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Wyszukujesz frazę "Du, G.-Y." wg kryterium: Autor


Tytuł:
Morphology and developmental traits of the trilobite Changaspis elongata from the Cambrian Series 2 of Guizhou, South China
Autorzy:
Du, G.-Y.
Peng, J.
Wang, D.-Z.
Wang, Q.-J.
Wang, Y.-F.
Zhang, H.
Wydawca:
Polska Akademia Nauk. Instytut Paleobiologii PAN
Powiązania:
https://bibliotekanauki.pl/articles/22906.pdf  Link otwiera się w nowym oknie
Opis:
The morphology and ontogeny of the trilobite Changaspis elongata based on 216 specimens collected from the Lazizhai section of the Balang Formation (Stage 4, Series 2 of the Cambrian) in Guizhou Province, South China are described. The relatively continuous ontogenetic series reveals morphological changes, and shows that the species has seventeen thoracic segments in the holaspid period, instead of the sixteen as previously suggested. The development of the pygidial segments shows that their number gradually decreases during ontogeny. A new dataset of well-preserved specimens offers a unique opportunity to investigate developmental traits after segment addition is completed. The ontogenetic size progressions for the lengths of cephalon and trunk show overall compliance with Dyar’s rule. As a result of different average growth rates for the lengths of cephalon, trunk and pygidium, the length of the thorax relative to the body shows a gradually increasing trend; however, the cephalon and pygidium follow the opposite trend. Morphometric analysis across fourteen post-embryonic stages reveals growth gradients with increasing values for each thoracic segment from anterior to posterior. The reconstruction of the development traits shows visualization of the changes in relative growth and segmentation for the different body parts. The new dataset and growth gradient of the trunk suggest that the thoracic segment growth dynamics of early Cambrian to Silurian trilobites follow the same general continuous, steady-state growth gradient decreasing from posterior to anterior.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
One shot profilometry using iterative two-step temporal phase-unwrapping
Autorzy:
Du, G.
Wang, M.
Zhou, C.
Si, S.
Li, H.
Lei, Z.
Li, Y.
Tematy:
phase unwrapping
composite fringe pattern
Fourier transform
two-step temporal phase-unwrapping
Pokaż więcej
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Powiązania:
https://bibliotekanauki.pl/articles/173912.pdf  Link otwiera się w nowym oknie
Opis:
This paper reviews two techniques that have been recently published for three-dimensional profilometry and proposes one shot profilometry using iterative two-step temporal phase-unwrapping by combining the composite fringe projection and the iterative two-step temporal phase unwrapping algorithm. In temporal phase unwrapping, many images with different frequency fringe pattern are needed to project, which would take much time. In order to solve this problem, Ochoa proposed a phase unwrapping algorithm based on phase partitions using a composite fringe. However, we found that the fringe order determined through the construction of phase partitions tended to be imprecise. Recently, we proposed an iterative two-step temporal phase unwrapping algorithm, which can achieve high sensitivity and high precision shape measurement. But it needs multiple frames of fringe images which would take much time. In order to take into account both the speed and accuracy of three-dimensional shape measurement, we get a new, and more accurate unwrapping method based on a composite fringe pattern by combining these two techniques. This method not only retains the speed advantage of Ochoa’s algorithm, but also greatly improves its measurement accuracy. Finally, the experimental evaluation is conducted to prove the validity of the proposed method.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Improved method for phase wraps reduction in profilometry
Autorzy:
Du, G.
Wang, M.
Zhou, C.
Si, S.
Li, H.
Lei, Z.
Li, Y.
Tematy:
phase unwrapping
zero-padding
Fourier transform
carrier-frequency
profilometry
Pokaż więcej
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Powiązania:
https://bibliotekanauki.pl/articles/173793.pdf  Link otwiera się w nowym oknie
Opis:
In order to completely eliminate, or greatly reduce the number of phase wraps in 2D wrapped phase map, Gdeisat and co-workers proposed an algorithm, which uses shifting the spectrum towards the origin. But the spectrum can be shifted only by an integer number, meaning that the phase wraps reduction is often not optimal. In addition, Gdeisat’s method will take much time to make the Fourier transform, inverse Fourier transform, select and shift the spectral components. In view of the above problems, we proposed an improved method for phase wraps elimination or reduction. First, the wrapped phase map is padded with zeros, the carrier frequency of the projected fringe is determined by high resolution, which can be used as the moving distance of the spectrum. And then realize frequency shift in spatial domain. So it not only can enable the spectrum to be shifted by a rational number when the carrier frequency is not an integer number, but also reduce the execution time. Finally, the experimental results demonstrated that the proposed method is feasible.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Establishment of 5-Fluorouracil-resistant canine mammary tumor cell line
Autorzy:
Zhou, B.
