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Academic literature on the topic 'Nude in a rt'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Nude in a rt"

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Lu, Victor M., and Kerrie L. McDonald. "Lanthanum nanoparticles to target the brain: proof of biodistribution and biocompatibility with adjuvant therapies." Nanomedicine 15, no. 22 (September 2020): 2107–17. http://dx.doi.org/10.2217/nnm-2020-0165.

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Aim: To determine the biodistribution of lanthanum (III) oxide (La2O3) nanoparticle (NP) therapy to the brain and its biocompatibility with radiation therapy (RT) and chemotherapy (CT). Materials & methods: Healthy balb/c nude mice were administered 4 weekly doses of La2O3 NP therapy via tail vein injection. Organ weights and lanthanum concentrations were evaluated. Results: La2O3 NP penetrated the brain. Concentrations were found to peak in the brain at 24 h after injection and persisted at 8 weeks after injection. Neither RT nor CT affected biodistribution. No adverse events or safety concerns in other organs were noted. Conclusion: La2O3 NP can reach the brain to target neurological disease and is biocompatible with RT and CT in a biological system.

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Zhu, Xiangyu, Si-ping Ma, Dongxiang Yang, Yanlong Liu, Yong-peng Wang, Tao Lin, Yan-xi Li, Shi-hua Yang, Wan-chuan Zhang, and Xin-ling Wang. "miR-142-3p Suppresses Cell Growth by Targeting CDK4 in Colorectal Cancer." Cellular Physiology and Biochemistry 51, no. 4 (2018): 1969–81. http://dx.doi.org/10.1159/000495721.

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Background/Aims: Deregulation of microRNAs (miRNAs) has been associated with a variety of cancers, including colorectal cancer (CRC). Here, we investigated anomalous miR-142-3p expression and its possible functional consequences in primary CRC samples. Methods: The expression of miR-142-3p was measured by quantitative RT-PCR in 116 primary CRC tissues and adjacent non-tumor tissues. The effect of miR-142-3p up- or down-regulation in CRC-derived cells was evaluated in vitro by cell viability and colony formation assays and in vivo by growth assays in xenografted nude mice. Results: Using quantitative RT-PCR, we found that miR-142-3p was down-regulated in 78.4 % (91/116) of the primary CRC tissues tested when compared to the adjacent non-tumor tissues. We also found that the miR-142-3p mimic reduced in vitro cell viability and colony formation by inducing cell cycle arrest in CRC-derived cells, and inhibited in vivo tumor cell growth in xenografted nude mice. Inversely, we found that the miR-142-3p inhibitor increased the viability and colony forming capacity of CRC-derived cells and tumor cell growth in xenografted nude mice. In addition, we identified CDK4 as a potential target of miR-142-3p by predictions and dual-luciferase reporter assays. Concordantly, we found that miR-142-3p mimics and inhibitors could decrease and increase CDK4 protein levels in CRC-derived cells, respectively. Conclusion: From our results we conclude that miR-142-3p may act as a tumor suppressor in CRC and may serve as a tool for miRNA-based CRC therapy.

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Wang, R. F., W. L. Campbell, W. W. Cao, R. M. Colvert, M. A. Holland, and C. E. Cerniglia. "Diagnosis of mouse hepatitis virus contamination in mouse population by using nude mice and RT-PCR." Molecular and Cellular Probes 13, no. 1 (February 1999): 29–33. http://dx.doi.org/10.1006/mcpr.1998.0211.

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Zhao, Lijuan, Fei Wang, and Wei Fan. "Cisplatin Nano-Liposomes Promoting Apoptosis of Retinoblastoma Cells Both In Vivo and In Vitro." Nanoscience and Nanotechnology Letters 12, no. 4 (April 1, 2020): 536–42. http://dx.doi.org/10.1166/nnl.2020.3127.

