Articles
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Citation: Cilia 2015 4(Suppl 1):P89
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Pkd2 affects the architecture of zebrafish left-right organizer
Citation: Cilia 2015 4(Suppl 1):P84 -
Characterisation of homologues of known and putative dynein assembly factors in a Drosophila model
Citation: Cilia 2015 4(Suppl 1):P80 -
Structure of outer arm dynein molecule in respiratory cilia suggests an alternative mechanism of force generation
Citation: Cilia 2015 4(Suppl 1):P78 -
CSPP-L and EB3 localize to centriolar satellites and are required for satellite-dependent recruitment of ciliopathy proteins to the centrosome
Citation: Cilia 2015 4(Suppl 1):P76 -
Developing a live cell assay for the centriole-cilium transition in flies
Citation: Cilia 2015 4(Suppl 1):P74 -
A systematic proximity map of the centriole-cilia interface
Citation: Cilia 2015 4(Suppl 1):P72 -
The role of Rabconnectin3a in cilia length regulation
Citation: Cilia 2015 4(Suppl 1):P70 -
Paramecium tetraurelia basal body unit isolation for Cryo-electron tomography studies
Citation: Cilia 2015 4(Suppl 1):P68 -
Cep164, but not EB1, is critical for centriolar localization of TTBK2 and its function in ciliogenesis
Citation: Cilia 2015 4(Suppl 1):P66 -
Number of nexin links detectable at standard electron microscopy of normal human nasal cilia and at nexin link deficiency
Citation: Cilia 2015 4(Suppl 1):P64 -
A reference to assess cilium phenotype in ciliopathy patients
Citation: Cilia 2015 4(Suppl 1):P60 -
Meckel-Gruber syndrome patient cells exhibit alterations in cell-substrate interaction, deformation response, and gene expression consistent with defects leading to liver fibrosis
Citation: Cilia 2015 4(Suppl 1):P58 -
Identification of human mutations in TRAF3IP1 in patients with nephronophthisis and retinal degeneration
Citation: Cilia 2015 4(Suppl 1):P52 -
Recruitment of IFT proteins during flagellum construction in Trypanosoma brucei
Citation: Cilia 2015 4(Suppl 1):P47 -
FPC4: a new cytoskeletal component in T.brucei
Citation: Cilia 2015 4(Suppl 1):P45 -
Transgenic tools for proteomic analysis of ciliary transport
Citation: Cilia 2015 4(Suppl 1):P43 -
Evidence for a role of the ciliopathy protein MKS1 in cell polarity
Citation: Cilia 2015 4(Suppl 1):P42 -
Using the talpid 2 as novel model for determining the cellular and molecular etiology of Oral-facial-digital syndrome
Citation: Cilia 2015 4(Suppl 1):P41 -
Does stopping left-right nodal flow mirror impaired mechanosensation in the left-right organizer?
Citation: Cilia 2015 4(Suppl 1):P39 -
FOXA2 controls Pkd1l1 expression in the mouse node during left-right determination
Citation: Cilia 2015 4(Suppl 1):P37 -
NrCAM modulates sonic hedgehog signalling by controlling smoothened translocation in the cilium
Citation: Cilia 2015 4(Suppl 1):P35 -
Effects of the novel formin INF1 on ciliogenesis
Citation: Cilia 2015 4(Suppl 1):P33 -
Yeast as a simple eukaryotic model to study human diseases linked to membrane trafficking
Citation: Cilia 2015 4(Suppl 1):P31 -
Gene discovery for motile cilia disorders: mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151
Citation: Cilia 2015 4(Suppl 1):P30 -
OFD1 and VFL3/CCDC61 in basal body positioning and docking in Paramecium
Citation: Cilia 2015 4(Suppl 1):P29 -
MARK4 contributes to cilia formation by regulating the degradation of inhibitory OFD1 from the centriolar satellites
Citation: Cilia 2015 4(Suppl 1):P27 -
Integrative approaches to investigate the structure and assembly of Trypanosoma brucei BILBO1, a multidomain cytoskeletal protein at the flagellar pocket collar
Citation: Cilia 2015 4(Suppl 1):P25 -
Crumbs proteins control ciliogenesis and centrosome organization: what about the mechanism?
