(Q37836591)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21298518%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

review article

1 reference

title

The podocyte as a target: cyclosporin A in the management of the nephrotic syndrome caused by WT1 mutations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21298518%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

1 reference

Constantinos J Stefanidis

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21298518%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

author name string

Uwe Querfeld

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21298518%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

publication date

8 February 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21298518%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

21 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21298518%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

volume

170

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21298518%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21298518%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

page(s)

1377-1383

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21298518%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00431-011-1397-6

21 January 2020

exact match

0 references

cites work

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21 January 2018

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Mesangial cell apoptosis: the major mechanism for resolution of glomerular hypercellularity in experimental mesangial proliferative nephritis

21 January 2018

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

21 January 2018

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Membranoproliferative glomerulonephritis associated with a mutation in Wilms' tumour suppressor gene 1

21 January 2018

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Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome

21 January 2018

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Development of an siRNA-based method for repressing specific genes in renal organ culture and its use to show that the Wt1 tumour suppressor is required for nephron differentiation.

21 January 2018

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

21 January 2018

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In vivo induction of interleukin 10 by anti-CD3 monoclonal antibody or bacterial lipopolysaccharide: differential modulation by cyclosporin A

21 January 2018

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The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A.

21 January 2018

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GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS.

21 January 2018

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21 January 2018

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Podocyte differentiation and hereditary proteinuria/nephrotic syndromes

21 January 2018

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

21 January 2018

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An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

21 January 2018

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The role of the Wilms' tumour-suppressor protein WT1 in apoptosis

21 January 2018

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Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

21 January 2018

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Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

21 January 2018

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The many facets of the Wilms' tumour gene, WT1

21 January 2018

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Familial nephrotic syndrome: PLCE1 enters the fray

21 January 2018

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Interleukin-10 inhibits experimental mesangial proliferative glomerulonephritis

21 January 2018

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

21 January 2018

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WT-1 is required for early kidney development

21 January 2018

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WT1 influences apoptosis through transcriptional regulation of Bcl-2 family members

21 January 2018

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Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis--a review

21 January 2018

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Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation.

21 January 2018

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Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome.

21 January 2018

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WT1 and glomerular function.

21 January 2018

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21 January 2018

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The Wilms tumour suppressor protein WT1 (+KTS isoform) binds alpha-actinin 1 mRNA via its zinc-finger domain.

21 January 2018

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WT1 induces apoptosis through transcriptional regulation of the proapoptotic Bcl-2 family member Bak.

21 January 2018

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WT1 and glomerular diseases

21 January 2018

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

21 January 2018

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A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes.

21 January 2018

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Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.

21 January 2018

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Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.

21 January 2018

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A role for the Wilms' tumor protein WT1 in organ development

21 January 2018

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Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations

21 January 2018

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Wilms' tumor protein Wt1 regulates the Interleukin-10 (IL-10) gene

21 January 2018

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Podocyte cytoskeleton is connected to the integral membrane protein podocalyxin through Na+/H+-exchanger regulatory factor 2 and ezrin

21 January 2018

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NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

21 January 2018

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Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

21 January 2018

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WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes

21 January 2018

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Diffuse mesangial sclerosis: a congenital glomerulopathy with nephrotic syndrome.

21 January 2018

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12 December 2020

Mechanisms of cyclosporine A-induced apoptosis in rat hepatocyte primary cultures

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12 December 2020

Cell death in the diseased glomerulus

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12 December 2020

Frasier syndrome: early gonadoblastoma and cyclosporine responsiveness

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12 December 2020

A proteomic investigation of glomerular podocytes from a Denys-Drash syndrome patient with a mutation in the Wilms tumour suppressor gene WT1

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12 December 2020

Steroid-resistant idiopathic childhood nephrosis: overdiagnosed and undertreated

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12 December 2020

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12 December 2020

Altered signaling and regulatory mechanisms of apoptosis in focal and segmental glomerulosclerosis

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12 December 2020

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

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12 December 2020

Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations

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12 December 2020

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

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12 December 2020