(Q30978054)

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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

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Europe PubMed Central

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15 October 2017

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

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Europe PubMed Central

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15 October 2017

type 2 diabetes

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single-nucleotide polymorphism

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based on heuristic

inferred from title

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15 October 2017

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Anders Jorsal

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Torben Hansen

11

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Oluf Borbye Pedersen

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Oluf Pedersen

30

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Jessica N Cooke Bailey

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Jessica N Cooke

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Barry I Freedman

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15 October 2017

Donald W Bowden

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Donald W Bowden

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15 October 2017

Meredith A Bostrom

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Meredith A Bostrom

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15 October 2017

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Kyong Soo Park

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15 October 2017

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Shiro Maeda

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15 October 2017

Tetsuya Babazono

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Tetsuya Babazono

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15 October 2017

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Masa-aki Kobayashi

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15 October 2017

Shin-ichi Araki

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15 October 2017

Masao Toyoda

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15 October 2017

Tomoya Umezono

9

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15 October 2017

Peter Gaede

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15 October 2017

Daniel P K Ng

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Minoru Ikeda

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15 October 2017

Toru Yanagimoto

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Tatsuhiko Tsunoda

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15 October 2017

Hiroyuki Unoki

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Koichi Kawai

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Masahito Imanishi

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15 October 2017

Daisuke Suzuki

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15 October 2017

Hyoung Doo Shin

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15 October 2017

Atsunori Kashiwagi

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15 October 2017

Yasuhiko Iwamoto

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Kohei Kaku

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Ryuzo Kawamori

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Hans-Henrik Parving

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Yusuke Nakamura

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15 October 2017

publication date

12 February 2010

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15 October 2017

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15 October 2017

6

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2

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15 October 2017

e1000842

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Europe PubMed Central

PMC publication ID

15 October 2017

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Creative Commons Attribution 4.0 International

12 February 2010

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April 2022 Public Data File from Crossref

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

1 reference

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14 July 2018

Peroxisome proliferator-activated receptors in diabetic nephropathy

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14 July 2018

Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes

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14 July 2018

Variants in intron 13 of the ELMO1 gene are associated with diabetic nephropathy in African Americans

1 reference

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14 July 2018

Type 2 diabetes: new genes, new understanding

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14 July 2018

Genetic factors in diabetic nephropathy

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14 July 2018

Genome-wide association studies provide new insights into type 2 diabetes aetiology

1 reference

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14 July 2018

Obesity and obesity-initiated metabolic syndrome: mechanistic links to chronic kidney disease

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14 July 2018

Polymorphisms in the 3' UTR in the neurocalcin delta gene affect mRNA stability, and confer susceptibility to diabetic nephropathy

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14 July 2018

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

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14 July 2018

SLC12A3 (solute carrier family 12 member [sodium/chloride] 3) polymorphisms are associated with end-stage renal disease in diabetic nephropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

Glucose and fat metabolism in adipose tissue of acetyl-CoA carboxylase 2 knockout mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

Acetyl-CoA carboxylase 2 mutant mice are protected against obesity and diabetes induced by high-fat/high-carbohydrate diets

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

JSNP: a database of common gene variations in the Japanese population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

Continuous fatty acid oxidation and reduced fat storage in mice lacking acetyl-CoA carboxylase 2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

Human acetyl-CoA carboxylase 2. Molecular cloning, characterization, chromosomal mapping, and evidence for two isoforms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

Familial factors determine the development of diabetic nephropathy in patients with IDDM.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

A comparison of linkage disequilibrium measures for fine-scale mapping

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

Familial clustering of diabetic kidney disease. Evidence for genetic susceptibility to diabetic nephropathy

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820513

14 July 2018

Overview of regular dialysis treatment in Japan as of 31 December 2006.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000842

21 January 2018

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000842

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000842

21 January 2018

Polymorphism of the solute carrier family 12 (sodium/chloride transporters) member 3, SLC12A3, gene at exon 23 (+78G/A: Arg913Gln) is associated with elevation of urinary albumin excretion in Japanese patients with type 2 diabetes: a 10-year longitu

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000842

21 January 2018

Multifactorial intervention and cardiovascular disease in patients with type 2 diabetes

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000842

21 January 2018

SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000842

21 January 2018

Factors associated with frequent remission of microalbuminuria in patients with type 2 diabetes

1 reference

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Reduced GFR and albuminuria in Chinese type 2 diabetes mellitus patients are both independently associated with activation of the TNF-α system

1 reference

https://pubmed.ncbi.nlm.nih.gov/20168990

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based on heuristic

inferred from PubMed ID database lookup

Genetics of diabetic nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/20168990

12 December 2020

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inferred from PubMed ID database lookup

Serum adiponectin predicts all-cause mortality and end stage renal disease in patients with type I diabetes and diabetic nephropathy

1 reference

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1 reference

https://pubmed.ncbi.nlm.nih.gov/20168990

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based on heuristic

inferred from PubMed ID database lookup

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10.1371/JOURNAL.PGEN.1000842

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Europe PubMed Central

PMC publication ID

15 October 2017

release_tjjlbjvn5vexdoqagll52ngwka

1 reference

https://api.fatcat.wiki/v0/release/tjjlbjvn5vexdoqagll52ngwka

24 November 2022

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mapped directly with Wikidata item

PMC publication ID

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Europe PubMed Central

PMC publication ID

15 October 2017

PubMed publication ID

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Europe PubMed Central

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15 October 2017

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