19 results on '"DePalma, Steven"'
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2. Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease
3. Pathogenesis of Cardiomyopathy Caused by Variants in ALPK3 , an Essential Pseudokinase in the Cardiomyocyte Nucleus and Sarcomere
4. Contribution of Noncanonical Splice Variants toTTNTruncating Variant Cardiomyopathy
5. Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation
6. Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency
7. Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy
8. Abstract 785: Modeling Congenital Heart Disease-Associated Variants in GATA6 Using CRISPR/Cas9 and Human Induced Pluripotent Stem Cells
9. Abstract 202: The R21C Mutation in Troponin I Has a Founder Effect in South Lebanon and Causes Malignant Hypertrophic Cardiomyopathy
10. Abstract 104: Identification and Characterization of a Titin Enhancer using CRISPR/Cas9 Genome Editing and hiPSC-Derived Cardiomyocytes
11. Genetic Variants Associated With Cancer Therapy–Induced Cardiomyopathy
12. Abstract 231: Identification of a Titin Enhancer using hiPSC-Derived Cardiomyocytes and CRISPR/Cas9 Genome Editing
13. THSD1 (Thrombospondin Type 1 Domain Containing Protein 1) Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid Hemorrhage
14. Using Next-generation RNA Sequencing to Examine Ischemic Changes Induced by Cold Blood Cardioplegia on the Human Left Ventricular Myocardium Transcriptome
15. Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data
16. Nationwide Study on Hypertrophic Cardiomyopathy in Iceland
17. Increased Burden of Cardiovascular Disease in Carriers of APOL1 Genetic Variants
18. Genomewide Linkage in a Large Caucasian Family Maps a New Locus for Intracranial Aneurysms to Chromosome 13q
19. Novel Locus for an Inherited Cardiomyopathy Maps to Chromosome 7
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