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Article

Functional evaluation of Dent’s disease-causing mutations: implications for ClC-5 channel trafficking and internalization

13 May 2005

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15895257
DOI: 10.1007/s00439-005-1303-2

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Functional evaluation of Dent’s disease-causing mutations: implications for ClC-5 channel trafficking and internalizationPMID 15895257Read ↗

Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing.Semantic proximity Read ↗

Heterogeneity in the processing of CLCN5 mutants related to Dent disease.Semantic proximity Read ↗

Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structureSemantic proximity Read ↗

Functional and transport analyses of CLCN5 genetic changes identified in Dent disease patients.Semantic proximity Read ↗

ClC-5 mutations associated with Dent's disease: a major role of the dimer interface.Semantic proximity Read ↗

A novel likely pathogenic CLCN5 variant in Dent’s diseaseSemantic proximity Read ↗

Genetic Analysis of Dent's Disease and Functional Research of CLCN5 Mutations.Semantic proximity Read ↗

CLC Chloride Channels and Transporters: Structure, Function, Physiology, and Disease.Semantic proximity Read ↗

Novel Dent disease 1 cellular models reveal biological processes underlying ClC-5 loss-of-function.Semantic proximity Read ↗

Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease.Semantic proximity Read ↗

ClC transporters: discoveries and challenges in defining the mechanisms underlying function and regulation of ClC-5.Semantic proximity Read ↗

A role for CBS domain 2 in trafficking of chloride channel CLC-5.Semantic proximity Read ↗

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