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Wyszukujesz frazę "Cole, B." wg kryterium: Autor


Autorzy:
Solans, C.
Andre, K. D. J.
Spiesberger, H.
Cakir, O.
Denizli, H.
Cruz-Alaniz, E.
Ruan, X.
Camarda, S.
Olivier, G.
Luo, X.
Azuelos, G.
Lei, G.
Lappi, T.
Glover, N.
Zhang, J.
Flores-Sánchez, O.
Krelina, M.
Gonzalez-Sprinberg, G. A.
Nowakowski, M.
Yock, P.
Hessler, J.
Xiaohao, C.
Bertolucci, S.
Coleppa, B.
Jana, S.
Tudora, A.
Alekhin, S.
Yamaguchi, Y.
Turk Cakir, I.
Raicevic, N.
Pan, R.
Morreale, A.
Sinha, N.
Shipman, N.
Olry, G.
Tommasini, D.
Perez-Segurana, G.
Giuli, F.
Gehrmann-De Ridder, A.
Sahin, M.
Harland-Lang, L.
Jansova, M.
Godbole, R. M.
Lobodzinska, E.
Zomer, F.
Behnke, O.
Salgado, C. A.
Pietralla, N.
Granados, E.
Hayden, D.
Apsimon, R.
Khalek, R. A.
Martens, A.
Calıskan, A.
Li, X.
Wei, H.
Korostelev, M.
Kaabi, W.
Laycock, P.
Han, C. C.
Hesari, H.
Stanyard, J.
Rosado, A.
Smith, S.
Russenschuck, S.
Gunaydin, Y. O.
Mitra, M.
Daly, E.
Angal-Kalinin, D.
Trbojevic, D.
Mäntysaari, H.
Kretzschmar, J.
Liuti, S.
Newman, P.
Ratoff, P.
Moretti, S.
Catalan-Lasheras, N. C.
Corsini, R.
Poelker, M.
Litvinenko, V.
Wang, B.
Pires, J.
Paukkunen, H.
Zhang, R.
Armbruster, A.
Gilbert, A.
de Blas, J.
Sekine, T.
Liu, Y.
Sampayo, O. A.
Zhang, Z.
Wollmann, D.
Pire, B.
Nissen, E. A.
Kulipanov, G.
Wang, K.
Karadeniz, H.
Das, A.
Rezaeian, A. H.
Cooper-Sarkar, A.
Gehrmann, T.
Bailey, I.
Tsurin, I.
Kalinin, D. A.
Duarte, L.
Cormier, E.
Valloni, A.
Tanaka, M.
Bordry, F.
Auchmann, B.
Wallon, S.
Schenke, B.
Nergiz, Z.
Brüning, O.
Gerigk, F.
Słomiński, Wojciech
Tywoniuk, K.
Dutta, S.
Mohammadi Najafabadi, M.
Bogacz, A.
Huss, A.
Senol, A.
Nadolsky, P.
Köksal, M.
Osborne, J. A.
Rashed, A.
Aperio Bella, L.
Mondal, S.
Tapia-Takaki, D.
Bracinik, J.
Apolinario, L.
Latina, A.
Cassou, K.
Militsyn, B.
Yue, C. X.
Olness, F.
Zurita, P.
Queiroz, F. S.
Haug, F.
Cepila, J.
Repond, J.
Cetinkaya, V.
Raut, D.
Yang, H.
Honorato, C. G.
Kocak, F.
Hoffstaetter, G. H.
Stasto, A.
Eichhorn, R.
Trott, M.
Shang, L.
Peinaud, Y.
Klein, U.
Deshpande, K. S.
Satendra, K.
Marhauser, F.
Liu, M.
Eskola, K. J.
Schulte, D.
Patra, M.
Liang, H.
Balli, F.
Bruni, C.
Hug, F.
Dassa, L.
Kostka, P.
Holzer, B.
Levitchev, E.
Apyan, A.
Starostenko, A.
Gonçalves, V.
Hod, N.
Dainton, J.
Kado, M.