Zhang, D.
Pei, S.M.
Zhang, K.
Du, H.C.
Jin, Y.P.
Lin, D.G.
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Powiązania:
https://bibliotekanauki.pl/articles/30283.pdf  Link otwiera się w nowym oknie
Opis:
Canine mammary tumors are the most common neoplasms in intact female dogs. The surgery cannot always solve the problem, chemotherapy are recommend to these patients. However, chemotherapy could always fail because of multidrug resistance (MDR). Through stepwise increasing 5-Fluorouracil (5-FU) concentration in the culture medium, a 5-FU-resistant canine mammary tumor cell line CMT7364/5-FU was established to disclose the molecular mechanism of the drug resistance. Cell morphology, cell sensitivity to drugs, growth curves, expression of proteins, and chemo-sensitivity in vivo were compared between the parental cell line and resistant cell line. As compared it to its parental cell line (CMT7364), CMT7364/5-FU showed different morphology, cross-resistant to other chemo-drugs and a prolonged population doubling time (PDT). The drug efflux pump proteins (ABCB1 and ABCG2) in CMT7364/5-FU were up-regulated. In vivo, the similar result revealed that CMT7364/5-FU cell line was more resistant to 5-FU. In conclusion, a 5-FU-resistant canine mammary tumor cell line (CMT7364/5-FU) was successfully established, it can serve as a good model for researching the mechanism of MDR and screening effective agents to reverse drug resistance.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The unsteadiness of tip clearance flow and its effect to stability of transonic axial compressor
Nieustaloność przepływu w szczelinie wierzchołkowej i jej wpływ na stabilność pracy przydźwiękowej sprężarki osiowej
Autorzy:
Hu, J. F.
Zhu, X. C.
Ou-Yang, H.
Tian, J.
Wu, Y. D.
Qiang, X. Q.
Zhao, G.
Du, Z. H.
Tematy:
tip leakage flow
compressor
stability
Pokaż więcej
Wydawca:
Polskie Towarzystwo Mechaniki Teoretycznej i Stosowanej
Powiązania:
https://bibliotekanauki.pl/articles/281445.pdf  Link otwiera się w nowym oknie
Opis:
The steady and unsteady RANS simulations of a transonic compressor rotor (NASA rotor 37) are performed to investigate the tip clearance flow characteristic and correlations between tip leakage flow and compressor stability. For steady simulations, the results are compared with the aerodynamic probe and laser anemometer data. The speed lines and span-wise aerodynamic parameters agree well with the experimental data. On the other hand, the tip clearance flow of unsteady simulations are analysed clearly at a near stall condition. The results show that there is a mass flow rate boundary. The tip clearance flow oscillates substantially with a frequency about 50% BPF when the mass is less than that, which is caused by tip clearance flow, shock, and the interaction between them and the oncoming flow. The interface between the oncoming flow and clearance flow shifts forward, and the tip clearance flow may spill over into the adjacent blade passage as the mass flow decreases, which may results in the spike stall inception.
W pracy przedstawiono symulacje stanu ustalonego i nieustalonego przydźwiękowej sprężarki osiowej (turbina NASA 37) z zastosowaniem metody Reynoldsa uśredniania równań Naviera-Stokesa (RANS) w celu zbadania charakterystyki przepływu w szczelinie wierzchołkowej oraz określenia zależności pomiędzy stratami związanymi z upływem w tej szczelinie a stabilnością pracy sprężarki. Wyniki symulacji stanu ustalonego porównano z danymi doświadczalnymi uzyskanymi za pomocą sondy aerodynamicznej i laserowego wiatromierza. Wyznaczone wzdłuż rozpiętości sprężarki linie prędkości przepływu i jego parametry aerodynamiczne okazały się zgodne z danymi doświadczalnymi. W przypadku symulacji stanu nieustalonego, analizę przepływu w szczelinie wierzchołkowej przeprowadzono dla warunków bliskich oderwania, tj. utraty wydajności sprężarki, wyznaczając graniczny wydatek przepływu dla takiej sytuacji. Poniżej tej granicznej wartości, zmiany przepływu w szczelinie oscylują z częstotliwością sięgającą 50% częstotliwości przejścia łopatek (tzw. BPF), co jest konsekwencją interakcji wywołanej zderzeniem przepływu z falą napływową w szczelinie wierzchołkowej. Powierzchnia tej interakcji przesuwa się do przodu, a sam przepływ może rozpaść się na fragmenty znajdujące ujście w kanałach przyległych łopatek. Zjawisko to zachodzi przy malejącym wydatku, a to z kolei może indukować oderwanie przepływu skokowymi zmianami mocy współpracującego silnika.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Pooled safety analysis of zanubrutinib monotherapy in patients with B-cell malignancies
Autorzy:
Dimopoulos, Meletios A.
Ji, Meng
D'Sa, Shirley
Cohen, Aileen
Xu, Wei
Tam, Constantine S
Huang, Jane
Garcia-Sanz, Ramon
Roberts, Andrew W
Zhu, Jun
Li, Jianyong
Marlton, Paula
Guo, Haiyi
Song, Yuqin
Jurczak, Wojciech
Gottlieb, David J
Zhou, Lei
Munoz, Javier
Du, Chenmu
Phillips, Tycel
Novotny, William
Cull, Gavin
Owen, Roger G.
Zhu, Hongjie
Tedeschi, Alessandra
Trotman, Judith
Chan, Wai Y.
Qiu, Lugui
Opat, Stephen
Opis:
Zanubrutinib is a selective Bruton tyrosine kinase (BTK) inhibitor evaluated in multiple B-cell malignancy studies. We constructed a pooled safety analysis to better understand zanubrutinib-associated treatment-emergent adverse events (TEAEs) and identify treatment-limiting toxicities. Data were pooled from 6 studies (N=779). Assessments included type, incidence, severity, and outcome of TEAEs. Median age was 65 years; 20% were ≥75 years old. Most patients had Waldenström macroglobulinemia (33%), chronic lymphocytic leukemia/small lymphocytic lymphoma (29%), or mantle-cell lymphoma (19%). Median treatment duration was 26 months (range: 0.1-65); 16% of patients were treated for ≥3 years. Common nonhematologic TEAEs were upper respiratory tract infection (URI, 39%), rash (27%), bruising (25%), musculoskeletal pain (24%), diarrhea (23%), cough, pneumonia (21% each), urinary tract infection (UTI), fatigue (15% each). Most common grade ≥3 TEAEs were pneumonia (11%), hypertension (5%), URI, UTI, sepsis, diarrhea, and musculoskeletal pain (2% each). Atrial fibrillation and major hemorrhage occurred in 3% and 4% of patients, respectively. Atrial fibrillation, hypertension and diarrhea occurred at lower rates than those reported historically for ibrutinib. Grade ≥3 AEs included neutropenia (23%), thrombocytopenia (8%), and anemia (8%). Serious TEAEs included pneumonia (11%), sepsis (2%), and pyrexia (2%). Treatment discontinuations and dose reductions for AEs occurred in 10% and 8% of patients, respectively. Thirty-nine patients (4%) had fatal TEAEs, including pneumonia (n=9), sepsis (n=4), unspecified cause (n=4), and multiple organ dysfunction syndrome (n=5). This analysis demonstrates that zanubrutinib is generally well tolerated with a safety profile consistent with known BTK inhibitor toxicities; these were manageable and mostly reversible.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Hot QCD white paper
Autorzy:
Perepelitsa, D. V.
O'Brien, E.
Zajc, W. A.
Niida, T.
Yee, H. -U.
Wang, F.
Ratti, C.
Shi, Z.
Bock, F.
Schäfer, T.
Narde, A.
Koch, V.
Finger Jr., M.
Putschke, J.
Berdnikov, Y.
Ramasubramanian, N. V.
Bossi, H.
Drees, A.
Salur, S.
Voloshin, S. A.
Ye, Z.
Schenke, B.
Lajoie, J. G.
Morrison, D. P.
Judd, E. G.
Yao, X.
Shen, C.
Hong, B.
Caines, H.
Jacak, B. V.
Praszałowicz, Michał
Kotov, D.
Odyniec, G.
Evdokimov, O.
Timmins, A. R.
Bautista, I.
Jheng, H. R.
Karpenko, I.
Song, H.
Knospe, A. G.
Jahan, J.
Blair, J. T.