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This study was established to investigate the effects of cisplatin nano-liposomes on the apoptosis of the human retinoblastoma (RB) cell line Y79 in vitro and in vivo. Y79 cells were cultured and then exposed to Annexin V/PI to test their apoptosis, tested with the Caspase-3 activity detection kit to examine the change in activity of Caspase-3, and subjected to western blotting to test Bcl-2 and Bax protein expression. Y79-cell-transplanted tumor model in nude mice was also established and divided into three groups, with five nude mice in each. Cisplatin nano-liposomes were applied to the experimental group, cisplatin was injected into the control group, while saline was administered to the blank group, after which the nude mice were killed and the tumor was removed. Tumor volumes and weights in the three groups were compared. Nucleic acid extraction from magnetic beads was adopted to extract DNA, RT-PCR was employed to test Bcl-2 and Bax mRNA levels in tumor tissues, and in situ cell death assay kit was applied to test apoptotic cells. In comparison to the cisplatin solution and DMSO groups, the cisplatin liposome group showed higher Y79 apoptotic rate, Caspase-3 activity, and Bax protein expression, and lower Bcl-2 protein expression (all P < 0 05). In comparison with the control and blank groups, the experimental group showed lower tumor volume, weight, and Bcl-2 mRNA level of nude mice. In addition, in comparison with the control group, the experimental group showed higher cellular apoptotic rate and Bax mRNA level. In terms of the clinical effects of cisplatin nano-liposomes on a tumor transplant in nude mice with cervical cancer, they were shown to promote tumor apoptosis.

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Zhao, Qian, Xin Zhu, Jin-ming Ke, Xiao-yu Su, Jing Yi, De-long Wu, Jiang Lin, and Zhao-qun Deng. "Circular RNA BMI1 Serves as a Potential Target for Diagnosis and Treatment in Esophageal Cancer." Technology in Cancer Research & Treatment 20 (January 1, 2021): 153303382110330. http://dx.doi.org/10.1177/15330338211033075.

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Aims: Previous studies have confirmed that BMI1 is elevated in esophageal cancer, which is a potential therapeutic target for esophageal cancer. However, the clinical significance of circular RNA BMI1 (circ-BMI1) in esophageal cancer is not yet clear. Herein, we revealed the clinical implication of circ-BMI1 in esophageal cancer, and provided a theoretical basis for molecular diagnosis and potential targeted therapy of esophageal cancer. Methods: Firstly, 10 fresh paired esophageal cancer tissues and paracancer tissues, 49 esophageal cancer serum samples and 28 healthy control serum samples were involved in our study. Differential expression and clinical significance of circ-BMI1 in esophageal cancer patients and healthy controls were evaluated by quantitative Real-time RT-PCR (RT-qPCR). Secondly, effects of circ-BMI1 differential expression on biological function of esophageal cancer cell line Eca109 were analyzed. Effects of circ-BMI1 on cell proliferation, migration and colony forming ability were evaluated by CCK-8, wound healing, and colony-forming assay. Cell apoptosis, drug sensitivity tests were also be conducted. Finally, influence of Eca109 cells differentially expressed by circ-BMI1 on tumorigenicity in nude mice was studied. Results: Expression of circ-BMI1 in serum and tissues of esophageal cancer patients was significantly decreased compared to controls ( P < 0.001 and P = 0.003, respectively). Area under the receiver operating characteristic curve (ROC) was 0.726. Cell proliferation, migration and colony forming ability of circBMI1-Eca109 cells were obviously decreased than that of NC-Eca109 cells ( P < 0.05). circBMI1-Eca109 cells were more sensitive to 5-fluorouracil and cisplatin, and tumor volume of nude mice in circBMI1-Eca109 group was smaller ( P < 0.05). Conclusions: The study indicated that expression of circ-BMI1 was significantly down-regulated in esophageal cancer. Overexpression of circ-BMI1 inhibited proliferation, migration, colony formation of Eca109 cells, and tumor growth of Eca109 cells in nude mice. circ-BMI1 may be a potential target for diagnosis and treatment in esophageal cancer.

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Wang, Jishi, Yuan Yang, Wei Zhang, and Pengxiang Guo. "Targeted Anti-Tumor Research of Mesenchymal Stem Cells Delivered Enzyme-Prodrug Gene CYP450." Blood 114, no. 22 (November 20, 2009): 3582. http://dx.doi.org/10.1182/blood.v114.22.3582.3582.

