Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis
about
A complex of BBS1 and NPHP7 is required for cilia motility in zebrafishVisualisation of cerebrospinal fluid flow patterns in albino Xenopus larvae in vivoCharacterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet-Biedl syndromeBardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia functionMutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia.The Zn finger protein Iguana impacts Hedgehog signaling by promoting ciliogenesisNephrocystin-3 is required for ciliary function in zebrafish embryosCSAP localizes to polyglutamylated microtubules and promotes proper cilia function and zebrafish developmentThe kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypesLRRC50, a conserved ciliary protein implicated in polycystic kidney diseaseKtu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins.CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms.Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defectsLoss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesiaThe centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4CCDC41 is required for ciliary vesicle docking to the mother centrioleCiliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3miR-129-3p controls cilia assembly by regulating CP110 and actin dynamicsThe heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality.Fused has evolved divergent roles in vertebrate Hedgehog signalling and motile ciliogenesisCC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290Left-right determination: involvement of molecular motor KIF3, cilia, and nodal flowProduction of Basal Bodies in bulk for dense multicilia formationZebrafish: a vertebrate tool for studying basal body biogenesis, structure, and functionSpecialized Cilia in Mammalian Sensory SystemsMicroscale imaging of cilia-driven fluid flowCilia in vertebrate development and diseaseSalient features of the ciliated organ of asymmetryDirectional cerebrospinal fluid movement between brain ventricles in larval zebrafish.Loss of cftr function leads to pancreatic destruction in larval zebrafish.Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and functionJagged2a-notch signaling mediates cell fate choice in the zebrafish pronephric ductIntraciliary calcium oscillations initiate vertebrate left-right asymmetryIsolation and genetic characterization of mother-of-snow-white, a maternal effect allele affecting laterality and lateralized behaviors in zebrafishCilia are required for asymmetric nodal induction in the sea urchin embryoExpression and knockdown of zebrafish folliculin suggests requirement for embryonic brain morphogenesis.Wdr18 is required for Kupffer's vesicle formation and regulation of body asymmetry in zebrafishReciprocal signaling between the ectoderm and a mesendodermal left-right organizer directs left-right determination in the sea urchin embryoEvolutionarily ancient association of the FoxJ1 transcription factor with the motile ciliogenic programCollective cell migration drives morphogenesis of the kidney nephron
P2860
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P2860
Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis
description
2005 nî lūn-bûn
@nan
2005 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Cilia-driven fluid flow in the ...... uired for normal organogenesis
@ast
Cilia-driven fluid flow in the ...... uired for normal organogenesis
@en
type
label
Cilia-driven fluid flow in the ...... uired for normal organogenesis
@ast
Cilia-driven fluid flow in the ...... uired for normal organogenesis
@en
prefLabel
Cilia-driven fluid flow in the ...... uired for normal organogenesis
@ast
Cilia-driven fluid flow in the ...... uired for normal organogenesis
@en
P2093
P3181
P356
P1433
P1476
Cilia-driven fluid flow in the ...... uired for normal organogenesis
@en
P2093
Drummond IA
Haycraft CJ
Kramer-Zucker AG
P304
P3181
P356
10.1242/DEV.01772
P407
P577
2005-04-01T00:00:00Z