138 research outputs found
Jet energy measurement with the ATLAS detector in proton-proton collisions at root s=7 TeV
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdelalim AA
- Abdesselam A
- Abdinov O
- Abi B
- Abolins M
- Abramowicz H
- Abreu H
- Acerbi E
- Acharya BS
- Adams DL
- Addy TN
- Adelman J
- Aderholz M
- Adomeit S
- Adragna P
- Adye T
- Aefsky S
- Aguilar-Saavedra JA
- Aharrouche M
- Ahlen SP
- Ahles F
- Ahmad A
- Ahsan M
- Aielli G
- Akdogana T
- Akesson TPA
- Akimoto G
- Akimov AV
- Akiyama A
- Aktas A
- Alam MA
- Alam MS
- Albert J
- Albrand S
- Aleksa M
- Aleksandrov IN
- Alessandria F
- Alexa C
- Alexander G
- Alexandre G
- Alexopoulos T
- Alhroob M
- Aliev M
- Alimonti G
- Alison J
- Aliyev M
- Allport PP
- Allwood-Spiers SE
- Almenar CC
- Almond J
- Aloisio A
- Alon R
- Alonso A
- Alviggi MG
- Amako K
- Amaral P
- Amelung C
- Ammosov VV
- Amorim A
- Amoros G
- Amram N
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders G
- Anderson KJ
- Andreazza A
- Andrei V
- Andrieux M-L
- Anduaga XS
- Angerami A
- Anghinolfi F
- Anh TV
- Anjos N
- Annovi A
- Antonaki A
- Antonelli M
- Antonov A
- Antos J
- Anulli F
- Aoun S
- Apolle R
- Arabidze G
- Aracena I
- Arai Y
- Aranda CP
- Arce ATH
- Archambault JP
- Arfaoui S
- Arguin J-F
- Arik E
- Arik M
- Armbruster AJ
- Arnaez O
- Arnault C
- Artamonov A
- Artoni G
- Arutinov D
- Asai S
- Asfandiyarov R
- Ask S
- Asman B
- Asner D
- Asquith L
- Assamagan K
- Astbury A
- Astvatsatourov A
- Atoian G
- Aubert B
- Auge E
- Augsten K
- Aurousseau M
- Austin N
- Avolio G
- Avramidou R
- Axen D
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- Azuelos G
- Azuma Y
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- Baccaglioni G
- Bacci C
- Bach AM
- Bachacou H
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- Backhaus M
- Badescu E
- Bagnaia P
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- Bai Y
- Bailey DC
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- Baker OK
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- Boscherini D
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- Botterill D
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- Boudreau J
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- Buckingham RM
- Buckley AG
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- Budagov IA
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- Bueso XP
- Bugge L
- Buira-Clark D
- Bulekov O
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- Butterworth JM
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- Castanheira MTD
- Castillo LRF
- Castro NF
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- Cavasinni V
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- Cerqueira AS
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- Cerutti F
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- Chafaq A
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- Chapleau B
- Chapman JD
- Chapman JW
- Chareyre E
- Charlton DG
- Chavda V
- Cheatham S
- Chekanov S
- Chekulaev SV
- Chelkov GA
- Chelstowska MA
- Chen C
- Chen H
- Chen S
- Chen T
- Chen X
- Cheng S
- Cheong ALF
- Cheplakov A
- Chepurnov VF
- Chernyatin V
- Cheu E
- Cheung SL
- Chevalier L
- Chiefari G
- Chikovani L
- Childers JT
- Chilingarov A
- Chiodini G
- Chizhov MV
- Choudalakis G
- Chouridou S
- Christidi IA
- Christov A
- Chromek-Burckhart D
- Chu ML
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- Ciobotaru MD
- Cioccaa C
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- Collaboration ATLAS
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- Da Costa JBG
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- Damazio DO
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- De Graat J
- De Groot N
- De Jong P
- De la Hoz SG
- De la Taille C
- De la Torre H
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- Degenhardt J
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/03/2013
- Field of study
