The Wilms' tumour suppressor Wt1 is a major regulator of tumour angiogenesis and progression. (Q53668097)

17 May 2018

title

The Wilms' tumour suppressor Wt1 is a major regulator of tumour angiogenesis and progression. (English)

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17 May 2018

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4

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author name string

Kay-Dietrich Wagner

1

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17 May 2018

Julien Cherfils-Vicini

2

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17 May 2018

Naoki Hosen

3

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17 May 2018

Eric Gilson

5

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17 May 2018

Nicholas D Hastie

6

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Jean-François Michiels

7

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17 May 2018

Nicole Wagner

8

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language of work or name

English

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publication date

16 December 2014

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17 May 2018

published in

Nature Communications

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17 May 2018

volume

5

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17 May 2018

page(s)

5852

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17 May 2018

https://scigraph.springernature.com/pub.10.1038/ncomms6852

exact match

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cites work

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The Wilms' tumor gene product represses the transcription of thrombospondin 1 in response to overexpression of c-Jun

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WT1 protein directly regulates expression of vascular endothelial growth factor and is a mediator of tumor response to hypoxia

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Subnuclear localization of WT1 in splicing or transcription factor domains is regulated by alternative splicing

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WT1 interacts with the splicing factor U2AF65 in an isoform-dependent manner and can be incorporated into spliceosomes

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WT1 regulates angiogenesis in Ewing Sarcoma

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The Telomeric Protein TRF2 Regulates Angiogenesis by Binding and Activating the PDGFRβ Promoter.

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The Wilms' tumour suppressor WT1 is involved in endothelial cell proliferation and migration: expression in tumour vessels in vivo

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WT1 immunoreactivity in uterine papillary serous carcinomas is different from ovarian serous carcinomas

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The Wilms' tumor suppressor Wt1 is expressed in the coronary vasculature after myocardial infarction.

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Oxygen‐regulated expression of the Wilms’ tumor suppressorWt1involves hypoxia‐inducible factor‐1 (HIF‐1)

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Identifiers

DOI

10.1038/NCOMMS6852

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17 May 2018

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1 reference

17 May 2018