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1. Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart Transplantation

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

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

19. Novel Locus for an Inherited Cardiomyopathy Maps to Chromosome 7

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