The jet energy scale and its systematic uncertainty are determined for jets measured with the ATLAS detector at the LHC in proton-proton collision data at a centre-of-mass energy of √s = 7TeV corresponding to an integrated luminosity of 38 pb-1. Jets are reconstructed with the anti-kt algorithm with distance parameters R=0. 4 or R=0. 6. Jet energy and angle corrections are determined from Monte Carlo simulations to calibrate jets with transverse momenta pT≥20 GeV and pseudorapidities {pipe}η{pipe}<4. 5. The jet energy systematic uncertainty is estimated using the single isolated hadron response measured in situ and in test-beams, exploiting the transverse momentum balance between central and forward jets in events with dijet topologies and studying systematic variations in Monte Carlo simulations. The jet energy uncertainty is less than 2. 5 % in the central calorimeter region ({pipe}η{pipe}<0. 8) for jets with 60≤pT<800 GeV, and is maximally 14 % for pT<30 GeV in the most forward region 3. 2≤{pipe}η{pipe}<4. 5. The jet energy is validated for jet transverse momenta up to 1 TeV to the level of a few percent using several in situ techniques by comparing a well-known reference such as the recoiling photon pT, the sum of the transverse momenta of tracks associated to the jet, or a system of low-pT jets recoiling against a high-pT jet. More sophisticated jet calibration schemes are presented based on calorimeter cell energy density weighting or hadronic properties of jets, aiming for an improved jet energy resolution and a reduced flavour dependence of the jet response. The systematic uncertainty of the jet energy determined from a combination of in situ techniques is consistent with the one derived from single hadron response measurements over a wide kinematic range. The nominal corrections and uncertainties are derived for isolated jets in an inclusive sample of high-pT jets. Special cases such as event topologies with close-by jets, or selections of samples with an enhanced content of jets originating from light quarks, heavy quarks or gluons are also discussed and the corresponding uncertainties are determined. © 2013 CERN for the benefit of the ATLAS collaboration
Measurement of the inclusive and dijet cross-sections of b-jets in pp collisions at sqrt(s) = 7 TeV with the ATLAS detector
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- Willocq S
- Wilson A
- Wilson JA
- Wilson MG
- Wingerter-Seez I
- Winkelmann S
- Winklmeier F
- Wittgen M
- Wolter MW
- Wolters H
- Wooden G
- Wosiek BK
- Wotschack J
- Woudstra MJ
- Wraight K
- Wright C
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- Wu SL
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- Wulf E
- Wunstorf R
- Wynne BM
- Xaplanteris L
- Xella S
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- Yamamoto A
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- Yao W-M
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- Yildiz HD
- Yilmaz M
- Yoosoofmiya R
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- Yu D
- Yu J
- Yu J
- Yuan L
- Yurkewicz A
- Zaets VG
- Zaidan R
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- Zalite YK
- Zanello L
- Zarzhitsky P
- Zaytsev A
- Zdrazil M
- Zeitnitz C
- Zeller M
- Zema PF
- Zemla A
- Zendler C
- Zenin AV
- Zenin O
- Zenis T
- Zenonos Z
- Zenz S
- Zerwas D
- Zhan Z
- Zhang D
- Zhang H
- Zhang J
- Zhang X
- Zhang Z
- Zhao L
- Zhao T
- Zhao Z
- Zhemchugov A
- Zheng S
- Zhong J
- Zhou B
- Zhou N
- Zhou Y
- Zhu CG
- Zhu H
- Zhu Y
- Zhuang X
- Zhuravlov V
- Zieminska D
- Zilka B
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Ziolkowski M
- Zitoun R
- Zivkovic L
- Zmouchko VV
- Zobernig G
- Zoccoli A
- Zolnierowski Y
- Zsenei A
- zur Nedden M
- Zutshi V
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 31/12/2010
- Field of study
The inclusive and dijet production cross-sections have been measured for jets
containing b-hadrons (b-jets) in proton-proton collisions at a centre-of-mass
energy of sqrt(s) = 7 TeV, using the ATLAS detector at the LHC. The
measurements use data corresponding to an integrated luminosity of 34 pb^-1.
The b-jets are identified using either a lifetime-based method, where secondary
decay vertices of b-hadrons in jets are reconstructed using information from
the tracking detectors, or a muon-based method where the presence of a muon is
used to identify semileptonic decays of b-hadrons inside jets. The inclusive
b-jet cross-section is measured as a function of transverse momentum in the
range 20 < pT < 400 GeV and rapidity in the range |y| < 2.1. The bbbar-dijet
cross-section is measured as a function of the dijet invariant mass in the
range 110 < m_jj < 760 GeV, the azimuthal angle difference between the two jets
and the angular variable chi in two dijet mass regions. The results are
compared with next-to-leading-order QCD predictions. Good agreement is observed
between the measured cross-sections and the predictions obtained using POWHEG +
Pythia. MC@NLO + Herwig shows good agreement with the measured bbbar-dijet
cross-section. However, it does not reproduce the measured inclusive
