Xom interacts with and stimulates transcriptional activity of LEF1/TCFs: implications for ventral cell fate determination during vertebrate embryogenesis (Q80088740)

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scientific article published on 01 April 2007

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English	Xom interacts with and stimulates transcriptional activity of LEF1/TCFs: implications for ventral cell fate determination during vertebrate embryogenesis	scientific article published on 01 April 2007

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28 December 2019

Xom interacts with and stimulates transcriptional activity of LEF1/TCFs: implications for ventral cell fate determination during vertebrate embryogenesis (English)

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28 December 2019

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Hong Gao

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28 December 2019

Bin Wu

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28 December 2019

Roger Giese

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28 December 2019

Zhenglun Zhu

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28 December 2019

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1 April 2007

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28 December 2019

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28 December 2019

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28 December 2019

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28 December 2019

345-356

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28 December 2019

A Xenopus gene, Xbr-1, defines a novel class of homeobox genes and is expressed in the dorsal ciliary margin of the eye.

1 reference

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T-cell factors: turn-ons and turn-offs

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All Tcf HMG box transcription factors interact with Groucho-related co-repressors

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Drosophila Tcf and Groucho interact to repress Wingless signalling activity.

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Drosophila CBP represses the transcription factor TCF to antagonize Wingless signalling.

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LEF-1/TCF proteins mediate wnt-inducible transcription from the Xenopus nodal-related 3 promoter

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Differential expression of the HMG box transcription factors XTcf-3 and XLef-1 during early xenopus development

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Wnt3a-/--like phenotype and limb deficiency in Lef1(-/-)Tcf1(-/-) mice

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Lef-1 and Tcf-3 transcription factors mediate tissue-specific Wnt signaling during Xenopus development

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Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene dTCF

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Regulated proteolysis of Xom mediates dorsoventral pattern formation during early Xenopus development

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XTcf-3 transcription factor mediates beta-catenin-induced axis formation in Xenopus embryos

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An in vivo structure-function study of armadillo, the beta-catenin homologue, reveals both separate and overlapping regions of the protein required for cell adhesion and for wingless signaling

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Identifiers

10.1038/CR.2007.20

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17404593%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17404593%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

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