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  1. Rpgrip1l controls ciliary gating by ensuring the proper amount of Cep290 at the vertebrate transition zone
  2. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
  3. Treatment of Ciliopathies: Current Perspectives
  4. GLI3 repressor but not GLI3 activator is essential for mouse eye patterning and morphogenesis
  5. The ciliary protein Rpgrip1l in development and disease
  6. Cell type‐specific regulation of ciliary transition zone assembly in vertebrates
  7. The ciliary protein RPGRIP1L governs autophagy independently of its proteasome-regulating function at the ciliary base in mouse embryonic fibroblasts
  8. The Role of Hedgehog Signalling in the Formation of the Ventricular Septum
  9. Control of Hedgehog Signalling by the Cilia-Regulated Proteasome
  10. The cilia-regulated proteasome and its role in the development of ciliopathies and cancer
  11. The transition zone protein Rpgrip1l regulates proteasomal activity at the primary cilium
  12. The Ciliary Protein Ftm Is Required for Ventricular Wall and Septal Development
  13. Primary cilia control telencephalic patterning and morphogenesis via Gli3 proteolytic processing
  14. The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome