391 research outputs found
IL23 differentially regulates the Th1/Th17 balance in ulcerative colitis and Crohn’s disease
- Author
- Publication venue
- Publication date
- 01/01/2008
- Field of study
ABSTRACT Background: A novel T helper (Th) cell lineage, Th17, that exclusively produces the proinflammatory cytokine interleukin 17 (IL17) has been reported to play important roles in various inflammatory diseases. IL23 is also focused upon for its potential to promote Th17. Here, the roles of the IL23/IL17 axis in inflammatory bowel diseases such as ulcerative colitis (UC) and Crohn's disease (CD) were investigated. Methods: Mucosal samples were obtained from surgically resected specimens (controls, n = 12; UC, n = 17; CD, n = 22). IL17 production by isolated peripheral blood (PB) and lamina propria (LP) CD4 + cells was examined. Quantitative PCR amplification was performed to determine the mRNA expression levels of IL17, interferon c (IFNc), IL23 receptor (IL23R) and retinoic acid-related orphan receptor c (RORC) in LP CD4 + cells, and IL12 family members, such as IL12p40, IL12p35 and IL23p19, in whole mucosal specimens. The effects of exogenous IL23 on IL17 production by LP CD4 + cells were also examined. Results: IL17 production was higher in LP CD4 + cells than in PB. Significant IL17 mRNA upregulation in LP CD4 + cells was found in UC, while IFNc was increased in CD. IL23R and RORC were upregulated in LP CD4 + cells isolated from both UC and CD. IL17 production was significantly increased by IL23 in LP CD4 + cells from UC but not CD. Upregulated IL23p19 mRNA expression was correlated with IL17 in UC and IFNc in CD. Conclusions: IL23 may play important roles in controlling the differential Th1/Th17 balance in both UC and CD, although Th17 cells may exist in both diseases. Crohn's disease (CD) and ulcerative colitis (UC) are the two major forms of inflammatory bowel disease (IBD). Although the aetiology of IBD remains unclear, accumulating evidence suggests that dysfunction of the mucosal immune system plays important roles in IBD pathogenesis
Induction of JNK and c-Abl signalling by cisplatin and oxaliplatin in mismatch repair-proficient and -deficient cells
- Author
- A Eastman
- A Kat
- A Monks
- A Nehme
- A Umar
- A Umar
- B Derijard
- B Derijard
- CL Sawyers
- CP Saris
- D Fink
- D Fink
- DR Duckett
- ET Kipreos
- G Los
- JA Mello
- JM Woynarowski
- JYJ Wang
- K Orth
- LR Kelland
- M Cavigelli
- M Hibi
- M Koi
- MC Christian
- MT Hawn
- P Skehan
- R Baskaran
- R Baskaran
- R Fishel
- R Kolodner
- S Aebi
- S Aebi
- S Gupta
- S Kharbanda
- S Kharbanda
- SG Chaney
- T Mattioni
- T Shafman
- W Schmidt
- Z Chen
- Z-G Liu
- Z-G Liu
- ZM Yuan
- Publication venue
- Nature Publishing Group
- Publication date
- 01/03/1999
- Field of study
Loss of DNA mismatch repair has been observed in a variety of human cancers. Recent studies have shown that loss of DNA mismatch repair results in resistance to cisplatin but not oxaliplatin, suggesting that the mismatch repair proteins serve as a detector for cisplatin but not oxaliplatin adducts. To identify the signal transduction pathways with which the detector communicates, we investigated the effect of loss of DNA mismatch repair on activation of known damage-responsive pathways, and recently reported that cisplatin differentially activates c-Jun NH2-terminal kinase (JNK) and c-Abl in repair-proficient vs.-deficient cells. In the current study, we directly compared differential activation of these pathways by cisplatin vs. oxaliplatin. The results confirm that cisplatin activates JNK kinase 5.7 ± 1.5 (s.d.)-fold more efficiently in DNA mismatch repair-proficient than repair-deficient cells, and that the c-Abl response to cisplatin is completely absent in DNA mismatch repair-deficient cells. In contrast, there was no detectable activation of the JNK or c-Abl kinases in DNA mismatch repair-proficient or -deficient cells exposed to oxaliplatin. The present study demonstrates that, despite the similarity of the adducts produced by cisplatin and oxaliplatin, they appear to be recognized by different detectors. The DNA mismatch repair system plays an important part in the recognition of cisplatin adducts, and activation of both the JNK and c-Abl kinases in response to cisplatin damage is dependent on the detector function of the DNA mismatch repair proteins. In contrast, this detector does not respond to oxaliplatin adducts. © 1999 Cancer Research Campaig
Resveratrol Induces Growth Arrest and Apoptosis through Activation of FOXO Transcription Factors in Prostate Cancer Cells
- Author
- A Brunet
- A Jemal
- A Slusarz
- BM Burgering
- C Barthelemy
- C Urbich
- CJ Lau
- DR Calnan
- F Zanella
- FJ Barreyro
- G Xie
- GJ Kops
- H Daitoku
- H Huang
- H Huang
- H Jonsson
- H Li
- H Yang
- Irina Lebedeva
- J Gilley
- J Jiang
- JH Paik
- JJ Brosens
- JR Graff
- JY Wu
- K Maiese
- Karan P. Singh
- KB Harikumar
- KC Arden
- KE van der Vos
- MC Hu
- MH Lee
- O Puig
- PF Dijkers
- PF Dijkers
- Qinghe Chen
- R Davis
- Rakesh K. Srivastava
- RK Srivastava
- RL Lynch
- RR Alcendor
- S Kikuchi
- S Reagan-Shaw
- S Shankar
- S Shankar
- S Shankar
- SC Manolagas
- SH Kim
- Sharmila Shankar
- SK Roy
- SS Myatt
- Suthakar Ganapathy
- T Furuyama
- T Nakamura
- TB Dansen
- WJ Bakker
- Y Bai
- Y Furukawa-Hibi
- Y Sun
- Y Zou
- YD Rege
- Z Fu
- Publication venue
- Public Library of Science
- Publication date
