Detalhe da pesquisa
1.
The Translational Landscape of the Human Heart.
Cell;
178(1): 242-260.e29, 2019 06 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31155234
2.
Spatial multi-omic map of human myocardial infarction.
Nature;
608(7924): 766-777, 2022 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35948637
3.
Meeting report - Desmosome dysfunction and disease: Alpine desmosome disease meeting.
J Cell Sci;
136(1)2023 01 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36594662
4.
Enhanced Ca2+-Dependent SK-Channel Gating and Membrane Trafficking in Human Atrial Fibrillation.
Circ Res;
132(9): e116-e133, 2023 04 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36927079
5.
Blood taken immediately after fatal resuscitation attempts yields higher quality DNA for genetic studies as compared to autopsy samples.
Int J Legal Med;
137(5): 1569-1581, 2023 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36773088
6.
A Drosophila melanogaster model for TMEM43-related arrhythmogenic right ventricular cardiomyopathy type 5.
Cell Mol Life Sci;
79(8): 444, 2022 Jul 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35869176
7.
Compound Heterozygous FKTN Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern.
Int J Mol Sci;
23(12)2022 Jun 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35743126
8.
Increased susceptibility of human endothelial cells to infections by SARS-CoV-2 variants.
Basic Res Cardiol;
116(1): 42, 2021 07 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34224022
9.
ATPase Inhibitory Factor-1 Disrupts Mitochondrial Ca2+ Handling and Promotes Pathological Cardiac Hypertrophy through CaMKIIδ.
Int J Mol Sci;
22(9)2021 Apr 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33922643
10.
The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report.
Int J Mol Sci;
22(13)2021 Jun 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34202524
11.
Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.
Int J Mol Sci;
22(7)2021 Apr 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33917638
12.
De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents.
Int J Mol Sci;
22(17)2021 Sep 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34502534
13.
A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy.
J Mol Cell Cardiol;
141: 17-29, 2020 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32201174
14.
Cardiomyopathy-associated mutations in the RS domain affect nuclear localization of RBM20.
Hum Mutat;
41(11): 1931-1943, 2020 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32840935
15.
Quaking Inhibits Doxorubicin-Mediated Cardiotoxicity Through Regulation of Cardiac Circular RNA Expression.
Circ Res;
122(2): 246-254, 2018 01 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29133306
16.
In vitro analysis of arrhythmogenic cardiomyopathy associated desmoglein-2 (DSG2) mutations reveals diverse glycosylation patterns.
J Mol Cell Cardiol;
129: 303-313, 2019 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30885746
17.
Noncompaction cardiomyopathy is caused by a novel in-frame desmin (DES) deletion mutation within the 1A coiled-coil rod segment leading to a severe filament assembly defect.
Hum Mutat;
40(6): 734-741, 2019 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30908796
18.
Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia.
Circulation;
137(15): 1595-1610, 2018 04 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29212896
19.
Glucocorticoids preserve the t-tubular system in ventricular cardiomyocytes by upregulation of autophagic flux.
Basic Res Cardiol;
114(6): 47, 2019 10 31.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31673803
20.
Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies.
Int J Mol Sci;
20(18)2019 Sep 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31489928