329 research outputs found
Topical immunotherapy of severe alopecia areata with diphenylcyclopropenone (DPCP): experience in an Iranian population
- Author
- Publication venue
- BioMed Central
- Publication date
- 01/01/2005
- Field of study
BACKGROUND: Highly variable results of topical diphenylcyclopropenone (DPCP) in the treatment of alopecia areata have been reported so far. The purposes of the present study were to evaluate the efficacy and tolerability of DPCP treatment in severe alopecia areata. METHODS: Twenty-eight patients (16 female and 12 male, 10â35 years old, mean age 25 years) with extensive alopecia areata were enrolled in an open-label clinical trial. After sensitization with 2% DPCP, progressively higher concentrations beginning at 0.001% were applied weekly for 6 months to one side of the scalp, after which, if terminal hair growth was noted, the entire scalp was then treated under the same weekly protocol. The maximum concentration of DPCP in acetone was 2%. RESULTS: Twenty-seven of 28 patients completed therapy. The overall response rate was 81.5% (22/27), complete remission (90%-100% terminal hair re-growth) was obtained 22.2% (6/27) and partial remission (10%-90% terminal hair re-growth) in 59.3% (16/27). In all patients an eczematous reaction consisting of erythema, itching, and scaling at the site of application were observed. During therapy, other side effects including, occipital lymphadenopathy 40.7% (11/27), severe eczema/blister formation 40.7% (11/27), hyperpigmentation 18.5% (5/27) were observed, but no hypopigmentation, vitiligo, contact urticaria, and erythema multiforme-like reaction were seen in the patients. Nineteen of 27 (70.4%) patients had at least one side effect, other than eczematous reaction. Notably, partial recurrence was observed in 50.9% (13/22) of these patients after 6 to 12 months of follow-up. During the follow-up time the maintenance DPCP immunotherapy was continued. CONCLUSION: Topical DPCP treatment for alopecia areata is an effective therapy with a slightly high relapse rate during bilateral maintenance treatment. According to the author's knowledge this is the first experience with DPCP in Iran
Jet energy measurement with the ATLAS detector in proton-proton collisions at root s=7 TeV
- Author
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- Zarzhitsky P
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- Zhemchugov A
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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 âs = 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 pTâ„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 60â€pT<800 GeV, and is maximally 14 % for pT<30 GeV in the most forward region 3. 2â€{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
Search for high-mass resonances decaying to dilepton final states in pp collisions at sâ=7 TeV with the ATLAS detector
- Author
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- Zhemchugov A
- Zhong J
- Zhou B
- Zhou N
- Zhou Y
- Zhu CG
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhuravlov V
- Zibell A
- Zieminska D
- Zimin NI
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zitoun R
- Zivkovic L
- Zmouchko VV
- Zobernig G
- Zoccoli A
- zur Nedden M
- Zutshi V
- Zwalinski L
- Publication venue
- Springer
- Publication date
- 23/11/2012
- Field of study
