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Institution

University of Trento

EducationTrento, Italy
About: University of Trento is a education organization based out in Trento, Italy. It is known for research contribution in the topics: Population & Large Hadron Collider. The organization has 10527 authors who have published 30978 publications receiving 896614 citations. The organization is also known as: Universitá degli Studi di Trento & Universita degli Studi di Trento.


Papers
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Journal ArticleDOI
05 Dec 2012-PLOS ONE
TL;DR: This test is considered to be an accurate, fast and relatively cheap method for retroviral quantification that is easily implemented for use in routine and research laboratories.
Abstract: Quantification of retroviruses in cell culture supernatants and other biological preparations is required in a diverse spectrum of laboratories and applications. Methods based on antigen detection, such as p24 for HIV, or on genome detection are virus specific and sometimes suffer from a limited dynamic range of detection. In contrast, measurement of reverse transcriptase (RT) activity is a generic method which can be adapted for higher sensitivity using real-time PCR quantification (qPCR-based product-enhanced RT (PERT) assay). We present an evaluation of a modified SYBR Green I-based PERT assay (SG-PERT), using commercially available reagents such as MS2 RNA and ready-to-use qPCR mixes. This assay has a dynamic range of 7 logs, a sensitivity of 10 nU HIV-1 RT and outperforms p24 ELISA for HIV titer determination by lower inter-run variation, lower cost and higher linear range. The SG-PERT values correlate with transducing and infectious units in HIV-based viral vector and replication-competent HIV-1 preparations respectively. This assay can furthermore quantify Moloney Murine Leukemia Virus-derived vectors and can be performed on different instruments, such as Roche Lightcycler® 480 and Applied Biosystems ABI 7300. We consider this test to be an accurate, fast and relatively cheap method for retroviral quantification that is easily implemented for use in routine and research laboratories.

164 citations

Journal ArticleDOI
TL;DR: Although the study did not meet its primary endpoint, a subset of patients with advanced prostate cancer and molecular features supporting Aurora-A and N-myc activation achieved significant clinical benefit from single-agent alisertib.
Abstract: Purpose: Neuroendocrine prostate cancer (NEPC) is an aggressive variant of prostate cancer that may develop de novo or as a mechanism of treatment resistance. N-myc is capable of driving NEPC progression. Alisertib inhibits the interaction between N-myc and its stabilizing factor Aurora-A, inhibiting N-myc signaling, and suppressing tumor growth. Patients and Methods: Sixty men were treated with alisertib 50 mg twice daily for 7 days every 21 days. Eligibility included metastatic prostate cancer and at least one: small-cell neuroendocrine morphology; ≥50% neuroendocrine marker expression; new liver metastases without PSA progression; or elevated serum neuroendocrine markers. The primary endpoint was 6-month radiographic progression-free survival (rPFS). Pretreatment biopsies were evaluated by whole exome and RNA-seq and patient-derived organoids were developed. Results: Median PSA was 1.13 ng/mL (0.01–514.2), number of prior therapies was 3, and 68% had visceral metastases. Genomic alterations involved RB1 (55%), TP53 (46%), PTEN (29%), BRCA2 (29%), and AR (27%), and there was a range of androgen receptor signaling and NEPC marker expression. Six-month rPFS was 13.4% and median overall survival was 9.5 months (7.3–13). Exceptional responders were identified, including complete resolution of liver metastases and prolonged stable disease, with tumors suggestive of N-myc and Aurora-A overactivity. Patient organoids exhibited concordant responses to alisertib and allowed for the dynamic testing of Aurora–N-myc complex disruption. Conclusions: Although the study did not meet its primary endpoint, a subset of patients with advanced prostate cancer and molecular features supporting Aurora-A and N-myc activation achieved significant clinical benefit from single-agent alisertib.

163 citations

Journal ArticleDOI
TL;DR: Perelmouter et al. as mentioned in this paper have been teaching severely or totally paralyzed patients to successfully control the movements of a cursor on a computer screen by means of systematic changes in the amplitudes of their slow cortical potentials.
Abstract: Since 1996 we have been teaching more than 18 severely or totally paralyzed patients to successfully control the movements of a cursor on a computer screen by means of systematic changes in the amplitudes of their slow cortical potentials (SCPs; Birbaumer, Ghanayim, Hinterberger, Iversen, Kotchoubey et al., 1999). Patients learned regulation of their SCP amplitudes by means of a brain-computer interface (BCI) and on-line feedback about the time course of SCP amplitude shifts, represented by cursor movements on a computer screen. When patients were able to successfully regulate their SCP amplitude, they were trained to use this ability to communicate with friends and caregivers by means of a Language Support Program (Perelmouter, Kotchoubey, Kubler, Taub, & Birbaumer, 1999). Having a reliable predictor of progress in training would be particularly helpful because training patients at their homes requires substantial effort and a positive outcome is desirable given limited personal and financial re...

163 citations

Journal ArticleDOI
TL;DR: In this paper, the authors examined a network of charging stations equipped with an energy storage device and proposed a scheme that allocates power to them from the grid, as well as routes customers.
Abstract: In order to increase the penetration of electric vehicles, a network of fast charging stations that can provide drivers with a certain level of quality of service (QoS) is needed. However, given the strain that such a network can exert on the power grid, and the mobility of loads represented by electric vehicles, operating it efficiently is a challenging and complex problem. In this paper, we examine a network of charging stations equipped with an energy storage device and propose a scheme that allocates power to them from the grid, as well as routes customers. We examine three scenarios, gradually increasing their complexity. In the first one, all stations have identical charging capabilities and energy storage devices, draw constant power from the grid and no routing decisions of customers are considered. It represents the current state of affairs and serves as a baseline for evaluating the performance of the proposed scheme. In the second scenario, power to the stations is allocated in an optimal manner from the grid and in addition a certain percentage of customers can be routed to nearby stations. In the final scenario, optimal allocation of both power from the grid and customers to stations is considered. The three scenarios are evaluated using real traffic traces corresponding to weekday rush hour from a large metropolitan area in the US. The results indicate that the proposed scheme offers substantial improvements of performance compared to the current mode of operation; namely, more customers can be served with the same amount of power, thus enabling the station operators to increase their profitability. Further, the scheme provides guarantees to customers in terms of the probability of being blocked (and hence not served) by the closest charging station to their location. Overall, the paper addresses key issues related to the efficient operation, both from the perspective of the power grid and the drivers satisfaction, of a network of charging stations.

163 citations

Journal ArticleDOI
TL;DR: A significant influence of ovarian hormone level on emotion processing and an important neural correlate, the amygdala, may enable a higher social sensitivity in females during their follicular phase, thus facilitating socio-emotional behavior (and social interaction) which may possibly facilitate mating behavior as well.

163 citations


Authors

Showing all 10758 results

NameH-indexPapersCitations
Yi Chen2174342293080
Jie Zhang1784857221720
Richard B. Lipton1762110140776
Jasvinder A. Singh1762382223370
J. N. Butler1722525175561
Andrea Bocci1722402176461
P. Chang1702154151783
Bradley Cox1692150156200
Marc Weber1672716153502
Guenakh Mitselmakher1651951164435
Brian L Winer1621832128850
J. S. Lange1602083145919
Ralph A. DeFronzo160759132993
Darien Wood1602174136596
Robert Stone1601756167901
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023158
2022340
20212,399
20202,286
20192,129
20181,943