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Institution

University of Coimbra

EducationCoimbra, Portugal
About: University of Coimbra is a education organization based out in Coimbra, Portugal. It is known for research contribution in the topics: Population & Context (language use). The organization has 14318 authors who have published 43067 publications receiving 994733 citations. The organization is also known as: UC & Universidade dos Estudos Gerais.


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Journal ArticleDOI
08 Jul 2010-Nature
TL;DR: The root-mean-square charge radius, rp, has been determined with an accuracy of 2 per cent by electron–proton scattering experiments, and the present most accurate value of rp (with an uncertainty of 1 per cent) is given by the CODATA compilation of physical constants.
Abstract: Considering that the proton is a basic subatomic component of all ordinary matter — as well as being ubiquitous in its solo role as the hydrogen ion H+ — there are some surprising gaps in our knowledge of its structure and behaviour. A collaborative project to determine the root-mean-square charge radius of the proton to better than the 1% accuracy of the current 'best' value suggests that those knowledge gaps may be greater than was thought. The new determination comes from a technically challenging spectroscopic experiment — the measurement of the Lamb shift (the energy difference between a specific pair of energy states) in 'muonic hydrogen', an exotic atom in which the electron is replaced by its heavier twin, the muon. The result is unexpected: a charge radius about 4% smaller than the previous value. The discrepancy remains unexplained. Possible implications are that the value of the most accurately determined fundamental constant, the Rydberg constant, will need to be revised — or that the validity of quantum electrodynamics theory is called into question. Here, a technically challenging spectroscopic experiment is described: the measurement of the muonic Lamb shift. The results lead to a new determination of the charge radius of the proton. The new value is 5.0 standard deviations smaller than the previous world average, a large discrepancy that remains unexplained. Possible implications of the new finding are that the value of the Rydberg constant will need to be revised, or that the validity of quantum electrodynamics theory is called into question. The proton is the primary building block of the visible Universe, but many of its properties—such as its charge radius and its anomalous magnetic moment—are not well understood. The root-mean-square charge radius, rp, has been determined with an accuracy of 2 per cent (at best) by electron–proton scattering experiments1,2. The present most accurate value of rp (with an uncertainty of 1 per cent) is given by the CODATA compilation of physical constants3. This value is based mainly on precision spectroscopy of atomic hydrogen4,5,6,7 and calculations of bound-state quantum electrodynamics (QED; refs 8, 9). The accuracy of rp as deduced from electron–proton scattering limits the testing of bound-state QED in atomic hydrogen as well as the determination of the Rydberg constant (currently the most accurately measured fundamental physical constant3). An attractive means to improve the accuracy in the measurement of rp is provided by muonic hydrogen (a proton orbited by a negative muon); its much smaller Bohr radius compared to ordinary atomic hydrogen causes enhancement of effects related to the finite size of the proton. In particular, the Lamb shift10 (the energy difference between the 2S1/2 and 2P1/2 states) is affected by as much as 2 per cent. Here we use pulsed laser spectroscopy to measure a muonic Lamb shift of 49,881.88(76) GHz. On the basis of present calculations11,12,13,14,15 of fine and hyperfine splittings and QED terms, we find rp = 0.84184(67) fm, which differs by 5.0 standard deviations from the CODATA value3 of 0.8768(69) fm. Our result implies that either the Rydberg constant has to be shifted by −110 kHz/c (4.9 standard deviations), or the calculations of the QED effects in atomic hydrogen or muonic hydrogen atoms are insufficient.

1,152 citations

Journal ArticleDOI
01 Jul 2014-Allergy
TL;DR: This guideline covers the definition and classification of urticaria, taking into account the recent progress in identifying its causes, eliciting factors and pathomechanisms, and outlines evidence-based diagnostic and therapeutic approaches for the different subtypes ofUrticaria.
Abstract: This guideline is the result of a systematic literature review using the 'Grading of Recommendations Assessment, Development and Evaluation' (GRADE) methodology and a structured consensus conference held on 28 and 29 November 2012, in Berlin. It is a joint initiative of the Dermatology Section of the European Academy of Allergy and Clinical Immunology (EAACI), the EU-funded network of excellence, the Global Allergy and Asthma European Network (GA(2) LEN), the European Dermatology Forum (EDF), and the World Allergy Organization (WAO) with the participation of delegates of 21 national and international societies. Urticaria is a frequent, mast cell-driven disease, presenting with wheals, angioedema, or both. The life-time prevalence for acute urticaria is approximately 20%. Chronic spontaneous urticaria and other chronic forms of urticaria do not only cause a decrease in quality of life, but also affect performance at work and school and, as such, are members of the group of severe allergic diseases. This guideline covers the definition and classification of urticaria, taking into account the recent progress in identifying its causes, eliciting factors and pathomechanisms. In addition, it outlines evidence-based diagnostic and therapeutic approaches for the different subtypes of urticaria. This guideline was acknowledged and accepted by the European Union of Medical Specialists (UEMS).

1,150 citations

Journal ArticleDOI
TL;DR: In this article, the authors present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes.
Abstract: In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field.

