(Q34495087)

2 August 2017

1 reference

title

NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review (English)

1 reference

focal segmental glomerulosclerosis

2 August 2017

1 reference

Jeffrey B Kopp

3

0 references

Kari E North

series ordinal

2

object named as

Kari E North

1 reference

2 August 2017

1

Nora Franceschini

1 reference

2 August 2017

5

Cheryl Winkler

1 reference

2 August 2017

Louise McKenzie

4

1 reference

PubMed ID

16481888

2 August 2017

language of work or name

English

0 references

publication date

1 February 2006

1 reference

2 August 2017

1 reference

2 August 2017

8

1 reference

2 August 2017

2

1 reference

2 August 2017

63-75

1 reference

https://scigraph.springernature.com/pub.10.1097/01.gim.0000200947.09626.1c

2 August 2017

0 references

cites work

Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis.

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

In situ evaluation of podocin in normal and glomerular diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Podocin localizes in the kidney to the slit diaphragm area

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Podocin, a raft-associated component of the glomerular slit diaphragm, interacts with CD2AP and nephrin

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Early glomerular filtration defect and severe renal disease in podocin-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

NPHS2 R229Q functional variant is associated with microalbuminuria in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Identification of podocin (NPHS2) gene mutations in African Americans with nondiabetic end-stage renal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

The many masks of focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Clinical picture and outcome of primary focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Racial differences in the incidence and renal outcome of idiopathic focal segmental glomerulosclerosis in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Broadening the spectrum of diseases related to podocin mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Podocin and nephrotic syndrome: implications for the clinician.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000200947.09626.1C

10.1097/01.GIM.0000200947.09626.1C

21 January 2018

Identifiers

DOI

1 reference

PubMed ID

16481888

Dimensions Publication ID

2 August 2017

0 references

1 reference

PubMed ID

16481888