224 research outputs found
Signaling Networks Associated with AKT Activation in Non-Small Cell Lung Cancer (NSCLC): New Insights on the Role of Phosphatydil-Inositol-3 kinase
- Author
- A Carnero
- A Di Cristofano
- A Jemal
- Alessandro Weisz
- Alfredo Fusco
- AS Tsao
- B Vanhaesebroeck
- BR Balsara
- BR Balsara
- C Bouchard
- C Garnis
- Carmela De Marco
- CF Mountain
- CX Xu
- D Malanga
- DA Altomare
- DL Rimm
- Donatella Malanga
- F Loupakis
- Fernanda Fabiani
- FR Hirsh
- G Wang
- G Wu
- Gaetano Rocco
- Gerardo Botti
- Giuseppe Pirozzi
- Giuseppe Viglietto
- GJ Riely
- H Endoh
- H Yamamoto
- I Vivanco
- J Abubaker
- J Brognard
- J Gandhi
- J Sambrook
- J Tsurutani
- JD Minna
- JF Liu
- JL Marks
- JM Kurie
- JM Tang
- K Oda
- K Stemke-Hale
- KJ Livak
- M Hanada
- Maria Ravo
- Marianna Scrima
- Michele Ceccarelli
- N Amodio
- N Chalhoub
- O Kawano
- P Chomczynski
- PG Rychahou
- Pietro Zoppoli
- PP Massion
- R Zufferey
- Renato Franco
- RM Memmott
- RR Reddel
- S Carvalho
- S Rodenhuis
- SA Aziz
- SH Lee
- SR Datta
- SS Hecht
- T Kirkegaard
- WT Lim
- Y Benjamini
- Y Lin
- Y Samuels
- Y Wang
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
Aberrant activation of PI3K/AKT signalling represents one of the most common molecular alterations in lung cancer, though the relative contribution of the single components of the cascade to the NSCLC development is still poorly defined. In this manuscript we have investigated the relationship between expression and genetic alterations of the components of the PI3K/AKT pathway [KRAS, the catalytic subunit of PI3K (p110α), PTEN, AKT1 and AKT2] and the activation of AKT in 107 surgically resected NSCLCs and have analyzed the existing relationships with clinico-pathologic features. Expression analysis was performed by immunohistochemistry on Tissue Micro Arrays (TMA); mutation analysis was performed by DNA sequencing; copy number variation was determined by FISH. We report that activation of PI3K/AKT pathway in Italian NSCLC patients is associated with high grade (G3–G4 compared with G1–G2; n = 83; p<0.05) and more advanced disease (TNM stage III vs. stages I and II; n = 26; p<0.05). In addition, we found that PTEN loss (41/104, 39%) and the overexpression of p110α (27/92, 29%) represent the most frequent aberration observed in NSCLCs. Less frequent molecular lesions comprised the overexpression of AKT2 (18/83, 22%) or AKT1 (17/96, 18%), and KRAS mutation (7/63, 11%). Our results indicate that, among all genes, only p110α overexpression was significantly associated to AKT activation in NSCLCs (p = 0.02). Manipulation of p110α expression in lung cancer cells carrying an active PI3K allele (NCI-H460) efficiently reduced proliferation of NSCLC cells in vitro and tumour growth in vivo. Finally, RNA profiling of lung epithelial cells (BEAS-2B) expressing a mutant allele of PIK3 (E545K) identified a network of transcription factors such as MYC, FOS and HMGA1, not previously recognised to be associated with aberrant PI3K signalling in lung cancer
Design and implementation of the canadian kidney disease cohort study (CKDCS): A prospective observational study of incident hemodialysis patients
- Author
- A Meguid El Nahas
- AF De Vecchi
- AJ Collins
- Aminu K Bello
- Anonymous
- Anonymous
- AS Levey
- B Manns
- BR Hemmelgarn
- Brenda Hemmelgarn
- Christopher Chan
- D Heng
- Daniel Holmes
- Dawn Opgenorth
- Deborah Zimmerman
- DS Lee
- ED Weinhandl
- F Borovecki
- G Eknoyan
- G Tripepi
- George Cembrowski
- H Quan
- HC Rayner
- JE Hux
- JIT Himmelfarb
- JJ Snyder
- John Gill
- KJ Jager
- KW Hong
- L Ding
- LA Mermel
- Marcello Tonelli
- Mohammad Karkhaneh
- MV Rocco
- N van der Bijl
- Natasha Wiebe
- P Ronco
- PA McFarlane
- PC Austin
- R Paniagua
