13 research outputs found

    Concert recording 2016-11-09

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    [Tracks 1-3]. Sonata for piano and violin no. 1 in G major, op. 78 / Johannes Brahms -- [Track 4]. Selections from Dichterliebe, op. 48. Im wunderschönen Monat Mai [Track 5]. Aus meinen Tränen sprießen [Track 6]. Die Rose, die Lilie, die Taube, die Sonne [Track 7]. Ich will meine Seele tauchen [Track 8]. Im Rhein, im heiligen Strome [Track 9]. Ich grolle nicht [Track 10]. Das ist ein Flöten und Geigen [Track 11]. Am leuchtenden Sommermorgen [Track 12]. Ich hab\u27 im Traum geweinet [Track 13]. Aus alten Märchen winkt es / Robert Schumann -- [Track 14-16]. Sonata for clarinet and piano / Francis Poulenc

    Concert recording 2016-04-23a

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    [Track 01]. Interludes for percussion and trumpet. March ; [Track 02]. Elegy ; [Track 03]. Prayer ; [Track 04]. Finale / Marilyn J. Harris ; Mark E. Wolfram -- [Track 05]. Pastorale / Eric Ewazen -- [Track 06]. Animal ditties. The turtle ; [Track 07]. The python ; [Track 08]. The hog ; [Track 09]. The chipmunk ; [Track 10]. The canary ; [Track 11]. The elk / Anthony Plog -- [Track 12]. La revue de cuisine. Prologue ; [Track 13]. Tango ; [Track 14]. Charleston ; [Track 15]. Finale / Bohuslav Martinů

    Concert recording 2016-11-15

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    [Track 1]. Subjugation. Connection [Track 2]. Captivation / Durgan Maxey -- [Track 3]. Fight / Bryce Owens -- [Track 4]. Overture to Stay / Joshua Bland -- [Track 5]. A cellist\u27s legacy. Part I [Track 6]. Part II / Eric Dreggors -- [Track 7]. Evening prayer / Robbie Baker -- [Track 8]. Elegy / Brandon Wade -- [Track 9]. The grotesques trio. Gargoyles [Track 10]. Chimera [Track 11]. Grotesques / Marissa Johnson -- [Track 12]. Crosshair / Joshua Bland -- [Track 13]. Nightwind sings / L. Coley Pitchford -- [Track 14]. Six reflections through poetry. Memories (Walt Whitman) [Track 15]. The musician\u27s wife (Weldon Kees) [Track 16]. The road not taken (Robert Frost) [Track 17]. Lessons (Whitman) [Track 18]. Stronger lessons (Whitman) [Track 19]. O me! O life! (Whitman) / Nick Vecchio -- [Tracks 20-21]. String quartet #1 / Jeremiah Flannery -- [Track 22]. Tides. Morning tide [Track 23]. Bore tide / Elizabeth Greener -- [Track 24]. Shepherd\u27s contemplation / Robbie Baker -- Green grass / arranged by Eva Martin -- [Track 25]. Urbe fracta est II. A prayer for Jerusalem / Joshua Bland

    Concert recording 2016-04-03

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    [Track 01]. Fanfare pour précéder \u27La Péri\u27 / Paul Dukas -- [Track 02]. French dances revisted. I ; [Track 03]. II ; [Track 04]. III ; [Track 05]. IV ; [Track 06]. V ; [Track 07]. VI / Adam Gorb -- [Track 08]. Danses sacrée et profane / Claude Debussy -- [Track 09]. Dance mix / Rob Smith

    Conciencia fonológica y velocidad de denominación entre niños de 5 años de un colegio público y otro privado de Santiago de Surco

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    La presente investigación tiene como objetivo general comparar los predictores de Conciencia Fonológica y Velocidad de Denominación que están estrechamente relacionados con el proceso de la adquisición de la lectoescritura. El enfoque es cuantitativo, de diseño no experimental, de tipo descriptivo - comparativo, que se realiza en una muestra de 94 niños y niñas, de inicial de 5 años, de un colegio privado y otro público del distrito de Santiago de Surco. Para el recojo de datos se utilizan el Test de Habilidades Prelectoras (THP) para evaluar la conciencia fonológica y el Test de Denominación Rápida (TDR) para velocidad de denominación. Los resultados muestran que existen diferencias significativas en los niveles de conciencia silábica y fonémica. Asimismo, en velocidad de denominación de objetos, colores, letras y estímulos alternos. Sin embargo; no se hallan diferencias significativas en la conciencia de rimas y en velocidad de denominación de númerosThe general objective of this research is to compare the predictors of Phonological Awareness and Denomination Velocity that are closely related to the process of acquiring literacy. The approach is quantitative, of non- experimental design, of a descriptive - comparative type, which is carried out in a sample of 94 boys and girls, of initial 5 years, of a private school and another public of the district of Santiago de Surco. For data collection, the Pre-Reading Skills Test (THP) is used to assess phonological awareness and the Rapid Naming Test (TDR) for naming speed. The results show that there are significant differences in the levels of syllabic and phonemic consciousness. Also, in speed of naming objects, colors, letters and alternate stimuli. However; no significant differences are found in the awareness of rhymes and in the speed of number namin

    The surfaceome of multiple myeloma cells suggests potential immunotherapeutic strategies and protein markers of drug resistance.

