Frizzled5/8 is required in secondary mesenchyme cells to initiate archenteron invagination during sea urchin development.
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microRNA regulation of Wnt signaling pathways in development and diseaseReciprocal signaling between the ectoderm and a mesendodermal left-right organizer directs left-right determination in the sea urchin embryoDevelopment of the aboral domain in Nematostella requires β-catenin and the opposing activities of Six3/6 and Frizzled5/8A genomic view of the sea urchin nervous systemDissecting the PCP pathway: one or more pathways?: Does a separate Wnt-Fz-Rho pathway drive morphogenesis?Integration of canonical and noncanonical Wnt signaling pathways patterns the neuroectoderm along the anterior-posterior axis of sea urchin embryos.Strabismus-mediated primary archenteron invagination is uncoupled from Wnt/β-catenin-dependent endoderm cell fate specification in Nematostella vectensis (Anthozoa, Cnidaria): Implications for the evolution of gastrulation.Specific functions of the Wnt signaling system in gene regulatory networks throughout the early sea urchin embryo.A genome-wide survey of the evolutionarily conserved Wnt pathways in the sea urchin Strongylocentrotus purpuratus.Frizzled1/2/7 signaling directs β-catenin nuclearisation and initiates endoderm specification in macromeres during sea urchin embryogenesisAxial patterning interactions in the sea urchin embryo: suppression of nodal by Wnt1 signalingA global view of gene expression in lithium and zinc treated sea urchin embryos: new components of gene regulatory networks.Wnt to build a tube: contributions of Wnt signaling to epithelial tubulogenesis.The sea urchin animal pole domain is a Six3-dependent neurogenic patterning center.Evolution of the Wnt pathwaysShort-range Wnt5 signaling initiates specification of sea urchin posterior ectoderm.Apical constriction: a cell shape change that can drive morphogenesis.Morphogenesis in sea urchin embryos: linking cellular events to gene regulatory network states.Integration of anterior neural plate patterning and morphogenesis by the Wnt signaling pathway.Telling left from right: left-right asymmetric controls in sea urchins.Molecular characterization of the apical organ of the anthozoan Nematostella vectensis.Apical constriction and invagination downstream of the canonical Wnt signaling pathway require Rho1 and Myosin II.Blocking Dishevelled signaling in the noncanonical Wnt pathway in sea urchins disrupts endoderm formation and spiculogenesis, but not secondary mesoderm formationLarval body patterning and apical organs are conserved in animal evolution.Hedgehog signaling patterns mesoderm in the sea urchin.The involvement of lethal giant larvae and Wnt signaling in bottle cell formation in Xenopus embryos.A comprehensive survey of wnt and frizzled expression in the sea urchin Paracentrotus lividus.Characterization of sFRP2-like in amphioxus: insights into the evolutionary conservation of Wnt antagonizing function.New insights from a high-resolution look at gastrulation in the sea urchin, Lytechinus variegatus.
P2860
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P2860
Frizzled5/8 is required in secondary mesenchyme cells to initiate archenteron invagination during sea urchin development.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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name
Frizzled5/8 is required in sec ...... during sea urchin development.
@en
Frizzled5/8 is required in sec ...... during sea urchin development.
@nl
type
label
Frizzled5/8 is required in sec ...... during sea urchin development.
@en
Frizzled5/8 is required in sec ...... during sea urchin development.
@nl
prefLabel
Frizzled5/8 is required in sec ...... during sea urchin development.
@en
Frizzled5/8 is required in sec ...... during sea urchin development.
@nl
P2093
P356
P1433
P1476
Frizzled5/8 is required in sec ...... during sea urchin development.
@en
P2093
Christian Gache
David R McClay
Guy Lhomond
Jenifer Croce
Louise Duloquin
P304
P356
10.1242/DEV.02218
P407
P577
2006-01-05T00:00:00Z