The ATLAS detector at the Large Hadron Collider is used to search for high-mass resonances decaying to an electron-positron pair or a muon-antimuon pair. The search is sensitive to heavy neutral ZâČ gauge bosons, Randall-Sundrum gravitons, Z * bosons, techni-mesons, Kaluza-Klein Z/Îł bosons, and bosons predicted by Torsion models. Results are presented based on an analysis of pp collisions at a center-of-mass energy of 7 TeV corresponding to an integrated luminosity of 4.9 fbâ1 in the e + e â channel and 5.0 fbâ1 in the ÎŒ + ÎŒ âchannel. A Z âČ boson with Standard Model-like couplings is excluded at 95 % confidence level for masses below 2.22 TeV. A Randall-Sundrum graviton with coupling k/MPl=0.1 is excluded at 95 % confidence level for masses below 2.16 TeV. Limits on the other models are also presented, including Technicolor and Minimal ZâČ Models
The p38/MK2/Hsp25 Pathway Is Required for BMP-2-Induced Cell Migration
- Author
- A Kotlyarov
- A Moustakas
- A Moustakas
- A Philips
- A Sorrentino
- AJ Ridley
- AM Goldstein
- Antonio G. Susperregui
- AR Nebreda
- BA Eaton
- BW Bernstein
- C Gamell
- C Le Clainche
- C Sanchez-Camacho
- CE Eyers
- CK Huang
- Cristina Gamell
- Domingos Henrique
- E Perdiguero
- F Vinals
- Francesc Ventura
- H Shibuya
- HF Chen
- HR Dawe
- J Cau
- J Fiedler
- JC Hedges
- JH Hu
- José Luis Rosa
- K Engel
- K Miyazono
- K Yamauchi
- L Lamalice
- M Damarla
- M Dudas
- M Gaestel
- M Kobayashi
- M Lind
- M Raftopoulou
- M Yamashita
- MO Hannigan
- MT Uhlik
- N Kimura
- N Nomura
- N Ronkina
- NR Jog
- Ora Bernard
- R Ben-Levy
- R Benndorf
- R Wu
- RH Adams
- RH Insall
- S Edlund
- S Edlund
- S Edlund
- S Kostenko
- S Pichon
- S Rousseau
- S Singh
- SH Lee
- ST Lee-Hoeflich
- T Adachi-Yamada
- T Lopez-Rovira
- T Sotobori
- TD Pollard
- VA Beardmore
- VC Foletta
- X Xu
- Y Wu
- YE Zhang
- Z Wen
- Publication venue
- Public Library of Science
- Publication date
- 28/01/2011
- Field of study
Background: Bone morphogenetic proteins (BMPs) have been shown to participate in the patterning and specification of several tissues and organs during development and to regulate cell growth, differentiation and migration in different cell types. BMP-mediated cell migration requires activation of the small GTPase Cdc42 and LIMK1 activities. In our earlier report we showed that activation of LIMK1 also requires the activation of PAKs through Cdc42 and PI3K. However, the requirement of additional signaling is not clearly known. Methodology/Principal Findings: Activation of p38 MAPK has been shown to be relevant for a number of BMP-2Âżs physiological effects. We report here that BMP-2 regulation of cell migration and actin cytoskeleton remodelling are dependent on p38 activity. BMP-2 treatment of mesenchymal cells results in activation of the p38/MK2/Hsp25 signaling pathway downstream from the BMP receptors. Moreover, chemical inhibition of p38 signaling or genetic ablation of either p38Âż or MK2 blocks the ability to activate the downstream effectors of the pathway and abolishes BMP-2-induction of cell migration. These signaling effects on p38/MK2/Hsp25 do not require the activity of either Cdc42 or PAK, whereas p38/MK2 activities do not significantly modify the BMP-2-dependent activation of LIMK1, measured by either kinase activity or with an antibody raised against phospho-threonine 508 at its activation loop. Finally, phosphorylated Hsp25 colocalizes with the BMP receptor complexes in lamellipodia and overexpression of a phosphorylation mutant form of Hsp25 is able to abolish the migration of cells in response to BMP-2. Conclusions: These results indicate that Cdc42/PAK/LIMK1 and p38/MK2/Hsp25 pathways, acting in parallel and modulating specific actin regulatory proteins, play a critical role in integrating responses during BMP-induced actin reorganization and cell migration
