about
CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the ciliumNephrocystins and MKS proteins interact with IFT particle and facilitate transport of selected ciliary cargosThe coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formationLRRC50, a conserved ciliary protein implicated in polycystic kidney diseaseDrosophila asterless and vertebrate Cep152 Are orthologs essential for centriole duplicationInsights into kidney stem cell development and regeneration using zebrafishA unified model for left-right asymmetry? Comparison and synthesis of molecular models of embryonic lateralityCharacterization of tetratricopeptide repeat-containing proteins critical for cilia formation and functionThe exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypesFunctional Diversification of the Four MARCKS Family Members in Zebrafish Neural DevelopmentZebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants.Mutations in zebrafish leucine-rich repeat-containing six-like affect cilia motility and result in pronephric cysts, but have variable effects on left-right patterning.Zebrafish Tsc1 reveals functional interactions between the cilium and the TOR pathwayOda16/Wdr69 is essential for axonemal dynein assembly and ciliary motility during zebrafish embryogenesisSept7b is essential for pronephric function and development of left-right asymmetry in zebrafish embryogenesisCep70 and Cep131 contribute to ciliogenesis in zebrafish embryos.Cildb: a knowledgebase for centrosomes and cilia.Early, nonciliary role for microtubule proteins in left-right patterning is conserved across kingdoms.The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and functionIFT46 plays an essential role in cilia developmentDevelopmental localization of nephrin in zebrafish and medaka pronephric glomerulus.Who drives the ciliary highway?The emerging role of Wnt/PCP signaling in organ formation.It's never too early to get it Right: A conserved role for the cytoskeleton in left-right asymmetry.Laterality defects are influenced by timing of treatments and animal model.Consistent left-right asymmetry cannot be established by late organizers in Xenopus unless the late organizer is a conjoined twin.The Cdc14B phosphatase contributes to ciliogenesis in zebrafishThe actin nucleator Cordon-bleu is required for development of motile cilia in zebrafish.The cytoplasmic tail of rhodopsin triggers rapid rod degeneration in kinesin-2 mutants.Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafish.Autophagy activators suppress cystogenesis in an autosomal dominant polycystic kidney disease model.
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh-hant
name
Genetic defects of pronephric cilia in zebrafish.
@en
Genetic defects of pronephric cilia in zebrafish.
@nl
type
label
Genetic defects of pronephric cilia in zebrafish.
@en
Genetic defects of pronephric cilia in zebrafish.
@nl
prefLabel
Genetic defects of pronephric cilia in zebrafish.
@en
Genetic defects of pronephric cilia in zebrafish.
@nl
P1476
Genetic defects of pronephric cilia in zebrafish
@en
P2093
Chengtian Zhao
P304
P356
10.1016/J.MOD.2007.04.004
P577
2007-05-04T00:00:00Z