- RA Kokotailo
- Rafael Sibrian
- Ravi Thadhani
- RL Pisoni
- S Fukuhara
- Scott Klarenbach
- SM Sozio
- Sophanny Tiv
- VS Stel
- Publication venue
- BioMed Central
- Publication date
- 01/01/2011
- Field of study
<p>Abstract</p> <p>Background</p> <p>Many nephrology observational studies use renal registries, which have well known limitations. The Canadian Kidney Disease Cohort Study (CKDCS) is a large prospective observational study of patients commencing hemodialysis in five Canadian centers. This study focuses on delineating potentially reversible determinants of adverse outcomes that occur in patients receiving dialysis for end-stage renal disease (ESRD).</p> <p>Methods/Design</p> <p>The CKDCS collects information on risk factors and outcomes, and stores specimens (blood, dialysate, hair and fingernails) at baseline and in long-term follow-up. Such specimens will permit measurements of biochemical markers, proteomic and genetic parameters (proteins and DNA) not measured in routine care. To avoid selection bias, all consenting incident hemodialysis patients at participating centers are enrolled, the large sample size (target of 1500 patients), large number of exposures, and high event rates will permit the exploration of multiple potential research questions.</p> <p>Preliminary Results</p> <p>Data on the baseline characteristics from the first 1074 subjects showed that the average age of patients was 62 (range; 50-73) years. The leading cause of ESRD was diabetic nephropathy (41.9%), and the majority of the patients were white (80.0%). Only 18.7% of the subjects received dialysis in a satellite unit, and over 80% lived within a 50 km radius of the nearest nephrologist's practice.</p> <p>Discussion</p> <p>The prospective design, detailed clinical information, and stored biological specimens provide a wealth of information with potential to greatly enhance our understanding of risk factors for adverse outcomes in dialysis patients. The scientific value of the stored patient tissue will grow as new genetic and biochemical markers are discovered in the future.</p
Plasma and cellular fibronectin: distinct and independent functions during tissue repair
- Author
- A Czirok
- A Gabrielli
- A Leask
- A Maqueda
- A Morla
- A Morla
- A Oomura
- A Rivera-Torres
- A Van Vliet
- A Woods
- A Yoneda
- AC Kauf
- AE Allio
- AF Muro
- AF Muro
- AF Oberhauser
- AH Limper
- AK Chauhan
- AR Pickford
- AR Pickford
- AS Meshel
- AT Vitale
- B Carnemolla
- B Geiger
- B Geiger
- B Hinz
- B Hinz
- BA Hocevar
- BJ Dzamba
- BJ Dzamba
- BJ Dzamba
- BR Tomasini-Johansson
- BR Tomasini-Johansson
- BS Weston
- C ffrench-Constant
- C Natal
- C Spitzfaden
- C Wu
- C Wu
- C Zhong
- CA Lemmon
- CB Arrington
- CC Tate
- CJ Millard
- CJ Roberts
- CL Wilson
- CM Klass
- CN Rao
- CP Denton
- CW Kischer
- CY Chung
- CY Chung
- D Craig
- D Julich
- D Vial
- D Vial
- DC Hocking
- DC Hocking
- DC Hocking
- DC Hocking
- DF Mosher
- DJ Leahy
- DM Peters
- DM Ramos
- E Bazigou
- E Cukierman
- E Klotzsch
- E Monaghan-Benson
- E Tafolla
- E Zamir
- EF Plow
- EF Plow
- EG Hayman
- ES White
- ES White
- ES Wijelath
- F Curnis
- F Grinnell
- F Shi
- F Strutz
- G Baneyx
- G Baneyx
- G Gabbiani
- G Huang
- G Serini
- GS Chin
- GS Horan
- GW Kamykowski
- H Altroff
- H Bultmann
- H Chen
- H Ihn
- H Kosmehl
- H Ni
- H Ni
- H Ni
- HM van der Straaten
- HP Erickson
- HP Erickson
- HP Lorenz
- HY Chiang
- I Takasaki
- I Wierzbicka-Patynowski
- J Cho
- J Cho
- J Kaczmarek
- J Matuskova
- J Niewiarowska
- J Sottile
- J Sottile
- J Sottile
- J Sottile
- J Takagi
- J Zhang
- JA Green
- JA McDonald
- JA McDonald
- JA Quinn
- JC Friedland
- JD Wencel-Drake
- JE Schwarzbauer
- JH Oh
- JH Peters
- JJ Bravo-Cordero
- JJ Tomasek
- JL Guan
