Relevant bibliographies by topics / MCP-Counter

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  1. Journal articles
  2. Dissertations / Theses
  3. Conference papers

Academic literature on the topic 'MCP-Counter'

Author: Grafiati
Published: 25 May 2024

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Journal articles on the topic "MCP-Counter"

1

Inami, K. "MCP-PMT development for Belle-II TOP counter." Physics Procedia 37 (2012): 683–90. http://dx.doi.org/10.1016/j.phpro.2012.02.417.

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Inami, K., N. Kishimoto, Y. Enari, M. Nagamine, and T. Ohshima. "A 5 ps TOF-counter with an MCP–PMT." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 560, no. 2 (2006): 303–8. http://dx.doi.org/10.1016/j.nima.2006.01.027.

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Jung, Seok-Kyu, and Jung-Myung Lee. "(32) Effects of 1-MCP Treatments on Several Major Apple Cultivars Grown in Korea." HortScience 40, no. 4 (2005): 1004D—1004. http://dx.doi.org/10.21273/hortsci.40.4.1004d.

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Fruits of `Tsugaru' (an early maturing cultivar), `Hongro' (mid-season cultivar), and `Fuji' (late cultivar), were harvested at different times of the year, depending upon their maturity, and treated with 1-MCP at 0.0, 0.5, 1.0, and 2.0 ppm for 8-24 hours. Fruits were also treated with 1-MCP at different times after harvest. Portions of 1-MCP-treated apples were also treated with ethylene in order to study the interaction between 1-MCP and ethylene. In other experiments, fruits were treated with ethylene first and then treated again with 1-MCP. Major results are as follows. Treatment of 1-MCP
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Gruss, H. J., M. A. Brach, R. R. Schumann, and F. Herrmann. "Regulation of MCP-1/JE gene expression during monocytic differentiation." Journal of Immunology 153, no. 11 (1994): 4907–14. http://dx.doi.org/10.4049/jimmunol.153.11.4907.

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Abstract We examined the expression of the MCP-1/JE gene in freshly prepared human monocytes and again after either in vitro or in vivo maturation of these cells. We show that previously unstimulated blood monocytes of healthy individuals prepared by adherence procedures display high levels of MCP-1/JE mRNA and protein. Monocytes that were not previously exposed to activational plastic surfaces but were separated from other blood cells by counter-flow centrifugal elutriation expressed severalfold lower MCP-1/JE transcript and protein levels. Treatment of these cells with endotoxin was associat
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Calvi, M., S. Capelli, P. Carniti, C. Gotti, and G. Pessina. "Single photon counting performance of the Auratek-Square MCP-PMT." Journal of Instrumentation 17, no. 11 (2022): P11009. http://dx.doi.org/10.1088/1748-0221/17/11/p11009.

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Abstract This paper reports on the time resolution of the Auratek-Square MCP-PMT, a multi-anode microchannel plate photomultiplier produced by Photek. When operating as single photon counter at low photon rate and with a single pixel illuminated it shows a transit time spread (jitter) of ∼100 ps FWHM, saturating at high rate, above ∼100 kHz/mm2. The worsening of the timing performance depends on the bias voltage between the photocathode and the MCP input and between the MCP slabs. The charge sharing between neighbouring pixels can become a major crosstalk source if not accounted for, degrading
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Wierzbicki, Jarosław, Artur Lipiński, Iwona Bednarz-Misa, et al. "Monocyte Chemotactic Proteins (MCP) in Colorectal Adenomas Are Differently Expressed at the Transcriptional and Protein Levels: Implications for Colorectal Cancer Prevention." Journal of Clinical Medicine 10, no. 23 (2021): 5559. http://dx.doi.org/10.3390/jcm10235559.

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The expression of monocyte chemotactic proteins (MCPs) in colorectal polyps and their suitability as targets for chemoprevention is unknown, although MCP expression and secretion can be modulated by non-steroidal inflammatory drugs. This study was designed to determine the expression patterns of MCP-1/CCL2, MCP-2/CCL8, and MCP-3/CCL7 at the protein (immunohistochemistry; n = 62) and transcriptional levels (RTqPCR; n = 173) in colorectal polyps with reference to the polyp malignancy potential. All chemokines were significantly upregulated in polyps at the protein level but downregulated at the
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Nagaraju, Raju, Apurva Kumar R. Joshi, Sowmya Giriyapura Vamadeva, and Rajini Padmanabhan Sharda. "Plasma paraoxonase1 activity in rats treated with monocrotophos: a study of the effect of duration of exposure." Interdisciplinary Toxicology 12, no. 3 (2019): 129–35. http://dx.doi.org/10.2478/intox-2019-0015.

