Functional genomics of the cilium, a sensory organelle - sprookjes - yvandenbroek - TriplyDB

Functional genomics of the cilium, a sensory organelle

Functional genomics of the cilium, a sensory organelle

http://www.wikidata.org/entity/Q28118687

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A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescence Identification and characterization of novel human tissue-specific RFX transcription factors Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle Bug22p, a conserved centrosomal/ciliary protein also present in higher plants, is required for an effective ciliary stroke in Paramecium.Cep164, a novel centriole appendage protein required for primary cilium formation Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice MNS1 is essential for spermiogenesis and motile ciliary functions in mice The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins An intronic insertion in KPL2 results in aberrant splicing and causes the immotile short-tail sperm defect in the pig Joubert syndrome Arl13b functions at ciliary membranes and stabilizes protein transport in Caenorhabditis elegans The role of primary cilia in neuronal function CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290 Characterization of mouse IFT complex B Structure and function of mammalian cilia Loss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and function Systematic discovery of regulatory motifs in conserved regions of the human genome, including thousands of CTCF insulator sites The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization Cilia in vertebrate development and disease Compartments within a compartment: what C. elegans can tell us about ciliary subdomain composition, biogenesis, function, and disease Changes in cGMP levels affect the localization of EGL-4 in AWC in Caenorhabditis elegans An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes The nephronophthisis-related gene ift-139 is required for ciliogenesis in Caenorhabditis elegans Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain RFX transcription factor DAF-19 regulates 5-HT and innate immune responses to pathogenic bacteria in Caenorhabditis elegans Evolutionarily ancient association of the FoxJ1 transcription factor with the motile ciliogenic program High-throughput in vivo analysis of gene expression in Caenorhabditis elegans KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome Localization of a guanylyl cyclase to chemosensory cilia requires the novel ciliary MYND domain protein DAF-25 Sensory ciliogenesis in Caenorhabditis elegans: assignment of IFT components into distinct modules based on transport and phenotypic profiles.Retrograde intraflagellar transport mutants identify complex A proteins with multiple genetic interactions in Chlamydomonas reinhardtii.The small GTPases ARL-13 and ARL-3 coordinate intraflagellar transport and ciliogenesis MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis Architecture and function of IFT complex proteins in ciliogenesis Intraflagellar transport complex structure and cargo interactions.Transcriptional program of ciliated epithelial cells reveals new cilium and centrosome components and links to human disease Identification of genetic and chemical modulators of zebrafish mechanosensory hair cell death

P2860

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P2860

Functional genomics of the cilium, a sensory organelle

http://www.wikidata.org/entity/Q28118687

description

2005 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի մայիսին հրատարակված գիտական հոդված

@hy

artículu científicu espublizáu en 2005

@ast

im Mai 2005 veröffentlichter wissenschaftlicher Artikel

@de

scientific journal article

@en

vedecký článok (publikovaný 2005/05/24)

@sk

vědecký článek publikovaný v roce 2005

@cs

wetenschappelijk artikel (gepubliceerd op 2005/05/24)

@nl

наукова стаття, опублікована в травні 2005

@uk

مقالة علمية (نشرت في 24-5-2005)

@ar

name

Functional genomics of the cilium, a sensory organelle

@ast

Functional genomics of the cilium, a sensory organelle

@en

Functional genomics of the cilium, a sensory organelle

@nl

type

label

Functional genomics of the cilium, a sensory organelle

@ast

Functional genomics of the cilium, a sensory organelle

@en

Functional genomics of the cilium, a sensory organelle

@nl

prefLabel

Functional genomics of the cilium, a sensory organelle

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Functional genomics of the cilium, a sensory organelle

@en

Functional genomics of the cilium, a sensory organelle

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J.CUB.2005.04.059

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Current Biology

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Functional genomics of the cilium, a sensory organelle

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Adam Warner

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Allan K Mah

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Chunmei Li

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David L Baillie

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Elliot A Perens

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Guangshuo Ou

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Jaswinder Khattra

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Marco A Marra

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Michel R Leroux

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Peter Huang

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935-941

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scholarly article

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2830060

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10.1016/J.CUB.2005.04.059

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2005-05-01T00:00:00Z

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7824711

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15916950

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