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1,554 results on '"Ikegami M"'

1. Technological developments and accelerator improvements for the FRIB beam power ramp-up

Author

Wei, J, Alleman, C, Ao, H, Arend, B, Barofsky, D, Beher, S, Bollen, G, Bultman, N, Casagrande, F, Chang, W, Choi, Y, Cogan, S, Cole, P, Compton, C, Cortesi, M, Curtin, J, Davidson, K, Di Carlo, S, Du, X, Elliott, K, Ewert, B, Facco, A, Fila, A, Fukushima, K, Ganni, V, Ganshyn, A, Ginter, T, Glasmacher, T, Gonzalez, A, Hao, Y, Hartung, W, Hasan, N, Hausmann, M, Holland, K, Hseuh, HC, Ikegami, M, Jager, D, Jones, S, Joseph, N, Kanemura, T, Kim, SH, Knowles, C, Konomi, T, Kortum, B, Kulkarni, N, Kwan, E, Lange, T, Larmann, M, Larter, T, Laturkar, K, LaVere, M, Laxdal, RE, LeTourneau, J, Li, Z-Y, Lidia, S, Machicoane, G, Magsig, C, Manwiller, P, Marti, F, Maruta, T, Metzgar, E, Miller, S, Momozaki, Y, Mugerian, M, Morris, D, Nesterenko, I, Nguyen, C, Ostroumov, P, Patil, M, Plastun, A, Popielarski, L, Portillo, M, Powers, A, Priller, J, Rao, X, Reaume, M, Rodriguez, S, Rogers, S, Saito, K, Sherrill, BM, Smith, MK, Song, J, Steiner, M, Stolz, A, Tarasov, O, Tousignant, B, Walker, R, Wang, X, Wenstrom, J, West, G, Witgen, K, Wright, M, Xu, T, Yamazaki, Y, Zhang, T, Zhao, Q, Zhao, S, Hurh, P, Prestemon, S, and Shen, T

Subjects
Nuclear and Plasma Physics, Engineering, Synchrotrons and Accelerators, Physical Sciences, Nuclear & Particles Physics, Physical sciences
Abstract

The Facility for Rare Isotope Beams (FRIB) began operation with 1 kW beam power for scientific users in May 2022 upon completion of 8 years of project construction. The ramp-up to the ultimate beam power of 400 kW, planned over a 6-year period, will enable the facility to reach its full potential for scientific discovery in isotope science and applications. In December 2023, a record-high beam power of 10.4 kW uranium was delivered to the target. Technological developments and accelerator improvements are being made over the entire facility and are key to completion of the power ramp-up. Major technological developments entail the phased deployment of high-power beam-intercepting systems, including the charge strippers, the charge selection systems, the production target, and the beam dump, along with support systems, including non-conventional utilities (NCU) and remote handling facilities. Major accelerator improvements include renovations to aging legacy systems associated with experimental beam lines and system automation for improved operational efficiency and better machine availability. Experience must be gained to safely handle the increased radiological impacts associated with high beam power; extensive machine studies and advanced beam tuning procedures are needed to minimize uncontrolled beam losses for the desired operating conditions. This paper discusses the technological developments and accelerator improvements with emphasis on major R&D efforts.

