| scholarly article | Q13442814 |
| P50 | author | Tim Stearns | Q27734166 |
| P2093 | author name string | Timothy R Stowe | |
| Ramona A Hoh | |||
| Erin Turk | |||
| P2860 | cites work | Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function | Q21145277 |
| The Chlamydomonas genome reveals the evolution of key animal and plant functions | Q22065869 | ||
| The Ciliopathies: An Emerging Class of Human Genetic Disorders | Q22337032 | ||
| Targeting expression of a transgene to the airway surface epithelium using a ciliated cell-specific promoter | Q43671300 | ||
| Microtubule nucleation by gamma-tubulin-containing rings in the centrosome | Q46052298 | ||
| Functional genomics in Trypanosoma brucei identifies evolutionarily conserved components of motile flagella. | Q46151100 | ||
| Analysis of xbx genes in C. elegans | Q47069052 | ||
| Characterization of the Drosophila myeloid leukemia factor. | Q47070838 | ||
| Flagellar motility is required for the viability of the bloodstream trypanosome | Q47219440 | ||
| Regulated targeting of a protein kinase into an intact flagellum. An aurora/Ipl1p-like protein kinase translocates from the cell body into the flagella during gamete activation in chlamydomonas | Q47861207 | ||
| Intraflagellar transport particles participate directly in cilium-generated signaling in Chlamydomonas | Q48089194 | ||
| Insulin receptor-like proteins in Tetrahymena thermophila ciliary membranes | Q48263276 | ||
| Association studies and gene expression analyses of the DISC1-interacting molecules, pericentrin 2 (PCNT2) and DISC1-binding zinc finger protein (DBZ), with schizophrenia and with bipolar disorder. | Q51841577 | ||
| Growth and differentiation of mouse tracheal epithelial cells: selection of a proliferative population. | Q52547922 | ||
| DSAS-6 organizes a tube-like centriole precursor, and its absence suggests modularity in centriole assembly. | Q52682166 | ||
| Transcriptional profiling of mucociliary differentiation in human airway epithelial cells. | Q53573827 | ||
| Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion | Q57317077 | ||
| Elevated MLF1 expression correlates with malignant progression from myelodysplastic syndrome | Q73048175 | ||
| An improved method for Dictyostelium centrosome isolation | Q80223603 | ||
| Nucleophosmin/B23 is a target of CDK2/cyclin E in centrosome duplication | Q24290438 | ||
| The centrosomal protein C-Nap1 is required for cell cycle-regulated centrosome cohesion | Q24290514 | ||
| The Polo kinase Plk4 functions in centriole duplication | Q24292705 | ||
| The centriolar satellite protein Cep131 is important for genome stability | Q24293336 | ||
| Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods | Q24296940 | ||
| Asterless is a scaffold for the onset of centriole assembly | Q24300230 | ||
| Proteomic characterization of the human centrosome by protein correlation profiling | Q24301045 | ||
| Toward a confocal subcellular atlas of the human proteome | Q24301129 | ||
| Cep68 and Cep215 (Cdk5rap2) are required for centrosome cohesion | Q24301594 | ||
| DYX1C1 functions in neuronal migration in developing neocortex | Q24304124 | ||
| Roles of BRCA1 in centrosome duplication | Q24306201 | ||
| Cep152 acts as a scaffold for recruitment of Plk4 and CPAP to the centrosome | Q24306268 | ||
| Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons | Q24307517 | ||
| HAUS, the 8-subunit human Augmin complex, regulates centrosome and spindle integrity | Q24308769 | ||
| The augmin complex plays a critical role in spindle microtubule generation for mitotic progression and cytokinesis in human cells | Q24316058 | ||
| Motile cilia of human airway epithelia are chemosensory | Q24317210 | ||
| Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia | Q24317556 | ||
| Huntingtin-associated protein 1 (HAP1) interacts with the p150Glued subunit of dynactin | Q24324649 | ||
| Plk4-induced centriole biogenesis in human cells | Q24336451 | ||
| The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression | Q24337908 | ||
| Cep72 regulates the localization of key centrosomal proteins and proper bipolar spindle formation | Q24338704 | ||
| SAS-6 defines a protein family required for centrosome duplication in C. elegans and in human cells | Q24338767 | ||
| BioGRID: a general repository for interaction datasets | Q24538650 | ||
| The forkhead-associated domain protein Cep170 interacts with Polo-like kinase 1 and serves as a marker for mature centrioles | Q24556578 | ||
| Centriole evolution | Q24631122 | ||
