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Macaque genome analysis will help find human disease genes
04-12-2007 · EurekAlert!Cornell University experts in computational biology and bioinformatics have made key contributions to the analysis of the genome of the rhesus macaque.
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Keywords: macaque, genome, analysis, human, disease, genes, analysi, gene
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Similar news on "Macaque genome analysis will help find human disease genes":
- Analysis of rhesus monkey genome uncovers genetic differences with humans, chimps
04-12-2007 · EurekAlert!
An international consortium of researchers has published the genome sequence of the rhesus macaque monkey and aligned it with the chimpanzee and human genomes. Published April 13 in a special section of the journal Science, the analysis reveals that the three primate species share about 93 percent of their DNA, yet have some significant differences among their genes.
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- Fruit fly gene research may shed light on human disease processes
03-27-2007 · EurekAlert!
Those small fruit flies buzzing around your bananas are more than pests -- they may be allies in a fruitful search for clues to human diseases caused when genes malfunction.
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- Scientists find major susceptibility gene for Crohn's disease
04-15-2007 · EurekAlert!
Using a novel approach, researchers identified that the PHOX2B, NCF4 and ATG16L1 genes constitute genetic risk factors for Crohn's disease. In addition, their study identified two regions of the genome where genetic risk factors are located but no known genes were implicated -- further work will be necessary to identify the causal genes in these regions.
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- Genomics study provides insight into the evolution of unique human traits
07-30-2007 · EurekAlert!
Researchers report the results of a large-scale, genome-wide study to investigate gene copy number differences among ten primate species, including humans. In the report, the scientists speculate how unique, lineage-specific gene copy number expansions and contractions in humans may underlie traits such as endurance running, higher cognitive function, and susceptibility genetic disease.
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- University of Washington researchers play leading role in major study of human genome function
06-13-2007 · EurekAlert!
Scientists at the University of Washington and other members of an international consortium have completed a multi-year research effort that dramatically boosts understanding of how the human genome functions. While previous studies of the human genome have focused mainly on genes, this study provides insight into non-gene sequences and "regulatory elements" that control genes and may play a role in many common diseases.
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- Gene expression profiling of dengue virus infection in cell lines and patients
11-06-2007 · EurekAlert!
Researchers at the Novartis Institute for Tropical Diseases and the Genome Institute of Singapore have identified new host genes associated with dengue virus infection, which may open new avenues to developing a drug to treat the disease. The results suggest that drugs that target the host pathways may prove effective against dengue.
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- Which genome variants matter?
02-08-2007 · EurekAlert!
Findings published in Science will accelerate the search for genes involved in human disease. This first genome-wide view shows that activity of more than 1000 genes is affected by sequence variation. This is an important step to understanding links between genes and disease for individuals, and across populations. By defining those genetic variants with a biological effect, the results will help prioritise regions of the genome that are investigated for association with disease.
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- Scientists find major susceptibility genes for Crohn's disease
04-16-2007 · EurekAlert!
A consortium of Canadian and American researchers led by Dr. John D. Rioux, PhD, Associate Professor of Medicine at the Montreal Heart Institute and the Université de Montréal, report in the April 15 online edition of Nature Genetics the results from a search of the entire human genome for genetic risk factors leading to the development of Crohn's disease.
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- Gene regulation in humans is closer than expected to simple organisms
08-29-2007 · EurekAlert!
Using a novel method developed to identify reliably functional binding motifs, researchers from the Weizmann Institute of Science in Israel have performed a genome-wide study of functional human transcription factor binding sites that encompasses nearly ten thousand genes and four hundred known binding motifs. The study appears in the August 29 issue of the online, open-access journal PLoS ONE.
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- Gene hunters close in on Lou Gehrig’s disease
02-20-2007 · EurekAlert!
In the first genome-wide search for the genetic roots of the most common form of amyotrophic lateral sclerosis (ALS), Johns Hopkins scientists have newly identified 34 unique variations in the human genetic code among 276 unrelated subjects with ALS.
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