Published
2024

2. Antihyperalgesic effects of ProTx-II, a Nav1.7 antagonist, and A803467, a Nav1.8 antagonist, in diabetic mice

Author

Tanaka KI, Sekino S, Ikegami M, Ikeda H, and Kamei J

Subjects
Therapeutics. Pharmacology, RM1-950
Abstract

Ken-ichiro Tanaka,1,2, Shota Sekino,1 Megumi Ikegami,1 Hiroko Ikeda,1 Junzo Kamei11Department of Pathophysiology and Therapeutics, School of Pharmacy and Pharmaceutical Sciences, Hoshi University, Tokyo, Japan; 2Department of Endocrinology and Metabolism, Graduate School of Medicine, Yokohama City University, Yokohama, JapanAbstract: The present study investigated the effects of intrathecal administration of ProTx-II (tarantula venom peptide) and A803467 (5-[4-chloro-phenyl]-furan-2-carboxylic acid [3,5-dimethoxy-phenyl]-amide), selective Nav1.7 and Nav1.8 antagonists, respectively, on thermal hyperalgesia in a painful diabetic neuropathy model of mice. Intrathecal administration of ProTx-II at doses from 0.04 to 4 ng to diabetic mice dose-dependently and significantly increased the tail-flick latency. Intrathecal administration of A803467 at doses from 10 to 100 ng to diabetic mice also dose-dependently and significantly increased the tail-flick latency. However, intrathecal administration of either ProTx-II (4 ng) or A803467 (100 ng) had no effect on the tail-flick latency in nondiabetic mice. The expression of either the Nav1.7 or Nav1.8 sodium channel protein in the dorsal root ganglion in diabetic mice was not different from that in nondiabetic mice. The present results suggest that ProTx-II and A803467, highly selective blockers of Nav1.7 and Nav1.8 sodium channels, respectively, in the spinal cord, can have antihyperalgesic effects in diabetic mice.Keywords: painful diabetic neuropathy, Nav1.7, Nav1.8, ProTx-II, A803467

Published
2015

3. Advances of the FRIB project

Author

Wei, J, Ao, H, Beher, S, Bultman, N, Casagrande, F, Cogan, S, Compton, C, Curtin, J, Dalesio, L, Davidson, K, Dixon, K, Facco, A, Ganni, V, Ganshyn, A, Gibson, P, Glasmacher, T, Hao, Y, Hodges, L, Holland, K, Hosoyama, K, Hseuh, H-C, Hussain, A, Ikegami, M, Jones, S, Kanemura, T, Kelly, M, Knudsen, P, Laxdal, RE, LeTourneau, J, Lidia, S, Machicoane, G, Marti, F, Miller, S, Momozaki, Y, Morris, D, Ostroumov, P, Popielarski, J, Popielarski, L, Prestemon, S, Priller, J, Ren, H, Russo, T, Saito, K, Stanley, S, Wiseman, M, Xu, T, and Yamazaki, Y

Subjects
Nuclear and Plasma Physics, Synchrotrons and Accelerators, Physical Sciences, Affordable and Clean Energy, Mathematical Sciences, Nuclear & Particles Physics, Mathematical sciences, Physical sciences
Abstract

The Facility for Rare Isotope Beams (FRIB) Project has entered the phase of beam commissioning starting from the room-temperature front end and the superconducting linac segment of first 15 cryomodules. With the newly commissioned helium refrigeration system supplying 4.5K liquid helium to the quarter-wave resonators and solenoids, the FRIB accelerator team achieved the sectional key performance parameters as designed ahead of schedule accelerating heavy ion beams above 20MeV/u energy. Thus, FRIB accelerator becomes world's highest-energy heavy ion linear accelerator. We also validated machine protection and personnel protection systems that will be crucial to the next phase of commissioning. FRIB is on track towards a national user facility at the power frontier with a beam power two orders of magnitude higher than operating heavy-ion facilities. This paper summarizes the status of accelerator design, technology development, construction, commissioning as well as path to operations and upgrades.

Published
2019

4. The Fast Linear Accelerator Modeling Engine for FRIB Online Model Service

Author

He, Z., Bengtsson, J., Davidsaver, M., Fukushima, K., Shen, G., and Ikegami, M.

Subjects
Physics - Accelerator Physics
Abstract

Commissioning of a large accelerator facility like FRIB needs support from an online beam dynamics model. Considering the new physics challenges of FRIB such as modeling of non-axisymmetric superconducting RF cavities and multi-charge state acceleration, there is no readily available online beam tuning code. The design code of FRIB super-conducting linac, IMPACT-Z, is not suitable for online tuning because of its code design and running speed. Therefore, the Fast Linear Accelerator Modeling Engine (FLAME), specifically designed to fulfill FRIB's online modeling challenges, is proposed. The physics model of FLAME, especially its novel way of modeling non-axisymmetric superconducting RF cavities using a multipole expansion based thin-lens kick model, is discussed in detail, and the benchmark results against FRIB design code is presented, after which the software design strategy of FLAME and its execution speed is presented.

