NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children (Q34189740)

31 July 2017

title

NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children (English)

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31 July 2017

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Kyoko Maruyama

1

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31 July 2017

Kazumoto Iijima

2

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31 July 2017

Masahiro Ikeda

3

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31 July 2017

Akiko Kitamura

4

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31 July 2017

Hiroyasu Tsukaguchi

5

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31 July 2017

Kunihiko Yoshiya

6

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31 July 2017

Sakurako Hoshii

7

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31 July 2017

Naohiro Wada

8

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31 July 2017

Osamu Uemura

9

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31 July 2017

Kenichi Satomura

10

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31 July 2017

Masataka Honda

11

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31 July 2017

Norishige Yoshikawa

12

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31 July 2017

publication date

5 April 2003

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31 July 2017

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31 July 2017

volume

18

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31 July 2017

issue

5

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31 July 2017

page(s)

412-416

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https://scigraph.springernature.com/pub.10.1007/s00467-003-1120-6

31 July 2017

exact match

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cites work

The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. A report of the International Study of Kidney Disease in Children

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12 December 2020

Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome

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12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

Another autosomal recessive form of focal glomerulosclerosis with neurological findings

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

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12 December 2020

Interaction with podocin facilitates nephrin signaling

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12 December 2020

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

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12 December 2020

Treatment of the idiopathic nephrotic syndrome: regimens and outcomes in children and adults

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12 December 2020

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

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12 December 2020

Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.

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12 December 2020

A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31

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12 December 2020

Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome

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12 December 2020

Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children

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12 December 2020

PAX2 gene mutation in a family with isolated renal hypoplasia

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12 December 2020

The estimated incidence of cystic fibrosis in Japan

1 reference

12 December 2020

Association study of the 5-HT(2A) receptor gene polymorphism, T102C and essential hypertension

1 reference

12 December 2020

Hereditary variation in platelet integrin alpha 2 beta 1 density is associated with two silent polymorphisms in the alpha 2 gene coding sequence

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12 December 2020

The significance of pure diffuse mesangial proliferation in idiopathic nephrotic syndrome

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12 December 2020

A polymorphic marker in the leptin gene associated with Japanese morbid obesity

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12 December 2020

Two novel polymorphisms (c954T>C and c1038A>G) in exon8 of NPHS2 gene identified in Taiwan Chinese

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12 December 2020

Congenital nephrotic syndrome in mice lacking CD2-associated protein

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12 December 2020

10.1007/S00467-003-1120-6

Identifiers

DOI

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Dimensions Publication ID

1075267270

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