Human iPSC-Derived Cardiomyocyte Networks on Multiwell Micro-electrode Arrays for Recurrent Action Potential Recordings von Zlochiver, Viviana, Kroboth, Stacie L, Beal, Christopher R, Cook, Jonathan A, Joshi-Mukherjee, Rosy

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Molecular Identification and Functional Characterization of a Mitochondrial Sulfonylurea Receptor 2 Splice Variant Generated by Intraexonic Splicing von Ye, Bin, Kroboth, Stacie L, Pu, Jie-Lin, Sims, Jason J, Aggarwal, Nitin T, McNally, Elizabeth M, Makielski, Jonathan C, Shi, Nian-Qing

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Gain-of-function mutation S422L in the KCNJ8- encoded cardiac KATP channel Kir6.1 as a pathogenic substrate for J-wave syndromes von Medeiros-Domingo, Argelia, MD, PhD, Tan, Bi-Hua, MD, PhD, Crotti, Lia, MD, PhD, Tester, David J., BS, Eckhardt, Lee, MD, Cuoretti, Alessandra, BS, Kroboth, Stacie L., BS, Song, Chunhua, MD, PhD, Zhou, Qing, BS, Kopp, Doug, MD, Schwartz, Peter J., MD, Makielski, Jonathan C., MD, Ackerman, Michael J., MD, PhD

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Cardiac sulfonylurea receptor short form-based channels confer a glibenclamide-insensitive KATP activity von Pu, Jie-Lin, Ye, Bin, Kroboth, Stacie L, McNally, Elizabeth M, Makielski, Jonathan C, Shi, Nian-Qing

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A Flexible Loop in Tyrosine Hydroxylase Controls Coupling of Amino Acid Hydroxylation to Tetrahydropterin Oxidation von Colette Daubner, S., McGinnis, James Thomas, Gardner, Meredith, Kroboth, Stacie L., Morris, Adam R., Fitzpatrick, Paul F.

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Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K ATP channel Kir6.1 as a pathogenic substrate for J-wave syndromes von Medeiros-Domingo, Argelia, Tan, Bi-Hua, Crotti, Lia, Tester, David J., Eckhardt, Lee, Cuoretti, Alessandra, Kroboth, Stacie L., Song, Chunhua, Zhou, Qing, Kopp, Doug, Schwartz, Peter J., Makielski, Jonathan C., Ackerman, Michael J.

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Human iPSC-Derived Cardiomyocyte Networks on Multiwell Micro-electrode Arrays for Recurrent Action Potential Recordings von Zlochiver, Viviana, Kroboth, Stacie L., Beal, Christopher R., Cook, Jonathan A., Joshi-Mukherjee, Rosy

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Cardiac sulfonylurea receptor short form-based channels confer a glibenclamide-insensitive K ATP activity von Pu, Jie-Lin, Ye, Bin, Kroboth, Stacie L., McNally, Elizabeth M., Makielski, Jonathan C., Shi, Nian-Qing

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Functional Characterization of the Andersen-Tawil Syndrome Associated Mutation (M307I) in KCNJ2 von Tan, Bi-Hua, Song, Chunhua, Kroboth, Stacie L., Zhou, Qing, Dovat, Sinisa, Ackerman, Michael J., Makielski, Janathan C., Eckhardt, Lee L.

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Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes von Medeiros-Domingo, Argelia, Tan, Bi-Hua, Crotti, Lia, Tester, David J, Eckhardt, Lee, Cuoretti, Alessandra, Kroboth, Stacie L, Song, Chunhua, Zhou, Qing, Kopp, Doug, Schwartz, Peter J, Makielski, Jonathan C, Ackerman, Michael J

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