| scholarly article | Q13442814 |
| review article | Q7318358 |
| P6179 | Dimensions Publication ID | 1049704746 |
| P356 | DOI | 10.1186/2046-2530-1-7 |
| P932 | PMC publication ID | 3555707 |
| P698 | PubMed publication ID | 23351924 |
| P5875 | ResearchGate publication ID | 235374058 |
| P2093 | author name string | Matthew W Kelley | |
| Helen L May-Simera | |||
| P2860 | cites work | The Golgin GMAP210/TRIP11 anchors IFT20 to the Golgi complex | Q21145025 |
| Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein | Q22008584 | ||
| The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly | Q24293516 | ||
| BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly | Q24295491 | ||
| Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods | Q24296940 | ||
| Chibby, a nuclear beta-catenin-associated antagonist of the Wnt/Wingless pathway | Q24300418 | ||
| Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling | Q24301800 | ||
| Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways | Q24302034 | ||
| Centriolar kinesin Kif24 interacts with CP110 to remodel microtubules and regulate ciliogenesis | Q24304699 | ||
| Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics | Q24305196 | ||
| A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis | Q24311615 | ||
| Motile cilia of human airway epithelia are chemosensory | Q24317210 | ||
| Regulation of planar cell polarity by Smurf ubiquitin ligases | Q24317525 | ||
| APC binds to the novel protein EB1 | Q24317778 | ||
| Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3 | Q24337720 | ||
| Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease. | Q51953017 | ||
| Cdc42 controls the polarity of the actin and microtubule cytoskeletons through two distinct signal transduction pathways. | Q53673562 | ||
| Observations on axonemes and membranes of olfactory and respiratory cilia in frogs and rats using tannic acid-supplemented fixation and photographic rotation | Q72736596 | ||
| The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression | Q24337908 | ||
| Cep97 and CP110 suppress a cilia assembly program | Q24338361 | ||
| CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease | Q24568058 | ||
| Intraflagellar transport molecules in ciliary and nonciliary cells of the retina | Q24595309 | ||
| Scaffold proteins: hubs for controlling the flow of cellular information | Q24611517 | ||
| Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome | Q24622660 | ||
| Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes | Q24625476 | ||
| Intraflagellar transport motors in cilia: moving along the cell's antenna | Q24645583 | ||
| Centrioles in the cell cycle. I. Epithelial cells | Q24681444 | ||
| Spectrum of clinical diseases caused by disorders of primary cilia | Q27024881 | ||
| Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome | Q27919661 | ||
| MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis | Q28000044 | ||
| Ciliogenesis: building the cell's antenna | Q28000047 | ||
| Chibby cooperates with 14-3-3 to regulate beta-catenin subcellular distribution and signaling activity | Q28114807 | ||
| Intraflagellar transport | Q28131775 | ||
| Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination | Q28188363 | ||
| Critical role for the EB1 and APC interaction in the regulation of microtubule polymerization | Q28208418 | ||
| Depletion of centromeric MCAK leads to chromosome congression and segregation defects due to improper kinetochore attachments | Q28236606 | ||
| Cdc42--the centre of polarity | Q28250444 | ||
| FGF-dependent left-right asymmetry patterning in zebrafish is mediated by Ier2 and Fibp1 | Q28312172 | ||
| Intraflagellar transport protein 122 antagonizes Sonic Hedgehog signaling and controls ciliary localization of pathway components | Q28505068 | ||
| PCP effector gene Inturned is an important regulator of cilia formation and embryonic development in mammals | Q28505120 | ||
| Fuz controls the morphogenesis and differentiation of hair follicles through the formation of primary cilia | Q28505257 | ||
| Planar cell polarity effector gene Fuzzy regulates cilia formation and Hedgehog signal transduction in mouse | Q28505727 | ||
| Impaired Wnt-beta-catenin signaling disrupts adult renal homeostasis and leads to cystic kidney ciliopathy | Q28506100 | ||
| An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia | Q28506229 | ||
| Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates | Q28506652 | ||