cross-section well, particularly for central b-jets with large transverse
momenta.Comment: 10 pages plus author list (21 pages total), 8 figures, 1 table, final
version published in European Physical Journal
Micro-RNAs as diagnostic or prognostic markers in human epithelial malignancies
- Author
- A Budhu
- A Cimmino
- A Laios
- A Navarro
- AB Hui
- AB Hui
- AJ Schetter
- AM Krichevsky
- Angela Hui
- AS Ho
- AW Tong
- B Xiao
- B Zhang
- C Fan
- C Roth
- C Roth
- C Zhang
- CC Yang
- CH Lawrie
- Christine How
- CJ Liu
- CM Calin GA Croce
- D Bonci
- D Bresters
- D Hanahan
- D Lebanony
- DD Taylor
- E Cocucci
- EA Wiemer
- EK Ng
- Emma Ito
- F Meng
- F Moltzahn
- F Wang
- F Yaman Agaoglu
- Fei-Fei Liu
- G Rabinowits
- G Stefani
- GA Calin
- GA Calin
- H Valadi
- H Zhao
- HL Zhang
- HM Heneghan
- HM Heneghan
- I Bentwich
- IA Asangani
- J Gui
- J Kluiver
- J Lu
- J Silva
- J Takamizawa
- J Wang
- J Xu
- J Yu
- JA Chan
- JC Brase
- JQ Chen
- K Breving
- K Morita
- KE Resnick
- KZ Qu
- L Du
- LF Sempere
- LM Li
- LX Yan
- M Bloomston
- M Cronin
- M Macabeo-Ong
- M Raponi
- M Spahn
- M Tsujiura
- MC du Rieu
- MD Mattie
- MJ Lodes
- MJ Ratain
- ML Si
- MZ Michael
- N Habbe
- N Osman
- N Yanaihara
- PH Lange
- PS Mitchell
- PT Nelson
- R Eitan
- R Flavin
- R Garzon
- R Liu
- S Ali
- S Asaga
- S Griffiths-Jones
- S Paik
- S Saini
- S Volinia
- SC Lin
- SF Hausler
- SL Lin
- SL Yu
- SN Thomas
- SP Balk
- T Donnem
- TS Wong
- W Zhu
- WL Heyward
- WM Merritt
- X Chen
- X Hu
- X Hu
- X Kong
- X Li
- XB Shi
- XX Pu
- Y Dorsett
- Y Guo
- Y Hayashita
- Y Yamamoto
- Y Zhang
- Z Hagman
- Z Hu
- Z Huang
- Z Lu
- ZS Kai
- Publication venue
- BioMed Central
- Publication date
- 01/01/2011
- Field of study
Micro-RNAs (miRs) are important regulators of mRNA and protein expression; the ability of miR expression profilings to distinguish different cancer types and classify their sub-types has been well-described. They also represent a novel biological entity with potential value as tumour biomarkers, which can improve diagnosis, prognosis, and monitoring of treatment response for human cancers. This endeavour has been greatly facilitated by the stability of miRs in formalin-fixed paraffin-embedded (FFPE) tissues, and their detection in circulation. This review will summarize some of the key dysregulated miRs described to date in human epithelial malignancies, and their potential value as molecular bio-markers in FFPE tissues and blood samples. There remain many challenges in this domain, however, with the evolution of different platforms, the complexities of normalizing miR profiling data, and the importance of evaluating sufficiently-powered training and validation cohorts. Nonetheless, well-conducted miR profiling studies should contribute important insights into the molecular aberrations driving human cancer development and progression
Lysophosphatidic Acid Acyltransferase β (LPAATβ) Promotes the Tumor Growth of Human Osteosarcoma
- Author
- A Burton
- AA Sandberg
- AC Stamps
- AJ Chou
- Bai-Cheng He
- BC He
- BT Andresen
- C Eberhardt
- CS Diefenbach
- D Hollenback
- Deana Shenaq
- DW Leung
- E Furuta
- EE Pakos
- Enyi Huang
- Eric R. Wagner
- Farbod Rastegar
- Gaurav Luther
- GM Springett
- Guo-Wei Zuo
- H Cheng
- HH Luu
- HH Luu
- Hue H. Luu
- J Luo
- J Magre
- J West
- JA Menendez
- JA Menendez
- Jian-Li Gao
- Jikun Shen
- Jinyong Luo
- JM Pagel
- JS Whelan
- KA Sharff
- Ke Yang
- L Bonham
- L Chen
- Liang Chen
- Linyuan Wang
- M Coon
- MB Mintz
- MD Murphey
- MG Douvas
- Mi Li
- MP Link
- N Gordon
- N Tang
- N Tang
- Ning Hu
- O Feugeas
- P La Rosee
- PA Meyers
- Q Kang
- Q Kang
- Q Luo
- Q Luo
- Q Zhou
- Qing Luo
- Qiong Shi
- R Gorlick
- R Gorlick
- R Yokoyama
- RC Haydon
- RC Haydon
- RC Haydon
- Rex C. Haydon
- RS Gieni
- S Ghosh
- S Niesporek
- SC Kaste
- Stephanie H. Kim
- T Hideshima
- T Mashima
- T Yonemoto
- TC He
- TC He
- TC He
- Tong-Chuan He
- VA Cortes
- Vladimir N. Uversky
- W Si
- Wei Jiang
- WG Ward
- X Luo
- X Luo
- X Wang
- Xiaoji Luo
- Xing Liu
- Y Bi
- Y Fang
- Y Gazitt
- Y Su
- Yang Bi
- Yanhong Gao
- Publication venue
- Public Library of Science
- Publication date
- 01/12/2010
- Field of study
