The Swedish Genomes Program will focus on identifying genetic causes
of common human diseases.
Examples
of common human diseases caused by viruses include the common cold, the flu, chickenpox and cold sores.
Following the award presentation, Feinberg will deliver a lecture on the epigenetic basis
of common human disease.
Not exact matches
Since the
human genome was decoded in 2003, researchers have been developing a powerful method for comparing the genomes
of patients and healthy people, with the hope
of pinpointing the DNA changes responsible for
common diseases.
Let us properly dwell upon it, being convinced that for the deadly
disease of «busyness» there is no medicine so specific as the pondering
of the hard path
of the true sufferer and as a fellow
human being sharing with him in the
common lot
of suffering.
There are eight
human herpes viruses, and they cause a wide spectrum
of diseases, ranging from
common cold sores to cancer.
A joint work by EPFL, ETH Zürich and the CHUV has identified a pathological process that takes place in both mice and
humans towards one
of the most
common diseases that people face in the industrialized world: type 2 diabetes.
In the United States, some
of the most alarming outbreaks are occurring in the suburbs, where rising temperatures may help explain the spike in such tick - borne illnesses as babesiosis; hga (
human granulocytic anaplasmosis), a potentially lethal flulike infection; and Lyme
disease, the most
common vector - borne
disease in this country.
Adds Visscher: «This is entirely in line with theory and previous inference from SNP [variant] data, yet for some reason many researchers in
human genetics and epidemiology continue to believe that there is a lot
of non-additive genetic variation for
common diseases and quantitative traits.»
A
common antioxidant found in
human breast milk and foods like kiwi fruit can protect against nonalcoholic fatty liver
disease (NAFLD) in the offspring
of obese mice, according to researchers at the University
of Colorado Anschutz Medical Campus.
Invasive aspergillosis (IA) is a serious
disease of immune - compromised individuals and the most
common invasive mold infection in
humans.
Efforts include the National Institutes
of Health Diabetes Genome Anatomy Project and another NIH - sponsored venture, the International HapMap Project, which is creating a map
of regions in the
human genome called haplotypes, where the underlying DNA influences
common diseases like diabetes.
First, the researchers used mice that had been genetically modified to produce excess amounts
of the
human version
of ß amyloid — a
common Alzheimer's
disease model.
Elegant, dainty, and deadly, it is the most
common of all blood - sucking arthropods and the most important insect carrier
of human disease, transmitting not only malaria but also yellow fever, dengue, West Nile virus, encephalitis, and the tiny worms that cause elephantiasis.
«We compared the ability
of RSV and parainfluenza virus (PIV3)-- another
common virus in children that causes much less severe airway
disease — to infect and cause inflammatory responses in a cell culture model
of human epithelial cells, which compose the lining
of the lung airway.
Underlying the most
common human diseases, however, are entire networks
of genes.
A team at the University
of Oxford assessed 199 such programmes and found potential welfare issues in two - thirds
of them, the most
common being mortality,
disease and conflict with
humans.
Researchers at University
of California, San Diego School
of Medicine have induced this all - too -
common human experience — or a close version
of it — permanently in rats and from what is observed perhaps derive clues about why strokes and Alzheimer's
disease can destroy a person's sense
of direction.
The «old friends hypothesis» proposes that the
human immune system can not learn to regulate itself without exposure to
common pathogens like helminths that have coevolved with people and that modern hygienic practices deprive people
of this necessary exposure, possibly explaining the relatively higher and more recent prevalence
of immune
diseases in industrialized countries like the U.S. Loke plans to continue researching helminthic therapy in people and in monkeys.
Fecal contamination in water is one
of the most
common reasons for
human diseases.
The PHPN uses information in
human disease networks in conjunction with network science tools to show clusters
of related disorders sharing
common genetic backgrounds.
Enter a mutant mouse strain that is afflicted at a young age with many
of the
diseases common to older
humans.
A year later, Carlo Croce, now director
of the
Human Cancer Genetics Program at Ohio State University, reported that chronic lymphocytic leukemia (CLL), the most
common form
of the
disease, was caused by deletion
of two microRNA genes.
But INB found a way to trick spinach (along with Swiss chard and petunias) into producing harmless bits and pieces
of common human pathogens that cause
diseases like flu and plague (inset).
Professor Yoshihito Watanabe (WPI - ITbM, Cooperating Researcher), Associate Professor Osami Shoji, Ms. Chikako Shirataki
of Nagoya University and co-workers have found a new method using an artificial metalloprotein (a protein that contains a metal) to inhibit the growth
of Pseudomonas aeruginosa bacteria, which is a
common bacterium that can cause
diseases in
humans and evolves to exhibit multiple antibiotic resistance.
«It is now clear that
common risk variants fail to explain the vast majority
of genetic heritability for any
human disease,» they wrote in an essay, arguing that many
of the hundreds
of GWAS findings to date «stem from factors other than a true association with
disease risk.»
