Oda16/Wdr69 is essential for axonemal dynein assembly and ciliary motility during zebrafish embryogenesis - Test2 - elhamkhani - TriplyDB

Oda16/Wdr69 is essential for axonemal dynein assembly and ciliary motility during zebrafish embryogenesis

Oda16/Wdr69 is essential for axonemal dynein assembly and ciliary motility during zebrafish embryogenesis

http://www.wikidata.org/entity/Q30499660

about

Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia.CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base Wdr18 is required for Kupffer's vesicle formation and regulation of body asymmetry in zebrafish The coiled-coil domain containing protein CCDC151 is required for the function of IFT-dependent motile cilia in animals Small heat shock proteins are necessary for heart migration and laterality determination in zebrafish.NPHP4 variants are associated with pleiotropic heart malformations.Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography.Kupffer's vesicle size threshold for robust left-right patterning of the zebrafish embryo.The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function A NIMA-Related Kinase Suppresses the Flagellar Instability Associated with the Loss of Multiple Axonemal Structures.Mechanisms of otoconia and otolith development Evolution and Expression of Paxillin Genes in Teleost Fish Serotonin has early, cilia-independent roles in Xenopus left-right patterning.Regional cell shape changes control form and function of Kupffer's vesicle in the zebrafish embryo.Lethal giant larvae 2 regulates development of the ciliated organ Kupffer's vesicle.The Chlamydomonas mutant pf27 reveals novel features of ciliary radial spoke assembly.Cilia and coordination of signaling networks during heart development.Structural basis of outer dynein arm intraflagellar transport by the transport adaptor protein ODA16 and the intraflagellar transport protein IFT46.Mutations in zebrafish pitx2 model congenital malformations in Axenfeld-Rieger syndrome but do not disrupt left-right placement of visceral organs.The role of hair cells, cilia and ciliary motility in otolith formation in the zebrafish otic vesicle.Paxillin genes and actomyosin contractility regulate myotome morphogenesis in zebrafish.Wnt5a is necessary for normal kidney development in zebrafish and mice.C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia

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P2860

Oda16/Wdr69 is essential for axonemal dynein assembly and ciliary motility during zebrafish embryogenesis

http://www.wikidata.org/entity/Q30499660

description

2010 nî lūn-bûn

@nan

2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի օգոստոսին 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

Oda16/Wdr69 is essential for a ...... during zebrafish embryogenesis

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Oda16/Wdr69 is essential for a ...... during zebrafish embryogenesis

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Oda16/Wdr69 is essential for a ...... during zebrafish embryogenesis

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Developmental Dynamics

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Oda16/Wdr69 is essential for a ...... during zebrafish embryogenesis

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Chunlei Gao

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

David R Mitchell

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

Guangliang Wang

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

Jeffrey D Amack

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

P2860

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm

LRRC50, a conserved ciliary protein implicated in polycystic kidney disease

Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins.

Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia

Ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy

Stages of embryonic development of the zebrafish

ODA16 aids axonemal outer row dynein assembly through an interaction with the intraflagellar transport machinery

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2190-2197

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scholarly article

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10.1002/DVDY.22355

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8

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239

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2010-08-01T00:00:00Z

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44692683

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20568242

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3077675

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