- JL Sechler
- JL Sechler
- JL Sechler
- JM Gardner
- JN Rybak
- JR Couchman
- JT Yang
- JT Yang
- K Havrlikova
- K Koli
- K Shiozawa
- K Tominaga
- K Wennerberg
- KA Brenner
- KC Ingham
- KC Ingham
- KC Ingham
- KC Ongenae
- KE Kubow
- Kim S Midwood
- KJ Johnson
- KJ Langenbach
- KL De Jong
- KM Aguirre
- KS Midwood
- KS Song
- L Bloom
- L Gui
- L Sabatier
- L Zardi
- LA Davidson
- LA Repesh
- LL McCormick
- LM Schnapp
- M Antia
- M Babu
- M Castellanos
- M Gao
- M Hashimoto-Uoshima
- M Kusubata
- M Marsden
- M Palolahti
- M Pereira
- M Rocco
- M Rocco
- M Zheng
- MA Hospenthal
- MA Latijnhouwers
- MA Loots
- MC D'Ovidio
- MG Choi
- MG Tonnesen
- MH Disatnik
- MH Tan
- MK Magnusson
- ML Smith
- MT Birchler
- N Buyukbabani
- N Oliver
- NJ Trengove
- NW Karuri
- OE Olorundare
- P Claudepierre
- P Knox
- P Mhawech
- P Sabatelli
- P Singh
- P Sivakumar
- PB Armstrong
- PJ McKeown-Longo
- PJ McKeown-Longo
- PJ Thurlow
- PK Schick
- PR Somanath
- Q Zhang
- Q Zhang
- Q Zhang
- R Kalluri
- R Kinsey
- R Manabe
- R Pankov
- R Pankov
- R Wang
- R Winklbauer
- RA Clark
- RAF Clark
- RF Diegelmann
- RP Hershberger
- S Astrof
- S Bencharit
- S Bourdoulous
- S Fernandez-Sauze
- S Godyna
- S Huveneers
- S Johansson
- S Lam
- S Li
- S Matsui
- S Takahashi
- S Wakui
- SA Corbett
- SE Lee
- SL Dallas
- SL Dallas
- SP Watson
- ST Jiang
- T Darribere
- T Fujimoto
- T Fukuda
- T Ohashi
- T Ohashi
- T Ohashi
- T Rozario
- T Sakai
- T Sakai
- T Tressel
- T Velling
- TF Busby
- TM Maher
- VL Barnes
- W Chen
- W Qi
- Wing S To
- WM Maniscalco
- WR Jarnagin
- WS To
- X Zhou
- Y Abe
- Y Chen
- Y Liu
- Y Mao
- Y Mao
- YF Liao
- YR Kuo
- YV Matsuka
- ZA Khan
- Publication venue
- BioMed Central
- Publication date
- 01/01/2011
- Field of study
Fibronectin (FN) is a ubiquitous extracellular matrix (ECM) glycoprotein that plays vital roles during tissue repair. The plasma form of FN circulates in the blood, and upon tissue injury, is incorporated into fibrin clots to exert effects on platelet function and to mediate hemostasis. Cellular FN is then synthesized and assembled by cells as they migrate into the clot to reconstitute damaged tissue. The assembly of FN into a complex three-dimensional matrix during physiological repair plays a key role not only as a structural scaffold, but also as a regulator of cell function during this stage of tissue repair. FN fibrillogenesis is a complex, stepwise process that is strictly regulated by a multitude of factors. During fibrosis, there is excessive deposition of ECM, of which FN is one of the major components. Aberrant FN-matrix assembly is a major contributing factor to the switch from normal tissue repair to misregulated fibrosis. Understanding the mechanisms involved in FN assembly and how these interplay with cellular, fibrotic and immune responses may reveal targets for the future development of therapies to regulate aberrant tissue-repair processes
Commercial Nucleic-Acid Amplification Tests for Diagnosis of Pulmonary Tuberculosis in Respiratory Specimens: Meta-Analysis and Meta-Regression
- Author
- A Barrett
- A Catanzaro
- A Hadgu
- A Walsh
- AG Michos
- AH Viinanen
- AS Glas
- AV Zamora J
- AW Rutjes
- B Jonsson
- B Littenberg
- BR Roos
- C Abe
- C Collaboration
- C Dye
- C Piersimoni
- C Piersimoni
- C Piersimoni
- C Piersimoni
- C Scarparo
- CC Boehme
- CE O'Sullivan
- D Jungkind
- Daphne I. Ling
- DF Moore
- DF Moore
- DP Chin
- E Carpentier
- E Fegou
- E Tortoli
- E Tortoli
- EJ Oh
- F Artiles
- F Gamboa
- F Gamboa
- F Salajka
- F Stauffer
- FK Ribeiro
- G Miragliotta
- GE Pfyffer
- GE Pfyffer
- GE Pfyffer
- GL Woods
- H Soini
- I Putova
- I Rajalahti
- IS Jan
- J Bennedsen
- J Lau
- J Maugein
- JG Lijmer
- JG Lijmer
- JI Pounder
- JJ Deeks
