(Q39982494)

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Microarray analysis of multiple candidate genes and associated plasma proteins for nephropathy secondary to type 2 diabetes among Chinese individuals

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scholarly article

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Europe PubMed Central

PubMed publication ID

16 September 2017

Microarray analysis of multiple candidate genes and associated plasma proteins for nephropathy secondary to type 2 diabetes among Chinese individuals (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

type 2 diabetes

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author name string

S C Lim

1

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Europe PubMed Central

PubMed publication ID

16 September 2017

J J Liu

2

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16 September 2017

H Q Low

3

1 reference

Europe PubMed Central

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16 September 2017

N G Morgenthaler

4

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Europe PubMed Central

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16 September 2017

Y Li

5

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Europe PubMed Central

PubMed publication ID

16 September 2017

L Y Yeoh

6

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Europe PubMed Central

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16 September 2017

Y S Wu

7

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Europe PubMed Central

PubMed publication ID

16 September 2017

S K Goh

8

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Europe PubMed Central

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16 September 2017

C Y Chionh

9

1 reference

Europe PubMed Central

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16 September 2017

S H Tan

10

1 reference

Europe PubMed Central

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16 September 2017

Y C Kon

11

1 reference

Europe PubMed Central

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16 September 2017

P C Soon

12

1 reference

Europe PubMed Central

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16 September 2017

Y M Bee

13

1 reference

Europe PubMed Central

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16 September 2017

T Subramaniam

14

1 reference

Europe PubMed Central

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16 September 2017

C F Sum

15

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Europe PubMed Central

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16 September 2017

K S Chia

16

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Europe PubMed Central

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16 September 2017

publication date

5 May 2009

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Europe PubMed Central

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16 September 2017

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Europe PubMed Central

PubMed publication ID

16 September 2017

52

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16 September 2017

7

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16 September 2017

1343-1351

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Europe PubMed Central

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16 September 2017

https://scigraph.springernature.com/pub.10.1007/s00125-009-1368-x

0 references

Paradoxes of nitric oxide in the diabetic kidney

1 reference

https://api.crossref.org/works/10.1007%2FS00125-009-1368-X

21 January 2018

Systematic analysis of sequence variability of the endothelin-1 gene: a prerequisite for association studies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of diabetes and its complications

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of neuronal nitric oxide synthase (NOS1) in the pathogenesis of renal hemodynamic changes in diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of progressive renal failure in diabetic kidney disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of the endothelin-1 gene locus for renal impairment in the general nondiabetic population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heredity of endothelin secretion: human twin studies reveal the influence of polymorphism at the chromogranin A locus, a novel determinant of endothelial function

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variations in the gene encoding ELMO1 are associated with susceptibility to diabetic nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

From hyperglycemia to diabetic kidney disease: the role of metabolic, hemodynamic, intracellular factors and growth factors/cytokines

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Problems of reporting genetic associations with complex outcomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased oxidative stress in the streptozotocin-induced diabetic apoE-deficient mouse: changes in expression of NADPH oxidase subunits and eNOS

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ROS generation by nonphagocytic NADPH oxidase: potential relevance in diabetic nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human non-synonymous SNPs: server and survey

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A haplotype map of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common and rare variants in multifactorial susceptibility to common diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variants in the plasmacytoma variant translocation gene (PVT1) are associated with end-stage renal disease attributed to type 1 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic basis of complex traits: rare variants or "common gene, common disease"?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation in the endothelin system: do polymorphisms affect the therapeutic strategies?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic studies of diabetes following the advent of the genome-wide association study: where do we go from here?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional significance of a hereditary adenine insertion variant in the 5'-UTR of the endothelin-1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variability of the ET-1 and the ETA receptor genes in essential hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cu/Zn superoxide dismutase plasma levels as a new useful clinical biomarker of oxidative stress in patients with end-stage renal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunoluminometric assay for measurement of the C-terminal endothelin-1 precursor fragment in human plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of an insertion variant in the 5'UTR of the endothelin-1 gene on orthostatic intolerance.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural organization of the human neuronal nitric oxide synthase gene (NOS1).

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relative impact of nucleotide and copy number variation on gene expression phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimating coverage and power for genetic association studies using near-complete variation data

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic risk factors for diabetic nephropathy on chromosomes 6p and 7q identified by the set-association approach.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship between common functional polymorphisms of the p22phox gene (-930A > G and +242C > T) and nephropathy as a result of Type 2 diabetes in a Chinese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diabetes mellitus increases endothelin-1 gene transcription in rat kidney

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early diabetes as a model for testing the regulation of juxtaglomerular NOS I.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel sources of reactive oxygen species in the human body

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide search for linkage to renal function phenotypes in West Africans with type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association mapping via regularized regression analysis of single-nucleotide-polymorphism haplotypes in variable-sized sliding windows

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amino-terminal pro-B-type natriuretic peptide testing for inpatient monitoring and treatment guidance of acute destabilized heart failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population structure, differential bias and genomic control in a large-scale, case-control association study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of endothelin in chronic renal failure--developments in renal involvement

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessment of 115 candidate genes for diabetic nephropathy by transmission/disequilibrium test

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Endothelins: vasoactive modulators of renal function in health and disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of nitric oxide and endothelin in end-stage renal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mendelian randomization: prospects, potentials, and limitations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Superoxide dismutase multigene family: a comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The renal hemodynamic basis of diabetic nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis and classification of diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/19415232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00125-009-1368-X

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 September 2017

ResearchGate publication ID

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