Academic literature on the topic 'IPDR'

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Journal articles on the topic "IPDR"

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Saif, Muhammad Wasif, Greg Berk, Yung-Chi Cheng, and Timothy James Kinsella. "IPdR: a novel oral radiosensitizer." Expert Opinion on Investigational Drugs 16, no. 9 (August 22, 2007): 1415–24. http://dx.doi.org/10.1517/13543784.16.9.1415.

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Heine, Carmen. "Integrated Problem Decision Reports (IPDR) im DaF-Kontext." ÖDaF-Mitteilungen 34, no. 2 (November 16, 2018): 22–32. http://dx.doi.org/10.14220/odaf.2018.34.2.22.

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Leu, Jenq-Shiou, Wen-Bin Hsieh, and Yun-Sun Yee. "Implementing Billing as a Service by an IPDR Aggregator System." Wireless Personal Communications 87, no. 4 (August 25, 2015): 1223–40. http://dx.doi.org/10.1007/s11277-015-3050-6.

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Ceron, Jesus D., Christine F. Martindale, Diego M. López, Felix Kluge, and Bjoern M. Eskofier. "Indoor Trajectory Reconstruction of Walking, Jogging, and Running Activities Based on a Foot-Mounted Inertial Pedestrian Dead-Reckoning System." Sensors 20, no. 3 (January 24, 2020): 651. http://dx.doi.org/10.3390/s20030651.

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The evaluation of trajectory reconstruction of the human body obtained by foot-mounted Inertial Pedestrian Dead-Reckoning (IPDR) methods has usually been carried out in controlled environments, with very few participants and limited to walking. In this study, a pipeline for trajectory reconstruction using a foot-mounted IPDR system is proposed and evaluated in two large datasets containing activities that involve walking, jogging, and running, as well as movements such as side and backward strides, sitting, and standing. First, stride segmentation is addressed using a multi-subsequence Dynamic Time Warping method. Then, detection of Toe-Off and Mid-Stance is performed by using two new algorithms. Finally, stride length and orientation estimation are performed using a Zero Velocity Update algorithm empowered by a complementary Kalman filter. As a result, the Toe-Off detection algorithm reached an F-score between 90% and 100% for activities that do not involve stopping, and between 71% and 78% otherwise. Resulting return position errors were in the range of 0.5% to 8.8% for non-stopping activities and 8.8% to 27.4% otherwise. The proposed pipeline is able to reconstruct indoor trajectories of people performing activities that involve walking, jogging, running, side and backward walking, sitting, and standing.
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Kinsella, Timothy J., Michael T. Kinsella, Seongwon Hong, Jerry P. Johnson, Brian Burback, and Patricia J. Tosca. "Toxicology and pharmacokinetic study of orally administered 5-iodo-2-pyrimidinone-2′deoxyribose (IPdR) × 28 days in Fischer-344 rats: impact on the initial clinical phase I trial design of IPdR-mediated radiosensitization." Cancer Chemotherapy and Pharmacology 61, no. 2 (June 12, 2007): 323–34. http://dx.doi.org/10.1007/s00280-007-0518-4.

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Wang Yang, 王杨, and 赵红东 Zhao Hongdong. "VLC/PDR Particle Filter Fusion Indoor Positioning Based on Smartphone." Chinese Journal of Lasers 47, no. 7 (2020): 0706001. http://dx.doi.org/10.3788/cjl202047.0706001.

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Yu, J., X. Zheng, and P. Jeppesen. "80 Gbit/s OTDM signal amplification in SOA and improvement of IPDR by shifting optical filter in wavelength." Electronics Letters 37, no. 7 (2001): 445. http://dx.doi.org/10.1049/el:20010290.

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Kummar, S., L. Anderson, K. Hill, E. Majerova, D. Allen, Y. Horneffer, P. Ivy, P. Harris, J. H. Doroshow, and J. Collins. "592 First-in-human Phase 0 Trial of Oral 5-iodo-2-pyrimidinone-2′-deoxyribose (IPdR) in Patients with Advanced Malignancies." European Journal of Cancer 48 (November 2012): 181–82. http://dx.doi.org/10.1016/s0959-8049(12)72389-4.

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Kinsella, Timothy, Howard Safran, Susan Wiersma, Thomas DiPetrillo, Andrew Schumacher, Kayla Rosati, John Vatkevich, et al. "Phase I and Pharmacology Study of Ropidoxuridine (IPdR) as Prodrug for Iododeoxyuridine-Mediated Tumor Radiosensitization in Advanced GI Cancer Undergoing Radiation." Clinical Cancer Research 25, no. 20 (July 23, 2019): 6035–43. http://dx.doi.org/10.1158/1078-0432.ccr-19-0862.

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Kinsella, Timothy J., Kathleen A. Vielhuber, and Keith A. Kunugi. "Pre-clinical toxicity and efficacy study of oral IPDR (QD X 14D) as a prodrug for IUDR-radiosensitization in U25 human glioblastoma xenografts." International Journal of Radiation Oncology*Biology*Physics 42, no. 1 (January 1998): 191. http://dx.doi.org/10.1016/s0360-3016(98)80235-6.

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Dissertations / Theses on the topic "IPDR"

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Chaudry, Kashif, and Elma Karadza. "End-to-End Application Billing in 3G." Thesis, Linköping University, Department of Science and Technology, 2002. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-1654.

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We have 3G on the doorstep but nothing seems to attract ordinary people to this technology. To attract the mass market the telecom industry must show something beyond high bit rates. They must show how ordinary people can take advantage of this new technology. This is done by showing the possibilities of the new technology and by demonstrating applications that it will handle. The telecom industry must convince the telecom operators to invest in this technology and the only thing that matters to them is how much revenue they can make by adopting the upcoming technology.

To convince the operators industry must show how the operators can charge for the new types of applications that will be introduced soon. This is the main reason why this Master's Thesis has been conducted. The purpose of this thesis is to provide a demonstration to Ericsson's 3G lab in Katrineholm in the form of an IP application with a billing solution. This thesis describes the migration from 1G to 3G and examines existing and future billing strategies as well.

The IP application is an application that uses progressive streaming in order to stream multimedia content to a PDA connected to a 3G phone. This application is platform independent because it is placed on leading Web servers, Apache and IIS.

The billing application consists of a number of steps. The first step is logging, which is performed by the Web server on which the streaming application is placed. The second step, processing and billing, is performed in the BGw, which is Ericsson's mediation tool, and the SQL server.The third step is displaying the bill, which is done by using ASP to create an active HTML page.

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Löffler, Daniel. "Eigenschaften und Reaktivität von IPR und non-IPR Fullerenfilmen." [S.l. : s.n.], 2008. http://digbib.ubka.uni-karlsruhe.de/volltexte/1000009893.

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Sconza, Sarah <1976&gt. "Quadri clinici in situazioni di: acidosi metabolica, iper L-lattacidemia e iper D-lattacidemia sperimentalmente indotte nel vitello lattante." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2007. http://amsdottorato.unibo.it/546/.

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Criollo-Cespedes, Alfredo. "Regulation of autophagy by IP3R and IKK complex." Paris 11, 2009. http://www.theses.fr/2009PA11T099.

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Astutik, Wynda. "IPR Modeling for Coning Wells." Thesis, Norges teknisk-naturvitenskapelige universitet, Institutt for petroleumsteknologi og anvendt geofysikk, 2012. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-19518.

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In this study, based on the work of Vogel, we generated the Inflow Performance Relationship (IPR) curves and its dimensionless form at any stage of depletion using black-oil simulator results. The IPR was generated for horizontal well with gas and water coning problems, producing from thin oil reservoir sandwiched between gas cap and aquifer. Two empirical IPR equations adopted from SPE paper by Whitson was also presented here. The first empirical relationship was developed based on simulated data for each reservoir pressure (stage of depletion) while the second relationship was developed based on all generated data.A fully implicit black-oil Cartesian model with total grid number of 1480 and 150 ft total thickness was used as reservoir model. The horizontal well extends through the full length of reservoir in y-direction with only one grid number along the horizontal section which makes the model a 2D problem. Sensor reservoir simulator and Pipe-It software were utilized to generate the IPR data.This work also includes a sensitivity study to understand the effect of several parameters to gas and water coning behavior, well placement optimization, coning collapse study, and the effect of coning to maximum well production rate. In coning collapse study, a relationship between flowing bottom-hole pressure and reservoir pressure when the cone collapse is provided in graphical form. This could be useful in field application where chocking the well to lower flowing bottom-hole pressure has become one alternative to reduce coning problems.
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Maslauskaitė, Eglė. "Intelektinės nuosavybės teisių (IPR) muitinis užtikrinimas." Master's thesis, Lithuanian Academic Libraries Network (LABT), 2010. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20100224_134005-74323.

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Baigiamojo magistro darbo tema - „Intelektinės nuosavybės teisių muitinis užtikrinimas“. Darbe keliama problema – intelektinės nuosavybės teisės pažeidimų skaičiaus augimas. Pastebėtina, jog, esant prastai ekonominei padėčiai, intelektinės nuosavybės teisių pažeidėjai pradėjo klastoti ne tik prabangos prekes. Patekusios į rinką klastotos prekės gali pakenkti vartotojui. Tačiau esant blogai ekonominei padėčiai, valstybės institucijoms gaunant mažesnį finansavimą nei įprastai, gali iškilti šių teisių užtikrinimo problema. Darbe keliama hipotezė: Didėjant Lietuvos muitinės veiklos efektyvumui ginant intelektinės nuosavybės teises bei stiprinant kovą prieš klastojimą ir piratavimą, nėra pasiekiamas laukiamas ekonominis efektas. Darbo tikslas: atskleisti intelektinės nuosavybės teisių muitinio užtikrinimo savitumus ir pateikti pasiūlymus dėl veiklos ekonominio efektyvinimo. Darbo uždaviniai: apibūdinti intelektinės nuosavybės svarbą tarptautinėje prekyboje; Išanalizuoti intelektinės nuosavybės apsaugos teisės aktus tarptautiniu ir nacionaliniu lygmeniu bei apžvelgti institucijas, atsakingas už jos įgyvendinimą; apžvelgti muitinės priežiūros priemones, taikomas intelektinės nuosavybės teisių apsaugos srityje; atlikti intelektinės nuosavybės teisių muitinio užtikrinimo Lietuvoje analizę; atliktos analizės pagrindu suformuoti išvadas ir pasiūlymus. pateikti intelektinės nuosavybės teisių muitinio užtikrinimo perspektyvas . Magistro baigiamąjį darbą sudaro keturios dalys:... [toliau žr. visą tekstą]
In order the subjects of intellectual property could participate actively in the international trade, and seeking to avoid unfair competence, their rights must be protected. To this purpose international organizations have been established and a number of international conventions have been signed. Customs plays a very important role while protecting the property that participates in the international trade. The topic of the final master’s thesis is “Customs Protection of Intellectual Property Rights”. The problem raised in the thesis is the increment in number of violation of intellectual property right. It should be noted that in the presence of depressed economic situation the violators of intellectual property rights started falsifying not only luxury goods. Falsified goods, which enter the market, may make harm to the consumers. However, in the presence of depressed economic situation and when national authorities receive lower financing than usually, there may arise a problem of intellectual property rights protection. The thesis has raised hypothesis: While the activity effectiveness of Lithuanian customs is increasing, having protection the rights of intellectual ownership and strengthening the high against falsification and piracy, the expected economic effect is not achieved. The aim of the thesis is to reveal how effectively and economically the Customs of the Republic of Lithuania protects intellectual property rights. The objectives of the thesis are as... [to full text]
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Bentham, J. "The IPPR & Demos : think tanks of the new social democracy." Thesis, University of Sheffield, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.408362.