Association of angiopoietin-2, C-reactive protein and markers of obesity and insulin resistance with survival outcome in colorectal cancer
- Author
- A Mantovani
- AA Moghaddam
- AMM Haydon
- AS Greenberg
- B A Robinson
- BM Wolpin
- C Murdoch
- C Porta
- CS Fuchs
- D Cao
- D Komninou
- DM Parkin
- E Giovannucci
- E Volkova
- EJ Park
- F Frizelle
- FL Greene
- G Bello
- G Gonullu
- G U Dachs
- GK Reeves
- H Morrin
- H Yang
- HG Moon
- I Helfrich
- J A Willis
- J E Wells
- JA Meyerhardt
- JA Meyerhardt
- JH Park
- JJ Dignam
- JK Litton
- JM Birmingham
- KA Rmali
- M J Currie
- M Trevisan
- MI Koukourakis
- MM Center
- MM Turu
- MS Sandhu
- N Reinmuth
- P Dandona
- PM Ridker
- R Pais
- RP Merkow
- S Sarraf-Yazdi
- S Tsujinaka
- SA Ahmad
- SA Ahmad
- SB Coffelt
- T Kadowaki
- T Nozoe
- T Nozoe
- U Fiedler
- V Goede
- VC Ganta
- XM Nguyen
- YC Chung
- Publication venue
- Nature Publishing Group
- Publication date
- Field of study
Critical Assessment of Metagenome Interpretation:A benchmark of metagenomics software
- Author
- A Mikheenko
- Aaron E Darling
- Adrian Fritz
- Alexander Sczyrba
- Alexey Gurevich
- Alice C McHardy
- Andreas Bremges
- B Liu
- Bernhard Y Renard
- Bertrand Denis
- Burton K H Chia
- C Lozupone
- Charles Deltel
- Chirag Jain
- Christopher Quince
- Claire Lemaitre
- D Coil
- D Koslicki
- D Koslicki
- D Koslicki
- D Li
- D Turaev
- Daniel A Cuevas
- David Koslicki
- DD Kang
- DE Wood
- DH Huson
- Dmitrij Turaev
- Dominique Lavenier
- Dongwan Don Kang
- E Pruesse
- Edward M Rubin
- Eik Dahms
- Fernando Meyer
- Genivaldo Gueiros Z Silva
- GG Silva
- Guillaume Rizk
- H Klingenberg
- Hans-Peter Klenk
- Heiner Klingenberg
- HH Lin
- Hsin-Hung Lin
- I Gregor
- Ivan Gregor
- J Alneberg
- J Dröge
- JA Chapman
- Jeff L Froula
- Jeffrey J Cook
- Jessika Fiedler
- Johannes Dröge
- Julia A Vorholt
- K Mavromatis
- KT Konstantinidis
- Lars Hestbjerg Hansen
- M Arumugam
- M BalvoÄiĆ«tÄ
- M Strous
- M Yassour
- Marc Strous
- Markus Göker
- Matthew Z DeMaere
- Michael Beckstette
- Michael D Barton
- Mihai Pop
- ML Bendall
- Monika BalvoÄiĆ«tÄ
- N Kashtan
- N Sangwan
- N Segata
- Nicole Shapiro
- Nikos C Kyrpides
- Niranjan Nagarajan
- NP Nguyen
- O Koren
- P Belmann
- Paul Schulze-Lefert
- Peter Belmann
- Peter Hofmann
- Peter Meinicke
- Philip D Blood
- Pierre Peterlongo
- R Chikhi
- R Ounit
- Rayan Chikhi
- Robert A Edwards
- Robert Egan
- RR Miller
- Ruben Garrido-Oter
- S Boisvert
- S Chatterjee
- S Gao
- S Lindgreen
- S Sunagawa
- Stefan Janssen
- Stephan Majda
- Steven W Singer
- Surya Saha
- SĂžren J SĂžrensen
- T Thomas
- Tanja Woyke
- Thomas Lingner
- Thomas Rattei
- Tue Sparholt JĂžrgensen
- V Marx
- VC Piro
- Vitor C Piro
- Y Bai
- Yang Bai
- Yu-Chieh Liao
- Yu-Wei Wu
- YW Wu
- Zhong Wang
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2017
- Field of study