1,129 citations

Journal ArticleDOI
19 Dec 2013-Cell
TL;DR: It is shown that, during aging, there is a specific loss of mitochondrial, but not nuclear, encoded OXPHOS subunits, and an alternate PGC-1α/β-independent pathway of nuclear-mitochondrial communication contributes to the decline in mitochondrial function with age.

1,101 citations

Journal ArticleDOI
Elena Aprile1, Jelle Aalbers2, F. Agostini, M. Alfonsi3, F. D. Amaro4, M. Anthony1, F. Arneodo5, P. Barrow6, Laura Baudis6, Boris Bauermeister7, M. L. Benabderrahmane5, T. Berger8, P. A. Breur2, April S. Brown2, Ethan Brown8, S. Bruenner9, Giacomo Bruno, Ran Budnik10, L. Bütikofer11, J. Calvén7, João Cardoso4, M. Cervantes12, D. Cichon9, D. Coderre11, Auke-Pieter Colijn2, Jan Conrad7, Jean-Pierre Cussonneau13, M. P. Decowski2, P. de Perio1, P. Di Gangi14, A. Di Giovanni5, Sara Diglio13, G. Eurin9, J. Fei15, A. D. Ferella7, A. Fieguth16, W. Fulgione, A. Gallo Rosso, Michelle Galloway6, F. Gao1, M. Garbini14, Robert Gardner17, C. Geis3, Luke Goetzke1, L. Grandi17, Z. Greene1, C. Grignon3, C. Hasterok9, E. Hogenbirk2, J. Howlett1, R. Itay10, B. Kaminsky11, Shingo Kazama6, G. Kessler6, A. Kish6, H. Landsman10, R. F. Lang12, D. Lellouch10, L. Levinson10, Qing Lin1, Sebastian Lindemann9, Manfred Lindner9, F. Lombardi15, J. A. M. Lopes4, A. Manfredini10, I. Mariș5, T. Marrodán Undagoitia9, Julien Masbou13, F. V. Massoli14, D. Masson12, D. Mayani6, M. Messina1, K. Micheneau13, A. Molinario, K. Morâ7, M. Murra16, J. Naganoma18, Kaixuan Ni15, Uwe Oberlack3, P. Pakarha6, Bart Pelssers7, R. Persiani13, F. Piastra6, J. Pienaar12, V. Pizzella9, M.-C. Piro8, Guillaume Plante1, N. Priel10, L. Rauch9, S. Reichard6, C. Reuter12, B. Riedel17, A. Rizzo1, S. Rosendahl16, N. Rupp9, R. Saldanha17, J.M.F. dos Santos4, Gabriella Sartorelli14, M. Scheibelhut3, S. Schindler3, J. Schreiner9, Marc Schumann11, L. Scotto Lavina19, M. Selvi14, P. Shagin18, E. Shockley17, Manuel Gameiro da Silva4, H. Simgen9, M. V. Sivers11, A. Stein20, S. Thapa17, Dominique Thers13, A. Tiseni2, Gian Carlo Trinchero, C. Tunnell17, M. Vargas16, N. Upole17, Hui Wang20, Zirui Wang, Yuehuan Wei6, Ch. Weinheimer16, J. Wulf6, J. Ye15, Yanxi Zhang1, T. Zhu1 
TL;DR: The first dark matter search results from XENON1T, a ∼2000-kg-target-mass dual-phase (liquid-gas) xenon time projection chamber in operation at the Laboratori Nazionali del Gran Sasso in Italy, are reported and a profile likelihood analysis shows that the data are consistent with the background-only hypothesis.
Abstract: We report the first dark matter search results from XENON1T, a ∼2000-kg-target-mass dual-phase (liquid-gas) xenon time projection chamber in operation at the Laboratori Nazionali del Gran Sasso in Italy and the first ton-scale detector of this kind The blinded search used 342 live days of data acquired between November 2016 and January 2017 Inside the (1042±12)-kg fiducial mass and in the [5,40] keVnr energy range of interest for weakly interacting massive particle (WIMP) dark matter searches, the electronic recoil background was (193±025)×10-4 events/(kg×day×keVee), the lowest ever achieved in such a dark matter detector A profile likelihood analysis shows that the data are consistent with the background-only hypothesis We derive the most stringent exclusion limits on the spin-independent WIMP-nucleon interaction cross section for WIMP masses above 10 GeV/c2, with a minimum of 77×10-47 cm2 for 35-GeV/c2 WIMPs at 90% CL

1,061 citations


Authors

Showing all 14693 results

NameH-indexPapersCitations
P. Chang1702154151783
Yang Gao1682047146301
Bin Liu138218187085
P. Sinervo138151699215
Filipe Veloso12888775496
Panagiotis Kokkas128123481051
Nuno Filipe Castro12896076945
Robert Gardner128101577619
Francois Corriveau128102275729
Peter Krieger128117181368
João Carvalho126127877017
Helmut Wolters12685175721
Nicola Venturi12679669518
Sai-Juan Chen121121173991
Harinder Singh Bawa12079866120
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20241
2023112
2022530
20213,238
20203,193
20193,090