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  • 26 Hits
  • Search Condition : Filter (Species = C.elegans AND Resource = tm925)
Species Resource Title
C.elegans tm925 , tm3100 CiliaCarta: An integrated and validated compendium of ciliary genes.
C.elegans tm925 , tm2705 , tm3100 , tm2452 A Screen for Modifiers of Cilia Phenotypes Reveals Novel MKS Alleles and Uncovers a Specific Genetic Interaction between osm-3 and nphp-4.
C.elegans tm5624 , tm3100 , tm4182 , tm925 , tm5963 MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone.
C.elegans tm1830 , tm324 , tm925 , tm2322 , tm3100 KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome.
C.elegans tm925 , tm2547 , tm3100 , tm2452 Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport.
C.elegans tm2597 , tm6235 , tm925 PACRG, a protein linked to ciliary motility, mediates cellular signaling.
C.elegans tm3067 , tm324 , tm925 Primary Cilium Formation and Ciliary Protein Trafficking Is Regulated by the Atypical MAP Kinase MAPK15 in Caenorhabditis elegans and Human Cells.
C.elegans tm2452 , tm3067 , tm3433 , tm3951 , tm4927 , tm925 Centrioles initiate cilia assembly but are dispensable for maturation and maintenance in C. elegans.
C.elegans tm1925 , tm2705 , tm2452 , tm2547 , tm925 , tm3083 Ciliogenesis in Caenorhabditis elegans requires genetic interactions between ciliary middle segment localized NPHP-2 (inversin) and transition zone-associated proteins.
C.elegans tm1703 , tm2322 , tm925 , tm1939 , tm2705 , tm2452 , tm2526 Cell- and subunit-specific mechanisms of CNG channel ciliary trafficking and localization in C. elegans.
C.elegans tm925 , tm2452 Assessing the pathogenic potential of human Nephronophthisis disease-associated NPHP-4 missense mutations in C. elegans.
C.elegans tm925 , tm3100 Caenorhabditis elegans ciliary protein NPHP-8, the homologue of human RPGRIP1L, is required for ciliogenesis and chemosensation.
C.elegans tm2452 , tm3100 , tm2547 , tm925 TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone.
C.elegans tm2322 , tm324 , tm3100 , tm2452 , tm925 Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain.
C.elegans tm2526 , tm1703 , tm2322 , tm3100 , tm2705 , tm2452 , tm925 , tm1746 , tm1946 Diverse cell type-specific mechanisms localize G protein-coupled receptors to Caenorhabditis elegans sensory cilia.
C.elegans tm925 , tm2705 , tm2452 , tm2547 Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling.
C.elegans tm5963 , tm3100 , tm925 TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone.
C.elegans tm925 , tm3083 TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome.
C.elegans tm5848 , tm925 Myristoylated CIL-7 regulates ciliary extracellular vesicle biogenesis.
C.elegans tm925 , tm3100 , mks-1/xbx-7 , tza-1/mksr-2 , tza-2/mksr-1 , mks-3 , mks-5 , mks-6 , nphp-1 , ... MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis.