The effectiveness of psychodrama for adolescents who have experienced trauma

This study focuses on the effectiveness of psychodrama as a treatment for adolescents who have experienced trauma. This study looked extensively at adolescent trauma and three treatment frameworks designed to treat it, The Neurosequential Model of Therapeutics, Attachment Self Regulation and Competency, and Trauma Focused Cognitive Behavioral Therapy. This study also looked at psychodrama and psychodrama frameworks that are intended for use with trauma survivors. Psychodrama is an action- based treatment framework, where clients engage in therapeutic enactments. The effectiveness of psychodrama was researched through qualitative interviews with seven clinicians who practice psychodrama with adolescents. Participants were asked specific questions about the effectiveness of psychodrama as well as how they measure effectiveness. Within this study all participants spoke to the effectiveness of psychodrama as a treatment for adolescents who have experienced trauma. Participants identified many ways in which they measure the success of their work, however only one participant spoke about using scientific measurements when measuring success

Pre-mRNA processing enhancer (PPE) elements from intronless genes play additional roles in mRNA biogenesis than do ones from intron-containing genes

Most mRNA-encoding genes require introns for efficient expression in high eukaryotes. However, mRNAs can efficiently accumulate in the cytoplasm without intron excision if they contain cis-acting elements such as the post-transcriptional regulatory element (PRE) of hepatitis B virus (HBV), the constitutive transport element (CTE) of Mason–Pfizer monkey virus (MPMV), or the pre-mRNA processing enhancer (PPE) of herpes simplex virus' thymidine kinase (HSV-TK) gene. We compared the activities of these viral elements, the Rev-responsive element (RRE) of the human immunodeficiency virus (HIV), and the human c-Jun gene's enhancer (CJE), an element newly identified here, to enable expression of an intronless variant of the human β-globin gene. The PRE, PPE and CJE from naturally intronless genes, but not the CTE or RRE from intron-containing genes, significantly enhanced stability, 3′ end processing and cytoplasmic accumulation. When the transcripts included the β-globin gene's first intron, the PRE, PPE and CJE still enhanced mRNA biogenesis, in some cases without intron excision. Thus, elements enabling stability, 3′ end formation and nucleocytoplasmic export, not the presence of introns or their excision per se, are necessary for mRNA biogenesis. While the CTE and RRE primarily enhance nucleocytoplasmic export, PPE-like elements from naturally intronless genes facilitate polyadenylation as well

Twin polaritons in semiconductor microcavities

The quantum correlations between the beams generated by polariton pair scattering in a semiconductor microcavity above the parametric oscillation threshold are computed analytically. The influence of various parameters like the cavity-exciton detuning, the intensity mismatch between the signal and idler beams and the amount of spurious noise is analyzed. We show that very strong quantum correlations between the signal and idler polaritons can be achieved. The quantum effects on the outgoing light fields are strongly reduced due to the large mismatch in the coupling of the signal and idler polaritons to the external photons

The Ursinus Weekly, December 3, 1909

Football number • Credit due coach • The scrubs • Football rules discussed • A review of the football season • Comment • Choral concert • Seminary notes • Personals • Latin-Maths and Math-Phys meet • Slonaker hurt • Football managers electedhttps://digitalcommons.ursinus.edu/weekly/2817/thumbnail.jp

Wall thinning criteria for low temperature-low pressure piping

This acceptance criteria is intended to prevent gross rupture or rapidly propagating failure during normal and abnormal operating conditions. Pitting may be present in the carbon steel piping. While the acceptance criteria have provisions to preclude gross rupture through a pitted region, they do not protect against throughwall pit growth and subsequent leakage. Potential leakage through a pit in low pressure piping is less than the post-DBE design basis leakage. Both the uniform thinning and LTA criteria protect against leakage, since their potential for leakage is larger. The acceptance criteria protects against gross rupture due to general wall thinning, local wall thinning (LTA's), pitting, and fracture through weld defects. General wall thinning calculations are based on the restart criteria, SEP-24. LTA criteria for hoop stresses are based on ASME Code Case N-480 [open quotes]Examination Requirements for Pipe Wall Thinning Due to Single Phase Erosion and Corrosion[close quotes]. The LTA criteria for axial stress is based on an effective average thickness concept, which prevents plastic collapse of a locally thinned pipe. Limits on pit density, based on an effective cross section concept, are used to prevent gross rupture through a group of pits. The CEGB R-6 failure assessment diagram is used in the fracture evaluation, along with postulated weld defects. This criteria is intended for low temperature, low pressure piping systems. Corrosion and/or weld defects increase the peak stresses during normal operation and may lead to a reduction in fatigue life. Piping systems subject to significant thermal or mechanical fatigue will require additional analysis which is beyond the scope of this document

