(Q54373732)

28 May 2018

title

Matrix metalloproteinase-9 functional promoter polymorphism 1562C>T increased risk of early-onset coronary artery disease. (English)

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28 May 2018

author

Asad Vaisi-Raygani

2

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28 May 2018

Zohreh Rahimi

7

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28 May 2018

Parvin Pasalar

6

object named as

Parvin Pasalar

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28 May 2018

author name string

Massoud Saedi

1

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28 May 2018

Shahnaz Khaghani

3

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28 May 2018

Ahmad Shariftabrizi

4

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28 May 2018

M Rezaie

5

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28 May 2018

Tayebeh Pourmotabbed

8

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28 May 2018

publication date

11 May 2011

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28 May 2018

Molecular Biology Reports

published in

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28 May 2018

volume

39

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28 May 2018

issue

1

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28 May 2018

page(s)

555-562

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28 May 2018

Serum butyrylcholinesterase activity and phenotype associations with lipid profile in stroke patients

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21 January 2018

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Peripheral blood levels of matrix metalloproteases-2 and -9 are elevated in patients with acute coronary syndromes

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Disruption of the myocardial extracellular matrix leads to cardiac dysfunction

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A polymorphism in the matrix metalloproteinase-9 promoter is associated with increased risk of preterm premature rupture of membranes in African Americans.

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C-reactive protein gene polymorphisms affect plasma CRP and homocysteine concentrations in subjects with and without angiographically confirmed coronary artery disease.

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Genetic variants on apolipoprotein gene cluster influence triglycerides with a risk of coronary artery disease among Indians

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Coronary artery complicated lesion area is related to functional polymorphism of matrix metalloproteinase 9 gene: an autopsy study

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Association between apolipoprotein E polymorphism and coronary artery disease in the Kermanshah population in Iran

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Matrix metalloproteinase-9 is necessary for the regulation of smooth muscle cell replication and migration after arterial injury

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The frequency of factor V Leiden mutation, ACE gene polymorphism, serum ACE activity and response to ACE inhibitor and angiotensin II receptor antagonist drugs in Iranians type II diabetic patients with microalbuminuria

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Association between apolipoprotein ε4 allele, factor V Leiden, and plasma lipid and lipoprotein levels with sickle cell disease in southern Iran

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Plasma lipids and lipoproteins in children and young adults with major β-thalassemia from western Iran: influence of genotype

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Butyrylcholinesterase K variants increase the risk of coronary artery disease in the population of western Iran

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Butyrylcholinesterase K variant and the APOE-ε4 allele work in synergy to increase the risk of coronary artery disease especially in diabetic patients

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10.1007/S11033-011-0770-X

Identifiers

DOI

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28 May 2018

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28 May 2018