| Fused has evolved divergent roles in vertebrate Hedgehog signalling and motile ciliogenesis | Q24633064 | ||
| Shuttling imbalance of MLF1 results in p53 instability and increases susceptibility to oncogenic transformation | Q24642177 | ||
| Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1. | Q24671718 | ||
| A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain | Q24673084 | ||
| Cyclin-dependent kinase control of centrosome duplication | Q24673544 | ||
| Centriolar satellites: molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesis | Q24680892 | ||
| Radial spoke proteins of Chlamydomonas flagella | Q24685097 | ||
| Sensory reception is an attribute of both primary cilia and motile cilia | Q27687126 | ||
| Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources | Q27860739 | ||
| The nonmotile ciliopathies | Q27967648 | ||
| Functional genomics of the cilium, a sensory organelle | Q28118687 | ||
| The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration | Q28306226 | ||
| Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene | Q28506396 | ||
| The mammalian SPD-2 ortholog Cep192 regulates centrosome biogenesis | Q28585043 | ||
| Tissue expression patterns identify mouse cilia genes | Q28585969 | ||
| Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene | Q28590359 | ||
| The primary cilium: a signalling centre during vertebrate development | Q29547197 | ||
| Proteomic analysis of a eukaryotic cilium | Q29614823 | ||
| Nucleation of microtubule assembly by a gamma-tubulin-containing ring complex | Q29615059 | ||
| Centrioles, centrosomes, and cilia in health and disease | Q29615173 | ||
| The primary cilium as a complex signaling center | Q29615254 | ||
| The ciliary proteome database: an integrated community resource for the genetic and functional dissection of cilia | Q29615741 | ||
| Decoding cilia function: defining specialized genes required for compartmentalized cilia biogenesis | Q29618534 | ||
| The proteome of the mouse photoreceptor sensory cilium complex | Q29619586 | ||
| Calcium influx regulates antibody-induced glycoprotein movements within the Chlamydomonas flagellar membrane | Q30456724 | ||
| Progress towards a cellular neurobiology of reading disability | Q30475697 | ||
| Identification of ciliary and ciliopathy genes in Caenorhabditis elegans through comparative genomics | Q30478961 | ||
| TRPV4 channel participates in receptor-operated calcium entry and ciliary beat frequency regulation in mouse airway epithelial cells | Q30483343 | ||
| Dilatory is a Drosophila protein related to AZI1 (CEP131) that is located at the ciliary base and required for cilium formation | Q30502585 | ||
| A proteomic analysis of human cilia: identification of novel components | Q30841923 | ||
| limmaGUI: a graphical user interface for linear modeling of microarray data | Q33205531 | ||
| Cell cycle progression and de novo centriole assembly after centrosomal removal in untransformed human cells | Q33269437 | ||
| An ATM- and ATR-dependent checkpoint inactivates spindle assembly by targeting CEP63. | Q33404354 | ||
| Cep70 and Cep131 contribute to ciliogenesis in zebrafish embryos | Q33413993 | ||
| Primary microcephaly: do all roads lead to Rome? | Q33629131 | ||
| Genome-wide transcriptional analysis of flagellar regeneration in Chlamydomonas reinhardtii identifies orthologs of ciliary disease genes | Q33928536 | ||
| Role of f-box factor foxj1 in differentiation of ciliated airway epithelial cells | Q34207601 | ||
| Cep120 is asymmetrically localized to the daughter centriole and is essential for centriole assembly. | Q34218804 | ||
| The centrosome cycle: Centriole biogenesis, duplication and inherent asymmetries | Q34221115 | ||
| Exploring the transcriptome of ciliated cells using in silico dissection of human tissues | Q34256530 | ||
| Cep152 interacts with Plk4 and is required for centriole duplication. | Q34317054 | ||
| SAK/PLK4 is required for centriole duplication and flagella development | Q34472675 | ||
| The air-liquid interface and use of primary cell cultures are important to recapitulate the transcriptional profile of in vivo airway epithelia | Q34502170 | ||
| The genetics of developmental dyslexia | Q34529947 | ||
| Flies without centrioles | Q34543650 | ||
| On the role of aurora-A in centrosome function | Q34818218 | ||
| Foxj1 transcription factors are master regulators of the motile ciliogenic program | Q34881332 | ||
| SnapShot: centriole biogenesis | Q34919184 | ||
