(Q30416011)

English

Revising the M235T polymorphism position for the AGT gene and reporting a modifying variant in the Brazilian population with potential cardiac and neural impact

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scholarly article

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Europe PubMed Central

PubMed publication ID

21 June 2017

Revising the M235T polymorphism position for the AGT gene and reporting a modifying variant in the Brazilian population with potential cardiac and neural impact (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

author name string

R R Lemos

1

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

S G de Lima

2

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

J E Gomes da Cunha

3

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

D F Oliveira

4

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

M B Rodrigues de Souza

5

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

C F J Ayres

6

1 reference

Europe PubMed Central

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21 June 2017

M F P M Albuquerque

7

1 reference

Europe PubMed Central

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21 June 2017

J R M Oliveira

8

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Europe PubMed Central

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21 June 2017

publication date

25 April 2012

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Europe PubMed Central

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21 June 2017

Journal of Molecular Neuroscience

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Europe PubMed Central

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21 June 2017

48

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Europe PubMed Central

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21 June 2017

1

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Europe PubMed Central

PubMed publication ID

21 June 2017

253-256

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Europe PubMed Central

PubMed publication ID

21 June 2017

Renin-angiotensin-aldosterone system in brain infarction and vascular death

1 reference

https://api.crossref.org/works/10.1007%2FS12031-012-9768-7

21 January 2018

Major heart disease genes prove elusive.

1 reference

https://api.crossref.org/works/10.1007%2FS12031-012-9768-7

21 January 2018

AGT M235T genotype/anxiety interaction and gender in the HyperGEN study

1 reference

https://api.crossref.org/works/10.1007%2FS12031-012-9768-7

21 January 2018

Left ventricular mass in relation to genetic variation in angiotensin II receptors, renin system genes, and sodium excretion.

1 reference

https://api.crossref.org/works/10.1007%2FS12031-012-9768-7

21 January 2018

Genetic heterogeneity in human disease

1 reference

https://api.crossref.org/works/10.1007%2FS12031-012-9768-7

21 January 2018

Angiotensinogen and angiotensin converting enzyme gene polymorphisms and the risk of bipolar affective disorder in humans

1 reference

https://api.crossref.org/works/10.1007%2FS12031-012-9768-7

21 January 2018

Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations

1 reference

https://api.crossref.org/works/10.1007%2FS12031-012-9768-7

21 January 2018

Novel multi-nucleotide polymorphisms in the human genome characterized by whole genome and exome sequencing

1 reference

https://api.crossref.org/works/10.1007%2FS12031-012-9768-7

21 January 2018

Polymorphisms of the renin-angiotensin system are associated with blood pressure, atherosclerosis and cerebral white matter pathology

1 reference

https://api.crossref.org/works/10.1007%2FS12031-012-9768-7

21 January 2018

Genotype-phenotype analysis of angiotensinogen polymorphisms and essential hypertension: the importance of haplotypes

1 reference

https://api.crossref.org/works/10.1007%2FS12031-012-9768-7

21 January 2018

Renin angiotensin system polymorphisms in patients with metabolic syndrome (MetS)

1 reference

https://pubmed.ncbi.nlm.nih.gov/22531885

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide polymorphism of p73 gene is associated with a reduced risk of lung cancer in a Chinese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/22531885

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensinogen gene polymorphism as a risk factor for ischemic stroke

1 reference

https://pubmed.ncbi.nlm.nih.gov/22531885

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12031-012-9768-7

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

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