Academic literature on the topic 'Cure'

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Journal articles on the topic "Cure"

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Kim, Y.-S., S.-H. Choi, B.-N. Lee, Y.-C. Hwang, I.-N. Hwang, W.-M. Oh, JL Ferracane, and H.-S. Chang. "Effect of Tack Cure on Polymerization Shrinkage of Resin-based Luting Cements." Operative Dentistry 45, no. 4 (April 3, 2020): E196—E206. http://dx.doi.org/10.2341/19-159-l.

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Clinical Relevance Self-cure after tack cure could result in a lower polymerization shrinkage in some resin-based luting cements, which is closely related to lower degree of cure. SUMMARY Objectives: To evaluate the effect of tack cure on polymerization shrinkage (PS) of resin-based luting cements. Methods and Materials: One composite resin cement, Duo-Link (Duolink); two self-adhesive resin cements, RelyX U200 (U200) and G-CEM LinkAce (GCem); and one resin-modified glass ionomer cement, RelyX Luting Plus (Luting+), were used for measuring PS in light-cure (LC group), self-cure (SC group), and two tack-cure modes that were light cured (TC-LC group) or self-cured (TC-SC group) after tack cure. PS was measured by a modified bonded disc method for 1600 seconds and analyzed with two-way analysis of variance and Tukey honestly significant difference test. To investigate the effect of tack cure on light cure or self-cure, data were analyzed with an independent-samples t-test with tack cure as a variable. The significance level was 5%. Results: Regarding cure mode, Duolink showed a significantly lower PS in the TC-SC group compared with the other groups. Luting+ showed a significantly lower PS in the TC-SC group than in the SC group. U200 showed a significantly lower PS in the self-cure groups compared with that in the light-cure groups. The PS of GCem was not affected by cure mode. Regarding cements, Luting+ showed the highest PS, followed by GCem, Duolink, and U200 (p<0.05). Self-cure of Duolink and Luting+ was negatively affected by tack cure, while light cure was not affected. U200 and GCem were not affected by tack cure either in the self-cure or light-cure groups. Conclusion: For the tested cements, tack cure decreased the PS of Duolink and Luting+ when they were self-cured after tack cure. When the cements were light cured after tack cure, PS was not affected by tack cure in any cement.
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Satyam, Abhigyan, and George C. Tsokos. "Curb complement to cure COVID-19." Clinical Immunology 221 (December 2020): 108603. http://dx.doi.org/10.1016/j.clim.2020.108603.

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Kowalski, Jennifer R., Geoffrey C. Hoops, and R. Jeremy Johnson. "Implementation of a Collaborative Series of Classroom-Based Undergraduate Research Experiences Spanning Chemical Biology, Biochemistry, and Neurobiology." CBE—Life Sciences Education 15, no. 4 (December 2016): ar55. http://dx.doi.org/10.1187/cbe.16-02-0089.

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Classroom undergraduate research experiences (CUREs) provide students access to the measurable benefits of undergraduate research experiences (UREs). Herein, we describe the implementation and assessment of a novel model for cohesive CUREs focused on central research themes involving faculty research collaboration across departments. Specifically, we implemented three collaborative CUREs spanning chemical biology, biochemistry, and neurobiology that incorporated faculty members’ research interests and revolved around the central theme of visualizing biological processes like Mycobacterium tuberculosis enzyme activity and neural signaling using fluorescent molecules. Each CURE laboratory involved multiple experimental phases and culminated in novel, open-ended, and reiterative student-driven research projects. Course assessments showed CURE participation increased students’ experimental design skills, attitudes and confidence about research, perceived understanding of the scientific process, and interest in science, technology, engineering, and mathematics disciplines. More than 75% of CURE students also engaged in independent scientific research projects, and faculty CURE contributors saw substantial increases in research productivity, including increased undergraduate student involvement and academic outputs. Our collaborative CUREs demonstrate the advantages of multicourse CUREs for achieving increased faculty research productivity and traditional CURE-associated student learning and attitude gains. Our collaborative CURE design represents a novel CURE model for ongoing laboratory reform that benefits both faculty and students.
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Poorabdollah, Mehdi, and Arezoo Kamran. "Optimising cure cycle of unsaturated polyester nanocomposites using directed grid search method." Polymers and Polymer Composites 27, no. 5 (February 5, 2019): 253–61. http://dx.doi.org/10.1177/0967391119826650.