Tribedy, P.
Yang, Y.
Luo, X.
Teaney, D.
Videbæk, F.
Durham, J. M.
Boimska, B.
Liu, M. X.
Khachatryan, V.
Dexheimer, V.
Lim, S. H.
Okorokov, V. A.
Schmidt, N. V.
Loizides, C.
Csanád, M.
Osborn, J. D.
Reed, R.
Kharzeev, D. E.
Thomas, D.
Ruan, L.
Jeon, S.
Majumder, A.
Seger, J.
Gonzalez, V.
Soudi, I.
Chen, Y.
Minafra, N.
Menon, A. S.
Xie, W.
Nagle, J. L.
Kimelman, B.
Dash, A. P.
Schmier, A.
Bielcik, J.
Becattini, F.
Rueda, O. V.
Stephanov, M.
Luzum, M.
Tapia Takaki, D.
Venugopalan, R.
Nouicer, R.
Royon, C.
Steinberg, P.
Hachiya, T.
Dehmelt, K.
Mueller, B.
Dong, X.
Ma, R.
Mehtar-Tani, Y.
Petreczky, P.
Greene, S. V.
Frawley, A. D.
Geurts, F.
Chien, Y. -T.
He, X.
Sumbera, M.
Klein, S. R.
Rosati, M.
Tu, Z.
Heinz, U.
Klay, J. L.
Strickland, M.
Weyhmiller, S.
Stahl Leiton, A. G.
Noronha-Hostler, J.
Krintiras, G. K.
Rinn, T.
Read, K. F.
Tang, A. H.
Mak, S.
Novitzky, N.
Gale, C.
Ivanishchev, D.
Ehlers, R. J.
Likmeta, I.
Mignerey, A. C.
Arslandok, M.
Noronha, J.
Sakaguchi, T.
Frantz, J.
Grau, N.
Singh, M.
Smith, K. L.
Sarsour, M.
Bellwied, R.
Seto, R
Smirnov, N.
Park, S.
Vovchenko, V.
Humanic, T. J.
Liao, J.
Elfner, H.
Sickles, A. M.
Singh, B. K.
Bass, S. A.
Beattie, C.
Kim, M.
Kuo, C. M.
Grossberndt, S. K.
Baty, A. A.
Wang, X. -N.
Kapusta, J. I.
Berdnikov, A.
Nattrass, C. E.
Vujanovic, G.
Shulga, E.
Velkovska, J.
Chiu, M.
Finger, M.
Sunar Cerci, D.
Connors, M. E.
Rebello Teles, P.
Jia, J.
Wang, X.
David, G.
Paquet, J. -F.
Rapp, R.
Tuo, S.
Du, L.
Kunnawalkam Elayavalli, R.
Lee, Y. -J.
Longo, R.
Xu, N.
Markert, C.
Pruneau, C.
Parotto, P.
Pinkenburg, C.
Sheibani, Oveis
Tachibana, Y.
da Silva, C. L.
Li, W.
Roland, G.
Opis:
Hot QCD physics studies the nuclear strong force under extreme temperature and densities. Experimentally these conditions are achieved via high-energy collisions of heavy ions at the Relativistic Heavy Ion Collider (RHIC) and the Large Hadron Collider (LHC). In the past decade, a unique and substantial suite of data was collected at RHIC and the LHC, probing hydrodynamics at the nucleon scale, the temperature dependence of the transport properties of quark-gluon plasma, the phase diagram of nuclear matter, the interaction of quarks and gluons at different scales and much more. This document, as part of the 2023 nuclear science long range planning process, was written to review the progress in hot QCD since the 2015 Long Range Plan for Nuclear Science, as well as highlight the realization of previous recommendations, and present opportunities for the next decade, building on the accomplishments and investments made in theoretical developments and the construction of new detectors. Furthermore, this document provides additional context to support the recommendations voted on at the Joint Hot and Cold QCD Town Hall Meeting, which are reported in a separate document.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
FCC physics opportunities : future circular collider conceptual design report, volume 1
Autorzy:
McCullough, M.
Incandela, J.
Canepa, A.
Hoehn, T.
Lechner, A.
Li, S.
Cantore-Cavalli, D.
Fox, J.
Rivkin, L.
Cibinetto, G.
Grudiev, A.
Bruzzone, P.
Sahin, M.
Gallo, E.
McIntosh, P. A.
Olness, F. I.
Ibarrola, N.
Delmastro, M.