Osteosarcoma is the most common primary malignancy of bone with poorly characterized molecular pathways important in its pathogenesis. Increasing evidence indicates that elevated lipid biosynthesis is a characteristic feature of cancer. We sought to investigate the role of lysophosphatidic acid acyltransferase β (LPAATβ, aka, AGPAT2) in regulating the proliferation and growth of human osteosarcoma cells. LPAATβ can generate phosphatidic acid, which plays a key role in lipid biosynthesis as well as in cell proliferation and survival. Although elevated expression of LPAATβ has been reported in several types of human tumors, the role of LPAATβ in osteosarcoma progression has yet to be elucidated.Endogenous expression of LPAATβ in osteosarcoma cell lines is analyzed by using semi-quantitative PCR and immunohistochemical staining. Adenovirus-mediated overexpression of LPAATβ and silencing LPAATβ expression is employed to determine the effect of LPAATβ on osteosarcoma cell proliferation and migration in vitro and osteosarcoma tumor growth in vivo. We have found that expression of LPAATβ is readily detected in 8 of the 10 analyzed human osteosarcoma lines. Exogenous expression of LPAATβ promotes osteosarcoma cell proliferation and migration, while silencing LPAATβ expression inhibits these cellular characteristics. We further demonstrate that exogenous expression of LPAATβ effectively promotes tumor growth, while knockdown of LPAATβ expression inhibits tumor growth in an orthotopic xenograft model of human osteosarcoma.Our results strongly suggest that LPAATβ expression may be associated with the aggressive phenotypes of human osteosarcoma and that LPAATβ may play an important role in regulating osteosarcoma cell proliferation and tumor growth. Thus, targeting LPAATβ may be exploited as a novel therapeutic strategy for the clinical management of osteosarcoma. This is especially attractive given the availability of selective pharmacological inhibitors
Approaches in biotechnological applications of natural polymers
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Natural polymers, such as gums and mucilage, are biocompatible, cheap, easily available and non-toxic materials of native origin. These polymers are increasingly preferred over synthetic materials for industrial applications due to their intrinsic properties, as well as they are considered alternative sources of raw materials since they present characteristics of sustainability, biodegradability and biosafety. As definition, gums and mucilages are polysaccharides or complex carbohydrates consisting of one or more monosaccharides or their derivatives linked in bewildering variety of linkages and structures. Natural gums are considered polysaccharides naturally occurring in varieties of plant seeds and exudates, tree or shrub exudates, seaweed extracts, fungi, bacteria, and animal sources. Water-soluble gums, also known as hydrocolloids, are considered exudates and are pathological products; therefore, they do not form a part of cell wall. On the other hand, mucilages are part of cell and physiological products. It is important to highlight that gums represent the largest amounts of polymer materials derived from plants. Gums have enormously large and broad applications in both food and non-food industries, being commonly used as thickening, binding, emulsifying, suspending, stabilizing agents and matrices for drug release in pharmaceutical and cosmetic industries. In the food industry, their gelling properties and the ability to mold edible films and coatings are extensively studied. The use of gums depends on the intrinsic properties that they provide, often at costs below those of synthetic polymers. For upgrading the value of gums, they are being processed into various forms, including the most recent nanomaterials, for various biotechnological applications. Thus, the main natural polymers including galactomannans, cellulose, chitin, agar, carrageenan, alginate, cashew gum, pectin and starch, in addition to the current researches about them are reviewed in this article.. }To the Conselho Nacional de Desenvolvimento Cientfíico e Tecnológico (CNPq) for fellowships (LCBBC and MGCC) and the Coordenação de Aperfeiçoamento de Pessoal de Nvíel Superior (CAPES) (PBSA). This study was supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/BIO/04469/2013 unit, the Project RECI/BBB-EBI/0179/2012 (FCOMP-01-0124-FEDER-027462) and COMPETE 2020 (POCI-01-0145-FEDER-006684) (JAT)
Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis
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- Al Turki S
- Amuzu A
- Anderson CA
- Anney R
- Antony D
- Artigas MS
- Ayub M
- Balasubramanian S
- Banton MC
- Barrett JC
- Barrett JC
- Barroso I
- Beales P
- Benn M
- Bentham J
- Bhattacharya S
- Birney E
- Blackwood D
- Bobrow M
- Bochukova E
- Bochukova EG
- Bolton PF
- Bolton PF
- Bounds R
- Boustred C
- Breen G
- Brion M-J
- Cacciottolo TM
