Pages that link to "Q24298367"
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The following pages link to Cep164, a novel centriole appendage protein required for primary cilium formation (Q24298367):
Displaying 50 items.
- Centrosomal protein 164 (Q21113998) (← links)
- Centrosome dysfunction contributes to chromosome instability, chromoanagenesis, and genome reprograming in cancer (Q21129300) (← links)
- Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome (Q21144903) (← links)
- Basal body stability and ciliogenesis requires the conserved component Poc1 (Q22001530) (← links)
- Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling (Q24294774) (← links)
- Primary ciliogenesis requires the distal appendage component Cep123. (Q24296378) (← links)
- Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods (Q24296940) (← links)
- Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy (Q24299464) (← links)
- Poc1A and Poc1B act together in human cells to ensure centriole integrity (Q24299615) (← links)
- Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731 (Q24299855) (← links)
- Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy (Q24300726) (← links)
- CEP90 is required for the assembly and centrosomal accumulation of centriolar satellites, which is essential for primary cilia formation (Q24302145) (← links)
- The deubiquitinating enzyme CYLD controls apical docking of basal bodies in ciliated epithelial cells (Q24302203) (← links)
- Ofd1, a human disease gene, regulates the length and distal structure of centrioles (Q24303311) (← links)
- The spinocerebellar ataxia-associated gene Tau tubulin kinase 2 controls the initiation of ciliogenesis (Q24303418) (← links)
- RBM14 prevents assembly of centriolar protein complexes and maintains mitotic spindle integrity (Q24306609) (← links)
- CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium (Q24310530) (← links)
- Centriole distal appendages promote membrane docking, leading to cilia initiation (Q24310904) (← links)
- The microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis (Q24316470) (← links)
- OCRL localizes to the primary cilium: a new role for cilia in Lowe syndrome (Q24318114) (← links)
- Early steps in primary cilium assembly require EHD1/EHD3-dependent ciliary vesicle formation (Q24319185) (← links)
- The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly (Q24319889) (← links)
- CCDC41 is required for ciliary vesicle docking to the mother centriole (Q24337341) (← links)
- Pitchfork regulates primary cilia disassembly and left-right asymmetry (Q24339279) (← links)
- CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base (Q24339550) (← links)
- CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease (Q24568058) (← links)
- CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290 (Q24644138) (← links)
- Plk1-dependent and -independent roles of an ODF2 splice variant, hCenexin1, at the centrosome of somatic cells (Q24657508) (← links)
- Cep164 is a mediator protein required for the maintenance of genomic stability through modulation of MDC1, RPA, and CHK1 (Q24657907) (← links)
- A primer on the mouse basal body (Q26750292) (← links)
- Human basal body basics (Q26765127) (← links)
- Cellular Mechanisms of Ciliary Length Control (Q26769756) (← links)
- Current topics of functional links between primary cilia and cell cycle (Q26771488) (← links)
- Building a ninefold symmetrical barrel: structural dissections of centriole assembly (Q26798315) (← links)
- The role of the cilium in normal and abnormal cell cycles: emphasis on renal cystic pathologies (Q27026481) (← links)
- The Seckel syndrome and centrosomal protein Ninein localizes asymmetrically to stem cell centrosomes but is not required for normal development, behavior, or DNA damage response in Drosophila (Q27305012) (← links)
- p53 protects against genome instability following centriole duplication failure (Q27310018) (← links)
- Centrosomal nucleolin is required for microtubule network organization (Q27311410) (← links)
- Nephronophthisis-associated CEP164 regulates cell cycle progression, apoptosis and epithelial-to-mesenchymal transition (Q27313602) (← links)
- Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes (Q27319882) (← links)
- Cep57 is a Mis12-interacting kinetochore protein involved in kinetochore targeting of Mad1-Mad2. (Q27339442) (← links)
- Intraflagellar transport (IFT) role in ciliary assembly, resorption and signalling. (Q27967638) (← links)
- Trafficking to the ciliary membrane: how to get across the periciliary diffusion barrier? (Q27967655) (← links)
- The ciliary membrane (Q27967675) (← links)
- A septin diffusion barrier at the base of the primary cilium maintains ciliary membrane protein distribution (Q28000024) (← links)
- ARL13B, PDE6D, and CEP164 form a functional network for INPP5E ciliary targeting (Q28000117) (← links)
- Cep164 mediates vesicular docking to the mother centriole during early steps of ciliogenesis (Q28000119) (← links)
- Assembling a primary cilium (Q28000134) (← links)
- CP110 and its network of partners coordinately regulate cilia assembly (Q28000138) (← links)
- Transition fibre protein FBF1 is required for the ciliary entry of assembled intraflagellar transport complexes (Q28000146) (← links)