(Q36200142)

English

Familial aggregation of albuminuria and arterial hypertension in an Aboriginal Australian community and the contribution of variants in ACE and TP53.

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Familial aggregation of albuminuria and arterial hypertension in an Aboriginal Australian community and the contribution of variants in ACE and TP53. (English)

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

arterial hypertension

1 reference

based on heuristic

inferred from title

Natalia L Duarte

object named as

Natalia L Duarte

8

0 references

object named as

David L Duffy

1

0 references

10

object named as

Wendy E Hoy

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

author name string

Stephen P McDonald

2

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Beverley Hayhurst

3

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Sianna Panagiotopoulos

4

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Trudy J Smith

5

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Xing L Wang

6

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

David E Wilcken

7

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

John Mathews

9

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

21 November 2016

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

17

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

1

1 reference

Europe PubMed Central

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12 August 2017

183

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

The P72R Polymorphism of p53 Predisposes to Obesity and Metabolic Dysfunction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Targeted deletion of p53 in the proximal tubule prevents ischemic renal injury

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

The role of the glomerular endothelium in albumin handling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Associations of estimated glomerular filtration rate and albuminuria with mortality and renal failure by sex: a meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Combined association of creatinine, albuminuria, and cystatin C with all-cause mortality and cardiovascular and kidney outcomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

p53 is renoprotective after ischemic kidney injury by reducing inflammation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Association of APOL1 variants with mild kidney disease in the first-degree relatives of African American patients with non-diabetic end-stage renal disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Genome-wide association and functional follow-up reveals new loci for kidney function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Codon 72 polymorphism (rs1042522) of TP53 is associated with changes in diastolic blood pressure over time

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Genetic association for renal traits among participants of African ancestry reveals new loci for renal function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

The human Tp53 Arg72Pro polymorphism explains different functional prognosis in stroke.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

CUBN is a gene locus for albuminuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Studies of the association of Arg72Pro of tumor suppressor protein p53 with type 2 diabetes in a combined analysis of 55,521 Europeans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

A genome-wide association study for diabetic nephropathy genes in African Americans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Genetic associations in diabetic nephropathy: a meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Mouse models for the p53 R72P polymorphism mimic human phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Association of estimated glomerular filtration rate and albuminuria with all-cause and cardiovascular mortality in general population cohorts: a collaborative meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

New loci associated with kidney function and chronic kidney disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Genetic loci influencing kidney function and chronic kidney disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

WOMBAT: a tool for mixed model analyses in quantitative genetics by restricted maximum likelihood (REML)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Genetic variation at the ACE gene is associated with persistent microalbuminuria and severe nephropathy in type 1 diabetes: the DCCT/EDIC Genetics Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Albuminuria: marker or target in indigenous populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

The codon 72 polymorphic variants of p53 have markedly different apoptotic potential

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Childhood post-streptococcal glomerulonephritis as a risk factor for chronic renal disease in later life

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Variance components for statistical genetics: applications in medical research to characteristics related to human diseases and health

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Gm3;5,13,14 and type 2 diabetes mellitus: an association in American Indians with genetic admixture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

1 October 2017

Methylenetetrahydrofolate reductase gene polymorphism as a risk factor for diabetic nephropathy in NIDDM patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

2 July 2018

Modelling the Influence of Risk Factors on Familial Aggregation of Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

2 July 2018

Familial aggregation of a disease consequent upon correlation between relatives in a risk factor measured on a continuous scale

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

2 July 2018

Decreasing rates of natural deaths in a remote Australian Aboriginal community, 1996-2010.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

Acquisition of complement factor H is important for pathogenesis of Streptococcus pyogenes infections: evidence from bacterial in vitro survival and human genetic association

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

An updated meta-analysis of methylenetetrahydrofolate reductase gene 677C/T polymorphism with diabetic nephropathy and diabetic retinopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

Glu298Asp and NOS4ab polymorphisms in diabetic nephropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

Low-grade albuminuria and incidence of cardiovascular disease events in nonhypertensive and nondiabetic individuals: the Framingham Heart Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

Genome-wide linkage analysis to urinary microalbuminuria in a community-based sample: the Framingham Heart Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

The natural history of renal disease in Australian Aborigines. Part 2. Albuminuria predicts natural death and renal failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

The natural history of renal disease in Australian Aborigines. Part 1. Changes in albuminuria and glomerular filtration rate over time.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

Glomerular size and glomerulosclerosis in Australian aborigines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5117595

22 September 2018

The multidimensional nature of renal disease: Rates and associations of albuminuria in an Australian Aboriginal community

1 reference

https://api.crossref.org/works/10.1186%2FS12882-016-0396-2

21 January 2018

Post-streptococcal glomerulonephritis is a strong risk factor for chronic kidney disease in later life

1 reference

https://api.crossref.org/works/10.1186%2FS12882-016-0396-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2FS12882-016-0396-2

21 January 2018

Quantifying the excess risk for proteinuria, hypertension and diabetes in Australian Aborigines: comparison of profiles in three remote communities in the Northern Territory with those in the AusDiab study

1 reference

https://api.crossref.org/works/10.1186%2FS12882-016-0396-2

21 January 2018

Low birthweight and renal disease in Australian aborigines

1 reference

https://api.crossref.org/works/10.1186%2FS12882-016-0396-2

21 January 2018

Segregation analysis of urinary albumin excretion in families with type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/27871254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The p53Pro72Arg polymorphism is associated with albuminuria among aboriginal Australians

1 reference

https://pubmed.ncbi.nlm.nih.gov/27871254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritability of GFR and albuminuria in Caucasians with type 2 diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/27871254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Australian Burden of Disease Study: impact and causes of illness and death in Aboriginal and Torres Strait Islander people, 2011.

1 reference

https://pubmed.ncbi.nlm.nih.gov/27871254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation C677T of methylenetetrahydrofolate reductase gene is not associated with coronary artery disease, but possibly with albuminuria, in type 2 diabetic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/27871254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/S12882-016-0396-2

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

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