- Calissano M
- Carss K
- Casas JP
- Chambers JC
- Charlton R
- Chatterjee K
- Chen L
- Ciampi A
- Cirak S
- Clapham P
- Clement G
- Coates G
- Cocca M
- Collier DA
- Consortium U
- Cosgrove C
- Cox T
- Craddock N
- Crooks L
- Curran S
- Curtis D
- Daly A
- Danecek P
- Danecek P
- Day INM
- Day-Williams A
- Dedoussis G
- Dominiczak A
- Down T
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- Publication venue
- Publication date
- 01/01/2019
- Field of study
Hypothalamic neurons expressing the anorectic peptide Pro-opiomelanocortin (Pomc) regulate food intake and body weight. Here, we show that Steroid Receptor Coactivator-1 (SRC-1) interacts with a target of leptin receptor activation, phosphorylated STAT3, to potentiate Pomc transcription. Deletion of SRC-1 in Pomc neurons in mice attenuates their depolarization by leptin, decreases Pomc expression and increases food intake leading to high-fat diet-induced obesity. In humans, fifteen rare heterozygous variants in SRC-1 found in severely obese individuals impair leptin-mediated Pomc reporter activity in cells, whilst four variants found in non-obese controls do not. In a knock-in mouse model of a loss of function human variant (SRC-1L1376P), leptin-induced depolarization of Pomc neurons and Pomc expression are significantly reduced, and food intake and body weight are increased. In summary, we demonstrate that SRC-1 modulates the function of hypothalamic Pomc neurons, and suggest that targeting SRC-1 may represent a useful therapeutic strategy for weight loss.Peer reviewe
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- Zhuang H
- Zhuang X
- Zientara-Rytter K
- Zimmermann CM
- Ziviani E
- Zoladek T
- Zong W-X
- Zorov DB
- Zorzano A
- Zou W
- Zou Z
- Zou Z
- Zuryn S
- Zwerschke W
- Álvarez ÉMC
- Ávalos Y
- Önal G
- Üstün S
- Čolić M
- Đokić J
- Žerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
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
Iron Behaving Badly: Inappropriate Iron Chelation as a Major Contributor to the Aetiology of Vascular and Other Progressive Inflammatory and Degenerative Diseases
- Author
- A Abbott
- A Abou-Raya
- A Aljandali
- A Ambesi-Impiombato
- A Aydin
- A Balcerczyk
- A Besarab
- A Brzezinski
- A Campbell
- A Carrillo-Vico
- A Cavalli
- A Chattopadhyay
- A Chattopadhyay
- A Cherubini
- A Dey
- A Doms
- A Donovan
- A Donovan
- A Dávalos
- A Gaeta
- A Garny
- A Gnjec
- A Gomes
- A Gopalakrishnan
- A Hald
- A Henney
- A Hirayama
- A Hoffmann
- A Huber
- A Hugman
- A Iannetti
- A Ide-Ektessabi
- A Jacobs
- A Jeyabalan
- A Kahvejian
- A Karrar
- A Kasztler
- A Kibel
- A Kocyigit
- A Kotha
- A Kumral
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- A Lecube
- A Lewén
- A Lotery
- A Maggio
- A Malek
- A Malik
- A Mantovani
- A Matsuzawa
- A Mitra
- A Monge
- A Murakami
- A Murakami
- A Murakami
- A Murakami
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- A Nijnik
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- A Persson
- A Pietrangelo
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- A Rattner
- A Ravati
- A Rehman
- A Reynolds
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- A Roetto
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- A Saltelli
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- A Sassano
- A Scalbert
- A Scalbert
- A Scalbert
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- A Smahi
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- A Stintzi
- A Szewczyk
- A Taguchi
- A Tedgui
- A Terman
- A Terman
- A Terman
- A Undas
- A Virdis
- A Wagner
- A Wagner
- A Wagner
- A Wagner
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- A Wong
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- Ad hoc committee on systemic lupus erythematosus response criteria for fatigue
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- Publication venue
- Publication date
- 09/08/2008
- Field of study
The production of peroxide and superoxide is an inevitable consequence of
aerobic metabolism, and while these particular "reactive oxygen species" (ROSs)
can exhibit a number of biological effects, they are not of themselves
excessively reactive and thus they are not especially damaging at physiological
concentrations. However, their reactions with poorly liganded iron species can
lead to the catalytic production of the very reactive and dangerous hydroxyl
radical, which is exceptionally damaging, and a major cause of chronic
inflammation. We review the considerable and wide-ranging evidence for the
