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ADCK4 "reenergizes" nephrotic syndrome
scientific article published on 25 November 2013
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3859427
retrieved
15 October 2017
title
ADCK4 "reenergizes" nephrotic syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3859427
retrieved
15 October 2017
author
Laura Malaga-Dieguez
object named as
Laura Malaga-Dieguez
series ordinal
1
0 references
Katalin Susztak
object named as
Katalin Susztak
series ordinal
2
0 references
language of work or name
English
0 references
publication date
25 November 2013
1 reference
stated in
Europe PubMed Central
PMCID
3859427
retrieved
15 October 2017
published in
Journal of Clinical Investigation
1 reference
stated in
Europe PubMed Central
PMCID
3859427
retrieved
15 October 2017
volume
123
1 reference
stated in
Europe PubMed Central
PMCID
3859427
retrieved
15 October 2017
issue
12
1 reference
stated in
Europe PubMed Central
PMCID
3859427
retrieved
15 October 2017
page(s)
4996-4999
1 reference
stated in
Europe PubMed Central
PMCID
3859427
retrieved
15 October 2017
cites work
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
Signaling from the podocyte intercellular junction to the actin cytoskeleton
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
Focal segmental glomerulosclerosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
Role of mTOR in podocyte function and diabetic nephropathy in humans and mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
A systematic approach to mapping recessive disease genes in individuals from outbred populations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
Coenzyme Q10 supplementation rescues renal disease in Pdss2kd/kd mice with mutations in prenyl diphosphate synthase subunit 2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
The spectrum of podocytopathies: a unifying view of glomerular diseases.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
5 June 2018
The Notch pathway in podocytes plays a role in the development of glomerular disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
17 August 2018
Glucose-induced reactive oxygen species cause apoptosis of podocytes and podocyte depletion at the onset of diabetic nephropathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
17 August 2018
Coenzyme Q10 prevents GDP-sensitive mitochondrial uncoupling, glomerular hyperfiltration and proteinuria in kidneys from db/db mice as a model of type 2 diabetes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859427
retrieved
2 December 2018
Ubiquinone (coenzyme Q10) prevents renal mitochondrial dysfunction in an experimental model of type 2 diabetes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24270414
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1172/JCI73168
1 reference
stated in
Europe PubMed Central
PMCID
3859427
retrieved
15 October 2017
PMCID
3859427
1 reference
stated in
Europe PubMed Central
PMCID
3859427
retrieved
15 October 2017
PubMed ID
24270414
1 reference
stated in
Europe PubMed Central
PMCID
3859427
retrieved
15 October 2017
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