82 research outputs found
Mother Courage and Her Children Poster
Providence College Department of Theatre, Dance & Film
Harkin\u27s Hall Auditorium
Mother Courage and Her Children by Bertolt Brecht
March 26-30, 1980, 8PMhttps://digitalcommons.providence.edu/courage_pubs/1002/thumbnail.jp
Joseph and the Amazing Technicolor Dreamcoat Open Auditions Poster
Providence College Department of Theatre, Dance & Film
Joseph and the Amazing Technicolor Dreamcoat open auditions
Mon. & Tues, Jan. 7 & 8, 1980 - 7PM
Callbacks: Wed., Jan 9, 1980 - 7PMhttps://digitalcommons.providence.edu/dreamcoat_pubs/1000/thumbnail.jp
Mother Courage and Her Children Playbill
Providence College Department of Theatre, Dance & Film
Harkin\u27s Hall Auditorium
Mother Courage and Her Children, a chronicle of the Thirty Years War by Bertolt Brecht, translation by Ralph Manheim, Music by Paul Dessau, adapted and arranged by R.B. Haller, O.P.
March 26-30, 1980
Director, Mary G. Farrell
Scenery, Elizabeth Popiel-Delp
Costumes, Peter J. Cameron
Lighting, Carl F. Gudenius
Theatre Arts Program Director, John Garrity
Cast: Mother Courage - Kate Farrell, Kattrin - Wilma Mondi, Elif - Peter J. Cameron, Swiss Cheese - Jim Maher, Cook - Daniel E. Otero, Chaplain - Wally Dunn, Yvette - Mary Ellen Baxter, COMPANY: Matthew Hilgreen, Frank Toti, Frank Gorrell, Matt Oliverio, Joe D\u27Antuono, Martina Flynn, Susan Schaeferhttps://digitalcommons.providence.edu/courage_pubs/1000/thumbnail.jp
Joseph and the Amazing Technicolor Dreamcoat Poster
Providence College Department of Theatre, Dance & Film
Harkin\u27s Hall Auditorium
Joseph and the Amazing Technicolor Dreamcoat
February 13-17, 1980
Curtain - 8PMhttps://digitalcommons.providence.edu/dreamcoat_pubs/1005/thumbnail.jp
Joseph and the Amazing Technicolor Dreamcoat Playbill
Providence College Department of Theatre, Dance & Film
Harkin\u27s Hall Auditorium
Joseph and the Amazing Technicolor Dreamcoat, created by Tim Rice and Andrew Lloyd Webber
February 13 - 17, 1980
Director, John Garrity
Choreography, Sharon Jenkins
Scenery & Lighting, Carl F. Gudenius
Musical Direction, Reginald B. Haller, O.P.
Costumes, Mary Farrell
Cast: Joseph - Peter Cameron, Jacob - John F. Cunningham, Potiphar - Wally Dunn, Potiphar\u27s Wife - Kate Farrell, Pharaoh - Joe Gianni, Narrators - Jane Dillon & Danny Otero, BROTHERS: Reuben - Peter Thomson, Simeon - Luke Rheaume, Levi - Matt Oliverio, Napthali - Lewis DiPrete, Isaacher - Dan Foster, Asher - Joe Gianni, Dan - Richard Lawrence, Zebulum - Wally Dunn, Gad - Jim Maher, Benjamin - Don Walker, Judah - Joe D\u27Antuono, ENSEMBLE: Mary Ellen Baxter, Wilma Mondi, Chris Paul, Sheryl Hanley, Debbie Haberlin, Judy Weaver & Debbie Thiberthttps://digitalcommons.providence.edu/dreamcoat_pubs/1006/thumbnail.jp
School Sense of Community, Teacher Support, and Students\u2019 School Safety Perceptions
This study examined the association between two characteristics of school climate (sense of community and teacher support, measured both at the individual and at the school level) and students\u2019 feelings of being unsafe at school. The study involved a sample of 49,638 students aged 10\u201318 years who participated in the 2010\u20132012 California Healthy Kids Survey. Using hierarchical linear modeling (HLM), our findings revealed that, at the individual level, students perceiving higher levels of sense of community and teacher support at school were less likely to feel unsafe within the school environment. At the school level, sense of community was negatively associated with unsafe feelings, whereas there was no association between school-level teacher support and feelings of being unsafe at school
Feeling Healthy? A Survey of Physical and Psychological Wellbeing of Students from Seven Universities in the UK
University students’ physical and psychological health and wellbeing are important and comprise many variables. This study assessed perceived health status in addition to a range of physical and psychological wellbeing indicators of 3,706 undergraduate students from seven universities in England, Wales and Northern Ireland. We compared differences in these variables across males and females, and across the participating universities. The data was collected in 2007–2008. A self-administered questionnaire assessed socio-demographic information (e.g., gender, age), self-reported physical and psychological health data, as well as questions on health awareness, health service use, social support, burdens and stressors and university study related questions. While females generally reported more health problems and psychological burdens, male students felt that they received/had fewer persons to depend on for social support. The comparisons of health and wellbeing variables across the different universities suggested some evidence of ‘clustering’ of the variables under study, whereby favourable situations would be exhibited by a cluster of the variables that is encountered at some universities; and conversely, the clustering of less favourable variables as exhibited at other universities. We conclude that the level of health complaints and psychological problems/burdens is relatively high and calls for increased awareness of university administrators, leaders and policy makers to the health and well-being needs of their students. The observed clustering effects also indicated the need for local (university-specific) health and wellbeing profiles as basis and guidance for relevant health promotion programmes at universities
Gene expression profiling identifies inflammation and angiogenesis as distinguishing features of canine hemangiosarcoma
