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Institution

Université libre de Bruxelles

EducationBrussels, Belgium
About: Université libre de Bruxelles is a education organization based out in Brussels, Belgium. It is known for research contribution in the topics: Population & Breast cancer. The organization has 24974 authors who have published 56969 publications receiving 2084303 citations. The organization is also known as: ULB.


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Journal ArticleDOI
Stephen G. Oliver1, Q. J. M. van der Aart2, M. L. Agostoni-Carbone3, Michel Aigle, Lilia Alberghina3, Despina Alexandraki, G. Antoine4, Rashida Anwar1, Juan P. G. Ballesta, Paule Bénit4, Gilbert Berben, Elisabetta Bergantino, N. Biteau, P. A. Bolle, Monique Bolotin-Fukuhara5, Anthony G. A. Brown1, Alistair J. P. Brown6, J. M. Buhler, C. Carcano3, Giovanna Carignani, Håkan Cederberg, R. Chanet4, Roland Contreras, Marc Crouzet, B. Daignan-Fornier5, E. Defoor7, M. Delgado, Jan Demolder, C. Doira5, Evelyne Dubois, Bernard Dujon8, A. Düsterhöft, D. Erdmann, M. Esteban, F. Fabre4, Cécile Fairhead8, Gérard Faye4, Horst Feldmann9, Walter Fiers, M. C. Francingues-Gaillard5, L. Franco, Laura Frontali10, H. Fukuhara4, L. J. Fuller11, P. Galland, Manda E. Gent1, D. Gigot, Véronique Gilliquet, Glansdorff Nn, André Goffeau12, M. Grenson13, P. Grisanti10, Leslie A. Grivell14, M. de Haan14, M. Haasemann, D. Hatat15, Janet Hoenicka, Johannes H. Hegemann, C. J. Herbert16, François Hilger, Stefan Hohmann, Cornelis P. Hollenberg, K. Huse, F. Iborra5, K. J. Indje1, K. Isono17, C. Jacq15, M. Jacquet5, C. M. James1, J. C. Jauniaux13, Y. Jia16, Alberto Jiménez, A. Kelly18, U. Kleinhans, P Kreisl, G. Lanfranchi, C Lewis11, C. G. vanderLinden19, G Lucchini3, K Lutzenkirchen, M.J. Maat14, L. Mallet5, G. Mannhaupet9, Enzo Martegani3, A. Mathieu4, C. T. C. Maurer19, David J. McConnell18, R. A. McKee11, F. Messenguy, Hans-Werner Mewes, Francis Molemans, M. A. Montague18, M. Muzi Falconi3, L. Navas, Carol S. Newlon20, D. Noone18, C. Pallier5, L. Panzeri3, Bruce M. Pearson11, J. Perea15, Peter Philippsen, A. Pierard, Rudi J. Planta19, Paolo Plevani3, B. Poetsch, Fritz M. Pohl21, B. Purnelle12, M. Ramezani Rad, S. W. Rasmussen, A. Raynal5, Miguel Remacha, P. Richterich21, Aki Roberts6, F. Rodriguez3, E. Sanz, I. Schaaff-Gerstenschlager, Bart Scherens, Bertold Schweitzer, Y. Shu15, J. Skala12, Piotr P. Slonimski16, F. Sor4, C. Soustelle5, R. Spiegelberg, Lubomira Stateva1, H. Y. Steensma2, S. Steiner, Agnès Thierry8, George Thireos, Maria Tzermia, L. A. Urrestarazu13, Giorgio Valle, I. Vetter9, J. C. van Vliet-Reedijk19, Marleen Voet7, Guido Volckaert7, P. Vreken19, H. Wang18, John R. Warmington1, D. von Wettstein, Barton Luke Wicksteed6, C. Wilson10, H. Wurst21, G. Xu, A. Yoshikawa17, Friedrich K. Zimmermann, J. G. Sgouros 
07 May 1992-Nature
TL;DR: The entire DNA sequence of chromosome III of the yeast Saccharomyces cerevisiae has been determined, which is the first complete sequence analysis of an entire chromosome from any organism.
Abstract: The entire DNA sequence of chromosome III of the yeast Saccharomyces cerevisiae has been determined. This is the first complete sequence analysis of an entire chromosome from any organism. The 315-kilobase sequence reveals 182 open reading frames for proteins longer than 100 amino acids, of which 37 correspond to known genes and 29 more show some similarity to sequences in databases. Of 55 new open reading frames analysed by gene disruption, three are essential genes; of 42 non-essential genes that were tested, 14 show some discernible effect on phenotype and the remaining 28 have no overt function.