Published
2016

5. Commissioning Status of the Linac for the Facility for Rare Isotope Beams

Author

Lidia, S., Ao, H., Barnes, B., Bennett, R., Bernal-Ruiz, E., Bollen, G., Brandon, J., Bull, B., Bultman, N., Casagrande, F., Chabot, D., Cogan, S., Compton, C., Davidson, K., Daykin, E., Georgiobani, D., Gibson, P., Grender, I., Kim, S.-H., Hartung, W., Hausmann, M., Hodges, L., Holland, K., Hussain, A., Ikegami, M., Konrad, M., Kiupel, G., Larter, T., Li, Z., Malloch, I., Machicoane, G., Maniar, H., Manwiller, P., Martins, B., Maruta, T., Morris, D., Morrison, P., Morton, C., Nesterenko, I., Omitto, D., Ostroumov, P., Pellemoine, F., Plastun, A., Popielarski, J., Popielarski, L., Pozdeyev, E., Ren, H., Rodriguez, P., Rodriguez, S., Russo, T., Saito, K., Shane, R., Stanley, S., Stolz, A., Timko, G., Wei, J., Xu, M., Xu, T., Yamazaki, Y., Yashimoto, T., Zhao, Q., and Zhao, S.

Published
2020
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6. Impacts of sea level rise and climate change on coastal plant species in the central California coast

Author

Garner, KL, Chang, MY, Fulda, MT, Berlin, JA, Freed, RE, Soo-Hoo, MM, Revell, DL, Ikegami, M, Flint, LE, Flint, AL, and Kendall, BE

Abstract

© 2015 Garner et al. Local increases in sea level caused by global climate change pose a significant threat to the persistence of many coastal plant species through exacerbating inundation, flooding, and erosion. In addition to sea level rise (SLR), climate changes in the form of air temperature and precipitation regimes will also alter habitats of coastal plant species. Although numerous studies have analyzed the effect of climate change on future habitats through species distribution models (SDMs), none have incorporated the threat of exposure to SLR. We developed a model that quantified the effect of both SLR and climate change on habitat for 88 rare coastal plant species in San Luis Obispo, Santa Barbara, and Ventura Counties, California, USA (an area of 23,948 km2). Our SLR model projects that by the year 2100, 60 of the 88 species will be threatened by SLR. We found that the probability of being threatened by SLR strongly correlates with a species' area, elevation, and distance from the coast, and that 10 species could lose their entire current habitat in the study region. We modeled the habitat suitability of these 10 species under future climate using a species distribution model (SDM). Our SDM projects that 4 of the 10 species will lose all suitable current habitats in the region as a result of climate change. While SLR accounts for up to 9.2 km2 loss in habitat, climate change accounts for habitat suitability changes ranging from a loss of 1,439 km2 for one species to a gain of 9,795 km2 for another species. For three species, SLR is projected to reduce future suitable area by as much as 28% of total area. This suggests that while SLR poses a higher risk, climate changes in precipitation and air temperature represents a lesser known but potentially larger risk and a small cumulative effect fromboth.

Published
2015

8. Consequences of Climate Change for Native Plants and Conservation

Author

Hannah, L., Shaw, M. R., Roehrdanz, P., Ikegami, M., Soong, O., and Thorne, J.

Abstract

Species ranges are dynamic, and often respond to changes in global climate. Recorded increases of global average temperatures through the twentieth century have already resulted in observed shifts of species ranges within California. Projections of future species distributions under climate change are possible through models that correlate known species occurrences with observed historical climate, then project this correlation onto scenarios of climate change. Previous work in California has focused on modeling changes in the distribution of vegetation and species. This study expands on this work through (1) modeling species at finer spatial scales than previously possible, (2) applying those models in advanced conservation planning tools, and (3) illustrating the intersection of human adaptation and conservation under climate change. Section 1 presents a suite of species distribution models created with climate and water balance data that has been statistically downscaled to finer horizontal resolutions than previous statewide modeling efforts. The models encompass range simulations for over 2,000 native California plant species at scales of 90 meters, 270 meters, 800 meters, 4 kilometers, and 16 kilometers, using three time periods, two global climate models, and two emissions scenarios. Section 2 presents Network Flow Analysis that has been developed as a conservation planning tool to assess landscape connectivity for species to respond to climate change. California is a particularly challenging application for Network Flow Analysis because of its large size and diverse flora. This paper presents methods that have been developed to overcome these challenges and applied as proof-of-concept for use in California. Section 3 presents changing suitability for wine grape cultivation in California using fine-scale (270 meter) climatology. Results from this study show that projected future distributions of climates currently associated with California viticulture may result in cropping changes or other adaptive responses from wine grape growers, with potentially serious implications for land and water conservation.

