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- Publication . Article . 2014Open AccessAuthors:Aad, G.; Abbott, B.; Abdallah, J.; Abdel Khalek, S.; Abdinov, O.; Aben, R.; Abi, B.; Abolins, M.; Abouzeid, O. S.; Abramowicz, H.; +190 moreAad, G.; Abbott, B.; Abdallah, J.; Abdel Khalek, S.; Abdinov, O.; Aben, R.; Abi, B.; Abolins, M.; Abouzeid, O. S.; Abramowicz, H.; Abreu, H.; Abreu, R.; Abulaiti, Y.; Acharya, B. S.; Adamczyk, L.; Adams, D. L.; Adelman, J.; Adomeit, S.; Adye, T.; Agatonovic Jovin, T.; Aguilar Saavedra, J. A.; Agustoni, M.; Ahlen, S. P.; Ahmadov, F.; Aielli, G.; Akerstedt, H.; Åkesson, T. P. A.; Akimoto, G.; Akimov, A. V.; Albert, J.; Albrand, S.; Alconada Verzini, M. J.; Aleksa, M.; Aleksandrov, I. N.; Alexa, C.; Alexander, G.; Alexandre, G.; Alexopoulos, T.; Alhroob, M.; Alimonti, G.; Alio, L.; Alison, J.; Allbrooke, B. M. M.; Allison, L. J.; Allport, P. P.; Almond, J.; Aloisio, A.; Alonso, A.; Alonso, F.; Alpigiani, C.; Altheimer, A.; Alvarez Gonzalez, B.; Alviggi, M. G.; Amako, K.; Amaral Coutinho, Y.; Amelung, C.; Amidei, D.; Amor Dos Santos, S. P.; Amorim, A.; Amoroso, S.; Amram, N.; Amundsen, G.; Anastopoulos, C.; Ancu, L. S.; Andari, N.; Andeen, T.; Anders, C. F.; Anders, G.; Anderson, K. J.; Andreazza, A.; Andrei, V.; Anduaga, X. S.; Angelidakis, S.; Angelozzi, I.; Anger, P.; Angerami, A.; Anghinolfi, F.; Anisenkov, A. V.; Anjos, N.; Annovi, A.; Antonaki, A.; Antonelli, M.; Antonov, A.; Antos, J.; Anulli, F.; Aoki, M.; Aperio Bella, L.; Apolle, R.; Arabidze, G.; Aracena, I.; Arai, Y.; Araque, J. P.; Arce, A. T. H.; Arguin, J. F.; Argyropoulos, S.; Arik, M.; Armbruster, A. J.; Arnaez, O.; Arnal, V.; Arnold, H.; Arratia, M.; Arslan, O.; Artamonov, A.; Artoni, G.; Asai, S.; Asbah, N.; Ashkenazi, A.; Åsman, B.; Asquith, L.; Assamagan, K.; Astalos, R.; Atkinson, M.; Atlay, N. B.; Auerbach, B.; Augsten, K.; Aurousseau, M.; Avolio, G.; Azuelos, G.; Azuma, Y.; Baak, M. A.; Baas, A. E.; Bacci, C.; Bachacou, H.; Bachas, K.; Backes, M.; Backhaus, M.; Backus Mayes, J.; Badescu, E.; Bagiacchi, P.; Bagnaia, P.; Bai, Y.; Bain, T.; Baines, J. T.; Baker, O. K.; Balek, P.; Balli, F.; Banas, E.; Banerjee, S.w.; Bannoura, A. A. E.; Bansal, V.; Bansil, H. S.; Barak, L.; Baranov, S. P.; Barberio, E. L.; Barberis, D.; Barbero, M.; Barillari, T.; Barisonzi, M.; Barklow, T.; Barlow, N.; Barnett, B. M.; Barnett, R. M.; Barnovska, Z.; Baroncelli, A.; Barone, G.; Barr, A. J.; Barreiro, F.; Barreiro Guimarães da Costa, J.; Bartoldus, R.; Barton, A. E.; Bartos, P.; Bartsch, V.; Bassalat, A.; Basye, A.; Bates, R. L.; Batley, J. R.; Battaglia, M.; Battistin, M.; Bauer, F.; Bawa, H. S.; Beattie, M. D.; Beau, T.; Beauchemin, P. H.; Beccherle, R.; Bechtle, P.; Beck, H. P.; Becker, K.; Becker, S.; Beckingham, M.; Becot, C.; Beddall, A. J.; Beddall, A.; Bedikian, S.; Bednyakov, V. A.; Bee, C. P.; Beemster, L. J.; Beermann, T. A.; Begel, M.; Behr, K.; Belanger Champagne, C.; Bell, P. J.; Bell, W. H.; Bella, G.; Bellerive, A.; Bellomo, M.; Belotskiy, K.; Beltramello, O.; Benary, O.; Benchekroun, D.; Bendtz, K.;
pmid: 25814877
pmc: PMC4370854
Countries: Italy, United KingdomATLAS measurements of the azimuthal anisotropy in lead–lead collisions at \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\sqrt{s_{\mathrm {NN}}}=2.76$$\end{document}sNN=2.76 TeV are shown using a dataset of approximately 7 \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\upmu $$\end{document}μb\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$^{-1}$$\end{document}-1 collected at the LHC in 2010. The measurements are performed for charged particles with transverse momenta \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$0.5
Average/low popularityAverage/low popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Preprint . 2018Open Access EnglishAuthors:Hinderer, Tanja; Nissanke, Samaya; Foucart, Francois; Hotokezaka, Kenta; Vincent, Trevor; Kasliwal, Mansi; Schmidt, Patricia; Williamson, Andrew R.; Nichols, David; Duez, Matthew; +3 moreHinderer, Tanja; Nissanke, Samaya; Foucart, Francois; Hotokezaka, Kenta; Vincent, Trevor; Kasliwal, Mansi; Schmidt, Patricia; Williamson, Andrew R.; Nichols, David; Duez, Matthew; Kidder, Lawrence E.; Pfeiffer, Harald P.; Scheel, Mark A.;Project: NSERC , NSF | Gravitational Radiation a... (1404569), NSF | Gravitational Radiation a... (1708213), NSF | Mergers, Stars, and Disks... (1806207), NSF | Maximizing Science Output... (1708212), NSF | PIRE: GROWTH: Global Rela... (1545949), NWO | Precision Gravity: black ... (680-47-460)
The discovery of GW170817 with gravitational waves (GWs) and electromagnetic (EM) radiation is prompting new questions in strong-gravity astrophysics. Importantly, it remains unknown whether the progenitor of the merger comprised two neutron stars (NSs), or a NS and a black hole (BH). Using new numerical-relativity simulations and incorporating modeling uncertainties we produce novel GW and EM observables for NS-BH mergers with similar masses. A joint analysis of GW and EM measurements reveals that if GW170817 is a NS-BH merger, <40% of the binary parameters consistent with the GW data are compatible with EM observations. Comment: 8 pages
Average/low popularityAverage/low popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact. - Publication . Other literature type . 2018Open Access EnglishAuthors:Große, Fabian; Greenwood, Naomi; Kreus, Markus; Lenhart, Hermann-Josef; Machoczek, Detlev; Pätsch, Johannes; Salt, Lesley; Thomas, Helmuth;Große, Fabian; Greenwood, Naomi; Kreus, Markus; Lenhart, Hermann-Josef; Machoczek, Detlev; Pätsch, Johannes; Salt, Lesley; Thomas, Helmuth;
Low oxygen conditions, often referred to as oxygen deficiency, occur regularly in the North Sea, a temperate European shelf sea. Stratification represents a major process regulating the seasonal dynamics of bottom oxygen, yet, lowest oxygen conditions in the North Sea do not occur in the regions of strongest stratification. This suggests that stratification is an important prerequisite for oxygen deficiency, but that the complex interaction between hydrodynamics and the biological processes drives its evolution. In this study we use the ecosystem model HAMSOM-ECOHAM to provide a general characterisation of the different zones of the North Sea with respect to oxygen, and to quantify the impact of the different physical and biological factors driving the oxygen dynamics inside the entire sub-thermocline volume and directly above the bottom. With respect to oxygen dynamics, the North Sea can be subdivided into three different zones: (1) a highly productive, non-stratified coastal zone, (2) a productive, seasonally stratified zone with a small sub-thermocline volume, and (3) a productive, seasonally stratified zone with a large sub-thermocline volume. Type 2 reveals the highest susceptibility to oxygen deficiency due to sufficiently long stratification periods (> 60 days) accompanied by high surface productivity resulting in high biological consumption, and a small sub-thermocline volume implying both a small initial oxygen inventory and a strong influence of the biological consumption on the oxygen concentration. Year-to-year variations in the oxygen conditions are caused by variations in primary production, while spatial differences can be attributed to differences in stratification and water depth. The large sub-thermocline volume dominates the oxygen dynamics in the northern central and northern North Sea and makes this region insusceptible to oxygen deficiency. In the southern North Sea the strong tidal mixing inhibits the development of seasonal stratification which protects this area from the evolution of low oxygen conditions. In contrast, the southern central North Sea is highly susceptible to low oxygen conditions (type 2). We furthermore show that benthic diagenetic processes represent the main oxygen consumers in the bottom layer, consistently accounting for more than 50 % of the overall consumption. Thus, primary production followed by remineralisation of organic matter under stratified conditions constitutes the main driver for the evolution of oxygen deficiency in the southern central North Sea. By providing these valuable insights, we show that ecosystem models can be a useful tool for the interpretation of observations and the estimation of the impact of anthropogenic drivers on the North Sea oxygen conditions.
