The population genetics of chronic kidney disease: insights from the MYH9-APOL1 locus (Q34182007)

31 July 2017

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title

The population genetics of chronic kidney disease: insights from the MYH9-APOL1 locus (English)

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chronic renal insufficiency

31 July 2017

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4

Walter G Wasser

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31 July 2017

5

Karl Skorecki

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31 July 2017

2

Shay Tzur

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31 July 2017

3

Doron M Behar

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31 July 2017

1

Saharon Rosset

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PubMed ID

21537348

31 July 2017

language of work or name

English

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publication date

3 May 2011

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Nature Reviews Nephrology

31 July 2017

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31 July 2017

7

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31 July 2017

313-326

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6

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https://scigraph.springernature.com/pub.10.1038/nrneph.2011.52

31 July 2017

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cites work

Hereditary proteinuria syndromes and mechanisms of proteinuria

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis--a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

21 January 2018

Genetic kidney diseases

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

2008 Homer W. Smith Award: insights into the pathogenesis of polycystic kidney disease from gene discovery

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Hereditary renal tubular disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Multigene kinase network, kidney transport, and salt in essential hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Functional characterization of two naturally occurring mutations in the human sodium-phosphate cotransporter type IIa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

NPT2a gene variation in calcium nephrolithiasis with renal phosphate leak.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Common genetic variants associate with serum phosphorus concentration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

New loci associated with kidney function and chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Salt handling in the distal nephron: lessons learned from inherited human disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A genome-wide association study of hypertension and blood pressure in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genetic variations in the sodium balance-regulating genes ENaC, NEDD4L, NDFIP2 and USP2 influence blood pressure and hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide association study of blood pressure and hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Uncovering the roles of rare variants in common disease through whole-genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Multiple loci associated with indices of renal function and chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Susceptibility genes in common complex kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide association studies in nephrology research

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genetic epidemiology of chronic kidney disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

CKD in MYH9-related disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The spectrum of MYH9-associated nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The genome-wide structure of the Jewish people

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Reconstructing Indian population history

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide scans for footprints of natural selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A composite of multiple signals distinguishes causal variants in regions of positive selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide detection and characterization of positive selection in human populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A map of human genome variation from population-scale sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genomic medicine--an updated primer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genetic variation, classification and 'race'

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Common genetic variation and human traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Haplotype trees and modern human origins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Haplotype blocks and linkage disequilibrium in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Definition and clinical importance of haplotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Allelic association: linkage disequilibrium structure and gene mapping.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Common genetic variation and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genetic mapping in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

On the allelic spectrum of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide association studies: theoretical and practical concerns

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Common and rare variants in multifactorial susceptibility to common diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Rare variants create synthetic genome-wide associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Interpretation of association signals and identification of causal variants from genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genomewide association studies and assessment of the risk of disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Beyond genome-wide association studies: genetic heterogeneity and individual predisposition to cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

New approaches to population stratification in genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Quality control for genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Methods for high-density admixture mapping of disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Design and analysis of admixture mapping studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Admixture mapping of end stage kidney disease genetic susceptibility using estimated mutual information ancestry informative markers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The familial risk of end-stage renal disease in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Familial clustering of chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

To have and have not: Health and health care disparities in chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Chronic kidney disease incidence, and progression to end-stage renal disease, in HIV-infected individuals: a tale of two races

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Is there a genetic basis for health disparities in human immunodeficiency virus disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide patterns of population structure and admixture in West Africans and African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Charting the ancestry of African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The genetic structure and history of Africans and African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Panel construction for mapping in admixed populations via expected mutual information.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Single, Rapid Coastal Settlement of Asia Revealed by Analysis of Complete Mitochondrial Genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Accounting for ancestry: population substructure and genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Estimation of individual admixture: analytical and study design considerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A genomewide admixture map for Latino populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The African diaspora: mitochondrial DNA and the Atlantic slave trade

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Glomerular pathology in autosomal dominant MYH9 spectrum disorders: what are the clues telling us about disease mechanism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide linkage analysis of serum creatinine in three isolated European populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A comprehensive computational characterization of conserved mammalian intronic sequences reveals conserved motifs associated with constitutive and alternative splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Discovery and analysis of evolutionarily conserved intronic splicing regulatory elements