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Criollo, Céspedes Alfredo. "Regulación de la autofagia por el receptor del inositol trisfosfato (IP3R)." Tesis, Universidad de Chile, 2009. http://repositorio.uchile.cl/handle/2250/105178.

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Doctor en Bioquímica
La macroautofagia, comúnmente referida como “autofagia” es la principal vía de degradación de proteínas, organelos y material citoplasmático, permitiendo de este modo el reciclaje del material intracelular. Este proceso consiste en el englobamiento de fracciones citosólicas por una estructura multimembranar llamada “autofagosoma”, el cual posteriormente se fusiona con el lisosoma para formar el “autofagolisosoma”. Luego el material comprendido en el autofagolisosoma es degradado por enzimas hidrolíticas. Un estudio mostró que la inhibición de la enzima inositolmonofosfatasa (IMPasa) usando litio y L690.330, inducía una disminución de los niveles basales del IP3 y en consecuencia la generación de autofagia. Nuestros resultados confirmaron estos datos previos, demostrando que el pre tratamiento con mio-inositol revierte la autofagia inducida por litio y L-690.330. Además se demuestra que el pre tratamiento con mio-inositol también revertía la autofagia inducida por privación de nutrientes. IP3 es ligando de su receptor de IP3 (IP3R), el cual es el principal canal de Ca2+ a nivel del retículo endoplásmico. El principal objetivo de esta tesis es evaluar el rol del IP3R en la regulación de la autofagia. Los resultados mostraron que la disminución de los niveles proteicos del IP3R usando siRNA específicos, así como el tratamiento con antagonistas químicos del IP3R, tales como xestosponginas B y C, estimulaban significativamente el aumento en los niveles de autofagia. Además, xestospongina B, así como también la privación de nutrientes, indujo una pérdida en la interacción entre Bcl-2 y Beclin-1, los cuales interactúan en condiciones basales. El tratamiento con xestospongina B no perturbó los niveles de Ca2+, tanto en retículo endoplásmico como en el citosol, concluyendo que la autofagia inducida por xestospongina B es independiente de una fluctuación del Ca2+. Los experimentos de inmunoprecipitación mostraron que Beclin-1 (regulador clave en la inducción de la autofagia) interactúa tanto con IP3R así como con Bcl-2 en condiciones basales, y la interacción de este complejo es atenuado bajo condiciones de privación de nutrientes o por tratamiento con ABT737, el cual es un mimetizador de dominios BH3. Este resultado sugiere la presencia de un complejo proteico en la regulación de la autofagia. El papel del retículo endoplásmico en el desarrollo de la autofagia toma gran significancia debido al reclutamiento de proteínas clave (IP3R, Beclin-1 and Bcl-2). La relación entre autofagia y estrés de retículo no es clara y por lo tanto se evaluó el efecto de agentes inductores de estrés de retículo en la inducción de la autofagia. Los resultados mostraron que tunicamicina, tapsigargina y brefeldina-A (agentes inductores de estrés de retículo) activaron el UPR (respuesta a proteínas mal plegadas) e indujeron autofagia. La disminución de los niveles de proteínas claves en el desarrollo de la autofagia (Atg5, Atg10, Atg12, Vps34 y Beclin-1) usando específicos RNAs interferentes atenuaron la autofagia inducida por agentes inductores de estrés de retículo y xestospongina B. Además, la sobreexpresión de Bcl-2 y Bcl-XL con destinación a retículo endoplásmico atenuó la autofagia inducida por xestospongina B e inhibidores de la IMPasa. Esta tesis muestra novedosos resultados, los cuales dan cuenta de un complejo proteico IP3R/Beclin-1/Bcl-2 en la regulación de la autofagia.