- 01/12/2010
- Field of study
Resveratrol, a naturally occurring phytopolyphenol compound, has attracted extensive interest in recent years because of its diverse pharmacological characteristics. Although resveratrol possesses chemopreventive properties against several cancers, the molecular mechanisms by which it inhibits cell growth and induces apoptosis have not been clearly understood. The present study was carried out to examine whether PI3K/AKT/FOXO pathway mediates the biological effects of resveratrol.Resveratrol inhibited the phosphorylation of PI3K, AKT and mTOR. Resveratrol, PI3K inhibitors (LY294002 and Wortmannin) and AKT inhibitor alone slightly induced apoptosis in LNCaP cells. These inhibitors further enhanced the apoptosis-inducing potential of resveratrol. Overexpression of wild-type PTEN slightly induced apoptosis. Wild type PTEN and PTEN-G129E enhanced resveratrol-induced apoptosis, whereas PTEN-G129R had no effect on proapoptotic effects of resveratrol. Furthermore, apoptosis-inducing potential of resveratrol was enhanced by dominant negative AKT, and inhibited by wild-type AKT and constitutively active AKT. Resveratrol has no effect on the expression of FKHR, FKHRL1 and AFX genes. The inhibition of FOXO phosphorylation by resveratrol resulted in its nuclear translocation, DNA binding and transcriptional activity. The inhibition of PI3K/AKT pathway induced FOXO transcriptional activity resulting in induction of Bim, TRAIL, p27/KIP1, DR4 and DR5, and inhibition of cyclin D1. Similarly, resveratrol-induced FOXO transcriptional activity was further enhanced when activation of PI3K/AKT pathway was blocked. Over-expression of phosphorylation deficient mutants of FOXO proteins (FOXO1-TM, FOXO3A-TM and FOXO4-TM) induced FOXO transcriptional activity, which was further enhanced by resveratrol. Inhibition of FOXO transcription factors by shRNA blocked resveratrol-induced upregulation of Bim, TRAIL, DR4, DR5, p27/KIP1 and apoptosis, and inhibition of cyclin D1 by resveratrol.These data suggest that FOXO transcription factors mediate anti-proliferative and pro-apoptotic effects of resveratrol, in part due to activation of extrinsic apoptosis pathway
KRIT1 Regulates the Homeostasis of Intracellular Reactive Oxygen Species
- Author
- A Brunet
- A Essaghir
- A Follenzi
- A Fortuno
- A Glading
- A Pagenstecher
- A Rimessi
- A van der Horst
- A van der Horst
- AA Miller
- AL Akers
- AM Shah
- AR Subauste
- AV Gore
- B Kleaveland
- BM Hogan
- C Denier
- C Giorgi
- C Iadecola
- C Napoli
- C Weidinger
- CB Chiribau
- CD Anuradha
- CR Kuhlmann
- D Hoogeboom
- D Maritano
- D Zivadinovic
- DA Liebermann
- DA Marchuk
- DG Sedding
- DR Calnan
- DR Green
- E Owusu-Ansah
- EH Sarsour
- EH Sarsour
- EW Childs
- F Balzac
- F Di Lisa
- F Francalanci
- F Johnson
- Fiorella Balzac
- FM Faraci
- FM Faraci
- FM Faraci
- G Barreto
- G De Luca
- GG Leblanc
- GJ Kops
- GJ Kops
- GJ Todaro
- H Daitoku
- H Girouard
- H Girouard
- H Huang
- H Kehrer-Sawatzki
- H Matsuzaki
- HJ Helbock
- I Serebriiskii
- IN Zelko
- J Belik
- J Gault
- J Gault
- J Gault
- J Mattila
- J Sakamaki
- J Zhang
- JF Turrens
- JH Paik
- JM Dypbukt
- JR Berman
- KH Jung
- KJ Whitehead
- KJ Whitehead
- KM Robinson
- KM Schmitz
- L Martinez-Gac
- LS Jouaville
- Luca Goitre
- M Adachi
- M Alia
- M Giorgio
- M Potente
- M Schmidt
- M Valko
- M Yamamoto
- MA Essers
- MA Essers
- Maurizio C. Capogrossi
- MC Motta
- MD Evans
- MD Evans
- ML Modrick
- ML Schroeter
- MM Tarpey
- N Petit
- O Adam
- O Ekshyyan
- O Puig
- P de Candia
- P Labauge
- P Pacher
- P Pinton
- Paolo Degan
- Paolo Pinton
- PK Vogt
- PV Usatyuk
- R Shenkar
- R Uranishi
- RE Clatterbuck
- RH Medema
- RR Alcendor
- RS Frey
- S Chrissobolis
- S Laberge-le Couteulx
- S Machida
- S Nemoto
- S Yalcin
- Saverio Francesco Retta
- Saverio Marchi
- SF Retta
- SH Park
- Simona Degani
- SW Ryter
- T Furuyama
- T Hosaka
- T Kahles
- T Sahoo
- T Thum
- U Felbor
- U Sure
- V Nogueira
- VP Bindokas
- W Droge
- WC Aird
- WO Carter
- Y Furukawa-Hibi
- Y Honda
- Z Tothova
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2010
- Field of study
KRIT1 is a gene responsible for Cerebral Cavernous Malformations (CCM), a major cerebrovascular disease characterized by abnormally enlarged and leaky capillaries that predispose to seizures, focal neurological deficits, and fatal intracerebral hemorrhage. Comprehensive analysis of the KRIT1 gene in CCM patients has suggested that KRIT1 functions need to be severely impaired for pathogenesis. However, the molecular and cellular functions of KRIT1 as well as CCM pathogenesis mechanisms are still research challenges. We found that KRIT1 plays an important role in molecular mechanisms involved in the maintenance of the intracellular Reactive Oxygen Species (ROS) homeostasis to prevent oxidative cellular damage. In particular, we demonstrate that KRIT1 loss/down-regulation is associated with a significant increase in intracellular ROS levels. Conversely, ROS levels in KRIT1−/− cells are significantly and dose-dependently reduced after restoration of KRIT1 expression. Moreover, we show that the modulation of intracellular ROS levels by KRIT1 loss/restoration is strictly correlated with the modulation of the expression of the antioxidant protein SOD2 as well as of the transcriptional factor FoxO1, a master regulator of cell responses to oxidative stress and a modulator