| A role for the primary cilium in Notch signaling and epidermal differentiation during skin development | Q28510710 | ||
| Lack of cadherins Celsr2 and Celsr3 impairs ependymal ciliogenesis, leading to fatal hydrocephalus | Q28511503 | ||
| Planar polarization in embryonic epidermis orchestrates global asymmetric morphogenesis of hair follicles | Q28513824 | ||
| The planar cell polarity effector Fuz is essential for targeted membrane trafficking, ciliogenesis and mouse embryonic development | Q28584722 | ||
| The subcellular destinations of APC proteins | Q34623795 | ||
| Ciliopathies: an expanding disease spectrum | Q34626170 | ||
| Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry | Q34796294 | ||
| Centriole age underlies asynchronous primary cilium growth in mammalian cells | Q34997578 | ||
| Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome | Q35032831 | ||
| The small GTPase Cdc42 is necessary for primary ciliogenesis in renal tubular epithelial cells | Q35063130 | ||
| EB1 and EB3 promote cilia biogenesis by several centrosome-related mechanisms | Q35112285 | ||
| Cilium, centrosome and cell cycle regulation in polycystic kidney disease. | Q35112926 | ||
| Cell biological regulation of division fate in vertebrate neuroepithelial cells | Q35116856 | ||
| Accumulation of the Raf-1 kinase inhibitory protein (Rkip) is associated with Cep290-mediated photoreceptor degeneration in ciliopathies | Q35150162 | ||
| NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway | Q35196050 | ||
| Cilia and cell cycle re-entry: more than a coincidence | Q35559947 | ||
| ARF family G proteins and their regulators: roles in membrane transport, development and disease. | Q35632439 | ||
| STAM and Hrs down-regulate ciliary TRP receptors | Q35949117 | ||
| APC is a component of an organizing template for cortical microtubule networks | Q36012265 | ||
| Adenomatous polyposis coli and EB1 localize in close proximity of the mother centriole and EB1 is a functional component of centrosomes. | Q36012450 | ||
| Cdc42 and noncanonical Wnt signal transduction pathways cooperate to promote cell polarity | Q36119733 | ||
| The adenomatous polyposis coli tumor suppressor protein localizes to plasma membrane sites involved in active cell migration. | Q36237136 | ||
| Asymmetric centrosome behavior and the mechanisms of stem cell division | Q36404828 | ||
| Asymmetric stem cell division and function of the niche in the Drosophila male germ line | Q36420003 | ||
| Planar cell polarity acts through septins to control collective cell movement and ciliogenesis. | Q36433141 | ||
| Lucky 13-microtubule depolymerisation by kinesin-13 motors | Q36599332 | ||
| What is the function of centrioles? | Q36658029 | ||
| Wnt signalling and the actin cytoskeleton | Q36672682 | ||
| Centrosome duplication: of rules and licenses | Q36769585 | ||
| Intraflagellar transport: from molecular characterisation to mechanism | Q36992512 | ||
| Functional modules, mutational load and human genetic disease | Q37086760 | ||
| Assembly of primary cilia | Q37130367 | ||
| Building it up and taking it down: the regulation of vertebrate ciliogenesis | Q37147143 | ||
| Dampened Hedgehog signaling but normal Wnt signaling in zebrafish without cilia | Q37314322 | ||
| Planar cell polarity signaling: the developing cell's compass. | Q37412656 | ||
| Making sense of cilia in disease: the human ciliopathies. | Q37624563 | ||
| Planar cell polarity: keeping hairs straight is not so simple | Q37698284 | ||
| CEP290, a gene with many faces: mutation overview and presentation of CEP290base. | Q37778326 | ||
| Mechanisms of mammalian ciliary motility: Insights from primary ciliary dyskinesia genetics | Q37812789 | ||
| Strange as it may seem: the many links between Wnt signaling, planar cell polarity, and cilia | Q37834841 | ||
| Kinesins and protein kinases: key players in the regulation of microtubule dynamics and organization | Q37846270 | ||
| Regulating the transition from centriole to basal body | Q37871223 | ||
| Ultrastructure of cilia and flagella - back to the future! | Q37897615 | ||
| Inversin, Wnt signaling and primary cilia | Q37972186 | ||
| Polarity proteins control ciliogenesis via kinesin motor interactions | Q38337461 | ||
| Ciliary transition zone activation of phosphorylated Tctex-1 controls ciliary resorption, S-phase entry and fate of neural progenitors | Q39537369 | ||
| Primary cilia regulate mTORC1 activity and cell size through Lkb1. | Q39640418 | ||