811 citations

Journal ArticleDOI
TL;DR: Myalgic encephalomyelitis: International Consensus Criteria (Review).
Abstract: 12 FatigueConsultationClinic,SaltLake RegionalMedicalCenter; 13 InternalMedicine,FamilyPractice,UniversityofUtah,SaltLakeCity,UT,USA; 14 ME ⁄CFSCenter,OsloUniversity HospitalHF,Norway; 15 DepartmentofPaediatrics,StateUniversityofNewYork,Buffalo,NY,USA; 16 Independent,Pavia,Italy; 17 Harbor-UCLA MedicalCenter,UniversityofCalifornia,LosAngeles,CA; 18 EVMedResearch,Lomita,CA,USA; 19 UniversityofLimerick,Limerick,Ireland; 20 Pain Clinic,KonyangUniversityHospital,Daejeon,Korea; 21 DonvaleSpecialistMedicalCentre,Donvale,Victoria,Australia; 22 Departmentsof Anesthesiology,NeurobiologyandAnatomy,UniversityofUtah,SaltLakeCity,UT,USA; 23 DepartmentofMedicinaNuclear,ClinicaLasCondes, Santiago,Chile; 24 WhittemorePetersonInstitute,UniversityofNevada,Reno,NV,USA; 25 MiwaNaikaClinic,Toyama,Japan; 26 A.Kirchenstein InstituteofMicrobiologyandVirology,RigaStradinsUniversity,Riga,Latvia; 27 DepartmentofBiochemistryBand 28 DepartmentofSportsSciences,UniversityofthePacific,Stockton,CAUSA

810 citations

Journal ArticleDOI
TL;DR: The use of genomic grade can identify two clinically distinct ER-positive molecular subtypes in a simple and highly reproducible manner across multiple data sets and emphasizes the important role of proliferation-related genes in predicting prognosis in ER- positive BC.
Abstract: Purpose A number of microarray studies have reported distinct molecular profiles of breast cancers (BC), such as basal-like, ErbB2-like, and two to three luminal-like subtypes. These were associated with different clinical outcomes. However, although the basal and the ErbB2 subtypes are repeatedly recognized, identification of estrogen receptor (ER) –positive subtypes has been inconsistent. Therefore, refinement of their molecular definition is needed. Materials and Methods We have previously reported a gene expression grade index (GGI), which defines histologic grade based on gene expression profiles. Using this algorithm, we assigned ER-positive BC to either high–or low–genomic grade subgroups and compared these with previously reported ER-positive molecular classifications. As further validation, we classified 666 ER-positive samples into subtypes and assessed their clinical outcome. Results Two ER-positive molecular subgroups (high and low genomic grade) could be defined using the GGI. Despite trackin...

810 citations

Journal ArticleDOI
TL;DR: Evidence is obtained for maturation in vivo in response to the bacterial product lipopolysaccharide (LPS), which is interpreted to mean that LPS can cause DC in the marginal zone to mature and to migrate into and then out of the T cell areas.
Abstract: Dendritic cells (DC) are described as "nature's adjuvant," since they have the capacity to sensitize T cells in vivo upon first encounter with the antigen. The potent accessory properties of DC appear to develop sequentially. In particular, the ability to process antigens and to sensitize native T cells develops in sequence, a process termed "maturation" that is well described in vitro. Here, we obtain evidence for maturation in vivo in response to the bacterial product lipopolysaccharide (LPS). Before LPS treatment, many DC are found at the margin between the red and white pulp. These cells lack the M342 and DEC-205 markers, but process soluble proteins effectively. 6 h after LPS, DC with the M342 and DEC-205 markers are found in increased numbers in the T cell areas. These cells have a reduced capacity to process proteins, but show increases in the B7 costimulator and T cell stimulatory capacity. 48 h after LPS, the number of DC in the spleen is reduced markedly. We interpret these findings to mean that LPS can cause DC in the marginal zone to mature and to migrate into and then out of the T cell areas.