Published
2012

10. Comparison of particle simulation with j-parc linac mebt beam test results

Author

Ikegami, M., Kato, T., Igarashi, Z., Ueno, A., Kondo, Y., Ryne, R., and Qiang, J.

Abstract

The construction of the initial part of the J-PARC linac has been started at KEK for beam tests before moving to the JAERI Tokai campus, where J-PARC facility is finally to be constructed. The RFQ and MEBT (Medium Energy Beam Transport) has already been installed at KEK, and the beam test has been performed successfully. In this paper, the experimental results of the beam test are compared with simulation results with a 3D PIC (Particle-In-Cell) code, IMPACT. Copyright 2003 American Institute of Physics

Published
2003

12. Review on Recent High Intensity Physics Experiments Relevant to X-Ray and Quantum Beam Generation at JAEA

Author

Daido, H., Pirozhkov, A., Nishiuchi, M., Yogo, A., Orimo, S., Ogura, K., Sagisaka, A., Daito, I., Mori, M., Ikegami, M., Kiriyama, H., Okada, H., Bulanov, S., Esirkepov, T., Kanazawa, S., Kondo, S., Shimomura, T., Tanoue, M., Nakai, Y., Sasao, H., Wakai, D., Bolton, P., Fukuda, Y., Faenov, A., Pikuz, T., Suzuki, M., Tampo, M., Sakaki, H., Tajima, T., Kawanishi, S., Kawachi, T., Nishikino, M., Choi, I. W., Kim, C. M., Jeong, T. M., Hafz, N., Yu, T. J., Sung, J. H., Noh, Y. -C., Ko, D. -K., Lee, J., Oishi, Y., Nemoto, K., Nayuki, T., Fujii, T., Nagatomo, H., Nagai, K., Nishimura, H., Lewis, Ciaran L. S., editor, and Riley, Dave, editor

Published
2009
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16. Accelerator commissioning and rare isotope identification at the Facility for Rare Isotope Beams

Author

Wei, J., primary, Ao, H., additional, Arend, B., additional, Beher, S., additional, Bollen, G., additional, Bultman, N., additional, Casagrande, F., additional, Chang, W., additional, Choi, Y., additional, Cogan, S., additional, Compton, C., additional, Cortesi, M., additional, Curtin, J., additional, Davidson, K., additional, Du, X., additional, Elliott, K., additional, Ewert, B., additional, Facco, A., additional, Fila, A., additional, Fukushima, K., additional, Ganni, V., additional, Ganshyn, A., additional, Gao, J., additional, Glasmacher, T., additional, Guo, J., additional, Hao, Y., additional, Hartung, W., additional, Hasan, N., additional, Hausmann, M., additional, Holland, K., additional, Hseuh, H. C., additional, Ikegami, M., additional, Jager, D., additional, Jones, S., additional, Joseph, N., additional, Kanemura, T., additional, Kim, S.-H., additional, Knudsen, P., additional, Kortum, B., additional, Kwan, E., additional, Larter, T., additional, Laxdal, R. E., additional, Larmann, M., additional, Laturkar, K., additional, LeTourneau, J., additional, Li, Z.-Y., additional, Lidia, S., additional, Machicoane, G., additional, Magsig, C., additional, Manwiller, P., additional, Marti, F., additional, Maruta, T., additional, McCartney, A., additional, Metzgar, E., additional, Miller, S., additional, Momozaki, Y., additional, Morris, D., additional, Mugerian, M., additional, Nesterenko, I., additional, Nguyen, C., additional, O’Brien, W., additional, Openlander, K., additional, Ostroumov, P. N., additional, Patil, M., additional, Plastun, A. S., additional, Popielarski, J., additional, Popielarski, L., additional, Portillo, M., additional, Priller, J., additional, Rao, X., additional, Reaume, M., additional, Ren, H., additional, Saito, K., additional, Smith, M., additional, Steiner, M., additional, Stolz, A., additional, Tarasov, O. B., additional, Tousignant, B., additional, Walker, R., additional, Wang, X., additional, Wenstrom, J., additional, West, G., additional, Witgen, K., additional, Wright, M., additional, Xu, T., additional, Xu, Y., additional, Yamazaki, Y., additional, Zhang, T., additional, Zhao, Q., additional, Zhao, S., additional, Dixon, K., additional, Wiseman, M., additional, Kelly, M., additional, Hosoyama, K., additional, and Prestemon, S., additional

Published
2022
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37. Transient induction of TGF-[alpha] disrupts lung morphogenesis, causing pulmonary disease in adulthood

Author

Le Cras, T.D., Hardie, W.D., Deutsch, G.H., Albertine, K.H., Ikegami, M., Whitsett, J.A., and Korfhagen, T.R.