Braun-Munzinger, P.
Verducci, M.
Kara, S. O.
Infantino, A.
Graverini, E.
Duca, V. D.
Bayındır, C.
Sugita, K.
Ferdeghini, C.
Snoeys, W.
Zhuang, P.
Brüning, O.
Wang, R.
Perez, J. C.
Widorski, M.
Ilyina-Brunner, K.
Malgeri, L.
Maggiora, M.
Marinozzi, V.
Hrdinka, J.
Pieloni, T.
Luzum, M.
Testa, M.
Müller, A.-S.
Aielli, G.
Fonnesu, D.
Jensen, M.
Bauer, F.
Florio, M.
Dalena, B.
Drewes, M.
Felici, G.
Malyshev, O. B.
Tartarelli, G. F.
Auchmann, B.
Capeans, M.
Casalbuoni, S.
Milardi, C.
Kocak, F.
Weinzierl, S.
Gorine, G.
Tudora, A. A.
Ruehl, I.
Pontecorvo, L.
Chiarelli, G.
Hong, D. K.
Rimmer, R. A.
Ruhlmann-Kleider, V.
Furuseth, S. V.
Pittau, R.
Meignan, J.
Tesi, A.
Agrawal, P.
Vallone, G.
Nason, P.
Monge, R.
Giovannetti, M.
Pérez, F.
O’Callaghan, J. M.
Bernhardt, J. M.
Thaler, J.
Calvet, D.
Rinaldesi, R.
Lucchesi, D.
Casas, J.
Zanotto, L.
Iacobucci, G.
Scibile, L.
Gobbi, G.
du Pree, T.
Bovone, G.
Krammer, M.
García, J. B.
Rizzo, T.
Cardella, U.
Boos, E.
Burkart, F.
Syphers, M. J.
Barber, D. P.
Santiago, J.
Lunt, A. J. G.
Rafique, H.
Coccaro, A.
Beznosov, O.
Zernov, S. M.
Castorina, G.
Chevalier, L.
Salzburger, A.
Lorin, C.
Chernoded, A.
Knecht, M.
Ull, A. S.
Tommasini, D.
No, J. M.
Wu, X.
Panella, O.
Etzion, E.
Duda, P.
Koeberl, C.
Klein, U.
Sborlini, G. F. R.
Cakir, I. T.
Bartmann, W.
Bedeschi, F.
Riemann, S.
Goddard, B.
Li, R.
Papaphilippou, Y.
Cerri, A.
Rata, R.
Nisati, A.
Tikhomirov, V.
Stupakov, G.
Beaudette, F.
Hegglin, A.
Bologna, S.
Klute, M.
Lyubimtsev, D. A.
Poiron, A.
Quispe, M.
Laine, M.
Fernández-Téllez, A.
Dubovyk, I.
Curtin, D.
Spannowsky, M.
Abada, A.
Grau, A.
Guiducci, S.
Mentink, M.
Franchino, S.
Contino, R.
Abbrescia, M.
Garrido, I. C.
Yu, T.-T.
de Jauregui, D. S.
Chancé, A.
Ivanovs, A.
Bertarelli, A.
Neundorf, J.
Chala, M.
Barducci, D.
de Florian, D.
Schott, M.
Hug, F.
Lansberg, J. P.
Apollinari, G.
Suzuki, K.
Pérez, M. G.
Navarro, A. M. F.
Ciaccio, A. D.
Lançon, E.
Krkotic, P.
Andriatis, A.
Yao, W.-M.
Mulders, M.
Pampaloni, A.
Zanetti, M.
Skrzypek, M.
Gonçalo, R.
Cook, C. T. A.
Tock, J. P.
Hofer, M.
Sorbi, M.
Kilic, A.
Płaczek, Wiesław
Ravotti, F.
Rentería-Olivo, A. E.
Fowler, T.
Munilla, J.
Martínez-Hernández, M. I.
Takeuchi, M.
Jensen, E.
Velev, G.
Pugnat, T.
Trant, R.
Mertens, V.
Milanese, A.
Esposito, L. S.
Leogrande, E.
Parker, M. A.
Agaliotis, E. L.
Serin, L.
Crouch, M.
Fischer, E.
Zahnd, M.
Giunta, A.
Jones, M. A.
Perfilov, M.
Tejeda-Muñoz, G.
Bernardi, G.
Royon, C.
Niedziela, J.
Fiorendi, S.
