Molecular basis of epithelial Cl channels

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De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females.

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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.

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Integrating GlycoSHIELD Modeling and DNA-PAINT SMLM to Map the Glycosylation-Dependent Distribution of the Na,K-ATPase.

The Journal of membrane biology·2026

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In vitro Reconstitution of Syncytin-2 and MFSD2A Reveals their Functional Tethering in Membrane Fusion Initiation.

The Journal of membrane biology·2026

Spatially heterogeneous ionic remodelling promotes wavefront instability in simulated atrial tissue.

Frontiers in network physiology·2026

Molecular-Ratchet Like Cation-Anion Coupling Dynamics Assist Ion Migration in Room Temperature Ionic Conductors.

The journal of physical chemistry letters·2026

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Materials (Basel, Switzerland)·2026

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Journal of thoracic disease·2026

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Frontiers in neuroscience·2026

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Molecular basis of epithelial Cl channels

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