about
A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexesCCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms.CCDC41 is required for ciliary vesicle docking to the mother centriolemiR-129-3p controls cilia assembly by regulating CP110 and actin dynamicsWtip and Vangl2 are required for mitotic spindle orientation and cloaca morphogenesisKnockdown of bicaudal C in zebrafish (Danio rerio) causes cystic kidneys: a nonmammalian model of polycystic kidney disease.Functional redundancy between Cdc14 phosphatases in zebrafish ciliogenesis.A comparative analysis of glomerulus development in the pronephros of medaka and zebrafish.In vivo investigation of cilia structure and function using XenopusStructural disorganization of pronephric glomerulus in zebrafish mpp5a/nagie oko mutant.Developmental localization of nephrin in zebrafish and medaka pronephric glomerulus.OCRL1 modulates cilia length in renal epithelial cells.Dynamin Binding Protein (Tuba) Deficiency Inhibits Ciliogenesis and Nephrogenesis in Vitro and in VivoWtip is required for proepicardial organ specification and cardiac left/right asymmetry in zebrafish.Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development.Regulation of basal body and ciliary functions by Diversin.The Cdc14B phosphatase contributes to ciliogenesis in zebrafishA Comparative Study of Embedded and Anesthetized Zebrafish in vivo on Myocardiac Calcium Oscillation and Heart Muscle Contraction.Xenopus radial spoke protein 3 gene is expressed in the multiciliated cells of epidermis and otic vesicles and sequentially in the nephrostomes.Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse.Polycystin 1 loss of function is directly linked to an imbalance in G-protein signaling in the kidney.Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalus.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Fish and frogs: models for vertebrate cilia signaling.
@en
type
label
Fish and frogs: models for vertebrate cilia signaling.
@en
prefLabel
Fish and frogs: models for vertebrate cilia signaling.
@en
P2860
P356
P1476
Fish and frogs: models for vertebrate cilia signaling.
@en
P2093
Oliver Wessely
Tomoko Obara
P2860
P304
P356
10.2741/2806
P577
2008-01-01T00:00:00Z