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide association studies: contribution of genomics to understanding blood pressure and essential hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Chronic kidney disease in HIV infection: an urban epidemic

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Racial differences in end-stage renal disease rates in HIV infection versus diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

MYH9 genetic variants associated with glomerular disease: what is the role for genetic testing?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Absence of HIV-associated nephropathy in Ethiopians

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The function of apolipoproteins L.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Apolipoprotein L-I is the trypanosome lytic factor of human serum

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Activity of trypanosome lytic factor: a novel component of innate immunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Human innate immunity against African trypanosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Prophylactic antiparasitic transgenesis for human parasitic disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Human African trypanosomiasis

21 January 2018

2 references

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

21 January 2018

12 December 2020

C-terminal mutants of apolipoprotein L-I efficiently kill both Trypanosoma brucei brucei and Trypanosoma brucei rhodesiense

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Mechanism of Trypanosoma brucei gambiense (group 1) resistance to human trypanosome lytic factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Worldwide distribution of the MYH9 kidney disease susceptibility alleles and haplotypes: evidence of historical selection in Africa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Apolipoprotein L1, a novel Bcl-2 homology domain 3-only lipid-binding protein, induces autophagic cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The apolipoprotein L gene cluster has emerged recently in evolution and is expressed in human vascular tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Autophagy influences glomerular disease susceptibility and maintains podocyte homeostasis in aging mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A study of renal outcomes in African American living kidney donors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Racial variation in medical outcomes among living kidney donors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Living kidney donors requiring transplantation: focus on African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Posttransplant recurrence of primary glomerulonephritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Shattuck Lecture. The hypertension paradox--more uncontrolled disease despite improved therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Intensive blood-pressure control in hypertensive chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

BIOLOGY, MOLECULAR AND ORGANISMIC

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Clinical documentation of end-stage renal disease due to hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A controlled, prospective study of the effects of atorvastatin on proteinuria and progression of kidney disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A proposed taxonomy for the podocytopathies: a reassessment of the primary nephrotic diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

HIV-associated nephropathy: clinical presentation, pathology, and epidemiology in the era of antiretroviral therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

High prevalence of sickle cell trait in African Americans with ESRD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The non-muscle Myosin heavy chain 9 gene (MYH9) is not associated with lupus nephritis in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A second generation human haplotype map of over 3.1 million SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

The International HapMap Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

A haplotype map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Ascertainment bias in studies of human genome-wide polymorphism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Linkage disequilibrium: what history has to tell us.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Patterns of linkage disequilibrium in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Individual genomes on the horizon

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Genome-wide SNP genotyping study using pooled DNA to identify candidate markers mediating susceptibility to end-stage renal disease attributed to Type 1 diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Socioeconomic status and the incidence of ESRD

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Is the prevalence of HIV-associated nephropathy decreasing?

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Apolipoproteins and lipoprotein receptors in glomeruli in human kidney diseases

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

31 March 2020

The beauty of admixture

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Pathogenesis and therapy of focal segmental glomerulosclerosis: an update

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Hypothesis: Dent disease is an underrecognized cause of focal glomerulosclerosis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Pathology of HIV-associated nephropathy: a detailed morphologic and comparative study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2011.52

Only the serum-resistant bloodstream forms of Trypanosoma brucei rhodesiense express the serum resistance associated (SRA) protein.

31 March 2020

1 reference

12 December 2020

Unravelling the genetic basis of renal diseases; from single gene to multifactorial disorders

1 reference

12 December 2020

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

1 reference

12 December 2020

Apolipoproteins prevent glomerular albumin permeability induced in vitro by serum from patients with focal segmental glomerulosclerosis

1 reference

12 December 2020

Linkage disequilibrium as a gene-mapping tool.

1 reference

12 December 2020

Risk factors for the development of chronic kidney disease with HIV/AIDS.

1 reference

12 December 2020

1 reference

12 December 2020

Recurrent focal segmental glomerulosclerosis in the renal allograft: single center experience in the era of modern immunosuppression

1 reference

12 December 2020

Identifiers

DOI

10.1038/NRNEPH.2011.52

1 reference

31 July 2017

1 reference

PubMed ID

21537348