Pages that link to "Q36631120"
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The following pages link to Functional redundancy of the B9 proteins and nephrocystins in Caenorhabditis elegans ciliogenesis (Q36631120):
Displaying 50 items.
- TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone (Q24299114) (← links)
- Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways (Q24302034) (← links)
- Nephrocystins and MKS proteins interact with IFT particle and facilitate transport of selected ciliary cargos (Q24304173) (← links)
- Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins (Q24310078) (← links)
- Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3 (Q24337720) (← links)
- Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome (Q24622660) (← links)
- Identification of novel families and classification of the C2 domain superfamily elucidate the origin and evolution of membrane targeting activities in eukaryotes (Q24623162) (← links)
- The hydrolethalus syndrome protein HYLS-1 links core centriole structure to cilia formation (Q24647436) (← links)
- Compartments within a compartment: what C. elegans can tell us about ciliary subdomain composition, biogenesis, function, and disease (Q27025518) (← links)
- Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling (Q27310130) (← links)
- KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome (Q27336381) (← links)
- MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone (Q27343217) (← links)
- Intraflagellar transport (IFT) role in ciliary assembly, resorption and signalling. (Q27967638) (← links)
- The nonmotile ciliopathies (Q27967648) (← links)
- The small GTPases ARL-13 and ARL-3 coordinate intraflagellar transport and ciliogenesis (Q28000022) (← links)
- MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis (Q28000044) (← links)
- A ciliopathy complex at the transition zone protects the cilia as a privileged membrane domain (Q28000085) (← links)
- Transition fibre protein FBF1 is required for the ciliary entry of assembled intraflagellar transport complexes (Q28000146) (← links)
- Disruption of a ciliary B9 protein complex causes Meckel syndrome (Q28114969) (← links)
- TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome (Q28115647) (← links)
- A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling (Q28507443) (← links)
- Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome (Q28577857) (← links)
- Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel-Gruber syndrome (Q28591420) (← links)
- NePHronoPhthisis (human kidney disease) homolog CELE_R13H4.1 (Q29793460) (← links)
- MecKel Syndrome 1 (MKS1)-Related CELE_K03E6.4 (Q29799748) (← links)
- MecKel Syndrome 1 (MKS1)-Related CELE_Y38F2AL.2 (Q29803242) (← links)
- Intraflagellar transport protein che-13 CELE_F59C6.7 (Q29806285) (← links)
- Transmembrane protein OSTA-1 shapes sensory cilia morphology via regulation of intracellular membrane trafficking in C. elegans (Q30537573) (← links)
- The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity. (Q30540974) (← links)
- The Ciliary Transition Zone: Finding the Pieces and Assembling the Gate (Q33654636) (← links)
- From the cytoplasm into the cilium: bon voyage (Q33728229) (← links)
- Normal ciliogenesis requires synergy between the cystic kidney disease genes MKS-3 and NPHP-4. (Q33834326) (← links)
- Specific alpha- and beta-tubulin isotypes optimize the functions of sensory Cilia in Caenorhabditis elegans (Q34007934) (← links)
- Ancestral centriole and flagella proteins identified by analysis of Naegleria differentiation (Q34329576) (← links)
- NPHP4 controls ciliary trafficking of membrane proteins and large soluble proteins at the transition zone. (Q34433457) (← links)
- A migrating ciliary gate compartmentalizes the site of axoneme assembly in Drosophila spermatids (Q34625473) (← links)
- B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis (Q35030818) (← links)
- Assessing the pathogenic potential of human Nephronophthisis disease-associated NPHP-4 missense mutations in C. elegans (Q35090086) (← links)
- Ciliary diffusion barrier: the gatekeeper for the primary cilium compartment (Q35126782) (← links)
- Modeling human disease in humans: the ciliopathies (Q35453921) (← links)
- Stages of ciliogenesis and regulation of ciliary length (Q35718497) (← links)
- The ciliary transition zone: from morphology and molecules to medicine (Q35902400) (← links)
- A Screen for Modifiers of Cilia Phenotypes Reveals Novel MKS Alleles and Uncovers a Specific Genetic Interaction between osm-3 and nphp-4. (Q35919552) (← links)
- Scoring a backstage pass: mechanisms of ciliogenesis and ciliary access. (Q36027360) (← links)
- Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone (Q36056355) (← links)
- Ciliogenesis in Caenorhabditis elegans requires genetic interactions between ciliary middle segment localized NPHP-2 (inversin) and transition zone-associated proteins (Q36111257) (← links)
- Formation of the transition zone by Mks5/Rpgrip1L establishes a ciliary zone of exclusion (CIZE) that compartmentalises ciliary signalling proteins and controls PIP2 ciliary abundance (Q36172263) (← links)
- Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy (Q37111349) (← links)
- The hydrolethalus syndrome protein HYLS-1 regulates formation of the ciliary gate (Q37191828) (← links)
- Joubert syndrome: congenital cerebellar ataxia with the molar tooth (Q37257283) (← links)