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Abstract Abstract 3582 Poster Board III-519 Objective Cytochrome P450(CYP450-CYP1A2 /CYP2B6/CYP2C9) was transfected into human bone marrow-derived mesenchymal stem cells (hBMSCs), and the targed anti-tumor effect of BMSC-CYP450 cooperated with enzyme-prodrug(Dacarbazine (DTIC)/Cyclophosphamide (CPA)) was measured to provide laboratory data base for gene directed enzyme prodrug targeted anti-tumor therapy (GDEPT) which used BMSC as vehicles. Methods We respectively cloned CYP1A2/CYP2B6/CYP2C9 cDNA from human liver and constructed recombinant adenovirus vectors(pAd5CMV-NpA-CYP1A2/ pAd5CMV-NpA-CYP2B6/pAd5CMV-NpA-CYP2C9) which titer was 1×1012 pfu/mL. These hBMSCs were separated, cultured, purified, and detected by morphology, flow cytometry, osteogenic, adipogenic and chondrogenic induction, and RT-PCR(A surface marker for the identification of MSCs-the neural ganglioside GD2 gene). The tropism of BMSCs for cancer cells was detected by Transwell inserts technique. These recombinant vectors were transferred into BMSCs and A375/K562 cells, and the expression of EGFP and CYP1A2/CYP2B6/CYP2C9 was detected by fluorescence microscope, RT-PCR and Western blot respectively. Inverted microscope, MTT and Annexin V-FITC/PI detected the anti-tumor effect of CYP450 recombinant adenovirus vectors combined with chemotherapeutic prodrug DTIC/CPA in vitro. A human melanoma(A375) BALB/c nude mice model and a human myelocytic leukemia(K562) BALB/c nude mice model was constructed and detected by immuno-histochemistry analysis. The CYP1A2 gene tranfected BMSCs were injected into the A375 BALB/c nude mice model in combination with DTIC through caudal vein, while CYP2B6/CYP2C9 gene tranfected BMSCs were injected into K562 BALB/c nude mice model in combination with CPA in the same way. The measurement of tumors size, fluorescence microscope and TUNEL were used to detect anti-tumor effect of BMSCs-CYP1A2 cooperating with DTIC and BMSCs-CYP2B6/CYP2C9 with CPA in vivo. Results We constructed the recombinant adenovirus vectors pAd5CMV-NpA-CYP1A2/pAd5CMV-NpA-CYP2B6/pAd5CMV-NpA-CYP2C9 and pAd5CMV-NpA-EGFP successfully. BMSCs was separated successfully, and it respectively showed that BMSCs can migrate through the polycarbonate filter toward K562 and A375 cells in the lower chamber in vitro. Fluorescence microscope detected the expression of EGFP, while both RT-PCR and Western blot detected high expression of CYP1A2/CYP2B6/CYP2C9 in gene-transfected group cells. Inverted microscope, MTT and Annexin V-FITC/PI confirmed that BMSCs transferred with CYP1A2/CYP2B6/CYP2C9 recombinant adenovirus vectors could activate DTIC/CPA and increase its anti-tumor effect(In the DTIC/CPA concentration(0.05 mmol/L/2.5 mmol/L) which BMSCs was relatively safe, the cell apoptosis was (38.38±2.27)% (P<0.01), (42.69±2.03)% (P<0.01) and (39. 51±1.94)% (P<0.01) in BMSCs-CYP1A2+A375 group, BMSCs-CYP2B6+K562 group and BMSCs-CYP2C9+K562 group respectively. ). A375 and K562 BALB/c nude mice model was constructed successfully. The sizes of the tumor in the nude mice treated with transfected BMSCs and DTIC/CPA were significantly smaller than control case and changed along with concentration(P< 0.01, P< 0.05).BMSCs was congregated to tumor site in fluorescence microscope. Apoptosis of tumor cells was conspicuously more in BMSCs-CYP1A2+A375/BMSCs-CYP2B6+K562/BMSCs-CYP2C9+K562 treatment group than in control group by TUNEL. Conclusion BMSCs had the tropism for cancer cells in vitro and vivo. DTIC can be catalyzed by CYP2E1/CYP1A2, while CPA by CYP2B6/CYP2C9 in vitro and vivo. BMSC-based enzyme prodrug system of CYP2E1/CYP1A2 and DTIC can induce A375 cells apoptosis, while BMSC-based enzyme prodrug system of CYP2B6/CYP2C9 and CPA can induce K562 cells apoptosis in vitro and targetedly in vivo. Disclosures: No relevant conflicts of interest to declare.

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Wason, Melissa, Heng Lu, Lin Yu, Satadru Lahiri, Debarati Mukherjee, Chao Shen, Soumen Das, Sudipta Seal, and Jihe Zhao. "Cerium Oxide Nanoparticles Sensitize Pancreatic Cancer to Radiation Therapy through Oxidative Activation of the JNK Apoptotic Pathway." Cancers 10, no. 9 (September 1, 2018): 303. http://dx.doi.org/10.3390/cancers10090303.

