All Stories

  1. A goat-derived gamma-tubulin antibody for triple-channel imaging of primary cilia
  2. Oxidative stress causes a reversible decrease of deubiquitylases activity in old vertebrate brains
  3. In situ proximity ligation assay for analysing spatial interactions between ciliary proteins
  4. Editorial: Regulation of proteostasis and cellular energy homeostasis at the primary cilium
  5. Life-Saver or Undertaker: The Relationship between Primary Cilia and Cell Death in Vertebrate Embryonic Development
  6. Extracellular vesicles in ciliary signalling
  7. Publisher's Note: Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components
  8. Rpgrip1l controls ciliary gating by ensuring the proper amount of Cep290 at the vertebrate transition zone
  9. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
  10. A View on the Contribution of Hedgehog Signalling to Ventricular Septal Development
  11. Treatment of Ciliopathies: Current Perspectives
  12. GLI3 repressor but not GLI3 activator is essential for mouse eye patterning and morphogenesis
  13. The Role of Primary Cilia in the Crosstalk between the Ubiquitin–Proteasome System and Autophagy
  14. The ciliary protein Rpgrip1l in development and disease
  15. Cell type‐specific regulation of ciliary transition zone assembly in vertebrates
  16. The ciliary protein RPGRIP1L governs autophagy independently of its proteasome-regulating function at the ciliary base in mouse embryonic fibroblasts
  17. The Role of Hedgehog Signalling in the Formation of the Ventricular Septum
  18. Control of Hedgehog Signalling by the Cilia-Regulated Proteasome
  19. The cilia-regulated proteasome and its role in the development of ciliopathies and cancer
  20. The transition zone protein Rpgrip1l regulates proteasomal activity at the primary cilium
  21. The Ciliary Protein Ftm Is Required for Ventricular Wall and Septal Development
  22. Primary cilia control telencephalic patterning and morphogenesis via Gli3 proteolytic processing
  23. The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome