(Q34712797)

English

Frequency of COL4A3/COL4A4 mutations amongst families segregating glomerular microscopic hematuria and evidence for activation of the unfolded protein response. Focal and segmental glomerulosclerosis is a frequent development during ageing

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Frequency of COL4A3/COL4A4 mutations amongst families segregating glomerular microscopic hematuria and evidence for activation of the unfolded protein response. Focal and segmental glomerulosclerosis is a frequent development during ageing (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

1 reference

based on heuristic

inferred from title

glomerulosclerosis

1 reference

based on heuristic

inferred from title

Konstantinos Voskarides

30

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Constantinos Deltas

31

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

27

object named as

Ioanna Zouvani

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Yiannis Athanasiou

8

object named as

Yiannis Athanasiou

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

29

object named as

Alkis Pierides

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Gregory Papagregoriou

4

object named as

Gregory Papagregoriou

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Louiza Papazachariou

1

object named as

Louiza Papazachariou

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

21

object named as

Maria Arsali

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

26

object named as

Avraam Elia

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

3

object named as

Myrtani Pieri

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

5

object named as

Isavella Savva

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Charalambos Patsias

10

object named as

Charalambos Patsias

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

author name string

Panayiota Demosthenous

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Christoforos Stavrou

6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Michael Zavros

7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Kyriakos Ioannou

9

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Alexia Panagides

11

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Costas Potamitis

12

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Kyproula Demetriou

13

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Marios Prikis

14

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Michael Hadjigavriel

15

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Maria Kkolou

16

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Panayiota Loukaidou

17

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Androulla Pastelli

18

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Aristos Michael

19

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Akis Lazarou

20

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Loukas Damianou

22

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Ioanna Goutziamani

23

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Andreas Soloukides

24

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Lakis Yioukas

25

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Polycarpos Polycarpou

28

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

language of work or name

0 references

publication date

16 December 2014

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

9

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

12

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

e115015

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

copyright license

Creative Commons Attribution 4.0 International

16 December 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4267773/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Alport syndrome from bench to bedside: the potential of current treatment beyond RAAS blockade and the horizon of future therapies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Familial haematuria: when to consider genetic testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Evidence for activation of the unfolded protein response in collagen IV nephropathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

ClinVar: public archive of relationships among sequence variation and human phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Molecular genetics of familial hematuric diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

A mathematical model of the unfolded protein stress response reveals the decision mechanism for recovery, adaptation and apoptosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

How benign is hematuria? Using genetics to predict prognosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Measuring ER stress and the unfolded protein response using mammalian tissue culture system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

A method and server for predicting damaging missense mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Mutant-type alpha5(IV) collagen in a mild form of Alport syndrome has residual ability to form a heterotrimer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Endoplasmic reticulum stress as a progression factor for kidney injury

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

The unfolded protein response and its relevance to connective tissue diseases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Basement membranes and human disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Screening for mutations in kidney-related genes using SURVEYOR nuclease for cleavage at heteroduplex mismatches.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Cellular origins of type IV collagen networks in developing glomeruli.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Mutations in FN1 cause glomerulopathy with fibronectin deposits.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Inherited diseases of the glomerular basement membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Familial hematuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Structure and function of basement membranes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Signal integration in the endoplasmic reticulum unfolded protein response

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Collagens at a glance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

ER stress and diseases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

SNPs3D: candidate gene and SNP selection for association studies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Thin basement membrane nephropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

The risks of thin basement membrane nephropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Characterization of assembly of recombinant type IV collagen alpha3, alpha4, and alpha5 chains in transfected cell strains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

A conditionally immortalized human podocyte cell line demonstrating nephrin and podocin expression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Goodpasture antigen: expression of the full-length alpha3(IV) chain of collagen IV and localization of epitopes exclusively to the noncollagenous domain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Formation of recombinant triple-helical [alpha 1(IV)]2 alpha 2(IV) collagen molecules in CHO cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Benign familial hematuria due to mutation of the type IV collagen alpha4 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Amino acid difference formula to help explain protein evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Single base mutation in α5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

7 July 2018

Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0115015

21 January 2018

Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidn

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0115015

21 January 2018

X-linked Alport syndrome in Hellenic families: phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0115015

21 January 2018

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0115015

21 January 2018

The 2014 International Workshop on Alport Syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

26 October 2018

Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4267773

26 October 2018

Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/25514610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sixteen novel mutations identified in COL4A3, COL4A4, and COL4A5 genes in Slovenian families with Alport syndrome and benign familial hematuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/25514610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thin basement membrane nephropathy and coincidental renal biopsy lesions

1 reference

https://pubmed.ncbi.nlm.nih.gov/25514610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The R229Q mutation in NPHS2 may predispose to proteinuria in thin-basement-membrane nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25514610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Persistent familial hematuria in children and the locus for thin basement membrane nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25514610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25514610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NPHS2 screening with SURVEYOR in Hellenic children with steroid-resistant nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25514610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence that NPHS2-R229Q predisposes to proteinuria and renal failure in familial hematuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/25514610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0115015

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

2014PLoSO...9k5015P

0 references

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25514610%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34712797&oldid=1859077815"