Subjects
Lungs -- Research, Transforming growth factors -- Research, Biological sciences
Abstract

Transient induction of TGF-[alpha] disrupts lung morphogenesis, causing pulmonary disease in adulthood. Am J Physiol Lung Cell Mol Physiol 287: L718-L729, 2004. First published April 16, 2004; 10.1152/ajplung. 00084.2004.--Clinical studies have associated increased transforming growth factor (TGF)-[alpha] and EGF receptor with lung remodeling in diseases including bronchopulmonary dysplasia (BPD). BPD is characterized by disrupted alveolar and vascular morphogenesis, inflammation, and remodeling. To determine whether transient increases in TGF-[alpha] are sufficient to disrupt postnatal lung morphogenesis, we utilized neonatal transgenic mice conditionally expressing TGF-[alpha]. Expression of TGF-[alpha] from postnatal days 3 to 5 disrupted postnatal alveologenesis, causing permanent enlargement of distal air spaces in neonatal and adult mice. Lung volume-to-body weight ratios and lung compliance were increased in adult TGF-a transgenic mice, whereas tissue and airway elastance were reduced. Elastin fibers in the alveolar septae were fragmented and disorganized. Pulmonary vascular morphogenesis was abnormal in TGF-[alpha] mice, with attenuated and occasionally tortuous arterial branching, The ratios of right ventricle weight to left ventricle plus septal weight were increased in TGF-[alpha] mice, indicating pulmonary hypertension. Electron microscopy showed gaps in the capillary endothelium and extravasation of erythrocytes into the alveolar space of TGF-[alpha] mice. Hemorrhage and inflammatory cells were seen in distal air spaces at 1 mo of age. In adult TGF-[alpha] mice. alveolar remodeling, nodules, proteinaceous deposits, and inflammatory cells were seen. Immunostaining for prosurfactant protein C showed that type II cells were abundant in the nodules, as well as neutrophils and macrophages. Trichrome staining showed that pulmonary fibrosis was minimal, apart from areas of nodular remodeling in adult TGF-[alpha] mice. Transient induction of TGF-[alpha] during early alveologenesis permanently disrupted lung structure and function and caused chronic lung disease. bronchopulmonary dysplasia; neonatal lung development; epidermal growth factor receptor; pulmonary hypertension; lung remodeling

Published
2004

39. Genetic evolution of α fetoprotein producing gastric cancer

Author

Fujii, H., Ichikawa, K., Takagaki, T., Nakanishi, Y., Ikegami, M., Hirose, S., and Shimoda, T.

Subjects
Health
Abstract

J Clin Pathol 2003;56:942-949 Background: α Fetoprotein (AFP) producing gastric cancer is an unusual form of aggressive adenocarcinoma with a complex histological picture, including enteroblastic and hepatoid differentiation. Aims: To [...]

Published
2003

44. Does infill outperform climate-adaptive growth policies in meeting sustainable urbanization goals? A scenario-based study in California, USA

Author

Thorne, James, Ferreira Dos Santos, M.J., Bjorkman, Jacquelyn H., Soong, O, Ikegami, M, Seo, C, Hannah, Lee, and Environmental Sciences

Subjects
0106 biological sciences, Climate mitigation and adaptation, 010504 meteorology & atmospheric sciences, Urban growth model, Management, Monitoring, Policy and Law, 010603 evolutionary biology, 01 natural sciences, Ecosystem services, Urban climate, Urbanization, Infill, 0105 earth and related environmental sciences, Nature and Landscape Conservation, Sustainable development, Ecology, Land use, business.industry, Sustainable urbanization, Environmental resource management, Urban Studies, Geography, UPlan, Redevelopment, Sustainability, Scenario modeling, business
Abstract

