Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies

Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome

(2008) Vincent Cantagrel et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Membrane traffic in the secretory pathway

(2008) M. Vicinanza et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium

(2008) Joon Kim et al.   HUMAN MOLECULAR GENETICS

ProliferationVersusMigration in Platelet-derived Growth Factor Signaling

(2008) Alina De Donatis et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

CELL BIOLOGY: Arrestin' Movement in Cilia

(2008) R. Rohatgi et al.   SCIENCE

Genotypes and phenotypes of Joubert syndrome and related disorders

(2007) Enza Maria Valente et al.   European Journal of Medical Genetics