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In this research, a method is proposed for optimising cure cycle of neat unsaturated polyester (UP) resins, and UP resins containing Cloisite 20A (UP/20A), in thin parts. Using the proposed optimisation method, optimised cure cycles for both neat UP resin system and UP/20A were calculated. Results of dynamic mechanical analysis tests show that samples cured by the optimised cure cycles are slightly different from those samples cured using a long-term cure cycle in terms of structural relaxation. This confirms that the proposed optimisation method not only reduces the cure cycle duration efficiently but also preserves the quality of the samples.
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Parthasarathy, Sanjay, Susan C. Mantell, and Kim A. Stelson. "Estimation, Control and Optimization of Curing in Thick-Sectioned Composite Parts." Journal of Dynamic Systems, Measurement, and Control 126, no. 4 (December 1, 2004): 824–33. http://dx.doi.org/10.1115/1.1850536.

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A nonlinear model-based control method is proposed and validated for controlling, estimating and optimizing the cure in composite parts. During the cure, the exothermic reaction causes temperature gradients through the thickness that can lead to a nonuniform cure and high residual stress. A predictive control and optimization approach is proposed to ensure that temperature gradients are kept within acceptable limits and the cure state is fairly uniform, regardless of the part thickness. A reduced order process model is derived and used to formulate a dynamic inversion controller. A nonlinear observer is constructed to estimate the unknown temperature and cure states within the composite. An on-line optimizer determines the maximum allowable heating rate. The optimizer is run at discrete intervals throughout the process to account for process and part variability. The control, estimation and optimization algorithms were validated through a series of simulations and experiments of composite parts cured in a press. Parts that were cured with the proposed control method were compared with parts cured following a manufacturer’s recommended cure cycle. The results demonstrate the success of the proposed control method in achieving uniform temperature and cure, and in decreasing the residual stress, without increasing cycle time.
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Gorkovskiy, Anton, Michael Reidy, Daniel C. Masison, and Reed B. Wickner. "Hsp104 disaggregase at normal levels cures many [PSI+] prion variants in a process promoted by Sti1p, Hsp90, and Sis1p." Proceedings of the National Academy of Sciences 114, no. 21 (May 8, 2017): E4193—E4202. http://dx.doi.org/10.1073/pnas.1704016114.

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Overproduction or deficiency of many chaperones and other cellular components cure the yeast prions [PSI+] (formed by Sup35p) or [URE3] (based on Ure2p). However, at normal expression levels, Btn2p and Cur1p eliminate most newly arising [URE3] variants but do not cure [PSI+], even after overexpression. Deficiency or overproduction of Hsp104 cures the [PSI+] prion. Hsp104 deficiency curing is a result of failure to cleave the Sup35p amyloid filaments to make new seeds, whereas Hsp104 overproduction curing occurs by a different mechanism. Hsp104(T160M) can propagate [PSI+], but cannot cure it by overproduction, thus separating filament cleavage from curing activities. Here we show that most [PSI+] variants arising spontaneously in anhsp104(T160M)strain are cured by restoration of just normal levels of the WT Hsp104. Both strong and weak [PSI+] variants are among those cured by this process. This normal-level Hsp104 curing is promoted by Sti1p, Hsp90, and Sis1p, proteins previously implicated in the Hsp104 overproduction curing of [PSI+]. The [PSI+] prion arises inhsp104(T160M)cells at more than 10-fold the frequency in WT cells. The curing activity of Hsp104 thus constitutes an antiprion system, culling many variants of the [PSI+] prion at normal Hsp104 levels.
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Xu, Wei, Haoyang Li, Qian Wang, Chen Hua, Hanzhen Zhang, Weihua Li, Shibo Jiang, and Lu Lu. "Advancements in Developing Strategies for Sterilizing and Functional HIV Cures." BioMed Research International 2017 (2017): 1–12. http://dx.doi.org/10.1155/2017/6096134.