Average/low popularityAverage/low popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact. - Publication . Article . Other literature type . 2021Open AccessAuthors:Denisa Hathazi; Dan Cox; Adele D'Amico; Giorgio Tasca; Richard Charlton; Robert-Yves Carlier; Jennifer Baumann; Laxmikanth Kollipara; René P. Zahedi; Ingo Feldmann; +18 moreDenisa Hathazi; Dan Cox; Adele D'Amico; Giorgio Tasca; Richard Charlton; Robert-Yves Carlier; Jennifer Baumann; Laxmikanth Kollipara; René P. Zahedi; Ingo Feldmann; Jean-François Deleuze; Annalaura Torella; Ronald D. Cohn; Emily Robinson; Francesco Ricci; Heinz Jungbluth; Fabiana Fattori; Anne Boland; Emily O'Connor; Rita Horvath; Rita Barresi; Hanns Lochmüller; Andoni Urtizberea; Marie-Line Jacquemont; Isabelle Nelson; Laura E. Swan; Gisèle Bonne; Andreas Roos;Publisher: Oxford University Press (OUP)Countries: United Kingdom, France, Germany, ItalyProject: CIHR , UKRI | Exosomal protein deficien... (MR/N025431/1)
Abstract Marinesco-Sjögren syndrome is a rare human disorder caused by biallelic mutations in SIL1 characterized by cataracts in infancy, myopathy and ataxia, symptoms which are also associated with a novel disorder caused by mutations in INPP5K. While these phenotypic similarities may suggest commonalties at a molecular level, an overlapping pathomechanism has not been established yet. In this study, we present six new INPP5K patients and expand the current mutational and phenotypical spectrum of the disease showing the clinical overlap between Marinesco-Sjögren syndrome and the INPP5K phenotype. We applied unbiased proteomic profiling on cells derived from Marinesco-Sjögren syndrome and INPP5K patients and identified alterations in d-3-PHGDH as a common molecular feature. d-3-PHGDH modulates the production of l-serine and mutations in this enzyme were previously associated with a neurological phenotype, which clinically overlaps with Marinesco-Sjögren syndrome and INPP5K disease. As l-serine administration represents a promising therapeutic strategy for d-3-PHGDH patients, we tested the effect of l-serine in generated sil1, phgdh and inpp5k a+b zebrafish models, which showed an improvement in their neuronal phenotype. Thus, our study defines a core phenotypical feature underpinning a key common molecular mechanism in three rare diseases and reveals a common and novel therapeutic target for these patients.
Top 10% in popularityTop 10% in popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2018Open AccessAuthors:K. Abe; C. Bronner; Yoshinari Hayato; M. Ikeda; K. Iyogi; J. Kameda; Y. Kato; Yasuhiro Kishimoto; Ll. Marti; M. Miura; +153 moreK. Abe; C. Bronner; Yoshinari Hayato; M. Ikeda; K. Iyogi; J. Kameda; Y. Kato; Yasuhiro Kishimoto; Ll. Marti; M. Miura; Shigetaka Moriyama; Masayuki Nakahata; Y. Nakajima; Yuuki Nakano; S. Nakayama; A. Orii; G. Pronost; Hiroyuki Sekiya; Masato Shiozawa; Y. Sonoda; A. Takeda; A. Takenaka; Hiromasa Tanaka; S. Tasaka; T. Yano; Ryosuke Akutsu; Takaaki Kajita; Yasuhiro Nishimura; Kimihiro Okumura; K. M. Tsui; Luis Labarga; P. Fernandez; F. d. M. Blaszczyk; C. Kachulis; E. Kearns; J. L. Raaf; Jl Stone; Lawrence Sulak; S. Berkman; S. Tobayama; J. Bian; M. Elnimr; W. R. Kropp; S. Locke; S. Mine; P. Weatherly; M. B. Smy; Henry W. Sobel; Volodymyr Takhistov; K. S. Ganezer; John Hill; J. Y. Kim; I. T. Lim; R. G. Park; Z. Li; E. O’Sullivan; Kate Scholberg; C. W. Walter; M. Gonin; J. Imber; Th. A. Mueller; T. Ishizuka; T. Nakamura; J. S. Jang; K. Choi; J. G. Learned; S. Matsuno; J. Amey; R. P. Litchfield; W. Y. Ma; Y. Uchida; M. O. Wascko; M. G. Catanesi; R. A. Intonti; E. Radicioni; G. De Rosa; A. Ali; G. Collazuol; L. Ludovici; S. V. Cao; M. Friend; T. Hasegawa; T. Ishida; T. Ishii; Takashi Kobayashi; T. Nakadaira; K. Nakamura; Y. Oyama; Ken Sakashita; T. Sekiguchi; T. Tsukamoto; K. Abe; Makoto Hasegawa; A. Suzuki; Y. Takeuchi; T. Hayashino; S. Hirota; M. Jiang; M. Mori; K. E. Nakamura; Tsuyoshi Nakaya; R. A. Wendell; L. H. V. Anthony; N. McCauley; A. Pritchard; Y. Fukuda; Yoshitaka Itow; M. Murase; Francesco Muto; P. Mijakowski; K. Frankiewicz; C. K. Jung; Xiaoning Li; J. L. Palomino; G. Santucci; C. Viela; M. J. Wilking; C. Yanagisawa; D. Fukuda; Hirokazu Ishino; Shintaro Ito; A. Kibayashi; Yusuke Koshio; H. Nagata; Makoto Sakuda; C. Xu; Yoshitaka Kuno; D. L. Wark; F. Di Lodovico; B. Richards; S. Molina Sedgwick; R. Tacik; Soo-Bong Kim; A. Cole; Lester D.R. Thompson; H. Okazawa; Y. Choi; K. Ito; Kyoshi Nishijima; M. Koshiba; Y. Suda; Masashi Yokoyama; R. G. Calland; M. Hartz; K. Martens; M. Murdoch; B. Quilain; C. Simpson; Yoshihiro Suzuki; Mark R. Vagins; D. Hamabe; Masahiro Kuze; Y. Okajima; Takashi Yoshida; Masaki Ishitsuka; J. F. Martin; C. M. Nantais; H. A. Tanaka; T. Towstego; A. Konaka; S. Chen; L. Wan; A. Minamino;Publisher: American Astronomical SocietyCountries: United Kingdom, United Kingdom, Italy, France, ItalyProject: EC | SKPLUS (641540), NSERC
We report the results of a neutrino search in Super-Kamiokande for coincident signals with the first detected gravitational wave produced by a binary neutron star merger, GW170817, which was followed by a short gamma-ray burst, GRB170817A, and a kilonova/macronova. We searched for coincident neutrino events in the range from 3.5 MeV to $\sim$100 PeV, in a time window $\pm$500 seconds around the gravitational wave detection time, as well as during a 14-day period after the detection. No significant neutrino signal was observed for either time window. We calculated 90% confidence level upper limits on the neutrino fluence for GW170817. From the upward-going-muon events in the energy region above 1.6 GeV, the neutrino fluence limit is $16.0^{+0.7}_{-0.6}$ ($21.3^{+1.1}_{-0.8}$) cm$^{-2}$ for muon neutrinos (muon antineutrinos), with an error range of $\pm5^{\circ}$ around the zenith angle of NGC4993, and the energy spectrum is under the assumption of an index of $-2$. The fluence limit for neutrino energies less than 100 MeV, for which the emission mechanism would be different than for higher-energy neutrinos, is also calculated. It is $6.6 \times 10^7$ cm$^{-2}$ for anti-electron neutrinos under the assumption of a Fermi-Dirac spectrum with average energy of 20 MeV. 8 pages, 4 figures
Top 10% in popularityTop 10% in popularityTop 10% in influencePopularity: Citation-based measure reflecting the current impact.Top 10% in influenceInfluence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2014RestrictedAuthors:Alexander V. Louie; Suresh Senan; Max Dahele; Ben J. Slotman; Wilko F.A.R. Verbakel;Alexander V. Louie; Suresh Senan; Max Dahele; Ben J. Slotman; Wilko F.A.R. Verbakel;
pmid: 25585783
