Associated Papers
NEK8, a NIMA-family protein kinase at the core of the ciliary INV complex.
Roig J
Cell Communication and Signaling : Ccs, 2025
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.
Claus LR et al.
Kidney International, 2023
Renal-hepatic-pancreatic dysplasia type 2: Perinatal lethal condition or a multisystemic disorder with variable expressivity.
Gunther K et al.
Molecular Genetics & Genomic Medicine, 2023
Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation.
Grampa V et al.
Plos Genetics, 2016
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