of SOD2 levels. Furthermore, we show that the KRIT1-dependent maintenance of low ROS levels facilitates the downregulation of cyclin D1 expression required for cell transition from proliferative growth to quiescence. Finally, we demonstrate that the enhanced ROS levels in KRIT1−/− cells are associated with an increased cell susceptibility to oxidative DNA damage and a marked induction of the DNA damage sensor and repair gene Gadd45α, as well as with a decline of mitochondrial energy metabolism. Taken together, our results point to a new model where KRIT1 limits the accumulation of intracellular oxidants and prevents oxidative stress-mediated cellular dysfunction and DNA damage by enhancing the cell capacity to scavenge intracellular ROS through an antioxidant pathway involving FoxO1 and SOD2, thus providing novel and useful insights into the understanding of KRIT1 molecular and cellular functions
Dijet Resonance Search with Weak Supervision Using root S=13 TeV pp Collisions in the ATLAS Detector
- Author
- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abud AA
- Abulaiti Y
- Acharya BS
- Achkar B
- Adam L
- Adamczyk L
- Adamek L
- Adelman J
- Adersberger M
- Adiguzel A
- Adorni S
- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra JA
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ai X
- Aielli G
- Akatsuka S
- Akesson TPA
- Akilli E
- Akimov A
- Al Khoury K
- Alberghi GL
- Albert J
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi A
- Alfonsi F
- Alhroob M
- Ali B
- Ali S
- Aliev M
- Alimonti G
- Allaire C
- Allbrooke BMM
- Allen BW
- Allport PP
- Aloisio A
- Alonso F
- Alpigiani C
- Alshehri AA
- Alvarez Estevez M
- Alviggi MG
- Amaral Coutinho Y
- Ambler A
- Ambroz L
- Amelung C
- Amidei D
- Amor Dos Santos SP
- Amoroso S
- Amrouche CS
- An F
- Anastopoulos C
- Andari N
- Andeen T
- Anders CF
- Anders JK
- Andrean SY
- Andreazza A
- Andrei V
- Anelli CR
- Angelidakis S
- Angerami A
- Anisenkov A
- Annovi A
- Antel C
- Anthony MT
- Antipov E
- Antonelli M
- Antrim DJA
- Anulli F
- Aoki M
- Aparisi Pozo JA
- Aparo MA
- Aperio Bella L
- Araujo Ferraz V
- Araujo Pereira R
- Araya ST
- Arcangeletti C
- Arce ATH
- Arduh FA
- Arguin J-F
- Argyropoulos S
- Arling J-H
- Armbruster AJ
- Armstrong A
- Arnaez O
- Arnold H
- Artoni G
- Artz S
- Asai S
- Asawatavonvanich T
- Asbah N
- Asimakopoulou EM
- Asquith L
- Assahsah J
- Assamagan K
- Astalos R
- Astigarraga MEP
- Atkin RJ
- Atkinson M
- Atlay NB
- Atmani H
- Augsten K
- Avolio G
- Ayoub MK
- Azuelos G
- Bachacou H
- Bachas K
- Backes M
- Backman F
- Bagnaia P
- Bahmani M
- Bahrasemani H
- Bailey AJ
- Bailey VR
- Baines JT
- Bakalis C
- Baker OK
- Bakker PJ
- Balaji S
- Baldin EM
- Balek P
- Balli F
- Balunas WK
- Balz J
- Banas E
- Bandieramonte M
- Bandyopadhyay A
- Banerjee S
- Barak L
- Barbe WM
- Barberio EL
- Barberis D
- Barbero M
- Barbour G
- Barillari T
- Barisits M-S
- Barkeloo J
- Barklow T
- Barnea R
- Barnett BM
- Barnett RM
- Barnovska-Blenessy Z
- Baroncelli A
- Barone G
- Barr AJ
- Barranco Navarro L
- Barreiro F
- Barron U
- Barsov S
- Bartels F
- Bartoldus R
- Bartolini G
- Barton AE
- Bartos P
- Basalaev A
- Basan A
- Bassalat A
- Basso MJ
- Bates RL
- Batlamous S
- Batley JR
- Batool B
- Battaglia M
- Bauce M
- Bauer F
- Bauer KT
- Bawa HS
- Beacham JB
- Beau T
- Beauchemin PH
- Becherer F
- Bechtle P
- Beck HC
- Beck HP
- Becker K
- Becot C
- Beddall A
- Beddall AJ
- Bednyakov VA
- Bedognetti M
- Bee CP
- Beermann TA
- Begalli M
- Begel M
- Behera A
- Behr JK
- Beisiegel F
- Belfkir M
- Bell AS
- Bella G
- Bellagamba L
- Bellerive A
- Bellos P
- Beloborodov K
- Belotskiy K
- Belyaev NL
- Benchekroun D
- Benekos N
- Benhammou Y
- Benjamin DP
- Benoit M
- Bensinger JR
- Bentvelsen S
- Beresford L
- Beretta M
- Berge D
- Berger N
- Bergmann B
- Bergsten LJ
- Beringer J
- Berlendis S
- Berlingen JM
- Bernardi G
- Bernius C
- Bernlochner FU
- Berry T
- Berta P
- Bertella C
- Berthold A
- Bertram IA
- Besson N
- Bethani A
- Bethke S
- Betti A
- Bevan AJ
- Beyer J
- Bhattacharya DS
- Bhattarai P
- Bi R
- Bianchi RM
- Biebel O
- Biedermann D
- Bielski R
- Bierwagen K
- Biesuz N
- Biglietti M
- Billoud TR
- Bindi M
- Bingul A
- Bini C
- Biondi S
- Birman M
- Bisanz T
- Biswal JP
- Biswas D
- Bitadze A
- Bittrich C
- Bjorke K
- Blazek T
- Bloch I
- Blocker C
- Blue A
- Blumenschein U
- Bobbink GJ
- Bobrovnikov VS
- Bocchetta SS
- Bocci A
- Boeriu OEV
- Boerner D
- Bogavac D
- Bogdanchikov AG
- Bohm C
- Boisvert V
- Bokan P
- Bold T
- Bolz AE
- Bomben M
- Bona M
- Bonilla JS
- Boonekamp M
- Booth CD
- Borecka-Bielska HM
- Borgna LS
- Borisov A
- Borissov G
- Bortfeldt J
- Bortoletto D
- Boscherini D
- Bosman M
- Bostanabad MG
- Bouaouda K
- Boudreau J
- Bouhova-Thacker E
- Boumediene D
- Bourdarios CA
- Boutle SK
- Boveia A
- Boyd J
- Boye D
- Boyko IR
- Bozson AJ
- Bracinik J
- Brahimi N
- Brandt G
- Brandt O
- Braren F
- Brau B
- Brau JE
- Brendlinger K
- Brenner L
- Brenner R
- Bressler S
- Bret MC
- Brickwedde B
- Briglin DL
- Britton D
- Britzger D
- Brock I
- Brock R
- Brooijmans G
- Brooks WK
- Brost E
- Bruncko D
- Bruni A
- Bruni G
- Bruni LS
- Bruno S
- Bruschi M
- Bruscino N
- Bryngemark L
- Buanes T
- Buat Q
- Buchholz P
- Buckley AG
- Budagov IA
- Buehrer F
- Buescher V
- Bugge MK
- Bulekov O
- Bullard BA
- Burch TJ
- Burdin S
- Burgard CD
- Burger AM
- Burghgrave B
- Burr JTP
- Burton CD
- Burzynski JC
- Buschmann E