| Aberrant activation of fatty acid synthesis suppresses primary cilium formation and distorts tissue development. | Q39648686 | ||
| Flow modulates centriole movements in tubular epithelial cells | Q39990068 | ||
| MCAK associates with EB1. | Q40060454 | ||
| Adenomatous polyposis coli (APC) protein moves along microtubules and concentrates at their growing ends in epithelial cells | Q40901818 | ||
| Fine mapping of regulatory loci for mammalian gene expression using radiation hybrids | Q41588995 | ||
| Asymmetric inheritance of mother versus daughter centrosome in stem cell division | Q41956545 | ||
| The PCP pathway instructs the planar orientation of ciliated cells in the Xenopus larval skin | Q42113899 | ||
| The Microtubule plus end-tracking protein EB1 is localized to the flagellar tip and basal bodies in Chlamydomonas reinhardtii | Q42452654 | ||
| Coupling between hydrodynamic forces and planar cell polarity orients mammalian motile cilia | Q42469073 | ||
| Bbs8, together with the planar cell polarity protein Vangl2, is required to establish left-right asymmetry in zebrafish. | Q42474570 | ||
| Ciliogenesis defects in embryos lacking inturned or fuzzy function are associated with failure of planar cell polarity and Hedgehog signaling | Q42491186 | ||
| Sperm ultrastructure and spermiogenesis of Coniopterygidae (Neuroptera, Insecta). | Q43772808 | ||
| Adenomatous polyposis coli associates with the microtubule-destabilizing protein XMCAK. | Q45158402 | ||
| Regulation of primary cilia formation and left-right patterning in zebrafish by a noncanonical Wnt signaling mediator, duboraya | Q46486197 | ||
| FGF-induced vesicular release of Sonic hedgehog and retinoic acid in leftward nodal flow is critical for left-right determination. | Q46486386 | ||
| Defective planar cell polarity in polycystic kidney disease | Q46845250 | ||
| Genome-wide analysis identifies a general requirement for polarity proteins in endocytic traffic | Q47068800 | ||
| Planar cell polarity signalling regulates cell adhesion properties in progenitors of the zebrafish laterality organ | Q47073220 | ||
| Vangl2 directs the posterior tilting and asymmetric localization of motile primary cilia. | Q47073501 | ||
| Cystic kidney gene seahorse regulates cilia-mediated processes and Wnt pathways | Q47073543 | ||
| Dishevelled promotes axon differentiation by regulating atypical protein kinase C. | Q48142245 | ||
| Inactivation of Chibby affects function of motile airway cilia | Q28585930 | ||
| Ciliary proteins link basal body polarization to planar cell polarity regulation | Q28585995 | ||
| Disruption of IFT complex A causes cystic kidneys without mitotic spindle misorientation | Q28587960 | ||
| Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking | Q28588535 | ||
| Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure | Q28588549 | ||
| Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease | Q28592609 | ||
| Hedgehog signalling in the mouse requires intraflagellar transport proteins | Q28593010 | ||
| Identification of Vangl2 and Scrb1 as planar polarity genes in mammals | Q28593071 | ||
| Identification and partial characterization of mitotic centromere-associated kinesin, a kinesin-related protein that associates with centromeres during mitosis | Q28633869 | ||
| The primary cilium: a signalling centre during vertebrate development | Q29547197 | ||
| Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms | Q29614613 | ||
| PDGFRalphaalpha signaling is regulated through the primary cilium in fibroblasts | Q29614616 | ||
| Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways | Q29614619 | ||
| CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content. | Q29614822 | ||
| The primary cilium as the cell's antenna: signaling at a sensory organelle | Q29615165 | ||
| Towards an integrated view of Wnt signaling in development | Q29615175 | ||
| The primary cilium as a complex signaling center | Q29615254 | ||
| Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response | Q29617051 | ||
| Two populations of node monocilia initiate left-right asymmetry in the mouse | Q29617071 | ||
| Centrosome composition and microtubule anchoring mechanisms | Q29619588 | ||
| Centrioles and the formation of rudimentary cilia by fibroblasts and smooth muscle cells | Q29620499 | ||
| Par3 functions in the biogenesis of the primary cilium in polarized epithelial cells | Q30441567 | ||
| The von Hippel-Lindau tumor suppressor protein controls ciliogenesis by orienting microtubule growth | Q30480543 | ||
