Association of Common Variants of APOE, CETP, and the 9p21.3 Chromosomal Region with the Risk of Myocardial Infarction: A Prospective Study
S Semaev, E Shakhtshneider, L Shcherbakova… - International Journal of …, 2023 - mdpi.com
The individual risk of an unfavorable cardiovascular outcome is determined by genetic
factors in addition to lifestyle factors. This study was aimed at analyzing possible …
factors in addition to lifestyle factors. This study was aimed at analyzing possible …
[PDF][PDF] The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease.
Objective: Recent genome-wide association studies have established that polymorphisms
within CDKN2B-AS1 of chr9p21. 3 locus increased susceptibility to coronary artery disease …
within CDKN2B-AS1 of chr9p21. 3 locus increased susceptibility to coronary artery disease …
Association between rs3088440 (G> A) polymorphism at 9p21. 3 locus with the occurrence and severity of coronary artery disease in an Iranian population
M Pourgholi, O Abazari, L Pourgholi… - Molecular Biology …, 2021 - Springer
Background Several genome-wide association studies showed that a series of genetic
variants located at the chromosome 9p21 locus are strongly associated with coronary artery …
variants located at the chromosome 9p21 locus are strongly associated with coronary artery …
Analysis of polymorphism rs1333049 (Located at 9P21. 3) in the white population of Western Siberia and associations with clinical and biochemical markers
E Shakhtshneider, P Orlov, S Semaev, D Ivanoshchuk… - Biomolecules, 2019 - mdpi.com
The 9p21. 3 chromosomal region is a marker of the risk of cardiovascular diseases. The aim
of this study was to analyze single-nucleotide polymorphism rs1333049 (chr9: 22125504) in …
of this study was to analyze single-nucleotide polymorphism rs1333049 (chr9: 22125504) in …
Homozygosity of the TT methylenetetrahydrofolate reductase C677T genotype is an independent long-term predictor of cardiac death in patients with premature …
Abstract Background Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism is
the main genetic modulator of homocysteine. Data suggest a potential association of …
the main genetic modulator of homocysteine. Data suggest a potential association of …
Clinical study of serum procalcitonin level in patients with myocardial infarction complicated by pulmonary infection
S Sun, F Wang, M Yu, J Kang - Experimental and …, 2018 - spandidos-publications.com
This study determined the serum procalcitonin (PCT) levels in patients with myocardial
infarction complicated by pulmonary infection and explore its clinical significance and …
infarction complicated by pulmonary infection and explore its clinical significance and …
The association of methylene tetrahydrofolate reductase (MTHFR) A1298C gene polymorphism, homocysteine, vitamin B12, and folate with coronary artery disease …
Background We pursued to find out the possible association of Methylene tetrahydrofolate
reductase (MTHFR) A1298C gene polymorphism, blood homocysteine, vitamin B12, and …
reductase (MTHFR) A1298C gene polymorphism, blood homocysteine, vitamin B12, and …
Role of neutrophil-derived s100b in acute myocardial infarction patients from the han chinese population
M Cheng, X Su, D Liu, X Tian, C Yan… - Frontiers in …, 2021 - frontiersin.org
Objective: This study aimed to clarify the novel role of homeostatic calmodulin S100B and
determined whether S100B genetic variants affected atherosclerosis progression in acute …
determined whether S100B genetic variants affected atherosclerosis progression in acute …
Ассоциация вариантов генов АРОЕ, СЕТР и хромосомного региона 9Р21. 3 с ишемической болезнью сердца, инфарктом миокарда и острой сердечной …
СЕ Семаев, ЛВ Щербакова, ПС Орлов… - …, 2024 - ateroskleroz.elpub.ru
Аннотация Актуальной задачей для системы здравоохранения служит выявление
слоев населения, наиболее предрасположенных к сердечно-сосудистым …
слоев населения, наиболее предрасположенных к сердечно-сосудистым …
[PDF][PDF] Полиморфные варианты генов PIK3CA, CDKN2B-AS1 и AGTR1 ассоциированы с возрастом дебюта инфаркта миокарда
АР Сидько, ГЖ Осьмак, БВ Титов… - Кардиологический …, 2021 - cardioweb.ru
РЕЗЮМЕ Ранее мы показали возможность возраст-зависимого подхода к оценке риска
развития инфаркта миокарда (ИМ), основанного на анализе носительства аллельных …
развития инфаркта миокарда (ИМ), основанного на анализе носительства аллельных …