Light dark forces at flavor factories

SuperB experiment could represent an ideal environment to test a new U (1) symmetry related to light dark forces candidates. A promising discovery channel is represented by the resonant production of a boson U, followed by its decay into lepton pairs. Beyond approximations adopted in the literature, an exact tree level calculation of the radiative processes $e+ e- \rightarrow \gamma, U \rightarrow \mu^+ \mu^- \gamma, e^+ e^- \gamma$ and corresponding QED backgrounds is performed, including also the most important higher-order corrections. The calculation is implemented in a release of the generator BabaYaga@NLO useful for data analysis and interpretation. The distinct features of U boson production are shown and the statistical significance is analysed

The importance of high-throughput cell separation technologies for genomics/proteomics-based clinical diagnostics

Gene expression microarray analyses of mixtures of cells approximate a weighted average of the gene expression profiles (GEPs) of each cell type according to its relative abundance in the overall cell sample being analyzed. If the targeted subpopulation of cells is in the minority, or the expected perturbations are marginal, then such changes will be masked by the GEP of the normal/unaffected cells. We show that the GEP of a minor cell subpopulation is often lost when that cell subpopulation is of a frequency less than 30 percent. The GEP is almost always masked by the other cell subpopulations when that frequency drops to 10 percent or less. On the basis of these results one should always assume that the GEP of a given cell subpopulation is probably seriously affected by, the presence of significant numbers of other "contaminating" cell types. Several methodologies can be employed to enrich the target cells submitted for microarray analyses. These include magnetic sorting and laser capture microdissection. If a cell subpopulation of interest is small, very high-throughput cell separation technologies are needed to separate enough cells for conventional microarrays. However, high-throughput flow cytometry/cell sorting overcomes many restrictions of experimental enrichment conditions. This technology can also be used to sort smaller numbers of cells of specific cell subpopulations and subsequently amplify their mRNAs before microarray analyses. When purification techniques are applied to unfixed samples, the potential for changes in gene levels during the process of collection is an additional concern. Since RNA rapidly degrades, and specific mRNAs turn over in minutes or hours, the cell separation process must be very rapid. Hence, high-throughput cell separation (HTS) technologies are needed that can process the necessary number of cells expeditiously in order to avoid such uncontrolled changes in the target cells GEP. In cases where even the use of HTS yields only a small number of cells, the mRNAs (after reverse transcription to cDNA's) must be amplified to yield enough material for conventional microarray analyses. However, the problem of using "microamplification" PCR methods to expand the amount of cDNAs (from mRNAs) is that it is very difficult to amplify equally all of the mRNAs. Unequal amplification leads to a distorted gene expression profile on the microarray. Linear amplifications is difficult to achieve. Unfortunately, present-day gene-chips need to be about 100 times more sensitive than they are now to be able to do many biologically and biomedically meaningful experiments and clinical tests

Sensitivity of wide band detectors to quintessential gravitons

There are no reasons why the energy spectra of the relic gravitons, amplified by the pumping action of the background geometry, should not increase at high frequencies. A typical example of this behavior are quintessential inflationary models where the slopes of the energy spectra can be either blue or mildly violet. In comparing the predictions of scenarios leading to blue and violet graviton spectra we face the problem of correctly deriving the sensitivities of the interferometric detectors. Indeed, the expression of the signal-to-noise ratio not only depends upon the noise power spectra of the detectors but also upon the spectral form of the signal and, therefore, one can reasonably expect that models with different spectral behaviors will produce different signal-to-noise ratios. By assuming monotonic (blue) spectra of relic gravitons we will give general expressions for the signal-to-noise ratio in this class of models. As an example we studied the case of quintessential gravitons. The minimum achievable sensitivity to $h^2_{0} \Omega_{GW}$ of different pairs of detectors is computed, and compared with the theoretical expectations.Comment: 10 pages in Revtex style, 3 figure

Design Principles for Aqueous Interactive Materials: Lessons from Small Molecules and Stimuli-Responsive Systems.

Interactive materials are at the forefront of current materials research with few examples in the literature. Researchers are inspired by nature to develop materials that can modulate and adapt their behavior in accordance with their surroundings. Stimuli-responsive systems have been developed over the past decades which, although often described as "smart," lack the ability to act autonomously. Nevertheless, these systems attract attention on account of the resultant materials' ability to change their properties in a predicable manner. These materials find application in a plethora of areas including drug delivery, artificial muscles, etc. Stimuli-responsive materials are serving as the precursors for next-generation interactive materials. Interest in these systems has resulted in a library of well-developed chemical motifs; however, there is a fundamental gap between stimuli-responsive and interactive materials. In this perspective, current state-of-the-art stimuli-responsive materials are outlined with a specific emphasis on aqueous macroscopic interactive materials. Compartmentalization, critical for achieving interactivity, relies on hydrophobic, hydrophilic, supramolecular, and ionic interactions, which are commonly present in aqueous systems and enable complex self-assembly processes. Relevant examples of aqueous interactive materials that do exist are given, and design principles to realize the next generation of materials with embedded autonomous function are suggested.JAM thanks ESPRC for an IAA KTF M is grateful for a Newton International Fellowship OAS is thankful to ERC Consolidator Grant CAM-RI

Biosensor-controlled gene therapy/drug delivery with nanoparticles for nanomedicine

Nanomedicine involves cell-by-cell regenerative medicine, either repairing cells one at a time or triggering apoptotic pathways in cells that are not repairable. Multilayered nanoparticle systems are being constructed for the targeted delivery of gene therapy to single cells. Cleavable shells containing targeting, biosensing, and gene therapeutic molecules are being constructed to direct nanoparticles to desired intracellular targets. Therapeutic gene sequences are controlled by biosensor-activated control switches to provide the proper amount of gene therapy on a single cell basis. The central idea is to set up gene therapy "nanofactories" inside single living cells. Molecular biosensors linked to these genes control their expression. Gene delivery is started in response to a biosensor detected problem; gene delivery is halted when the cell response indicates that more gene therapy is not needed