Cryogen spray cooling (CSC) has been used effectively to protect the epidermis during laser dermatologie surgery. However, the temperature reduction in human skin induced by CSC has not been reliably determined due to the short cooling period and significant temperature gradient in the skin. Therefore, CSC has not been optimized for different laser dermatologie surgery procedures. Although it would be desirable to measure in situ human skin temperature, embedding a sensor within 100 μm beneath the skin surface is not feasible. In addition, infrared skin temperature measurement is also not workable because the skin is covered with a cryogen layer of unknown thickness. In this study, we selected an epoxy which has similar thermal properties to that of human skin as our cooling target. Thin-film thermocouples (TFTC) were deposited directly onto the epoxy substrate using micro-fabrication techniques to minimize the thermal contact resistance between TFTC and the substrate. The negligible mass of TFTC also creates a minimal disturbance to heat flow across the surface. Due to the difference in thermoelectric property between thin film and leading wire, special sensor design and calibration procedures were developed. TFTC were calibrated from -46 to 50°C The thermoelectric sensitivity is around 50-60% of that of bulk material. Skin phantom temperature reductions produced by a commercial medical laser nozzle at different spray durations were measured using the TFTC The results not only help to elucidate the mechanisms involved in interaction between cryogen spray and human skin but also provide a thermal boundary condition for numerical modeling of laser dermatologie surgery. Copyright © 2007 by ASME.

A variety of genetic techniques have been devised to determine cell lineage relationships during tissue development. Some of these systems monitor cell lineages spatially and/or temporally without regard to gene expression by the cells, whereas others correlate gene expression with the lineage under study. The GAL4 Technique for Real-time and Clonal Expression (G-TRACE) system allows for rapid, fluorescent protein-based visualization of both current and past GAL4 expression patterns and is therefore amenable to genome-wide expression-based lineage screens. Here we describe the results from such a screen, performed by undergraduate students of the University of California, Los Angeles (UCLA) Undergraduate Research Consortium for Functional Genomics (URCFG) and high school summer scholars as part of a discovery-based education program. The results of the screen, which reveal novel expression-based lineage patterns within the brain, the imaginal disc epithelia, and the hematopoietic lymph gland, have been compiled into the G-TRACE Expression Database (GED), an online resource for use by the Drosophila research community. The impact of this discovery-based research experience on student learning gains was assessed independently and shown to be greater than that of similar programs conducted elsewhere. Furthermore, students participating in the URCFG showed considerably higher STEM retention rates than UCLA STEM students that did not participate in the URCFG, as well as STEM students nationwide.