140 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
- Ay C
- Azuelos G
- Azuma Y
- Baak MA
- Baccaglioni G
- Bacci C
- Bach AM
- Bachacou H
- Bachas K
- Bachy G
- Backes M
- Backhaus M
- Badescu E
- Bagnaia P
- Bahinipati S
- Bai Y
- Bailey DC
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- Baker MD
- Baker OK
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- Bangert A
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- Boorman G
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- Boscherini D
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- Botterill D
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- Chapman JD
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- Chekanov S
- Chekulaev SV
- Chelkov GA
- Chelstowska MA
- Chen C
- Chen H
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- 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
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- Collaboration ATLAS
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- Damazio DO
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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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- 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
- Wrona B
- Wu SL
- Wu X
- Wu Y
- Wulf E
- Wunstorf R
- Wynne BM
- Xaplanteris L
- Xella S
- Xie S
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- Xu C
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- Xu G
- Yabsley B
- Yagci KD
- Yamada M
- Yamamoto A
- Yamamoto K
- Yamamoto S
- Yamamura T
- Yamaoka J
- Yamazaki T
- Yamazaki Y
- Yan Z
- Yang H
- Yang S
- Yang UK
- Yang Y
- Yang Y
- Yang Z
- Yanush S
- Yao W-M
- Yao Y
- Yasu Y
- Ye J
- Ye S
- Yildiz HD
- Yilmaz M
- Yoosoofmiya R
- Yorita K
- Yoshida R
- Young C
- Youssef S
- Yu D
- Yu J
- Yu J
- Yuan L
- Yurkewicz A
- Zaets VG
- Zaidan R
- Zaitsev AM
- Zajacova Z
- 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
Single hadron response measurement and calorimeter jet energy scale uncertainty with the ATLAS detector at the LHC
- Author
- A. A. Abdelalim
- A. A. Carter
- A. A. Grillo
- A. A. Komar
- A. A. Minaenko
- A. A. Nepomuceno
- A. A. Snesarev
- A. A. Solodkov
- A. Abdesselam
- A. Ahmad
- A. Akiyama
- A. Aloisio
- A. Alonso
- A. Amorim
- A. Andreazza
- A. Angerami
- A. Anisenkov
- A. Annovi
- A. Antonaki
- A. Antonov
- A. Artamonov
- A. Astbury
- A. Astvatsatourov
- A. B. Fenyuk
- A. B. Lazarev
- A. Bangert
- A. Barashkou
- A. Barbaro Galtieri
- A. Baroncelli
- A. Battaglia
- A. Beddall
- A. Belloni
- A. Bertin
- A. Bingul
- A. Blondel
- A. Bocci
- A. Bogdanchikov
- A. Bogouch
- A. Borisov
- A. Boveia
- A. Braem
- A. Brandt
- A. Bruni
- A. C. König
- A. C. Martyniuk
- A. C. Schaffer
- A. Canepa
- A. Catinaccio
- A. Cattai
- A. Cerri
- A. Chafaq
- A. Cheplakov
- A. Chilingarov
- A. Christov
- A. Ciocio
- A. Clark
- A. Coccaro
- A. Cortes-Gonzalez
- A. D. Doxiadis
- A. D. Hawkins
- A. D. Hershenhorn
- A. D. Pilkington
- A. De Salvo
- A. De Santo
- A. Dell’Acqua
- A. Dewhurst
- A. Di Ciaccio
- A. Di Girolamo
- A. Di Mattia
- A. Di Simone
- A. Do Valle Wemans
- A. Doria
- A. Dos Anjos
- A. Dotti
- A. Dudarev
- A. D’Orazio
- A. E. Barton
- A. E. Kiryunin
- A. Engl
- A. Eppig
- A. Ereditato
- A. F. Saavedra
- A. Farbin
- A. Farilla
- A. Favareto
- A. Ferrari
- A. Ferrer
- A. Ferretto Parodi
- A. Filippas
- A. Filipčič
- A. Firan
- A. Floderus
- A. Formica
- A. Forti
- A. Foussat
- A. G. Buckley
- A. G. Goussiou
- A. G. Kholodenko
- A. G. Myagkov
- A. G. Olchevski
- A. G. Schamov
- A. Gaponenko
- A. Gemmell
- A. Gershon
- A. Gibson
- A. Glazov
- A. Gomes
- A. Gonidec
- A. Gorišek
- A. Guida
- A. Gupta
- A. Haas
- A. Hamilton
- A. Harvey
- A. Henrichs
- A. Hoecker
- A. Hoummada
- A. Huettmann
- A. I. Etienvre
- A. I. Kononov
- A. I. Mincer
- A. Irles Quiles
- A. Ishikawa
- A. J. Armbruster
- A. J. Barr
- A. J. Beddall
- A. J. Fowler
- A. J. Lankford
- A. J. Lowe
- A. J. Martin
- A. J. Tanasijczuk
- A. Jantsch
- A. Jeremie
- A. Juste Rozas
- A. K. Ciftci
- A. K. Morley
- A. Kaczmarska
- A. Kapliy
- A. Kasmi
- A. Kastanas
- A. Khanov
- A. Khodinov
- A. Khomich
- A. Khoroshilov
- A. Kiryunin
- A. Klier
- A. Klimentov
- A. Knue
- A. Kootz
- A. Korn
- A. Korol
- A. Kotwal
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- A.-E. Nuncio-Quiroz
- ATLAS Collaboration
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- W. S. Lockman
- W. T. Meyer
- W. Taylor
- W. Trischuk
- W. Vandelli
- W. Verkerke
- W. Wagner
- W. Walkowiak
- W. Wiedenmann
- W. Willis
- X. Chen
- X. Espinal Curull
- X. Ju
- X. Lei
- X. Li
- X. Lou
- X. Portell Bueso
- X. Prudent
- X. Ruan
- X. S. Anduaga
- X. Sun
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- Y. Benhammou
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- Y. Doi
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- Y. Gusakov
- Y. Hasegawa
- Y. Hernández Jiménez
- Y. Homma
- Y. Ikegami
- Y. Ilchenko
- Y. Jiang
- Y. Kataoka
- Y. Komori
- Y. Kulchitsky
- Y. Liu
- Y. Mahalalel
- Y. Makida
- Y. Ming
- Y. Munwes
- Y. Nagasaka
- Y. Nakahama
- Y. Ninomiya
- Y. Okumura
- Y. Oren
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- Y. Rozen
- Y. S. Gao
- Y. Silver
- Y. Smirnov
- Y. Sugaya
- Y. Suzuki
- Y. Suzuki
- Y. Takahashi
- Y. Takubo
- Y. Tanaka
- Y. Tayalati
- Y. Unno
- Y. V. Grishkevich
- Y. Wu
- Y. Xie
- Y. Yamazaki
- Y. Yang
- Y. Yang
- Y. Yao
- Y. Yasu
- Y. Zhou
- Y. Zhu
- Y. Zolnierowski
- Yu. M. Sviridov
- Z. Czyczula
- Z. D. Greenwood
- Z. Dolezal
- Z. Drasal
- Z. Hajduk
- Z. Hubacek
- Z. Kohout
- Z. L. Ren
- Z. Liang
- Z. Marshall
- Z. Meng
- Z. Qian
- Z. Qin
- Z. Rurikova
- Z. V. Krumshteyn
- Z. van Kesteren
- Z. Weng
- Z. Yan
- Z. Yang
- Z. Zajacova
- Z. Zenonos
- Z. Zhan
- Z. Zhang
- Z. Zhao
- Z. Zinonos
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 06/03/2012
- Field of study
The uncertainty on the calorimeter energy response to jets of particles is
derived for the ATLAS experiment at the Large Hadron Collider (LHC). First, the
calorimeter response to single isolated charged hadrons is measured and
compared to the Monte Carlo simulation using proton-proton collisions at
centre-of-mass energies of sqrt(s) = 900 GeV and 7 TeV collected during 2009
and 2010. Then, using the decay of K_s and Lambda particles, the calorimeter
response to specific types of particles (positively and negatively charged
pions, protons, and anti-protons) is measured and compared to the Monte Carlo
predictions. Finally, the jet energy scale uncertainty is determined by
propagating the response uncertainty for single charged and neutral particles
to jets. The response uncertainty is 2-5% for central isolated hadrons and 1-3%
for the final calorimeter jet energy scale.Comment: 24 pages plus author list (36 pages total), 23 figures, 1 table,
submitted to European Physical Journal
In vitro nuclear interactome of the HIV-1 Tat protein
- Author
- A Clery
- A Gatignol
- A Kuzmichev
- A Kuzmichev
- A Marchler-Bauer
- A Mazumdar
- A Munnia
- A Pumfery
- A You
- AB Makar
- AJ Ruthenburg
- AM Hidalgo-Estevez
- AM Pyle
- AS Neish
- AY Nikolaev
- B Kalverda
- BB Singh
- BJ Breitkreutz
- BJ Wilson
- BK Das
- BM Lunde
- BP Ashburner
- C Alfarano
- C Delphin
- C Franz
- C Hetzer
- C Morris-Desbois
- C Musahl
- C Schwerk
- C Treand
- C Underhill
- CA Hassig
- CA Hassig
- CA Johnson
- CA Johnson
- CA Parada
- CD Laherty
- CG Lee
- CH Herrmann
- CK Dreger
- CL Jiang
- CL Will
- CM Grozinger
- D Dorner
- D Gorlich
- D Li
- D Maiorano
- D Reinberg
- D Schulte
- D Yasui
- DA Bochar
- DC Bharucha
- DD Fischer
- DG Quintana
- DR Schmidt
- E Agbottah
- E Cavellan
- E Craig
- E Nagoshi
- E Nicolas
- E Nicolas
- EK Sullivan
- EP Kransdorf
- ER Griffis
- F Kashanchi
- F Macian
- F Peruzzi
- FR Bischoff
- G Dellaire
- G He
- G Jiang
- G Lattanzi
- GL Mayeur
- H Cho
- H Fujita
- H Kato
- H Kitagawa
- H Sakai
- H Takeuchi
- H Xiao
- H Zhang
- H Zhang
- HH Ng
- HL Kiefer
- HT Adler
- I Letunic
- I Olave
- J Becker
- J Boeke
- J Brady
- J Harborth
- J Joseph
- J Kamine
- J Koipally
- J Koipally
- J Koipally
- J Marango
- J Moroianu
- J Park
- J Taplick
- J van der Vlag
- J Zhou
- JA Schmiesing
- JA Schmiesing
- JF Rual
- JH Lee
- JH Liu
- JJ Coull
- JK Tong
- JM Bridger
- JR Dobosy
- JW Critchfield
- K Furukawa
- K Imai
- K Scheffzek
- K Yoder
- K Zhao
- K Zhou
- KC Moraes
- KI Tatematsu
- KL Block
- KM Lounsbury
- KS McKeegan
- L Corsini
- L Deng
- L Finch
- L Mohrmann
- L Tickenbrock
- L Yang
- LA Boyer
