Two splice variants of the Wilms' tumor 1 gene have distinct functions during sex determination and nephron formation (Q28509874)

24 January 2017

title

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

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Wilms tumor protein homolog

24 January 2017

main subject

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GOA release 2020-03-11

sex-determination system

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A. Schedl

8

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Marie-Claire Gubler

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ORCID Public Data File 2021

author name string

A. Hammes

1

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24 January 2017

J. K. Guo

2

1 reference

24 January 2017

G. Lutsch

3

1 reference

24 January 2017

J. R. Leheste

4

1 reference

24 January 2017

D. Landrock

5

1 reference

24 January 2017

U. Ziegler

6

1 reference

24 January 2017

M. C. Gubler

7

1 reference

24 January 2017

language of work or name

English

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publication date

10 August 2001

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24 January 2017

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24 January 2017

volume

106

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24 January 2017

issue

3

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24 January 2017

page(s)

319–329

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Targeted mutagenesis of the endogenous mouse Mis gene promoter: in vivo definition of genetic pathways of vertebrate sexual development

24 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryo.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

1 reference

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7 January 2021

RNA binding by the Wilms tumor suppressor zinc finger proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

Did nucleotides or amino acids drive evolutionary conservation of the WT1 +/-KTS alternative splice?

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

Direct interaction of SRY-related protein SOX9 and steroidogenic factor 1 regulates transcription of the human anti-Müllerian hormone gene

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

Truncated WT1 mutants alter the subnuclear localization of the wild-type protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

1 reference

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7 January 2021

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

1 reference

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7 January 2021

The human sex-determining gene SRY is a direct target of WT1.

1 reference

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7 January 2021

Nephrotic syndrome and end-stage renal disease with WT1 mutation detected at 3 years

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7 January 2021

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

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7 January 2021

An RNA recognition motif in Wilms' tumour protein (WT1) revealed by structural modelling.

1 reference

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7 January 2021

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

1 reference

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7 January 2021

Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

The Wilms' tumor suppressor gene (wt1) product regulates Dax-1 gene expression during gonadal differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

WT-1 is required for early kidney development

1 reference

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7 January 2021

Presence of WT1, the Wilm's tumor suppressor gene product, in nuclear poly(A)(+) ribonucleoprotein

1 reference

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7 January 2021

Molecular basis for modulation of biological function by alternate splicing of the Wilms' tumor suppressor protein

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

The Wilms tumor suppressor WT1 encodes a transcriptional activator of amphiregulin

1 reference

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7 January 2021

Complete sequencing of the Fugu WAGR region from WT1 to PAX6: dramatic compaction and conservation of synteny with human chromosome 11p13.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

Sox9 expression during gonadal development implies a conserved role for the gene in testis differentiation in mammals and birds

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

Wilms' tumor 1 and Dax-1 modulate the orphan nuclear receptor SF-1 in sex-specific gene expression

1 reference

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7 January 2021

Sex reversal caused by Mus musculus domesticus Y chromosomes linked to variant expression of the testis-determining gene Sry

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7 January 2021

A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Denys-Drash syndrome

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7 January 2021

Congenital nephrotic syndrome in mice lacking CD2-associated protein

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7 January 2021

Mouse Dax1 expression is consistent with a role in sex determination as well as in adrenal and hypothalamus function

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7 January 2021

Dax1 antagonizes Sry action in mammalian sex determination

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900453-6

7 January 2021

Homologous recombination for gene replacement in mouse cell lines.

1 reference

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7 January 2021

10.1016/S0092-8674(01)00453-6

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017