involvement of this combination of (su)peroxide and poorly liganded iron in a
large number of physiological and indeed pathological processes and
inflammatory disorders, especially those involving the progressive degradation
of cellular and organismal performance. These diseases share a great many
similarities and thus might be considered to have a common cause (i.e.
iron-catalysed free radical and especially hydroxyl radical generation). The
studies reviewed include those focused on a series of cardiovascular, metabolic
and neurological diseases, where iron can be found at the sites of plaques and
lesions, as well as studies showing the significance of iron to aging and
longevity. The effective chelation of iron by natural or synthetic ligands is
thus of major physiological (and potentially therapeutic) importance. As
systems properties, we need to recognise that physiological observables have
multiple molecular causes, and studying them in isolation leads to inconsistent
patterns of apparent causality when it is the simultaneous combination of
multiple factors that is responsible. This explains, for instance, the
decidedly mixed effects of antioxidants that have been observed, etc...Comment: 159 pages, including 9 Figs and 2184 reference
Measurement of the cross-section for b-jets produced in association with a Z boson at root s=7 TeV with the ATLAS detector ATLAS Collaboration
- Author
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- Yao Y
- Yasu Y
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- Yilmaz M
- Yoosoofmiya R
- Yorita K
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- Youssef S
- Yu D
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- Yu J
- Yuan L
- Yurkewicz A
- Zaets VG
- Zaidan R
- Zaitsev AM
- Zajacova Z
- Zalite YK
- Zanello L
- Zarzhitsky P
- Zaytsev A
- Zeitnitz C
- Zeller M
- Zeman M
- Zemla A
- Zendler C
- Zenin O
- Zenis T
- Zenonos Z
- Zenz S
- Zerwas D
- Zhan Z
- Zhang D
- Zhang H
- Zhang J
- Zhang X
- Zhang Z
- Zhao L
- Zhao T
- Zhao Z
- Zhemchugov A
- Zheng S
- Zhong J
- Zhou B
- Zhou N
- Zhou Y
- Zhu CG
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhuravlov V
- Zieminska D
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Ziolkowski M
- Zitoun R
- Zivkovic L
- Zmouchko VV
- Zobernig G
- Zoccoli A
- Zolnierowski Y
- Zsenei A
- zur Nedden M
- Zutshi V
- Zwalinski L
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2011
- Field of study
A measurement is presented of the inclusive cross-section for b-jet production in association with a Z boson in pp collisions at a centre-of-mass energy of root s = 7 TeV. The analysis uses the data sample collected by the ATLAS experiment in 2010, corresponding to an integrated luminosity of approximately 36 pb(-1). The event selection requires a Z boson decaying into high P-T electrons or muons, and at least one b-jet, identified by its displaced vertex, with transverse momentum p(T) > 25 GeV and rapidity vertical bar y vertical bar < 2.1. After subtraction of background processes, the yield is extracted from the vertex mass distribution of the candidate b-jets. The ratio of this cross-section to the inclusive Z cross-section (the average number of b-jets per Z event) is also measured. Both results are found to be in good agreement with perturbative QCD predictions at next-to-leading order
Search for heavy resonances decaying into a vector boson and a Higgs boson in final states with charged leptons, neutrinos, and b quarks
- Author
- A. Abdulsalam
- A. Ackert
- A. Adair
- A. Adiguzel
- A. Agapitos
- A. Ahmad
- A. Al-bataineh
- A. Albert
- A. Aleksandrov
- A. Apresyan
- A. Apyan
- A. Askew
- A. Attikis
- A. Aubin
- A. Avetisyan
- A. Baden
- A. Barker
- A. Baskakov
- A. Baty
- A. Bean
- A. Belloni
- A. Belyaev
- A. Belyaev
- A. Beretvas
- A. Bhardwaj
- A. Bocci
- A. Bodek
- A. Boletti
- A. Bonato
- A. Bornheim
- A. Borzou
- A. Braghieri
- A. Brinkerhoff
- A. Bundock
- A. Bylinkin
- A. Byszuk
- A. Cabrera
- A. Cakir
- A. Calderon
- A. Campbell
- A. Carnes
- A. Carvalho Antunes De Oliveira
- A. Castro
- A. Caudron
- A. Celik
- A. Cimmino
- A. Cocoros
- A. Colaleo
- A. Custódio
- A. Dabrowski
- A. David
- A. De Cosa
- A. De Roeck
- A. De Wit
- A. Degano
- A. Delgado
- A. Delgado Peris
- A. Dermenev
- A. Di Francesco
- A. Di Mattia
- A. Dierlamm
- A. Dimitrov
- A. Dishaw
- A. Dominguez
- A. Elliott-Peisert
- A. Elwood
- A. Escalante Del Valle
- A. Evans
- A. Fagot
- A. Fahim
- A. Fanfani
- A. Finkel
- A. Florent
- A. Garabedian
- A. Garcia-Bellido
- A. Geiser
- A. Ghezzi
- A. Giammanco
- A. Giassi