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Combined antiretroviral therapy (cART) has been successful in prolonging lifespan and reducing mortality of patients infected with human immunodeficiency virus (HIV). However, the eradication of latent HIV reservoirs remains a challenge for curing HIV infection (HIV cure) because of HIV latency in primary memory CD4+ T cells. Currently, two types of HIV cures are in development: a “sterilizing cure” and a “functional cure.” A sterilizing cure refers to the complete elimination of replication-competent proviruses in the body, while a functional cure refers to the long-term control of HIV replication without treatment. Based on these concepts, significant progress has been made in different areas. This review focuses on recent advancements and future prospects for HIV cures.
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Swain, Prafulla Kumar, Gurprit Grover, and Komal Goel. "Mixture and Non-Mixture Cure Fraction Models Based on Generalized Gompertz Distribution under Bayesian Approach." Tatra Mountains Mathematical Publications 66, no. 1 (June 1, 2016): 121–35. http://dx.doi.org/10.1515/tmmp-2016-0025.

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Abstract The cure fraction models are generally used to model lifetime data with long term survivors. In a cohort of cancer patients, it has been observed that due to the development of new drugs some patients are cured permanently, and some are not cured. The patients who are cured permanently are called cured or long term survivors while patients who experience the recurrence of the disease are termed as susceptibles or uncured. Thus, the population is divided into two groups: a group of cured individuals and a group of susceptible individuals. The proportion of cured individuals after the treatment is typically known as the cure fraction. In this paper, we have introduced a three parameter Gompertz (viz. scale, shape and acceleration) or generalized Gompertz distribution in the presence of cure fraction, censored data and covariates for estimating the proportion of cure fraction through Bayesian Approach. Inferences are obtained using the standard Markov Chain Monte Carlo technique in openBUGS software.
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Rejman, Daniel John, Theodore Eliades, Thomas G. Bradley, and George Eliades. "Polymerization Efficiency of Glass-Ionomer and Resin Adhesives under Molar Bands." Angle Orthodontist 78, no. 3 (May 1, 2008): 549–52. http://dx.doi.org/10.2319/022207-88.1.

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Abstract Objective: To determine the degree of cure of a light-cured resin-modified glass ionomer (RMGI) under molar bands compared with a light-cured resin and a dual-cured resin. Materials and Methods: The 3 cements used were Fuji Ortho LC, Eagle Spectrum resin, and Variolink II dual-cure. Each sample was indirectly light cured for 20 seconds (10 seconds occlusally, 10 seconds cervically) under sections of molar bands, and the degree of cure was evaluated with micro-MIR FTIR spectroscopy. Results: The RMGI exhibited a significantly higher mean degree of cure (55.31%) than both of the resins (Eagle 19.23%; Variolink II, 25.42%), which did not differ significantly at α = .05 level of significance. Conclusion: Higher degree of conversion can be obtained from RMGIs under molar bands compared with composite resin adhesives provided the proper curing technique is used.
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Sloane, Michael E. "Is There a Cure for Desperate Cures?" Contemporary Psychology: A Journal of Reviews 33, no. 1 (January 1988): 13–14. http://dx.doi.org/10.1037/025269.

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Dissertations / Theses on the topic "Cure"

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Lograsso, Anthony. "Cure/Repeat/Cure." Bowling Green State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1556546784827036.

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DeStefano, Michele, Hendrik Schneider, and Michael Lindemann. "Editorial: Cure or curse? Compliance in digital healthcare." Universität Leipzig, 2018. https://ul.qucosa.de/id/qucosa%3A32050.

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The edition features first-rate articles by specialists in the field of healthcare and data security. Apart from that we will face some classical compliance topics and last but not least CEJ Founder Michele DeStefanos new book Legal Upheaval will be introduced and reviewed.
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Tsakoumagos, Nicole. "Fight/Cure." Cleveland State University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=csu1622640775978268.

