Preparation -- Isaac Vasserman (left) and Matt Kasa of Argonne's Accelerator Systems Division prepare an undulator for magnetic tuning and verification. Argonne reached another milestone in the design and construction of the Linac Coherent Light Source (LCLS) undulator system.

Virginia Tech researchers have received $1.2 million to study protein-protein interactions associated with biomass production in poplar wood. The U.S. Department of Energy (DOE) and the U.S. Department of Agriculture (USDA) jointly selected the Virginia Tech project and 10 others for awards totaling $8.3 million for biofuel research that may increase the availability and use of alternative fuels.

Researchers in Delft University of Technology’s Kavli Institute of Nanoscience in The Netherlands have cast new light on the workings of the important cancer inhibitor topotecan. Little had been known about the underlying molecular mechanism, but the Delft scientists can now view the effects of the medicine live at the levelin of a single DNA molecule. The research is being published this week in the journal Nature. The lead author of the article, Daniel Koster, will receive his PhD at TU Delft on Monday June 25, partly on the results described in the article.

Tokyo, Japan -- Researchers have shown that bone marrow stem cells injected into a damaged inner ear can speed hearing recovery after partial hearing loss. The related report by Kamiya et al, “Mesenchymal stem cell transplantation accelerates hearing recovery through the repair of injured cochlear fibrocytes,” appears in the July issue of The American Journal of Pathology.

Studies show that the incidence of mental illness on college campuses is rising, and a new survey of 2,785 college students indicates that more than half of students with significant symptoms of anxiety or depression do not seek help.

An X-ray of a case of scoliosis showing the abnormal curvature of the spine. Physicians have recognized scoliosis, the abnormal curvature of the spine, since the time of Hippocrates, but its causes have remained a mystery -- until now. For the first time, researchers have discovered a gene that underlies the condition, which affects about 3 percent of all children.