Associated Papers
Primary Cilia Signaling Promotes Axonal Tract Development and Is Disrupted in Joubert Syndrome-Related Disorders Models.
Guo J et al.
Developmental Cell, 2019
A novel homozygous ARL13B variant in patients with Joubert syndrome impairs its guanine nucleotide-exchange factor activity.
Rafiullah R et al.
European Journal of Human Genetics : Ejhg, 2017
Primary Cilia Signaling Shapes the Development of Interneuronal Connectivity.
Guo J et al.
Developmental Cell, 2017
Deletion of ADP Ribosylation Factor-Like GTPase 13B Leads to Kidney Cysts.
Li Y et al.
Journal of the American Society of Nephrology : Jasn, 2016
MKS1 regulates ciliary INPP5E levels in Joubert syndrome.
Slaats GG et al.
Journal of Medical Genetics, 2016
Identification of a novel ARL13B variant in a Joubert syndrome-affected patient with retinal impairment and obesity.
Thomas S et al.
European Journal of Human Genetics : Ejhg, 2015
Arl13b in primary cilia regulates the migration and placement of interneurons in the developing cerebral cortex.
Higginbotham H et al.
Developmental Cell, 2012
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