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Side effects of radiation therapy (RT) remain the most challenging issue for pancreatic cancer treatment. Cerium oxide nanoparticles (CONPs) are currently being tested in pre-clinical trials as an adjuvant to sensitize pancreatic cancer cells to RT and protect normal tissues from the harmful side effects. CONPs were not able to significantly affect RT-induced DNA damage in cancer cells, thereby ruling out sensitization through increased mitotic catastrophe. However, activation of c-Jun terminal kinase (JNK), a key driver of RT-induced apoptosis, was significantly enhanced by co-treatment with CONPs and RT in pancreatic cancer cells in vitro and human pancreatic tumors in nude mice in vivo compared to CONPs or RT treatment alone. Further, CONP-driven increase in RT-induced JNK activity was associated with a marked increase in Caspase 3/7 activation, indicative of apoptosis. We have previously shown that CONPs increase reactive oxygen species (ROS) production in cancer cells. ROS has been shown to drive the oxidation of thioredoxin 1 (TRX1) which results in the activation of apoptosis signaling kinase 1 (ASK1). The increase in ASK1 activation following the co-treatment with CONPs followed by RT suggests that the increased JNK activation is the result of increased TRX1 oxidation. The ability of CONPs to sensitize pancreatic cancer cells to RT was mitigated when the TRX1 oxidation was prevented by mutagenesis of a cysteine residue or when the JNK activation was blocked by an inhibitor. Taken together, these data demonstrate an important mechanism for CONPs in specifically killing cancer cells and provide novel insights into the utilization of CONPs as a radiosensitizer and therapeutic agent for pancreatic cancer.

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Tang, Renyan, Jianmin Zhu, Ying Liu, Ning Wu, and Jinbin Han. "Formulation Comprising Arsenic Trioxide and Dimercaprol Enhances Radiosensitivity of Pancreatic Cancer Xenografts." Technology in Cancer Research & Treatment 20 (January 1, 2021): 153303382110363. http://dx.doi.org/10.1177/15330338211036324.

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Objective: To investigate the efficacy of a formula comprising arsenic trioxide and dimercaprol (BAL-ATO) as a radiosensitizing agent in model mice with pancreatic cancer xenografts. Methods: Female BALB/c nude mice bearing SW1990 human pancreatic cancer xenografts were divided into four treatment arms, including control, radiotherapy (RT), BAL-ATO, and RT + BAL-ATO groups. Survival and tumor volume were analyzed. We also assessed apoptosis in tumor samples by live imaging and detected hypoxia by confocal laser microscope observation. We further investigated the mechanisms of BAL-ATO action in RT by detecting affected proteins by western blot and immunohistochemistry assays. Results: Median survival was significantly longer in the RT + BAL-ATO group (64.5 days) compared with the control (49.5 days), RT (39 days), and BAL-ATO (48 days) groups ( P < 0.001). RT + BAL-ATO inhibited the growth of tumors in mice by 73% compared with the control group, which was significantly higher than the rate of inhibition following RT alone (59%) ( P < 0.01). Further analysis showed an improved microenvironment in terms of hypoxia in tumors treated with BAL-ATO alone or RT + BAL-ATO. Expression of signaling molecules associated with pancreatic cancer stem cells, including CD24, CD44, ALDH1A1, Gli-1, and Nestin, was detected in tumors treated with BAL-ATO alone or in combination with RT. Conclusion: These data suggest that BAL-ATO function as a radiosensitizer in mice with pancreatic cancer xenografts, via mechanisms involving hypoxia reduction and inhibition of signaling pathways associated with pancreatic cancer stem cells. BAL-ATO may thus be a promising radiosensitizing agent in patients with pancreatic cancer.

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Li, Xian, Long Xia, Xiaohui Ouyang, Qimuge Suyila, Liya Su, and Xiulan Su. "Bioactive Peptides Sensitize Cells to Anticancer Effects of Oxaliplatin in Human Colorectal Cancer Xenografts in Nude Mice." Protein & Peptide Letters 26, no. 7 (July 22, 2019): 512–22. http://dx.doi.org/10.2174/0929866526666190405124955.