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Game, R. L. "A depth of cure test for visible light cured restorative resins /." Title page, contents and abstract only, 1991. http://web4.library.adelaide.edu.au/theses/09DM/09dmg192.pdf.

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Wood, William E. "Depression a cure /." Portland, Or. : Theological Research Exchange Network (TREN), 2005. http://www.tren.com.

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Somanath, Nagendra. "A finite element cure model and cure cycle optimization for composite structures." Thesis, This resource online, 1987. http://scholar.lib.vt.edu/theses/available/etd-04272010-020304/.

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Contini, Andrea. "Où "habite" la cure ? : la conception de la cure dans la Daseinanalyse." Paris 12, 2006. https://athena.u-pec.fr/primo-explore/search?query=any,exact,990002460040204611&vid=upec.

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Plus on cherche à approcher l'essence de la cure par la raison plus la raison elle-même nous montre ses limites. Le symptôme et sa genèse à partir du corps-sujet, autrement dit de la "chair (Leib", ce n'est qu'après qu'il devient manifeste dans le corps-objet ("Körper"). Cela nous fait comprendre que la disparition du symptôme au niveau du corps-objet ne présuppose pas la disparition du "symptôme au niveau de la chair". La cure est alors invisible. Pour nous orienter vers la cure, il est nécessaire de se pencher sur la "Lebenswelt", soit sur la pré-réflexivité et sur l'affectivité en même temps. Il est nécessaire de réfléchir sur le rythme du patient et du médecin durant la relation thérapeutique. Leurs rythmes s'entrecoisent à un niveau pré-réflexif : cela permet au patient l' "incarnation du sens" vécu dans la relation thérapeutique
The more we search for the essence of the cure through reason, the more the reason itself shows its limits. To understand what a cure is, it's necessary to study the "Lebenswelt". The symptom are born in the body and in the flesh ("chair") and only later it will be express in the body as "Körper". We understand that the disappearance of the "Körper" symptom does not necessary lead to the disappearance of the flesh symptom. Then, it appears that cure is invisible. For understanding the cure, we have to study the "Lebenswelt", the pre-reflexivity, and the affect in the same time. It is necessary to reflect on the rhythm of the patient and the doctor during the therapeutic relation. Their rhythms intersect on a pre-reflexive level : that allows to the patient the "incarnation of the meaning" lived in the therapeutic relation
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Contini, Andrea Naudin Jean Escoubas Éliane. "Où "habite" la cure ? la conception de la cure dans la Daseinanalyse /." Créteil : Université de Paris-Val-de-Marne, 2006. http://doxa.scd.univ-paris12.fr:80/theses/th0246004.pdf.

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Tang, Yanyan. "Stereolithography Cure Process Modeling." Diss., Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/7235.

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Although stereolithography (SL) is a remarkable improvement over conventional prototyping production, it is being pushed aggressively for improvements in both speed and resolution. However, it is not clear currently how these two features can be improved simultaneously and what the limits are for such optimization. In order to address this issue a quantitative SL cure process model is developed which takes into account all the sub-processes involved in SL: exposure, photoinitiation, photopolymerizaion, mass and heat transfer. To parameterize the model, the thermal and physical properties of a model compound system, ethoxylated (4) pentaerythritol tetraacrylate (E4PETeA) with 2,2-dimethoxy-2-phenylacetophenone (DMPA) as initiator, are determined. The free radical photopolymerization kinetics is also characterized by differential photocalorimetry (DPC) and a comprehensive kinetic model parameterized for the model material. The SL process model is then solved using the finite element method in the software package, FEMLAB, and validated by the capability of predicting fabricated part dimensions. The SL cure process model, also referred to as the degree of cure (DOC) threshold model, simulates the cure behavior during the SL fabrication process, and provides insight into the part building mechanisms. It predicts the cured part dimension within 25% error, while the prediction error of the exposure threshold model currently utilized in SL industry is up to 50%. The DOC threshold model has been used to investigate the effects of material and process parameters on the SL performance properties, such as resolution, speed, maximum temperature rise in the resin bath, and maximum DOC of the green part. The effective factors are identified and parameter optimization is performed, which also provides guidelines for SL material development as well as process and laser improvement.
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Tang, Yanyan. "Sterolithography (SL) cure modeling." Thesis, Georgia Institute of Technology, 2002. http://hdl.handle.net/1853/10143.

