Pages that link to "Q33909617"
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The following pages link to Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis (Q33909617):
Displaying 50 items.
- Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17 (Q21145265) (← links)
- A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population (Q24297364) (← links)
- Molecular genetics of coronary artery disease (Q24674808) (← links)
- Advances in the genetic basis of coronary artery disease (Q24682029) (← links)
- Aging syndrome genes and premature coronary artery disease (Q24811421) (← links)
- Absence of association between atherosclerotic cerebral infarction and TNFSF4/TNFRSF4 single nucleotide polymorphisms rs1234313, rs1234314 and rs17568 in a Chinese population (Q28235238) (← links)
- New quantitative trait loci for carotid atherosclerosis identified in an intercross derived from apolipoprotein E-deficient mouse strains (Q30413841) (← links)
- A functionally significant polymorphism in ID3 is associated with human coronary pathology (Q30414349) (← links)
- Id3 is a novel atheroprotective factor containing a functionally significant single-nucleotide polymorphism associated with intima-media thickness in humans (Q30432659) (← links)
- GATA2 is associated with familial early-onset coronary artery disease (Q33255348) (← 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)
- Mutation in KERA identified by linkage analysis and targeted resequencing in a pedigree with premature atherosclerosis (Q33690049) (← links)
- Lack of MEF2A mutations in coronary artery disease (Q33726939) (← links)
- Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease (Q33906092) (← links)
- A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study (Q33910046) (← links)
- Apolipoprotein E receptor-2 deficiency enhances macrophage susceptibility to lipid accumulation and cell death to augment atherosclerotic plaque progression and necrosis (Q34016939) (← links)
- Identifying novel genes for atherosclerosis through mouse-human comparative genetics (Q34021005) (← links)
- A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene. (Q34076234) (← links)
- A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study (Q34137411) (← 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)
- Genomics of heart failure (Q34588881) (← links)
- Genome-wide linkage scan identifies two novel genetic loci for coronary artery disease: in GeneQuest families (Q34654020) (← links)
- Association of SNP rs17465637 on Chromosome 1q41 and rs599839 on 1p13.3 with Myocardial Infarction in an American Caucasian Population (Q35046461) (← links)
- Transcription factor MEF2A mutations in patients with coronary artery disease (Q35054057) (← links)
- The power of Pasteur's quadrant: cardiovascular disease at the turn of the century (Q35559072) (← links)
- VAMP-8 gene variant is associated with increased risk of early myocardial infarction. (Q35674159) (← links)
- Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease (Q35752509) (← links)
- The genetics of heart attack (Q35770844) (← links)
- EphA2 activation promotes the endothelial cell inflammatory response: a potential role in atherosclerosis (Q35885608) (← links)
- Update of the G2D tool for prioritization of gene candidates to inherited diseases (Q35914140) (← links)
- Genetic and genomic insights into the molecular basis of atherosclerosis (Q36155114) (← links)
- Identification of shared genetic susceptibility locus for coronary artery disease, type 2 diabetes and obesity: a meta-analysis of genome-wide studies (Q36347919) (← links)
- Genetic susceptibility to coronary artery disease: from promise to progress. (Q36389322) (← links)
- An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction (Q36430809) (← links)
- Nonconventional genetic risk factors for cardiovascular disease (Q36461077) (← links)
- Identification of a novel locus for triglyceride on chromosome 1p31-32 in families with premature CAD and MI (Q36558312) (← links)
- Personalized genomic medicine: a future prerequisite for the prevention of coronary artery disease. (Q36559160) (← links)
- Genetic susceptibility to myocardial infarction and coronary artery disease (Q36599259) (← links)
- Identification of atherosclerosis-modifying genes: pathogenic insights and therapeutic potential (Q36642686) (← links)
- Challenges in the phenotypic characterisation of patients in genetic studies of coronary artery disease (Q36678689) (← links)
- Connexin37: a potential modifier gene of inflammatory disease. (Q36743696) (← links)
- Molecular genetics of myocardial infarction (Q36843011) (← links)
- Identifying genes for coronary artery disease: An idea whose time has come (Q36898731) (← links)
- Mechanisms of disease: The genetic basis of coronary heart disease. (Q36950890) (← links)
- Genetic epidemiology of subclinical cardiovascular disease in the diabetes heart study (Q36962260) (← links)
- Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest). (Q37081240) (← links)
- Functional organization of the yeast proteome by a yeast interactome map (Q37083698) (← links)
- Identifying the susceptibility genes for coronary artery disease: from hyperbole through doubt to cautious optimism (Q37138039) (← links)