Land allocation for urban growth is central to sustainable development strategy because urban growth can impact space available for food production, ecosystem services and biodiversity conservation. Urbanization is a growing stressor due the 2.5 billion additional people projected to live in urban areas by 2050. Potential climate change impacts to natural systems increase the need for sustainable urbanization, which should integrate land use needs for urban growth with climate adaptation objectives such as maintaining biodiversity, food production and ecosystem services. Here we compare climate-neutral and climate-adaptive urbanization scenarios to see which produces the most sustainable urbanization, defined as being the most effective at meeting development, conservation, and two climate adaptation objectives. We modeled five urban growth scenarios portraying an increase of 25.8 million people by 2050 for California, USA comprising three climate-neutral scenarios: business-as-usual, compact-new-growth and infill (redevelopment); and two climate-adaptive scenarios: preservation of agricultural climate refugia or future plant dispersal corridors. Infill was the least impacting for the multiple objectives tested; preserving 46–57% more land for other uses. Each climate-adaptive scenario reduced land consumption for its respective target, but increased impacts to the opposite climate-adaptive scenario target. Infill has the potential to contribute towards sustainable urbanization, particularly if combined with other climate adaptation targets.

Published
2017
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45. Abstracts of presentations on plant protection issues at the xth international congress of virology: August 11–16,1996 Binyanei haOoma, Jerusalem, Israel Part 2 Plenary Lectures

