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Team reveals molecular mechanism underlying a form of diabetes
By investigating a rare and severe form of diabetes in children, University of Iowa researchers have discovered a new molecular mechanism that regulates specialized pancreatic cells and insulin secretion. view more (2009-09-09)
Linking 2 molecular pieces of the Alzheimer's puzzle
Researchers have uncovered a biological link between the protein whose mutation causes early-onset Alzheimer's disease (AD) and a gene variant linked to late-onset AD. The researchers said their finding could lead to new approaches to treating AD. view more (2007-10-04)
'Best of both worlds' — Targeting a single gene could inhibit bone decay and stimulate bone growth
Researchers at the University of Pennsylvania's School of Medicine have found by targeting the function of a single gene that it is possible to inhibit bone decay while simultaneously stimulating bone formation. view more (2006-12-11)
McMaster researchers discover new mode of how diseases evolve
Researchers of the Michael G. DeGroote Institute for Infectious Disease Research have discovered a new way that bacteria evolve into something that can make you sick. view more (2009-02-17)
Mutation in renin gene linked to inherited kidney disease
A mutation in a gene that helps regulate high blood pressure is a cause of inherited kidney disease, according to a new study by researchers at Wake Forest University School of Medicine, Charles University in Prague and colleagues. view more (2009-08-19)
Participative risk regulation and the reform of the UK food safety regime
Henry Rothstein explores the impact of contemporary trends towards participative risk regulation on policy processes and outcomes. view more (2004-11-18)
A novel explanation for a floral genetic mystery
Scientists at the University of Jena, Germany have put forth a novel explanation of the evolutionary driving force behind a genetic switching circuit that regulates flower development and survival. view more (2009-01-16)
Typhoid carriers: a Salmonella gene mutation?
Salmonella enterica causes approximately 16 million cases of typhoid fever worldwide, killing around 500,000 per year. One in thirty of the survivors, however, become carriers, such as Typhoid Mary who caused several typhoid outbreaks in New York City at the beginning of the last century. In carriers the bacteria remain hidden inside cells and the... view more... (2002-06-25)
Oxford Biomedica Obtains Further Fundamental Patent For Lentiviral Gene Therapy Technology
Oxford BioMedica plc announced today that it has received allowance from the US Patent Office for a further patent covering its proprietary LentiVector technology. This additional patent compliments the US patent 6,312,682 issued in November 2001 and both include broad composition of matter claims and methods of production claims for lentiviral... view more... (2003-08-13)
NYU, Rutgers study shows how using mental strategies can alter the brain's reward circuitry
The cognitive strategies humans use to regulate emotions can determine both neurological and physiological responses to potential rewards, a team of New York University and Rutgers University neuroscientists has discovered. view more (2008-06-30)
Probability Controls The Molecule Of Life
Thanks to biophysicists, statistics has reached the most intimate aspect of life - regulation of genes' activity. Investigation on probabilistic aspects of molecular biology has been supported by the Russian Foundation for Basic Research and the INTAS Foundation. Regulation of genes' activity is one of the most important biological problems which... view more... (2004-05-24)
Animal Experiments Are Necessary, But Government And Industry Should Do More To Develop Non-animal Alternatives
A Lords report published today by the Select Committee on Animals in Scientific Procedures found that animal experiments are currently necessary to develop human and veterinary medicine, and to protect humans and the environment. However, the report says that more should be done to fund and promote "alternative" methods known as the... view more... (2002-07-24)
Ironing out the genetic cause of hemoglobin problems
A gene with a significant effect on regulating hemoglobin in the body has been identified as part of a genome-wide association study, which looked at the link between genes and hemoglobin level in 16,000 people. view more (2009-10-12)
Mutation responsible for cystic fibrosis also involved in muscle atrophy
Patients with cystic fibrosis (CF) usually experience significant muscle loss, a symptom traditionally considered to be a secondary complication of the devastating genetic disease. view more (2009-07-31)
Life Cycle of Operons Yields New Look at Bacterial Genetics
In a breakthrough that will immediately benefit biologists who study bacteria, and could in the future have bearing on the advancement of synthetic biology, a team of researchers has determined the life cycle of operons, small groups of genes with related functions that are co-transcribed in a single strand of messenger RNA. view more (2006-07-06)
Searching for shut eye: Penn study identifies possible sleep gene
While scientists and physicians know what happens if you don't get six to eight hours of shut-eye a night, investigators have long been puzzled about what controls the actual need for sleep. Researchers at the University of Pennsylvania School of Medicine might have an answer, at least in fruit flies. In a recent study of fruit flies, they... view more... (2008-07-30)
New light shed on the enigma of salt intake and hypertension
A high salt intake has been implicated in cardiovascular disease risk for 5000 years. But salt-sensitive hypertension still remains an enigma. view more (2009-05-04)
Gene linked to lupus might explain gender difference in disease risk
In an international human genetic study, researchers at UT Southwestern Medical Center have identified a gene linked to the autoimmune disease lupus, and its location on the X chromosome might help explain why females are 10 times more susceptible to the disease than males. view more (2009-03-30)
Seasonal Affective Disorder May Be Linked to Genetic Mutation, Study Suggests
With the days shortening toward winter, many people will begin to experience the winter blahs. For some, the effect can be devastating. view more (2008-11-04)
Linchpin gene may be useful target for new breast cancer therapies
University of Iowa researchers have discovered a gene that plays a linchpin role in the ability of breast cancer cells to respond to estrogen. The finding may lead to improved therapies for hormone-responsive breast cancers and may explain differences in the effectiveness of current treatments. view more (2007-09-17)
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