«Lab - grown
human colons change study
of GI
disease: Stem cell derived organoids fill gap in modeling
common ailments.»
On the negative side, the researchers found that many
of the genes whose activity is unique to modern
humans are linked to
diseases like Alzheimer's
disease, autism and schizophrenia, suggesting that these recent changes in our brain may underlie some
of the psychiatric disorders that are so
common in
humans today.
The pigs showed both movement problems and respiratory difficulties
common to
human patients, and it is hoped that this model will assist in the creation
of new treatments for Huntington's — a genetically inherited and fatal
disease which affects tens
of thousands
of people.
About deCODE deCODE is a biopharmaceutical company applying its discoveries in
human genetics to the development
of diagnostics and drugs for
common diseases.
Telomeres have recently emerged as a read - out
of human cellular aging and their shortening actually contributes, along with other factors, to various
common age - associated
diseases.
for example, no HD mouse model shows signs
of «chorea», the dance - like movements that are a
common feature
of the
human disease.
The condition is more
common than muscular dystrophy and cystic fibrosis, but the development
of new therapeutic concepts is hindered by the fact that unlike muscular dystrophy and cystic fibrosis, where a single mutated gene causing the
disease is known, the entire
human chromosome 21 (containing around 300 genes) still has to be dissected into individual gene - dose contributions to the DS symptoms.
Human genetic studies strongly point to apolipoprotein E (APOE) and microglia (the immune cells
of the brain) as, respectively, the most important gene and cell type in the chain
of events leading to Alzheimer's
disease (AD), a
common disorder in the elderly in which the brain is damaged and memories falter.
Our wet - lab research is focused on the study
of Brucella, a facultative intracellular bacterium that causes brucellosis, one
of the most
common zoonotic
diseases in the world in
humans and a variety
of animal species.
Investigators in the CRGGH will develop genetic epidemiology models that will explore the patterns and determinants
of common complex
diseases in populations in the United States and other
human populations around the world.
His lab develops isogenic
human pluripotent stem cells and transgenic animals to model
disease, with the goal
of delineating novel approaches to influence outcomes for Huntington
disease (HD) and Fragile X Syndrome (FXS), the most
common genetic causes
of dementia and intellectual disability, respectively.
The quality and scale
of deCODE's in - house, CLIA - registered genotyping laboratory underpins deCODE's global leadership in the discovery
of variations in the sequence
of the
human genome conferring risk
of common diseases.
This study
of human genetic variation and its relationship to health and
disease involves a large number
of study participants and will capture not only
common single nucleotide variations but also rare copy number and structural variants that are increasingly thought to play an important role in complex
disease.
In
human disease, a mutation from G to A is extremely
common; these alterations have been implicated in, for example, cases
of focal epilepsy, Duchenne muscular dystrophy, and Parkinson's
disease.
The idea behind a â $ œHuman Vaccine Projectâ $ is to combine efforts at developing vaccines for major (but very different)
diseases such as influenza, dengue, HIV, hepatitis C, tuberculosis and malaria, with the rationale that what scientists working on those
diseases have in
common is the Ray Ban outlet challenge
of working with the
human immune system.
deCODE is a biopharmaceutical company applying its discoveries in
human genetics to the development
of drugs and diagnostics for
common diseases.
«Although we first became aware
of prions because they cause several bizarre neurological
diseases, the discovery that something so awesomely similar happens in organisms as different as
humans and yeast makes us suspect that there is a fundamental,
common biochemical process at work here,» said study director Susan Lindquist, PhD, professor
of molecular genetics and cell biology and an investigator in the Howard Hughes Medical Institute at the University
of Chicago.
Not so long ago, there was a hope in the research community that
common genetic variation, i.e. variants present at minor allele frequencies > 5 % in
human populations, might explain most or all
of the heritability
of common complex
disease.
About deCODE genetics deCODE is a biopharmaceutical company applying its discoveries in
human genetics to the development
of drugs for
common diseases.
In
humans, PKD is one
of the most
common diseases caused by a mutation in a single gene.
Potential projects include identifying
common pathways that modify retinal degenerative
disease from a large collection
of actively maintained mouse models; determining molecular networks implicated in pathological disruption
of the retinal pigment epithelium; identifying molecular pathways that regulate postnatal ocular growth; and using mouse models to assess the pathogenic role
of gene variants that increase the risk
of age - related macular degeneration as identified by
human genome - wide association studies.
Performing genetic studies in multiple
human populations can identify
disease risk alleles that are
common in one population but rare in others, with the potential to illuminate pathophysiology, health disparities, and the population genetic origins
of disease alleles.
Human Genetic Variation and
Common Disease David Altshuler, MD, PhD Professor
of Genetics and
of Medicine, Harvard Medical School and Massachusetts General Hospital Deputy Director and Chief Academic Officer, The Broad Institute
of MIT and Harvard
About deCODE deCODE is a biopharmaceutical company applying its discoveries in
human genetics to the development
of drugs and diagnostics for
common diseases.