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Books on the topic "Cure"

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Robin, Cook. Cure. New York: G. P. Putnam's Sons, 2010.

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Robin, Cook. Cure. New York: G. P. Putnam's Sons, 2010.

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Robin, Cook. Cure. Waterville, Me: Thorndike Press, 2010.

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Robin, Cook. Cure. New York: G. P. Putnam's Sons, 2010.

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Robin, Cook. Cure. New York: Berkley Books, 2011.

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Robin, Cook. Cure. Detroit: Large Print Press, 2011.

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Robin, Cook. Cure. Waterville, Me: Thorndike Press, 2010.

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Azzolina, Gaetano. Il libro del cuore: Malattie e cure. Milano: A. Mondadori, 1990.

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The Cure: De A à Z. Paris: Goupe Express éd., 2005.

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Levitin, Sonia. The cure. San Diego, Calif: Harcourt Brace, 1999.

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Book chapters on the topic "Cure"

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Brueckner, Martin, Angela Durey, Robyn Mayes, and Christof Pforr. "Confronting the ‘Resource Curse or Cure’ Binary." In Resource Curse or Cure ?, 3–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53873-5_1.

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Pforr, Christof, Ross Dowling, and David Newsome. "Geotourism: A Sustainable Development Alternative for Remote Locations in Western Australia?" In Resource Curse or Cure ?, 153–62. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53873-5_10.

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Chandler, Lisa. "Regulating the Resource Juggernaut." In Resource Curse or Cure ?, 165–77. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53873-5_11.

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Roche, Charles, and Gavin Mudd. "An Overview of Mining and the Environment in Western Australia." In Resource Curse or Cure ?, 179–94. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53873-5_12.

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Majer, Jonathan D. "Mining and Biodiversity: Are They Compatible?" In Resource Curse or Cure ?, 195–205. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53873-5_13.

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Broderick, Gemma, and Pierre Horwitz. "Sustainability Mining: Water for Mining, and Mining Water." In Resource Curse or Cure ?, 207–19. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53873-5_14.

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Mayes, Robyn. "Mining and (Sustainable) Local Communities: Transforming Ravensthorpe, Western Australia." In Resource Curse or Cure ?, 223–37. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53873-5_15.

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Brueckner, Martin. "On the Social Sustainability of Development in Western Australia: A Community Perspective." In Resource Curse or Cure ?, 239–55. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53873-5_16.

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Scott, Kim, and Angela Durey. "‘Not Taking, But Giving’: A Paradox of Cross-Cultural Empowerment." In Resource Curse or Cure ?, 257–70. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53873-5_17.

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Brueckner, Martin, Angela Durey, Robyn Mayes, and Christof Pforr. "Curse or Cure? Revisiting State, Capital and Resources." In Resource Curse or Cure ?, 273–90. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53873-5_18.

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Conference papers on the topic "Cure"

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Guha, Sudipto, Rajeev Rastogi, and Kyuseok Shim. "CURE." In the 1998 ACM SIGMOD international conference. New York, New York, USA: ACM Press, 1998. http://dx.doi.org/10.1145/276304.276312.

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Wang, Yi, Luis Angel D. Bathen, Nikil D. Dutt, and Zili Shao. "Meta-Cure." In the 49th Annual Design Automation Conference. New York, New York, USA: ACM Press, 2012. http://dx.doi.org/10.1145/2228360.2228401.

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Aishvarya, S. M., D. Charu, S. Haripriya, and T. P. Rani. "Charging Commotion Cure." In 2019 3rd International Conference on Computing and Communications Technologies (ICCCT). IEEE, 2019. http://dx.doi.org/10.1109/iccct2.2019.8824810.

