Nephrocystin-3 is required for ciliary function in zebrafish embryos
about
An ARL3-UNC119-RP2 GTPase cycle targets myristoylated NPHP3 to the primary ciliumCOQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotypeReference gene selection for quantitative real-time RT-PCR normalization in the half-smooth tongue sole (Cynoglossus semilaevis) at different developmental stages, in various tissue types and on exposure to chemicalsThe ciliary protein Nek8/Nphp9 acts downstream of Inv/Nphp2 during pronephros morphogenesis and left-right establishment in zebrafishKnockdown of Bardet-Biedl syndrome gene BBS9/PTHB1 leads to cilia defectsInducible podocyte injury and proteinuria in transgenic zebrafish.The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity.NPHP4 variants are associated with pleiotropic heart malformations.Ciliopathies: the trafficking connection.FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair.Senior-Løken syndrome: a syndromic form of retinal dystrophy associated with nephronophthisis.Genetic background of nonmutant Piebald-Virol-Glaxo rats does not influence nephronophthisis phenotypes.Little fish, big catch: zebrafish as a model for kidney diseaseANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3Zebrafish cytosolic carboxypeptidases 1 and 5 are essential for embryonic development.Functional modelling of a novel mutation in BBS5.Cystic kidney disease: the role of Wnt signaling.Zebrafish kidney development: basic science to translational research.Visualizing renal primary cilia.Cilia and coordination of signaling networks during heart development.From zebrafish heart jogging genes to mouse and human orthologs: using Gene Ontology to investigate mammalian heart development.Zebrafish assays of ciliopathies.Association of kidney structure-related gene variants with type 2 diabetes-attributed end-stage kidney disease in African Americans.Effects of acceleration in the Gz axis on human cardiopulmonary responses to exercise.Homozygous mutation in the NPHP3 gene causing foetal nephronophthisis.Zebrafish as a Model for Drug Screening in Genetic Kidney Diseases.Genetic Renal Diseases: The Emerging Role of Zebrafish ModelsThe nucleoside-diphosphate kinase NME3 associates with nephronophthisis proteins and is required for ciliary function during renal development
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Nephrocystin-3 is required for ciliary function in zebrafish embryos
description
2010 nî lūn-bûn
@nan
2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@ast
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@en
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@en-gb
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@nl
type
label
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@ast
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@en
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@en-gb
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@nl
prefLabel
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@ast
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@en
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@en-gb
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@nl
P2093
P2860
P1476
Nephrocystin-3 is required for ciliary function in zebrafish embryos
@en
P2093
Massimo Attanasio
Weibin Zhou
P2860
P304
P356
10.1152/AJPRENAL.00043.2010
P407
P577
2010-07-01T00:00:00Z