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You searched for: Author/Creator Meder, Benjamin

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1. A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy. (15th October 2021)

2. A kinome-wide RNAi screen identifies ALK as a target to sensitize neuroblastoma cells for HDAC8-inhibitor treatment. Issue 12 (December 2018)

3. A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank–Starling mechanism. Issue 1 (5th August 2016)

4. A novel risk model for predicting potentially life-threatening arrhythmias in non-ischemic dilated cardiomyopathy (DCM-SVA risk). (15th September 2021)

5. Alterations in cardiac DNA methylation in human dilated cardiomyopathy. Issue 3 (22nd January 2013)

7. Biomarker Changes after Strenuous Exercise Can Mimic Pulmonary Embolism and Cardiac Injury—A Metaanalysis of 45 Studies. (6th January 2020)

9. Clinical and Genetic Investigations of 109 Index Patients With Dilated Cardiomyopathy and 445 of Their Relatives. (October 2020)

10. Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology. Issue 10 (23rd May 2018)