Li, R.
Strikman, M.
Brodsky, S. J.
Goddard, B.
Liu, T.
Satyanarayan, N.
Wang, X.
Gaddi, A.
Perrot, L.
Hutton, A.
Kumar, M.
Fischer, O.
Zhang, C.
Pellegrini, D.
Rahaman, R.
Szymanowski, L.
Marquet, C.
Currie, J.
Sutton, M.
Bousson, S.
Milhano, J. G.
Tasci, A. T.
Kawaguchi, S.
McFayden, J.
Hounsell, B.
Hernandez-Sanchez, J.
Allport, P. P.
Backovic, S.
Okada, N.
Tomas-Garcia, R.
Welsch, C.
Willering, G.
Britzger, D.
Agostini, P.
Tapan, I.
Verney, D.
Grassellino, A.
Aulenbacher, K.
Niehues, J.
Bernauer, J.
Pownall, G.
Yilmaz, A.
Ma, W.
Efremov, A. V.
Schwanenberger, C.
Biswal, S. S.
Rai, S. K.
Williams, P. H.
Ozansoy, A.
Grames, J.
Setiniyaz, S.
Jensen, E.
Rabbertz, K.
Delle Rose, L.
Bouzas, A. O.
Andari, N.
Burkhardt, H.
Larios, F.
Benedikt, M.
Das, S. P.
Ben-Zvi, I.
Longuevergne, D.
Levy, A.
Caldwell, A.
Parker, B.
Meot, F.
Stuart, M. J.
Zadeh, S. G.
Goyal, A.
Helenius, I.
Raychaudhuri, S.
Machado, M.
Milanese, A.
Mandal, S.
Polini, A.
Gao, J.
Islam, R.
Zimmermann, F.
Chetvertkova, V.
Yamazaki, Y.
Rinolfi, L.
Blümlein, J.
Polifka, R.
Armesto, N.
Dupraz, K.
Sultansoy, S.
Cornell, A. S.
Wang, Z. S.
Boonekamp, M.
Kaya, U.
Moch, S.
Kilic, A.
Marzani, S.
Aksakal, H.
Schirm, K.
Mcintosh, P.
Perini, D.
D’Onofrio, M.
Rimmer, R.
Boroun, G. R.
Radescu, V.
Martin, R.
Guzey, V.
Thonet, P.
Navarra, F.
Stocchi, A.
Bracco, C.
Henry, J.
Schopper, H.
Bottura, L.
Ari, V.
Shen, X.
Levonian, S.
Sun, H.
Douglas, D.
Ten-Kate, A. T.
Tang, Y.
Zhu, G.
Zurita, J.
Cole, B.
Poulose, P.
Ferreiro, E. G.
Hu, N.
Forte, S.
Xu, T.
Klein, M.
Guo, Y. C.
Seryi, A.
Vallerand, C.
Bonvini, M.
Kluth, S.
Morgan, T.
Zhu, S.
Glazov, A.
Zenaiev, O.
Pupkov, Y. A.
Gwenlan, C.
Calaga, R.
Kuze, M.
Placakyte, R.
Pilicer, E.
Bailey, S.
Hammad, A.
Hautmann, F.
Arduini, G.
Liu, W.
Walker, D.
Jones, T.
Song, M.
Kuday, S.
Hobbs, T. J.
Rojo, J.
Curtin, D.
Antusch, S.
Mellado, B.
Yaguna, C. E.
Khanpour, H.
Schott, M.
Behera, S.
Vilella, E.
Iwamoto, S.
Jowett, J. M.