- A. Gilbert
- A. Givernaud
- A. Gizhko
- A. Godshalk
- A. Gozzelino
- A. Grebenyuk
- A. Gude
- A. Gurrola
- A. Güth
- A. Harb
- A. Hart
- A. Heister
- A. Hernandez-Almada
- A. Hervé
- A. Hinzmann
- A. Holzner
- A. Hortiangtham
- A. Ivanov
- A. Jafari
- A. Johnson
- A. Junkes
- A. Juodagalvis
- A. Kalinin
- A. Kalinowski
- A. Kalogeropoulos
- A. Kamenev
- A. Kapoor
- A. Karneyeu
- A. Kaur
- A. Kayis Topaksu
- A. Khan
- A. Kharchilava
- A. Khatiwada
- A. Khukhunaishvili
- A. Khvedelidze
- A. Kornmayer
- A. Korytov
- A. Kropivnitskaya
- A. Kubik
- A. Kumar
- A. Kumar
- A. Kyriakis
- A. König
- A. Künsken
- A. Lanaro
- A. Lanev
- A. Lath
- A. Ledovskoy
- A. Lee
- A. Lelek
- A. Leonidov
- A. Levin
- A. Levine
- A. Lobanov
- A. Lopez Virto
- A. Léonard
- A. Magitteri
- A. Magnani
- A. Makovec
- A. Malakhov
- A. Malta Rodrigues
- A. Marinov
- A. Martelli
- A. Massironi
- A. Mehta
- A. Melo
- A. Mertens
- A. Messineo
- A. Mestvirishvili
- A. Meyer
- A. Modak
- A. Moeller
- A. Mohamed
- A. Mohammadi
- A. Montanari
- A. Moraes
- A. Morelos Pineda
- A. Mott
- A. Mussgiller
- A. Nayak
- A. Nehrkorn
- A. Nikitenko
- A. Nowack
- A. Olbrechts
- A. Ostapchuk
- A. Ovcharova
- A. Panagiotou
- A. Parker
- A. Pashenkov
- A. Penzo
- A. Perieanu
- A. Perloff
- A. Perrotta
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- A. Pfeiffer
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- A. Soha
- A. Solano
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- C. Zorbilmez
- C.-E. Wulz
- C.A. Bernardes
- C.A. Carrillo Montoya
- C.E. Gerber
- C.F. González Hernández
- C.H. Jiang
- C.H. Shepherd-Themistocleous
- C.M. Kuo
- C.S. Moon
- C.W. Chen
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- Cacciari
- Cacciari
- Contino
- Cowan
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- D. Abercrombie
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- D. Anderson
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- D. Barney
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- D. Bonacorsi
- D. Bourilkov
- D. Burns
- D. Burns
- D. Burton
- D. Ciangottini
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- D. Colling
- D. Contardo
- D. Creanza
- D. Curry
- D. Cussans
- D. Cutts
- D. d'Enterria
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- D. Del Re
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- D. Eckstein
- D. Elumakhov
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- D. Fehling
- D. Ferencek
- D. Futyan
- D. Gastler
- D. Gelé
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- R.D. Field
- R.G. Kellogg
- R.K. Dewanjee
- R.M. Brown
- R.M. Chatterjee
- R.M. Harris
- R.P. Gandrajula
- R.P. Kenny III
- R.R. Betts
- R.Y. Zhu
- Read
- S. Abdullin
- S. Abu Zeid
- S. Ahuja
- S. Albergo
- S. Alderweireldt
- S. Argiro
- S. Baffioni
- S. Bahinipati
- S. Banerjee
- S. Banerjee
- S. Bansal
- S. Baur
- S. Beauceron
- S. Bein
- S. Belforte
- S. Beranek
- S. Bhattacharya
- S. Bhattacharya
- S. Bhowmik
- S. Bianco
- S. Bilmis
- S. Bitioukov
- S. Boren
- S. Braibant-Giacomelli
- S. Brandt
- S. Brochet
- S. Buontempo
- S. Carpinteyro
- S. Carrillo Moreno
- S. Casasso
- S. Chauhan
- S. Chauhan
- S. Chenarani
- S. Cho
- S. Choi
- S. Choudhury
- S. Cihangir
- S. Cittolin
- S. Colafranceschi
- S. Cooperstein
- S. Costa
- S. Czellar
- S. Damarseckin
- S. Das
- S. Dasu
- S. De Visscher
- S. Dey
- S. Di Guida
- S. Dildick
- S. Dittmer
- S. Dogra
- S. Donato
- S. Dube
- S. Dugad
- S. Durgut
- S. Duric
- S. Dutt
- S. Dutta
- S. Elgammal
- S. Erdweg
- S. Fartoukh
- S. Fink
- S. Fiorendi
- S. Flowers
- S. Folgueras
- S. Fonseca De Souza
- S. Gadrat
- S. Ganguly
- S. Ganjour
- S. Gascon
- S. Gelli
- S. Gennai
- S. Ghosh
- S. Ghosh
- S. Girgis
- S. Gninenko
- S. Goy Lopez
- S. Greene
- S. Grünendahl
- S. Gundacker
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- S. Harper
- S. Hasegawa
- S. Jabeen
- S. Jindariani
- S. Kalafut
- S. Kaplan
- S. Keshri
- S. Kesisoglou
- S. Khalil
- S. Knutzen
- S. Kudella
- S. Kumar
- S. Kunori
- S. Kyriacou
- S. Lacaprara
- S. Lammel
- S. Lee
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- S. Lehti
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- S. Malhotra
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- S. Malvezzi
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- S. Maruyama
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- S. Meola
- S. Mersi
- S. Micanovic
- S. Mitra
- S. Moortgat
- S. Morovic
- S. Mrenna
- S. Mukherjee
- S. Mukhopadhyay
- S. My
- S. Nahn
- S. Nandan
- S. Narayanan
- S. Nourbakhsh
- S. Nuzzo
