(Q47400156)

15 January 2018

title

WT1 is a modifier of the Pax2 mutant phenotype: cooperation and interaction between WT1 and Pax2 (English)

1 reference

https://api.crossref.org/works/10.1038/SJ.ONC.1206997

29 March 2024

1 reference

1 reference

https://api.crossref.org/works/10.1038/SJ.ONC.1206997

29 March 2024

6

Paul Goodyer

1 reference

15 January 2018

Michael Eccles

7

object named as

Michael Eccles

1 reference

15 January 2018

author name string

Maria Teresa Discenza

1

1 reference

15 January 2018

Shujie He

2

1 reference

15 January 2018

Tae Ho Lee

3

1 reference

15 January 2018

Lee Lee Chu

4

1 reference

15 January 2018

Brad Bolon

5

1 reference

15 January 2018

Jerry Pelletier

8

1 reference

15 January 2018

language of work or name

English

0 references

publication date

1 November 2003

1 reference

15 January 2018

6 November 2003

1 reference

National Center for Biotechnology Information

PubMed ID

14603255

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14603255

full work available at URL

29 March 2024

https://www.nature.com/articles/1206997.pdf

file format

Portable Document Format

online access status

open access

1 reference

PubMed ID

14603255

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14603255

https://www.nature.com/articles/1206997.pdf

29 March 2024

file format

Portable Document Format

1 reference

https://api.crossref.org/works/10.1038/SJ.ONC.1206997

https://www.nature.com/articles/1206997

29 March 2024

1 reference

https://api.crossref.org/works/10.1038/SJ.ONC.1206997

29 March 2024

1 reference

15 January 2018

volume

22

1 reference

15 January 2018

page(s)

8145-8155

1 reference

15 January 2018

issue

50

1 reference

15 January 2018

https://scigraph.springernature.com/pub.10.1038/sj.onc.1206997

exact match

0 references

cites work

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Pax genes and organogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Pax-2 is a DNA-binding protein expressed in embryonic kidney and Wilms tumor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Transcriptional repression by Pax5 (BSAP) through interaction with corepressors of the Groucho family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

The role of PAX2 in normal and abnormal development of the urinary tract.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Two splice variants of the Wilms' tumor 1 gene have distinct functions during sex determination and nephron formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

The Wilms tumor suppressor gene wt1 is required for development of the spleen.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Modulation of EWS/WT1 activity by the v-Src protein tyrosine kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

WT-1 is required for early kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

PTIP, a novel BRCT domain-containing protein interacts with Pax2 and is associated with active chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Wilms tumor and the WT1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Inhibition of Wilms tumor 1 transactivation by bone marrow zinc finger 2, a novel transcriptional repressor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Functional characterization of WT1 binding sites within the human vitamin D receptor gene promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Differential regulation of the human Wilms tumour suppressor gene (WT1) promoter by two isoforms of PAX2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

WT1 regulates the expression of the major glomerular podocyte membrane protein Podocalyxin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Cross-talk in kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Wnt-4 regulation by the Wilms' tumour suppressor gene, WT1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

The regulation of IGF-I receptor gene expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

Inhibition of cellular proliferation by the Wilms' tumor suppressor WT1 is associated with suppression of insulin-like growth factor I receptor gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

The highly conserved beta-hairpin of the paired DNA-binding domain is required for assembly of Pax-Ets ternary complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

A non-AUG translational initiation event generates novel WT1 isoforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

7 January 2021

Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

7 January 2021

Microwave-stimulated antigen retrieval is pH and temperature dependent

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

7 January 2021

The new stereological tools: disector, fractionator, nucleator and point sampled intercepts and their use in pathological research and diagnosis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

7 January 2021

Coordinate action of Wt1 and a modifier gene supports embryonic survival in the oviduct

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

7 January 2021

WT1: what has the last decade told us?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206997

7 January 2021

WT1 suppresses synthesis of the epidermal growth factor receptor and induces apoptosis

10

1 reference

https://api.crossref.org/works/10.1038/SJ.ONC.1206997

29 March 2024

Identifiers

1 reference

15 January 2018

PubMed ID

14603255

1 reference

15 January 2018