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<P>Background: Despite new agent development and short-term benefits in patients with Colorectal Cancer (CRC), metastatic CRC cure rates have not improved due to high rates of oxaliplatin resistance and toxicity. There is an urgent need for effective tools to prevent and treat CRC and reduce morbidity and mortality of CRC patients. Exploring the effects of bioactive peptides on the antitumor to CRC was of vital importance to the clinical application. </P><P> Objective: This study aimed to investigate the therapeutic impact of Anticancer Bioactive Peptides (ACBP) on anticancer effect of oxaliplatin (LOHP) in human colorectal cancer xenografts models in nude mice. </P><P> Methods: HCT-116 cells were cultured in vitro via CCK-8 assays and the absorbance was measured at 450 nm. Apoptosis and cell cycle were assessed by Flow Cytometry (FCM) in vitro. HCT-116 human colorectal cancer cells inoculated subcutaneously in nude mice of treatment with PBS (GG), ACBP, LOHP, ACBP+LOHP (A+L) in vivo. The quality of life was assessed by dietary amount of nude mice, the weight of nude mice, inhibition rates, tumor weight and tumor volume. Immunohistochemistry and RT-qPCR method was conducted to determine the levels of apoptosisregulating proteins/genes in transplanted tumors. </P><P> Results: ACBP induced substantial reductions in viable cell numbers and apoptosis of HCT116 cells in combined with LOHP in vitro. Compared with the control GG group, ACBP combined low dose oxaliplatin (U) group demonstrated significantly different tumor volume, the rate of apoptosis, the expression levels of Cyt-C, caspase-3,8,9 proteins and corresponding RNAs (P<0.05). The expression of pro-apoptotic proteins in the cytoplasm around the nucleus was significantly enhanced by ACBP. Short term intermittent use of ACBP alone indicted a certain inhibitory effect on tumor growth, and improve the quality of life of tumor bearing nude mice. </P><P> Conclusion: ACBP significantly increased the anti-cancer responses of low dose oxaliplatin (L-LOHP), thus, significantly improving the quality of life of tumor-bearing nude mice.</P>

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Liu, Yang. "Detection of blood AFPmRNA in nude mice bearing human HCC using nested RT-PCR and its significance." World Journal of Gastroenterology 4, no. 3 (1998): 268. http://dx.doi.org/10.3748/wjg.v4.i3.268.

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Dissertations / Theses on the topic "Nude in a rt"

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Stubblefield, Shannon. "The nude female performer." Thesis, Mills College, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=1562505.

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A live nude female performer can occupy a powerful identity equal to a man because she willingly places herself in front of an audience. She commits to this state of profound vulnerability as a means of gaining ownership of her body that men by virtue of their power in society take for granted. The female body occupies physical space, unlike how a body image seen on a television or in a magazine does. The actuality of the live female nude creates a transformation from the purely sexualized body to an authentic female nude body. This authentic female nude body, via her control of her physicality, is a “loud” and often rejected body. The acknowledgement of her authenticity is an acknowledgement of her power and this is common ground on which the female audience member and performer can relate intersubjectively. On the surface, it seems the most effective solution to eliminating objectification and this obstruction of the female body would be to take focus away from her body. Yet paradoxically, female subjects have altered these culturally shaped identity norms of objectification through nude performance, liberating the hyper-sexualized projections attached to the female body and replacing them with symbols of innocence, creativity and power.

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Filgueiras, Tatiana Pereira. "RT-JADE." Florianópolis, SC, 2011. http://repositorio.ufsc.br/xmlui/handle/123456789/95866.

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Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro Tecnológico, Programa de Pós-Graduação em Engenharia de Automação e Sistemas, Florianópolis, 2011
Made available in DSpace on 2012-10-26T06:39:32Z (GMT). No. of bitstreams: 1 294604.pdf: 2124450 bytes, checksum: 0b81771135979b58563a2b4d4c5675c3 (MD5)
Com o crescimento das redes de computadores mundiais e o aumento do uso de aplicações distribuídas, surge um aumento significativo no tráfego de dados no enlace, demonstrando, assim, a necessidade de primoramento - ou substituição das atuais técnicas de transmissão de dados - do modelo tradicional cliente-servidor. A tecnologia de agentes móveis tem sido alvo de diversas pesquisas na área, por permitir que apenas um código mova--se entre os nós da rede e retorne com os resultados, diminuindo, assim, a carga na rede. Para que um agente móvel possa cumprir sua missão, é necessário que se atenda a um deadline. Entretanto, em um sistema distribuído, há a possibilidade de concorrência por um mesmo recurso. Tratar de forma adequada tal concorrência é de suma importância, especialmente em um ambiente em tempo real. Em face disso, um modelo de execução em que agentes móveis disputam um mesmo recurso em um mesmo host é proposto, o RT-JADE: uma extensão de middleware que possibilita agentes móveis concorrentes cumprirem suas missões, usando métodos de escalonamento em tempo real sobre a plataforma JADE. A eficácia do modelo proposto foi demonstrada através de simulações e comparações entre diversas políticas de escalonamento, com distintas cargas de trabalho (quantidade de agentes concorrentes).
With the growth of worldwide computer networks and increased use of distributed applications, there is a significant increase in data traffic in the link, thus demonstrating the need for improvement # or replacement of existing techniques for data transmission # of the traditional client-server one. The mobile agent technology has been the subject of several researches in area, because it only allows a code to move between network nodes and return with the results, reducing the network#s load. For a mobile agent to accomplish its mission, it is necessary for it to meet a deadline. However, in a distributed system there is the possibility of competition for the same resource. Treating such competition adequately is very important, especially in a real-time environment. In this view, an execution model in which mobile agents compete for the same resource in the same host is proposed # RT-JADE: a middleware extension that allows concurrent mobile agents to achieve their missions, using real-time scheduling methods on the JADE platform. We demonstrate the effectiveness of the proposed model through simulation and comparison of different scheduling policies under different workloads (number of competing agents).