- JS Bergmann
- JS Bergmann
- JS Bergmann
- JS Bergmann
- JY Wang
- JY Wang
- K Al Zahrani
- K Rantakokko-Jalava
- K Welch
- KG Beavis
- KK Abu-Amero
- KM Jackson
- KP Hengstler M
- KR Steingart
- KR Steingart
- L Alcala
- L Irwig
- L Kivihya-Ndugga
- Laura L. Flores
- Lee W. Riley
- LL Flores
- M Bogard
- M Gallina
- M Pai
- M Pai
- M Pai
- M Pai
- M Pai
- M Pai
- M Pai
- M Pai
- M Viveiros
- M Zolnir-Dovc
- Madhukar Pai
- MB Smith
- MB Smith
- MD Perkins
- MG Garrino
- MJ Ruiz-Serrano
- MSG Egger
- MT La Rocco
- N Miller
- N Shetty
- O Denis
- O Gurkan
- OL Sarmiento
- P Chedore
- P Coll
- P Della-Latta
- P Rohner
- P Vuorinen
- P Whiting
- PC Basta
- PM Small
- PTS Daley
- R Cartuyvels
- R Lumb
- RA Cohen
- RF D'Amato
- S Ehlers
- S Ehlers
- S Greco
- S Ichiyama
- S Ichiyama
- S Levidiotou
- S Mitarai
- S Rusch-Gerdes
- S Sheehan
- S Takakura
- SD Walter
- SE Hoffner
- SE Hoffner
- SP Bradley
- Srikanth Tripathy
- SX Wang
- SY Kim
- T Bodmer
- T Bodmer
- T Tonjum
- TD McHugh
- TK Lim
- TK Lim
- TS Shim
- U Ni Riain
- V Ausina
- V Jonas
- VO Thomsen
- WH Goessens
- WL Deville
- WL Wobeser
- Y Iinuma
- Y Iinuma
- YC Yee
- Publication venue
- Public Library of Science
- Publication date
- 06/02/2008
- Field of study
BACKGROUND: Hundreds of studies have evaluated the diagnostic accuracy of nucleic-acid amplification tests (NAATs) for tuberculosis (TB). Commercial tests have been shown to give more consistent results than in-house assays. Previous meta-analyses have found high specificity but low and highly variable estimates of sensitivity. However, reasons for variability in study results have not been adequately explored. We performed a meta-analysis on the accuracy of commercial NAATs to diagnose pulmonary TB and meta-regression to identify factors that are associated with higher accuracy. METHODOLOGY/PRINCIPAL FINDINGS: We identified 2948 citations from searching the literature. We found 402 articles that met our eligibility criteria. In the final analysis, 125 separate studies from 105 articles that reported NAAT results from respiratory specimens were included. The pooled sensitivity was 0.85 (range 0.36-1.00) and the pooled specificity was 0.97 (range 0.54-1.00). However, both measures were significantly heterogeneous (p<.001). We performed subgroup and meta-regression analyses to identify sources of heterogeneity. Even after stratifying by type of commercial test, we could not account for the variability. In the meta-regression, the threshold effect was significant (p = .01) and the use of other respiratory specimens besides sputum was associated with higher accuracy. CONCLUSIONS/SIGNIFICANCE: The sensitivity and specificity estimates for commercial NAATs in respiratory specimens were highly variable, with sensitivity lower and more inconsistent than specificity. Thus, summary measures of diagnostic accuracy are not clinically meaningful. The use of different cut-off values and the use of specimens other than sputum could explain some of the observed heterogeneity. Based on these observations, commercial NAATs alone cannot be recommended to replace conventional tests for diagnosing pulmonary TB. Improvements in diagnostic accuracy, particularly sensitivity, need to be made in order for this expensive technology to be worthwhile and beneficial in low-resource countries
Recovery of high mountain Alpine lakes after the eradication of introduced brook trout Salvelinus fontinalis using non-chemical methods
- Author
- A Bellati
- A Miró
- A Miró
- Achaz von Hardenberg
- AS McNaught
- BG Ludgate
- BR Parker
- BR Parker
- Bruno Bassano
- C Pacas
- DE Schindler
- DF Bradford
- DS Pilliod
- EK Kenison
- EL Cooper
- EO Casamayor
- G Alessio
- G Howald
- G Orizaola
- Giuseppe Bogliani
