Pages that link to "Q36430809"
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The following pages link to An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction (Q36430809):
Displaying 44 items.
- Sequencing and analysis of a South Asian-Indian personal genome (Q21266697) (← links)
- Apolipoprotein E receptors in the nervous system (Q24607165) (← links)
- Identification of association of common AGGF1 variants with susceptibility for Klippel-Trenaunay syndrome using the structure association program (Q24645040) (← links)
- Genetic and functional association of FAM5C with myocardial infarction (Q33330164) (← links)
- Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study (Q33445395) (← links)
- Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease (Q33906092) (← links)
- Apolipoprotein E receptor-2 deficiency enhances macrophage susceptibility to lipid accumulation and cell death to augment atherosclerotic plaque progression and necrosis (Q34016939) (← links)
- A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene. (Q34076234) (← links)
- Genetic variants of ApoE and ApoER2 differentially modulate endothelial function (Q34218155) (← links)
- A genome-wide linkage scan identifies multiple quantitative trait loci for HDL-cholesterol levels in families with premature CAD and MI. (Q34559909) (← links)
- Genome-wide linkage scan identifies two novel genetic loci for coronary artery disease: in GeneQuest families (Q34654020) (← links)
- Genome-wide association studies in atherosclerosis (Q34902005) (← links)
- Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population (Q35046461) (← links)
- Platelet CD36 surface expression levels affect functional responses to oxidized LDL and are associated with inheritance of specific genetic polymorphisms (Q35067424) (← links)
- CANDID: a flexible method for prioritizing candidate genes for complex human traits. (Q35571604) (← links)
- Suppression of cell division-associated genes by Helicobacter pylori attenuates proliferation of RAW264.7 monocytic macrophage cells (Q35745709) (← links)
- A Subregion of Reelin Suppresses Lipoprotein-Induced Cholesterol Accumulation in Macrophages (Q35758654) (← links)
- Up-regulation of ATP binding cassette transporter A1 expression by very low density lipoprotein receptor and apolipoprotein E receptor 2. (Q35763151) (← links)
- Apolipoprotein E receptor 2 is involved in the thrombotic complications in a murine model of the antiphospholipid syndrome (Q35874202) (← links)
- Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US population (Q36445247) (← links)
- Identification of a novel locus for triglyceride on chromosome 1p31-32 in families with premature CAD and MI (Q36558312) (← links)
- Molecular genetics of myocardial infarction (Q36843011) (← links)
- Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest). (Q37081240) (← links)
- Deficiency of LRP8 in mice is associated with altered platelet function and prolonged time for in vivo thrombosis (Q37141835) (← links)
- Pathogenic role of antiphospholipid antibodies (Q37168017) (← links)
- Molecular signatures of cardiovascular disease risk: potential for test development and clinical application (Q37273667) (← links)
- Platelets and the antiphospholipid syndrome (Q37283013) (← links)
- Novel roles of GATA1 in regulation of angiogenic factor AGGF1 and endothelial cell function (Q37358087) (← links)
- Integrative mutation, haplotype and G × G interaction evidence connects ABGL4, LRP8 and PCSK9 genes to cardiometabolic risk (Q37419254) (← links)
- Athsq1 is an atherosclerosis modifier locus with dramatic effects on lesion area and prominent accumulation of versican (Q37445003) (← links)
- Family-based and population-based association studies validate PTPRD as a risk factor for restless legs syndrome (Q37492251) (← links)
- The role of LRP8 (ApoER2') in the pathophysiology of the antiphospholipid syndrome (Q37721602) (← links)
- The role of maternal-fetal cholesterol transport in early fetal life: current insights. (Q38059934) (← links)
- New Insights in the Pathophysiology of Antiphospholipid Syndrome. (Q39106759) (← links)
- Multi-allelic haplotype association identifies novel information different from single-SNP analysis: a new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI. (Q41941614) (← links)
- The cloning, characterization, and expression profiling of the LRP8 gene in duck (Anas platyrhynchos). (Q42680183) (← links)
- Protein C supports platelet binding and activation under flow: role of glycoprotein Ib and apolipoprotein E receptor 2. (Q47698131) (← links)
- Significant genetic association of a functional TFPI variant with circulating fibrinogen levels and coronary artery disease (Q47999144) (← links)
- Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population. (Q50920089) (← links)
- Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction (Q56458636) (← links)
- Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population (Q83543008) (← links)
- Identification of rare variants in cardiac sodium channel β4-subunit gene SCN4B associated with ventricular tachycardia (Q90291333) (← links)
- Analysis of causal effect of APOA5 variants on premature coronary artery disease (Q90336572) (← links)
- Phenotypic severity in a family with MEND syndrome is directly associated with the accumulation of potentially functional variants of cholesterol homeostasis genes (Q92516847) (← links)