Macroautophagy (herein referred to as “autophagy”) is the major catabolic pathway for entire organelles, long-lived/ aberrant proteins and superfluous portions of the cytosol. It consists of the stepwise engulfment of substrate elements into distinctive multimembraned “autophagosomes”, which after fusion with lysosomes form singlemembraned autophagolysosomes. Into the autophagolysosome, the engulfed material is degradated by lisosomal hidrolytic enzymes, leading the recyclage of intracellular material. A study has suggested that myo-inositol-1,4,5-trisphosphate (IP3) could regulate autophagy because inhibition of inositol monophosphatase (IMPasa) by lithium or L-690.330 stimulates autophagy through the depletion of IP3. Our results have confirmed that the reduction of intracellular IP3 levels by IMPasa inhibitors (lithium and L.690.330) stimulates autophagy, whereas the enhancement of IP3 levels by pre treatment whit mio-inositol inhibits the lithium and L.690.330 effect. Moreover we have demostred that autophagy induced by nutrient privation was also inhibited by treatment with mio-inositol, but the effect of nutrient privation in the intracellular IP3 basal levels was not evaluated. IP3 acts on the IP3 receptor (IP3R), an IP3‑activated Ca2+ channel of the endoplasmic reticulum membrane and consequently we wanted to evaluate de roll of IP3R in the regulation of autophagy. The results obtained in this thesis show that knockdown of the IP3 receptor (IP3R) with specifics small interfering RNAs and pharmacological IP3R antagonist (xestospongin B and C) are a strong stimulus for the induction of autophagy, in addition, xestospongin B (like nutrient starvation) induced loss in the interaction between Beclin-1 and Bcl-2. Moreover, the autophagy promoted by xestospongin B not produced alterations in the steady-state Ca2+ levels in the ER or in the cytosol, therefore the autophagy induced by xestospongin B was Ca2+-independent. Immunoprecipitation assays shown that Beclin- 1 (key protein in the regulation of autophagy) interacts with IP3R and Bcl-2 in basal conditions, and this interaction may be attenuated both by nutrient starvation or ABT737 treatment, which is a mimetic compound of BH3. These results suggest the presence of a protein complex in the regulation of autophagy. The treatment whit ER stressors such as tunicamycin, thapsigargin and brepheldine A induced Unfolded Protein Responses (UPR) and autophagy. The autophagy induced by these agents showed to be IRE1α dependent, but the inhibition of autophagy showed an increase in the cell death, indicating a pro survival function of the autophagy upon endoplasmic reticumum stress conditions. The autophagy induced by treatment with xestospongin B and ER stressors was inhibited by knockdown of Atg5, Atg10, Atg12, Vps34 and Beclin-1, which are keys proteins in the autophagic process. We have also evaluated the roll of Bcl-2 and Bcl-XL in the inhibition of autophgy, and the results showed that Autophagy triggered by IMPasa inhibitors and xestospongin B was inhibited by Bcl-2 and Bcl-XL over expression specifically targeted to ER but not Bcl-2 or Bcl-XL proteins targeted to mitocondria. Altogether, these results suggest that IP3R form a regulator complex with Bcl-2 and Beclin-1, which exerts a major role in the physiological control of autophagy
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Koleszar, Thomas W. "The generation of IPDP micropulsations, with special attention to frequency shift mechanisms." Thesis, University of British Columbia, 1988. http://hdl.handle.net/2429/29132.

