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Article

Reptin/Ruvbl2 is a Lrrc6/Seahorse interactor essential for cilia motility.

Proceedings of the National Academy of Sciences of the United States of America - 30 Jul 2013

Zhao Lu, Yuan Shiaulou, Cao Ying, Kallakuri Sowjanya, Li Yuanyuan, Kishimoto Norihito, DiBella Linda, Sun Zhaoxia

Abstract excerpt

Primary ciliary dyskinesia (PCD) is an autosomal recessive disease caused by defective cilia motility. The identified PCD genes account for about half of PCD incidences and the underlying mechanisms remain poorly understood. We demonstrate that Reptin/Ruvbl2, a protein known to be involved in epi...

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Identifiers

PMID: 23858445
DOI: 10.1073/pnas.1300968110
PMCID: PMC3732945

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23858445-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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