Scientists find new genes linked to lung cancer. Discovery opens door to individualized treatment strategies. – Working as part of a multi-institutional collaboration, scientists at Washington University School of Medicine in St. Louis have assembled the most complete catalog to date of the genetic changes underlying the most common form of lung cancer.
Three genes are associated with increased risk of higher levels of uric acid in the blood, which can lead to gout. – Researchers have identified two new genes ? and confirmed the role of a third gene ? associated with increased risk of higher levels of uric acid in the blood, which can lead to gout, a common, painful form of arthritis.
Results published today from a study led by researchers from The Translational Genomic Research Institute (TGen) in Phoenix, Arizona and The Queensland Institute of Medical Research (QIMR), Queensland, Australia, however, may yet change these statistics. The team is close to discovering a new gene that could help explain variation in melanoma risk. – The researchers are close to discovering a new gene that could help explain variation in melanoma risk. They have identified a region on chromosome 20 (20q11.22) that influences a person’s risk of developing melanoma.
Researchers from four continents announced the launch of the International Cancer Genome Consortium (ICGC), a major collaboration designed to identify the key genetic mutations involved in up to 50 types of cancer. – The International Cancer Genome Consortium (ICGC), which includes the Wellcome Trust and the Wellcome Trust Sanger Institute in the UK, will generate a valuable resource enabling the development of new and better ways of diagnosing, treating and preventing cancer.
Six new genes identified which play a role in the development of type 2 diabetes, and among the group is the second gene known to also play a role in prostate cancer. – Scientists have identified six new genes which play a role in the development of type 2 diabetes, and among the group is the second gene known to also play a role in prostate cancer.
A team of researchers at the University of Washington and Cold Spring Harbor Laboratories has uncovered genetic errors that may shed light on the causes of schizophrenia. The scientists found that deletions and duplications of DNA are more common in people with the mental disorder, and that many of those errors occur in genes related to brain development and neurological function. – Schizophrenia, a debilitating psychiatric disorder, is caused by some genetic errors due to deletions and duplications of DNA are more common in people with the mental disorders, revealed by researchers at the University of Washington and Cold Spring Harbor Laboratories.
NIH Collaborates with EPA to Improve the Safety Testing of Chemicals; New Strategy Aims to Reduce Reliance on Animal Testing. – Testing the safety of chemicals ranging from pesticides to household cleaners will benefit from new technologies and a plan for collaboration, according to federal scientists from the National Institutes of Health (NIH) and the U.S. Environmental Protection Agency (EPA), who announced a new toxicity testing agreement.
One thousand people are to have their genomes mapped in a major effort to understand how genes influence disease. – An international research consortium announced the 1000 Genomes Project, an ambitious effort that will involve sequencing the genomes of at least a thousand people from around the world to create the most detailed and medically useful picture to date of human genetic variation.
Chromosomal abnormalities play substantial role in autism, revealed in a study. Noting this change would help early diagnosis for autism or autism spectrum disorder (ASD) – a kind of developmental disorder. – Genome-wide scans of families affected by autism spectrum disorder (ASD) have revealed new evidence that previously unknown chromosomal abnormalities have a substantial role in the prevalent developmental disorder, according to a report published online Jan. 17th in the American Journal of Human Genetics, a publication of Cell Press.
Researchers applied a variety of genetic and analytic techniques to identify a chromosomal region, and ultimately a gene, associated with alcohol preference.
– A variant of a gene involved in communication among brain cells has a direct influence on alcohol consumption in mice, according to a new study by scientists supported by the National Institute on Alcohol Abuse and Alcoholism (NIAAA), part of the National Institutes of Health (NIH), and the U.S. Army.
