(Q37118487)

18 August 2017

1 reference

title

Primer: strategies for identifying genes involved in renal disease (English)

1 reference

18 August 2017

Ariela Benigni

2

0 references

Giuseppe Remuzzi

object named as

Giuseppe Remuzzi

series ordinal

3

0 references

author name string

Martin H de Borst

series ordinal

1

1 reference

18 August 2017

publication date

25 March 2008

1 reference

Nature Clinical Practice Nephrology

18 August 2017

published in

1 reference

18 August 2017

volume

4

1 reference

18 August 2017

issue

5

1 reference

18 August 2017

page(s)

265-276

1 reference

Chronic kidney disease: the global challenge

18 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

Congenic substitution mapping excludes Sa as a candidate gene locus for a blood pressure quantitative trait locus on rat chromosome 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

Local hypomethylation in atherosclerosis found in rabbit ec-sod gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

Podocyte-associated molecules in puromycin aminonucleoside nephrosis of the rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

Kidney failure rates end 20-year climb

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Mechanisms of progression and regression of renal lesions of chronic nephropathies and diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Molecular pathomechanisms of membranous nephropathy: from Heymann nephritis to alloimmunization

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Prognostic factors in idiopathic membranous nephropathy

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Clinical and morphological prognostic factors in membranous nephropathy: significance of focal segmental glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Meta-analysis of association of insertion/deletion polymorphism of angiotensin I-converting enzyme gene with diabetic nephropathy and retinopathy

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

The deletion/insertion polymorphism of the angiotensin converting enzyme gene and cardiovascular-renal risk

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Role of the deletion of polymorphism of the angiotensin converting enzyme gene in the progression and therapeutic responsiveness of IgA nephropathy

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Perspectives and limitations of microarray-based gene expression profiling of thyroid tumors.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Quantitative monitoring of gene expression patterns with a complementary DNA microarray

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Large-scale identification of genes implicated in kidney glomerulus development and function

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Global gene expression analysis reveals a role for the alpha 1 integrin in renal pathogenesis.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Significance analysis of time course microarray experiments

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Evaluation of gene expression measurements from commercial microarray platforms

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Application of genome-wide expression analysis to human health and disease

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Evaluation of DNA microarray results with quantitative gene expression platforms

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Experimental comparison and cross-validation of the Affymetrix and Illumina gene expression analysis platforms

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

A sequence-oriented comparison of gene expression measurements across different hybridization-based technologies

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Large scale real-time PCR validation on gene expression measurements from two commercial long-oligonucleotide microarrays

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Gene expression in the normal adult human kidney assessed by complementary DNA microarray

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

A panoramic view of gene expression in the human kidney

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Absolute protein expression profiling estimates the relative contributions of transcriptional and translational regulation.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Profiling of the renal kinome: a novel tool to identify protein kinases involved in angiotensin II-dependent hypertensive renal damage

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Transcription factor profiling in individual hematopoietic progenitors by digital RT-PCR

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

DNA methylation profiling of human chromosomes 6, 20 and 22

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genome-wide high-resolution mapping and functional analysis of DNA methylation in arabidopsis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Combined proteome and metabolite-profiling analyses reveal surprising insights into yeast sulfur metabolism

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Analysis of shotgun proteomics and RNA profiling data from Arabidopsis thaliana chloroplasts.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

A comprehensive survey of the Plasmodium life cycle by genomic, transcriptomic, and proteomic analyses

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Identification of coexpressed gene clusters in a comparative analysis of transcriptome and proteome in mouse tissues.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Identification of 14-3-3sigma mutation causing cutaneous abnormality in repeated-epilation mutant mouse

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genetic dissection of complex traits

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

A common variant on chromosome 9p21 affects the risk of myocardial infarction

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Multiple regions within 8q24 independently affect risk for prostate cancer

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

A genome-wide association study identifies novel risk loci for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

The future of genetic studies of complex human diseases

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genome sequence of the Brown Norway rat yields insights into mammalian evolution

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Finding genes that underlie complex traits

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Strategies for mapping and cloning quantitative trait genes in rodents

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

QTL fine mapping by measuring and testing for Hardy-Weinberg and linkage disequilibrium at a series of linked marker loci in extreme samples of populations

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Experimental strategies for the genetic dissection of complex traits in animal models

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genetic dissection of complex traits with chromosome substitution strains of mice.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Dissection of a genetic locus influencing renal function in the rat and its concordance with kidney disease loci on human chromosome 1q21

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

The genetic dissection of essential hypertension

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Meta-analysis of genome-wide linkage studies of systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Gene for susceptibility to diabetic nephropathy in type 2 diabetes maps to 18q22.3-23

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Linkage analysis of candidate loci for end-stage renal disease due to diabetic nephropathy

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

A genome-wide linkage scan for genes controlling variation in urinary albumin excretion in type II diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genome-Wide Linkage Scan of a Large Family with IgA Nephropathy Localizes a Novel Susceptibility Locus to Chromosome 2q36

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Pathophysiology of Progressive Nephropathies

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Carnosine as a protective factor in diabetic nephropathy: association with a leucine repeat of the carnosinase gene CNDP1.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

L-carnosine, a substrate of carnosinase-1, influences glucose metabolism.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Induction of TRPC6 channel in acquired forms of proteinuric kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Expression of podocyte-associated molecules in acquired human kidney diseases

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Permselective dysfunction of podocyte-podocyte contact upon angiotensin II unravels the molecular target for renoprotective intervention

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

The Connectivity Map: using gene-expression signatures to connect small molecules, genes, and disease

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

The Collaborative Cross, a community resource for the genetic analysis of complex traits

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

The diploid genome sequence of an individual human

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Genome-wide analysis of Arabidopsis thaliana DNA methylation uncovers an interdependence between methylation and transcription.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Beyond the sequence: cellular organization of genome function

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

X-inactivation profile reveals extensive variability in X-linked gene expression in females

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Angiotensin-converting enzyme 2 is an essential regulator of heart function

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Loss of angiotensin-converting enzyme-2 leads to the late development of angiotensin II-dependent glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Age- and gender-related difference of ACE2 expression in rat lung

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Impact of inflammation on epigenetic DNA methylation - a novel risk factor for cardiovascular disease?

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Comprehensive analysis of CpG islands in human chromosomes 21 and 22

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Assessment of gene promoter hypermethylation for detection of cervical neoplasia.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Parallel SUMOylation-dependent pathways mediate gene- and signal-specific transrepression by LXRs and PPARgamma

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

E4F1 is an atypical ubiquitin ligase that modulates p53 effector functions independently of degradation.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Mapping DNA interaction sites of chromosomal proteins using immunoprecipitation and polymerase chain reaction.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

The epigenomics of cancer

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

The fundamental role of epigenetic events in cancer

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Methylation of the estrogen receptor gene is associated with aging and atherosclerosis in the cardiovascular system

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Methylation of the estrogen receptor-alpha gene promoter is selectively increased in proliferating human aortic smooth muscle cells.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Inhibition of histone deacetylase activity suppresses epithelial-to-mesenchymal transition induced by TGF-beta1 in human renal epithelial cells

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

The Bradykinin B2 receptor gene is a target of angiotensin II type 1 receptor signaling

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEPH0785

7 January 2021

Identifiers

DOI

10.1038/NCPNEPH0785

1 reference

18 August 2017

1 reference