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Short period geomagnetic micropulsations termed IPDPs (Intervals of Pulsations of Diminishing Period) are investigated using ground station data, geosynchronous satellite magnetograms, and the Kp and Dst geomagnetic indices. A model for the generation of IPDPs is described, and consideration is given to three mechanisms which could be responsible for the IPDP frequency rise: the inward motion, azimuthal drift, and increasing background magnetic field mechanisms. A simplified IPDP generation model containing the first two of these mechanisms is tested by computer simulation. Results from this simulation indicate the possibility of significant source region inward motion without actual plasmapause displacement, and the possibility of eastward developing IPDPs. Using amplitude variations along a north-south line of ground stations, two methods, each applicable under different ionospheric propagation conditions, are developed for quantitatively determining the inward motion of the IPDP source region. A system for qualitatively determining the potential influence of the increasing background field mechanism on an IPDP using the Dst index and geosynchronous satellite magnetograms is also formulated. Lastly, a technique for the assessment of the effects of the azimuthal drift mechanism, in conjunction with the inward motion mechanism, is developed. This technique assumes that only these two mechanisms are operating. In addition to addressing the frequency shift mechanisms, it provides estimates of the injection boundary position and the magnitude of any (ring current created) magnetic field depression in the IPDP source region. The frequency rises of two IPDPs are analyzed in detail using these methods. In both cases, the inward motion effect is the dominant factor in producing the frequency rise, with the increasing background field mechanism having no significant effect. The azimuthal drift mechanism is a secondary factor in creating one event's frequency rise, and actually suppresses the frequency rise of the other event. The computer simulation calculations also generally show the inward motion mechanism to be the dominant effect in producing IPDP frequency rises. Longitudinal variations within an IPDP event are also examined. The results of this examination are consistent with the IPDP generation model used here, which includes showing significant variations between stations spaced comparatively closely in longitude.
Science, Faculty of
Earth, Ocean and Atmospheric Sciences, Department of
Graduate
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Gottschalk, Eckart [Verfasser]. "Allgemeine Lehren des IPR in kollisionsrechtlichen Staatsverträgen. / Eckart Gottschalk." Berlin : Duncker & Humblot, 2020. http://d-nb.info/1238318150/34.

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Books on the topic "IPDR"

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Soesilo. Tragedi IPDN' 07: Menyingkap kezaliman kampus maut IPDN. Malang: Yayasan Yusula, 2007.

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Krypto-ipr. Deventer: Kluwer, 1985.

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Bukhman, Naḥum. Me-aḥore ha-ipur. T.A. [z.o. Tel Aviv]: Yaron Golan, 1994.

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Annamária, Inzelt. Rendellenességek az ipar szervezetében. Budapest: Közgazdasági és Jogi Könyvkiadó, 1988.

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Zeʼev, Ḥamuṭal Ben. Tsipor be-ipur afor. Tel-Aviv: Tamuz, 1992.

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Zeʾev, Ḥamuṭal Ben. Tsipor be-ipur afor. Tel-Aviv: Tamuz, 1992.

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Stäheli, Thomas. Persönlichkeitsverletzungen im IPR. Basel: Helbing & Lichtenhahn, 1990.

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Boonk, H. Zeerecht en IPR. Deventer: Kluwer, 1998.

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Syafiie, Inu Kencana. IPDN undercover: Sebuah kesaksian bernurani. Kiaracondong, Bandung: Progressio, 2007.

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Efrian. Lebih dekat dengan STPDN /IPDN. Jakarta: Kerjasama Forum Alumni Sekolah Pamong Praja (FKASPP) dan Wadi Press, 2005.

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Book chapters on the topic "IPDR"

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Borgianni, Yuri, Gaetano Cascini, and Federico Rotini. "IPPR Implementation." In Springer Series in Advanced Manufacturing, 47–85. London: Springer London, 2012. http://dx.doi.org/10.1007/978-1-4471-4017-7_3.

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Anderl, Reiner, and Martin Arlt. "IPDM Systems." In IFIP Advances in Information and Communication Technology, 523–30. Boston, MA: Springer US, 2001. http://dx.doi.org/10.1007/978-0-387-35399-9_51.

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Bährle-Rapp, Marina. "IPD." In Springer Lexikon Kosmetik und Körperpflege, 283. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_5270.