A global view of shifting cultivation: Recent, current, and future extent

Mosaic landscapes under shifting cultivation, with their dynamic mix of managed and natural land covers, often fall through the cracks in remote sensing–based land cover and land use classifications, as these are unable to adequately capture such landscapes’ dynamic nature and complex spectral and spatial signatures. But information about such landscapes is urgently needed to improve the outcomes of global earth system modelling and large-scale carbon and greenhouse gas accounting. This study combines existing global Landsat-based deforestation data covering the years 2000 to 2014 with very high-resolution satellite imagery to visually detect the specific spatio-temporal pattern of shifting cultivation at a one-degree cell resolution worldwide. The accuracy levels of our classification were high with an overall accuracy above 87%. We estimate the current global extent of shifting cultivation and compare it to other current global mapping endeavors as well as results of literature searches. Based on an expert survey, we make a first attempt at estimating past trends as well as possible future trends in the global distribution of shifting cultivation until the end of the 21st century. With 62% of the investigated one-degree cells in the humid and sub-humid tropics currently showing signs of shifting cultivation—the majority in the Americas (41%) and Africa (37%)—this form of cultivation remains widespread, and it would be wrong to speak of its general global demise in the last decades. We estimate that shifting cultivation landscapes currently cover roughly 280 million hectares worldwide, including both cultivated fields and fallows. While only an approximation, this estimate is clearly smaller than the areas mentioned in the literature which range up to 1,000 million hectares. Based on our expert survey and historical trends we estimate a possible strong decrease in shifting cultivation over the next decades, raising issues of livelihood security and resilience among people currently depending on shifting cultivation

The effects of exposure to a rotating environment /10 rpm/ on four aviators for a period of twelve days

Motion sickness studies of aviators exposed to rotating environment - Aerospace medicin

Complete reversal of epithelial to mesenchymal transition requires inhibition of both ZEB expression and the Rho pathway

<p>Abstract</p> <p>Background</p> <p>Epithelial to Mesenchymal Transition (EMT) induced by Transforming Growth Factor-β (TGF-β) is an important cellular event in organogenesis, cancer, and organ fibrosis. The process to reverse EMT is not well established. Our purpose is to define signaling pathways and transcription factors that maintain the TGF-β-induced mesenchymal state.</p> <p>Results</p> <p>Inhibitors of five kinases implicated in EMT, TGF-β Type I receptor kinase (TβRI), p38 mitogen-activated protein kinase (p38 MAPK), MAP kinase kinase/extracellular signal-regulated kinase activator kinase (MEK1), c-Jun NH-terminal kinase (JNK), and Rho kinase (ROCK), were evaluated for reversal of the mesenchymal state induced in renal tubular epithelial cells. Single agents did not fully reverse EMT as determined by cellular morphology and gene expression. However, exposure to the TβRI inhibitor SB431542, combined with the ROCK inhibitor Y27632, eliminated detectable actin stress fibers and mesenchymal gene expression while restoring epithelial E-cadherin and Kidney-specific cadherin (Ksp-cadherin) expression. A second combination, the TβRI inhibitor SB431542 together with the p38 MAPK inhibitor SB203580, was partially effective in reversing EMT. Furthermore, JNK inhibitor SP600125 inhibits the effectiveness of the TβRI inhibitor SB431542 to reverse EMT. To explore the molecular basis underlying EMT reversal, we also targeted the transcriptional repressors ZEB1 and ZEB2/SIP1. Decreasing ZEB1 and ZEB2 expression in mouse mammary gland cells with shRNAs was sufficient to up-regulate expression of epithelial proteins such as E-cadherin and to re-establish epithelial features. However, complete restoration of cortical F-actin required incubation with the ROCK inhibitor Y27632 in combination with ZEB1/2 knockdown.</p> <p>Conclusions</p> <p>We demonstrate that reversal of EMT requires re-establishing both epithelial transcription and structural components by sustained and independent signaling through TβRI and ROCK. These findings indicate that combination small molecule therapy targeting multiple kinases may be necessary to reverse disease conditions.</p

ZEB1 Regulates the Latent-Lytic Switch in Infection by Epstein-Barr Virus

The immediate-early (IE) BZLF1 gene of Epstein-Barr virus (EBV) regulates the switch between latent and lytic infection by EBV. We previously showed that the cellular transcription factor ZEB1 binds to a sequence element, ZV, located at nt −17 to −12 relative to the transcription initiation site of the BZLF1 promoter, Zp, repressing transcription from Zp in a transient transfection assay. Here, we report the phenotype in the context of a whole EBV genome of a variant of EBV strain B95.8 containing a 2-bp substitution mutation in the ZV element of Zp that reduced, but did not eliminate, ZEB1 binding to Zp. Strikingly, epithelial 293 cells latently infected with the EBV ZV mutant spontaneously produced IE-, early-, and late-gene products and infectious virus, while wild-type (WT)-infected 293 cells did not and have never been reported to do so. Furthermore, treatment with the chemical inducers sodium butyrate and 12-O-tetradecanoyl-phorbol-13-acetate (TPA) led to an additional order-of-magnitude production of infectious virus in the ZV mutant–infected 293 cells, but still no virus in the WT-infected 293 cells. Similarly, ZV mutant–infected Burkitt's lymphoma BJAB cells accumulated at least 10-fold more EBV IE mRNAs than did WT-infected BJAB cells, with TPA or sodium butyrate treatment leading to an additional 5- to 10-fold accumulation of EBV IE mRNAs in the ZV mutant–infected cells. Thus, we conclude that ZEB1 binding to Zp plays a central role in regulating the latent-lytic switch in EBV-infected epithelial and B cells, suggesting ZEB1 as a target for lytic-induction therapies in EBV-associated malignancies