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    The myeloma surface proteome (surfaceome) determines tumor interaction with the microenvironment and serves as an emerging arena for therapeutic development. Here, we use glycoprotein capture proteomics to define the myeloma surfaceome at baseline, in drug resistance, and in response to acute drug treatment. We provide a scoring system for surface antigens and identify CCR10 as a promising target in this disease expressed widely on malignant plasma cells. We engineer proof-of-principle chimeric antigen receptor (CAR) T-cells targeting CCR10 using its natural ligand CCL27. In myeloma models we identify proteins that could serve as markers of resistance to bortezomib and lenalidomide, including CD53, CD10, EVI2B, and CD33. We find that acute lenalidomide treatment increases activity of MUC1-targeting CAR-T cells through antigen upregulation. Finally, we develop a miniaturized surface proteomic protocol for profiling primary plasma cell samples with low inputs. These approaches and datasets may contribute to the biological, therapeutic, and diagnostic understanding of myeloma

    Cabozantinib in advanced non-clear-cell renal cell carcinoma: a multicentre, retrospective, cohort study

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    BACKGROUND: Cabozantinib is approved for patients with metastatic renal cell carcinoma on the basis of studies done in clear-cell histology. The activity of cabozantinib in patients with non-clear-cell renal cell carcinoma is poorly characterised. We sought to analyse the antitumour activity and toxicity of cabozantinib in advanced non-clear-cell renal cell carcinoma. METHODS: We did a multicentre, international, retrospective cohort study of patients with metastatic non-clear-cell renal cell carcinoma treated with oral cabozantinib during any treatment line at 22 centres: 21 in the USA and one in Belgium. Eligibility required patients with histologically confirmed non-clear-cell renal cell carcinoma who received cabozantinib for metastatic disease during any treatment line roughly between 2015 and 2018. Mixed tumours with a clear-cell histology component were excluded. No other restrictive inclusion criteria were applied. Data were obtained from retrospective chart review by investigators at each institution. Demographic, surgical, pathological, and systemic therapy data were captured with uniform database templates to ensure consistent data collection. The main objectives were to estimate the proportion of patients who achieved an objective response, time to treatment failure, and overall survival after treatment. FINDINGS: Of 112 identified patients with non-clear-cell renal cell carcinoma treated at the participating centres, 66 (59%) had papillary histology, 17 (15%) had Xp11.2 translocation histology, 15 (13%) had unclassified histology, ten (9%) had chromophobe histology, and four (4%) had collecting duct histology. The proportion of patients who achieved an objective response across all histologies was 30 (27%, 95% CI 19-36) of 112 patients. At a median follow-up of 11 months (IQR 6-18), median time to treatment failure was 6·7 months (95% CI 5·5-8·6), median progression-free survival was 7·0 months (5·7-9·0), and median overall survival was 12·0 months (9·2-17·0). The most common adverse events of any grade were fatigue (58 [52%]), and diarrhoea (38 [34%]). The most common grade 3 events were skin toxicity (rash and palmar-plantar erythrodysesthesia; five [4%]) and hypertension (four [4%]). No treatment-related deaths were observed. Across 54 patients with available next-generation sequencing data, the most frequently altered somatic genes were CDKN2A (12 [22%]) and MET (11 [20%]) with responses seen irrespective of mutational status. INTERPRETATION: While we await results from prospective studies, this real-world study provides evidence supporting the antitumour activity and safety of cabozantinib across non-clear-cell renal cell carcinomas. Continued support of international collaborations and prospective ongoing studies targeting non-clear-cell renal cell carcinoma subtypes and specific molecular alterations are warranted to improve outcomes across these rare diseases with few evidence-based treatment options. FUNDING: None.status: publishe

    Association between convalescent plasma treatment and mortality in COVID-19: a collaborative systematic review and meta-analysis of randomized clinical trials

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    Abstract Background Convalescent plasma has been widely used to treat COVID-19 and is under investigation in numerous randomized clinical trials, but results are publicly available only for a small number of trials. The objective of this study was to assess the benefits of convalescent plasma treatment compared to placebo or no treatment and all-cause mortality in patients with COVID-19, using data from all available randomized clinical trials, including unpublished and ongoing trials (Open Science Framework, https://doi.org/10.17605/OSF.IO/GEHFX ). Methods In this collaborative systematic review and meta-analysis, clinical trial registries (ClinicalTrials.gov, WHO International Clinical Trials Registry Platform), the Cochrane COVID-19 register, the LOVE database, and PubMed were searched until April 8, 2021. Investigators of trials registered by March 1, 2021, without published results were contacted via email. Eligible were ongoing, discontinued and completed randomized clinical trials that compared convalescent plasma with placebo or no treatment in COVID-19 patients, regardless of setting or treatment schedule. Aggregated mortality data were extracted from publications or provided by investigators of unpublished trials and combined using the Hartung–Knapp–Sidik–Jonkman random effects model. We investigated the contribution of unpublished trials to the overall evidence. Results A total of 16,477 patients were included in 33 trials (20 unpublished with 3190 patients, 13 published with 13,287 patients). 32 trials enrolled only hospitalized patients (including 3 with only intensive care unit patients). Risk of bias was low for 29/33 trials. Of 8495 patients who received convalescent plasma, 1997 died (23%), and of 7982 control patients, 1952 died (24%). The combined risk ratio for all-cause mortality was 0.97 (95% confidence interval: 0.92; 1.02) with between-study heterogeneity not beyond chance (I2 = 0%). The RECOVERY trial had 69.8% and the unpublished evidence 25.3% of the weight in the meta-analysis. Conclusions Convalescent plasma treatment of patients with COVID-19 did not reduce all-cause mortality. These results provide strong evidence that convalescent plasma treatment for patients with COVID-19 should not be used outside of randomized trials. Evidence synthesis from collaborations among trial investigators can inform both evidence generation and evidence application in patient care
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