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Robinson, James, and Steven G. E. Marsh. "IPD." In Methods in Molecular Biology, 61–74. Totowa, NJ: Humana Press, 2007. http://dx.doi.org/10.1007/978-1-60327-118-9_4.

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Bährle-Rapp, Marina. "Dimethiconol/IPDI Copolymer." In Springer Lexikon Kosmetik und Körperpflege, 161. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3099.

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Borgianni, Yuri, Gaetano Cascini, and Federico Rotini. "IPPR Methodological Foundations." In Springer Series in Advanced Manufacturing, 29–46. London: Springer London, 2012. http://dx.doi.org/10.1007/978-1-4471-4017-7_2.

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Bährle-Rapp, Marina. "Glycereth-7/IPDI Copolymer." In Springer Lexikon Kosmetik und Körperpflege, 226. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_4313.

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Bährle-Rapp, Marina. "Dihydroxyethyl Tallowamine/IPDI Copolymer." In Springer Lexikon Kosmetik und Körperpflege, 158. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3010.

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Bährle-Rapp, Marina. "Dilinoleyl Alcohol/IPDI Copolymer." In Springer Lexikon Kosmetik und Körperpflege, 159. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3049.

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Ju, Fengkui, Nana Cui, and Shujiao Li. "Trace Semantics for IPDL." In Logic, Rationality, and Interaction, 169–81. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-48561-3_14.

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Conference papers on the topic "IPDR"

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Guo, Wenxuan, Adam Dunstan, and Jeff Finkelstein. "Using IPDR to transfer network management and measurement information." In 2011 IEEE International Workshop Technical Committee on Communications Quality and Reliability (CQR 2011). IEEE, 2011. http://dx.doi.org/10.1109/cqr.2011.5996085.

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Ha, Jinyong, Kevin A. Williams, Richard V. Penty, Ian H. White, and Madeleine Glick. "IPDR improvement and gain reduction in a beam holding SOA." In Photonics Europe, edited by Daan Lenstra, Markus Pessa, and Ian H. White. SPIE, 2006. http://dx.doi.org/10.1117/12.662875.

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Joshi, Adya, Madan Oberoi, and Ranjan Bose. "Analyzing CDR/IPDR Data to Find People Network from Encrypted Messaging Services." In 2018 IEEE 4th International Conference on Collaboration and Internet Computing (CIC). IEEE, 2018. http://dx.doi.org/10.1109/cic.2018.00013.

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Ding, M., Q. Cheng, A. Wonfor, R. V. Penty, and I. H. White. "Routing Algorithm to Optimize Loss and IPDR for Rearrangeably Non-Blocking Integrated Optical Switches." In CLEO: Applications and Technology. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/cleo_at.2015.jth2a.60.

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Rampurwala, MM, A. Choudhary, and ME Burkard. "Abstract P6-13-16: Ropidoxuridine (IPdR) potentiates alisertib (MLN8237) activity in triple-negative breast cancer." In Abstracts: Thirty-Eighth Annual CTRC-AACR San Antonio Breast Cancer Symposium; December 8-12, 2015; San Antonio, TX. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.sabcs15-p6-13-16.

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Rampurwala, Murtuza M., Alka Choudhary, and Mark E. Burkard. "Abstract 2638: Novel synergy of radiosensitizer prodrug IPdR with Aurora kinase inhibitors in triple-negative breast cancer." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-2638.

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Karajz, Sándor. "A digitalizáció és a társadalmi innovációk összefüggései." In Társadalmi és gazdasági folyamatok elemzésének kérdései a XXI. században. Szeged: Szegedi Tudományegyetem Gazdaságtudományi Kar, 2020. http://dx.doi.org/10.14232/tgfek21sz.13.