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Tolley, Rebecca. "Review of Exposed: The Victorian Nude." Digital Commons @ East Tennessee State University, 2002. https://dc.etsu.edu/etsu-works/5712.

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Pennings, Mark W. "Charles Wheeler and the nude in Australia." Connect to thesis, 1991. http://repository.unimelb.edu.au/10187/1432.

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The place for Charles Wheeler’s nudes in Australian art history has not been adequately gauged by art historians. He was one of Australia’s most notable painters of the nude, not perhaps because his vision was particularly inventive or original, but rather because he was an important, conservative conduit of that European tradition. Wheeler was very popular with the buying public over many decades, but success with his nudes was fundamentally a critical one. The positive response to Wheeler’s nudes, paintings which combined elements of the academic tradition and more fashionable conventions, presents an intriguing reflection on the nature of art criticism in Australia. The style of Wheeler’s discourse is indebted not only to late nineteenth century British models, as it was represented in the writings of critics such as R.A.M. Stevenson, who was primarily concerned with technique, but also to current debates about art and morality. One of the determining characteristics of this discourse was an interest in defining the limits between naked and nude. Critics were particularly concerned to protect the nude as a genre against moral attack by refusing to engage in a discussion of its sensual aspects. While the public was keen to debate the moral problems associated with the nude, the critics were anxious to avoid these issues. They felt that questions of morality were not central to artistic merit, and sensed that by engaging in discussion of this kind, the nude was on danger of being brought into disrepute.

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Smith, Alison. "The nude in Victorian painting : 1850-1885." Thesis, Courtauld Institute of Art (University of London), 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297081.

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Wyatt, Malinda. "William Rimmer's Concept of the Heroic Male Nude." VCU Scholars Compass, 1986. http://hdl.handle.net/10156/1443.

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Assano, Mauro Eidi Villela. "Guides for CCS to UML-RT and UML-RT to CCS conversions." Instituto Tecnológico de Aeronáutica, 2009. http://www.bd.bibl.ita.br/tde_busca/arquivo.php?codArquivo=940.

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CCS (Communicating and Concurrent Systems) is the process algebra to specify and verify concurrent and communicating systems. This work proposes a transformation guide of the CCS equations into to the UML-RT (Unified Modeling Language for Real-Time) model and a transformation guide of the UML-RT model into a set of CCS equations. The UML-RT model is a software design language, which supports code generation and the construction of executable systems. The UML-RT is an UML extension, and it does not have a formal semantics; therefore it is not possible to verify UMLRT models. The transformation guide of UML-RT models into CCS equations allows verifying the models. We argue that the transformation of CCS models into UML-RT models allows an alternative way of correctly building systems. This work details the transformation guides from CCS equations to UML-RT models and from UML-RT models to CSS equations and it discusses the limitations and benefits.

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Blount, Jennifer Lynn. "The black male nude a study of John Singer Sargent's Thomas McKeller nude within the context of nineteenth-century art and culture /." Birmingham, Ala. : University of Alabama at Birmingham, 2009. https://www.mhsl.uab.edu/dt/2009m/blount.pdf.

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Thesis (M.A.)--University of Alabama at Birmingham, 2009.
Title from PDF title page (viewed Sept. 2, 2009). Degree earned with the cooperation of additional faculty from the University of Alabama. Includes bibliographical references (p. 88-91).

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Smither, Devon. "Identity crisis : the nude in 1930s modern Canadian art." Thesis, University of British Columbia, 2010. http://hdl.handle.net/2429/27693.