- IUCN
- JC Finlay
- JD Hadfield
- Kevin Liautaud
- KL Pope
- KL Pope
- KR Matthews
- L Orsini
- L Winandy
- LA Eby
- LB Kats
- M Bomford
- M Denoël
- M Denoël
- M Denoël
- M Rolla
- M Toro
- M Ventura
- Matteo Rolla
- MJ Vanni
- N Ling
- NPS [National Park Service]
- O Sarnelle
- PN Epanchin
- R Schabetsberger
- R Schabetsberger
- R Tiberti
- R Tiberti
- R Tiberti
- R Tiberti
- R Tiberti
- R Tiberti
- R Tiberti
- R Tiberti
- RA Knapp
- RA Knapp
- RA Knapp
- RA Knapp
- RA Knapp
- RA Knapp
- RH Baayen
- RJ Whittaker
- Rocco Iacobuzio
- Rocco Tiberti
- S Bertolino
- Stefano Brighenti
- TM Rout
- TM Rout
- TW Armstrong
- U Magnea
- VT Vredenburg
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
The final publication is available at Springer via http://dx.doi.org/10.1007/s10530-018-1867-0Fish stocking is a serious threat to originally fishless mountain lakes. We used non-chemical eradication methods (i.e. gillnetting and electrofishing) in four high mountain lakes in the Gran Paradiso National Park (Western Italian Alps) to eradicate alien brook trout Salvelinus fontinalis. Data of amphibians, macroinvertebrates, zooplankton, chlorophyll-a, nutrient concentrations, and water transparency were used as indicators of the recovery process. All treated lakes were returned to their original fishless condition in spite of their different sizes and habitat complexity, without permanent negative side-effects for native species. Several ecological indicators showed that many impacts of introduced fish can be reversed over a short time period following eradication. The present study adds to a still growing body of specialized literature on the recovery of habitats after the eradication of alien species and provides further evidence that physical eradication methods are effective and can be part of a more general strategy for the conservation of high mountain lake biota
Combination therapy analysis of ezetimibe and statins in Chinese patients with acute coronary syndrome and type 2 diabetes
- Author
- A Undas
- B Goldfine Allison
- BR Rocco Michael
- C Neal Ryan
- CM Ballantyne
- CP Cannon
- D Necati
- Daqing Zhang
- DP Mikhailidis
- E Moutzouri
- EA Amsterdam
- F Chenot
- Fuxiang Su
- GG Schwartz
- H Takase
- HPS2-THRIVE Collaborative Group
- J He
- Jie Shen
- Joint committee for developing Chinese guidelines on Prevention and Treatment of Dyslipidemia in Adults
- Lulu Li
- M Nomura
- Minli Zhang
- P Deharo
- PJ Delahoy
- S Zhao
- SM Haffner
- TR Pedersen
- Yali Shen
- Yang Li
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Combined measurement of differential and total cross sections in the H → γγ and the H → ZZ* → 4ℓ decay channels at s=13 TeV with the ATLAS detector
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdinov O
- Abeloos B
- Abhayasinghe DK
- Abidi SH
- Abouzeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abulaiti Y
- Acharya BS
- Adachi S
- Adamczyk L
- Adelman J
- Adersberger M
- Adiguzel A
- Adye T
- Affolder AA
- Afik Y
- Agheorghiesei C
- Aguilar-Saavedra JA
- Ahmadov F
- Aielli G
- Akatsuka S
- Akilli E
- Akimov AV
- Alberghi GL
- Albert J
- Albicocco P
- Alconada Verzini MJ
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alhroob M
- Ali B
- Alimonti G
- Alison J
- Alkire SP
- Allaire C
- Allbrooke BMM
- Allen BW
- Allport PP
- Aloisio A
- Alonso A
- Alonso F
- Alpigiani C
- Alshehri AA
- Alstaty MI
- Alvarez Gonzalez B
- Alviggi MG
- Amadio BT
- Amaral Coutinho Y
- Ambroz L
- Amelung C
- Amidei D
- Amor Dos Santos SP
- Amoroso S
- Amrouche CS
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders JK
- Anderson KJ
- Andreazza A
- Andrei V
- Anelli CR
- Angelidakis S
- Angelozzi I
- Angerami A
- Anisenkov AV
- Annovi A
- Antel C
- Anthony MT
- