(Q28259503)

Crossref

https://api.crossref.org/works/10.1007%2FS00467-006-0208-1

DNA recognition by splicing variants of the Wilms' tumor suppressor, WT1

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00467-006-0208-1

WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00467-006-0208-1

Diffuse mesangial sclerosis: a congenital glomerulopathy with nephrotic syndrome.

21 January 2018

1 reference

12 December 2020

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

1 reference

12 December 2020

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

1 reference

12 December 2020

Further evidence that imbalance of WT1 isoforms may be involved in Denys – Drash syndrome

1 reference

12 December 2020

Gonadoblastoma and dysgerminoma associated with XY gonadal dysgenesis in an adolescent with chronic renal failure: a case of Frasier syndrome

1 reference

12 December 2020

The Denys-Drash syndrome

1 reference

12 December 2020

Wilms' tumor suppressor gene WT1: from structure to renal pathophysiologic features

1 reference

12 December 2020

Software and database for the analysis of mutations in the human WT1 gene

1 reference

12 December 2020

A clinical overview of WT1 gene mutations

1 reference

12 December 2020

Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinicopathologic review of twelve children with nephropathy, Wilms tumor, and genital abnormalities (Drash syndrome).

1 reference

12 December 2020

Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases

1 reference

12 December 2020

Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations.

1 reference

12 December 2020

Isolated diffuse mesangial sclerosis and Wilms tumor suppressor gene

1 reference

12 December 2020

Familial Wilms' tumor associated with a WT1 zinc finger mutation

1 reference

12 December 2020

A girl with bilateral ovarian tumours: Frasier syndrome.

1 reference

12 December 2020

WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumour

1 reference

12 December 2020

Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT

1 reference

12 December 2020

The nephropathy associated with male pseudohermaphroditism and Wilms' tumor (Drash syndrome): a distinctive glomerular lesion--report of 10 cases

1 reference

12 December 2020

Evidence for the genetic heterogeneity of nephropathic phenotypes associated with Denys-Drash and Frasier syndromes

1 reference

12 December 2020

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

1 reference

12 December 2020

Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene

1 reference

12 December 2020

46,XY phenotypic male with focal segmental glomerulosclerosis caused by the WT1 splice site mutation

1 reference

12 December 2020

Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?

1 reference

12 December 2020

Renal failure in the Denys-Drash and Wilms' tumor-aniridia syndromes

1 reference

12 December 2020

WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis.

1 reference

12 December 2020

A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease

1 reference

12 December 2020

A non-AUG translational initiation event generates novel WT1 isoforms

1 reference

12 December 2020

The WT1 Wilms tumor gene product: a developmentally regulated transcription factor in the kidney that functions as a tumor suppressor

1 reference

12 December 2020

Chronic renal failure and XY gonadal dysgenesis: "Frasier" syndrome--a commentary on reported cases

1 reference

12 December 2020

The same mutation affecting the splicing ofWT1 gene is present on Frasier syndrome patients with or without Wilms' tumor

1 reference

12 December 2020

Frasier syndrome: a cause of focal segmental glomerulosclerosis in a 46,XX female.

1 reference

12 December 2020

WT1 mutations associated with incomplete Denys-Drash syndrome define a domain predicted to behave in a dominant-negative fashion

1 reference

12 December 2020

Differential function of Wilms' tumor gene WT1 splice isoforms in transcriptional regulation

1 reference

12 December 2020

The Wilms' tumor gene product WT1 activates or suppresses transcription through separate functional domains

1 reference

12 December 2020

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

1 reference

12 December 2020

Antagonism of WT1 activity by protein self-association.

1 reference

12 December 2020

A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome

1 reference

12 December 2020

Nephropathy-gonadal dysgenesis, type 2: renal failure in three siblings with XY dysgenesis in one

1 reference

12 December 2020

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

1 reference

12 December 2020

Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities.

1 reference

12 December 2020

Inherited WT1 mutation in Denys-Drash syndrome

1 reference

12 December 2020

Constitutional WT1 mutations in Wilms' tumor patients

1 reference

12 December 2020

Prophylactic bilateral nephrectomies in two paediatric patients with missense mutations in the WT1 gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Absent pubertal development in a child with chronic renal failure: the case of Frasier syndrome

1 reference

12 December 2020

The genomic organization and expression of the WT1 gene

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Diaphragmatic hernia in Denys-Drash syndrome

1 reference

12 December 2020

Frasier syndrome comes full circle: genetic studies performed in an original patient.

1 reference

12 December 2020

Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism

1 reference

12 December 2020

A Japanese case with Frasier syndrome caused by the splice junction mutation of WT1 gene

1 reference

12 December 2020

A novel missense mutation of the Wt1 gene causing Denys-Drash syndrome with exceptionally mild renal manifestations

1 reference

12 December 2020

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

1 reference

12 December 2020

Two cases of isolated diffuse mesangial sclerosis with WT1 mutations

1 reference

12 December 2020

In utero nephropathy, Denys-Drash syndrome and Potter phenotype

1 reference

12 December 2020

End stage renal disease in patients with Wilms tumor: results from the National Wilms Tumor Study Group and the United States Renal Data System

1 reference

12 December 2020

Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion

1 reference

12 December 2020

Gonadal mosaicism of Frasier syndrome in 3 Chinese siblings with donor splice site mutation of Wilms' tumour gene

1 reference

12 December 2020

WT1 is a key regulator of podocyte function: reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis

1 reference

12 December 2020

GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS.

1 reference

12 December 2020

Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms, are also responsible for Frasier syndrome

1 reference

12 December 2020

Frasier syndrome with childhood-onset renal failure

1 reference

12 December 2020

WT1, renal development, and glomerulopathies

1 reference

12 December 2020

The role of WT1 in Wilms tumorigenesis

1 reference

12 December 2020

The WT1 Wilms' tumor suppressor gene: how much do we really know?

1 reference

12 December 2020

RNA editing in the Wilms' tumor susceptibility gene, WT1

1 reference

12 December 2020

Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

1 reference

12 December 2020

Novel familial WT1 read-through mutation associated with Wilms tumor and slow progressive nephropathy.

1 reference

12 December 2020

Alternative splicing and genomic structure of the Wilms tumor gene WT1

1 reference

12 December 2020

Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.

1 reference

12 December 2020

10.1007/S00467-006-0208-1

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3685240

Dimensions Publication ID

1022484112

0 references

OpenCitations bibliographic resource ID

3685240

1 reference