Yohei Katoh
Kyoto, Japan
Last Updated: 09/26/2026
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Found 53 publications
Assembly and mother centriole recruitment of IFT-B subcomplexes to form IFT-B holocomplex.
Journal: Cell structure and function
Published: June 26, 2025
Coordinated roles of the CEP164 homodimer and TTBK2 are required for recruitment of the IFT machinery to the mother centriole for ciliogenesis.
Journal: Molecular biology of the cell
Published: April 30, 2025
Mutually independent and cilia-independent assembly of IFT-A and IFT-B complexes at mother centriole.
Journal: Molecular biology of the cell
Published: February 28, 2025
β-Arrestin mediates the export of ciliary GPR161 but not Smoothened together with the BBSome and intraflagellar transport machinery.
Journal: Journal of cell science
Published: December 12, 2024
Lipid flippases ATP9A and ATP9B form a complex and contribute to the exocytic pathway from the Golgi.
Journal: Life science alliance
Published: December 06, 2024
Skeletal ciliopathy variants of the dynein-2 DYNC2LI1 subunit impair osteogenic differentiation of mesenchymal stem cells.
Journal: Journal of cell science
Published: November 19, 2024
Counterregulatory roles of GLI2 and GLI3 in osteogenic differentiation via Gli1 expression.
Journal: Journal of cell science
Published: September 20, 2024
Positive regulation of Hedgehog signaling via phosphorylation of GLI2/GLI3 by DYRK2 kinase.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: July 05, 2024
TXNDC15, an ER-localized thioredoxin-like transmembrane protein, contributes to ciliary transition zone integrity.
Journal: Journal of cell science
Published: March 18, 2024
Defects in diffusion barrier function of ciliary transition zone caused by ciliopathy variations of TMEM218.
Journal: Human molecular genetics
Published: March 15, 2024
Mirror-Image Single-Domain Antibody for a Novel Nonimmunogenic Drug Scaffold.
Journal: Bioconjugate chemistry
Published: October 26, 2023
Compound heterozygous IFT81 variations in a skeletal ciliopathy patient cause Bardet-Biedl syndrome-like ciliary defects.
Journal: Human molecular genetics
Published: April 28, 2023
Last Updated: 09/26/2026