Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.

Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.

Item
http://www.wikidata.org/entity/Q33840124
The rs1333049 polymorphism on locus 9p21.3 and extreme longevity in Spanish and Japanese cohorts.Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarctionHigher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21.Four pairs of gene-gene interactions associated with increased risk for type 2 diabetes (CDKN2BAS-KCNJ11), obesity (SLC2A9-IGF2BP2, FTO-APOA5), and hypertension (MC4R-IGF2BP2) in Chinese women.Differential associations of depressive symptom dimensions with cardio-vascular disease in the community: results from the Gutenberg health study.Association of Angiotensin Converting Enzyme Insertion-Deletion Polymorphism with Hypertension in Emiratis with Type 2 Diabetes Mellitus and Its Interaction with Obesity Status.The rs10757278 polymorphism of the 9p21.3 locus is associated with premature coronary artery disease in Polish patients.Polymorphisms in ApoB gene are associated with risk of myocardial infarction and serum ApoB levels in a Chinese population.Association Study of rs1333040 and rs1004638 Polymorphisms in the 9p21 Locus with Coronary Artery Disease in Southwest of Iran.Chromosome 9p21 and ABCA1 Genetic Variants and Their Interactions on Coronary Heart Disease and Ischemic Stroke in a Chinese Han PopulationLong noncoding RNA dysregulation in ischemic heart failure.Association between rs10757274 and rs2383206 SNPs as Genetic Risk Factors in Iranian Patients with Coronary Artery Disease.Variant at 9p21 rs1333049 is associated with age of onset of coronary artery disease in a Western Indian population: a case control association study.Familial genetic risk factors in premature cardiovascular disease: a family study.Ameliorating effects of Inonotus obliquus on high fat diet-induced obese rats.Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarction.
P2860

Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.

Item
http://www.wikidata.org/entity/Q33840124
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
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2011年論文
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2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Six sequence variants on chrom ...... ction: a multicenter registry.
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Six sequence variants on chrom ...... ction: a multicenter registry.
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Six sequence variants on chrom ...... ction: a multicenter registry.
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Six sequence variants on chrom ...... ction: a multicenter registry.
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Six sequence variants on chrom ...... ction: a multicenter registry.
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Six sequence variants on chrom ...... ction: a multicenter registry.
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Six sequence variants on chrom ...... ction: a multicenter registry.
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P2093
P2860
P2888
P304
P31
P356
P478
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P5875
P6179
P698
P921
P932