p38 MAPK is essential for secondary axis specification and patterning in sea urchin embryos.
about
A perturbation model of the gene regulatory network for oral and aboral ectoderm specification in the sea urchin embryoCilia are required for asymmetric nodal induction in the sea urchin embryoAncestral regulatory circuits governing ectoderm patterning downstream of Nodal and BMP2/4 revealed by gene regulatory network analysis in an echinodermThe Maternal Maverick/GDF15-like TGF-β Ligand Panda Directs Dorsal-Ventral Axis Formation by Restricting Nodal Expression in the Sea Urchin EmbryoBranching out: origins of the sea urchin larval skeleton in development and evolutionEvolutionary crossroads in developmental biology: sea urchinsp38 MAPK-dependent shaping of the keratin cytoskeleton in cultured cells.Hydroxyurea exposure triggers tissue-specific activation of p38 mitogen-activated protein kinase signaling and the DNA damage response in organogenesis-stage mouse embryos.The evolution of nervous system patterning: insights from sea urchin development.Pantropic retroviruses as a transduction tool for sea urchin embryos.A missing link in the sea urchin embryo gene regulatory network: hesC and the double-negative specification of micromeres.Oral-aboral axis specification in the sea urchin embryo III. Role of mitochondrial redox signaling via H2O2.Short-range Wnt5 signaling initiates specification of sea urchin posterior ectoderm.Mitochondria and metazoan epigenesis.Long-chain Acyl-CoA synthetase 4A regulates Smad activity and dorsoventral patterning in the zebrafish embryo.Developmental gene regulatory network evolution: insights from comparative studies in echinoderms.Asymmetric distribution of hypoxia-inducible factor α regulates dorsoventral axis establishment in the early sea urchin embryo.Crosstalk between Nodal/activin and MAPK p38 signaling is essential for anterior-posterior axis specification.Cis-regulatory control of the nodal gene, initiator of the sea urchin oral ectoderm gene network.The Snail repressor is required for PMC ingression in the sea urchin embryo.Chordin is required for neural but not axial development in sea urchin embryos.Early asymmetric cues triggering the dorsal/ventral gene regulatory network of the sea urchin embryo.Specification to biomineralization: following a single cell type as it constructs a skeleton.The newly characterized Pl-jun is specifically expressed in skeletogenic cells of the Paracentrotus lividus sea urchin embryo.MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo
P2860
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P2860
p38 MAPK is essential for secondary axis specification and patterning in sea urchin embryos.
description
2005 nî lūn-bûn
@nan
2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի նոյեմբերին 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
p38 MAPK is essential for seco ...... terning in sea urchin embryos.
@ast
p38 MAPK is essential for seco ...... terning in sea urchin embryos.
@en
type
label
p38 MAPK is essential for seco ...... terning in sea urchin embryos.
@ast
p38 MAPK is essential for seco ...... terning in sea urchin embryos.
@en
prefLabel
p38 MAPK is essential for seco ...... terning in sea urchin embryos.
@ast
p38 MAPK is essential for seco ...... terning in sea urchin embryos.
@en
P356
P1433
P1476
p38 MAPK is essential for seco ...... terning in sea urchin embryos.
@en
P2093
Cynthia A Bradham
David R McClay
P356
10.1242/DEV.02160
P407
P577
2005-11-30T00:00:00Z