- Bussey PJ
- Butler JM
- Buttar CM
- Butterworth JM
- Butti P
- Buttinger W
- Buzatu A
- Buzykaev AR
- Bylund OB
- Cabras G
- Cabrera Urban S
- Caforio D
- Cai H
- Cairo VMM
- Cakir IT
- Cakir O
- Calace N
- Calafiura P
- Calderini G
- Calfayan P
- Callea G
- Caloba LP
- Caltabiano A
- Calvente Lopez S
- Calvet D
- Calvet S
- Calvet TP
- Calvetti M
- Camarda S
- Camarero Munoz D
- Camarri P
- Camelia EA
- Camerlingo MT
- Cameron D
- Camincher C
- Campana S
- Campanelli M
- Camplani A
- Campoverde A
- Canale V
- Canesse A
- Cantero J
- Cao T
- Cao Y
- Capriles FGD
- Capua M
- Cardarelli R
- Cardillo F
- Carducci G
- Carli I
- Carli T
- Carlino G
- Carlson BT
- Carlson EM
- Carminati L
- Carney RMD
- Caron S
- Carquin E
- Carra S
- Carter JWS
- Carter TM
- Casado MP
- Casha AF
- Castillo Garcia L
- Castillo Gimenez V
- Castillo FL
- Castillo LRF
- Castro NF
- Catinaccio A
- Catmore JR
- Cattai A
- Cavaliere V
- Cavallaro E
- Cavasinni V
- Celebi E
- Celli F
- Cerda Alberich L
- Cerny K
- Cerqueira AS
- Cerri A
- Cerrito L
- Cerutti F
- Cervelli A
- Cetin SA
- Chadi Z
- Chakraborty D
- Chan J
- Chan WS
- Chan WY
- Chapman JD
- Chargeishvili B
- Charlton DG
- Charman TP
- Chau CC
- Che S
- Chekanov S
- Chekulaev S
- Chelkov GA
- Chen B
- Chen C
- Chen CH
- Chen H
- Chen J
- Chen S
- Chen SJ
- Chen X
- Chen Y
- Chen Y-H
- Cheng HC
- Cheng HJ
- Cheplakov A
- Cheremushkina E
- Cheu E
- Cheung K
- Chevalerias TJA
- Chevalier L
- Chiarella V
- Chiarelli G
- Chiodini G
- Chisholm AS
- Chitan A
- Chiu I
- Chiu YH
- Chizhov M
- Choi K
- Chomont AR
- Chouridou S
- Chow YS
- Christopher LD
- Chu MC
- Chu X
- Chudoba J
- Chwastowski JJ
- Chytka L
- Cieri D
- Ciesla KM
- Cinca D
- Cindro V
- Cioara IA
- Ciocio A
- Cirotto F
- Citron ZH
- Citterio M
- Ciubotaru DA
- Ciungu BM
- Clark A
- Clark MR
- Clark PJ
- Clawson SE
- Clement C
- Coadou Y
- Cobal M
- Coccaro A
- Cochran J
- Cohen H
- Coimbra AEC
- Cole B
- Colijn AP
- Collot J
- Conde Muino P
- Connell SH
- Connelly IA
- Constantinescu S
- Conventi F
- Cooper-Sarkar KAM
- Cormier F
- Cormier KJR
- Cornell SD
- Corpe LD
- Corradi M
- Corrado JG
- Correia AMH
- Corrigan EE
- Corriveau F
- Costa MJ
- Costanza F
- Costanzo D
- Cowan G
- Cowley JW
- Crane J
- Cranmer K
- Crawley SJ
- Creager RA
- Crepe-Renaudin S
- Crescioli F
- Cristinziani M
- Croft V
- Crosetti G
- Cueto A
- Cukierman AR
- Cunningham WR
- Czekierda S
- Czodrowski P
- Czurylo MM
- D'amen G
- D'Amico V
- D'Auria S
- D'Eramo L
- D'onofrio A
- D'Onofrio M
- Da Via C
- Dabrowski W
- Dachs F
- Dado T
- Dahbi S
- Dai T
- Dallapiccola C
- Dam M
- Damazio DO
- Damp J
- Dandoy JR
- Daneri MF
- Dann NS
- Danninger M
- Dao V
- Darbo G
- Dartsi O
- Dattagupta A
- Daubney T
- David C
- Davidek T
- Davis DR
- Dawson I
- de Andrade Filho LM
- De Asmundis R
- De Beurs M
- De Castro S
- De Cecco S
- De Groot N
- de Jong P
- De la Torre H
- de Lima DEF
- De Lima RT
- De Maria A
- De Pedis D
- De Regie JBDV
- de Renstrom PAB
- De Salvo A
- De Sanctis U
- De Santis M
- De Santo A
- De Sousa MJDCS
- De K
- Debenedetti C
- Dedovich D
- Deiana AM
- Del Peso J
- Delgove D
- Deliot F
- Delitzsch CM
- Dell'Acqua A
- Dell'Asta L
- Della Pietra M
- Della Volpe D
- Delmastro M
- Delporte C
- Delsart PA
- DeMarco DA
- Demers S
- Demichev M
- Demontigny G
- Denisov SP
- Derendarz D
- Derkaoui JE
- Derue F
- Dervan P
- Desch K
- Deterre C
- Dette K
- Deuren M
- Deutsch C
- Devesa MR
- Deviveiros PO
- Di Bello FA
- Di Ciaccio A
- Di Ciaccio L
- Di Clemente WK
- Di Donato C
- Di Girolamo A
- Di Gregorio G
- Di Micco B
- Di Nardo R
- Di Petrillo KF
- Di Sipio R
- Diaconu C
- Dias Do Vale T
- Dias FA
- Diaz LP
- Diaz MA
- Diaz YD
- Dickinson J
- Diehl EB
- Dietrich J
- Dimitrievska A
- Ding W
- Dingfelder J
- Dittus F
- Djama F
- Djobava T
- Djuvsland J
- Do Vale MAB
- Dobre M
- Dodsworth D
- Doglioni C
- Dolejsi J
- Dolezal Z
- Dominguez LP
- Don MMR
- Donadelli M
- Donaldson CP
- Dong B
- Donini J
- Donszelmann TC
- Dopke J
- Doria A
- Dova MT
- Doyle AT
- Drechsler E
- Dreyer E
- Dreyer T
- Drobac AS
- du Pree TA
- Du D
- Duan Y
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- Zaripovas DR
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- Zemaityte G
- Zeng JC
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- Zhemchugov A
- Zheng Z
- Zhong D
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- Zhulanov V
- Zieminska D
- Zimine N
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zu Theenhausen HM
- Zwalinski L
- Publication venue
- AMER PHYSICAL SOC
- Publication date
- 25/09/2020
- Field of study
This Letter describes a search for narrowly resonant new physics using a machine-learning anomaly
detection procedure that does not rely on signal simulations for developing the analysis selection. Weakly
supervised learning is used to train classifiers directly on data to enhance potential signals. The targeted
topology is dijet events and the features used for machine learning are the masses of the two jets. The
resulting analysis is essentially a three-dimensional search A → BC, for mA ∼ OðTeVÞ, mB; mC ∼
Oð100 GeVÞ and B, C are reconstructed as large-radius jets, without paying a penalty associated with
a large trials factor in the scan of the masses of the two jets. The full run 2 ffiffi
s p ¼ 13 TeV pp collision
dataset of 139 fb−1 recorded by the ATLAS detector at the Large Hadron Collider is used for the search.
There is no significant evidence of a localized excess in the dijet invariant mass spectrum between 1.8 and
8.2 TeV. Cross-section limits for narrow-width A, B, and C particles vary with mA, mB, and mC. For
example, when mA ¼ 3 TeV and mB ≳ 200 GeV, a production cross section between 1 and 5 fb is
excluded at 95% confidence level, depending on mC. For certain masses, these limits are up to 10 times
more sensitive than those obtained by the inclusive dijet search. These results are complementary to the
dedicated searches for the case that B and C are standard model boson
Measurement of the energy asymmetry in t(t)over-barj production at 13 TeV with the ATLAS experiment and interpretation in the SMEFT framework
- Author
- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- Aboulhorma A
- Abramowicz H
- Abreu H
- Abud A Abed
- Abulaiti Y
- Abusleme Hoffman AC
- Acharya BS
- Achkar B
- Adam L
- Adamczyk L
- Adamek L
- Addepalli S
- Adelman J
- Adiguzel A
- Adorni S
- Adye T
- Affolder AA
- Afik Y
- Agapopoulou C
- Agaras MN
- Agarwala J
- Aggarwal A
- Agheorghiesei C
- Aguilar-Saavedra JA
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ai X
- Aielli G
- Aizenberg I
- Akatsuka S
- Akbiyik M
- Akesson TPA
- Akimov A
- Al Khoury K
- Alberghi GL
- Albert J
- Albicocco P
- Alconada Verzini MJ
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi A
- Alfonsi F
- Alhroob M
- Ali B
- Ali S
- Aliev M
- Alimonti G
- Allaire C
- Allbrooke BMM
- Allport PP
- Aloisio A
- Alonso F
- Alpigiani C
- Alvarez Estevez M
- Alves FL Lucio
- Alviggi MG
- Ambler A
- Ambroz L
- Amelung C
- Amidei D
- Amor Dos Santos SP
- Amoroso S
- Amos KR
- Amrouche CS
- Ananiev V
- Anastopoulos C
- Andari N
- Andeen T
- Anders JK
- Andrean SY
- Andreazza A
- Angelidakis S
- Angerami A
- Anisenkov A
- Annovi A
- Antel C
- Anthony MT
- Antipov E
- Antonelli M
- Antrim DJA
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- Aparo MA
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- Astigarraga ME Pozo
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- Austrup VA
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- Zhemchugov A
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- Publication venue
- 'Springer Fachmedien Wiesbaden GmbH'
- Publication date
- 28/04/2022
- Field of study
A measurement of the energy asymmetry in jet-associated top-quark pair production is presented using 139fb−1
139
fb
-
1
of data collected by the ATLAS detector at the Large Hadron Collider during pp collisions at s=13TeV
s
=
13
TeV
. The observable measures the different probability of top and antitop quarks to have the higher energy as a function of the jet scattering angle with respect to the beam axis. The energy asymmetry is measured in the semileptonic ttˉ
t
t
¯
decay channel, and the hadronically decaying top quark must have transverse momentum above 350GeV
350
GeV
. The results are corrected for detector effects to particle level in three bins of the scattering angle of the associated jet. The measurement agrees with the SM prediction at next-to-leading-order accuracy in quantum chromodynamics in all three bins. In the bin with the largest expected asymmetry, where the jet is emitted perpendicular to the beam, the energy asymmetry is measured to be −0.043±0.020
-
0.043
±
0.020
, in agreement with the SM prediction of −0.037±0.003
-
0.037
±
0.003
. Interpreting this result in the framework of the Standard Model effective field theory (SMEFT), it is shown that the energy asymmetry is sensitive to the top-quark chirality in four-quark operators and is therefore a valuable new observable in global SMEFT fits
Configuration and performance of the ATLAS b-jet triggers in Run 2
- Author
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- Abbott B
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- Zhemchugov A
- Zheng Z
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- Publication venue
- 'Springer Fachmedien Wiesbaden GmbH'
- Publication date
- 01/12/2021
- Field of study
Several improvements to the ATLAS triggers used to identify jets containing b-hadrons (b-jets) were implemented for data-taking during Run 2 of the Large Hadron Collider from 2016 to 2018. These changes include reconfiguring the b-jet trigger software to improve primary-vertex finding and allow more stable running in conditions with high pile-up, and the implementation of the functionality needed to run sophisticated taggers used by the offline reconstruction in an online environment. These improvements yielded an order of magnitude better light-flavour jet rejection for the same b-jet identification efficiency compared to the performance in Run 1 (2011–2012). The efficiency to identify b-jets in the trigger, and the conditional efficiency for b-jets that satisfy offline b-tagging requirements to pass the trigger are also measured. Correction factors are derived to calibrate the b-tagging efficiency in simulation to match that observed in data. The associated systematic uncertainties are substantially smaller than in previous measurements. In addition, b-jet triggers were operated for the first time during heavy-ion data-taking, using dedicated triggers that were developed to identify semileptonic b-hadron decays by selecting events with geometrically overlapping muons and jets
Measurements of W+W−+ ≥ 1 jet production cross-sections in pp collisions at s = 13 TeV with the ATLAS detector
- Author
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- Zeißner SV
- Zemaityte G
- Zeng JC
- Zenin O
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- Zerradi S
- Zerwas D
- Zgubič M
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- Zhang G
- Zhang J
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- Zhang R
- Zhang S
- Zhang X
- Zhang X
- Zhang Z
- Zhao P
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zheng Z
- Zhong D
- Zhou B
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- Zhu C
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- Zhukov K
- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zou W
- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/06/2021
- Field of study
Fiducial and differential cross-section measurements of W+W− production in
association with at least one hadronic jet are presented. These measurements are sensitive
to the properties of electroweak-boson self-interactions and provide a test of perturbative
quantum chromodynamics and the electroweak theory. The analysis is performed using
proton-proton collision data collected at p
s = 13TeV with the ATLAS experiment, corresponding
