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Author

A. Ratan

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Open access Sep 2026

Biallelic DAW1 variants reveal a tissue-specific role in heterotaxy without primary ciliary dyskinesia.

Defects in motile cilia cause a range of disorders, including heterotaxy (HTX), congenital heart disease (CHD), and primary ciliary dyskinesia (PCD). Although these conditions often co-occur, the genetic and mechanistic bases for tissue-specific manifestations remain poorly understood. Here, we identify compound hetero...

Dana Urbatsch, Anburaj Jeyaraj, Shruti Bedekar et al. · 0 citations
Review Open access Aug 2026

G-quadruplex structures as regulators of cellular processes and drivers of genome instability in cancer.

Therapeutically targeting G4s requires balancing their essential regulatory roles with their pathological effects, and understanding this tension is essential for exploiting G4s as therapeutic targets across cancer types.

Anna R. Bartosik, Magda Bujnowska, D. B. Stovall et al. · 0 citations

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