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  • 23 Hits
  • Search Condition : Filter (MeSH = Cilia / genetics)
Species Resource Title
C.elegans tm3310 , tm3360 , tm4059 , tm4910 Mutation of NEKL-4/NEK10 and TTLL genes suppress neuronal ciliary degeneration caused by loss of CCPP-1 deglutamylase function.
C.elegans tm3067 , tm7883 TALPID3 and ANKRD26 selectively orchestrate FBF1 localization and cilia gating.
C.elegans tm324 Optimal sidestepping of intraflagellar transport kinesins regulates structure and function of sensory cilia.
DNA material pMRX-bsr-EGFP-P2A-Rab34  (RDB18392) , pEF-FLAG-Rab34-S1A  (RDB18393) , pEF-FLAG-Rab34-deltaN (RDB18394) , pEGFP-C1-Rab34-T66N  (RDB18395) A comprehensive analysis of Rab GTPases reveals a role for Rab34 in serum starvation-induced primary ciliogenesis.
Zebrafish off-limit rw689 Microtubules are required for the maintenance of planar cell polarity in monociliated floorplate cells.
Human and Animal Cells 10T1/2(RCB0247) Down-regulated WDR35 contributes to fetal anomaly via regulation of osteogenic differentiation.
C.elegans tm1215 , tm0246 Endosome maturation factors Rabenosyn-5/VPS45 and caveolin-1 regulate ciliary membrane and polycystin-2 homeostasis.
Zebrafish Tg(sox17:EGFP) Myosin1D is an evolutionarily conserved regulator of animal left-right asymmetry.
Mice RBRC02369 Mice with a Deletion of Rsph1 Exhibit a Low Level of Mucociliary Clearance and Develop a Primary Ciliary Dyskinesia Phenotype.
C.elegans tm4314 Accelerating Gene Discovery by Phenotyping Whole-Genome Sequenced Multi-mutation Strains and Using the Sequence Kernel Association Test (SKAT).
C.elegans tm6493 A Conserved Role for Girdin in Basal Body Positioning and Ciliogenesis.
C.elegans tm1830 , tm324 , tm925 , tm2322 , tm3100 KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome.
C.elegans tm324 The nephronophthisis-related gene ift-139 is required for ciliogenesis in Caenorhabditis elegans.
C.elegans tm1653 , tm901 , tm2411 , tm4300 , tm2669 , tm1449 , tm2816 , tm2364 , tm324 Mutations in a guanylate cyclase GCY-35/GCY-36 modify Bardet-Biedl syndrome-associated phenotypes in Caenorhabditis elegans.
C.elegans tm925 , tm3100 Caenorhabditis elegans ciliary protein NPHP-8, the homologue of human RPGRIP1L, is required for ciliogenesis and chemosensation.
C.elegans tm5234 , tm4878 , tm4888 An ER complex of ODR-4 and ODR-8/Ufm1 specific protease 2 promotes GPCR maturation by a Ufm1-independent mechanism.
DNA material pCAGGSII-mICK (RDB13108) , pCAGGSII-hICK (RDB13109) , pCAGGSII-mICK-K33R (RDB13110) , pCAGGSII-hICK-R272Q (RDB13111) , pCAGGSII-mIFT57 (RDB13112) , pCAGGSII-mBBS8 (RDB13113) , pCAGGSII-mKIF3A (RDB13114) , pCAGGSII-mIFT88 (RDB13115) , pCAGGSII-mIFT140 (RDB13116) , pGEX-4T-1-mKIF3A (delta 1-454 aa) (RDB13117) , ... ICK is essential for cell type-specific ciliogenesis and the regulation of ciliary transport.
Medaka abc (MT144) , Cab Pkd1l1 complexes with Pkd2 on motile cilia and functions to establish the left-right axis.
Medaka Cab inbred strain The LIM protein Ajuba is required for ciliogenesis and left-right axis determination in medaka.
C.elegans tm2322 Joubert syndrome Arl13b functions at ciliary membranes and stabilizes protein transport in Caenorhabditis elegans.