Publisher: Elsevier BVCountry: NetherlandsPurpose Use of stereotactic ablative radiation therapy (SABR) for subcentimeter lung tumors is controversial. We report our outcomes for tumors with diameter ≤1 cm and their visibility on cone beam computed tomography (CBCT) scans and retrospectively evaluate the planned dose using a deterministic dose calculation algorithm (Acuros XB [AXB]). Methods and Materials We identified subcentimeter tumors from our institutional SABR database. Tumor size was remeasured on an artifact-free phase of the planning 4-dimensional (4D)-CT. Clinical plan doses were generated using either a pencil beam convolution or an anisotropic analytic algorithm (AAA). All AAA plans were recalculated using AXB, and differences among D95 and mean dose for internal target volume (ITV) and planning target volume (PTV) on the average intensity CT dataset, as well as for gross tumor volume (GTV) on the end respiratory phases were reported. For all AAA patients, CBCT scans acquired during each treatment fraction were evaluated for target visibility. Progression-free and overall survival rates were calculated using the Kaplan-Meier method. Results Thirty-five patients with 37 subcentimeter tumors were eligible for analysis. For the 22 AAA plans recalculated using AXB, Mean D95 ± SD values were 2.2 ± 4.4% (ITV) and 2.5 ± 4.8% (PTV) lower using AXB; whereas mean doses were 2.9 ± 4.9% (ITV) and 3.7 ± 5.1% (PTV) lower. Calculated AXB doses were significantly lower in one patient (difference in mean ITV and PTV doses, as well as in mean ITV and PTV D95 ranged from 22%-24%). However, the end respiratory phase GTV received at least 95% of the prescription dose. Review of 92 CBCT scans from all AAA patients revealed that the tumor was visualized in 82 images, and its position could be inferred in other images. The 2-year local progression-free survival was 100%. Conclusions Patients with subcentimeter lung tumors are good candidates for SABR, given the dosimetry, ability to localize tumors with image guidance, and excellent local control.
Average/low popularityAverage/low popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . Other literature type . 2013Open AccessAuthors:Montserrat Garcia-Closas; Sara Lindström; Kyriaki Michailidou; Marjanka K. Schmidt; Mark N. Brook; Elio Riboli; Loic Le Marchand; Diana Eccles; Penelope Miron; Peter A. Fasching; +201 moreMontserrat Garcia-Closas; Sara Lindström; Kyriaki Michailidou; Marjanka K. Schmidt; Mark N. Brook; Elio Riboli; Loic Le Marchand; Diana Eccles; Penelope Miron; Peter A. Fasching; Hiltrud Brauch; Jenny Chang-Claude; Jane Carpenter; Andrew K. Godwin; Heli Nevanlinna; Graham G. Giles; Angela Cox; John L. Hopper; Manjeet K. Bolla; Qin Wang; Joe Dennis; Ed Dicks; Nils Schoof; Stig E. Bojesen; Diether Lambrechts; Annegien Broeks; Pascal Guénel; Barbara Burwinkel; Elinor J. Sawyer; Antoinette Hollestelle; Olivia Fletcher; Robert Winqvist; Hermann Brenner; Arto Mannermaa; Ute Hamann; Alfons Meindl; Annika Lindblom; Wei Zheng; Peter Devillee; Mark S. Goldberg; Jan Lubinski; Anthony J. Swerdlow; Hoda Anton-Culver; Thilo Dörk; Keitaro Matsuo; Anna H. Wu; Paolo Radice; Soo Hwang Teo; Xiao-Ou Shu; William Blot; Daehee Kang; Mikael Hartman; Suleeporn Sangrajrang; Chen-Yang Shen; Melissa C. Southey; Daniel J. Park; Jennifer Stone; Laura J. van't Veer; Emiel J. Th. Rutgers; Artitaya Lophatananon; Sarah Stewart-Brown; Pornthep Siriwanarangsan; Julian Peto; Arif B. Ekici; Isabel dos Santos Silva; Nichola Johnson; Helen R. Warren; Ian Tomlinson; Michael J. Kerin; Nicola Miller; Thérèse Truong; Pierre Laurent-Puig; Børge G. Nordestgaard; Sune F. Nielsen; Henrik Flyger; Jose Ignacio Arias Perez; Primitiva Menéndez; Heiko Müller; Magdalena Lochmann; Christina Justenhoven; Yon Ko; Kristiina Aittomäki; Carl Blomqvist; Dario Greco; Tuomas Heikkinen; Hidemi Ito; Yasushi Yatabe; Sara Margolin; Vesa Kataja; Veli-Matti Kosma; Jaana M. Hartikainen; Rosemary L. Balleine; Chiu-Chen Tseng; Patrick Neven; Anne Sophie Dieudonne; Karin Leunen; Anja Rudolph; Stefan Nickels; Dieter Flesch-Janys; Paolo Peterlongo; Bernard Peissel; Loris Bernard; Janet E. Olson; Xianshu Wang; Gianluca Severi; Laura Baglietto; Catriona McLean; Gerhard A. Coetzee; Ye Feng; Fredrick R. Schumacher; Cheng Har Yip; Nur Aishah Taib; Ching-Yu Cheng; Martha J. Shrubsole; Jirong Long; Katri Pylkäs; Arja Jukkola-Vuorinen; Julia A. Knight; Gord Glendon; Anna Marie Mulligan; R.A.E.M. Tollenaar; Mieke Kriege; Carolien H.M. van Deurzen; Wei Lu; Yu Tang Gao; Hui Cai; Sabapathy P. Balasubramanian; Simon S. Cross; Malcolm W.R. Reed; Qiuyin Cai; Hui Miao; Ching Wan Chan; Kee Seng Chia; Anna Jakubowska; Katarzyna Jaworska; Katarzyna Durda; Chia-Ni Hsiung; Pei Ei Wu; Alan Ashworth; Michael Jones; Anna González-Neira; Guillermo Pita; M. Rosario Alonso; Daniel Vincent; Francois Bacot; Christine B. Ambrosone; Elisa V. Bandera; Gary K. Chen; Jorge L. Rodriguez-Gil; Leslie Bernstein; Michael F. Press; Regina G. Ziegler; Sarah J. Nyante; Sue A. Ingles; Quinten Waisfisz; Helen Tsimiklis; Enes Makalic; Minh Bui; Rita K. Schmutzler; Norbert Dahmen; Lars Beckmann; Kirsimari Aaltonen; Kamila Czene; Astrid Irwanto; Jianjun Liu; Clare Turnbull; Nazneen Rahman; Hanne Meijers-Heijboer; André G. Uitterlinden; Fernando Rivadeneira; Curtis Olswold; Robert Pilarski; Foluso O. Ademuyiwa; Irene Konstantopoulou; Nicholas G. Martin; Grant W. Montgomery; Dennis J. Slamon; Claudia Rauh; Michael P. Lux; Sebastian M. Jud; Thomas Brüning; Priyanka Sharma; Harsh B. Pathak; William J. Tapper; Sue Gerty; Lorraine Durcan; Dimitrios Trichopoulos; Rosario Tumino; Petra H.M. Peeters; Rudolf Kaaks; Daniele Campa; Federico Canzian; Elisabete Weiderpass; Mattias Johansson; Ruth C. Travis; Françoise Clavel-Chapelon; Laurence N. Kolonel; Andrew H. Beck; Susan E. Hankinson; Christine D. Berg; Jolanta Lissowska; Jonine D. Figueroa; Daniel I. Chasman; W. Ryan Diver; Jacques Simard; Alison M. Dunning; Mark E. Sherman; Georgia Chenevix-Trench; Stephen J. Chanock; Celine M. Vachon; Peter Kraft;Publisher: Springer Science and Business Media LLCCountries: Netherlands, United Kingdom, Italy, IrelandProject: NIH | Characterizing Genetic Su... (5U01CA098710-06), WT , NIH | Breast &prostate cancer &... (1U01CA098216-01), NIH | Characterizing Genetic Su... (5U01CA098233-06), NIH | Genetic epidemiology of c... (3R01CA122340-03S1), EC | COGS (223175), CIHR , NIH | Discovery Expansion and R... (5U19CA148065-04), NIH | Breast &Prostate Cancer &... (1U01CA098758-01)