Author

Ramirez, E., Hernádez, A., Ham, E., Barrón, B. L., Ding, S. W., Li, W. X., Shi, B. J., Symons, R. H., Li, Q., Ryu, K. H., Palukaitis, P., Kaplan, I. B., Palukaitis, P., Kaplan, I. B., Palukaitis, P., Gal-On, A., Kunhara, J., Otsubo, T., Tomaru, K., Tsuda, S., Kinta, M., Lin, T., Johnson, J. E., Porta, C., Taylor, K. M., Spall, V. E., Lomonossoff, G. P., Spall, V. E., Porta, C., Lomonossoff, G. P., Gal-On, A., Meiri, E., Raccah, B., Gaba, V., Ikegami, M., Kawashima, H., Murayama, A., Natsuaki, T., Kageyama, Y., Sugimura, N., Thole, V., Bol, J. F., Deiman, B. A. L. M., Koenen, A. K., Pleij, C. W. A., Chaleeprom, W., Bateson, M. F., Dale, J. L., Badge, J. L., Foster, G. D., Brunt, A. A., Robinson, D., Schubert, J., Rabenstein, F., Merits, A., Yeh, Shyi-Dong, Chiang, Chu-Hui, Wang, Ching-Hsien, Chiang, Chu-Hui, Yeh, Shyi-Dong, Golshani, A., Ivanov, I. G., AbouHaidar, M. G., Rodoni, B. C., Harding, R. M., Bateson, M. F., Dale, J. L., Oertel, U., Fuchs, E., Schubert, J., Yang, S. J., Revere, F., Walter, J., Le Gall, O., Dunez, J., Candresse, T., Lot, H., Souche, S., Kasschau, Kristin D., Carrington, James C., Chiang, A. N., Turner, N. E., Hwang, D. J., Chachulska, A. M., Zagórski, W., Robaglia, C., Chrzanowska, M., Truve, E., Tamm, T., Saarma, M., Makinen, K., Wang, Aiming, Carrier, Karma, Wieczorek, Andrew, Huguenot, Claire, Sanfacon, Helene, Wurscher, M. A., Christensen, F. E., Prody, G. A., Sanchez-Navarro, J. A., Pallas, V., Carson, R., Dagless, E., Lock, S., Turner, R., Foster, G. D., Badge, J. L., Adams, M., Antoniw, J., Brunt, A. A., Phillips, S., Kashiwazaki, S., Seal, S., Karamagioli, M., Druka, Amis, Makhdoom, Rahat, Yitang, Yan, Hull, Roger, Kikkert, M., Bodegom, P., Storms, M., van Lent, J., Kormelink, R., Goldbach, R., De Haan, P., De Rover, A. R., Van Schepen, A., Gielen, J. J. L., Van Grinsven, M. Q. J. M., Livneh, O., Vardi, E., Kuznetsova, L., Aliskevicius, E., Stram, Y., Sela, I., Dinant, S., Kusiak, C., Blaise, F., Chupeau, Y., Astier, S., Albouy, J., Clifford, T. B., Taylor, S. C., Stratford, R., Foster, G. D., Xiao, X. W., Frenkel, M. J., Chu, P., Tabe, L., Shukla, D. D., Ward, C. W., Hwang, Duk-Ju, Turner, Nilgun, Taylor, S. C., Mooney, A., MacFarlane, S. A., Twell, D., Foster, G. D., Jacquet, C., Ravelonandro, M., Bachelier, J. C., Dunez, J., Almási, A., Böddi, B., Szigeti, Z., Ekes, M., Gaborianvi, R., Yankulova, Margarita, Ivanova, Lidia, Adam, G., Guelemerov, S., Nikolaeva, Velitchka, Atanassov, A., Prins, Marcel, de Haan, Peter, Goldbach, Rob, Duan, Y. P., Powell, C. A., Purcifull, D. E., Hiebert, E., Levine, B., Faktor, O., Zeituny, Silvy, Edelbaum, Orit, Sela, L., Marano, Maria-Rosa, Ratcliff, Frank, Baulcombe, David C., van Oers, Monique M., Linthorst, Huub J. M., Bol, John F., Schillberg, S., Zimmermann, S., Drossard, J., Schumann, D., Nahring, J., Fischer, R., Lapidot, Moshe, Arce-Johnson, Patricio, Rivera-Bustamante, Rafael, Beachy, Roger N., Cassidy, Brandt G., Flasinski, Stanislaw, Hajimorad, M. R., Wesley, Varsha, Angel-Diaz, J., Mayo, M. A., Hafner, G. J., May, G. D., Becker, D. K., Harding, R. M., Arntzen, C. J., Dale, J. L., Taylor, S. C., Porter, J., Foster, G. D., Palukaitis, P., Hellwald, K. H., Banerjee, N., Zaitlin, M., Gal-On, A., Wolf, D., Faure, J. E., Pilowsky, M., Cohen, S., Zelcer, A., Hardi, V., Tomassoli, L., Kaniewski, W. K., Mitsky, T., Barba, M., Hou, Y. -M., Ursin, V. M., Sanders, R., Gilbertson, R. L., Gruden, Kristina, Štrukelj, Borut, Brzin, Joze, Ravnikar, Maja, Maganja, Darja Barlič, Kregar, Igor, Maki-Valkama, T., Pehu, T., Valkonen, J., Lento, K., Pehu, E., Zaitlin, M., Kaniewski, W. K., Lawson, E. C., Feldman, J., Zalewski, J., Saarma, M., Kuittinen, T., Valkonen, J., Atiri, G. I., Romero, A., Arroyo, R., Soto, M. J., Martínez-Zapater, J. M., Ponz, F., Gilardi, P., López, L., García-Luque, I., Serra, M. T., Pang, Sheng-Zhi, Jan, Fuh-Jyh, Carney, Kim, Tricoli, David M., Quemada, Hector D., Gonsalves, Dennis, Aboul-Ata, A. E., Thouvenel, J. -C., Marshall, D., Abo-El-Saad, Sh., Satour, M., Mazithulela, G., Mehlo, L., Gahakwa, D., Leech, M., Boulton, M. I., Davies, J. W., Christou, P., Huet, H., Sivamani, E., Ong, C. A., Chen, L., de Kochko, A., Beachy, R. N., Fauquet, C. M., Sithisarn-Burns, P., Maugeri, M. M., Dale, J. L., Smith, G. R., Harding, R. M., Handley, J. A., Harding, R. M., Smith, G. R., Dale, J. L., Graichen, K., Peterka, J., Chu, Paul, Larkin, Phil, Higgins, T. J., Wylie, S., Jones, M. G. K., Somsap, V., Loo, H. P., Li, D., Mathews, A., Jones, M. G. K., Dwyer, G. I., Jones, M. G. K., McCarthy, P. L., Hansen, J., Shiel, P. J., Zemetra, R. S., Wyatt, S. D., Berger, P. H., Ford, C., Collins, N., Rathjen, J., Shams-Bakhsh, M., Paltridge, N., Symons, R. 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1997
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