International audienceIn metagenome analysis, computational methods for assembly, taxonomic profilingand binning are key components facilitating downstream biological datainterpretation. However, a lack of consensus about benchmarking datasets andevaluation metrics complicates proper performance assessment. The CriticalAssessment of Metagenome Interpretation (CAMI) challenge has engaged the globaldeveloper community to benchmark their programs on datasets of unprecedentedcomplexity and realism. Benchmark metagenomes were generated from newlysequenced ~700 microorganisms and ~600 novel viruses and plasmids, includinggenomes with varying degrees of relatedness to each other and to publicly availableones and representing common experimental setups. Across all datasets, assemblyand genome binning programs performed well for species represented by individualgenomes, while performance was substantially affected by the presence of relatedstrains. Taxonomic profiling and binning programs were proficient at high taxonomicranks, with a notable performance decrease below the family level. Parametersettings substantially impacted performances, underscoring the importance ofprogram reproducibility. While highlighting current challenges in computationalmetagenomics, the CAMI results provide a roadmap for software selection to answerspecific research questions
Wnt signaling in triple-negative breast cancer
- Author
- A Ciupek
- A De
- A Esquela-Kerscher
- A Gucalp
- A Prat
- A Prat
- A Prat
- A Schech
- A Suzuki
- AI Khramtsov
- AL Stiegler
- AS Cleary
- B Cui
- B Howard
- B Kaufman
- B Samatanga
- BD Lehmann
- BT MacDonald
- BT MacDonald
- C Arce-Salinas
- C Gao
- C Henry
- C Laezza
- C Lindvall
- C Lindvall
- C Liu
- C Wang
- C Wang
- C-C Liu
- C-M Cruciat
- CA Hudis
- CC Huard
- CJ Creighton
- CM Perou
- CP Prasad
- CR Tate
- CY Janda
- D Castiglia
- D Wang
- DJ Sussman
- DV Tauriello
- E Bourhis
- E Gomez-Orte
- E Hilborn
- EF Byrne
- EM Shin
- F Chiacchiera
- FC Geyer
- FV Fuller-Pace
- G Corda
- G Wang
- G Wu
- G-B Jang
- GB Jang
- Group EBCTC.
- H Clevers
- H Farmer
- H Taipaleenmaki
- H Wang
- H Wang
- H Xu
- HC Moore
- HC Wong
- HE Bryant
- I Jarmoskaite
- J Cai
- J Dejmek
- J Roose
- J Schlessinger
- J Xu
- J-P Borg
- JA Sparano
- JD Kormish
- JN Goh
- JP Dijksterhuis
- JP Medema
- JP Solzak
- K Kast
- K Kikuchi
- K Pogoda
- K Tamai
- K Willert
- KA Avery-Kiejda
- KKN Guturi
- KM Cadigan
- KR Greenow
- L Azzolin
- L Azzolin
- L Cheng
- L Li
- L Li
- L Livraghi
- L Pusztai
- L Yang
- L Zhang
- M Botlagunta
- M Fiedler
- M Habu
- M Kai
- M Nishita
- M Peiris-Pages
- M Pistelli
- M Xie
- M Xu
- MC Rangel
- MD Burstein
- MK Mohammed
- MV Gammons
- N Dey
- N Takebe
- NM Badders
- O Tudoran
- P Eroles
- P Eroles
- P Linder
- P Polakis
- PS Weisman
- Q Jiang
- Q Yu
- R Bao
- R Chakrabarti
- R Habas
- R Takada
- R van Amerongen
- R Yasuhara
- RD Sicchieri
- RL Atkinson
- S Chen
- S Mohammadi Yeganeh
- S Mohammadi-Yeganeh
- S Rocak
- S Yin
- S Yin
- S Yin
- S Zhang
- S Zhang
- SA Ibrahim
- SM Huang
- SP Shah
- T Ishitani
- T Ishitani
- T Isobe
- T Ovcaricek
- T Phesse
- T Schwarz-Romond
- TC He
- TK Noah
- U Weierstall
- UD Kahlert
- V Lefebvre
- V Nikolova
- VC Jordan
- VE Ahn
- VF Merino
- VF Taelman
- VG Abramson
- VS Golubkov
- VS Li
- WD Foulkes
- WH Conrad
- X Gao
- X Jiang
- X Zeng
- Y Gong
- Y Liu
- Y Minami
- Y Shimono
- Y-R Liu
- YA Zeng
- YL Huang
- Z Cheng
- ZS Wu
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2017
- Field of study
Wnt signaling regulates a variety of cellular processes, including cell fate, differentiation, proliferation and stem cell pluripotency. Aberrant Wnt signaling is a hallmark of many cancers. An aggressive subtype of breast cancer, known as triple-negative breast cancer (TNBC), demonstrates dysregulation in canonical and non-canonical Wnt signaling. In this review, we summarize regulators of canonical and non-canonical Wnt signaling, as well as Wnt signaling dysfunction that mediates the progression of TNBC. We review the complex molecular nature of TNBC and the emerging therapies that are currently under investigation for the treatment of this disease