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Abstract We have earlier demonstrated the potential of monocrotophos (MCP), a highly toxic organophosphorus insecticide (OPI), to elicit insulin resistance in rats after chronic exposure. Given the understanding of role of paraoxonase1 (PON1) in OPI toxicity and diabetes pathology, this study was envisaged to understand the effect of duration of exposure to MCP on plasma PON1 activity in rats. Rats were administered MCP per os at 1/20 and 1/10th LD50 as daily doses for 180 days. Interim blood samples were collected at 15, 30, 45, 90 and 180 d for analysis of plasma parameters. Exposure to MCP
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Akiyoshi, Takashi, Zhe Wang, Tomoko Kaneyasu, et al. "Transcriptomic Analyses of Pretreatment Tumor Biopsy Samples, Response to Neoadjuvant Chemoradiotherapy, and Survival in Patients With Advanced Rectal Cancer." JAMA Network Open 6, no. 1 (2023): e2252140. http://dx.doi.org/10.1001/jamanetworkopen.2022.52140.

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ImportanceNeoadjuvant chemoradiotherapy (CRT) is the standard of care for advanced rectal cancer. Yet, estimating response to CRT remains an unmet clinical challenge.ObjectiveTo investigate and better understand the transcriptomic factors associated with response to neoadjuvant CRT and survival in patients with advanced rectal cancer.Design, Setting, and ParticipantsA single-center, retrospective, case series was conducted at a comprehensive cancer center. Pretreatment biopsies from 298 patients with rectal cancer who were later treated with neoadjuvant CRT between April 1, 2004, and September
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Matsuoka, K. "Development and production of the MCP-PMT for the Belle II TOP counter." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 766 (December 2014): 148–51. http://dx.doi.org/10.1016/j.nima.2014.05.003.

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White, Kieron, Maxime Meylan, Antoine Bougoüin, et al. "TAMI-51. IDENTIFYING NEW TUMOR MICROENVIRONMENT (TME) CONTEXTS OF VULNERABILITY IN GLIOBLASTOMA." Neuro-Oncology 22, Supplement_2 (2020): ii224. http://dx.doi.org/10.1093/neuonc/noaa215.938.

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Abstract Glioblastoma (GBM) is the most frequent and aggressive adult brain tumor with 85% of patients dying within two years. New effective precision medicine therapies are urgently required, especially for isocitrate dehydrogenase wild-type (IDHwt) disease. Despite efforts to subtype patients based on molecular profiles, this approach has yet failed to direct treatment strategies. Further interrogation of the tumor microenvironment (TME) across molecular subtypes and identification of new TME specific subtypes may guide new directions for future therapies. Here, we analysed transcriptomic da
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Dissertations / Theses on the topic "MCP-Counter"

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De, Vries-Brilland Manon. "Caractérisation du microenvironnement immunitaire des carcinomes papillaires du rein." Electronic Thesis or Diss., Angers, 2023. http://www.theses.fr/2023ANGE0017.

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Article 1 : Inhibiteurs de points de contrôle dans le carcinome rénal papillaire métastatique : le carcinome papillaire à cellules rénales (pRCC) est le CCR à cellules non claires (nccRCC) le plus courant et une entité distincte, bien qu'hétérogène, associée à de mauvais pronostics. Le paysage thérapeutique du pRCC métastatique (mpRCC) reposait jusqu'à présent sur des thérapies ciblées, imitant les développements antérieurs dans le carcinome rénal métastatique à cellules claires. Cependant, les antiangiogéniques ainsi que les inhibiteurs de mTOR ne conservent qu'une activité limitée dans le mp
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Conference papers on the topic "MCP-Counter"

1

Matsuoka, Kodai, Shigeki Hirose, Toru Iijima, et al. "Performance of the MCP-PMT for the Belle II TOP counter." In International Conference on New Photo-detectors. Sissa Medialab, 2016. http://dx.doi.org/10.22323/1.252.0028.

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Cho, Doo Jin, and G. Michael Morris. "Dead-time effects in curved-channel microchannel plates." In OSA Annual Meeting. Optica Publishing Group, 1989. http://dx.doi.org/10.1364/oam.1989.wq4.

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Dead-time effects of microchannel plates (MCPs) are due to the recharging time of the semiconducting inner wall of individual microchannels. To study the dependence of dead-time effects on the area of illumination, circular apertures of different size are imaged onto the curved-channel microchannel plate (C-MCP) using ultraviolet light (257.3 nm). It is found that an independent paralyzable counter (IPC) model, which assumes that individual microchannels of the C-MCP behave as independent paralyzable counters with a fixed dead time, agrees well with experimental results. Except for the case of
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YONEKURA, Takuya. "Performance of the MCP-PMTs for the TOP counter in the Belle II experiment." In Technology and Instrumentation in Particle Physics 2014. Sissa Medialab, 2015. http://dx.doi.org/10.22323/1.213.0082.

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Matsuoka, Kodai. "Performance of the MCP-PMTs of the TOP Counter in the First Beam Operation of the Belle II Experiment." In Proceedings of the 5th International Workshop on New Photon-Detectors (PD18). Journal of the Physical Society of Japan, 2019. http://dx.doi.org/10.7566/jpscp.27.011020.

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