Ge, S.-F.
Klyukhin, V. I.
Biarrotte, J.-L.
Pyarelal, A.
Liu, Z.
Malvezzi, S.
Han, C.
Foppiani, N.
Leroy, O.
Chorowski, M.
Low, I.
Bhat, P.
Rinolfi, L.
Akhundov, A.
Chetvertkova, V.
Ellison, J. A.
Merk, M.
Aiba, M.
Wagner, U.
Antinori, F.
Murray, M. J.
Ratoff, P.
Lobko, A.
Dünser, M.
Gorini, E.
Miralles, L. S.
Viehhauser, G.
Debono, C. J.
Eisenhardt, S.
Faus-Golfe, A.
Martin, O.
Su, S.
Oide, K.
Vecchi, L.
Karaventzas, V.
Usovitsch, J.
Valchkova, F.
Sidorov, S.
Yermolchik, V.
Massironi, A.
Srivastava, T.
da Costa, J. B. G.
Robens, T.
Hod, E. T.
Rescigno, M.
Veness, R.
Sauvain, M.
Bertolucci, S.
Allanach, B. C.
Meier, A.
Sian, T.
Tabarés, L. G.
Biagini, M. E.
Staśto, A. M.
Baudouy, B.
Bogacz, S. A.
Sarpün, I. H.
Ruiz, R.
Humann, B.
Salgado, C. A.
Sirvinskaite, R.
Risselada, T.
Khechen, D. E.
Osland, P.
Polini, A.
Sulak, L.
Salam, G. P.
Mahmoud, M. A.
Glukhov, S.
Sublet, A.
Gaudio, G.
Pinto, P. C.
Cogan, J.
Magnin, N.
Farilla, A.
Komppula, J.
Barjhoux, P.
Krämer, M.
Blanco-García, O. R.
Tang, K.
Keinz, P. A.
Rolandi, G.
Kollegger, A.
Elsing, M.
Rosaz, G.
Bramante, J.
Britzger, D.
Podlech, H.
Barr, A.
Fawcett, W. J.
Zadeh, S. G.
Morretta, V.
Eskola, K. J.
Gupta, R. S.
Cobal, M.
Butterworth, A.
Vysotsky, V.
Kumar, M.
Tavian, L.
Cardarelli, R.
Sarasola, X.
Tehrani, N. A.
Kowalski, S.
Papadopoulos, C. G.
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Ball, A. H.
Blekman, F.
Varasteh, M.
Valassi, A.
Craig, N.
Kramer, T.
Savelyeva, S.
Hacışahinoğlu, B.
Catalano, G.
Borgonovi, L.
Spira, M.
Bai, Y.
Maitre, J.
Kim, Y.-K.
Giagu, S.
Peruzzi, M.
Deliot, F.
Montenero, G.
Deghaye, S.
Zhao, Z.
Shirkov, G. D.
Louzguiti, A.
Millet, F.
Holdener, F.
Albacete, J. L.
Pont, M.
Skordis, E.
Pankov, A. A.
Dziewit, B.
Korjik, M.
Dominjon, A.
Roda, C.
Keintzel, J.
Guyot, C.
Cantergiani, E.
Malclés, J.
Torre, R.
Jarry, P.
Bernini, C.
Martinez, T.
Rubiras, O. R.
Giudice, G. F.
Bolukbasi, O.
Spallino, L.
Barzi, E.
Sallese, J. M.
Roloff, P.
Islam, R.
Proudfoot, J.
Cavasinni, V.
Taroni, S.
Penttinen, J.-P.
Rousset, B.
Morley, A. K.
Arbuzov, A.
Kretzschmar, L.
Krasnov, A. A.
Primavera, M.
Ogur, S.
Adzic, P. R.
Morales, J. P.
Grancagnolo, F.
Heinemann, K.
Romanenko, A.
Mele, B.
Senatore, C.
Andris, C.
Duval, F.
Lombardo, M. P.
Nie, Y.
Opis:
We review the physics opportunities of the Future Circular Collider, covering its e+e-, pp, ep and heavy ion programmes. We describe the measurement capabilities of each FCC component, addressing the study of electroweak, Higgs and strong interactions, the top quark and flavour, as well as phenomena beyond the Standard Model. We highlight the synergy and complementarity of the different colliders, which will contribute to a uniquely coherent and ambitious research programme, providing an unmatchable combination of precision and sensitivity to new physics.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł

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