| Cell biology of normal and abnormal ciliogenesis in the ciliated epithelium | Q35739149 | ||
| Molecular characterization of centriole assembly in ciliated epithelial cells | Q36118747 | ||
| Controlling centrosome number: licenses and blocks | Q36345293 | ||
| Piecing together a ciliome | Q36543698 | ||
| Centriole/basal body morphogenesis and migration during ciliogenesis in animal cells | Q36689663 | ||
| Centriole and basal body formation during ciliogenesis revisited | Q36847218 | ||
| Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy | Q37111349 | ||
| Photoreceptor sensory cilia and inherited retinal degeneration | Q37711181 | ||
| 1001 model organisms to study cilia and flagella | Q37833124 | ||
| Centrosomes and cilia in human disease. | Q37890619 | ||
| Ultrastructure of cilia and flagella - back to the future! | Q37897615 | ||
| Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteins | Q39265866 | ||
| Proteomic analysis of isolated chlamydomonas centrioles reveals orthologs of ciliary-disease genes | Q39720851 | ||
| Human Protein Reference Database and Human Proteinpedia as discovery tools for systems biology. | Q39950844 | ||
| The forkhead protein Foxj1 specifies node-like cilia in Xenopus and zebrafish embryos | Q42158837 | ||
| FoxJ1-dependent gene expression is required for differentiation of radial glia into ependymal cells and a subset of astrocytes in the postnatal brain | Q42462822 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | limma | Q112236343 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Tetratricopeptide repeat domain 12 | Q21123520 |
| Myeloid leukemia factor 1 | Q21491064 | ||
| Transformed mouse 3T3 cell double minute 1 | Q21982568 | ||
| Tetratricopeptide repeat domain 12 | Q21987049 | ||
| P304 | page(s) | e52166 | |
| P577 | publication date | 2012-12-31 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Transcriptional program of ciliated epithelial cells reveals new cilium and centrosome components and links to human disease | |
| P478 | volume | 7 |
| Q26750292 | A primer on the mouse basal body |
| Q93021066 | ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits |
| Q64917283 | Atypical function of a centrosomal module in WNT signalling drives contextual cancer cell motility. |
| Q38642368 | BCAP is a centriolar satellite protein and inhibitor of ciliogenesis. |
| Q47248840 | Building the right centriole for each cell type |
| Q29871115 | CFAP157 is a murine downstream effector of FOXJ1 that is specifically required for flagellum morphogenesis and sperm motility |
| Q36412975 | Ccdc11 is a novel centriolar satellite protein essential for ciliogenesis and establishment of left-right asymmetry |
| Q41929273 | Centriole amplification by mother and daughter centrioles differs in multiciliated cells. |
| Q26851178 | Centriole structure |
| Q99546574 | Centrioles are amplified in cycling progenitors of olfactory sensory neurons |
| Q27309098 | Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and function |
| Q39983088 | Chibby functions to preserve normal ciliary morphology through the regulation of intraflagellar transport in airway ciliated cells |
| Q35734837 | Cilia dysfunction in lung disease |
| Q37258809 | Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs |
| Q58697477 | Cyclin-dependent kinase control of motile ciliogenesis |
| Q27309156 | DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia |
| Q24310331 | DYX1C1 is required for axonemal dynein assembly and ciliary motility |
| Q36452437 | De novo centriole formation in human cells is error-prone and does not require SAS-6 self-assembly. |
| Q41896783 | Decreased FOXJ1 expression and its ciliogenesis programme in aggressive ependymoma and choroid plexus tumours |
| Q92883444 | Dynein tails: how to hitch a ride on an IFT train |
| Q52739053 | Expanding the phenotype associated with biallelic WDR60 mutations: Siblings with retinal degeneration and polydactyly lacking other features of short rib thoracic dystrophies. |
| Q52584777 | Fank1 and Jazf1 promote multiciliated cell differentiation in the mouse airway epithelium. |
| Q42501984 | Foxn4 promotes gene expression required for the formation of multiple motile cilia. |
| Q37551640 | GEMC1 is a critical regulator of multiciliated cell differentiation |
| Q41120448 | Genetic and genomic approaches to identify genes involved in flagellar assembly in Chlamydomonas reinhardtii |
| Q42510561 | Human DNA helicase, RuvBL1 and its Chlamydomonas homologue, CrRuvBL1 plays an important role in ciliogenesis |
