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Molecular Basis of Decreased Kir4.1 Function in SeSAME/EAST Syndrome
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KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function
Markus Reichold et al.
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Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations.
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Regulation of magnesium reabsorption in DCT
Qi Xi et al.
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IK1 channel activity contributes to cisplatin sensitivity of human epidermoid cancer cells
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Conditional knock-out of Kir4.1 leads to glial membrane depolarization, inhibition of potassium and glutamate uptake, and enhanced short-term synaptic Potentiation
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Differential assembly of inwardly rectifying K+ channel subunits, Kir4.1 and Kir5.1, in brain astrocytes
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KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential
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An inward rectifier K+ channel at the basolateral membrane of the mouse distal convoluted tubule:: similarities with Kir4-Kir5.1 heteromeric channels
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