Pages that link to "Q24630394"
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The following pages link to Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk (Q24630394):
Displaying 50 items.
- arterial hypertension (Q41861) (← links)
- HFE (Q14890978) (← links)
- MOV10 (Q18029250) (← links)
- PLCE1 (Q18040087) (← links)
- SLC39A8 (Q18045573) (← links)
- Genetic studies of body mass index yield new insights for obesity biology (Q22305005) (← links)
- Pathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variants (Q24273409) (← links)
- GWAS of 126,559 individuals identifies genetic variants associated with educational attainment (Q24289119) (← links)
- KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron (Q24307394) (← links)
- Genetic implication of a novel thiamine transporter in human hypertension (Q24336342) (← links)
- Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (Q24620065) (← links)
- Blood pressure loci identified with a gene-centric array (Q24630508) (← links)
- Platt versus Pickering: what molecular insight to primary hyperaldosteronism tells us about hypertension (Q24632816) (← links)
- Riociguat: Mode of action and clinical development in pulmonary hypertension (Q26748684) (← links)
- The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease (Q26748869) (← links)
- The Functions of Metallothionein and ZIP and ZnT Transporters: An Overview and Perspective (Q26766916) (← links)
- MicroRNAs and Endothelial (Dys) Function (Q26775547) (← links)
- Genomic and Proteomic Characterization of Acute Kidney Injury (Q26780469) (← links)
- Genetics and genomics of psychiatric disease (Q26781213) (← links)
- Current Applications of Genetic Risk Scores to Cardiovascular Outcomes and Subclinical Phenotypes (Q26798259) (← links)
- A review of genetics, arterial stiffness, and blood pressure in African Americans. (Q26825571) (← links)
- Natriuretic Peptides and Cardiometabolic Health (Q26827702) (← links)
- Are there genetic paths common to obesity, cardiovascular disease outcomes, and cardiovascular risk factors? (Q26829259) (← links)
- The contribution of genomic research to explaining racial disparities in cardiovascular disease: a systematic review (Q26829341) (← links)
- The discovery of hypertension: evolving views on the role of the kidneys, and current hot topics (Q26830489) (← links)
- Regulators of Slc4 bicarbonate transporter activity (Q26851045) (← links)
- Phenotyping the microcirculation (Q26851686) (← links)
- Emerging directions in the genetics of atrial fibrillation (Q26852051) (← links)
- STK39 polymorphism is associated with essential hypertension: a systematic review and meta-analysis (Q26859180) (← links)
- Mendelian randomization studies do not support a causal role for reduced circulating adiponectin levels in insulin resistance and type 2 diabetes (Q26861535) (← links)
- Regulation of intraocular pressure by soluble and membrane guanylate cyclases and their role in glaucoma (Q26861763) (← links)
- Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes (Q26991686) (← links)
- Challenges in elucidating the genetics of diabetic retinopathy (Q26998699) (← links)
- Understanding the genetics of coronary artery disease through the lens of noninvasive imaging (Q26999418) (← links)
- Genetic modification of hypertension by sGCα1 (Q27001632) (← links)
- Mendelian randomization: genetic anchors for causal inference in epidemiological studies (Q27002487) (← links)
- Neutral endopeptidase inhibition and the natriuretic peptide system: an evolving strategy in cardiovascular therapeutics (Q27004000) (← links)
- Two patients walk into a clinic...a genomics perspective on the future of schizophrenia (Q27004669) (← links)
- Cardiac target organ damage in hypertension: insights from epidemiology (Q27007701) (← links)
- Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants (Q27008212) (← links)
- Mendelian and trans-generational inheritance in hypertensive renal disease (Q27009363) (← links)
- Genome-wide association studies of late-onset cardiovascular disease (Q27012711) (← links)
- SLC transporters as therapeutic targets: emerging opportunities (Q27014726) (← links)
- Extending the translational potential of targeting NO/cGMP-regulated pathways in the CVS (Q27021649) (← links)
- Variant Near FGF5 Has Stronger Effects on Blood Pressure in Chinese With a Higher Body Mass Index (Q27304646) (← links)
- Peripancreatic fat necrosis worsens acute pancreatitis independent of pancreatic necrosis via unsaturated fatty acids increased in human pancreatic necrosis collections. (Q27318338) (← links)
- Soluble guanylate cyclase α1-deficient mice: a novel murine model for primary open angle glaucoma (Q27331498) (← links)
- Systems Medicine as an Emerging Tool for Cardiovascular Genetics (Q28069197) (← links)
- Novel Approaches to Investigate One-Carbon Metabolism and Related B-Vitamins in Blood Pressure (Q28074234) (← links)
- Genetic Risk Factors for Ischemic and Hemorrhagic Stroke (Q28079249) (← links)