807 citations

Journal ArticleDOI
Fengpeng An1, Guangpeng An, Qi An2, Vito Antonelli3  +226 moreInstitutions (55)
TL;DR: The Jiangmen Underground Neutrino Observatory (JUNO) as mentioned in this paper is a 20kton multi-purpose underground liquid scintillator detector with the determination of neutrino mass hierarchy (MH) as a primary physics goal.
Abstract: The Jiangmen Underground Neutrino Observatory (JUNO), a 20 kton multi-purpose underground liquid scintillator detector, was proposed with the determination of the neutrino mass hierarchy (MH) as a primary physics goal. The excellent energy resolution and the large fiducial volume anticipated for the JUNO detector offer exciting opportunities for addressing many important topics in neutrino and astro-particle physics. In this document, we present the physics motivations and the anticipated performance of the JUNO detector for various proposed measurements. Following an introduction summarizing the current status and open issues in neutrino physics, we discuss how the detection of antineutrinos generated by a cluster of nuclear power plants allows the determination of the neutrino MH at a 3–4σ significance with six years of running of JUNO. The measurement of antineutrino spectrum with excellent energy resolution will also lead to the precise determination of the neutrino oscillation parameters ${\mathrm{sin}}^{2}{\theta }_{12}$, ${\rm{\Delta }}{m}_{21}^{2}$, and $| {\rm{\Delta }}{m}_{{ee}}^{2}| $ to an accuracy of better than 1%, which will play a crucial role in the future unitarity test of the MNSP matrix. The JUNO detector is capable of observing not only antineutrinos from the power plants, but also neutrinos/antineutrinos from terrestrial and extra-terrestrial sources, including supernova burst neutrinos, diffuse supernova neutrino background, geoneutrinos, atmospheric neutrinos, and solar neutrinos. As a result of JUNO's large size, excellent energy resolution, and vertex reconstruction capability, interesting new data on these topics can be collected. For example, a neutrino burst from a typical core-collapse supernova at a distance of 10 kpc would lead to ∼5000 inverse-beta-decay events and ∼2000 all-flavor neutrino–proton ES events in JUNO, which are of crucial importance for understanding the mechanism of supernova explosion and for exploring novel phenomena such as collective neutrino oscillations. Detection of neutrinos from all past core-collapse supernova explosions in the visible universe with JUNO would further provide valuable information on the cosmic star-formation rate and the average core-collapse neutrino energy spectrum. Antineutrinos originating from the radioactive decay of uranium and thorium in the Earth can be detected in JUNO with a rate of ∼400 events per year, significantly improving the statistics of existing geoneutrino event samples. Atmospheric neutrino events collected in JUNO can provide independent inputs for determining the MH and the octant of the ${\theta }_{23}$ mixing angle. Detection of the (7)Be and (8)B solar neutrino events at JUNO would shed new light on the solar metallicity problem and examine the transition region between the vacuum and matter dominated neutrino oscillations. Regarding light sterile neutrino topics, sterile neutrinos with ${10}^{-5}\,{{\rm{eV}}}^{2}\lt {\rm{\Delta }}{m}_{41}^{2}\lt {10}^{-2}\,{{\rm{eV}}}^{2}$ and a sufficiently large mixing angle ${\theta }_{14}$ could be identified through a precise measurement of the reactor antineutrino energy spectrum. Meanwhile, JUNO can also provide us excellent opportunities to test the eV-scale sterile neutrino hypothesis, using either the radioactive neutrino sources or a cyclotron-produced neutrino beam. The JUNO detector is also sensitive to several other beyondthe-standard-model physics. Examples include the search for proton decay via the $p\to {K}^{+}+\bar{ u }$ decay channel, search for neutrinos resulting from dark-matter annihilation in the Sun, search for violation of Lorentz invariance via the sidereal modulation of the reactor neutrino event rate, and search for the effects of non-standard interactions. The proposed construction of the JUNO detector will provide a unique facility to address many outstanding crucial questions in particle and astrophysics in a timely and cost-effective fashion. It holds the great potential for further advancing our quest to understanding the fundamental properties of neutrinos, one of the building blocks of our Universe.

807 citations


Authors

Showing all 25206 results

NameH-indexPapersCitations
Karl J. Friston2171267217169
Yi Chen2174342293080
David Miller2032573204840
Jing Wang1844046202769
H. S. Chen1792401178529
Jie Zhang1784857221720
Jasvinder A. Singh1762382223370
D. M. Strom1763167194314
J. N. Butler1722525175561
Andrea Bocci1722402176461
Bradley Cox1692150156200
Marc Weber1672716153502
Hongfang Liu1662356156290
Guenakh Mitselmakher1651951164435
Yang Yang1642704144071
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023119
2022412
20213,195
20203,051
20192,751
20182,609