Genetic variation at the ACE gene is associated with persistent microalbuminuria and severe nephropathy in type 1 diabetes: the DCCT/EDIC Genetics Study (Q35107546)

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

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scholarly article

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Europe PubMed Central

PubMed publication ID

6 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

type-1 diabetes

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1 reference

based on heuristic

inferred from title

genetic variation

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based on heuristic

inferred from title

Andrew D. Paterson

object named as

Andrew D Paterson

2

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Stephen W. Scherer

6

object named as

Stephen W Scherer

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Europe PubMed Central

PubMed publication ID

6 August 2017

7

object named as

Bernard Zinman

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Europe PubMed Central

PubMed publication ID

6 August 2017

author name string

Andrew P Boright

1

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Europe PubMed Central

PubMed publication ID

6 August 2017

Lucia Mirea

3

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Europe PubMed Central

PubMed publication ID

6 August 2017

Shelley B Bull

4

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Alireza Mowjoodi

5

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Europe PubMed Central

PubMed publication ID

6 August 2017

DCCT/EDIC Research Group

8

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Europe PubMed Central

PubMed publication ID

6 August 2017

language of work or name

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publication date

1 April 2005

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Europe PubMed Central

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6 August 2017

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Europe PubMed Central

PubMed publication ID

6 August 2017

54

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Europe PubMed Central

PubMed publication ID

6 August 2017

4

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Europe PubMed Central

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6 August 2017

1238-1244

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Europe PubMed Central

PubMed publication ID

6 August 2017

Declining incidence of severe retinopathy and persisting decrease of nephropathy in an unselected population of Type 1 diabetes-the Linköping Diabetes Complications Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

9 July 2018

Genetically increased angiotensin I-converting enzyme level and renal complications in the diabetic mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

9 July 2018

Contribution of genetic polymorphism in the renin-angiotensin system to the development of renal complications in insulin-dependent diabetes: Genetique de la Nephropathie Diabetique (GENEDIAB) study group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

9 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=1621110

9 July 2018

The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. The Diabetes Control and Complications Trial Research Group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

9 July 2018

The changing natural history of nephropathy in type I diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

9 July 2018

Familial resemblance of plasma angiotensin-converting enzyme level: the Nancy Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

9 July 2018

Familial clustering of diabetic kidney disease. Evidence for genetic 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=1621110

9 July 2018

The angiotensin converting enzyme in the kidney.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

9 July 2018

An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

9 July 2018

Is diabetic nephropathy an inherited complication?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

9 July 2018

Decreasing incidence of severe diabetic microangiopathy in type 1 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

27 September 2018

Sequence variation in the human angiotensin converting enzyme

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

27 September 2018

Diabetic nephropathy in type 1 (insulin-dependent) diabetes: An epidemiological study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1621110

27 September 2018

[Polymorphism of the insertion/deletion type in the angiotensin-converting enzyme gene in normal subjects and among patients with vascular complications]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15793268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15793268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15793268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta analysis. Diabetic nephropathy and the insertion/deletion polymorphism of the angiotensin-converting enzyme gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/15793268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/15793268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of glomerular filtration rate by renin-angiotensin system

1 reference

https://pubmed.ncbi.nlm.nih.gov/15793268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Diabetes Control and Complications Trial (DCCT). Design and methodologic considerations for the feasibility phase. The DCCT Research Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/15793268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationships between angiotensin I converting enzyme gene polymorphism, plasma levels, and diabetic retinal and renal complications

1 reference

https://pubmed.ncbi.nlm.nih.gov/15793268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensin I-converting enzyme (ACE): estimation of DNA haplotypes in unrelated individuals using denaturing gradient gel blots

1 reference

https://pubmed.ncbi.nlm.nih.gov/15793268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clustering of long-term complications in families with diabetes in the diabetes control and complications trial. The Diabetes Control and Complications Trial Research Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/15793268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.2337/DIABETES.54.4.1238

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

ResearchGate publication ID

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