IndraLab

Statements



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"The PIP 2 inhibition of hEAG1 channels is physiologically relevant as evidenced by the observation that neuronal transmitter 5-HT noticeably increased the whole-cell current from the hEAG1 channels coexpressed with the serotonin receptor HTR 2A in HEK293 cells, suggesting that endogenous PIP 2 may exert a detectable tonic inhibitory influence on hEAG1 channels in intact neurons."

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"We found that depletion of endogenous PIP 2 by activation of the voltage sensing phosphatase from Danio rerio (Dr-VSP) or the human muscarinic type-1 receptor (hM1R) inhibits hEAG1 currents; however, the application of exogenous PIP 2 to increase the level of this lipid on the plasma membrane, also induced an inhibition of hEAG1."

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"Molecular determinants of hEAG1 channel inhibition by PIP 2 ."

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"The PIP 2 inhibition of hEAG1 channels is physiologically relevant as evidenced by the observation that neuronal transmitter 5-HT noticeably increased the whole-cell current from the hEAG1 channels coexpressed with the serotonin receptor HTR 2A in HEK293 cells, suggesting that endogenous PIP 2 may exert a detectable tonic inhibitory influence on hEAG1 channels in intact neurons."

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"The PIP 2 inhibition of hEAG1 channels is physiologically relevant as evidenced by the observation that neuronal transmitter 5-HT noticeably increased the whole-cell current from the hEAG1 channels coexpressed with the serotonin receptor HTR 2A in HEK293 cells, suggesting that endogenous PIP 2 may exert a detectable tonic inhibitory influence on hEAG1 channels in intact neurons."

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"In this case, PIP 2 inhibits hEAG1 channels through a mechanism that requires an intact CaM BD-N region."

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"Inhibition of hEAG1 channels by PIP 2."

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"PIP 2 quickly inhibited the hEAG1 channel when the membrane potential was held at 40mV (XREF_FIG, D)."

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"Physiological relevance of the tonic inhibitory influence of PIP 2 as an endogenous modulator of hEAG1 is further suggested by the finding that activation of serotonin HTR 2A receptors, known to activate PLC XREF_BIBR to promote hydrolysis of PIP 2, also increases hEAG1 currents at negative voltages."

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"Molecular determinants of hEAG1 channel inhibition by PIP 2 ."