<p>Abstract</p> <p>Background</p> <p>The etiology of hemangiosarcoma remains incompletely understood. Its common occurrence in dogs suggests predisposing factors favor its development in this species. These factors could represent a constellation of heritable characteristics that promote transformation events and/or facilitate the establishment of a microenvironment that is conducive for survival of malignant blood vessel-forming cells. The hypothesis for this study was that characteristic molecular features distinguish hemangiosarcoma from non-malignant endothelial cells, and that such features are informative for the etiology of this disease.</p> <p>Methods</p> <p>We first investigated mutations of VHL and Ras family genes that might drive hemangiosarcoma by sequencing tumor DNA and mRNA (cDNA). Protein expression was examined using immunostaining. Next, we evaluated genome-wide gene expression profiling using the Affymetrix Canine 2.0 platform as a global approach to test the hypothesis. Data were evaluated using routine bioinformatics and validation was done using quantitative real time RT-PCR.</p> <p>Results</p> <p>Each of 10 tumor and four non-tumor samples analyzed had wild type sequences for these genes. At the genome wide level, hemangiosarcoma cells clustered separately from non-malignant endothelial cells based on a robust signature that included genes involved in inflammation, angiogenesis, adhesion, invasion, metabolism, cell cycle, signaling, and patterning. This signature did not simply reflect a cancer-associated angiogenic phenotype, as it also distinguished hemangiosarcoma from non-endothelial, moderately to highly angiogenic bone marrow-derived tumors (lymphoma, leukemia, osteosarcoma).</p> <p>Conclusions</p> <p>The data show that inflammation and angiogenesis are important processes in the pathogenesis of vascular tumors, but a definitive ontogeny of the cells that give rise to these tumors remains to be established. The data do not yet distinguish whether functional or ontogenetic plasticity creates this phenotype, although they suggest that cells which give rise to hemangiosarcoma modulate their microenvironment to promote tumor growth and survival. We propose that the frequent occurrence of canine hemangiosarcoma in defined dog breeds, as well as its similarity to homologous tumors in humans, offers unique models to solve the dilemma of stem cell plasticity and whether angiogenic endothelial cells and hematopoietic cells originate from a single cell or from distinct progenitor cells.</p
Ten-year mortality, disease progression, and treatment-related side effects in men with localised prostate cancer from the ProtecT randomised controlled trial according to treatment received
Background
The ProtecT trial reported intention-to-treat analysis of men with localised prostate cancer randomly allocated to active monitoring (AM), radical prostatectomy, and external beam radiotherapy.
Objective
To report outcomes according to treatment received in men in randomised and treatment choice cohorts.
Design, setting, and participants
This study focuses on secondary care. Men with clinically localised prostate cancer at one of nine UK centres were invited to participate in the treatment trial comparing AM, radical prostatectomy, and radiotherapy.
Intervention
Two cohorts included 1643 men who agreed to be randomised and 997 who declined randomisation and chose treatment.
Outcome measurements and statistical analysis
Analysis was carried out to assess mortality, metastasis and progression and health-related quality of life impacts on urinary, bowel, and sexual function using patient-reported outcome measures. Analysis was based on comparisons between groups defined by treatment received for both randomised and treatment choice cohorts in turn, with pooled estimates of intervention effect obtained using meta-analysis. Differences were estimated with adjustment for known prognostic factors using propensity scores.
Results and limitations
According to treatment received, more men receiving AM died of PCa (AM 1.85%, surgery 0.67%, radiotherapy 0.73%), whilst this difference remained consistent with chance in the randomised cohort (p = 0.08); stronger evidence was found in the exploratory analyses (randomised plus choice cohort) when AM was compared with the combined radical treatment group (p = 0.003). There was also strong evidence that metastasis (AM 5.6%, surgery 2.4%, radiotherapy 2.7%) and disease progression (AM 20.35%, surgery 5.87%, radiotherapy 6.62%) were more common in the AM group. Compared with AM, there were higher risks of sexual dysfunction (95% at 6 mo) and urinary incontinence (55% at 6 mo) after surgery, and of sexual dysfunction (88% at 6 mo) and bowel dysfunction (5% at 6 mo) after radiotherapy. The key limitations are the potential for bias when comparing groups defined by treatment received and changes in the protocol for AM during the lengthy follow-up required in trials of screen-detected PCa.
Conclusions
Analyses according to treatment received showed increased rates of disease-related events and lower rates of patient-reported harms in men managed by AM compared with men managed by radical treatment, and stronger evidence of greater PCa mortality in the AM group.
Patient summary
More than 95 out of every 100 men with low or intermediate risk localised prostate cancer do not die of prostate cancer within 10 yr, irrespective of whether treatment is by means of monitoring, surgery, or radiotherapy. Side effects on sexual and bladder function are better after active monitoring, but the risks of spreading of prostate cancer are more common
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