- LF Garcia-Martinez
- Lili Gu
- LR Racki
- M Ashburner
- M Barboric
- M Benkirane
- M Bienz
- M Brackertz
- M Brackertz
- M Brand
- M Bukrinsky
- M Chibi
- M Fornerod
- M Fuchs
- M Fujita
- M Kneissl
- M Kohler
- M Meurer
- M Ohnishi
- M Ott
- M Saito
- M Sorin
- M Stros
- M Tyagi
- M Yanagida
- MA Bhat
- MA Hakimi
- MA Hakimi
- MA Hakimi
- MJ Bottomley
- ML Phelan
- MR Rountree
- MV Natsiuk
- MY Chou
- N Bonifaci
- N Epie
- N Fujita
- N Methot
- N Wagner
- N Yabuta
- Niaobh O'Donoghue
- NJ Watkins
- Noreen Sheehy
- NR Yaseen
- NR Yaseen
- O Rohr
- O Rozenblatt-Rosen
- P Cramer
- P Gacesa
- PA Tucker
- PG Young
- PM Dehe
- PM Dehe
- Q Ye
- R Berro
- R Gamsjaeger
- R Mahajan
- R Murr
- R Truant
- R Van Duyne
- R Van Duyne
- RA Sclafani
- RA Silverstein
- RC Hillig
- RD Adzerikho
- RD Finn
- RE Kiernan
- RH Kehlenbach
- RM Ewing
- S Bannwarth
- S Debernardi
- S Mujtaba
- S Mujtaba
- S Nakielny
- S Nekhai
- S Nekhai
- S Pagans
- S Peri
- S Shaklai
- S Sif
- S Takezawa
- S Vashee
- SA Ansari
- SA Denslow
- SA Williams
- SC Tsai
- SK Dhar
- SL Forsburg
- SM Nicol
- Stephen Pennington
- T Ammosova
- T Hirano
- T Mahmoudi
- T Otsuki
- T Sasaki
- T Tasara
- T Yoshida
- TC Fleischer
- TE Harris
- TP Cujec
- TP Cujec
- TW Reichman
- U Kutay
- U Stelzl
- V Bres
- VB Cismasiu
- VF Zhupan
- Virginie W Gautier
- VW Gautier
- W Antonin
- W Fischle
- W Fischle
- W Fu
- W Wang
- WE Muller
- WE Muller
- William W Hall
- WM Yang
- X Yang
- Y Ariumi
- Y Bennasser
- Y Doyon
- Y Ishimi
- Y Ishimi
- Y Shi
- Y Xue
- Y Zhang
- Y Zhang
- Y Zhang
- Y Zhang
- Y Zhang
- Y Zhang
- Y Zhu
- YJ Hsieh
- YL Yao
- YL Yao
- YP Li
- YP Li
- Z Nie
- Z You
- Z You
- ZB Xia
- Publication venue
- BioMed Central
- Publication date
- 01/01/2009
- Field of study
<p>Abstract</p> <p>Background</p> <p>One facet of the complexity underlying the biology of HIV-1 resides not only in its limited number of viral proteins, but in the extensive repertoire of cellular proteins they interact with and their higher-order assembly. HIV-1 encodes the regulatory protein Tat (86–101aa), which is essential for HIV-1 replication and primarily orchestrates HIV-1 provirus transcriptional regulation. Previous studies have demonstrated that Tat function is highly dependent on specific interactions with a range of cellular proteins. However they can only partially account for the intricate molecular mechanisms underlying the dynamics of proviral gene expression. To obtain a comprehensive nuclear interaction map of Tat in T-cells, we have designed a proteomic strategy based on affinity chromatography coupled with mass spectrometry.</p> <p>Results</p> <p>Our approach resulted in the identification of a total of 183 candidates as Tat nuclear partners, 90% of which have not been previously characterised. Subsequently we applied <it>in silico </it>analysis, to validate and characterise our dataset which revealed that the Tat nuclear interactome exhibits unique signature(s). First, motif composition analysis highlighted that our dataset is enriched for domains mediating protein, RNA and DNA interactions, and helicase and ATPase activities. Secondly, functional classification and network reconstruction clearly depicted Tat as a polyvalent protein adaptor and positioned Tat at the nexus of a densely interconnected interaction network involved in a range of biological processes which included gene expression regulation, RNA biogenesis, chromatin structure, chromosome organisation, DNA replication and nuclear architecture.</p> <p>Conclusion</p> <p>We have completed the <it>in vitro </it>Tat nuclear interactome and have highlighted its modular network properties and particularly those involved in the coordination of gene expression by Tat. Ultimately, the highly specialised set of molecular interactions identified will provide a framework to further advance our understanding of the mechanisms of HIV-1 proviral gene silencing and activation.</p
Global, regional, and national burden of neurological disorders, 1990–2016 : a systematic analysis for the Global Burden of Disease Study 2016
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- Abbasi Nooshin
- Abd-Allah Foad
- Abdelalim Ahmed
- Abdollahpour Ibrahim
- Aboyans Victor
- Abraha Haftom N.
