The transition zone: an essential functional compartment of cilia. - Wikidata - thesis-toulmin - TriplyDB

The transition zone: an essential functional compartment of cilia.

The transition zone: an essential functional compartment of cilia.

http://www.wikidata.org/entity/Q42966406

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Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies Unique properties of Drosophila spermatocyte primary cilia Ciliary subcompartments: how are they established and what are their functions?MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration NINL and DZANK1 Co-function in Vesicle Transport and Are Essential for Photoreceptor Development in Zebrafish Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome Chemically inducible diffusion trap at cilia reveals molecular sieve-like barrier.TGF-β Signaling Regulates the Differentiation of Motile Cilia.Protein arginine methyltransferases interact with intraflagellar transport particles and change location during flagellar growth and resorption.From the cytoplasm into the cilium: bon voyage.Diverse cell type-specific mechanisms localize G protein-coupled receptors to Caenorhabditis elegans sensory cilia A migrating ciliary gate compartmentalizes the site of axoneme assembly in Drosophila spermatids.A high-resolution morphological and ultrastructural map of anterior sensory cilia and glia in Caenorhabditis elegans.Developmental disruptions underlying brain abnormalities in ciliopathies.Joubert Syndrome in French Canadians and Identification of Mutations in CEP104 Gated entry into the ciliary compartment.Transition zone assembly and its contribution to axoneme formation in Drosophila male germ cells.INPP5E regulates phosphoinositide-dependent cilia transition zone function.Primary cilia in neurodevelopmental disorders.Cilia and coordination of signaling networks during heart development.Role of cilia in structural birth defects: insights from ciliopathy mutant mouse models.Hearing molecules, mechanism and transportation: modeled in Drosophila melanogaster.Chemical and Physical Sensors in the Regulation of Renal Function.Unmasking the ciliopathies: craniofacial defects and the primary cilium.Ciliopathies: Genetics in Pediatric Medicine.The cilium: a cellular antenna with an influence on obesity risk.Structural and molecular bases of rod photoreceptor morphogenesis and disease.Regulation of Hedgehog Signalling Inside and Outside the Cell.Primary Cilia and Coordination of Receptor Tyrosine Kinase (RTK) and Transforming Growth Factor β (TGF-β) Signaling.Motile and non-motile cilia in human pathology: from function to phenotypes.Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes.CILIA: before and after.Routes and machinery of primary cilium biogenesis.Biophysics and Biofluiddynamics of Primary Cilia: evidence for and against the flow-sensing function.Motile cilia defects in diseases other than primary ciliary dyskinesia: The contemporary diagnostic and research role for transmission electron microscopy.Proteomic analysis of isolated ciliary transition zones reveals the presence of ESCRT proteins.The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway.Rab GTPases in cilium formation and function.Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center.

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P2860

The transition zone: an essential functional compartment of cilia.

http://www.wikidata.org/entity/Q42966406

description

2012 nî lūn-bûn

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2012年論文

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2012年论文

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name

The transition zone: an essential functional compartment of cilia.

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The transition zone: an essential functional compartment of cilia.

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The transition zone: an essential functional compartment of cilia.

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The transition zone: an essential functional compartment of cilia.

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Colin A Johnson

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Katarzyna Szymanska

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P2860

The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly

Cep164, a novel centriole appendage protein required for primary cilium formation

TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone

Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies

CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium

A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia

Functional dissection of Rab GTPases involved in primary cilium formation

The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia

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10.1186/2046-2530-1-10

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axonemal basal plate

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