Related references
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Intracellular localization of ClC chloride channels and their ability to form hetero-oligomers
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Ion-binding properties of the ClC chloride selectivity filter
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CLC chloride channels and transporters
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Cysteine accessibility in ClC-0 supports conservation of the ClC intracellular vestibule
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Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration
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ClC-3 chloride channels facilitate endosomal acidification and chloride accumulation
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Secondary active transport mediated by a prokaryotic homologue of ClC Cl- channels
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Ionic currents mediated by a prokaryotic homologue of CLC Cl- channels
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Molecular determinants of differential pore blocking of kidney CLC-K chloride channels
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Electrostatic control and chloride regulation of the fast gating of ClC-0 chloride channels
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Conformational changes in the pore of CLC-0
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Conservation of chloride channel structure revealed by an inhibitor binding site in CIC-1
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X-ray structure of a CIC chloride channel at 3.0 Å reveals the molecular basis of anion selectivity
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The chloride channel ClC-4 co-localizes with cystic fibrosis transmembrane conductance regulator and may mediate chloride flux across the apical membrane of intestinal epithelia
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Loss of the CIC-7 chloride channel leads to osteopetrosis in mice and man
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Mice lacking renal chloride channel, CLC-5, are a model for Dent's disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosis
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CIC-5Cl--channel disruption impairs endocytosis in a mouse model for Dent's disease
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