The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase. (Q39522092)

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scientific article published on 17 June 2011

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English	The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase.	scientific article published on 17 June 2011

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5 February 2020

The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase (English)

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5 February 2020

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Christian Johannes Gloeckner

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Susanne Roosing

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Jeroen van Reeuwijk

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Jeroen van Reeuwijk

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Marius Ueffing

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Dorus A Mans

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Karsten Boldt

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Emine Bolat

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Stef J F Letteboer

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Frans P M Cremers

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Ronald Roepman

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publication date

17 June 2011

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Human Molecular Genetics

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3592-3605

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5 February 2020

The primary cilium: a signalling centre during vertebrate development

1 reference

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The Ciliopathies: An Emerging Class of Human Genetic Disorders

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Null RPGRIP1 alleles in patients with Leber congenital amaurosis

1 reference

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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

1 reference

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The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

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The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors

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A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

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Retinitis pigmentosa GTPase regulator (RPGRr)-interacting protein is stably associated with the photoreceptor ciliary axoneme and anchors RPGR to the connecting cilium

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The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: subserving RPGR function and participating in disk morphogenesis

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Species-specific subcellular localization of RPGR and RPGRIP isoforms: implications for the phenotypic variability of congenital retinopathies among species

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The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin

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A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution

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Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations

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A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies

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NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development

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Murine models of polycystic kidney disease: molecular and therapeutic insights

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Mutations in a NIMA-related kinase gene, Nek1, cause pleiotropic effects including a progressive polycystic kidney disease in mice

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NEK1 mutations cause short-rib polydactyly syndrome type majewski

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The ciliary proteome database: an integrated community resource for the genetic and functional dissection of cilia

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Proteomic analysis of a eukaryotic cilium

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The proteome of the mouse photoreceptor sensory cilium complex

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A novel tandem affinity purification strategy for the efficient isolation and characterisation of native protein complexes

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Transcriptional profile analysis of RPGRORF15 frameshift mutation identifies novel genes associated with retinal degeneration

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The ciliary rootlet maintains long-term stability of sensory cilia

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Rootletin, a novel coiled-coil protein, is a structural component of the ciliary rootlet

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Comparison of 12 reference genes for normalization of gene expression levels in Epstein-Barr virus-transformed lymphoblastoid cell lines and fibroblasts

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Functional genomic screen for modulators of ciliogenesis and cilium length

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Nek4 status differentially alters sensitivity to distinct microtubule poisons

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Never say never. The NIMA-related protein kinases in mitotic control

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NEK11 regulates CDC25A degradation and the IR-induced G2/M checkpoint

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Members of the NIMA-related kinase family promote disassembly of cilia by multiple mechanisms

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A NIMA-related kinase, Cnk2p, regulates both flagellar length and cell size in Chlamydomonas

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NIMA-related kinase TbNRKC is involved in basal body separation in Trypanosoma brucei.

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A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish

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NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis

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Caught Nek-ing: cilia and centrioles

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Rootletin forms centriole-associated filaments and functions in centrosome cohesion

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Cell regulation: determined to signal discrete cooperation

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Activity and substrate specificity of the murine STK2 Serine/Threonine kinase that is structurally related to the mitotic regulator protein NIMA of Aspergillus nidulans

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Nek2B stimulates zygotic centrosome assembly in Xenopus laevis in a kinase-independent manner

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The NIMA-family kinase, Nek1 affects the stability of centrosomes and ciliogenesis

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Nek11, a new member of the NIMA family of kinases, involved in DNA replication and genotoxic stress responses

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MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis

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