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- Adamu Abdu A.
- Adebayo Oladimeji M.
- Adeoye Abiodun M.
- Adsuar Jose C.
- Afarideh Mohsen
- Agrawal Sutapa
- Ahmadi Alireza
- Ahmed Muktar B.
- Aichour Amani N.
- Aichour Ibtihel
- Aichour Miloud T.
- Akinyemi Rufus O.
- Akseer Nadia
- Al-Eyadhy Ayman
- Al-Shahi Salman Rustam
- Alahdab Fares
- Alam Tahiya
- Alene Kefyalew A.
- Aljunid Syed M.
- Altirkawi Khalid A.
- Alvis-Guzman Nelson
- Anber Nahla H.
- Antonio Carl Abelardo T.
- Arabloo Jalal
- Aremu Olatunde
- Arnlov Johan
- Asayesh Hamid
- Asghar Rana J.
- Atalay Hagos T.
- Awasthi Ashish
- Ayala Quintanilla Beatriz P.
- Ayuk Tambe B.
- Badawi Alaa
- Banach Maciej
- Bannick Marlena S.
- Banoub Joseph A.
- Barboza Miguel A.
- Barker-Collo Suzanne L.
- Barnighausen Till W.
- Baune Bernhard T.
- Bedi Neeraj
- Beghi Ettore
- Behzadifar Masoud
- Behzadifar Meysam
- Bejot Yannick
- Bekele Bayu B.
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- Berhane Adugnaw
- Beuran Mircea
- Bhattacharyya Krittika
- Bhutta Zulfiqar A.
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- Bin Sayeed Muhammad S.
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- Meretoja Atte
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- Morrison Shane D.
- Mountjoy-Venning Cliff
- Mousavi Seyyed M.
- Muhammed Oumer S.
- Muruet Walter
- Musa Kamarul I.
- Mustafa Ghulam
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- Nagel Gabriele
- Naheed Aliya
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- Najafi Farid
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- Negoi Ionut
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- Ogbo Felix A. (R18978)
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- Olivares Pedro R.
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- 01/01/2019
- Field of study
Background: Neurological disorders are increasingly recognised as major causes of death and disability worldwide. The aim of this analysis from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2016 is to provide the most comprehensive and up-to-date estimates of the global, regional, and national burden from neurological disorders. Methods: We estimated prevalence, incidence, deaths, and disability-adjusted life-years (DALYs; the sum of years of life lost [YLLs] and years lived with disability [YLDs]) by age and sex for 15 neurological disorder categories (tetanus, meningitis, encephalitis, stroke, brain and other CNS cancers, traumatic brain injury, spinal cord injury, Alzheimer's disease and other dementias, Parkinson's disease, multiple sclerosis, motor neuron diseases, idiopathic epilepsy, migraine, tension-type headache, and a residual category for other less common neurological disorders) in 195 countries from 1990 to 2016. DisMod-MR 2.1, a Bayesian meta-regression tool, was the main method of estimation of prevalence and incidence, and the Cause of Death Ensemble model (CODEm) was used for mortality estimation. We quantified the contribution of 84 risks and combinations of risk to the disease estimates for the 15 neurological disorder categories using the GBD comparative risk assessment approach. Findings: Globally, in 2016, neurological disorders were the leading cause of DALYs (276 million [95% UI 247–308]) and second leading cause of deaths (9·0 million [8·8–9·4]). The absolute number of deaths and DALYs from all neurological disorders combined increased (deaths by 39% [34–44] and DALYs by 15% [9–21]) whereas their age-standardised rates decreased (deaths by 28% [26–30] and DALYs by 27% [24–31]) between 1990 and 2016. The only neurological disorders that had a decrease in rates and absolute numbers of deaths and DALYs were tetanus, meningitis, and encephalitis. The four largest contributors of neurological DALYs were stroke (42·2% [38·6–46·1]), migraine (16·3% [11·7–20·8]), Alzheimer's and other dementias (10·4% [9·0–12·1]), and meningitis (7·9% [6·6–10·4]). For the combined neurological disorders, age-standardised DALY rates were significantly higher in males than in females (male-to-female ratio 1·12 [1·05–1·20]), but migraine, multiple sclerosis, and tension-type headache were more common and caused more burden in females, with male-to-female ratios of less than 0·7. The 84 risks quantified in GBD explain less than 10% of neurological disorder DALY burdens, except stroke, for which 88·8% (86·5–90·9) of DALYs are attributable to risk factors, and to a lesser extent Alzheimer's disease and other dementias (22·3% [11·8–35·1] of DALYs are risk attributable) and idiopathic epilepsy (14·1% [10·8–17·5] of DALYs are risk attributable). Interpretation: Globally, the burden of neurological disorders, as measured by the absolute number of DALYs, continues to increase. As populations are growing and ageing, and the prevalence of major disabling neurological disorders steeply increases with age, governments will face increasing demand for treatment, rehabilitation, and support services for neurological disorders. The scarcity of established modifiable risks for most of the neurological burden demonstrates that new knowledge is required to develop effective prevention and treatment strategies. Funding: Bill & Melinda Gates Foundation
Parasitic fauna of domestic cavies in the western highlands of Cameroon (Central Africa)
- Author
- A Permin
- AM Zajac
- Anonymous
- AO Bush
- BE Kumsa
- C Mans
- CH Yiva
- CJ García
- D d'Ovidio
- D d'Ovidio
- D Thienpont
- DP Humber
- Emile Miegoué
- ET Pamo
- F Audebert
- Felix Meutchieye
- Georgios Theodoropoulos
- HF Hintz
- J Massoni
- J Tchoumboue
- JF William
- JL Dunnum
- JM Dzik
- Joseph Tchoumboué
- K Dittmar
- K Wilson
- LT Gressler
- M Iseki
- MA Basombrio
- Marc K. Kouam
- N Pantchev
- NI Ogo
- PA Ellis
- PH Bayemi
- R Franz
- R Fujisaki
- RG Gamarra
- RM Pinto
- S Coman
- T Muto
- TA Niba
- Terence T. Nguafack
- TL Rothwell
- Y Manjeli
- Z Banda
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
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
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- Zanello L
- Zarzhitsky P
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- Zeman M
- Zemla A
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- Zenin O
- Zenis T
- Zenonos Z
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- Zerwas D
- Zhan Z
- Zhang D
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- Zhang Z
- Zhao L
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- Zhao Z
- Zhemchugov A
- Zheng S
- Zhong J
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- Zhu CG
- Zhu H
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- 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
Measurement of event-shape observables in Z→ℓ+ℓ− events in pp collisions at √ s=7 TeV with the ATLAS detector at the LHC
- Author
- Aad G.
- Abbott B.
- Abdallah J.
- Abdelalim A.A.
- Abdesselam A.
- Abdinov O.
- Abi B.
- Abolins M.
- Abramowicz H.
- Abreu H.
- Acerbi E.
- Acerbi E.
- Acharya B.S.
- Acharya B.S.
- Adams D.L.
- Addy T.N.
- Adelman J.
- Aderholz M.
- Adomeit S.
- Adragna P.
- Adye T.
- Aefsky S.
- Aguilar-Saavedra J.A.
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- Alison J.
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- Allport P.P.
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- Zimmermann R.
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- Zitoun R.
- Zmouchko V.V.
- Zobernig G.
- Zoccoli A.
- Zoccoli A.
- Zoccoli A.
- Zolnierowski Y.
- Zsenei A.
- Zur Nedden M.
- Zutshi V.
- Zwalinski L.
- Åkesson T.P.A.
- Åsman B.
- Åsman B.
- Ženiš T.
- Živković L.
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Event-shape observables measured using charged particles in inclusive
Z-boson events are presented, using the electron and muon decay modes of the
Z bosons. The measurements are based on an integrated luminosity of 1.1fb−1 of proton--proton collisions recorded by the ATLAS detector at the
LHC at a centre-of-mass energy s=7 TeV. Charged-particle
distributions, excluding the lepton--antilepton pair from the Z-boson decay,
are measured in different ranges of transverse momentum of the Z boson.