to an integrated luminosity of 139 fb−1. Events are selected with exactly one oppositely
charged electron-muon pair and at least one hadronic jet with a transverse momentum
of pT > 30 GeV and a pseudorapidity of |�| < 4.5. After subtracting the background
contributions and correcting for detector effects, the jet-inclusive W+W−+ � 1 jet fiducial
cross-section and W+W−+ jets differential cross-sections with respect to several kinematic
variables are measured. These measurements include leptonic quantities, such as the lepton
transverse momenta and the transverse mass of the W+W− system, as well as jet-related
observables such as the leading jet transverse momentum and the jet multiplicity. Limits on
anomalous triple-gauge-boson couplings are obtained in a phase space where interference
between the Standard Model amplitude and the anomalous amplitude is enhanced
Measurement of the tt¯tt¯ production cross section in pp collisions at √s=13 TeV with the ATLAS detector
- Author
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- Zeißner SV
- Zemaityte G
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- Zhemchugov A
- Zheng Z
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- Zhukov K
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- Zieminska D
- Zimine NI
- Zimmermann S
- Ziolkowski M
- Zoccoli A
- Zoch K
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- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 16/11/2021
- Field of study
A measurement of four-top-quark production using proton-proton collision data at a centre-of-mass energy of 13 TeV collected by the ATLAS detector at the Large Hadron Collider corresponding to an integrated luminosity of 139 fb−1 is presented. Events are selected if they contain a single lepton (electron or muon) or an opposite-sign lepton pair, in association with multiple jets. The events are categorised according to the number of jets and how likely these are to contain b-hadrons. A multivariate technique is then used to discriminate between signal and background events. The measured four-top-quark production cross section is found to be 26+17−15 fb, with a corresponding observed (expected) significance of 1.9 (1.0) standard deviations over the background-only hypothesis. The result is combined with the previous measurement performed by the ATLAS Collaboration in the multilepton final state. The combined four-top-quark production cross section is measured to be 24+7−6 fb, with a corresponding observed (expected) signal significance of 4.7 (2.6) standard deviations over the background-only predictions. It is consistent within 2.0 standard deviations with the Standard Model expectation of 12.0 ± 2.4 fb
Muon reconstruction and identification efficiency in ATLAS using the full Run 2 pp collision data set at \sqrt{s}=13 TeV
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- Milosavljevic MV
- Milov A
- Milstead DA
- Minaenko AA
- Minashvili IA
- Mince L
- Mincer AI
- Mindur B
- Mineev M
- Minegishi Y
- Mino Y
- Miotto GL
- Mir LM
- Mironova M
- Mitani T
- Mitrevski J
- Mitsou VA
- Mittal M
- Miu O
- Miucci A
- Miyagawa PS
- Mizukami A
- Mjoernmark JU
- Mkrtchyan T
- Mlynarikova M
- Moa T
- Mobius S
- Mochizuki K
- Moder P
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- Mohamed ATA
- Mohapatra S
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- Monnier E
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- Monzani S
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- Morgenstern S
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- Morii M
- Morinaga M
- Morisbak V
- Morley AK
- Mornacchi G
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- Moschovakos P
- Moser B
- Mosidze M
- Moskalets T
- Moskvitina P
- Moss J
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- Muenstermann D
- Muino PC
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- Munoz DC
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- Murrone A
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- Muskinja M
- Mwewa C
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- Myers G
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- Nanjo H
- Napolitano F
- Narayan R
- Naryshkin I
- Naseri M
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- Navarro G
- Navarro JEG
- Navarro LB
- Nechaeva PY
- Nechansky F
- Neep TJ
- Negri A
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- Nellist C
- Nelson C
- Nelson ME
- Nemecek S
- Nessi M
- Neubauer MS
- Neuhaus F
- Neumann M
- Newhouse R
- Newman PR
- Ng CW
- Ng YS
- Ng YWY
- Ngair B
- Nguyen HDN
- Nibigira E
- Nickerson RB
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- Nielsen J
- Niemeyer M
- Nikiforou N
- Nikolaenko V
- Nikolic-Audit I
- Nikolopoulos K
- Nilsson P
- Nindhito HR
- Nisati A
- Nishu N
- Nisius R
- Nitsche I
- Nitta T
- Nobe T
- Noel DL
- Noguchi Y
- Nomidis I
- Nomura MA
- Nordberg M
- Novak J
- Novak T
- Novgorodova O
- Novotny R
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- Nurse E
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- O'neill AP
- O'Shea V
- Oakham FG
- Ocariz J
- Ochi A
- Ochoa I
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- Oda S
- Odaka S
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- Ogrodnik A
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- Oishi R
- Ojeda ML
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- Okazaki Y
- Okumura Y
- Olariu A
- Oliveira MVS
- Oliver JL
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- Onofre A
- Onyisi PUE
- Oppen H
- Oreglia MJ
- Orellana GE
- Orestano D
- Orlando N
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- Otero y Garzon G
- Otono H
- Ott PS
- Ottino GJ
- Ouchrif M
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- Palacino G
- Palazzo S
- Palestini S
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- Papadatos C
- Papageorgiou K
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- Paramonov A
- Paraskevopoulos C
- Pardos CD
- Parida B
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- Parsons JA
- Parzefall U
- Pascual JAG
- Pascuzzi VR
- Pasner JMP
- Pasquali F
- Pasqualucci E
- Passaggio S
- Pastor ET
- Pastor OE
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- Pasuwan P
- Pataraia S
- Pater JR
- Pathak A
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- Paz IL
- Pearkes J
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- Peixoto APP
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- Pereira RA
- Perepelitsa DV
- Perez MV
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- Pernegger H
- Perrella S
- Perrevoort A