| Dual role of Cdc42 in spindle orientation control of adherent cells | Q30487617 | ||
| Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells | Q30491381 | ||
| Loss of oriented cell division does not initiate cyst formation | Q30493527 | ||
| Intraflagellar transport is required for polarized recycling of the TCR/CD3 complex to the immune synapse | Q30493645 | ||
| Planar cell polarity breaks bilateral symmetry by controlling ciliary positioning | Q30499162 | ||
| The cilia protein IFT88 is required for spindle orientation in mitosis | Q30499405 | ||
| Planar cell polarity enables posterior localization of nodal cilia and left-right axis determination during mouse and Xenopus embryogenesis. | Q30977459 | ||
| Patterns of expression of Bardet-Biedl syndrome proteins in the mammalian cochlea suggest noncentrosomal functions | Q33435460 | ||
| Primary cilia are not required for normal canonical Wnt signaling in the mouse embryo. | Q33498502 | ||
| Wnt regulates spindle asymmetry to generate asymmetric nuclear β-catenin in C. elegans | Q34021395 | ||
| Primary cilia regulate branching morphogenesis during mammary gland development. | Q34047857 | ||
| KIF17 stabilizes microtubules and contributes to epithelial morphogenesis by acting at MT plus ends with EB1 and APC. | Q34069997 | ||
| Control of vertebrate multiciliogenesis by miR-449 through direct repression of the Delta/Notch pathway | Q34186612 | ||
| The intraflagellar transport component IFT88/polaris is a centrosomal protein regulating G1-S transition in non-ciliated cells | Q34607735 | ||
| P275 | copyright license | Creative Commons Attribution 2.0 Generic | Q19125117 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P921 | main subject | cytoskeleton | Q154626 |
| P304 | page(s) | 7 | |
| P577 | publication date | 2012-05-02 | |
| P1433 | published in | Cilia | Q27724298 |
| P1476 | title | Cilia, Wnt signaling, and the cytoskeleton | |
| P478 | volume | 1 |
| Q92617626 | A CEP104-CSPP1 Complex Is Required for Formation of Primary Cilia Competent in Hedgehog Signaling |
| Q56978235 | A Novel Mouse Model for Cilia-Associated Cardiovascular Anomalies with a High Penetrance of Total Anomalous Pulmonary Venous Return |
| Q50911466 | A novel role of KIF3b in the seminoma cell cycle. |
| Q36125919 | A transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the Sea anemone Nematostella vectensis |
| Q98564827 | An interphase pool of KIF11 localizes at the basal bodies of primary cilia and a reduction in KIF11 expression alters cilia dynamics |
| Q34211767 | Atmin mediates kidney morphogenesis by modulating Wnt signaling. |
| Q26865107 | Autophagy and regulation of cilia function and assembly |
| Q38748824 | Basal cell carcinoma pathogenesis and therapy involving hedgehog signaling and beyond |
| Q64094557 | Basalin is an evolutionarily unconstrained protein revealed via a conserved role in flagellum basal plate function |
| Q50116067 | CDKL Family Kinases Have Evolved Distinct Structural Features and Ciliary Function |
| Q50421643 | Centrosomal protein Dzip1l binds Cby, promotes ciliary bud formation, and acts redundantly with Bromi to regulate ciliogenesis in the mouse |
| Q38979853 | Chronic pancreatitis and lipomatosis are associated with defective function of ciliary genes in pancreatic ductal cells |
| Q50457524 | Cilia and Ciliopathies in Congenital Heart Disease |
| Q28512858 | Ciliary proteins Bbs8 and Ift20 promote planar cell polarity in the cochlea |
| Q59620272 | Cilium structure, assembly, and disassembly regulated by the cytoskeleton |
| Q93043521 | Clinical Implications of Primary Cilia in Skin Cancer |
| Q38729320 | Concise Review: Primary Cilia: Control Centers for Stem Cell Lineage Specification and Potential Targets for Cell-Based Therapies |
| Q92146556 | Convergence of Canonical and Non-Canonical Wnt Signal: Differential Kat3 Coactivator Usage |
| Q90703591 | Coordination of WNT signaling and ciliogenesis during odontogenesis by piezo type mechanosensitive ion channel component 1 |
| Q90239236 | Deregulation of Neuro-Developmental Genes and Primary Cilium Cytoskeleton Anomalies in iPSC Retinal Sheets from Human Syndromic Ciliopathies |
| Q90277564 | Effects of FSS on the expression and localization of the core proteins in two Wnt signaling pathways, and their association with ciliogenesis |
| Q42133585 | Egr-5 is a post-mitotic regulator of planarian epidermal differentiation |