Measurement of Higgs boson production in the diphoton decay channel in pp collisions at center-of-mass energies of 7 and 8 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Aben R
- Abi B
- Abolins M
- AbouZeid OS
- Abramowicz H
- Abreu H
- Abreu R
- Abulaiti Y
- Acharya BS
- Adam ER
- Adamczyk L
- Adams DL
- Adelman J
- Adomeit S
- Adye T
- Agatonovic-Jovina T
- Aguilar-Saavedra JA
- Agustoni M
- Ahlen SP
- Ahmadov F
- Aielli G
- Akerstedt H
- Akesson TP
- Akimoto G
- Akimov AV
- Alberghi GL
- Albert J
- Albrand S
- Alconada Verzini MJ
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexander G
- Alexandre G
- Alexopoulos T
- Alhroob M
- Alimonti G
- Alio L
- Alison J
- Allbrooke BMM
- Allison LJ
- Allport PP
- Aloisio A
- Alonso A
- Alonso F
- Alpigiani C
- Altheimer A
- Alviggi MG
- Amako K
- Amaral Coutinho Y
- Amelung C
- Amidei D
- Amor Dos Santos SP
- Amorim A
- Amoroso S
- Amram N
- Amundsen G
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders G
- Anderson KJ
- Andreazza A
- Andrei V
- Anduaga XS
- Angelidakis S
- Angelozzi I
- Anger P
- Angerami A
- Anghinolfi F
- Anh TV
- Anisenkov AV
- Anjos N
- Annovi A
- Antonaki A
- Antonelli M
- Antonov A
- Antos J
- Anulli F
- Aoki M
- Apolle R
- Arabidze G
- Aracena I
- Arai Y
- Aranda CP
- Araque JP
- Arce ATH
- Arguin J-F
- Argyropoulos S
- Arik M
- Armadans RC
- Armbruster AJ
- Arnaez O
- Arnal V
- Arnold H
- Arratia M
- Arslan O
- Artamonov A
- Artoni G
- Asai S
- Asbah N
- Ashkenazi A
- Asman B
- Asquith L
- Assamagan K
- Astalos R
- Atkinson M
- Atlay NB
- Auerbach B
- Augsten K
- Aurousseau M
- Avolio G
- Azuelos G
- Azuma Y
- Baak MA
- Baas AE
- Bacci C
- Bachacou H
- Bachas K
- Backes M
- Backhaus M
- Badescu E
- Bagiacchi P
- Bagnaia P
- Bai Y
- Bain T
- Baines JT
- Baker OK
- Balek P
- Balli F
- Banas E
- Banerjee S
- Bannoura AAE
- Bansal V
- Bansil HS
- Barajas CAC
- Barak L
- Baranov P
- Barberio EL
- Barberis D
- Barbero M
- Barillari T
- Barisonzi M
- Barklow T
- Barlow N
- Barnett BM
- Barnett RM
- Barnovska Z
- Baroncelli A
- Barone G
- Barr AJ
- Barreiro F
- Barrera CO
- Bartoldus R
- Barton AE
- Bartos P
- Bartsch V
- Bassalat A
- Basye A
- Bates RL
- Batley JR
- Battaglia M
- Battistin M
- Bauer F
- Bawa HS
- Beattie MD
- Beau T
- Beauchemin PH
- Beccherle R
- Bechtle P
- Beck HP
- Becker K
- Becker S
- Beckingham M
- Becot C
- Beddall A
- Beddall AJ
- Bedikian S
- Bednyakov VA
- Bee CP
- Beemster LJ
- Beermann TA
- Begel M
- Behr K
- Belanger-Champagne C
- Belenguer MJ
- Bell PJ
- Bell WH
- Bella G
- Bella LA
- Bellagamba L
- Bellerive A
- Bellomo M
- Belotskiy K
- Beltramello O
- Benary O
- Benchekroun D
- Bendtz K
- Benekos N
- Benhammou Y
- Benjamin DP
- Bensinger JR
- Benslama K
- Bentvelsen S
- Berge D
- Berger N
- Berghaus F
- Beringer J
- Berlingen JM
- Bernard C
- Bernat P
- Bernius C
- Bernlochner FU
- Berry T
- Berta P
- Bertella C
- Bertoli G
- Bertolucci F
- Bertsche C
- Bertsche D
- Besana MI
- Besjes GJ
- Bessidskaia O
- Bessner M
- Besson N
- Betancourt C
- Bethke S
- Bhimji W
- Bianchi RM
- Bianchini L
- Bianco M
- Biebel O
- Bieniek SP
- Bierwagen K
- Biesiada J
- Biglietti M
- Bilokon H
- Bindi M
- Binet S
- Bingul A
- Bini C
- Black CW
- Black JE
- Black KM
- Blackburn D
- Blair RE
- Blanchard J-B
- Blazek T
- Bloch I
- Blocker C
