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181 results on '"Christoforou, Nicolas"'

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4. KCNQ1 suppression-replacement gene therapy in transgenic rabbits with type 1 long QT syndrome.

8. Development and validation of a high throughput screening platform to enable target identification in skeletal muscle cells from Duchenne Muscular Dystrophy (DMD) patients

10. BS-452758-1 SUPPRESSION-REPLACEMENT GENE THERAPY REVERSE REMODELS THE INTRACELLULAR CALCIUM HANDLING DISEASE PHENOTYPE OF -MEDIATED HYPERTROPHIC CARDIOMYOPATHY

11. PO-02-210 AAV9-MEDIATED -SUPPRESSION-REPLACEMENT GENE THERAPY IN TRANSGENIC RABBITS WITH TYPE 1 LONG QT SYNDROME

15. DUX4 expression activates JNK and p38 MAP kinases in myoblasts

19. PO-CES-03 AAV9-MEDIATED KCNQ1-SUPPRESSION-REPLACEMENT GENE THERAPY IN TRANSGENIC RABBITS WITH TYPE 1 LONG QT SYNDROME (LQT1)

20. PO-05-191 AAV9-MEDIATED KCNQ1-SUPPRESSION-REPLACEMENT GENE THERAPY IN TRANSGENIC RABBITS WITH TYPE 1 LONG QT SYNDROME (LQT1)

21. EN-482891-004 AAV9-MEDIATED KCNH2-SUPPRESSION-REPLACEMENT GENE THERAPY PROLONGS THE PATHOLOGICALLY SHORTENED QT/APD IN SHORT QT SYNDROME TYPE 1 RABBIT MODELS

24. CRISPR-mediated correction of skeletal muscle Ca2+handling in a novel DMD patient-derived pluripotent stem cell model

25. List of Contributors

32. Mouse ES cell--derived cardiac precursor cells are multipotent and facilitate identification of novel cardiac genes

34. PO-02-210 AAV9-MEDIATED KCNQ1-SUPPRESSION-REPLACEMENT GENE THERAPY IN TRANSGENIC RABBITS WITH TYPE 1 LONG QT SYNDROME

38. Stem Cell Culture

41. Transdifferentiation of human endothelial progenitors into functional smooth muscle cells for tissue engineered blood vessel assembly

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