| Q54936023 | Endothelial dysfunction in pulmonary arterial hypertension: loss of cilia length regulation upon cytokine stimulation. |
| Q53087377 | Etiologies of uterine malformations. |
| Q34685089 | Evaluating the role of PTH in promotion of chondrosarcoma cell proliferation and invasion by inhibiting primary cilia expression |
| Q50528573 | Evaluation of Planar-Cell-Polarity Phenotypes in Ciliopathy Mouse Mutant Cochlea. |
| Q41931303 | Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype. |
| Q47919079 | Expression profiles of NPHP1 in the germ cells in the semen of men with male factor infertility |
| Q61845606 | FGFR1-mediated protocadherin-15 loading mediates cargo specificity during intraflagellar transport in inner ear hair-cell kinocilia |
| Q36441268 | Genetic screening reveals a link between Wnt signaling and antitubulin drugs |
| Q92327415 | Genetics of Congenital Heart Disease |
| Q37698831 | Identification of Elongated Primary Cilia with Impaired Mechanotransduction in Idiopathic Scoliosis Patients |
| Q36947278 | Identification of cilia genes that affect cell-cycle progression using whole-genome transcriptome analysis in Chlamydomonas reinhardtti |
| Q34672726 | Inversin/Nephrocystin-2 is required for fibroblast polarity and directional cell migration |
| Q38895233 | Ionizing radiation increases primary cilia incidence and induces multiciliation in C2C12 myoblasts |
| Q27310217 | LINE-1 Mediated Insertion into Poc1a (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice |
| Q27343217 | MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone |
| Q27320543 | Measuring the primary cilium length: improved method for unbiased high-throughput analysis. |
| Q90427508 | Mechanical loading induces primary cilia disassembly in tendon cells via TGFβ and HDAC6 |
| Q33991899 | MicroRNAs in Cholangiopathies |
| Q37348018 | Mutations in the Motile Cilia Gene DNAAF1 Are Associated with Neural Tube Defects in Humans. |
| Q64110277 | Neural control of body-plan axis in regenerating planaria |
| Q92157976 | Novel functions of the primary cilium in bone disease and cancer |
| Q38973454 | Oscillatory fluid flow influences primary cilia and microtubule mechanics |
| Q28082204 | Physiological mechanisms and therapeutic potential of bone mechanosensing. |
| Q27001174 | Polycystic liver diseases: advanced insights into the molecular mechanisms |
| Q64067818 | Primary Cilia-An Underexplored Topic in Major Mental Illness |
| Q45932817 | Primary Cilium-Dependent Signaling Mechanisms. |
| Q47234929 | Primary Cilium-Mediated Retinal Pigment Epithelium Maturation Is Disrupted in Ciliopathy Patient Cells. |
| Q64233855 | Primary cilia and their role in cancer |
| Q89605874 | Primary cilia: Versatile regulator in cartilage development |
| Q36382780 | Prion protein localizes at the ciliary base during neural and cardiovascular development, and its depletion affects α-tubulin post-translational modifications |
| Q90576089 | Prominins control ciliary length throughout the animal kingdom: New lessons from human prominin-1 and zebrafish prominin-3 |
| Q38639930 | Proper ciliary assembly is critical for restricting Hedgehog signaling during early eye development in mice |
| Q55100657 | RPGR protein complex regulates proteasome activity and mediates store-operated calcium entry. |
| Q64269462 | Roles of Primary Cilia in the Developing Brain |
| Q39380506 | Routes and machinery of primary cilium biogenesis |
| Q39377571 | The (pro)renin receptor and its interaction partners. |
| Q55430488 | The E3 ubiquitin ligase SMURF1 regulates cell-fate specification and outflow tract septation during mammalian heart development. |
| Q37179516 | The ciliary GTPase Arl13b regulates cell migration and cell cycle progression |
| Q39457168 | The connections of Wnt pathway components with cell cycle and centrosome: side effects or a hidden logic? |
| Q47681227 | The primary cilium as a signaling nexus for growth plate function and subsequent skeletal development. |
| Q38430088 | Transcriptomic analysis comparing mouse strains with extreme total lung capacities identifies novel candidate genes for pulmonary function |
| Q37588325 | Tris DBA palladium is highly effective against growth and metastasis of pancreatic cancer in an orthotopic model. |
| Q37564942 | Zonal variation in primary cilia elongation correlates with localized biomechanical degradation in stress deprived tendon |
| Q36264739 | nlz1 is required for cilia formation in zebrafish embryogenesis |
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