- Blum W
- Blumenschein U
- Bobbink GJ
- Bobrovnikov VS
- Bocchetta SS
- Bocci A
- Bock C
- Boddy CR
- Boehler M
- Boek TT
- Boeriu OEV
- Bogaerts JA
- Bogdanchikov AG
- Bogouch A
- Bohm C
- Bohm J
- Boisvert V
- Bold T
- Boldea V
- Boldyrev AS
- Bomben M
- Bona M
- Boonekamp M
- Borisov A
- Borissov G
- Borri M
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- Bortfeldt J
- Bortolotto V
- Bos K
- Boscherini D
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- Boyko R
- Bozic I
- Bracinik J
- Brandt A
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- Brau B
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- Bret MC
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- Bristow TM
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- Brock I
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- Bromberg C
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- Brooijmans G
- Brooks T
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- Brosamer J
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- Brown J
- Bruncko D
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- Bruni A
- Bruni G
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- Bryngemark L
- Buanes T
- Buat Q
- Bucci F
- Buchholz P
- Buckingham RM
- Buckley AG
- Buda SI
- Budagov IA
- Buehrer F
- Buescher D
- Buescher V
- Bueso XP
- Bugge L
- Bugge MK
- Bulekov O
- Bundock AC
- Burckhart H
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- Burghgrave B
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- Burmeister I
- Busato E
- Bussey P
- Bustos ACF
- Buszello CP
- Butler B
- Butler JM
- Butt AI
- Buttar CM
- Butterworth JM
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- Buttinger W
- Buzatu A
- Byszewski M
- Caforio D
- Cakir IT
- Cakir O
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- Calandri A
- Calderini G
- Calfayan P
- Calkins R
- Caloba LP
- Calvet D
- Calvet S
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- Caminada LM
- Campana S
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- Campoverde A
- Canale V
- Canepa A
- Cantero J
- Cantrill R
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- Caprini I
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- Capua M
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- Carlino G
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- Carrillo-Montoya GD
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- Carvalho J
- Casadei D
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- Castanheira MTD
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- Castillo LRF
- Castro NF
- Catastini P
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- Catmore JR
- Cattai A
- Cattani G
- Caudron J
- Cavaliere V
- Cavalli D
- Cavalli-Sforza M
- Cavasinni V
- Ceradini F
- Cerio BC
- Cerny K
- Cerqueira AS
- Cerri A
- Cerrito L
- Cerutti F
- Cerv M
- Cervelli A
- Cetin SA
- Chafaq A
- Chakraborty D
- Chalupkova I
- Chang P
- Chapleau B
- Chapman JD
- Charfeddine D
- Charlton DG
- Chau CC
- Cheatham S
- Chegwidden A
- Chekanov S
- Chekulaev SV
- Chelkov GA
- Chelstowska MA
- Chen C
- Chen H
- Chen K
- Chen L
- Chen S
- Chen X
- Chen Y
- Chen Y
- Cheng HC
- Cheng Y
- Cheplakov A
- Chernyatin V
- Cheu E
- Chevalier L
- Chiarella V
- Chiefari G
- Childers JT
- Chilingarov A
- Chiodini G
- Chisholm AS
- Chislett RT
- Chitan A
- Chizhov MV
- Chouridou S
- Chow BKB
- Chromek-Burckhart D
- Chu ML
- Chudoba J
- Chwastowski JJ
- Chytka L
- Ciapetti G
- Ciftci AK
