| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Søren T Christensen | Q39189891 |
| Lotte Bang Pedersen | Q47296734 | ||
| P2093 | author name string | Peter Satir | |
| Linda Schneider | |||
| P2860 | cites work | Decoding cilia function: defining specialized genes required for compartmentalized cilia biogenesis | Q29618534 |
| P433 | issue | 2 | |
| P304 | page(s) | 97-109 | |
| P577 | publication date | 2007-02-01 | |
| P1433 | published in | Traffic | Q1572846 |
| P1476 | title | Sensory cilia and integration of signal transduction in human health and disease | |
| P478 | volume | 8 |
| Q46536737 | A novel case of natural killer cell deficiency associated with Joubert syndrome |
| Q45058431 | A novel role for primary cilia in airway remodeling. |
| Q38657660 | Aberrant protein trafficking in retinal degenerations: The initial phase of retinal remodeling. |
| Q88814878 | Advances in the Genetics of Primary Ciliary Dyskinesia: Clinical Implications |
| Q27313933 | An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes |
| Q30487418 | An essential role for dermal primary cilia in hair follicle morphogenesis. |
| Q50025735 | Arl3 and RP2 regulate the trafficking of ciliary tip kinesins |
| Q43110896 | Assay for in vitro budding of ciliary-targeted rhodopsin transport carriers |
| Q37130367 | Assembly of primary cilia |
| Q34782639 | Asymmetric mitosis: Unequal segregation of proteins destined for degradation |
| Q36523549 | Autophagy and primary cilia: dual interplay |
| Q26865107 | Autophagy and regulation of cilia function and assembly |
| Q38602968 | BBS4 regulates the expression and secretion of FSTL1, a protein that participates in ciliogenesis and the differentiation of 3T3-L1. |
| Q38558495 | Bardet-Biedl syndrome: Is it only cilia dysfunction? |
| Q37763105 | Basal cell carcinoma and the carcinogenic role of aberrant Hedgehog signaling |
| Q35195922 | Bioinformatic analysis of ciliary transition zone proteins reveals insights into the evolution of ciliopathy networks. |
| Q57022242 | CCDC114 is mutated in patient with a complex phenotype combining primary ciliary dyskinesia, sensorineural deafness, and renal disease |
| Q47579681 | Calcium-axonemal microtubuli interactions underlie mechanism(s) of primary cilia morphological changes. |
| Q30541981 | Carcinogens induce loss of the primary cilium in human renal proximal tubular epithelial cells independently of effects on the cell cycle |
| Q26769756 | Cellular Mechanisms of Ciliary Length Control |
| Q39961011 | Characterization of primary cilia and Hedgehog signaling during development of the human pancreas and in human pancreatic duct cancer cell lines |
| Q57367164 | Chemically-mediated communication in self-oscillating, biomimetic cilia |
| Q36277264 | Cholangiocyte cilia express TRPV4 and detect changes in luminal tonicity inducing bicarbonate secretion. |
| Q28577465 | Cholangiocyte primary cilia are chemosensory organelles that detect biliary nucleotides via P2Y12 purinergic receptors |
| Q36953076 | Cholangiocyte primary cilia in liver health and disease |
| Q26865112 | Cilia/Ift protein and motor -related bone diseases and mouse models |
| Q35537057 | Ciliary ectosomes: transmissions from the cell's antenna |
| Q24621121 | Ciliary entry of the kinesin-2 motor KIF17 is regulated by importin-beta2 and RanGTP |
| Q27967640 | Ciliary targeting motif VxPx directs assembly of a trafficking module through Arf4. |
| Q33514006 | Clinical and molecular features of Joubert syndrome and related disorders |
| Q37820312 | Clinical and molecular insights into tuberous sclerosis complex renal disease. |
| Q28592696 | Directional cell migration and chemotaxis in wound healing response to PDGF-AA are coordinated by the primary cilium in fibroblasts |
| Q35990019 | Disruption of Kif3a in osteoblasts results in defective bone formation and osteopenia |
| Q36011180 | Dopamine receptor 1 localizes to neuronal cilia in a dynamic process that requires the Bardet-Biedl syndrome proteins |
| Q42684966 | Dynein-deficient flagella respond to increased viscosity with contrasting changes in power and recovery strokes |
| Q35112285 | EB1 and EB3 promote cilia biogenesis by several centrosome-related mechanisms |
| Q42914197 | Enteric neurons show a primary cilium |
| Q34256530 | Exploring the transcriptome of ciliated cells using in silico dissection of human tissues |
| Q24321757 | Functional dissection of Rab GTPases involved in primary cilium formation |
| Q24310078 | Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins |
| Q36665960 | Gene expression profiling of flagellar disassembly in Chlamydomonas reinhardtii |
| Q33795641 | Geometry-specific heterogeneity of the apparent diffusion rate of materials inside sperm cells |
| Q92578258 | Group IID, IIE, IIF and III secreted phospholipase A2s |
| Q37369321 | How did the cilium evolve? |
| Q42510561 | Human DNA helicase, RuvBL1 and its Chlamydomonas homologue, CrRuvBL1 plays an important role in ciliogenesis |
| Q36491735 | Human embryonic stem cells in culture possess primary cilia with hedgehog signaling machinery |
| Q36023714 | Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons |
| Q42957171 | IGF-1 activates a cilium-localized noncanonical Gβγ signaling pathway that regulates cell-cycle progression |
| Q24323384 | INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse |
| Q35055414 | Identification of genes involved in the ciliary trafficking of C. elegans PKD-2. |
| Q33479917 | Identification of novel antigens with induced immune response in monoclonal gammopathy of undetermined significance |
| Q33801226 | In situ deflection of tendon cell-cilia in response to tensile loading: an in vitro study |
| Q28585930 | Inactivation of Chibby affects function of motile airway cilia |
| Q34057290 | Insect stage-specific receptor adenylate cyclases are localized to distinct subdomains of the Trypanosoma brucei Flagellar membrane |
| Q27967638 | Intraflagellar transport (IFT) role in ciliary assembly, resorption and signalling. |
| Q40810769 | Intraflagellar transport: a new player at the immune synapse |
| Q37644949 | Intraflagellar transport: it's not just for cilia anymore |
| Q39900371 | Isolation of primary cilia for morphological analysis |
| Q24614362 | Joubert syndrome Arl13b functions at ciliary membranes and stabilizes protein transport in Caenorhabditis elegans |
| Q36840844 | Keeping an eye on I1: I1 dynein as a model for flagellar dynein assembly and regulation |
| Q33743633 | Laminin-511 and integrin beta-1 in hair follicle development and basal cell carcinoma formation |
| Q28000042 | Localization of retinitis pigmentosa 2 to cilia is regulated by Importin beta2. |
| Q64236771 | Loss of Primary Cilia Results in the Development of Cancer in the Murine Thyroid Gland |
| Q24315070 | Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia |
| Q24297023 | MIP-T3 is a negative regulator of innate type I IFN response |
| Q47398675 | Maintaining centrosomes and cilia. |
| Q28834419 | Mechanical dynamics in live cells and fluorescence-based force/tension sensors |
| Q37923514 | Mechanisms of Hedgehog signalling in cancer |
| Q58895773 | Metachronal Waves in Cellular Automata: Cilia-Like Manipulation in Actuator Arrays |
| Q26860718 | Molecular complexes that direct rhodopsin transport to primary cilia |
| Q34914024 | Morphology of non-sensory epithelium during post-natal development of the rabbit vomeronasal organ |
| Q27692039 | Mouse models of ciliopathies: the state of the art. |
| Q33405892 | Nanobiology of the primary cilium--paradigm of a multifunctional nanomachine complex |
| Q35952274 | Neuronal ciliary signaling in homeostasis and disease |
| Q36105568 | Non-Overlapping Distributions and Functions of the VDAC Family in Ciliogenesis |
| Q41161853 | Novel Biochemical and Structural Insights into the Interaction of Myristoylated Cargo with Unc119 Protein and Their Release by Arl2/3. |
| Q39339465 | Nuclear roles for cilia-associated proteins |
| Q24303311 | Ofd1, a human disease gene, regulates the length and distal structure of centrioles |
| Q37052753 | PACRG, a protein linked to ciliary motility, mediates cellular signaling |
| Q37358449 | PACS-1 mediates phosphorylation-dependent ciliary trafficking of the cyclic-nucleotide-gated channel in olfactory sensory neurons |
| Q36564940 | Paramecium BBS genes are key to presence of channels in Cilia |
| Q38768808 | Phosphorylation-dependent Akt-Inversin interaction at the basal body of primary cilia. |
| Q37711181 | Photoreceptor sensory cilia and inherited retinal degeneration |
| Q33949172 | Polycystic liver diseases. |
| Q37242240 | Potassium channels keep mobile cells on the go. |
| Q37080411 | Preformed cell structure and cell heredity |
| Q52717980 | Primary Cilia as a Signaling Platform for Control of Energy Metabolism. |
| Q33894574 | Primary Cilia in Tumor Biology: The Primary Cilium as a Therapeutic Target in Cholangiocarcinoma |
| Q90206038 | Primary Cilium, An Unsung Hero in Maintaining Functional β-cell Population |
| Q34959225 | Primary cilia and coordination of receptor tyrosine kinase (RTK) signalling |
