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"We demonstrate that intracellular ATP is a more potent modulator of I Ks activity than PIP 2, supporting the notion that direct binding of ATP to the KCNQ1 and KCNE1 channel is essential for channel a[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"Furthermore, the second component of IKs inhibition by Ci-VSP was reduced by AMP-PCP in the pipette filling solution, indicating that direct binding of ATP to the KCNQ1 and KCNE1 complex is required for voltage activation of IKs."