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- Cinca D
- Cindro V
- Ciocio A
- Cirkovic P
- Citron ZH
- Citterio M
- Ciubancan M
- Clark A
- Clark PJ
- Clarke RN
- Cleland W
- Clemens JC
- Clement C
- Coadou Y
- Cobal M
- Coccaro A
- Cochran J
- Codina EP
- Coffey L
- Cogan JG
- Coggeshall J
- Cole B
- Cole S
- Colijn AP
- Collaboration ATLAS
- Collot J
- Colombo T
- Colon G
- Compostella G
- Coniavitis E
- Conidi MC
- Connell SH
- Connelly IA
- Consonni SM
- Consorti V
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- Conti G
- Conventi F
- Cooke M
- Cooper BD
- Cooper-Sarkar AM
- Cooper-Smith NJ
- Copic K
- Cornelissen T
- Corradi M
- Correia AMH
- Corriveau F
- Corso-Radu A
- Cortes-Gonzalez A
- Cortiana G
- Costa G
- Costa MJ
- Costanzo D
- Cote D
- Cottin G
- Cowan G
- Cox BE
- Cranmer K
- Cree G
- Crepe-Renaudin S
- Crescioli F
- Cribbs WA
- Cristinziani M
- Croft V
- Crosetti G
- Cuciuc C-M
- Cummings J
- Curatolo M
- Cuthbert C
- Czirr H
- Czodrowski P
- Czyczula Z
- D'Auria S
- D'Onofrio M
- da Costa JBG
- Da Costa JGPF
- Da Via C
- Dabrowski W
- Dafinca A
- Dai T
- Dale O
- Dallaire F
- Dallapiccola C
- Dam M
- Damazio DO
- Daniells AC
- Dao V
- Darbo G
- Darmora S
- Dassoulas JA
- Dattagupta A
- Davey W
- David C
- Davidek T
- Davies E
- Davies M
- Davignon O
- Davison AR
- Davison P
- Davygora Y
- Dawe E
- Dawson I
- Daya-Ishmukhametova RK
- de Andrade Filho LM
- de Asmundis R
- De Bruin PHS
- De Castro S
- De Cecco S
- De Groot N
- De Jong P
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- Zhemchugov A
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- Zhukov K
- Zibell A
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- Zimine NI
- Zimmermann C
- Zimmermann R
- Zimmermann S
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- Zurzolo G
- Zutshi V
- Zwalinski L
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2014
- Field of study
A measurement of the production processes of the recently discovered Higgs boson is performed in the two-photon final state using 4.5ââfb[superscript â1] of proton-proton collisions data at âs=7ââTeV and 20.3ââfb[superscript â1] at âs=8ââTeV collected by the ATLAS detector at the Large Hadron Collider. The number of observed Higgs boson decays to diphotons divided by the corresponding Standard Model prediction, called the signal strength, is found to be ÎŒ=1.17±0.27 at the value of the Higgs boson mass measured by ATLAS, m[subscript H]=125.4ââGeV. The analysis is optimized to measure the signal strengths for individual Higgs boson production processes at this value of m[subscript H]. They are found to be ÎŒ[subscript ggF]=1.32±0.38, ÎŒ[subscript VBF]=0.8±0.7, ÎŒ[subscript WH]=1.0±1.6, ÎŒ[subscript ZH]=0.1[superscript +3.7 subscript â0.1], and ÎŒ[subscript t [bar over t] H] =1.6[superscript +2.7 subscript â1.8], for Higgs boson production through gluon fusion, vector-boson fusion, and in association with a W or Z boson or a top-quark pair, respectively. Compared with the previously published ATLAS analysis, the results reported here also benefit from a new energy calibration procedure for photons and the subsequent reduction of the systematic uncertainty on the diphoton mass resolution. No significant deviations from the predictions of the Standard Model are found.European Organization for Nuclear ResearchUnited States. Dept. of EnergyNational Science Foundation (U.S.)Brookhaven National Laborator
Charged-particle distributions at low transverse momentum in âs=13 13 TeV pp interactions measured with the ATLAS detector at the LHC
