Polycystin-2 immunolocalization and function in zebrafish - Wikidata - awgldk - TriplyDB

Polycystin-2 immunolocalization and function in zebrafish

Polycystin-2 immunolocalization and function in zebrafish

http://www.wikidata.org/entity/Q36973881

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A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes Nephrocystin-3 is required for ciliary function in zebrafish embryos Cilia functions in development The luminal connection: from animal development to lumopathies Intraciliary calcium oscillations initiate vertebrate left-right asymmetry Collective cell migration drives morphogenesis of the kidney nephron The exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypes Pkd1 regulates lymphatic vascular morphogenesis during development Function and regulation of TRPP2 ion channel revealed by a gain-of-function mutant Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants.Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene.The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretch Wtip and Vangl2 are required for mitotic spindle orientation and cloaca morphogenesis Polycystin-2 mutations lead to impaired calcium cycling in the heart and predispose to dilated cardiomyopathy Sept7b is essential for pronephric function and development of left-right asymmetry in zebrafish embryogenesis Phosphodiesterase 1A modulates cystogenesis in zebrafish.Polycystic kidney disease in the medaka (Oryzias latipes) pc mutant caused by a mutation in the Gli-Similar3 (glis3) gene.Knockdown of bicaudal C in zebrafish (Danio rerio) causes cystic kidneys: a nonmammalian model of polycystic kidney disease.A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in mice.Modulation of the secretory pathway rescues zebrafish polycystic kidney disease pathology.The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development.The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function Inhibition of the P2X7 receptor reduces cystogenesis in PKD.Immunostaining Phospho-epitopes in Ciliated Organs of Whole Mount Zebrafish Embryos.Xenopus Bicaudal-C is required for the differentiation of the amphibian pronephros.The orphan G protein-coupled receptor 161 is required for left-right patterning The subcellular localization of TRPP2 modulates its function.TRPP2 and TRPV4 form a polymodal sensory channel complex.Fish and frogs: models for vertebrate cilia signaling.Cdc42 deficiency causes ciliary abnormalities and cystic kidneys.Function and regulation of TRPP2 at the plasma membrane.Calcium signaling: a common thread in vertebrate left-right axis development.PACS-1 mediates phosphorylation-dependent ciliary trafficking of the cyclic-nucleotide-gated channel in olfactory sensory neurons A new model system swims into focus: using the zebrafish to visualize intestinal metabolism in vivo.Zebrafish kidney development: basic science to translational research.The zebrafish as a model for nociception studies.Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency.Disease modeling in genetic kidney diseases: zebrafish.Zebrafish Pronephros Development.Comparative transcriptomic analysis identifies evolutionarily conserved gene products in the vertebrate renal distal convoluted tubule.

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P2860

Polycystin-2 immunolocalization and function in zebrafish

http://www.wikidata.org/entity/Q36973881

description

2006 nî lūn-bûn

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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2006年论文

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2006年论文

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name

Polycystin-2 immunolocalization and function in zebrafish

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Polycystin-2 immunolocalization and function in zebrafish

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Polycystin-2 immunolocalization and function in zebrafish

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P1433

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P1433

Journal of the American Society of Nephrology

P1476

Polycystin-2 immunolocalization and function in zebrafish

@en

P2093

Albrecht G Kramer-Zucker

http://www.w3.org/2001/XMLSchema#string

Alexander F Schier

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Felix Olale

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Iain A Drummond

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Jinhua Zhao

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Stephanie Wiessner

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Steven Mangos

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Tomoko Obara

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Yan Liu

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P2860

The polycystic kidney disease protein PKD2 interacts with Hax-1, a protein associated with the actin cytoskeleton

Cellular and subcellular distribution of polycystin-2, the protein product of the PKD2 gene

Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel

Polycystin-2 is an intracellular calcium release channel

Trafficking of TRPP2 by PACS proteins represents a novel mechanism of ion channel regulation

TRPV4 channel is involved in the coupling of fluid viscosity changes to epithelial ciliary activity

Homo- and heterodimeric interactions between the gene products of PKD1 and PKD2

PKD1 interacts with PKD2 through a probable coiled-coil domain

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

PKD2 interacts and co-localizes with mDia1 to mitotic spindles of dividing cells: role of mDia1 IN PKD2 localization to mitotic spindles

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2706-2718

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scholarly article

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10.1681/ASN.2006040412

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10

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17

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2006-08-30T00:00:00Z

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16943304

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3698611

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