Estrogen receptor (ER)-negative tumors represent 20-30% of all breast cancers, with a higher proportion occurring in younger women and women of African ancestry. The etiology and clinical behavior of ER-negative tumors are different from those of tumors expressing ER (ER positive), including differences in genetic predisposition. To identify susceptibility loci specific to ER-negative disease, we combined in a metaanalysis 3 genome-wide association studies of 4,193 ER-negative breast cancer cases and 35,194 controls with a series of 40 follow-up studies (6,514 cases and 41,455 controls), genotyped using a custom Illumina array, iCOGS, developed by the Collaborative Oncological Gene-environment Study (COGS). SNPs at four loci, 1q32.1 (MDM4, P= 2.1 x 10(-12) and LGR6, P = 1.4 x 10(-8)), 2p24.1 (P = 4.6 x 10(-8)) and 16q12.2 (FTO, P = 4.0 x 10(-8)), were associated with ER-negative but not ER-positive breast cancer (P> 0.05). These findings provide further evidence for distinct etiological pathways associated with invasive ER-positive and ER-negative breast cancers.
Top 1% in popularityTop 1% in popularityTop 1% in influencePopularity: Citation-based measure reflecting the current impact.Top 1% in influenceInfluence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2021Open AccessAuthors:Rosalie A. Scholtes; Michaël J.B. van Baar; Megan D. Kok; Petter Bjornstad; David Z.I. Cherney; Jaap A. Joles; Daniël H. van Raalte;Rosalie A. Scholtes; Michaël J.B. van Baar; Megan D. Kok; Petter Bjornstad; David Z.I. Cherney; Jaap A. Joles; Daniël H. van Raalte;Publisher: WileyCountry: Netherlands
Abstract Diabetic kidney disease remains the leading cause of end‐stage kidney disease and a major risk factor for cardiovascular disease. Large cardiovascular outcome trials and dedicated kidney trials have shown that sodium‐glucose cotransporter (SGLT)2 inhibitors reduce cardiovascular morbidity and mortality and attenuate hard renal outcomes in patients with type 2 diabetes (T2D). Underlying mechanisms explaining these renal benefits may be mediated by decreased glomerular hypertension, possibly by vasodilation of the post‐glomerular arteriole. People with T2D often receive several different drugs, some of which could also impact the renal vasculature, and could therefore modify both renal efficacy and safety of SGLT2 inhibition. The most commonly prescribed drugs that could interact with SGLT2 inhibitors on renal haemodynamic function include renin‐angiotensin system inhibitors, calcium channel blockers and diuretics. Herein, we review the effects of these drugs on renal haemodynamic function in people with T2D and focus on studies that measured glomerular filtration rate (GFR) and effective renal plasma flow (ERPF) with gold‐standard techniques. In addition, we posit, based on these observations, potential interactions with SGLT2 inhibitors with an emphasis on efficacy and safety. SUMMARY AT A GLANCE This invited review describes the renal haemodynamic and protective effects of commonly prescribed drugs in people with type 2 diabetes and their interaction with SGLT2 inhibitors.
Top 10% in popularityTop 10% in popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . Other literature type . 2011Open AccessAuthors:Robin Pourzal; Isabelle Catelas; Ralf Theissmann; C. Kaddick; Alfons Fischer;Robin Pourzal; Isabelle Catelas; Ralf Theissmann; C. Kaddick; Alfons Fischer;Publisher: Elsevier BVCountry: Germany
Biological effects of wear products (particles and metal ions) generated by metal-on-metal (MoM) hip replacements made of CoCrMo alloy remain a major cause of concern. Periprosthetic osteolysis, potential hypersensitivity response and pseudotumour formation are possible reactions that can lead to early revisions. To accurately analyse the biological response to wear particles from MoM implants, the exact nature of these particles needs to be characterized. Most previous studies used energy-dispersive X-ray spectroscopy (EDS) analysis for characterization. The present study used energy filtered transmission electron microscopy (TEM) and electron diffraction pattern analysis to allow for a more precise determination of the chemical composition and to gain knowledge of the crystalline structure of the wear particles.Particles were retrieved from two different test rigs: a reciprocating sliding wear tribometer (CoCrMo cylinder vs. bar) and a hip simulator according to ISO 14242-1 (CoCrMo head vs. CoCrMo cup). All tests were conducted in bovine serum. Particles were retrieved from the test medium using a previously published enzymatic digestion protocol.Particles isolated from tribometer samples had a size of 100 - 500 nm. Diffraction pattern analysis clearly revealed the lattice structure of strain induced hcp ε-martensite. Hip simulator samples revealed numerous particles of 15 - 30 nm and 30 - 80 nm size. Most of the larger particles appeared to be only partially oxidized and exhibited cobalt locally. The smallest particles were Cr(2)O(3) with no trace of cobalt. It optically appeared that these Cr(2)O(3) particles were flaking off the surface of larger particles that depicted a very high intensity of oxygen, as well as chromium, and only background noise of cobalt. The particle size difference between the two test rigs is likely related to the conditions of the two tribosystems, in particular the difference in the sample geometry and in the type of sliding (reciprocating vs. multidirectional).Results suggest that there may be a critical particle size at which chromium oxidation and cobalt ionization is accelerated. Since earlier studies have shown that wear particles are covered by organic residue which may act as a passive layer inhibiting further oxidation, it would suggest that this organic layer may be removed during the particle isolation process, resulting in a change of the particle chemical composition due to their pyrophoric properties. However, prior to being isolated from the serum lubricant, particles remain within the contact area of head and cup as a third-body. It is therefore possible that during that time, particles may undergo significant transformation and changes in chemical composition in the contact area of the head and cup within the tribological interface due to mechanical interaction with surface asperities.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Conference object . 2004RestrictedAuthors:Mark S. Ackerman; Marlene Huysman; John M. Carroll; Barry Wellman; Giorgio DeMichelis; Volker Wulf;Mark S. Ackerman; Marlene Huysman; John M. Carroll; Barry Wellman; Giorgio DeMichelis; Volker Wulf;Publisher: ACMCountry: Netherlands
Communities are social entities whose actors share common needs, interests, or practices: they constitute the basic units of social experience. With regard to communities, social capital captures the structural, relational and cognitive aspects of the relationships among their members. Social capital is defined as a set of properties of a social entity (e.g. norms, level of trust, and intensive social networking) which enables joint activities and cooperation for mutual benefit. It can be understood as the glue which holds communities together. On this panel we will discuss whether and how information technology can strengthen communities by fostering social capital.
