluripotent Stem Cells to Dopaminergic Neurons.
Int J Mol Sci;
24(2)2023 Jan 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36674941
2.
Impact of the DSP-H1684R Genetic Variant on Ion Channels Activity in iPSC-Derived Cardiomyocytes.
Cell Physiol Biochem;
54(4): 696-706, 2020 Jul 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32706220
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.
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
5.
Generation of iPSC line FAMRCi010-A from patient with restrictive cardiomyopathy carrying genetic variant FLNC p.Gly2011Arg.
Stem Cell Res;
59: 102639, 2022 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34971931
6.
Generation of iPSC line (FAMRCi009-A) from patient with familial progressive cardiac conduction disorder carrying genetic variant FLNC p.Val2264Met.
Stem Cell Res;
59: 102640, 2022 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34971933
7.
LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient.
Front Cardiovasc Med;
9: 932956, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35935653
8.
Use of hiPSC-Derived Cardiomyocytes to Rule Out Proarrhythmic Effects of Drugs: The Case of Hydroxychloroquine in COVID-19.
Front Physiol;
12: 730127, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35153806
9.
Different Expressions of Pericardial Fluid MicroRNAs in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy and Ischemic Heart Disease Undergoing Ventricular Tachycardia Ablation.
Front Cardiovasc Med;
8: 647812, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33816578
10.
FLNC Expression Level Influences the Activity of TEAD-YAP/TAZ Signaling.
Genes (Basel);
11(11)2020 11 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33202721
11.
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
12.
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
13.
Generation of two iPSC lines (FAMRCi004-A and FAMRCi004-B) from patient with familial progressive cardiac conduction disorder carrying genetic variant DSP p.His1684Arg.
Stem Cell Res;
43: 101720, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32062131
14.
Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p.Asp357Val.
Stem Cell Res;
43: 101719, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32062135
15.
Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro.
Stem Cell Res;
43: 101714, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32059175
16.
Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln.
Stem Cell Res;
47: 101895, 2020 Jun 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32659731
17.
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
18.
Transfer of Synthetic Human Chromosome into Human Induced Pluripotent Stem Cells for Biomedical Applications.
Cells;
7(12)2018 Dec 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30544831
19.
Generation of iPSC line from desmin-related cardiomyopathy patient carrying splice site mutation of DES gene.
Stem Cell Res;
24: 77-80, 2017 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29034897
20.
Generation of iPSC line from patient with arrhythmogenic right ventricular cardiomyopathy carrying mutations in PKP2 gene.
Stem Cell Res;
24: 85-88, 2017 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29034900