Cargando…
Ciliopathy-Associated Protein Kinase ICK Requires Its Non-Catalytic Carboxyl-Terminal Domain for Regulation of Ciliogenesis
Loss-of-function mutations in the human ICK (intestinal cell kinase) gene cause dysfunctional primary cilia and perinatal lethality which are associated with human ciliopathies. The enzyme that we herein call CAPK (ciliopathy-associated protein kinase) is a serine/threonine protein kinase that has a...
Autores principales: | Oh, Yoon Seon, Wang, Eric J., Gailey, Casey D., Brautigan, David L., Allen, Benjamin L., Fu, Zheng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678984/ https://www.ncbi.nlm.nih.gov/pubmed/31277411 http://dx.doi.org/10.3390/cells8070677 |
Ejemplares similares
-
Functional Alterations in Ciliogenesis-Associated Kinase 1 (CILK1) that Result from Mutations Linked to Juvenile Myoclonic Epilepsy
por: Wang, Eric J., et al.
Publicado: (2020) -
Mice Harboring a Non-Functional CILK1/ICK Allele Fail to Model the Epileptic Phenotype in Patients Carrying Variant CILK1/ICK
por: Salvati, Kathryn A., et al.
Publicado: (2021) -
A ciliopathy complex builds distal appendages to initiate ciliogenesis
por: Kumar, Dhivya, et al.
Publicado: (2021) -
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
por: Wheway, Gabrielle, et al.
Publicado: (2015) -
Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling
por: Yee, Laura E., et al.
Publicado: (2015)