A mutation in the Gsk3-binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon - Wikidata - wikimedia - TriplyDB

A mutation in the Gsk3-binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon

A mutation in the Gsk3-binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon

http://www.wikidata.org/entity/Q35079035

about

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer Transcription factor Zic2 inhibits Wnt/β-catenin protein signaling Six3 repression of Wnt signaling in the anterior neuroectoderm is essential for vertebrate forebrain development The ankyrin repeat protein Diversin recruits Casein kinase Iepsilon to the beta-catenin degradation complex and acts in both canonical Wnt and Wnt/JNK signaling Neurogenesis in zebrafish - from embryo to adult Hsp90 selectively modulates phenotype in vertebrate development Smooth muscle tension induces invasive remodeling of the zebrafish intestine Zebrafish foxo3b negatively regulates canonical Wnt signaling to affect early embryogenesis Pleiotropic effects of Sox2 during the development of the zebrafish epithalamus Transcriptional regulation of cranial sensory placode development Emerging roles of Axin in cerebral cortical development Habenula circuit development: past, present, and future The β-catenin destruction complex Regulation of slow and fast muscle myofibrillogenesis by Wnt/beta-catenin and myostatin signaling Anteriorization of neural fate by inhibitor of beta-catenin and T cell factor (ICAT), a negative regulator of Wnt signaling Wnt/Axin1/beta-catenin signaling regulates asymmetric nodal activation, elaboration, and concordance of CNS asymmetries Epithelial cell proliferation in the developing zebrafish intestine is regulated by the Wnt pathway and microbial signaling via Myd88.The ventral habenulae of zebrafish develop in prosomere 2 dependent on Tcf7l2 function.Neurodevelopment genes in lampreys reveal trends for forebrain evolution in craniates Differential regulation of the zebrafish orthopedia 1 gene during fate determination of diencephalic neurons.The tumor suppressor PRDM5 regulates Wnt signaling at early stages of zebrafish development.Characterization and development of novel small-molecules inhibiting GSK3 and activating Wnt signaling.Correct anteroposterior patterning of the zebrafish neurectoderm in the absence of the early dorsal organizer.A median third eye: pineal gland retraces evolution of vertebrate photoreceptive organs.Lhx2 and Lhx9 determine neuronal differentiation and compartition in the caudal forebrain by regulating Wnt signaling.Loss of eyes in zebrafish caused by mutation of chokh/rx3.Genes and signaling networks regulated during zebrafish optic vesicle morphogenesis Differential role of Axin RGS domain function in Wnt signaling during anteroposterior patterning and maternal axis formation Constructing the hindbrain: insights from the zebrafish.Embryonic origin of the eyes in teleost fish.Dopaminergic neuronal cluster size is determined during early forebrain patterning Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa.Parsing the prosencephalon.Keeping an eye on SOXC proteins.Evolution of photosensory pineal organs in new light: the fate of neuroendocrine photoreceptors HESX1- and TCF3-mediated repression of Wnt/β-catenin targets is required for normal development of the anterior forebrain.The visual system of zebrafish and its use to model human ocular diseases.Early steps in the development of the forebrain Regionally specific induction by the Spemann-Mangold organizer.

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P2860

A mutation in the Gsk3-binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon

http://www.wikidata.org/entity/Q35079035

description

2001 nî lūn-bûn

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2001 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2001 թվականի հունիսին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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name

A mutation in the Gsk3-binding ...... halon and eyes to diencephalon

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A mutation in the Gsk3-binding ...... halon and eyes to diencephalon

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type

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A mutation in the Gsk3-binding ...... halon and eyes to diencephalon

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A mutation in the Gsk3-binding ...... halon and eyes to diencephalon

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A mutation in the Gsk3-binding ...... halon and eyes to diencephalon

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A mutation in the Gsk3-binding ...... halon and eyes to diencephalon

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A mutation in the Gsk3-binding ...... halon and eyes to diencephalon

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P2093

C P Heisenberg

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D L Stemple

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G J Rauch

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M L Concha

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P2860

DIX domains of Dvl and axin are necessary for protein interactions and their ability to regulate beta-catenin stability

Axin, a negative regulator of the Wnt signaling pathway, forms a complex with GSK-3beta and beta-catenin and promotes GSK-3beta-dependent phosphorylation of beta-catenin.

Constitutive transcriptional activation by a beta-catenin-Tcf complex in APC-/- colon carcinoma

A molecular mechanism for the effect of lithium on development

Establishment of the dorso-ventral axis in Xenopus embryos is presaged by early asymmetries in beta-catenin that are modulated by the Wnt signaling pathway

The mouse Fused locus encodes Axin, an inhibitor of the Wnt signaling pathway that regulates embryonic axis formation

Effective targeted gene 'knockdown' in zebrafish

Mechanisms of Wnt signaling in development

beta-catenin is a target for the ubiquitin-proteasome pathway

Neuronal specification in the spinal cord: inductive signals and transcriptional codes

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