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- Publication . Article . 2014Open AccessAuthors:Aad, G.; Abbott, B.; Abdallah, J.; Abdel Khalek, S.; Abdinov, O.; Aben, R.; Abi, B.; Abolins, M.; Abouzeid, O. S.; Abramowicz, H.; +190 moreAad, G.; Abbott, B.; Abdallah, J.; Abdel Khalek, S.; Abdinov, O.; Aben, R.; Abi, B.; Abolins, M.; Abouzeid, O. S.; Abramowicz, H.; Abreu, H.; Abreu, R.; Abulaiti, Y.; Acharya, B. S.; Adamczyk, L.; Adams, D. L.; Adelman, J.; Adomeit, S.; Adye, T.; Agatonovic Jovin, T.; Aguilar Saavedra, J. A.; Agustoni, M.; Ahlen, S. P.; Ahmadov, F.; Aielli, G.; Akerstedt, H.; Åkesson, T. P. A.; Akimoto, G.; Akimov, A. V.; Albert, J.; Albrand, S.; Alconada Verzini, M. J.; Aleksa, M.; Aleksandrov, I. N.; Alexa, C.; Alexander, G.; Alexandre, G.; Alexopoulos, T.; Alhroob, M.; Alimonti, G.; Alio, L.; Alison, J.; Allbrooke, B. M. M.; Allison, L. J.; Allport, P. P.; Almond, J.; Aloisio, A.; Alonso, A.; Alonso, F.; Alpigiani, C.; Altheimer, A.; Alvarez Gonzalez, B.; Alviggi, M. G.; Amako, K.; Amaral Coutinho, Y.; Amelung, C.; Amidei, D.; Amor Dos Santos, S. P.; Amorim, A.; Amoroso, S.; Amram, N.; Amundsen, G.; Anastopoulos, C.; Ancu, L. S.; Andari, N.; Andeen, T.; Anders, C. F.; Anders, G.; Anderson, K. J.; Andreazza, A.; Andrei, V.; Anduaga, X. S.; Angelidakis, S.; Angelozzi, I.; Anger, P.; Angerami, A.; Anghinolfi, F.; Anisenkov, A. V.; Anjos, N.; Annovi, A.; Antonaki, A.; Antonelli, M.; Antonov, A.; Antos, J.; Anulli, F.; Aoki, M.; Aperio Bella, L.; Apolle, R.; Arabidze, G.; Aracena, I.; Arai, Y.; Araque, J. P.; Arce, A. T. H.; Arguin, J. F.; Argyropoulos, S.; Arik, M.; Armbruster, A. J.; Arnaez, O.; Arnal, V.; Arnold, H.; Arratia, M.; Arslan, O.; Artamonov, A.; Artoni, G.; Asai, S.; Asbah, N.; Ashkenazi, A.; Åsman, B.; Asquith, L.; Assamagan, K.; Astalos, R.; Atkinson, M.; Atlay, N. B.; Auerbach, B.; Augsten, K.; Aurousseau, M.; Avolio, G.; Azuelos, G.; Azuma, Y.; Baak, M. A.; Baas, A. E.; Bacci, C.; Bachacou, H.; Bachas, K.; Backes, M.; Backhaus, M.; Backus Mayes, J.; Badescu, E.; Bagiacchi, P.; Bagnaia, P.; Bai, Y.; Bain, T.; Baines, J. T.; Baker, O. K.; Balek, P.; Balli, F.; Banas, E.; Banerjee, S.w.; Bannoura, A. A. E.; Bansal, V.; Bansil, H. S.; Barak, L.; Baranov, S. P.; Barberio, E. L.; Barberis, D.; Barbero, M.; Barillari, T.; Barisonzi, M.; Barklow, T.; Barlow, N.; Barnett, B. M.; Barnett, R. M.; Barnovska, Z.; Baroncelli, A.; Barone, G.; Barr, A. J.; Barreiro, F.; Barreiro Guimarães da Costa, J.; Bartoldus, R.; Barton, A. E.; Bartos, P.; Bartsch, V.; Bassalat, A.; Basye, A.; Bates, R. L.; Batley, J. R.; Battaglia, M.; Battistin, M.; Bauer, F.; Bawa, H. S.; Beattie, M. D.; Beau, T.; Beauchemin, P. H.; Beccherle, R.; Bechtle, P.; Beck, H. P.; Becker, K.; Becker, S.; Beckingham, M.; Becot, C.; Beddall, A. J.; Beddall, A.; Bedikian, S.; Bednyakov, V. A.; Bee, C. P.; Beemster, L. J.; Beermann, T. A.; Begel, M.; Behr, K.; Belanger Champagne, C.; Bell, P. J.; Bell, W. H.; Bella, G.; Bellerive, A.; Bellomo, M.; Belotskiy, K.; Beltramello, O.; Benary, O.; Benchekroun, D.; Bendtz, K.;
pmid: 25814877
pmc: PMC4370854
Countries: Italy, United KingdomATLAS measurements of the azimuthal anisotropy in lead–lead collisions at \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\sqrt{s_{\mathrm {NN}}}=2.76$$\end{document}sNN=2.76 TeV are shown using a dataset of approximately 7 \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\upmu $$\end{document}μb\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$^{-1}$$\end{document}-1 collected at the LHC in 2010. The measurements are performed for charged particles with transverse momenta \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$0.5
Average/low popularityAverage/low popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Preprint . 2018Open Access EnglishAuthors:Hinderer, Tanja; Nissanke, Samaya; Foucart, Francois; Hotokezaka, Kenta; Vincent, Trevor; Kasliwal, Mansi; Schmidt, Patricia; Williamson, Andrew R.; Nichols, David; Duez, Matthew; +3 moreHinderer, Tanja; Nissanke, Samaya; Foucart, Francois; Hotokezaka, Kenta; Vincent, Trevor; Kasliwal, Mansi; Schmidt, Patricia; Williamson, Andrew R.; Nichols, David; Duez, Matthew; Kidder, Lawrence E.; Pfeiffer, Harald P.; Scheel, Mark A.;Project: NSERC , NSF | Gravitational Radiation a... (1404569), NSF | Gravitational Radiation a... (1708213), NSF | Mergers, Stars, and Disks... (1806207), NSF | Maximizing Science Output... (1708212), NSF | PIRE: GROWTH: Global Rela... (1545949), NWO | Precision Gravity: black ... (680-47-460)
The discovery of GW170817 with gravitational waves (GWs) and electromagnetic (EM) radiation is prompting new questions in strong-gravity astrophysics. Importantly, it remains unknown whether the progenitor of the merger comprised two neutron stars (NSs), or a NS and a black hole (BH). Using new numerical-relativity simulations and incorporating modeling uncertainties we produce novel GW and EM observables for NS-BH mergers with similar masses. A joint analysis of GW and EM measurements reveals that if GW170817 is a NS-BH merger, <40% of the binary parameters consistent with the GW data are compatible with EM observations. Comment: 8 pages
Average/low popularityAverage/low popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact. - Publication . Other literature type . 2018Open Access EnglishAuthors:Große, Fabian; Greenwood, Naomi; Kreus, Markus; Lenhart, Hermann-Josef; Machoczek, Detlev; Pätsch, Johannes; Salt, Lesley; Thomas, Helmuth;Große, Fabian; Greenwood, Naomi; Kreus, Markus; Lenhart, Hermann-Josef; Machoczek, Detlev; Pätsch, Johannes; Salt, Lesley; Thomas, Helmuth;
Low oxygen conditions, often referred to as oxygen deficiency, occur regularly in the North Sea, a temperate European shelf sea. Stratification represents a major process regulating the seasonal dynamics of bottom oxygen, yet, lowest oxygen conditions in the North Sea do not occur in the regions of strongest stratification. This suggests that stratification is an important prerequisite for oxygen deficiency, but that the complex interaction between hydrodynamics and the biological processes drives its evolution. In this study we use the ecosystem model HAMSOM-ECOHAM to provide a general characterisation of the different zones of the North Sea with respect to oxygen, and to quantify the impact of the different physical and biological factors driving the oxygen dynamics inside the entire sub-thermocline volume and directly above the bottom. With respect to oxygen dynamics, the North Sea can be subdivided into three different zones: (1) a highly productive, non-stratified coastal zone, (2) a productive, seasonally stratified zone with a small sub-thermocline volume, and (3) a productive, seasonally stratified zone with a large sub-thermocline volume. Type 2 reveals the highest susceptibility to oxygen deficiency due to sufficiently long stratification periods (> 60 days) accompanied by high surface productivity resulting in high biological consumption, and a small sub-thermocline volume implying both a small initial oxygen inventory and a strong influence of the biological consumption on the oxygen concentration. Year-to-year variations in the oxygen conditions are caused by variations in primary production, while spatial differences can be attributed to differences in stratification and water depth. The large sub-thermocline volume dominates the oxygen dynamics in the northern central and northern North Sea and makes this region insusceptible to oxygen deficiency. In the southern North Sea the strong tidal mixing inhibits the development of seasonal stratification which protects this area from the evolution of low oxygen conditions. In contrast, the southern central North Sea is highly susceptible to low oxygen conditions (type 2). We furthermore show that benthic diagenetic processes represent the main oxygen consumers in the bottom layer, consistently accounting for more than 50 % of the overall consumption. Thus, primary production followed by remineralisation of organic matter under stratified conditions constitutes the main driver for the evolution of oxygen deficiency in the southern central North Sea. By providing these valuable insights, we show that ecosystem models can be a useful tool for the interpretation of observations and the estimation of the impact of anthropogenic drivers on the North Sea oxygen conditions.
