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Items for "genetics"

Stroke: epidemiology, risk factors, and genetics

Stroke constitutes a major global challenge for health policy and healthcare economics. Reducing stroke burden requires extensive knowledge of risk factors and, if applicable, preventive control...

Keywords: Schlaganfall, Epidemiologie, Risikofaktoren, Genetik

01/2006 | Hämostaseologie, Schattauer
Genetic Epidemiology in Germany From Biobanking to Genetic Statistics

Objectives: Genetic epidemiology investigates the role of genetic factors and their interaction with environmental factors (in a broad meaning) for the occurrence of diseases in human populations...

Keywords: Biobanking, genetics, epidemiology, bioethics

01/2005 | Methods of Information in Medicine, Schattauer
Genetic analysis of CAV1 gene in hypertension and metabolic syndrome

Recently, we reported that the polymorphism 1132T>C (Gene-Bank: AF519768.1) of the NOS3 gene was associated with susceptibility to metabolic syndrome (MS) in hypertensive patients...

Keywords: CAV1, MNOS3, genetics, hypertension, metabolic syndrome

04/2006 | Thrombosis and Haemostasis, Schattauer
Haplotypes of the plasminogen activator gene associated with ischemic stroke

Ischemic stroke (IS) is thought to be a multifactorial disorder associated with genetic backgrounds and environmental factors...

Keywords: Tissue plasminogen activator, ischemic stroke, haplotypes, association studies, genetics

09/2006 | Thrombosis and Haemostasis, Schattauer
Identification of functional polymorphisms of the thromboxane A2 receptor gene in healthy volunteers

Thromboxane A2 receptor (TP) is an important actor in vascular physiology and plays a crucial role in the platelet activation process...

Keywords: genetics, Platelet, polymorphisms, thromboxane, TP

09/2006 | Thrombosis and Haemostasis, Schattauer
Assessment of genetic risk for myocardial infarction

Although lifestyle and environmental factors influence the prevalence of myocardial infarction, genetic epidemiological studies have suggested that several genetic variants increase the risk for this condition...

Keywords: genetics, Polymorphism, myocardial infarction, coronary heart disease, atherosclerosis

08/2006 | Thrombosis and Haemostasis, Schattauer
Fibrinogen gene haplotypes in relation to risk of coronary events and coronary and extracoronary atherosclerosis: The Rotterdam Study

Fibrin network structure has been correlated with coronary disease. Fibrinogen and (FGG and FGA) gene haplotypes (chromosome 4q28) may be associated with fibrin network structure, and thereby with rigidity of the fibrin clot and sensitivity of the fibrin clot to the fibrinolytic system...

Keywords: Coronary disease, atherosclerosis, epidemiology, genetics, fibrinogen

00/0000 | Thrombosis and Haemostasis, Schattauer
Distribution, morphology, and genetic affinities of dwarf embedded Fucus populations from the Northwest Atlantic Ocean

Dwarf embedded Fucus populations in the Northwest Atlantic Ocean are restricted to the upper intertidal zone in sandy salt marsh environments; they lack holdfasts and are from attached parental populations of F...

Keywords: distribution, dwarf embedded Fucus, ecology, genetics, morphology, salt marsh fucoid algae

09/2006 | Botanica Marina, Walter de Gruyter
Understanding hyperlipidemia and atherosclerosis: lessons from genetically modified apoe and ldlr mice

Hyperlipidemia is the most important risk factor for atherosclerosis, which is the major cause of cardiovascular disease...

Keywords: apolipoprotein E (ApoE), gene targeting, genetics, Genomics, hyperlipoproteinemia, low-density protein receptor (LDLR), transgenesis

05/2005 | Clinical Chemical Laboratory Medicine, Walter de Gruyter
Nutrigenomics – 2006 update

The Human Genome and HapMap projects have provided the tools and information that will aid in understanding how nutrients alter the expression of an individual's genetic information and why individuals differ in metabolism of foods at the molecular level...

Keywords: Epistasis, gene-nutrient interactions, genetics, nutrigenomics, nutrition

03/2007 | Clinical Chemical Laboratory Medicine, Walter de Gruyter
Mother-to-infant vertical transmission of transfusion transmitted virus in South China

A nested PCR was used to detect TTV DNA in serum from 490 mother-infant pairs to determine the rate of vertical transmission of TTV in Guangzhou City, P.R...

Keywords: genetics, infant, nested polymerase chain reaction, pregnancy, transfusion transmitted virus, vertical transmission

09/2004 | Journal of Perinatal Medicine, Walter de Gruyter
A pediatric perspective on hemochromatosis: not just “an old man's disease” Eine pädiatrische Sichtweise der Hämochromatosis: nicht nur ein Altersleiden

Hemochromatosis, once considered to be an autosomal recessive disorder of increased iron absorption, predominantly affecting men after the fourth decade of life, is now known to be a syndrome caused by mutations in at least five different genes, one of which results in an autosomal dominant form of the disease...

Keywords: Genetik, Hämochromatose, juvenil, Kind

03/2006 | LaboratoriumsMedizin, Walter de Gruyter
Biobanks in Genetic-epidemiological Research such as KORA-gen

Biobanks are an important tool of genetic epidemiology, which investigates the role of genetic factors and their interaction with environmental factors (in a broad meaning) for the occurrence of diseases in human populations...

Keywords: biobanks, genetics, epidemiology, biostatistics, bioethics

06/2007 | it – Information Technology (vormals it+ti), Oldenbourg Wissenschaftsverlag