News tagged with medical genomics
Gene therapy is a 'disruptive science' ready for commercial development
The time for commercial development of gene therapy has come. Patients with diseases treatable and curable with gene therapy deserve access to the technology, which has demonstrated both its effectiveness ...
Jan 24, 2012 |
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Finding the silent killer -- a biomarker test for atherosclerosis
Furring of the arteries, atherosclerosis, is a leading cause of death across the world. Atherosclerosis leads to peripheral arterial disease, coronary heart disease, stroke and heart attacks. However, atherosclerosis is a ...
Jan 13, 2012 |
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Single gene links rare and unrelated cancers
Scientists at the BC Cancer Agency, Vancouver Coastal Health Research Institute, and the University of British Columbia are excited over a discovery made while studying rare tumour types.
Dec 21, 2011 |
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Institute presses for greater use of gene sequencing in medicine
Almost a year after researchers in Wisconsin published a groundbreaking paper describing their use of genetic sequencing to diagnose and treat a 4-year-old boy, a national health agency is shifting its focus to put $416 ...
Dec 07, 2011 |
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The power to help, hurt and confuse: Direct-to-consumer whole genome testing
The era of widely available next generation personal genomic testing has arrived and with it the ability to quickly and relatively affordably learn the sequence of your entire genome. This would include what ...
Dec 06, 2011 |
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New research gives hope to women with deadliest breast cancer
Women with the deadliest and rarest form of breast cancer now have a chance of treatment where once their options were severely limited, thanks to a new discovery by George Mason University researchers.
Nov 14, 2011 |
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Biotech start-up brings DNA-sequencing to the medical market
What started back in 2004 as a three-person start-up may well be on its way to becoming a multi-million euro success story. Advanced by a team of young Dutch scientists pushing disruptive biotech innovations onto the market, ...
Nov 08, 2011 |
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Modern genetics answers age-old question on Garrod's fourth inborn error of metabolism
Fifty years after participating in studies of pentosuria, an inherited disorder once mistaken for diabetes, 15 families again welcomed medical geneticists into their lives. Their willingness to have their DNA analyzed with ...
Oct 31, 2011 |
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Scripps launches whole genome sequencing study to find root causes of idiopathic diseases
Scripps Health announced today it has launched an innovative clinical research study that is using whole genome sequencing to help determine the causes of idiopathic human diseases -- those serious, rare and perplexing health ...
Oct 18, 2011 |
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Small island nation to sequence genome of entire population
(Medical Xpress) -- The small island nation of the Faroe Islands is planning to offer free full genome sequencing to all of its 50,000 citizens. Though only partially sponsored as yet (by genome-sequencing company Illumina) ...
Study gauges emotional toll of direct-to-consumer genetic testing
Among the latest health care trends seeking to advance "individualized medicine" are private companies marketing genetic testing directly to patients. The mail-in kits, with price tags as high as $2,500, use a saliva specimen ...
Oct 03, 2011 |
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Mom, dad and kids undergo novel genome analyses for medical risks in new study
Stanford University School of Medicine researchers have predicted the inherited health risks of a four-person family by analyzing their whole genome sequences. With the DNA sequences of both parents and children, the team ...
Sep 15, 2011 |
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Genetic link to Barrett's esophagus, esophageal cancer discovered
Mutations in three genes have been identified that are more prevalent in patients with esophageal cancer and Barrett esophagus, a premalignant metaplasia (change in cells or tissue) caused by chronic gastroesophageal reflux ...
Jul 26, 2011 |
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Personalized medicine
Although personalized medicine is a term used in science and medicine that holds significant promise of improved treatment, it may set up unrealistic expectations in patients, states an editorial in CMAJ (Canadian Medical A ...
Jul 18, 2011 |
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Computational software provides rapid identification of disease-causing gene variations
Scientists from the University of Utah and Omicia, Inc., a privately held company developing tools to interpret personal genome sequences, today announced the publication in Genome Research of a new software tool called VAAST, ...
Jun 23, 2011 |
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