Distributions include multiplicity, scalar sum of transverse momenta, beam
thrust, transverse thrust, spherocity, and F-parameter, which are
in particular sensitive to properties of the underlying event at small values
of the Z-boson transverse momentum. The Sherpa event generator shows larger
deviations from the measured observables than Pythia8 and Herwig7. Typically,
all three Monte Carlo generators provide predictions that are in better
agreement with the data at high Z-boson transverse momenta than at low
Z-boson transverse momenta and for the observables that are less sensitive to
the number of charged particles in the event.Comment: 36 pages plus author list + cover page (54 pages total), 14 figures,
4 tables, submitted to EPJC, All figures including auxiliary figures are
available at
http://atlas.web.cern.ch/Atlas/GROUPS/PHYSICS/PAPERS/STDM-2014-0
Global, regional, and national incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990–2017: A systematic analysis for the Global Burden of Disease Study 2017
- Author
- Abate Degu
- Abate Lkidan Hassen
- Abay Solomon M
- Abbafati Cristiana
- Abbasi Nooshin
- Abbastabar Hcdayat
- Abd El Razek Hassan Magdy
- Abd El Razek Muhammed Magdy
- Abd-Allah Foad
- Abdel-Rahman Omar
- Abdela Jeinal
- Abdelalim Ahmed
- Abdi Alireza
- Abdollahpour Ibrahim
- Abdulkader Rizwan Suliankatchi
- Abdurahman Ahmed Abdulahi
- Abebe Haftom Temesgen
- Abebe Molla
- Abebe Zegeye
- Abebo Teshome Abuka
- Aboyans Victor
- Abraha Haftom Niguse
- Abrham Aklilu Roba
- Abu-Raddad Laith Jamal
- Abu-Rmeileh Niveen Ml
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- Shams-Beyranvand Mehran
- Shamsi MohammadBagher
- Shamsizadeh Modena
- Sharafi Heidar
- Sharafi Kiomars
- Sharif-Alhoseini Mahdi
- Sharit Mehdi
- Sharma Jayendra
- Sharma Meenakshi
- Sharma Rajesh
- She Jun
- Sheikh Aziz
- Sheth Kevin N
- Shi Peilin
- Shiadeh Malihe Nourollahpour
- Shibuya Kenji
- Shifa Gimia Temam
- Shiferaw Mekonnen Sissy
- Shigematsu Mika
- Shiri Rahman
- Shirkoohi Reza
- Shiue Ivy
- Shokraneh Farhad
- Shrime Mark C
- Shukla Sharvari Rahul
- Si Si
- Siabani Soraya
- Siddiqi Tariq J
- Sigfusdottir Inga Dora
- Sigurvinsdottir Rannveig
- Silpakit Nazis
- Silva Diego Augusto Santos
- Silva Joao Pedro
- Silveira Dayane Gabriele Alves
- Singam Narayana Sarma Venkata
- Singh Jasvinder A
- Singh Virendra
- Sinha Anju Pradhan
- Sinha Dhirendra Narain
- Sitas Freddy
- Skirbekk Vegard
- Sliwa Karen
- Soares Filho Adauto Martins
- Sobaih Badr Hasan
- Sobhani Soheila
- Soofi Moslem
- Soriano Joan B
- Soyiri Ireneous N
- Sposato Luciano A
- Sreeramareddy Chandrashekhar T
- Srinivasan Vinay
- Srivastava Rakesh Kumar
- Starodubov Vladimir I
- Stathopoulou Vasiliki
- Steel Nicholas
- Stein Dan J
- Steiner Caitlyn
- Stewart Leo G
- Stokes Mark A
- Sudaryanto Agus
- Sufiyan Mu'awiyyah Babale
- Sulo Gerhard
- Sunguya Bruno F
- Sur Patrick John
- Sutradhar Ipsita
- Sykes Bryan L
- Sylaja PN
- Sylte Dillon O
- Szoeke Cassandra FI
- Tabares-Seisdedos Rafael
- Tabuchi Takahiro
- Tadakamadla Santosh Kumar
- Takahashi Ken
- Tandon Nikhil
- Tassew Aberash Abay
- Tassew Segen Gebremeskel
- Tavakkoli Mohammad
- Taveira Nuno
- Tawye Vega Yimer
- Tehrani-Banihashemi Arash
- Tekalign Tigist Gashaw
- Tekle Merhawi Gebremedhin
- Temesgen Habtamu
- Temsah Mohamad-Hani
- Temsah Omar
- Terkawi Abdullah Sulieman
- Teshale Manaye Yihune
- Tessema Belay
- Teweldemedhin Mebrahtu
- Thakur Jarnail Singh
- Thankappan Kavumpurathu Raman
- Thinmavukkarasu Sathish
- Thomas Laura Anne
- Thomas Nihal
- Thou Maigeng
- Thrift Amanda G
- TIavani-Palone Marcos Roberto
- Tilahun Binyam
- To Quyen G
- Tobe-Gai Ruoyan
- Tonelli Marcello
- Topor-Madry Roman
- Topouzis Fotis
- Torisky Sonia
- Torre Anna E
- Tortajada-Girbes Miguel
- Towbin Jeffrey A
- Tran Bach Xuan
- Tran Khanh Ban
- Tripathi Suryakant
- Tripathy Srikanth Prasad
- Truelsen Thomas Clement
- Truong Nu Thi
- Tsadik Afewerki Gehremeskel
- Tsilimparis Nikolaos
- Tuzcu E Murat
- Tyrovolas Stefanos
- Ukwaja Kingsley Nnanna
- Ullah Irfan
- Usman Muhammad Shaniq
- Uthman Olalekan A
- Uzun Selen Begun
- Vaduganathan Muthiah
- Vaezi Afsane
- Vaidya Gaurang
- Valdez Pascual R
- Varavikova Elena
- Varughese Santosh
- Vasankari Tommi Juhani
- Vasconcelos Ana Maria Nogales
- Velasquez This Moreno
- Venketasubramanian Narayanaswamy
- Vidavalur Ramesh
- Villafaina Santos
- Violante Francesco S
- Vladimirov Sergey Konstantinovitch
- Vlassov Vasily
- Vollset Stein Emil
- Vos Theo
- Vosoughi Kia
- Vujcic Isidora S
- Wagner Gregory R
- Wagnew Fasil Shiferaw Wagnew
- Waheed Yasir
- Wang Yanping
- Wang Yuan-Pang
- Wassie Molla Mesele
- Weaver Nicole Davis
