EAST LANSING, Mich. — Catching terrorists who detonate bombs may be easier by testing the containers that hide the bombs rather than the actual explosives, according to pioneering research led by Michigan State University.
Currently, law enforcement labs tend to test for DNA on the exploded bomb fragments – but this has a low success rate, said David Foran, an MSU forensic biologist and lead investigator on the research project. (more…)
Researchers from UCLA’s cancer and stem cell centers have demonstrated for the first time that blood stem cells can be engineered to create cancer-killing T-cells that seek out and attack a human melanoma. The researchers believe the approach could be useful in about 40 percent of Caucasians with this malignancy.
Yale School of Medicine researchers have discovered that a variant of a gene linked to heart disease also increases the risk of deadly aneurysms of blood vessels in the brain. The discovery of this link raises hopes for new treatments for intracranial aneurysms, which affect more than a half million people worldwide annually.
“Existing drugs already target this common pathway and, in the future, could help treat or prevent aneurysms in people who are at risk,” said Murat Gunel, professor of neurosurgery, genetics and neurobiology and senior author of the study, published the week of Nov. 21 in the Proceedings of the National Academy of Sciences. (more…)
Researchers at Yale University have discovered new chemical compounds that prevent HIV from replicating in human T-cells. These compounds could result in new, highly effective HIV treatments that are 10 to 2000 times more potent than HIV drugs now on the market.
“The current compounds or slight variants could become drugs,” said Professor William L. Jorgensen, one of two principal investigators behind the research. The other is Karen S. Anderson, a pharmacology professor at Yale School of Medicine. They reported their results online Nov. 15 in the Journal of Medicinal Chemistry. (more…)
*New analytical method approaches the unstudied 99% of the human genome*
WASHINGTON, D.C., – 02 Nov 2011: Evolutionary history shows that human populations likely originated in Africa, and the Genographic Project, the most extensive survey of human population genetic data to date, suggests where they went next. A study by the Project finds that modern humans migrated out of Africa via a southern route through Arabia, rather than a northern route by way of Egypt. These findings will be highlighted today at a conference at the National Geographic Society.
National Geographic and IBM’s Genographic Project scientific consortium have developed a new analytical method that traces the relationship between genetic sequences from patterns of recombination – the process by which molecules of DNA are broken up and recombine to form new pairs. Ninety-nine percent of the human genome goes through this shuffling process as DNA is being transmitted from one generation to the next. These genomic regions have been largely unexplored to understand the history of human migration. (more…)
In the results of a new study, scientists explain how they used DNA to identify microbes present in the Gulf of Mexico following the Deepwater Horizon oil spill–and the particular microbes responsible for consuming natural gas immediately after the spill.
Water temperature played a key role in the way bacteria reacted to the spill, the researchers found. (more…)
Cell-penetrating peptides, such as the HIV TAT peptide, are able to enter cells using a number of mechanisms, from direct entry to endocytosis, a process by which cells internalize molecules by engulfing them.
Further, these cell-penetrating peptides, or CPPs, can facilitate the cellular transfer of various molecular cargoes, from small chemical molecules to nano-sized particles and large fragments of DNA. Because of this ability, CPPs hold great potential as in vitro and in vivo delivery vehicles for use in research and for the targeted delivery of therapeutics to individual cells. (more…)
*The genomes of 17 common strains of lab mice were sequenced to advance genetic studies of human diseases*
Scientists have sequenced the genomes (genetic codes) of 17 strains of common lab mice–an achievement that lays the groundwork for the identification of genes responsible for important traits, including diseases that afflict both mice and humans.
Mice represent the premier genetic model system for studying human diseases. What’s more, the 17 strains of mice included in this study are the most common strains used in lab studies of human diseases. By enabling scientists to list all DNA differences between the 17 strains, the new genome sequences will speed the identification of subsets of mutations and genes that contribute to disease. (more…)