(Q36773270)

English

Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy

scientific article published on 17 June 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

left ventricular hypertrophy

1 reference

based on heuristic

inferred from title

genetic variation

1 reference

based on heuristic

inferred from title

object named as

Miriam Revera

3

0 references

Lize van der Merwe

object named as

Lize van der Merwe

1

0 references

author name string

Ruben Cloete

2

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Marshall Heradien

4

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Althea Goosen

5

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Valerie A Corfield

6

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Paul A Brink

7

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Johanna C Moolman-Smook

8

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

publication date

17 June 2008

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

124

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

57-61

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

https://scigraph.springernature.com/pub.10.1007/s00439-008-0524-6

0 references

Heritability of cardiovascular and personality traits in 6,148 Sardinians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

29 September 2017

Genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

29 September 2017

Interpretation of genetic association studies in complex disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

29 September 2017

Modifier genes for hypertrophic cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

29 September 2017

A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

29 September 2017

The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

29 September 2017

Recommendations for quantitation of the left ventricle by two-dimensional echocardiography. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

29 September 2017

Polymorphisms of angiotensin-converting enzyme 2 gene associated with magnitude of left ventricular hypertrophy in male patients with hypertrophic cardiomyopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

5 September 2018

Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

5 September 2018

[Association of angiotensin I converting enzyme 2 gene polymorphism with essential hypertension in Chinese].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

5 September 2018

No association of angiotensin-converting enzyme 2 gene (ACE2) polymorphisms with essential hypertension.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

5 September 2018

Measured haplotype analysis of the aldosterone synthase gene and heart size.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

5 September 2018

Transesophageal Echocardiography

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0524-6

21 January 2018

Association of angiotensin-converting enzyme 2 (ACE2) gene polymorphisms with parameters of left ventricular hypertrophy in men

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2469277

4 December 2018

Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass

1 reference

https://pubmed.ncbi.nlm.nih.gov/18560893

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association study of ACE2 (angiotensin I-converting enzyme 2) gene polymorphisms with coronary heart disease and myocardial infarction in a Chinese Han population

1 reference

https://pubmed.ncbi.nlm.nih.gov/18560893

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin

1 reference

https://pubmed.ncbi.nlm.nih.gov/18560893

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-008-0524-6

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

ResearchGate publication ID

0 references

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