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KCNQ1 activates KCN. 7 / 7
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"It is caused by mutations in the KCNQ1 gene, encoding for the α-subunit of the voltage-dependent potassium channel responsible for the delayed rectifier potassium current (I Ks ), one of the repolariz[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
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"It is caused by mutations in the KCNQ1 gene, encoding for the α-subunit of the voltage-dependent potassium channel responsible for the delayed rectifier potassium current (I Ks ), one of the repolariz[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
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"1 It is caused by mutations in the KCNQ1 gene that impair the slow acting potassium channel that gives rise to I Ks."
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"XREF_BIBR, XREF_BIBR Rare mutations in KCNQ1 are known to cause potassium channel dysfunction leading to a form of cardiac long QT syndrome (LQT1) and serious arrhythmias, ventricular fibrillation and cardiac arrest."
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"It is caused by mutations in the KCNQ1 gene, encoding for the α-subunit of the voltage-dependent potassium channel responsible for the delayed rectifier potassium current (I Ks ), one of the repolariz[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
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"E2 (100 nM) reduced the currents mediated by the KCNQ1 : KCNE3 potassium channel and had no effect on currents via KCNQ1 : KCNE1 or KCNQ1 alone."
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"In vitro, the co-expression of SGK3 and KCNE1/KCNQ1(Kv7.1) in Xenopus oocytes could up-regulate the activity of the potassium channel KCNE1/KCNQ1 (Embark et al., 2003)."
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