Average/low popularityAverage/low popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact. - Publication . Article . Other literature type . 2021Open AccessAuthors:Denisa Hathazi; Dan Cox; Adele D'Amico; Giorgio Tasca; Richard Charlton; Robert-Yves Carlier; Jennifer Baumann; Laxmikanth Kollipara; René P. Zahedi; Ingo Feldmann; +18 moreDenisa Hathazi; Dan Cox; Adele D'Amico; Giorgio Tasca; Richard Charlton; Robert-Yves Carlier; Jennifer Baumann; Laxmikanth Kollipara; René P. Zahedi; Ingo Feldmann; Jean-François Deleuze; Annalaura Torella; Ronald D. Cohn; Emily Robinson; Francesco Ricci; Heinz Jungbluth; Fabiana Fattori; Anne Boland; Emily O'Connor; Rita Horvath; Rita Barresi; Hanns Lochmüller; Andoni Urtizberea; Marie-Line Jacquemont; Isabelle Nelson; Laura E. Swan; Gisèle Bonne; Andreas Roos;Publisher: Oxford University Press (OUP)Countries: United Kingdom, France, Germany, ItalyProject: CIHR , UKRI | Exosomal protein deficien... (MR/N025431/1)
Abstract Marinesco-Sjögren syndrome is a rare human disorder caused by biallelic mutations in SIL1 characterized by cataracts in infancy, myopathy and ataxia, symptoms which are also associated with a novel disorder caused by mutations in INPP5K. While these phenotypic similarities may suggest commonalties at a molecular level, an overlapping pathomechanism has not been established yet. In this study, we present six new INPP5K patients and expand the current mutational and phenotypical spectrum of the disease showing the clinical overlap between Marinesco-Sjögren syndrome and the INPP5K phenotype. We applied unbiased proteomic profiling on cells derived from Marinesco-Sjögren syndrome and INPP5K patients and identified alterations in d-3-PHGDH as a common molecular feature. d-3-PHGDH modulates the production of l-serine and mutations in this enzyme were previously associated with a neurological phenotype, which clinically overlaps with Marinesco-Sjögren syndrome and INPP5K disease. As l-serine administration represents a promising therapeutic strategy for d-3-PHGDH patients, we tested the effect of l-serine in generated sil1, phgdh and inpp5k a+b zebrafish models, which showed an improvement in their neuronal phenotype. Thus, our study defines a core phenotypical feature underpinning a key common molecular mechanism in three rare diseases and reveals a common and novel therapeutic target for these patients.
Top 10% in popularityTop 10% in popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2018Open AccessAuthors:K. Abe; C. Bronner; Yoshinari Hayato; M. Ikeda; K. Iyogi; J. Kameda; Y. Kato; Yasuhiro Kishimoto; Ll. Marti; M. Miura; +153 moreK. Abe; C. Bronner; Yoshinari Hayato; M. Ikeda; K. Iyogi; J. Kameda; Y. Kato; Yasuhiro Kishimoto; Ll. Marti; M. Miura; Shigetaka Moriyama; Masayuki Nakahata; Y. Nakajima; Yuuki Nakano; S. Nakayama; A. Orii; G. Pronost; Hiroyuki Sekiya; Masato Shiozawa; Y. Sonoda; A. Takeda; A. Takenaka; Hiromasa Tanaka; S. Tasaka; T. Yano; Ryosuke Akutsu; Takaaki Kajita; Yasuhiro Nishimura; Kimihiro Okumura; K. M. Tsui; Luis Labarga; P. Fernandez; F. d. M. Blaszczyk; C. Kachulis; E. Kearns; J. L. Raaf; Jl Stone; Lawrence Sulak; S. Berkman; S. Tobayama; J. Bian; M. Elnimr; W. R. Kropp; S. Locke; S. Mine; P. Weatherly; M. B. Smy; Henry W. Sobel; Volodymyr Takhistov; K. S. Ganezer; John Hill; J. Y. Kim; I. T. Lim; R. G. Park; Z. Li; E. O’Sullivan; Kate Scholberg; C. W. Walter; M. Gonin; J. Imber; Th. A. Mueller; T. Ishizuka; T. Nakamura; J. S. Jang; K. Choi; J. G. Learned; S. Matsuno; J. Amey; R. P. Litchfield; W. Y. Ma; Y. Uchida; M. O. Wascko; M. G. Catanesi; R. A. Intonti; E. Radicioni; G. De Rosa; A. Ali; G. Collazuol; L. Ludovici; S. V. Cao; M. Friend; T. Hasegawa; T. Ishida; T. Ishii; Takashi Kobayashi; T. Nakadaira; K. Nakamura; Y. Oyama; Ken Sakashita; T. Sekiguchi; T. Tsukamoto; K. Abe; Makoto Hasegawa; A. Suzuki; Y. Takeuchi; T. Hayashino; S. Hirota; M. Jiang; M. Mori; K. E. Nakamura; Tsuyoshi Nakaya; R. A. Wendell; L. H. V. Anthony; N. McCauley; A. Pritchard; Y. Fukuda; Yoshitaka Itow; M. Murase; Francesco Muto; P. Mijakowski; K. Frankiewicz; C. K. Jung; Xiaoning Li; J. L. Palomino; G. Santucci; C. Viela; M. J. Wilking; C. Yanagisawa; D. Fukuda; Hirokazu Ishino; Shintaro Ito; A. Kibayashi; Yusuke Koshio; H. Nagata; Makoto Sakuda; C. Xu; Yoshitaka Kuno; D. L. Wark; F. Di Lodovico; B. Richards; S. Molina Sedgwick; R. Tacik; Soo-Bong Kim; A. Cole; Lester D.R. Thompson; H. Okazawa; Y. Choi; K. Ito; Kyoshi Nishijima; M. Koshiba; Y. Suda; Masashi Yokoyama; R. G. Calland; M. Hartz; K. Martens; M. Murdoch; B. Quilain; C. Simpson; Yoshihiro Suzuki; Mark R. Vagins; D. Hamabe; Masahiro Kuze; Y. Okajima; Takashi Yoshida; Masaki Ishitsuka; J. F. Martin; C. M. Nantais; H. A. Tanaka; T. Towstego; A. Konaka; S. Chen; L. Wan; A. Minamino;Publisher: American Astronomical SocietyCountries: United Kingdom, United Kingdom, Italy, France, ItalyProject: EC | SKPLUS (641540), NSERC
We report the results of a neutrino search in Super-Kamiokande for coincident signals with the first detected gravitational wave produced by a binary neutron star merger, GW170817, which was followed by a short gamma-ray burst, GRB170817A, and a kilonova/macronova. We searched for coincident neutrino events in the range from 3.5 MeV to $\sim$100 PeV, in a time window $\pm$500 seconds around the gravitational wave detection time, as well as during a 14-day period after the detection. No significant neutrino signal was observed for either time window. We calculated 90% confidence level upper limits on the neutrino fluence for GW170817. From the upward-going-muon events in the energy region above 1.6 GeV, the neutrino fluence limit is $16.0^{+0.7}_{-0.6}$ ($21.3^{+1.1}_{-0.8}$) cm$^{-2}$ for muon neutrinos (muon antineutrinos), with an error range of $\pm5^{\circ}$ around the zenith angle of NGC4993, and the energy spectrum is under the assumption of an index of $-2$. The fluence limit for neutrino energies less than 100 MeV, for which the emission mechanism would be different than for higher-energy neutrinos, is also calculated. It is $6.6 \times 10^7$ cm$^{-2}$ for anti-electron neutrinos under the assumption of a Fermi-Dirac spectrum with average energy of 20 MeV. 8 pages, 4 figures
Top 10% in popularityTop 10% in popularityTop 10% in influencePopularity: Citation-based measure reflecting the current impact.Top 10% in influenceInfluence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2014RestrictedAuthors:Alexander V. Louie; Suresh Senan; Max Dahele; Ben J. Slotman; Wilko F.A.R. Verbakel;Alexander V. Louie; Suresh Senan; Max Dahele; Ben J. Slotman; Wilko F.A.R. Verbakel;
pmid: 25585783
