Science Resources RSS Feeds
|
 |
 |
 |
Genetics Current Events | Genetics News | 4
|
| Page
4 of
10 |
193 Results |
|
|
|
Sort By:
Page Views | Date |
Study uncovers mutation responsible for Noonan Syndrome
Scientists have discovered that mutations in a gene known as SOS1 account for many cases of Noonan syndrome (NS), a common childhood genetic disorder which occurs in one in 1,000-2,500 live births. view more (2006-12-05)
Genetic irregularities linked to higher risk of COPD among smokers
Scientists at Duke University Medical Center have discovered two genetic markers that appear to put some smokers at significantly higher risk of developing chronic obstructive pulmonary disease (COPD). view more (2009-03-20)
Bone specialists' hi-tech answer to patient care
Bone-disorder experts from across Europe have turned to the web in a unique alliance that will improve patient care. The European Skeletal Dysplasia Network (ESDN), which was developed by The University of Manchester, links eight institutions in six different countries by means of a secure web portal. The hi-tech referral system means a patient,... view more... (2005-01-05)
Rodent's bizarre traits deepen mystery of genetics, evolution
A shadowy rodent has potential to shed light on human genetics and the mysteries of evolution. view more (2006-09-18)
Scientists discover how smallpox may derail human immune system
University of Florida researchers have learned more about how smallpox conducts its deadly business - discoveries that may reveal as much about the human immune system as they do about one of the world's most feared pathogens. view more (2009-05-12)
Researchers discover gene behind devastating vitamin B12-related disorder
Swiss, British and Canadian researchers have identified the gene responsible for a rare but serious genetic disorder and have simultaneously provided more clues as to how vitamin B12 works in the body. Their results will be published April 3 in the New England Journal of Medicine. view more (2008-04-03)
UAB Researchers Discover a New Mechanism Involved in Predisposition to Cancer
A team of researchers at the Universitat Autònoma de Barcelona (UAB) has discovered a new mechanism that accelerates the shortening of telomeres (structures that protect the ends of chromosomes) involved in genetic instability and a predisposition to cancer. The research has been published in the journal Human Molecular Genetics. view more (2002-02-26)
Greatest thing since sliced bread: New data offer important clues toward improving wheat yields
Breed a better crop of wheat? That's exactly what a team of researchers from Kansas State University and the U.S. Department of Agriculture hope their research will lead to. view more (2009-03-11)
New genomic markers associated with risk of heart disease and early heart attack
Five short reports published simultaneously by the journal Nature Genetics have for the first time identified clusters of genetic markers associated with heart attack and coronary heart disease. view more (2009-02-19)
Manchester researchers identify gene behind rheumatoid arthritis
University of Manchester researchers have identified a genetic variant in a region on chromosome 6 that is associated with rheumatoid arthritis (RA), the most common inflammatory arthritis affecting 387,000 people in the UK. view more (2007-11-05)
GENETICS OF BLOOD CLOTTING FACTORS (pp 83, 101)
People with a family history of coronary heart disease are thought more likely to develop the disease themselves, because of a combination of genetic and shared environmental factors. Researchers use twin or adoption studies to establish whether genetic or environmental factors are more important in the development of a particular disease. There... view more... (2001-01-11)
Where there's muck there's grass
The oldest ecological experiment in the world, set up almost 150 years ago to see whether inorganic fertilisers could produce more grass than traditional animal manures, is becoming an important source of evidence on the impact of climate change on genetic variation in plants. Speaking at the British Ecological Society's Annual Meeting, being... view more... (2003-09-01)
Genetic test for spinal muscular atrophy should be offered to all couples, says the ACMG
Carrier screening for spinal muscular atrophy (SMA)-a serious genetic disease affecting approximately 1 in 10,000 infants that causes progressive muscle weakness and death-should be made available to all families, according to a new practice guideline issued by the American College of Medical Genetics (ACMG). view more (2008-12-10)
Environment influences when drinking begins; genes' role increases in transition to alcohol dependence
The influence of genetics increases as young women transition from taking their first drink to becoming alcoholics. view more (2008-04-24)
Genetic risk for anxiety does not have to be destiny
A growing body of basic animal research and studies of abused and neglected children provide a strong basis of support for the hypothesis that individuals with particular genotypes are at greater risk for depression, anxiety disorders, and problems with the abuse of alcohol and other substances. view more (2009-04-29)
UNC medical geneticist cautions against rushing into genetic testing
Just because scientific advances now allow individuals to learn their genetic make-up doesn't mean they should rush into genetic testing in hopes of making revolutionary improvements to their health, cautions a geneticist and practicing physician at the University of North Carolina at Chapel Hill. view more (2008-06-02)
Statistical tool could explain gene study variations
While scientists are using the human genome to associate certain genes with disease, Dr. Hongyan Xu wants to ensure they are accounting for natural variations in those genes. view more (2008-05-29)
MUHC-led international team identifies gene responsible for blindness in infants and children
A MUHC-led study identifies a gene responsible for Leber Congenital Amaurosis (LCA), the most common cause of congenital blindness in infants and small children. view more (2007-06-04)
MUHC and McGill scientists identify gene for debilitating vitamin B12 disease
Scientists at the MUHC and McGill University have identified a gene responsible for a disease that impairs the body's ability to handle vitamin B12 and that may contribute to heart disease, stroke and dementia. view more (2005-12-01)
Taking the P out of plants
Is there an alternative to using GM crops in agriculture to eradicate the need for applying excessive phosphate fertiliser? John Hammond of UK's Horticulture Research International thinks so. Working in collaboration with Nottingham University, he is developing a diagnostic test that tells when plants are low on phosphorus so they can be... view more... (2004-03-24)
|
|
| Page
4 of
10 |
193 Results |
|
|
|
Sort By:
Page Views | Date |
|
|
