(Q34475363)

2 August 2017

title

A systems view of genetics in chronic kidney disease (English)

1 reference

chronic renal insufficiency

2 August 2017

main subject

1 reference

4

Matthias Kretzler

1 reference

2 August 2017

Benjamin J Keller

1

1 reference

2 August 2017

Sebastian Martini

series ordinal

2

1 reference

2 August 2017

John R Sedor

series ordinal

3

1 reference

2 August 2017

language of work or name

English

0 references

publication date

19 October 2011

1 reference

2 August 2017

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2 August 2017

volume

81

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2 August 2017

issue

1

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2 August 2017

page(s)

14-21

1 reference

https://scigraph.springernature.com/pub.10.1038/ki.2011.359

2 August 2017

exact match

0 references

cites work

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6 July 2018

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Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases

6 July 2018

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6 July 2018

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Association of trypanolytic ApoL1 variants with kidney disease in African Americans

6 July 2018

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Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

6 July 2018

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Systematic analysis of a novel human renal glomerulus-enriched gene expression dataset

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

6 July 2018

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Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice

6 July 2018

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Systems genetics analysis of gene-by-environment interactions in human cells

6 July 2018

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A single nucleotide polymorphism within the acetyl-coenzyme A carboxylase beta gene is associated with proteinuria in patients with type 2 diabetes

6 July 2018

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6 July 2018

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Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX, SOX4, and IRX3

6 July 2018

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Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging

6 July 2018

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Targeting bone morphogenetic protein signaling on renal and vascular diseases.

6 July 2018

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6 July 2018

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A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia

6 July 2018

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Confirmation of genetic associations at ELMO1 in the GoKinD collection supports its role as a susceptibility gene in diabetic nephropathy

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

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6 July 2018

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Human and murine kidneys show gender- and species-specific gene expression differences in response to injury

6 July 2018

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6 July 2018

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6 July 2018

1 reference

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6 July 2018

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Hypoxia response and VEGF-A expression in human proximal tubular epithelial cells in stable and progressive renal disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Genetical genomics: spotlight on QTL hotspots

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

High-resolution mapping of expression-QTLs yields insight into human gene regulation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Integrating large-scale functional genomic data to dissect the complexity of yeast regulatory networks

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Mapping the genetic architecture of gene expression in human liver

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Gene regulation in the third dimension

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Variations in DNA elucidate molecular networks that cause disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Genetics of gene expression and its effect on disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Linking metabolic QTLs with network and cis-eQTLs controlling biosynthetic pathways

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Gene expression profiling analysis in nephrology: towards molecular definition of renal disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Comparative promoter analysis allows de novo identification of specialized cell junction-associated proteins

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

A familial risk of chronic renal failure among blacks on dialysis?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Apolipoprotein E polymorphism and the progression of diabetic nephropathy in type 2 diabetes.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Toll-like receptor 1 gene polymorphisms in childhood IgA nephropathy: a case-control study in the Korean population.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Effect of IL-6 C-572G polymorphism on idiopathic membranous nephropathy risk in a Han Chinese population

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Channelopathies: Decoding Disease Pathogenesis

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Muscle dysfunction caused by a KATP channel mutation in neonatal diabetes is neuronal in origin

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Genomic regulatory blocks encompass multiple neighboring genes and maintain conserved synteny in vertebrates

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

System-wide molecular evidence for phenotypic buffering in Arabidopsis

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4224965

Quantitative gene expression analysis in renal biopsies: a novel protocol for a high-throughput multicenter application

9 December 2018

1 reference

12 December 2020

Interaction of eNOS polymorphism with MTHFR variants increase the risk of diabetic nephropathy and its progression in type 2 diabetes mellitus patients

1 reference

12 December 2020

Angiotensin-I converting enzyme insertion/deletion polymorphism and its association with diabetic nephropathy: a meta-analysis of studies reported between 1994 and 2004 and comprising 14,727 subjects

1 reference

12 December 2020

Modular activation of nuclear factor-kappaB transcriptional programs in human diabetic nephropathy

1 reference

12 December 2020

Interstitial vascular rarefaction and reduced VEGF-A expression in human diabetic nephropathy.

1 reference

12 December 2020

Sequence variants in the PLEKHH2 region are associated with diabetic nephropathy in the GoKinD study population

1 reference

12 December 2020

Association of IRF5 gene polymorphisms and lupus nephritis in a Chinese population

1 reference

12 December 2020

Single nucleotide polymorphisms in the phospholipase A2 receptor gene are associated with genetic susceptibility to idiopathic membranous nephropathy

1 reference

12 December 2020

Identifiers

DOI

10.1038/KI.2011.359

1 reference

Dimensions Publication ID

2 August 2017

0 references

1 reference

2 August 2017

1 reference