Publisher: Elsevier BVCountry: NetherlandsPurpose Use of stereotactic ablative radiation therapy (SABR) for subcentimeter lung tumors is controversial. We report our outcomes for tumors with diameter ≤1 cm and their visibility on cone beam computed tomography (CBCT) scans and retrospectively evaluate the planned dose using a deterministic dose calculation algorithm (Acuros XB [AXB]). Methods and Materials We identified subcentimeter tumors from our institutional SABR database. Tumor size was remeasured on an artifact-free phase of the planning 4-dimensional (4D)-CT. Clinical plan doses were generated using either a pencil beam convolution or an anisotropic analytic algorithm (AAA). All AAA plans were recalculated using AXB, and differences among D95 and mean dose for internal target volume (ITV) and planning target volume (PTV) on the average intensity CT dataset, as well as for gross tumor volume (GTV) on the end respiratory phases were reported. For all AAA patients, CBCT scans acquired during each treatment fraction were evaluated for target visibility. Progression-free and overall survival rates were calculated using the Kaplan-Meier method. Results Thirty-five patients with 37 subcentimeter tumors were eligible for analysis. For the 22 AAA plans recalculated using AXB, Mean D95 ± SD values were 2.2 ± 4.4% (ITV) and 2.5 ± 4.8% (PTV) lower using AXB; whereas mean doses were 2.9 ± 4.9% (ITV) and 3.7 ± 5.1% (PTV) lower. Calculated AXB doses were significantly lower in one patient (difference in mean ITV and PTV doses, as well as in mean ITV and PTV D95 ranged from 22%-24%). However, the end respiratory phase GTV received at least 95% of the prescription dose. Review of 92 CBCT scans from all AAA patients revealed that the tumor was visualized in 82 images, and its position could be inferred in other images. The 2-year local progression-free survival was 100%. Conclusions Patients with subcentimeter lung tumors are good candidates for SABR, given the dosimetry, ability to localize tumors with image guidance, and excellent local control.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . Other literature type . 2013Open AccessAuthors:Montserrat Garcia-Closas; Sara Lindström; Kyriaki Michailidou; Marjanka K. Schmidt; Mark N. Brook; Elio Riboli; Loic Le Marchand; Diana Eccles; Penelope Miron; Peter A. Fasching; +201 moreMontserrat Garcia-Closas; Sara Lindström; Kyriaki Michailidou; Marjanka K. Schmidt; Mark N. Brook; Elio Riboli; Loic Le Marchand; Diana Eccles; Penelope Miron; Peter A. Fasching; Hiltrud Brauch; Jenny Chang-Claude; Jane Carpenter; Andrew K. Godwin; Heli Nevanlinna; Graham G. Giles; Angela Cox; John L. Hopper; Manjeet K. Bolla; Qin Wang; Joe Dennis; Ed Dicks; Nils Schoof; Stig E. Bojesen; Diether Lambrechts; Annegien Broeks; Pascal Guénel; Barbara Burwinkel; Elinor J. Sawyer; Antoinette Hollestelle; Olivia Fletcher; Robert Winqvist; Hermann Brenner; Arto Mannermaa; Ute Hamann; Alfons Meindl; Annika Lindblom; Wei Zheng; Peter Devillee; Mark S. Goldberg; Jan Lubinski; Anthony J. Swerdlow; Hoda Anton-Culver; Thilo Dörk; Keitaro Matsuo; Anna H. Wu; Paolo Radice; Soo Hwang Teo; Xiao-Ou Shu; William Blot; Daehee Kang; Mikael Hartman; Suleeporn Sangrajrang; Chen-Yang Shen; Melissa C. Southey; Daniel J. Park; Jennifer Stone; Laura J. van't Veer; Emiel J. Th. Rutgers; Artitaya Lophatananon; Sarah Stewart-Brown; Pornthep Siriwanarangsan; Julian Peto; Arif B. Ekici; Isabel dos Santos Silva; Nichola Johnson; Helen R. Warren; Ian Tomlinson; Michael J. Kerin; Nicola Miller; Thérèse Truong; Pierre Laurent-Puig; Børge G. Nordestgaard; Sune F. Nielsen; Henrik Flyger; Jose Ignacio Arias Perez; Primitiva Menéndez; Heiko Müller; Magdalena Lochmann; Christina Justenhoven; Yon Ko; Kristiina Aittomäki; Carl Blomqvist; Dario Greco; Tuomas Heikkinen; Hidemi Ito; Yasushi Yatabe; Sara Margolin; Vesa Kataja; Veli-Matti Kosma; Jaana M. Hartikainen; Rosemary L. Balleine; Chiu-Chen Tseng; Patrick Neven; Anne Sophie Dieudonne; Karin Leunen; Anja Rudolph; Stefan Nickels; Dieter Flesch-Janys; Paolo Peterlongo; Bernard Peissel; Loris Bernard; Janet E. Olson; Xianshu Wang; Gianluca Severi; Laura Baglietto; Catriona McLean; Gerhard A. Coetzee; Ye Feng; Fredrick R. Schumacher; Cheng Har Yip; Nur Aishah Taib; Ching-Yu Cheng; Martha J. Shrubsole; Jirong Long; Katri Pylkäs; Arja Jukkola-Vuorinen; Julia A. Knight; Gord Glendon; Anna Marie Mulligan; R.A.E.M. Tollenaar; Mieke Kriege; Carolien H.M. van Deurzen; Wei Lu; Yu Tang Gao; Hui Cai; Sabapathy P. Balasubramanian; Simon S. Cross; Malcolm W.R. Reed; Qiuyin Cai; Hui Miao; Ching Wan Chan; Kee Seng Chia; Anna Jakubowska; Katarzyna Jaworska; Katarzyna Durda; Chia-Ni Hsiung; Pei Ei Wu; Alan Ashworth; Michael Jones; Anna González-Neira; Guillermo Pita; M. Rosario Alonso; Daniel Vincent; Francois Bacot; Christine B. Ambrosone; Elisa V. Bandera; Gary K. Chen; Jorge L. Rodriguez-Gil; Leslie Bernstein; Michael F. Press; Regina G. Ziegler; Sarah J. Nyante; Sue A. Ingles; Quinten Waisfisz; Helen Tsimiklis; Enes Makalic; Minh Bui; Rita K. Schmutzler; Norbert Dahmen; Lars Beckmann; Kirsimari Aaltonen; Kamila Czene; Astrid Irwanto; Jianjun Liu; Clare Turnbull; Nazneen Rahman; Hanne Meijers-Heijboer; André G. Uitterlinden; Fernando Rivadeneira; Curtis Olswold; Robert Pilarski; Foluso O. Ademuyiwa; Irene Konstantopoulou; Nicholas G. Martin; Grant W. Montgomery; Dennis J. Slamon; Claudia Rauh; Michael P. Lux; Sebastian M. Jud; Thomas Brüning; Priyanka Sharma; Harsh B. Pathak; William J. Tapper; Sue Gerty; Lorraine Durcan; Dimitrios Trichopoulos; Rosario Tumino; Petra H.M. Peeters; Rudolf Kaaks; Daniele Campa; Federico Canzian; Elisabete Weiderpass; Mattias Johansson; Ruth C. Travis; Françoise Clavel-Chapelon; Laurence N. Kolonel; Andrew H. Beck; Susan E. Hankinson; Christine D. Berg; Jolanta Lissowska; Jonine D. Figueroa; Daniel I. Chasman; W. Ryan Diver; Jacques Simard; Alison M. Dunning; Mark E. Sherman; Georgia Chenevix-Trench; Stephen J. Chanock; Celine M. Vachon; Peter Kraft;Publisher: Springer Science and Business Media LLCCountries: Netherlands, United Kingdom, Italy, IrelandProject: NIH | Characterizing Genetic Su... (5U01CA098710-06), WT , NIH | Breast &prostate cancer &... (1U01CA098216-01), NIH | Characterizing Genetic Su... (5U01CA098233-06), NIH | Genetic epidemiology of c... (3R01CA122340-03S1), EC | COGS (223175), CIHR , NIH | Discovery Expansion and R... (5U19CA148065-04), NIH | Breast &Prostate Cancer &... (1U01CA098758-01)
