(Q81360096)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17899208%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17899208%20AND%20SRC:MED&resulttype=core&format=json

idiopathic nephrotic syndrome

8 January 2020

main subject

1 reference

1 reference

4

1 reference

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8 January 2020

author name string

Afig Berdeli

1

1 reference

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8 January 2020

Sevgi Mir

2

1 reference

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8 January 2020

Onder Yavascan

3

1 reference

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8 January 2020

Mustafa Bak

5

1 reference

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8 January 2020

Nejat Aksu

6

1 reference

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8 January 2020

Ayse Oner

7

1 reference

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8 January 2020

Ali Anarat

8

1 reference

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8 January 2020

Osman Donmez

9

1 reference

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8 January 2020

Nurhan Yildiz

10

1 reference

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8 January 2020

Lale Sever

11

1 reference

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8 January 2020

Yilmaz Tabel

12

1 reference

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8 January 2020

Ruhan Dusunsel

13

1 reference

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8 January 2020

Ferah Sonmez

14

1 reference

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8 January 2020

Nilgun Cakar

15

1 reference

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8 January 2020

publication date

25 September 2007

1 reference

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8 January 2020

1 reference

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8 January 2020

volume

22

1 reference

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8 January 2020

issue

12

1 reference

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8 January 2020

page(s)

2031-2040

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00467-007-0595-y

8 January 2020

exact match

0 references

cites work

Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood

1 reference

12 December 2020

Podocin and nephrotic syndrome: implications for the clinician.

1 reference

12 December 2020

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

1 reference

12 December 2020

A novel polymorphism (c288C>T) of the NPHS2 gene identified in a Taiwan Chinese family

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele

1 reference

12 December 2020

Clinical and genetic evaluation of familial steroid-responsive nephrotic syndrome in childhood.

1 reference

12 December 2020

Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome

1 reference

12 December 2020

Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin

1 reference

12 December 2020

NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children

1 reference

12 December 2020

NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms

1 reference

12 December 2020

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

1 reference

12 December 2020

Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity

1 reference

12 December 2020

Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Primary nephrotic syndrome in children: clinical significance of histopathologic variants of minimal change and of diffuse mesangial hypercellularity. A Report of the International Study of Kidney Disease in Children

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Short versus standard prednisone therapy for initial treatment of idiopathic nephrotic syndrome in children. Arbeitsgemeinschaft für Pädiatrische Nephrologie

1 reference

12 December 2020

Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Case Report. A novel NPHS2 gene mutation in Turkish children with familial steroid-resistant nephrotic syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Broadening the spectrum of diseases related to podocin mutations

1 reference

12 December 2020

Podocin localizes in the kidney to the slit diaphragm area

1 reference

12 December 2020

Pathologic classification of focal segmental glomerulosclerosis: a working proposal

1 reference

12 December 2020