Detalhe da pesquisa
1.
Epigenetics and microRNAs in cardiovascular diseases.
Genomics
; 113(2): 540-551, 2021 03.
Artigo
Inglês
| MEDLINE | ID: mdl-33482325
2.
Recent Advances in CRISPR/Cas9-Based Genome Editing Tools for Cardiac Diseases.
Int J Mol Sci
; 22(20)2021 Oct 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34681646
3.
Therapeutic Delivery of miR-148a Suppresses Ventricular Dilation in Heart Failure.
Mol Ther
; 27(3): 584-599, 2019 03 06.
Artigo
Inglês
| MEDLINE | ID: mdl-30559069
4.
Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures.
Int J Mol Sci
; 21(9)2020 May 11.
Artigo
Inglês
| MEDLINE | ID: mdl-32403456
5.
Genetics meets epigenetics: Genetic variants that modulate noncoding RNA in cardiovascular diseases.
J Mol Cell Cardiol
; 89(Pt A): 27-34, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26546166
6.
Arrhythmogenic cardiomyopathy: a disease of intercalated discs.
Cell Tissue Res
; 360(3): 491-500, 2015 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-25344329
7.
Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy.
Eur Heart J
; 34(3): 201-10, 2013 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-23136403
8.
The PRKAG2 gene and hypertrophic cardiomyopathy: an energetically imbalanced relationship.
Am J Physiol Heart Circ Physiol
; 313(2): H248-H250, 2017 08 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28626079
9.
Circulating miR-185-5p as a Potential Biomarker for Arrhythmogenic Right Ventricular Cardiomyopathy.
Cells
; 10(10)2021 09 28.
Artigo
Inglês
| MEDLINE | ID: mdl-34685557
10.
Circulating miR-216a as a biomarker of metabolic alterations and obesity in women.
Noncoding RNA Res
; 5(3): 144-152, 2020 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-32954093
11.
12.
Metabolic Alterations in Inherited Cardiomyopathies.
J Clin Med
; 8(12)2019 Dec 12.
Artigo
Inglês
| MEDLINE | ID: mdl-31842377
13.
A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signalling and miRNA dysregulation.
Cardiovasc Res
; 115(4): 739-751, 2019 03 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30304392
14.
A targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy.
Heart Rhythm
; 16(5): 773-780, 2019 05.
Artigo
Inglês
| MEDLINE | ID: mdl-30453078
15.
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy.
Circ Genom Precis Med
; 11(10): e002123, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-30354300
16.
Wnt/ß-catenin pathway in arrhythmogenic cardiomyopathy.
Oncotarget
; 8(36): 60640-60655, 2017 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28948000
17.
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy.
Eur J Hum Genet
; 25(10): 1165-1169, 2017 10.
Artigo
Inglês
| MEDLINE | ID: mdl-28699631
18.
Large Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients.
Circ Arrhythm Electrophysiol
; 10(10)2017 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-29038103
19.
Arrhythmogenic right-ventricular cardiomyopathy: molecular genetics into clinical practice in the era of next generation sequencing.
J Cardiovasc Med (Hagerstown)
; 17(6): 399-407, 2016 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-26990921
20.
Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology.
Circ Genom Precis Med
; 13(2): e002824, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-32004434