Estrogen receptor (ER)-negative tumors represent 20-30% of all breast cancers, with a higher proportion occurring in younger women and women of African ancestry. The etiology and clinical behavior of ER-negative tumors are different from those of tumors expressing ER (ER positive), including differences in genetic predisposition. To identify susceptibility loci specific to ER-negative disease, we combined in a metaanalysis 3 genome-wide association studies of 4,193 ER-negative breast cancer cases and 35,194 controls with a series of 40 follow-up studies (6,514 cases and 41,455 controls), genotyped using a custom Illumina array, iCOGS, developed by the Collaborative Oncological Gene-environment Study (COGS). SNPs at four loci, 1q32.1 (MDM4, P= 2.1 x 10(-12) and LGR6, P = 1.4 x 10(-8)), 2p24.1 (P = 4.6 x 10(-8)) and 16q12.2 (FTO, P = 4.0 x 10(-8)), were associated with ER-negative but not ER-positive breast cancer (P> 0.05). These findings provide further evidence for distinct etiological pathways associated with invasive ER-positive and ER-negative breast cancers.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . 2021Open AccessAuthors:Rosalie A. Scholtes; Michaël J.B. van Baar; Megan D. Kok; Petter Bjornstad; David Z.I. Cherney; Jaap A. Joles; Daniël H. van Raalte;Rosalie A. Scholtes; Michaël J.B. van Baar; Megan D. Kok; Petter Bjornstad; David Z.I. Cherney; Jaap A. Joles; Daniël H. van Raalte;Publisher: WileyCountry: Netherlands
Abstract Diabetic kidney disease remains the leading cause of end‐stage kidney disease and a major risk factor for cardiovascular disease. Large cardiovascular outcome trials and dedicated kidney trials have shown that sodium‐glucose cotransporter (SGLT)2 inhibitors reduce cardiovascular morbidity and mortality and attenuate hard renal outcomes in patients with type 2 diabetes (T2D). Underlying mechanisms explaining these renal benefits may be mediated by decreased glomerular hypertension, possibly by vasodilation of the post‐glomerular arteriole. People with T2D often receive several different drugs, some of which could also impact the renal vasculature, and could therefore modify both renal efficacy and safety of SGLT2 inhibition. The most commonly prescribed drugs that could interact with SGLT2 inhibitors on renal haemodynamic function include renin‐angiotensin system inhibitors, calcium channel blockers and diuretics. Herein, we review the effects of these drugs on renal haemodynamic function in people with T2D and focus on studies that measured glomerular filtration rate (GFR) and effective renal plasma flow (ERPF) with gold‐standard techniques. In addition, we posit, based on these observations, potential interactions with SGLT2 inhibitors with an emphasis on efficacy and safety. SUMMARY AT A GLANCE This invited review describes the renal haemodynamic and protective effects of commonly prescribed drugs in people with type 2 diabetes and their interaction with SGLT2 inhibitors.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Article . Other literature type . 2011Open AccessAuthors:Robin Pourzal; Isabelle Catelas; Ralf Theissmann; C. Kaddick; Alfons Fischer;Robin Pourzal; Isabelle Catelas; Ralf Theissmann; C. Kaddick; Alfons Fischer;Publisher: Elsevier BVCountry: Germany
Biological effects of wear products (particles and metal ions) generated by metal-on-metal (MoM) hip replacements made of CoCrMo alloy remain a major cause of concern. Periprosthetic osteolysis, potential hypersensitivity response and pseudotumour formation are possible reactions that can lead to early revisions. To accurately analyse the biological response to wear particles from MoM implants, the exact nature of these particles needs to be characterized. Most previous studies used energy-dispersive X-ray spectroscopy (EDS) analysis for characterization. The present study used energy filtered transmission electron microscopy (TEM) and electron diffraction pattern analysis to allow for a more precise determination of the chemical composition and to gain knowledge of the crystalline structure of the wear particles.Particles were retrieved from two different test rigs: a reciprocating sliding wear tribometer (CoCrMo cylinder vs. bar) and a hip simulator according to ISO 14242-1 (CoCrMo head vs. CoCrMo cup). All tests were conducted in bovine serum. Particles were retrieved from the test medium using a previously published enzymatic digestion protocol.Particles isolated from tribometer samples had a size of 100 - 500 nm. Diffraction pattern analysis clearly revealed the lattice structure of strain induced hcp ε-martensite. Hip simulator samples revealed numerous particles of 15 - 30 nm and 30 - 80 nm size. Most of the larger particles appeared to be only partially oxidized and exhibited cobalt locally. The smallest particles were Cr(2)O(3) with no trace of cobalt. It optically appeared that these Cr(2)O(3) particles were flaking off the surface of larger particles that depicted a very high intensity of oxygen, as well as chromium, and only background noise of cobalt. The particle size difference between the two test rigs is likely related to the conditions of the two tribosystems, in particular the difference in the sample geometry and in the type of sliding (reciprocating vs. multidirectional).Results suggest that there may be a critical particle size at which chromium oxidation and cobalt ionization is accelerated. Since earlier studies have shown that wear particles are covered by organic residue which may act as a passive layer inhibiting further oxidation, it would suggest that this organic layer may be removed during the particle isolation process, resulting in a change of the particle chemical composition due to their pyrophoric properties. However, prior to being isolated from the serum lubricant, particles remain within the contact area of head and cup as a third-body. It is therefore possible that during that time, particles may undergo significant transformation and changes in chemical composition in the contact area of the head and cup within the tribological interface due to mechanical interaction with surface asperities.
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You have already added works in your ORCID record related to the merged Research product. - Publication . Conference object . 2004RestrictedAuthors:Mark S. Ackerman; Marlene Huysman; John M. Carroll; Barry Wellman; Giorgio DeMichelis; Volker Wulf;Mark S. Ackerman; Marlene Huysman; John M. Carroll; Barry Wellman; Giorgio DeMichelis; Volker Wulf;Publisher: ACMCountry: Netherlands
Communities are social entities whose actors share common needs, interests, or practices: they constitute the basic units of social experience. With regard to communities, social capital captures the structural, relational and cognitive aspects of the relationships among their members. Social capital is defined as a set of properties of a social entity (e.g. norms, level of trust, and intensive social networking) which enables joint activities and cooperation for mutual benefit. It can be understood as the glue which holds communities together. On this panel we will discuss whether and how information technology can strengthen communities by fostering social capital.
Average/low popularityAverage/low popularityAverage/low influencePopularity: Citation-based measure reflecting the current impact.Average/low influenceInfluence: Citation-based measure reflecting the total impact.add Add to ORCIDPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.