31 results on '"Anson, Blake D"'
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2. Multiparametric assessment of networked electrical activity using induced pluripotent stem cell-derived glutamatergic neurons
3. Development of a 3D-spheroid culture system to assess drug induced liver injury using induced pluripotent stem cell-derived hepatocytes
4. Electrophysiological characterization of iCell 2 hiPSC derived cardiomyocytes: The new generation of CDI hiPSC-CMs
5. Identification of Drug–Drug InteractionsIn Vitro: A Case Study Evaluating the Effects of Sofosbuvir and Amiodarone on hiPSC-Derived Cardiomyocytes
6. Development and Characterization of a Scaffold-Free 3D Spheroid Model of Induced Pluripotent Stem Cell-Derived Human Cardiomyocytes
7. Loose-Patch Voltage-Clamp Technique
8. Combine use of Intracellular Calcium and Sarcolemma Voltage Measurements to Distinguish Mixed Channel Effects in Human Induced Plutipotent Stem Cells Derived Cardiomyocytes (HIPSC-CMS)
9. High purity human-induced pluripotent stem cell-derived cardiomyocytes: electrophysiological properties of action potentials and ionic currents
10. Human iPSC-derived cardiomyocytes (iCell™) and DrugPrint®: A suitable assay platform for cardiac electrophysiology
11. Stem Cells and Their Derivatives: A Renaissance in Cardiovascular Translational Research
12. Induced pluripotent stem cell derived cardiomyocytes and multivariate analysis for detection of potential QT perturbation
13. Properties of WT and mutant hERG K+ channels expressed in neonatal mouse cardiomyocytes
14. Mechanism Of IKr Loss In Mutant T421M-hERG Expressing Rat Ventricular Myocytes
15. Specific serine proteases selectively damage KCNH2 (hERG1) potassium channels and IKr
16. Comparison of HERG channel blocking effects of various β -blockers - implication for clinical strategy
17. Most LQT2 Mutations Reduce Kv11.1 (hERG) Current by a Class 2 (Trafficking-Deficient) Mechanism
18. N-linked glycosylation is not obligatory for rescue of trafficking-defective LQT2 mutations
19. Most LQT-linked KCNH2 mutations are trafficking-defective
20. Intragenic Suppression of Trafficking-Defective KCNH2 Channels Associated with Long QT Syndrome
21. Blockade of HERG channels by HIV protease inhibitors
22. An intronic mutation causes long QT syndrome
23. Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels
24. Thapsigargin Selectively Rescues the Trafficking Defective LQT2 Channels G601S and F805C
25. Molecular characterization, functional expression, and developmental profile of an ether à‐go‐go K+ channel in the tobacco hornworm Manduca sexta
26. Genetic basis for the origin of cardiac arrhythmias: Implications for therapy
27. Pharmacological Rescue of Human K + Channel Long-QT2 Mutations
28. Molecular autopsy for HERG defects in sudden infant death syndrome
29. Sodium channel distribution on uninnervated and innervated embryonic skeletal myotubes
30. A Novel Voltage Clamp Technique for Mapping Ionic Currents from Cultured Skeletal Myotubes
31. Effects of protein and juglone on gypsy moths: Growth performance and detoxification enzyme activity
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