(Q43146624)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20191369%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20191369%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

Constantinos J Stefanidis

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20191369%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

Jutta Gellermann

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20191369%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Andromachi Mitsioni

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20191369%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Uwe Querfeld

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20191369%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

27 February 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20191369%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20191369%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

25

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20191369%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

7

1 reference

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19 January 2020

page(s)

1285-1289

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00467-010-1468-3

19 January 2020

exact match

0 references

cites work

Cyclosporin therapy in patients with Alport syndrome.

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

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Early identification of frequent relapsers among children with minimal change nephrotic syndrome. A report of the International Study of Kidney Disease in Children

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

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

1 reference

12 December 2020

Steroid-resistant idiopathic childhood nephrosis: overdiagnosed and undertreated

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

A simple estimate of glomerular filtration rate in children derived from body length and plasma creatinine

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

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The Wt1+/R394W mouse displays glomerulosclerosis and early-onset renal failure characteristic of human Denys-Drash syndrome

1 reference

12 December 2020

WT1 and glomerular diseases

1 reference

12 December 2020

Primary focal segmental glomerular sclerosis in children: clinical course and prognosis

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

Cyclosporine a slows the progressive renal disease of alport syndrome (X-linked hereditary nephritis): results from a canine model

1 reference

12 December 2020

Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome.

1 reference

12 December 2020

New insights into the function of the Wilms tumor suppressor gene WT1 in podocytes

1 reference

12 December 2020

Direct effects of dexamethasone on human podocytes

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

The major podocyte protein nephrin is transcriptionally activated by the Wilms' tumor suppressor 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/S00467-010-1468-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20191369%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

19 January 2020

0 references

1 reference