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Abeloos B
- Aben R
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abreu R
- Abulaiti Y
- Acharya BS
- Adam ER
- Adamczyk L
- Adams DL
- Adelman J
- Adomeit S
- Adye T
- Affolder AA
- Agatonovic-Jovin T
- Agricola J
- Aguilar-Saavedra JA
- Ahlen SP
- Ahmadov F
- Aielli G
- Akerstedt H
- Akesson TPA
- Akimov AV
- Alberghi GL
- Alberich LC
- Albert J
- Albrand S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexander G
- Alexopoulos T
- Alhroob M
- Ali B
- Aliev M
- Alimonti G
- Alison J
- Alkire SP
- Allbrooke BMM
- Allen BW
- Allport PP
- Aloisio A
- Alonso A
- Alonso F
- Alpigiani C
- Alstaty M
- Alviggi MG
- Amadio BT
- Amako K
- Amelung C
- Amidei D
- Amorim A
- Amoroso S
- Amundsen G
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders G
- Anders JK
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- Zivkovic L
- Zobernig G
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- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Measurements of distributions of charged particles produced in protonâproton collisions with a centre-of-mass energy of 13 TeV are presented. The data were recorded by the ATLAS detector at the LHC and correspond to an integrated luminosity of 151 ÎŒb â1 ÎŒbâ1 . The particles are required to have a transverse momentum greater than 100 MeV and an absolute pseudorapidity less than 2.5. The charged-particle multiplicity, its dependence on transverse momentum and pseudorapidity and the dependence of the mean transverse momentum on multiplicity are measured in events containing at least two charged particles satisfying the above kinematic criteria. The results are corrected for detector effects and compared to the predictions from several Monte Carlo event generators
Measurement of W+Wâ production in association with one jet in protonâproton collisions at sqrt(s) = 8TeV with the ATLAS detector
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- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2016
- Field of study
The production of W boson pairs in association with one jet in pp collisions at View the MathML sources=8 TeV is studied using data corresponding to an integrated luminosity of 20.3 fbâ1 collected by the ATLAS detector during 2012 at the CERN Large Hadron Collider. The cross section is measured in a fiducial phase-space region defined by the presence of exactly one electron and one muon, missing transverse momentum and exactly one jet with a transverse momentum above 25 GeV and a pseudorapidity of |η|<4.5|η|<4.5. The leptons are required to have opposite electric charge and to pass transverse momentum and pseudorapidity requirements. The fiducial cross section is found to be View the MathML sourceÏWWfid,1-jet=136±6(stat)±14(syst)±3(lumi) fb. In combination with a previous measurement restricted to leptonic final states with no associated jets, the fiducial cross section of WW production with zero or one jet is measured to be View the MathML sourceÏWWfid,â€1-jet=511±9(stat)±26(syst)±10(lumi) fb. The ratio of fiducial cross sections in final states with one and zero jets is determined to be 0.36±0.050.36±0.05. Finally, a total cross section extrapolated from the fiducial measurement of WW production with zero or one associated jet is reported. The measurements are compared to theoretical predictions and found in good agreement
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