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In their unwillingness to fully assimilate or relate the human body to its surroundings, many artists who painted nudes in the 1930s in Canada found their works the subject of censure and moral debate. Rather than becoming the site of praise for a new Canadian sensibility in the visual arts, the nudes painted in this period would not come to be associated with a uniquely Canadian artistic practice, and the genre failed to assume a pivotal place within the canon of Canadian art history. Viewers could not imagine themselves as heroic pioneers in front of a painting like Lilias Torrance Newton’s Nude (1933), or could they see anything distinctly modern and revolutionary in its execution that would allow them to hold up such an image as an example of an inherently Canadian art. The nude in Canada did not incite the admiration of an art-going public who instead came to associate a national art movement with the landscape paintings of the Group of Seven. Censored, debated, praised, and criticized, the nude genre ultimately failed to have the same impact as landscape painting on the visual arts in Canada. Landscape painting was able to mediate the relationship between the natural world and its human inhabitants in a way not offered by the nude or figurative painting. In 1916, Saturday Night magazine published an article jocularly recounting how the typical Canadian artist was a “husky beggar” who pulled on a pair of Strathcona boots and set off into the woods with a rifle, a paddle, and enough baked beans for three months. Such assertions would lead a critic like Barker Fairley to complain later that, “[N]ot one Canadian in a hundred goes into an art gallery looking for anything but hills and trees and lakes and clouds and flowers and fruit.” Ultimately, the nude was not able to provide a collective viewing position that could embody a national sentiment. It was unable to penetrate the Canadian consciousness in a way that would win it a place alongside the rolling topography and pristine lakes of the Group of Seven.

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Missia, Frano G. "Painting the nude by male artists in Western art /." Access Digital Full Text version, 1993. http://pocketknowledge.tc.columbia.edu/home.php/bybib/11396210.

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Thesis (Ed.D.)--Teachers College, Columbia University, 1993.
Typescript; issued also on microfilm. Sponsor: Justin Schorr. Dissertation Committee: Rene Arcilla. Includes bibliographical references (leaves 112-113).

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Books on the topic "Nude in a rt"

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Chonchúir, Nuala Ní. Nude. London: Salt Pub., 2009.

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Nude. Boston: GemmaMedia, 2012.

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Nude. London: Salt Pub., 2009.

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Lindsay, Robert Bruce. Nude. Reno, NV: Other World Press, 2001.

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Harbunangin, Buntje. @rt energy. Jakarta: Kementerian ESDM, 2012.

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Pirandello, Luigi. Maschere nude. Milano: A. Mondadori, 1986.

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Nude men. New York: Viking, 1993.

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The nude. [United States]: Xlibris Corp, 2011.

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Taylor, Chuck. Naked nude. Austin, Tex. (Box 1385, Austin 78767): Naked Truth Media, 1990.

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Luigi, Pirandello. Maschere nude. Milano: Mondadori, 1993.

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Book chapters on the topic "Nude in a rt"

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Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "ScF3 rt." In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 327. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_143.

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Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "GdBO3 rt." In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 361. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_173.

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Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "Li2Ga6Te10 rt." In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 369. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_180.

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Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "Na5.5ZrSi0.5P2.5O12 rt." In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 384. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_193.

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Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "Na2Ca2Si3O9 rt." In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 476. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_270.

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Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "Na2Ca2Si3O9 rt." In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 477. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_271.

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Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "CrCl3 rt." In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 501. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_287.

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Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "NiTiO3 rt." In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 640. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_401.

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Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "PbxMo3S4 rt." In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 643–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_404.

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Villars, P., K. Cenzual, J. Daams, R. Gladyshevskii, O. Shcherban, V. Dubenskyy, V. Kuprysyuk, and I. Savysyuk. "PdAl rt." In Structure Types. Part 8: Space Groups (156) P3m1 – (148) R-3, 720. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-70892-6_476.

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Conference papers on the topic "Nude in a rt"

1

Knowlton, Ken. "Nude (studying in perception), 1996." In ACM SIGGRAPH 98 Electronic art and animation catalog. New York, New York, USA: ACM Press, 1998. http://dx.doi.org/10.1145/281388.281647.

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Chi-Yoon Jeong, Jong-Sung Kim, and Ki-Sang Hong. "Appearance-based nude image detection." In Proceedings of the 17th International Conference on Pattern Recognition, 2004. ICPR 2004. IEEE, 2004. http://dx.doi.org/10.1109/icpr.2004.1333803.

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Xin-Lu, Wang, Li Xiao-juan, and Liu Xiao-bo. "Nude Image Detection Based on SVM." In 2009 International Conference on Computational Intelligence and Natural Computing (CINC). IEEE, 2009. http://dx.doi.org/10.1109/cinc.2009.148.

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Belem, R. J. S., J. M. B. Cavalcanti, E. S. de Moura, and M. A. Nascimento. "SNIF: a simple nude image finder." In Proceedings. Third Latin American Web Congress (LA-WEB 2005). IEEE, 2005. http://dx.doi.org/10.1109/laweb.2005.32.

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Lieberman, Larry A. "Another look at the reclining nude." In Display Holography: Fifth International Symposium, edited by Tung H. Jeong. SPIE, 1995. http://dx.doi.org/10.1117/12.201902.

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Chishiro, Hiroyuki, Yuji Fujita, Akira Takeda, Yuta Kojima, Kenji Funaoka, Shinpei Kato, and Nobuyuki Yamasaki. "Extended RT-Component Framework for RT-Middleware." In 2009 IEEE International Symposium on Object/Component/Service-Oriented Real-Time Distributed Computing (ISORC). IEEE, 2009. http://dx.doi.org/10.1109/isorc.2009.40.

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DeAntoni, Julien, Frédéric Mallet, Frédéric Thomas, Gonzague Reydet, Jean-Philippe Babau, Chokri Mraidha, Ludovic Gauthier, Laurent Rioux, and Nicolas Sordon. "RT-simex." In the eighteenth ACM SIGSOFT international symposium. New York, New York, USA: ACM Press, 2010. http://dx.doi.org/10.1145/1882291.1882357.

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Owen, G. Scott. "RT Prolog." In the 1988 ACM sixteenth annual conference. New York, New York, USA: ACM Press, 1988. http://dx.doi.org/10.1145/322609.323151.

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Maeng, Ji Chan, Jung-Il Kwon, Min-Kyu Sin, and Minsoo Ryu. "RT-replayer." In the 2009 ACM symposium. New York, New York, USA: ACM Press, 2009. http://dx.doi.org/10.1145/1529282.1529656.

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Sahoo, Sampa, Bibhudatta Sahoo, and Ashok Kumar Turuk. "RT-PUSH." In the 3rd International Conference. New York, New York, USA: ACM Press, 2017. http://dx.doi.org/10.1145/3162957.3163026.

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Reports on the topic "Nude in a rt"

1

Wade, Jon, Mark S. Avnet, LiGuo Huang, Azad Madni, Kevin Sullivan, and Gary Witus. RT 128: New Project Incubator. Fort Belvoir, VA: Defense Technical Information Center, September 2015. http://dx.doi.org/10.21236/ada631782.

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Bryzik, Walter. Vehicle Systems Engineering and Integration (RT 26). Fort Belvoir, VA: Defense Technical Information Center, January 2012. http://dx.doi.org/10.21236/ada582688.

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Deshmukh, Abhi, Marty Wortman, Barry Boehm, Dave Jacques, Tom Housel, Kevin Sullivan, and Paul Collopy. RT-18: Value of Flexibility. Phase 1. Fort Belvoir, VA: Defense Technical Information Center, September 2010. http://dx.doi.org/10.21236/ada546778.

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Cook, John. Tactical Atmospheric Modeling System-Real Time (TAMS-RT). Fort Belvoir, VA: Defense Technical Information Center, September 1999. http://dx.doi.org/10.21236/ada630754.

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Buell, Krista. Aphrodite of Knidos, Trendsetter: Depictions of the Female Nude and Sexuality in Ancient Greek Sculpture. Portland State University Library, January 2016. http://dx.doi.org/10.15760/honors.265.

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Cook, John. Tactical Atmospheric Modeling System-Real Time (TAMS-RT) Transition. Fort Belvoir, VA: Defense Technical Information Center, September 1999. http://dx.doi.org/10.21236/ada630752.

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Masiello, Valeria. The role of radiotherapy (RT) in the treatment of Adenoid Cystic Carcinoma of the Breast: case report of RT retreatment and literature review. Science Repository OÜ, March 2019. http://dx.doi.org/10.31487/j.cor.2019.01.107.

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Xing, Huili G., and Debdeep Jena. Ultrascaled AIN/GaN HEMT Technology for mm-wave RT Applications. Fort Belvoir, VA: Defense Technical Information Center, February 2011. http://dx.doi.org/10.21236/ada538446.

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Salter, Margaret S., David E. Eakin, and Bruce W. Knerr. Dismounted Warrior Network Enhanced Restricted Terrain (DWN RT): An Independent Assessment. Fort Belvoir, VA: Defense Technical Information Center, May 1999. http://dx.doi.org/10.21236/ada364607.

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Narayan, Amit. Demand Response Optimization and Management System for Real-TIme (DROMS-RT). Office of Scientific and Technical Information (OSTI), June 2014. http://dx.doi.org/10.2172/1595092.

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