Citation: Cilia 2015 4(Suppl 1):P23 -
Developing stem cell therapy for retinal dystrophies
Citation: Cilia 2015 4(Suppl 1):O19 -
Pericentrin interacts with KASH domain-containing protein Syne-2
Citation: Cilia 2015 4(Suppl 1):P19 -
Uncoupling flagellum formation and maintenance
Citation: Cilia 2015 4(Suppl 1):O17 -
A novel form of PCD that impacts nodal, but not tracheal cilia
Citation: Cilia 2015 4(Suppl 1):O15 -
PDZD7 connects the Usher protein complex to the intraflagellar transport machinery
Citation: Cilia 2015 4(Suppl 1):P12 -
DNA Methylation and Ciliopathies: a way to be explored
Citation: Cilia 2015 4(Suppl 1):P10 -
Investigation into the Importance of genes encoding ciliary proteins in congenital heart disease using whole exome sequencing
Citation: Cilia 2015 4(Suppl 1):P9 -
Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy
Citation: Cilia 2015 4(Suppl 1):P7 -
The regulation of mechanosensory motile cilium formation
Citation: Cilia 2015 4(Suppl 1):O7 -
The study of a total and two hypothalamic-specific BBS10 knockout models highlights the importance of systemic inactivation in the obese phenotype in Bardet Biedl Syndrome
Citation: Cilia 2015 4(Suppl 1):P5 -
9+2 to 9+0 axoneme conversion in Leishmania
Citation: Cilia 2015 4(Suppl 1):O5 -
Kinesin-3 motor protein KIF13B localizes to centrosomes and primary cilia and regulates ciliary length and signaling
Citation: Cilia 2015 4(Suppl 1):O3 -
Phenotypic variability in Meckel-Gruber syndrome
Citation: Cilia 2015 4(Suppl 1):P1 -
PI3K-C2α regulates Polycystin-2 ciliary entry to prevent kidney cyst formation
Citation: Cilia 2015 4(Suppl 1):O1 -
The Drosophila homologue of Rootletin is required for mechanosensory function and ciliary rootlet formation in chordotonal sensory neurons
In vertebrates, rootletin is the major structural component of the ciliary rootlet and is also part of the tether linking the centrioles of the centrosome. Various functions have been ascribed to the rootlet, ...
Citation: Cilia 2015 4:9 -
Non-invasive sources of cells with primary cilia from pediatric and adult patients
Ciliopathies give rise to a multitude of organ-specific pathologies; obtaining relevant primary patient material is useful for both diagnostics and research. However, acquisition of primary ciliated cells from...
Citation: Cilia 2015 4:8 -
The primary cilium functions as a mechanical and calcium signaling nexus
The primary cilium is an antenna-like, nonmotile structure that extends from the surface of most mammalian cell types and is critical for chemosensing and mechanosensing in a variety of tissues including carti...
Citation: Cilia 2015 4:7 -
Calcium sensors of ciliary outer arm dynein: functions and phylogenetic considerations for eukaryotic evolution
The motility of eukaryotic cilia and flagella is modulated in response to several extracellular stimuli. Ca2+ is the most critical intracellular factor for these changes in motility, directly acting on the axonem...
Citation: Cilia 2015 4:6 -
The more we know, the more we have to discover: an exciting future for understanding cilia and ciliopathies
The Cilia 2014 conference was organised by four European networks: the Ciliopathy Alliance, the Groupement de Recherche CIL, the Nordic Cilia and Centrosome Network and the EU FP7 programme SYSCILIA. More than...
Citation: Cilia 2015 4:5 -
Ultrastructural visualization of trans-ciliary rhodopsin cargoes in mammalian rods
Cilia are vital to various cellular and sensory functions. The pathway by which ciliary membrane proteins translocate through the transition zone is not well understood. Direct morphological characterization o...
Citation: Cilia 2015 4:4 -
Cryo-electron tomography of motile cilia and flagella
Cryo-electron tomography has been a valuable tool in the analysis of 3D structures of cilia at molecular and cellular levels. It opened a way to reconstruct 3D conformations of proteins in cilia at 3-nm resolu...
Citation: Cilia 2015 4:3