| Q38439569 | Identification of FOXJ1 effectors during ciliogenesis in the foetal respiratory epithelium and embryonic left-right organiser of the mouse |
| Q36947278 | Identification of cilia genes that affect cell-cycle progression using whole-genome transcriptome analysis in Chlamydomonas reinhardtti |
| Q28672682 | Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments |
| Q52647764 | Integrated Lung and Tracheal mRNA-Seq and miRNA-Seq Analysis of Dogs with an Avian-Like H5N1 Canine Influenza Virus Infection. |
| Q37596072 | Integrative mechanisms of oriented neuronal migration in the developing brain |
| Q47929915 | Loss of zinc finger MYND-type containing 10 (zmynd10) affects cilia integrity and axonemal localization of dynein arms, resulting in ciliary dysmotility, polycystic kidney and scoliosis in medaka (Oryzias latipes). |
| Q28116536 | MDM1 is a microtubule-binding protein that negatively regulates centriole duplication |
| Q37614857 | Mechanisms of HsSAS-6 assembly promoting centriole formation in human cells |
| Q36141261 | Molecular Evolution of MDM1, a "Duplication-Resistant" Gene in Vertebrates |
| Q93091862 | Mucociliary Defense: Emerging Cellular, Molecular, and Animal Models |
| Q38942536 | Multiciliated Cells in Animals |
| Q30805039 | Multiciliated cell basal bodies align in stereotypical patterns coordinated by the apical cytoskeleton |
| Q33850562 | Multicilin drives centriole biogenesis via E2f proteins |
| Q36236090 | Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family |
| Q30416758 | Myb promotes centriole amplification and later steps of the multiciliogenesis program. |
| Q63979683 | Pan-cancer association of a centrosome amplification gene expression signature with genomic alterations and clinical outcome |
| Q92126517 | Parental centrioles are dispensable for deuterosome formation and function during basal body amplification |
| Q38222354 | Polo-like kinases: structural variations lead to multiple functions |
| Q30361244 | Primary Cilia as a Possible Link between Left-Right Asymmetry and Neurodevelopmental Diseases. |
| Q36482651 | Probing mammalian centrosome structure using BioID proximity-dependent biotinylation |
| Q26740651 | Production of Basal Bodies in bulk for dense multicilia formation |
| Q24301540 | Proteomic analysis of mammalian sperm cells identifies new components of the centrosome |
| Q41413017 | RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly. |
| Q94481960 | Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report |
| Q64084498 | Regulation of cilia abundance in multiciliated cells |
| Q30871699 | Remodeling Cildb, a popular database for cilia and links for ciliopathies |
| Q36253764 | Rfx2 Stabilizes Foxj1 Binding at Chromatin Loops to Enable Multiciliated Cell Gene Expression. |
| Q30858189 | Robust selection of cancer survival signatures from high-throughput genomic data using two-fold subsampling |
| Q29147553 | Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60 |
| Q94464438 | Single-Cell Transcriptomes Reveal a Complex Cellular Landscape in the Middle Ear and Differential Capacities for Acute Response to Infection |
| Q36746500 | Sonic Hedgehog promotes proliferation of Notch-dependent monociliated choroid plexus tumour cells. |
| Q58761846 | Strain-specific differences in brain gene expression in a hydrocephalic mouse model with motile cilia dysfunction |
| Q30592941 | Systematic discovery of novel ciliary genes through functional genomics in the zebrafish. |
| Q55102472 | TRRAP is a central regulator of human multiciliated cell formation. |
| Q36548933 | The Endoplasmic Reticulum Resident Protein AGR3. Required for Regulation of Ciliary Beat Frequency in the Airway. |
| Q28592935 | The Rilp-like proteins Rilpl1 and Rilpl2 regulate ciliary membrane content. |
| Q33959920 | The centriole duplication cycle |
| Q39235969 | The development and functions of multiciliated epithelia. |
| Q34708502 | The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function |
| Q24304929 | Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension |
| Q37131481 | WD60/FAP163 is a dynein intermediate chain required for retrograde intraflagellar transport in cilia |
| Q36215907 | Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport |
| Q36128862 | miR-34/449 control apical actin network formation during multiciliogenesis through small GTPase pathways |
| Q30585689 | miR-34/449 miRNAs are required for motile ciliogenesis by repressing cp110. |
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