- Weiderpass Elisabete
- Weintraub Robert G
- Weiss Daniel J
- Weiss Jordan
- Weldegebreal Fitsum
- Weldegwergs Kidu Gidey
- Werdecker Andrea
- Westerman Ronny
- Whiteford Harvey A
- Widecka Justyna
- Widecka Katarzyna
- Wijeratne Tissa
- Winkler Andrea Sylvia
- Wiysonge Charles Shey
- Wolfe Charles DA
- Wondemagegn Sintayehu Ambachew
- Wu Shouling
- Wyper Grant MA
- Xu Gelin
- Yadav Rajaram
- Yakob Bereket
- Yamada Tomohide
- Yan Lijing L
- Yano Yuichiro
- Yaseri Mehdi
- Yasin Jemal Yasin
- Ye Pengpeng
- Yearwood Jamal A
- Yentur Gokalp Kadri
- Yeshaneh Alex
- Yimer Ebrahim M
- Yip Paul
- Yisma Engida
- Yonemoto Naohiro
- Yoon Seok-Jun
- York Hunter W
- Yotebieng Marcel
- Younis Mustafa Z
- Yousefifard Mahmoud
- Yu Chuanhua
- Zachariah Geevar
- Zadnik Vesna
- Zafar Shamsa
- Zaidi Zoubida
- Zaki Maysaa El Sayed
- Zamani Mohammad
- Zare Zohreh
- Zeeb Hajo
- Zeleke Mulugeta Molla
- Zenebe Zerihun Menlkalew
- Zerfu Taddese Alemu
- Zhang Kai
- Zhang Xueying
- Zhu Jun
- Zodpey Sanjay
- Zucker Inbar
- Zuhlke Liesl Joanna J
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2018
- Field of study
Background: The Global Burden of Diseases, Injuries, and Risk Factors Study 2017 (GBD 2017) includes a comprehensive assessment of incidence, prevalence, and years lived with disability (YLDs) for 354 causes in 195 countries and territories from 1990 to 2017. Previous GBD studies have shown how the decline of mortality rates from 1990 to 2016 has led to an increase in life expectancy, an ageing global population, and an expansion of the non-fatal burden of disease and injury. These studies have also shown how a substantial portion of the world's population experiences non-fatal health loss with considerable heterogeneity among different causes, locations, ages, and sexes. Ongoing objectives of the GBD study include increasing the level of estimation detail, improving analytical strategies, and increasing the amount of high-quality data. Methods: We estimated incidence and prevalence for 354 diseases and injuries and 3484 sequelae. We used an updated and extensive body of literature studies, survey data, surveillance data, inpatient admission records, outpatient visit records, and health insurance claims, and additionally used results from cause of death models to inform estimates using a total of 68 781 data sources. Newly available clinical data from India, Iran, Japan, Jordan, Nepal, China, Brazil, Norway, and Italy were incorporated, as well as updated claims data from the USA and new claims data from Taiwan (province of China) and Singapore. We used DisMod-MR 2.1, a Bayesian meta-regression tool, as the main method of estimation, ensuring consistency between rates of incidence, prevalence, remission, and cause of death for each condition. YLDs were estimated as the product of a prevalence estimate and a disability weight for health states of each mutually exclusive sequela, adjusted for comorbidity. We updated the Socio-demographic Index (SDI), a summary development indicator of income per capita, years of schooling, and total fertility rate. Additionally, we calculated differences between male and female YLDs to identify divergent trends across sexes. GBD 2017 complies with the Guidelines for Accurate and Transparent Health Estimates Reporting. Findings: Globally, for females, the causes with the greatest age-standardised prevalence were oral disorders, headache disorders, and haemoglobinopathies and haemolytic anaemias in both 1990 and 2017. For males, the causes with the greatest age-standardised prevalence were oral disorders, headache disorders, and tuberculosis including latent tuberculosis infection in both 1990 and 2017. In terms of YLDs, low back pain, headache disorders, and dietary iron deficiency were the leading Level 3 causes of YLD counts in 1990, whereas low back pain, headache disorders, and depressive disorders were the leading causes in 2017 for both sexes combined. All-cause age-standardised YLD rates decreased by 3·9% (95% uncertainty interval [UI] 3·1-4·6) from 1990 to 2017; however, the all-age YLD rate increased by 7·2% (6·0-8·4) while the total sum of global YLDs increased from 562 million (421-723) to 853 million (642-1100). The increases for males and females were similar, with increases in all-age YLD rates of 7·9% (6·6-9·2) for males and 6·5% (5·4-7·7) for females. We found significant differences between males and females in terms of age-standardised prevalence estimates for multiple causes. The causes with the greatest relative differences between sexes in 2017 included substance use disorders (3018 cases [95% UI 2782-3252] per 100 000 in