The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5
Zakia A. Abdelhamed(Cincinnati Children's Hospital Medical Center), Colin A. Johnson(University of Leeds)
Cited by 27
Related Papers
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
|Nature Genetics|2007|495
Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome
|The American Journal of Human Genetics|2008|399
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
|Nature Genetics|2011|381
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
|Nature Genetics|2010|285
IFT27 Links the BBSome to IFT for Maintenance of the Ciliary Signaling Compartment
|Developmental Cell|2014|274