(Q33897098)

29 July 2017

title

NPHS2 variation in sporadic focal segmental glomerulosclerosis (English)

1 reference

focal segmental glomerulosclerosis

29 July 2017

main subject

1 reference

Howard Trachtman

12

0 references

Jeffrey B. Kopp

object named as

Jeffrey B Kopp

19

0 references

Gregory Kirk

18

object named as

Gregory D Kirk

1 reference

29 July 2017

20

Cheryl A Winkler

1 reference

29 July 2017

2

Sher L Hendrickson

1 reference

29 July 2017

7

Paul L Kimmel

1 reference

29 July 2017

Louise M McKenzie

1

1 reference

29 July 2017

William A Briggs

3

1 reference

29 July 2017

Richard A Dart

4

1 reference

29 July 2017

Stephen M Korbet

5

1 reference

29 July 2017

Michelle H Mokrzycki

6

1 reference

29 July 2017

Tejinder S Ahuja

8

1 reference

29 July 2017

Jeffrey S Berns

9

1 reference

29 July 2017

Eric E Simon

10

1 reference

29 July 2017

Michael C Smith

11

1 reference

29 July 2017

Donna M Michel

13

1 reference

29 July 2017

Jeffrey R Schelling

14

1 reference

29 July 2017

Monique Cho

15

1 reference

29 July 2017

Yu C Zhou

16

1 reference

29 July 2017

Elizabeth Binns-Roemer

17

1 reference

29 July 2017

publication date

17 October 2007

1 reference

Journal of the American Society of Nephrology

29 July 2017

published in

1 reference

29 July 2017

volume

18

1 reference

29 July 2017

issue

11

1 reference

29 July 2017

page(s)

2987-2995

1 reference

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

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

Haploview: analysis and visualization of LD and haplotype maps

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

A comparison of bayesian methods for haplotype reconstruction from population genotype data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

Statistical significance for genomewide studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

HIV-associated nephropathy in African Americans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

Broadening the spectrum of diseases related to podocin mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

Idiopathic focal segmental glomerulosclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

The genetic basis of FSGS and steroid-resistant nephrosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

Why the kidney glomerulus does not clog: a gel permeation/diffusion hypothesis of renal function

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

Interaction with podocin facilitates nephrin signaling

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

A New Statistical Method for Haplotype Reconstruction from Population Data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

Podocin and nephrotic syndrome: implications for the clinician

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096868

Is there an epidemic of HIV Infection in the US ESRD program?

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17942957

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial clustering of end-stage renal disease in blacks with HIV-associated nephropathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17942957

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17942957

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1681/ASN.2007030319

1 reference

29 July 2017

1 reference

29 July 2017

1 reference