Detalhe da pesquisa
1.
Phosphorylation of the chromatin remodeling factor DPF3a induces cardiac hypertrophy through releasing HEY repressors from DNA.
Nucleic Acids Res
; 44(6): 2538-53, 2016 Apr 07.
Artigo
Inglês
| MEDLINE | ID: mdl-26582913
2.
Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot.
Hum Mol Genet
; 23(12): 3115-28, 2014 Jun 15.
Artigo
Inglês
| MEDLINE | ID: mdl-24459294
3.
The cardiac transcription network modulated by Gata4, Mef2a, Nkx2.5, Srf, histone modifications, and microRNAs.
PLoS Genet
; 7(2): e1001313, 2011 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-21379568
4.
The SWI/SNF chromatin remodeling factor DPF3 regulates metastasis of ccRCC by modulating TGF-ß signaling.
Nat Commun
; 13(1): 4680, 2022 08 09.
Artigo
Inglês
| MEDLINE | ID: mdl-35945219
5.
MicroRazerS: rapid alignment of small RNA reads.
Bioinformatics
; 26(1): 123-4, 2010 Jan 01.
Artigo
Inglês
| MEDLINE | ID: mdl-19880369
6.
Evaluation of the LightCycler 1536 Instrument for high-throughput quantitative real-time PCR.
Methods
; 50(4): S19-22, 2010 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-20215016
7.
The Needle in the Haystack-Searching for Genetic and Epigenetic Differences in Monozygotic Twins Discordant for Tetralogy of Fallot.
J Cardiovasc Dev Dis
; 7(4)2020 Dec 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33276527
8.
Induced pluripotent stem cells of patients with Tetralogy of Fallot reveal transcriptional alterations in cardiomyocyte differentiation.
Sci Rep
; 10(1): 10921, 2020 07 02.
Artigo
Inglês
| MEDLINE | ID: mdl-32616843
9.
Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart.
Dis Model Mech
; 13(12)2020 12 18.
Artigo
Inglês
| MEDLINE | ID: mdl-33033063
10.
Altered microRNA and target gene expression related to Tetralogy of Fallot.
Sci Rep
; 9(1): 19063, 2019 12 13.
Artigo
Inglês
| MEDLINE | ID: mdl-31836860
11.
CRISPR correction of the PRKAG2 gene mutation in the patient's induced pluripotent stem cell-derived cardiomyocytes eliminates electrophysiological and structural abnormalities.
Heart Rhythm
; 15(2): 267-276, 2018 02.
Artigo
Inglês
| MEDLINE | ID: mdl-28917552
12.
Muscle-relevant genes marked by stable H3K4me2/3 profiles and enriched MyoD binding during myogenic differentiation.
PLoS One
; 12(6): e0179464, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28609469
13.
Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases.
Cardiovasc Res
; 112(1): 464-77, 2016 10.
Artigo
Inglês
| MEDLINE | ID: mdl-27496870
14.
Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies.
Arch Med Sci
; 12(2): 263-78, 2016 Apr 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27186169
15.
Application of high-throughput sequencing for studying genomic variations in congenital heart disease.
Brief Funct Genomics
; 13(1): 51-65, 2014 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-24095982
16.
Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot.
PLoS One
; 9(1): e85375, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-24400131
17.
Diverging roads to the heart.
Science
; 359(6380): 1098-1099, 2018 03 09.
Artigo
Inglês
| MEDLINE | ID: mdl-29590027
18.
Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy.
Eur J Hum Genet
; 21(3): 294-300, 2013 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-22892539
19.
Dynamics of Srf, p300 and histone modifications during cardiac maturation in mouse.
Mol Biosyst
; 8(2): 495-503, 2012 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-22101280
20.
Systems biology approaches to heart development and congenital heart disease.
Cardiovasc Res
; 91(2): 269-78, 2011 Jul 15.
Artigo
Inglês
| MEDLINE | ID: mdl-21527437