males vs 1400 [1279-1524] per 100 000 in females), transport injuries (3322 [3082-3583] vs 2336 [2154-2535]), and self-harm and interpersonal violence (3265 [2943-3630] vs 5643 [5057-6302]). Interpretation: Global all-cause age-standardised YLD rates have improved only slightly over a period spanning nearly three decades. However, the magnitude of the non-fatal disease burden has expanded globally, with increasing numbers of people who have a wide spectrum of conditions. A subset of conditions has remained globally pervasive since 1990, whereas other conditions have displayed more dynamic trends, with different ages, sexes, and geographies across the globe experiencing varying burdens and trends of health loss. This study emphasises how global improvements in premature mortality for select conditions have led to older populations with complex and potentially expensive diseases, yet also highlights global achievements in certain domains of disease and injury
Progress in gene therapy for neurological disorders
- Author
- A Donsante
- A Immonen
- AE Lang
- AH Nagahara
- AI den Hollander
- AI Freeman
- AL Peel
- AM Maguire
- AM Sandmair
- AP Kells
- AS Galanopoulou
- AT Berg
- AT Sorensen
- B Jarraya
- B Paradiso
- B Paradiso
- BK Berges
- BK Kaspar
- C Franz
- C Jomary
- C Richichi
- CH Vite
- CN Cearley
- CN Cearley
- CW Christine
- D Klatzmann
- D Lau
- D Wolfe
- David J. Fink
- DJ Fink
- DJ Watson
- DM Holtzman
- DP Woldbye
- E Thevenot
- EA Chiocca
- EA Chiocca
- EA Chiocca
- EJ Lin
- F Noe
- F Noe
- FF Lang
- FP Cremers
- G Lui
- G Palu
- G Vande Velde
- GJ Farrar
- GJ Farrar
- I Kanter-Schlifke
- IM Germano
- J Luo
- J Matrai
- J Yun
- JC Glorioso
- JC McIntyre
- Jean Bennett
- JF Curtin
- JH Kordower
- JH Wolfe
- JL McBride
- JM Laing
- JM Markert
- JM Markert
- John H. Wolfe
- Joseph C. Glorioso
- JR Goss
- JR Goss
- JR Goss
- JR Goss
- JW Bainbridge
- JY Qin
- K Wirdefeldt
- KD Foust
- KS Bankiewicz
- L Jiang
- Luk H. Vandenberghe
- M Ashtari
- M Azzouz
- M Castro
- M Chattopadhyay
- M Chattopadhyay
- M Chattopadhyay
- M Chattopadhyay
- M Chattopadhyay
- M Elsabahy
- M Izquierdo
- M Izumikawa
- M Mata
- M Simonato
- M Suzuki
- MA Goncalves
- Maria G. Castro
- MD Prados
- ME Emborg
- Michele Simonato
- N Cartier
- N Maheshri
- N Pulicherla
- N Shand
- NG Rainov
- Nicholas M. Boulis
- NM Ellinwood
- O Akil
- P Forsyth
- P Leone
- P Theofilas
- PA LeWitt
- Pedro R. Lowenstein
- PS Smitt
- R Bovolenta
- R Brookmeyer
- R Haberman
- R Levy
- R Rampling
- RA Smith
- RC Baek
- RC Wykes
- RP Haberman
- RS Fisher
- S Ali
- S Duque
- S Foti
- S Hao
- S Hao
- S Hao
- S Hermening
- S Kugler
- S Kügler
- S Millington-Ward
- S Muramatsu
- S Nayak
- S Ramaswamy
- S Worgall
- SA Grossman
- SE Leff
- SJ Gray
- SJ Gray
- SJ Gray
- SP Gubbels
- SQ Harper
- Steven J. Gray
- T Husain
- T Siddique
- Thomas J. Wilson
- TJ McCown
- TP Dryja
- TW Trask
- V Busskamp
- V Papanastassiou
- William F. Goins
- WJ Marks Jr.
- WJ Marks Jr.
- WW Hauswirth
- Y Lee
- Y Oiwa
- YH Chen
- YH Raol
- YK Lai
- Z Arvanitakis
- Z Ram
- Z Wu
- Z Zhou
- Publication venue
- Publication date
- 01/01/2013
- Field of study
Diseases of the nervous system have devastating effects and are widely distributed among the population, being especially prevalent in the elderly. These diseases are often caused by inherited genetic mutations that result in abnormal nervous system development, neurodegeneration, or impaired neuronal function. Other causes of neurological diseases include genetic and epigenetic changes induced by environmental insults, injury, disease-related events or inflammatory processes. Standard medical and surgical practice has not proved effective in curing or treating these diseases, and appropriate pharmaceuticals do not exist or are insufficient to slow disease progression. Gene therapy is emerging as a powerful approach with potential to treat and even cure some of the most common diseases of the nervous system. Gene therapy for neurological diseases has been made possible through progress in understanding the underlying disease mechanisms, particularly those involving sensory neurons, and also by improvement of gene vector design, therapeutic gene selection, and methods of delivery. Progress in the field has renewed our optimism for gene therapy as a treatment modality that can be used by neurologists, ophthalmologists and neurosurgeons. In this Review, we describe the promising gene therapy strategies that have the potential to treat patients with neurological diseases and discuss prospects for future development of gene therapy
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