Silke R. Sperling
Berlin, BE 13125, Germany
Last Updated: 09/26/2026
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Found 14 publications
The SWI/SNF chromatin remodeling factor DPF3 regulates metastasis of ccRCC by modulating TGF-β signaling.
Journal: Nature communications
Published: July 24, 2021
The Needle in the Haystack-Searching for Genetic and Epigenetic Differences in Monozygotic Twins Discordant for Tetralogy of Fallot.
Journal: Journal of cardiovascular development and disease
Published: November 03, 2020
CRISPR correction of the PRKAG2 gene mutation in the patient's induced pluripotent stem cell-derived cardiomyocytes eliminates electrophysiological and structural abnormalities.
Journal: Heart rhythm
Published: July 08, 2017
Beyond antibiotic therapy - Future antiinfective strategies - Update 2017
Journal: Der Unfallchirurg
Published: June 24, 2017
Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases.
Journal: Cardiovascular research
Published: February 16, 2016
Phosphorylation of the chromatin remodeling factor DPF3a induces cardiac hypertrophy through releasing HEY repressors from DNA.
Journal: Nucleic acids research
Published: August 07, 2015
Congenital coronary artery anomalies: a bridge from embryology to anatomy and pathophysiology--a position statement of the development, anatomy, and pathology ESC Working Group.
Journal: Cardiovascular research
Published: February 24, 2015
Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies.
Journal: Archives of medical science : AMS
Published: February 04, 2015
Application of high-throughput sequencing for studying genomic variations in congenital heart disease.
Journal: Briefings in functional genomics
Published: October 08, 2013
Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot.
Journal: PloS one
Published: September 12, 2013
Last Updated: 09/26/2026