- Peso JD
- Peters K
- Peters RFY
- Petersen BA
- Petersen TC
- Petit E
- Petousis V
- Petridou C
- Petrucci F
- Pettee M
- Pettersson NE
- Petukhova K
- Peyaud A
- Pezoa R
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- Pham T
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- Phipps MW
- Piacquadio G
- Pianori E
- Picazio A
- Pickles RH
- Piegaia R
- Pietreanu D
- Pilcher JE
- Pilkington AD
- Pinamonti M
- Pineda AS
- Pinfold JL
- Pino SAO
- Pitt M
- Pizzimento L
- Pizzini A
- Pleier M-A
- Plesanovs V
- Pleskot V
- Plotnikova E
- Podberezko P
- Poettgen R
- Poggi R
- Poggioli L
- Pogrebnyak I
- Pohl D
- Pokharel I
- Polesello G
- Poley A
- Policicchio A
- Polifka R
- Polini A
- Pollard CS
- Polychronakos V
- Ponce JMI
- Ponomarenko D
- Pontecorvo L
- Popa S
- Popeneciu GA
- Portales L
- Pospisil S
- Potamianos K
- Potrap IN
- Potter CJ
- Potti H
- Poulsen T
- Poveda J
- Powell TD
- Pownall G
- Pozo JAA
- Pralavorio P
- Prapa MM
- Pree TAD
- Prell S
- Price D
- Primavera M
- Proffitt ML
- Proklova N
- Prokofiev K
- Prokoshin F
- Protopopescu S
- Proudfoot J
- Przybycien M
- Pudzha D
- Puri A
- Puzo P
- Pyatiizbyantseva D
- Qian J
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- Quintero DMP
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- Ragusa F
- Rahal G
- Raine JA
- Rajagopalan S
- Ramos JM
- Ran K
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- Rauch DM
- Rauscher F
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- Ravina B
- Ravinovich I
- Rawling JH
- Raymond M
- Read AL
- Readioff NP
- Reale M
- Rebuzzi DM
- Redlinger G
- Reeves K
- Reikher D
- Reiss A
- Rej A
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- Renardi A
- Renda M
- Rendel MB
- Rennie AG
- Renous DS
- Renteria CG
- Resconi S
- Resseguie ED
- Rettie S
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- Reynolds E
- Rezanova OL
- Reznicek P
- Ricci E
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- Richter S
- Richter-Was E
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- Rieck P
- Rifki O
- Rijssenbeek M
- Rimoldi A
- Rimoldi M
- Rinaldi L
- Rinn TT
- Ripellino G
- Riu I
- Rivadeneira P
- Rizatdinova F
- Rizvi E
- Rizzi C
- Robertson SH
- Robin M
- Robinson D
- Robson A
- Rocchi A
- Roda C
- Rodriguez AR
- Rodriguez GRG
- Roe S
- Roehrig R
- Roggel J
- Rohne O
- Rojas JGRG
- Rojas RA
- Roland B
- Roland CPA
- Roloff J
- Romaniouk A
- Romano M
- Rompotis N
- Ronzani M
- Roos L
- Rosati S
- Rosin G
- Rosser BJ
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- Rossi E
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- Rossi LP
- Rossini L
- Rosten R
- Rotaru M
- Rottler B
- Rousseau D
- Rovelli G
- Roy A
- Roy D
- Rozanov A
- Rozas AJ
- Rozen Y
- Ruan X
- Ruehr F
- Ruettinger EM
- Ruggeri TA
- Ruiz-Martinez A
- Rummler A
- Rurikova Z
- Rusakovich NA
- Russell HL
- Rustige L
- Rutherfoord JP
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- Rybkin G
- Rye EB
- Ryzhov A
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- Sabetta L
- Sacerdoti S
- Sadrozinski HF-W
- Sadykov R
- Saenz SRP
- Safdari M
- Saha P
- Saha S
- Sahinsoy M
- Sahu A
- Saimpert M
- Saito M
- Saito T
- Sakamoto H
- Salamani D
- Salamanna G
- Salas AS
- Salnikov A
- Salt J
- Salvatore D
- Salvatore F
- Salvucci A
- Salzburger A
- Samani BS
- Samarati J
- Sammel D
- Sampsonidis D
- Sampsonidou D
- Sanchez CAS
- Sanchez FJM
- Sanchez J
- Sanchez LP
- Sandaker H
- Sander CO
- Sanderswood IG
- Sandhoff M
- Sandoval C
- Sankey DPC
- Sannino M
- Sano Y
- Sansoni A
- Santoni C
- Santos H
- Santos SPAD
- Santpur SN
- Santra A
- Santurio EV
- Saoucha KA
- Sapronov A
- Saraiva JG
- Sasaki O
- Sato K
- Sauerburger F
- Sauvan E
- Savard P
- Sawada R
- Sawyer C
- Sawyer L
- Sbarra C
- Sbrizzi A
- Scanlon T
- Schaarschmidt J
- Schacht P
- Schaefer D
- Schaefer L
- Schaefer U
- Schaffer AC
- Schaile D
- Schamberger RD
- Schanet E
- Scharf C
- Scharmberg N
- Schegelsky VA
- Scheirich D
- Schenck F
- Schernau M
- Schiavi C
- Schildgen LK
- Schillaci ZM
- Schioppa EJ
- Schioppa M
- Schleicher KE
- Schlenker S
- Schmidt-Sommerfeld KR
- Schmieden K
- Schmitt C
- Schmitt S
- Schoeffel L
- Schoening A
- Scholer PG
- Schopf E
- Schott M
- Schouwenberg JFP
- Schovancova J
- Schramm S
- Schroeder F
- Schroeder TV
- Schulte A
- Schultz-Coulon H-C
- Schumacher M
- Schumm BA
- Schune P
- Schwartzman A
- Schwarz TA
- Schwemling P
- Schwienhorst R
- Sciandra A
- Sciolla G
- Scuri F
- Scutti F
- Scyboz LM
- Seabra LFO
- Sebastiani CD
- Sedlaczek K
- Seema P
- Seidel SC
- Seiden A
- Seidlitz BD
- Seiss T
- Seitz C
- Seixas JM
- Sekhniaidze G
- Sekula SJ
- Semprini-Cesari N
- Sen S
- Serfon C
- Serin L
- Serkin L
- Sessa M
- Severini H
- Sevova S
- Sforza F
- Sfyrla A
- Shabalina E
- Shahinian JD
- Shaikh NW
- Shan LY
- Shapiro M
- Sharma A
- Sharma AS
- Shatalov PB
- Shaw K
- Shaw SM
- Shehade M
- Shen Y
- Sherman AD
- Sherwood P
- Shi L
- Shimmin CO
- Shimogama Y
- Shimojima M
- Shinner JD
- Shipsey IPJ
- Shirabe S
- Shiyakova M
- Shlomi J
- Shmeleva A
- Shochet MJ
- Shojaii J
- Shope DR
- Shrestha S
- Shrif EM
- Shroff MJ
- Shulga E
- Sicho P
- Sickles AM
- Sidiropoulou O
- Sidoti A
- Siegert F
- Sijacki D
- Silva MJ
- Silverstein SB
- Simion S
- Simoniello R
- Simpson-allsop CJ
- Simsek S
- Sinervo P
- Sinetckii V
- Singh S
- Sinha S
- Sioli M
- Siral I
- Sivoklokov SY
- Sjoelin J
- Skaf A
- Skorda E
- Skubic P
- Slawinska M
- Sliwa K
- Smakhtin V
- Smart BH
- Smiesko J
- Smirnov N
- Smirnov SY
- Smirnov Y
- Smirnova LN
- Smirnova O
- Smith EA
- Smith HA
- Smizanska M
- Smolek K
- Smykiewicz A
- Snesarev AA
- Snoek HL
- Snyder IM
- Snyder S
- Sobie R
- Soffer A
- Sogaard A
- Sohns F
- Sola JDB
- Soldatov EY
- Soldevila U
- Solis AL
- Solodkov AA
- Soloshenko A
- Solovyanov OV
- Solovyev V
- Sommer P
- Son H
- Sonay A
- Song W
- Song WY
- Sopczak A
- Sopio AL
- Sopkova F
- Sottocornola S
- Soualah R
- Soukharev AM
- South D
- Spagnolo S
- Spalla M
- Spangenberg M
- Spano F
- Sperlich D
- Spieker TM
- Spigo G
- Spina M
- Spiteri DP
- Spousta M
- Stabile A
- Staerz S
- Stamas BL
- Stamen R
- Stamenkovic M
- Stampekis A
- Stanecka E
- Stanislaus B
- Stanitzki MM
- Stankaityte M
- Stapf B
- Starchenko EA
- Stark GH
- Stark J
- Staroba P
- Starovoitov P
- Staszewski R
- Stavropoulos G
- Stegler M
- Steinberg P
- Steinhebel AL
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- Stelzer HJ
- Stelzer-Chilton O
- Stenzel H
- Stevenson TJ
- Stewart GA
- Stockton MC
- Stoicea G
- Stolarski M
- Stonjek S
- Straessner A
- Strandberg J
- Strandberg S
- Strauss M
- Strebler T
- Strizenec P
- Stroehmer R
- Strom DM