Opis:
The Large Hadron–Electron Collider (LHeC) is designed to move the field of deep inelastic scattering (DIS) to the energy and intensity frontier of particle physics. Exploiting energy-recovery technology, it collides a novel, intense electron beam with a proton or ion beam from the High-Luminosity Large Hadron Collider (HL-LHC). The accelerator and interaction region are designed for concurrent electron–proton and proton–proton operations. This report represents an update to the LHeC’s conceptual design report (CDR), published in 2012. It comprises new results on the parton structure of the proton and heavier nuclei, QCD dynamics, and electroweak and top-quark physics. It is shown how the LHeC will open a new chapter of nuclear particle physics by extending the accessible kinematic range of lepton–nucleus scattering by several orders of magnitude. Due to its enhanced luminosity and large energy and the cleanliness of the final hadronic states, the LHeC has a strong Higgs physics programme and its own discovery potential for new physics. Building on the 2012 CDR, this report contains a detailed updated design for the energy-recovery electron linac (ERL), including a new lattice, magnet and superconducting radio-frequency technology, and further components. Challenges of energy recovery are described, and the lower-energy, high-current, three-turn ERL facility, PERLE at Orsay, is presented, which uses the LHeC characteristics serving as a development facility for the design and operation of the LHeC. An updated detector design is presented corresponding to the acceptance, resolution, and calibration goals that arise from the Higgs and parton-density-function physics programmes. This paper also presents novel results for the Future Circular Collider in electron–hadron (FCC-eh) mode, which utilises the same ERL technology to further extend the reach of DIS to even higher centre-of-mass energies.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Thirteen new species of Chilecicada Sanborn, 2014 (Hemiptera: Auchenorrhyncha: Cicadidae: Tibicininae) expand the highly endemic cicada fauna of Chile
Autorzy:
Cole, Jeffrey A.
Veloso, Claudio
Simon, Chris
Gonzalez, Valorie A.
Sanborn, Allen F.
Karkar, Jessica B.
Stukel, Mark
Łukasik, Piotr
Opis:
The genus Chilecicada Sanborn, 2014 is shown to be a complex of closely related species rather than a monospecific genus. Chilecicada citatatemporaria Sanborn & Cole n. sp., C. culenesensis Sanborn & Cole n. sp., C. curacaviensis Sanborn & Cole n. sp., C. impartemporaria Sanborn & Cole n. sp., C. magna Sanborn & Cole n. sp., C. mapuchensis Sanborn n. sp., C. oraria Sanborn & Cole n. sp., C. parrajaraorum Sanborn n. sp., C. partemporaria Sanborn & Cole n. sp., C. pehuenchesensis Sanborn & Cole n. sp., C. trifascia Sanborn n. sp., C. trifasciunca Sanborn & Cole n. sp., and C. viridicitata Sanborn & Cole n. sp. are described as new. Chilecicada occidentis Walker, 1850 is re-described to facilitate separation of the new species from the only previously known species. Song and cytochrome oxidase I analysis available for most species support the separation of the new taxa from the type species of the genus. Known species distributions and a key to the species of the genus are also provided. The new species increases the known cicada diversity 61.9% to 34 species, 91.2% of which are endemic to Chile.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Migraine-associated common genetic variants confer greater risk of posterior vs. anterior circulation ischemic stroke
Autorzy:
Dalca, A.V.
Thijs, V.
Ryan, K.
Frid, P.
Meschia, J.F.
Schmidt, R.
Słowik, Agnieszka
Kissela, B.M.
Holmegaard, L.
Golland, P.
Broderick, J.P.
Worrall, B.B.
Wu, O.
Rundek, T.
Giralt-Steinhauer, E.
Drake, M.
Mcardle, P.F.
Woo, D.
Mocking, S.J.T.
Bouts, M.J.R.J.
Lemmens, R.
Sharma, P.
Xu, H.
Jood, K.
Cole, J.W.
Lindgren, A.
Irie, R.
Kleindorfer, D.O.
Rost, N.S.
Schirmer, M.
Roquer, J.
Kittner, S.J.
Donahue, K.L.
Gaynor, B.
Mitchell, B.D.
Sacco, R.L.
Jern, C.
Giese, A.K.
Wasselius, J.
Rosand, J.
Mcintosh, E.C.
Jimenez-Conde, J.
Petersson, J.