| Q55443025 | Primary cilia and signaling pathways in mammalian development, health and disease. |
| Q34141711 | Primary cilia are decreased in breast cancer: analysis of a collection of human breast cancer cell lines and tissues |
| Q33760974 | Primary cilia are highly oriented with respect to collagen direction and long axis of extensor tendon |
| Q28513509 | Primary cilia dynamics instruct tissue patterning and repair of corneal endothelium |
| Q80845872 | Primary cilia in osteoarthritic chondrocytes: from chondrons to clusters |
| Q37369343 | Primary cilia in planar cell polarity regulation of the inner ear |
| Q40003783 | Primary cilia modulate Ihh signal transduction in response to hydrostatic loading of growth plate chondrocytes |
| Q37252102 | Primary cilia: cellular sensors for the skeleton |
| Q80766703 | Primary cilia: integral to development and disease |
| Q35717888 | Primary cilium suppression by SREBP1c involves distortion of vesicular trafficking by PLA2G3. |
| Q95822241 | Proceedings of the 21st International Bile Acid Meeting. October 7-14, 2010, Freiburg, Germany |
| Q91966626 | Rare Human Diseases: Model Organisms in Deciphering the Molecular Basis of Primary Ciliary Dyskinesia |
| Q35043160 | Regulation of ciliary motility: conserved protein kinases and phosphatases are targeted and anchored in the ciliary axoneme |
| Q37337466 | Regulation of primary cilia formation by ceramide |
| Q27024881 | Spectrum of clinical diseases caused by disorders of primary cilia |
| Q24654284 | Structure and function of mammalian cilia |
| Q36056355 | Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone |
| Q37299245 | Swimming with protists: perception, motility and flagellum assembly |
| Q40522835 | TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23) |
| Q28571736 | Targeting of beta-arrestin2 to the centrosome and primary cilium: role in cell proliferation control |
| Q91802631 | The Centrosome and the Primary Cilium: The Yin and Yang of a Hybrid Organelle |
| Q33340686 | The NIMA-family kinase, Nek1 affects the stability of centrosomes and ciliogenesis |
| Q37237906 | The Na+/H+ exchanger NHE1 is required for directional migration stimulated via PDGFR-alpha in the primary cilium |
| Q39922904 | The Ran importin system in cilia trafficking |
| Q34094901 | The Role of Primary Cilia in Mesenchymal Stem Cell Differentiation: A Pivotal Switch in Guiding Lineage Commitment |
| Q38987762 | The Roles of the Secreted Phospholipase A2 Gene Family in Immunology |
| Q37035044 | The UNI1 and UNI2 genes function in the transition of triplet to doublet microtubules between the centriole and cilium in Chlamydomonas |
| Q37052472 | The cell biological basis of ciliary disease |
| Q39381392 | The cholangiocyte primary cilium in health and disease. |
| Q38111287 | The ciliary cytoskeleton |
| Q30558636 | The cilium secretes bioactive ectosomes |
| Q34307572 | The eukaryotic flagellum makes the day: novel and unforeseen roles uncovered after post-genomics and proteomics data |
| Q36522394 | The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically |
| Q42440588 | The nucleotide-binding proteins Nubp1 and Nubp2 are negative regulators of ciliogenesis. |
| Q37358103 | The primary cilia of secretory cells in the human oviduct mucosa |
| Q37025292 | The primary cilia, a 'Rab-id' transit system for hedgehog signaling |
| Q37690035 | The primary cilium at a glance |
| Q28507794 | The primary cilium coordinates early cardiogenesis and hedgehog signaling in cardiomyocyte differentiation |
| Q37369347 | The primary cilium coordinates signaling pathways in cell cycle control and migration during development and tissue repair |
| Q37369898 | The primary cilium: a small yet mighty organelle. |
| Q24297630 | The retinitis pigmentosa protein RP2 links pericentriolar vesicle transport between the Golgi and the primary cilium |
| Q35082225 | The role of cilia in the regulation of bile flow |
| Q56793763 | The spermatogenesis and sperm structure of Timema poppensis (Insecta: Phasmatodea) |
| Q37323142 | The ubiquitin conjugation system is involved in the disassembly of cilia and flagella |
| Q30420687 | Transport and localization of signaling proteins in ciliated cells |
| Q88917702 | Type I collagen-induced YAP nuclear expression promotes primary cilia growth and contributes to cell migration in confluent mouse embryo fibroblast 3T3-L1 cells |
| Q42804636 | Using quantitative PCR to identify kinesin-3 genes that are upregulated during growth arrest in mouse NIH3T3 cells |
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