Evidence of strong higher twist effects in diffractive DIS at HERA at moderate Q2

We study a twist decomposition of diffractive structure functions in the diffractive deep inelastic scattering (DDIS) at HERA. At low Q2 and at large energy the data exhibit a strong excess, up to about 100%, above the twist 2 NLO DGLAP description. The excess in consistent with higher twist effects. It is found, that complementing the DGLAP fit by twist 4 and 6 components of the GBW saturation model leads to a good description of data at low Q2. We conclude that the DDIS at HERA provides the first, strong evidence of higher twist effects in DIS.Comment: 4 pages, 2 PDF figure

General Mass Scheme for Jet Production in DIS

We propose a method for calculating DIS jet production cross sections in QCD at NLO accuracy with consistent treatment of heavy quarks. The scheme relies on the dipole subtraction method for jets, which we extend to all possible initial state splittings with heavy partons, so that the Aivazis-Collins-Olness-Tung massive collinear factorization scheme (ACOT) can be applied. As a first check of the formalism we recover the ACOT result for the heavy quark structure function using a dedicated Monte Carlo program.Comment: 6 pages, 2 figure

Phenomenology of the Electron Structure Function

Advantages of introducing the electron structure function (ESF) in electron induced processes are demonstrated. Contrary to the photon structure function it is directly measured in such processes. At present energies a simultaneous analysis of both the electron and the photon structure functions gives an important test of the experimentally applied methods. Estimates of the ESF at currently measured momenta are given. At very high momenta contributions from $W$ and $Z$ bosons together with $\gamma$-$Z$ interference can be observed. Predictions for next generation of experiments are given.Comment: 6 pages, 4 figures New version, new figures adde

Evidence for breakdown of the DGLAP description in diffractive DIS at HERA

HERA data on diffractive DIS show deviations from twist 2 DGLAP predictions below $Q^2\sim 5$ GeV$^2$ at low pomeron $\xi$, which may reach up to 100%. These deviations are consistent with higher twists effects extracted from the saturation model. It is a first direct evidence for the higher twists in DIS. This finding affects determination of the diffractive parton densities that are used for the predictions at the LHC.Comment: 5 pages, 2 figures, Based on the talk presented at the conference Deep-Inelastic Scattering and Related Subjects (DIS2012), Bonn, 201

Advanced Transport Operating System (ATOPS) color displays software description: MicroVAX system

This document describes the software created for the Display MicroVAX computer used for the Advanced Transport Operating Systems (ATOPS) project on the Transport Systems Research Vehicle (TSRV). The software delivery of February 27, 1991, known as the 'baseline display system', is the one described in this document. Throughout this publication, module descriptions are presented in a standardized format which contains module purpose, calling sequence, detailed description, and global references. The global references section includes subroutines, functions, and common variables referenced by a particular module. The system described supports the Research Flight Deck (RFD) of the TSRV. The RFD contains eight Cathode Ray Tubes (CRTs) which depict a Primary Flight Display, Navigation Display, System Warning Display, Takeoff Performance Monitoring System Display, and Engine Display

Advanced Transport Operating System (ATOPS) color displays software description microprocessor system

This document describes the software created for the Sperry Microprocessor Color Display System used for the Advanced Transport Operating Systems (ATOPS) project on the Transport Systems Research Vehicle (TSRV). The software delivery known as the 'baseline display system', is the one described in this document. Throughout this publication, module descriptions are presented in a standardized format which contains module purpose, calling sequence, detailed description, and global references. The global reference section includes procedures and common variables referenced by a particular module. The system described supports the Research Flight Deck (RFD) of the TSRV. The RFD contains eight cathode ray tubes (CRTs) which depict a Primary Flight Display, Navigation Display, System Warning Display, Takeoff Performance Monitoring System Display, and Engine Display

Characterization of a new pathway that activates lumisterol <i>in vivo</i> to biologically active hydroxylumisterols

Abstract Using LC/qTOF-MS we detected lumisterol, 20-hydroxylumisterol, 22-hydroxylumisterol, 24-hydroxylumisterol, 20,22-dihydroxylumisterol, pregnalumisterol, 17-hydroxypregnalumisterol and 17,20-dihydroxypregnalumisterol in human serum and epidermis, and the porcine adrenal gland. The hydroxylumisterols inhibited proliferation of human skin cells in a cell type-dependent fashion with predominant effects on epidermal keratinocytes. They also inhibited melanoma proliferation in both monolayer and soft agar. 20-Hydroxylumisterol stimulated the expression of several genes, including those associated with keratinocyte differentiation and antioxidative responses, while inhibiting the expression of others including RORA and RORC. Molecular modeling and studies on VDRE-transcriptional activity excludes action through the genomic site of the VDR. However, their favorable interactions with the A-pocket in conjunction with VDR translocation studies suggest they may act on this non-genomic VDR site. Inhibition of RORα and RORγ transactivation activities in a Tet-on CHO cell reporter system, RORα co-activator assays and inhibition of (RORE)-LUC reporter activity in skin cells, in conjunction with molecular modeling, identified RORα and RORγ as excellent receptor candidates for the hydroxylumisterols. Thus, we have discovered a new biologically relevant, lumisterogenic pathway, the metabolites of which display biological activity. This opens a new area of endocrine research on the effects of the hydroxylumisterols on different pathways in different cells and the mechanisms involved