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Li, Zhijun, Wei Huang, Mingqing Gan, Kuangsheng Zhang, Wenxiong Wang, Yongbin Shan, Donnie Burts, Dongbo Chen, and Jie Song. "Casing Leak Cure." In SPE Oil and Gas India Conference and Exhibition. Society of Petroleum Engineers, 2019. http://dx.doi.org/10.2118/194592-ms.

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Djordjevic, B. Boro. "Ultrasonic cure monitoring." In The ninth international symposium on nondestructive characterization of materials. AIP, 1999. http://dx.doi.org/10.1063/1.1302032.

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Krishnaswamy, Smita, Bernd Bodenmiller, and Dana Pe'er. "Can CAD cure cancer?" In the 50th Annual Design Automation Conference. New York, New York, USA: ACM Press, 2013. http://dx.doi.org/10.1145/2463209.2488910.

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Seeburger, Jan. "No cure for curiosity." In the 7th Nordic Conference. New York, New York, USA: ACM Press, 2012. http://dx.doi.org/10.1145/2399016.2399054.

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Hirata, Akihiro. "Nonpost mold cure compound." In ISMA '97 International Symposium on Microelectronics and Assembly, edited by Yong Khim Swee, HongYu Zheng, and Ray T. Chen. SPIE, 1997. http://dx.doi.org/10.1117/12.289503.

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Safari, Wende Clarence, Ignacio López-de-Ullibarri, and María Amalia Jácome. "Nonparametric Inference for Mixture Cure Model When Cure Information Is Partially Available." In XoveTIC Conference. Basel Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/engproc2021007017.

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Yi, Sung, Harry Hilton, M. Ahmad, and Kendall Pierson. "Cure cycle simulations of composites with temperature and cure dependent anisotropic viscoelastic properties." In 37th Structure, Structural Dynamics and Materials Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1996. http://dx.doi.org/10.2514/6.1996-1577.

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Reports on the topic "Cure"

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Buiter, Willem. Deflation: Prevention and Cure. Cambridge, MA: National Bureau of Economic Research, April 2003. http://dx.doi.org/10.3386/w9623.

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Ortiz-Acosta, Denisse. Sylgard? Cure Inhibition Characterization. Office of Scientific and Technical Information (OSTI), October 2012. http://dx.doi.org/10.2172/1053123.

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Spencer, J. Brock. Cure shrinkage in casting resins. Office of Scientific and Technical Information (OSTI), February 2015. http://dx.doi.org/10.2172/1170250.

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McClain, Dennis R. MEDEVAC: A Cure or Problem. Fort Belvoir, VA: Defense Technical Information Center, June 1997. http://dx.doi.org/10.21236/ada328166.

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Palmer, Charis, ed. Will we ever cure dementia? Monash University, November 2021. http://dx.doi.org/10.54377/4f0f-6832.

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Kropka, Jamie Michael, Mark E. Stavig, and Rex Jaramillo. Residual Stress Developed During the Cure of Thermosetting Polymers: Optimizing Cure Schedule to Minimize Stress. Office of Scientific and Technical Information (OSTI), June 2016. http://dx.doi.org/10.2172/1430479.

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Gillham, John K. Cure and Properties of Thermosetting Polymers. Fort Belvoir, VA: Defense Technical Information Center, August 1987. http://dx.doi.org/10.21236/ada184669.

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Bridget Eklund, Bridget Eklund. Can cockroaches help us cure tularemia? Experiment, December 2014. http://dx.doi.org/10.18258/4274.

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Hrushesy, William, Phillip Bulkhaults, and Shaojin You. Sage Gene Expression Profiles Characterizing Cure. Fort Belvoir, VA: Defense Technical Information Center, October 2006. http://dx.doi.org/10.21236/ada462344.

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Madhukar, Madhu S. Cure Cycle Optimization in Polymer Composites. Fort Belvoir, VA: Defense Technical Information Center, April 2000. http://dx.doi.org/10.21236/ada379701.

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