- S. Obraztsov
- S. Oliveros
- S. Orfanelli
- S. Ozturk
- S. Padhi
- S. Paktinat Mehdiabadi
- S. Paoletti
- S. Paramesvaran
- S. Perries
- S. Petrushanko
- S. Pigazzini
- S. Piperov
- S. Ragazzi
- S. Rahatlou
- S. Rappoccio
- S. Regnard
- S. Roy Chowdhury
- S. Röcker
- S. Sagir
- S. Salur
- S. Salva
- S. Sanchez Cruz
- S. Sanders
- S. Sarkar
- S. Schael
- S. Schnetzer
- S. Schumann
- S. Seif El Nasr-storey
- S. Sekmen
- S. Sen
- S. Shalhout
- S. Sharma
- S. Shmatov
- S. Shulha
- S. Simon
- S. Somalwar
- S. Spanier
- S. Spannagel
- S. Stoykova
- S. Stoynev
- S. Summers
- S. Taroni
- S. Tavernier
- S. Thakur
- S. Thomas
- S. Thüer
- S. Tkaczyk
- S. Toda
- S. Tosi
- S. Troshin
- S. Tuo
- S. Turkcapar
- S. Undleeb
- S. Viret
- S. Wang
- S. Wasserbaech
- S. Wayand
- S. Wertz
- S. Wilbur
- S. Williamson
- S. Wimpenny
- S. Xie
- S.B. Beri
- S.B. Oh
- S.C. Eno
- S.C. Kao
- S.C. Tonwar
- S.C. Zenz
- S.D. Mullin
- S.F. Novaes
- S.h. Seo
- S.I. Cooper
- S.J. Qian
- S.K. Park
- S.K. Swain
- S.M. Etesami
- S.M. Heindl
- S.M. Shaheen
- S.M. Tan
- S.M.A. Ghiasi Shirazi
- S.P. Ratti
- S.R. Wagner
- S.S. Chhibra
- S.S. Yu
- S.V. Rusakov
- S.W. Lee
- S.W. Lee
- Sa. Jain
- Salvioni
- Sandra S. Padula
- Schmaltz
- Sh. Jain
- Sjöstrand
- Sjöstrand
- Skands
- T. Adams
- T. Arndt
- T. Aziz
- T. Bergauer
- T. Boccali
- T. Bose
- T. Camporesi
- T. Cheng
- T. Chwalek
- T. Cornelis
- T. Dorigo
- T. Dreyer
- T. du Pree
- T. Eichhorn
- T. Esch
- T. Ferbel
- T. Ferguson
- T. Frueboes
- T. Geralis
- T. Hebbeker
- T. Hreus
- T. Huang
- T. James
- T. Järvinen
- T. Kamon
- T. Kolberg
- T. Kress
- T. Lampén
- T. Lapsien
- T. Lenz
- T. Lenzi
- T. Libeiro
- T. Lindén
- T. Liu
- T. Lomtadze
- T. Maerschalk
- T. Matsushita
- T. Medvedeva
- T. Mulholland
- T. Müller
- T. Orimoto
- T. Peiffer
- T. Peltola
- T. Perry
- T. Pook
- T. Reis
- T. Rodrigo
- T. Rohe
- T. Rovelli
- T. Roy
- T. Ruggles
- T. Sakuma
- T. Sarkar
- T. Schoerner-Sadenius
- T. Sculac
- T. Seva
- T. Sinthuprasith
- T. Strebler
- T. Susa
- T. Tabarelli de Fatis
- T. Tuuva
- T. Verlage
- T. Virdee
- T. Weiler
- T. Williams
- T. Yetkin
- T.A. Gómez Espinosa
- T.H. Doan
- T.J. Kim
- T.K. Aarrestad
- T.R. Fernandez Perez Tomei
- T.W. Wang
- Th. Müller
- U. Behrens
- U. Bhawandeep
- U. Dosselli
- U. Gasparini
- U. Goerlach
- U. Heintz
- U. Husemann
- U. Joshi
- U. Kiminsu
- U. Langenegger
- U. Sarica
- U.K. Yang
- V. Alexakhin
- V. Andreev
- V. Azzolini
- V. Bhatnagar
- V. Bhopatkar
- V. Blinov
- V. Blobel
- V. Brigljevic
- V. Bunichev
- V. Calvelli
- V. Candelise
- V. Cherepanov
- V. Ciulli
- V. Daponte
- V. Dudenas
- V. Dutta
- V. Epshteyn
- V. Gavrilov
- V. Golovtsov
- V. Gori
- V. Hagopian
- V. Hegde
- V. Innocente
- V. Jha
- V. Kachanov
- V. Karimäki
- V. Karjavin
- V. Khachatryan
- V. Khristenko
- V. Kim
- V. Klyukhin
- V. Knünz
- V. Krutelyov
- V. Krychkine
- V. Kumar
- V. Lemaitre
- V. Makarenko
- V. Matveev
- V. Monaco
- V. Mossolov
- V. Murzin
- V. O'Dell
- V. Oreshkin
- V. Palichik
- V. Perelygin
- V. Petrov
- V. Popov
- V. Re
- V. Rekovic
- V. Rusinov
- V. Savrin
- V. Sharma
- V. Sharma
- V. Smirnov
- V. Sola
- V. Sordini
- V. Sulimov
- V. Valuev
- V. Veckalns
- V. Veszpremi
- V. Zhukov
- V. Zhukova
- V. Zykunov
- V.A. Giakoumopoulou
- V.D. Elvira
- V.E. Barnes
- V.J. Smith
- V.M. Ghete
- V.R. Tavolaro
- W. Adam
- W. Bertl
- W. Busza
- W. Carvalho
- W. Clarida
- W. De Boer
- W. Erdmann
- W. Fang
- W. Funk
- W. Ji
- W. Johns
- W. Ko
- W. Lange
- W. Li
- W. Lin
- W. Lohmann
- W. Luo
- W. Lustermann
- W. Mcbrayer
- W. Si
- W. Van Doninck
- W. Van Driessche
- W. Waltenberger
- W. Xie
- W.-S. Hou
- W.A. Khan
- W.A.T. Wan Abdullah
- W.D. Zeuner
- W.H. Smith
- W.J. Spalding
- W.L. Aldá Júnior
- W.L. Prado Da Silva
- W.T. Ford
- X. Coubez
- X. Janssen
- X. Niu
- X. Shi
- X. Sun
- Y. Ban
- Y. Chao
- Y. Chen
- Y. Chen
- Y. Choi
- Y. Gershtein
- Y. Go
- Y. Guler
- Y. Haddad
- Y. Hsiung
- Y. Iiyama
- Y. Ivanov
- Y. Jo
- Y. Kim
- Y. Kubota
- Y. Lu
- Y. Mao
- Y. Maravin
- Y. Musienko
- Y. Onel
- Y. Pakhotin
- Y. Roh
- Y. Sirois
- Y. Skovpen
- Y. Takahashi
- Y. Wang
- Y. Xin
- Y. Yang
- Y. Yilmaz
- Y.-J. Lee
- Y.C. Yang
- Y.D. Oh
- Y.F. Liu
- Y.H. Chang
- Y.H. Chang
- Y.H. Shin
- Y.J. Lu
- Y.M. Tzeng
- Y.S. Lai
- Y.t. Duh
- Y.W. Chang
- Yu. Andreev
- Z. Antunovic
- Z. Chen
- Z. Demiragli
- Z. Hu
- Z. Lesko
- Z. Liu
- Z. Mao
- Z. Szillasi
- Z. Tao
- Z. Tsamalaidze
- Z. Tu
- Z. Wang
- Z. Wang
- Z. Wu
- Z. Xu
- Z. Zolkapli
- Z.A. Ibrahim
- Z.L. Trocsanyi
- Z.S. Demiroglu
- Publication venue
- Publication date
- 01/01/2016
- Field of study
Peer reviewe
- …