Opis:
Objective: To examine potential genetic relationships between migraine and the two distinct phenotypes posterior circulation ischemic stroke (PCiS) and anterior circulation ischemic stroke (ACiS), we generated migraine polygenic risk scores (PRSs) and compared these between PCiS and ACiS, and separately vs. non-stroke control subjects. Methods: Acute ischemic stroke cases were classified as PCiS or ACiS based on lesion location on diffusion-weighted MRI. Exclusion criteria were lesions in both vascular territories or uncertain territory; supratentorial PCiS with ipsilateral fetal posterior cerebral artery; and cases with atrial fibrillation. We generated migraine PRS for three migraine phenotypes (any migraine; migraine without aura; migraine with aura) using publicly available GWAS data and compared mean PRSs separately for PCiS and ACiS vs. non-stroke control subjects, and between each stroke phenotype. Results:Our primary analyses included 464 PCiS and 1079 ACiS patients with genetic European ancestry. Compared to non-stroke control subjects (n=15396), PRSs of any migraine were associated with increased risk of PCiS (p=0.01–0.03) and decreased risk of ACiS (p=0.010–0.039). Migraine without aura PRSs were significantly associated with PCiS (p=0.008–0.028), but not with ACiS. When comparing PCiS vs. ACiS directly, migraine PRSs were higher in PCiS vs. ACiS for any migraine (p=0.001–0.010) and migraine without aura (p=0.032–0.048). Migraine with aura PRS did not show a differential association in our analyses. Conclusions: Our results suggest a stronger genetic overlap between unspecified migraine and migraine without aura with PCiS compared to ACiS. Possible shared mechanisms include dysregulation of cerebral vessel endothelial function.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Interrupting sitting with moderate-intensity physical activity breaks improves inhibitory control in adults with overweight and obesity : findings from the SITLess pilot randomized crossover trial
Autorzy:
Quiroz, Flor B.
Kuang, Jin
Cannavale, Corinne N.
Burd, Nicholas A.
Pindus, Dominika M.
Herrera, Bryan Montero
Zou, Liye
Liang, Sharon
Hillman, Charles H.
Pickerill, Lauryn
Shanmugam, Ramiya
Bashir, Neha
Kramer, Arthur F.
Tewell, Paige
Syed, Talha
Stanfield, Cole
Khan, Naiman A.
Yu, Qian
Martin, Hannah
Lloyd, Katherine M.
Ligęza, Tomasz
Sharma, Arushi
Opis:
Introduction: Adults with overweight and obesity (OW/OB) show deficits in inhibitory control, which may be amplified by prolonged sitting. This study tested the acute effects of interrupting 3-h prolonged sitting every 30 min with 3.5-min moderate-intensity physical activity bouts (MPA +SIT) on inhibitory control relative to a sedentary social interaction condition (SOC +SIT) in young and middle-aged adults with OW/OB. Method: Data from 19 adults (63% females; 29.9 ±7.5 years; BMI =30.0 ±3.64 kg*m2) were analysed from the SITLess pilot randomized crossover trial. Inhibitory control was expressed as response accuracy and reaction time (RT) on incongruent trials of a flanker task. Choice RT was expressed as accuracy and RT on congruent trials. Attentional resource allocation and the speed of stimulus evaluation were measured using the amplitude and latency of the P3b component of event-related brain potentials, respectively. Intervention effects were tested using Generalized Linear Mixed Models with Time (pre, post) by Condition (MPA +SIT vs. SOC +SIT) interactions and simple effects within each time point. Results: Participants were faster on incongruent trials after MPA +SIT than SOC +SIT (F(18.0, 54) =5.59, p = 0.02; △M =16.7 ms, 95% CI: 1.64, 31.7). A similar trend (F(18.0, 54) =4.03, p =0.05) emerged for congruent trials (△M =17.3 ms, 95% CI: 5.66, 29.0). P3b amplitude and latency did not differ between conditions or time. Conclusion: Interrupting sitting with short MPA bouts is a viable strategy to prevent a decline in cognitive performance following a continuous bout of sitting in adults with OW/OB. A definitive trial should test its efficacy in enhancing cognitive and brain health in obesity.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł

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