- Stroynowski R
- Strubig A
- Stucci SA
- Stugu B
- Stupak J
- Styles NA
- Su D
- Su W
- Su X
- Suarez NB
- Suarez RG
- Sulin VV
- Sullivan MJ
- Sultan DMS
- Sultansoy S
- Sumida T
- Sun S
- Sun X
- Suster CJE
- Sutton MR
- Suzuki S
- svatos M
- Swiatlowski M
- Swift SP
- Swirski T
- Sydorenko A
- Sykora I
- Sykora M
- Sykora T
- Ta D
- Tackmann K
- Taenzer J
- Taffard A
- Tafirout R
- Tagiev E
- Taibah RHM
- Takashima R
- Takeda K
- Takeshita T
- Takeva EP
- Takubo Y
- Talby M
- Talyshev AA
- Tam KC
- Tame ZPA
- Tamir NM
- Tanaka J
- Tanaka R
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- Tarem S
- Tariq K
- Tarna G
- Tartarelli GF
- Tas P
- Tasevsky M
- Tassi E
- Tateno G
- Tayalati Y
- Taylor AJ
- Taylor GN
- Taylor W
- Teagle H
- Tee AS
- Tehrani FS
- Teixeira-Dias P
- Teoh JJ
- Terashi K
- Terron J
- Terzo S
- Testa M
- Teuscher RJ
- Themistokleous N
- Theveneaux-Pelzer T
- Thomas DW
- Thomas JP
- Thompson EA
- Thompson PD
- Thomson E
- Thorpe EJ
- Tikhomirov VO
- Tikhonov YA
- Timoshenko S
- Tipton P
- Tisserant S
- Todome K
- Todorova-Nova S
- Todt S
- Tojo J
- Tokar S
- Tokushuku K
- Tolley E
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- Torregrosa EF
- Torrence E
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- Tosciri C
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- Trigger IM
- Trincaz-Duvoid S
- Trischuk DA
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- Trocme B
- Trofymov A
- Troncon C
- Trovato F
- Truong L
- Trzebinski M
- Trzupek A
- Tsai F
- Tsiareshka PV
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- Tsiskaridze V
- Tskhadadze EG
- Tsopoulou M
- Tsukerman II
- Tsulaia V
- Tsuno S
- Tsybychev D
- Tu Y
- Tudorache A
- Tudorache V
- Tuna AN
- Turchikhin S
- Turgeman D
- Turner RJ
- Turra R
- Tuts PM
- Tzamarias S
- Tzovara E
- Uchida K
- Ukegawa F
- Unal G
- Unal M
- Undrus A
- Unel G
- Ungaro FC
- Unno Y
- Uno K
- Urban J
- Urban SC
- Urquijo P
- Usai G
- Uysal Z
- Vacek V
- Vachon B
- Vadla KOH
- Vafeiadis T
- Vaidya A
- Valderanis C
- Valente M
- Valentinetti S
- Valero A
- Valery L
- Vallance RA
- Vallier A
- Van Daalen TR
- Van Gemmeren P
- Van Stroud S
- Van Vulpen I
- Vanadia M
- Vandelli W
- Vandenbroucke M
- Vandewall ER
- Vannicola D
- Vari R
- Varnes EW
- Varni C
- Varol T
- Varouchas D
- Varvell KE
- Vasile ME
- Vasquez GA
- Vazeille F
- Vazquez CJB
- Vazquez JGP
- Veatch J
- Vecchio V
- Veen MJ
- Veloce LM
- Veloso F
- Veneziano S
- Ventura A
- Vera AMR
- Verbytskyi A
- Vercesi V
- Verducci M
- Vergara JCR
- Vergis C
- Verkerke W
- Vermeulen AT
- Vermeulen JC
- Vernieri C
- Verschuuren PJ
- Verzini MJA
- Vetterli MC
- Vickey T
- Viehhauser GHA
- Vigani L
- Villa M
- Villhauer EM
- Vilucchi E
- Vincter MG
- Virdee GS
- Vishwakarma A
- Vittori C
- Vivarelli I
- Vogel M
- Vokac P
- von Buddenbrock SE
- Von Toerne E
- Vorobel V
- Vorobev K
- Vos M
- Vossebeld JH
- Vozak M
- Vranjes N
- Vrba V
- Vreeswijk M
- Vu NK
- Vuillermet R
- Vukotic I
- Wada S
- Wagner P
- Wagner W
- Wagner-Kuhr J
- Wahdan S
- Wahlberg H
- Wakasa R
- Walbrecht VM
- Walder J
- Walker R
- Walker SD
- Walkowiak W
- Wallangen V
- Walls FMG
- Wang AM
- Wang AZ
- Wang C
- Wang C
- Wang H
- Wang H
- Wang J
- Wang P
- Wang Q
- Wang R
- Wang R
- Wang R-J
- Wang SM
- Wang W
- Wang WT
- Wang WX
- Wang Y
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- Wanotayaroj C
- Warburton A
- Ward CP
- Ward RJ
- Warrack N
- Watson AT
- Watson MF
- Watts G
- Waugh BM
- Webb AF
- Weber C
- Weber MS
- Weber SA
- Weber SM
- Wei Y
- Weidberg AR
- Weingarten J
- Weirich M
- Weiser C
- Wells PS
- Wenaus T
- Wendland B
- Wengler T
- Wenig S
- Wermes N
- Wessels M
- Weston TD
- Whalen K
- Wharton AM
- White A
- White AS
- White MJ
- Whiteson D
- Whitmore BW
- Wiedenmann W
- Wiel C
- Wielers M
- Wieseotte N
- Wiglesworth C
- Wiik-Fuchs LAM
- Wilkens HG
- Wilkins LJ
- Williams DM
- Williams HH
- Williams S
- Willocq S
- Windischhofer PJ
- Wingerter-Seez I
- Winkels E
- Winklmeier F
- Winter BT
- Wittgen M
- Wobisch M
- Woelker R
- Wolf A
- Wollrath J
- Wolter MW
- Wolters H
- Wong VWS
- Wongel AF
- Woods NL
- Worm SD
- Wosiek BK
- Wozniak KW
- Wraight K
- Wu SL
- Wu X
- Wu Y
- Wuerzinger J
- Wyatt TR
- Wynne BM
- Xella S
- Xiang J
- Xiao X
- Xie X
- Xiotidis I
- Xu D
- Xu H
- Xu H
- Xu L
- Xu R
- Xu T
- Xu W
- Xu Y
- Xu Z
- Xu Z
- Yabsley B
- Yacoob S
- Yallup DP
- Yamaguchi N
- Yamaguchi Y
- Yamamoto A
- Yamatani M
- Yamazaki T
- Yamazaki Y
- Yan J
- Yan Z
- Yang HJ
- Yang HT
- Yang S
- Yang T
- Yang X
- Yang X
- Yang Y
- Yang Z
- Yao W-M
- Yap YC
- Ye H
- Ye J
- Ye S
- Yeletskikh I
- Yexley MR
- Yigitbasi E
- Yildiz HD
- Yin P
- Yorita K
- Yoshihara K
- Young C
- Young CJS
- Yu J
- Yuan R
- Yue X
- Zaazoua M
- Zabinski B
- Zacharis G
- Zaffaroni E
- Zahreddine J
- Zaitsev AM
- Zakareishvili T
- Zakharchuk N
- Zambito S
- Zanzi D
- Zeissner SV
- Zeitnitz C
- Zemaityte G
- Zeng JC
- Zenin O
- Zenis T
- Zerwas D
- Zgubic M
- Zhang B
- Zhang DF
- Zhang G
- Zhang J
- Zhang K
- Zhang L
- Zhang L
- Zhang M
- Zhang R
- Zhang S
- Zhang X
- Zhang X
- Zhang Y
- Zhang Z
- Zhang Z
- Zhao P
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zheng Z
- Zhong D
- Zhou B
- Zhou C
- Zhou H
- Zhou M
- Zhou N
- Zhou Y
- Zhu C
- Zhu CG
- Zhu H
- Zhu HL
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zwalinski L
- Publication venue
- 'Springer Fachmedien Wiesbaden GmbH'
- Publication date
- 01/01/2021
- Field of study
This article documents the muon reconstruction and identification efficiency obtained by the ATLAS experiment for 139 \hbox {fb}^{-1} of pp collision data at \sqrt{s}=13 TeV collected between 2015 and 2018 during Run 2 of the LHC. The increased instantaneous luminosity delivered by the LHC over this period required a reoptimisation of the criteria for the identification of prompt muons. Improved and newly developed algorithms were deployed to preserve high muon identification efficiency with a low misidentification rate and good momentum resolution. The availability of large samples of Z\rightarrow \mu \mu and J/\psi \rightarrow \mu \mu decays, and the minimisation of systematic uncertainties, allows the efficiencies of criteria for muon identification, primary vertex association, and isolation to be measured with an accuracy at the per-mille level in the bulk of the phase space, and up to the percent level in complex kinematic configurations. Excellent performance is achieved over a range of transverse momenta from 3 GeV to several hundred GeV, and across the full muon detector acceptance of |\eta |<2.7
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