The vertebrate primary cilium in development, homeostasis, and disease - Test2 - elhamkhani - TriplyDB

The vertebrate primary cilium in development, homeostasis, and disease

The vertebrate primary cilium in development, homeostasis, and disease

http://www.wikidata.org/entity/Q29614609

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Live imaging of individual cell divisions in mouse neuroepithelium shows asymmetry in cilium formation and Sonic hedgehog response Basal body stability and ciliogenesis requires the conserved component Poc1 ICK is essential for cell type-specific ciliogenesis and the regulation of ciliary transport RTTN mutations link primary cilia function to organization of the human cerebral cortex Bug22p, a conserved centrosomal/ciliary protein also present in higher plants, is required for an effective ciliary stroke in Paramecium.Poc1A and Poc1B act together in human cells to ensure centriole integrity Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia Direct role of Bardet-Biedl syndrome proteins in transcriptional regulation Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics Functional genomic screen for modulators of ciliogenesis and cilium length Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons The Zn finger protein Iguana impacts Hedgehog signaling by promoting ciliogenesis Negative regulation of ciliary length by ciliary male germ cell-associated kinase (Mak) is required for retinal photoreceptor survival HIF1α deubiquitination by USP8 is essential for ciliogenesis in normoxia A SNX10/V-ATPase pathway regulates ciliogenesis in vitro and in vivo CCDC41 is required for ciliary vesicle docking to the mother centriole The role of RPGR in cilia formation and actin stability Casein kinase 1δ functions at the centrosome and Golgi to promote ciliogenesis Founder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families Ciliary entry of the kinesin-2 motor KIF17 is regulated by importin-beta2 and RanGTP Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome Wnt/beta-catenin signaling: components, mechanisms, and diseases Gli-similar (Glis) Krüppel-like zinc finger proteins: insights into their physiological functions and critical roles in neonatal diabetes and cystic renal disease Mammalian axoneme central pair complex proteins: Broader roles revealed by gene knockout phenotypes Photoreceptor Sensory Cilium: Traversing the Ciliary Gate Novel Insights into the Development and Function of Cilia Using the Advantages of the Paramecium Cell and Its Many Cilia Cilia in vertebrate development and disease Molecular complexes that direct rhodopsin transport to primary cilia Sensory functions of motile cilia and implication for bronchiectasis Axonemal positioning and orientation in three-dimensional space for primary cilia: what is known, what is assumed, and what needs clarification Kinesin motors and primary cilia Cell cycle progression by the repression of primary cilia formation in proliferating cells Scrutinizing ciliopathies by unraveling ciliary interaction networks The role of the cilium in normal and abnormal cell cycles: emphasis on renal cystic pathologies Spag17 deficiency results in skeletal malformations and bone abnormalities Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and function Basal body multipotency and axonemal remodelling are two pathways to a 9+0 flagellum.The Armadillo repeat protein PF16 is essential for flagellar structure and function in Plasmodium male gametes Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes Pitchfork and Gprasp2 Target Smoothened to the Primary Cilium for Hedgehog Pathway Activation

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The vertebrate primary cilium in development, homeostasis, and disease

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2009 nî lūn-bûn

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2009 թվականի ապրիլին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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P2860

Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function

The Ciliopathies: An Emerging Class of Human Genetic Disorders

Recruitment and activation of caspase-8 by the Huntingtin-interacting protein Hip-1 and a novel partner Hippi

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

Role of the kinesin-2 family protein, KIF3, during mitosis

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

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

The autosomal recessive polycystic kidney disease protein is localized to primary cilia, with concentration in the basal body area

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

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