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A társadalmi innovációk folyamatát és eredményességét nagymértékben befolyásolja a technikai fejlődés. E fejlődés aktuális folyamatát Ipar 4.0-nak nevezzük. Az ipar 4.0 legfontosabb jellemzője a digitalizáció, amely jelentősen átalakítja a hagyományos társadalmi struktúrákat, befolyásolja az értékteremtő folyamatokat. A digitalizáció napjainkban egyre többször megjelenik a társadalmi innovációkban, megváltoztatva az ilyen típusú innovációs folyamatokat. Az Ipar 4.0 eredményei alapján a társadalmi innovációk területén is egyre több olyan megoldást találunk, amely a digitalizációra, az automatizálásra épül. A tanulmány célja a digitalizáció és a társadalmi innováció ismertetése és jellemzése, a két folyamat kapcsolatának értelmezése, illetve a digitális társadalmi innováció bemutatása nemzetközi példákon keresztül.
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Song, Shuaiwen Leon, and Torsten Hoefler. "IPDRM Workshop Introduction." In 2017 IEEE International Parallel and Distributed Processing Symposium Workshops (IPDPSW). IEEE, 2017. http://dx.doi.org/10.1109/ipdpsw.2017.184.

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"IPDS Author Index." In Proceedings International Conference on Dependable Systems and Networks. IEEE, 2002. http://dx.doi.org/10.1109/dsn.2002.1029031.

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Hoffmann, Henry. "IPDRM 2016 Keynote." In 2016 IEEE International Parallel and Distributed Processing Symposium Workshops (IPDPSW). IEEE, 2016. http://dx.doi.org/10.1109/ipdpsw.2016.256.

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Reports on the topic "IPDR"

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Terp, Susan. Integrated Project Review (IPR) Program. Office of Scientific and Technical Information (OSTI), June 2021. http://dx.doi.org/10.2172/1798093.

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Dulikravich, George S. IPDO-2007: Inverse Problems, Design and Optimization Symposium. Fort Belvoir, VA: Defense Technical Information Center, August 2007. http://dx.doi.org/10.21236/ada483042.

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Dulikravich, George S. IPDO-2007 - Inverse Problems, Design and Optimization Symposium. Fort Belvoir, VA: Defense Technical Information Center, December 2007. http://dx.doi.org/10.21236/ada475106.

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Carpenter, B., and L. Lynch, eds. BCP 101 Update for IPR Trust. RFC Editor, January 2006. http://dx.doi.org/10.17487/rfc4371.

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Hall, David L., and Carl S. Byington. MURI IPD Introduction and Project Overview. Fort Belvoir, VA: Defense Technical Information Center, August 2000. http://dx.doi.org/10.21236/ada389929.

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Huang, Xinxin, and Shin-Ichi Izumi. Neural Alterations in Interpersonal Distance (IPD) Cognition and its Correlation with IPD Behavior: A Systematic Review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, July 2021. http://dx.doi.org/10.37766/inplasy2021.7.0074.

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Sathaye, Jayant A., Elmer C. Holt, and Stephane De La Rue du Can. Overview of IPR Practices for Publicly-funded Technologies. Office of Scientific and Technical Information (OSTI), October 2005. http://dx.doi.org/10.2172/919927.

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Maldonado, G. Ivan. Enhanced Accident-Tolerant Fuel Performance and Reliability for Aggressive iPWR/SMR Operation. Office of Scientific and Technical Information (OSTI), August 2018. http://dx.doi.org/10.2172/1470224.

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King, Ron, Sola Talabi, Peter Hastings, and Gregory Zysk. Advanced Nuclear Technology: Integrated Pressurized Water Reactor (iPWR) Containment Aerosol Deposition Behavior. Office of Scientific and Technical Information (OSTI), July 2018. http://dx.doi.org/10.2172/1459651.

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Polk, T., and P. Saint-Andre. Promoting Compliance with Intellectual Property Rights (IPR) Disclosure Rules. RFC Editor, August 2012. http://dx.doi.org/10.17487/rfc6702.

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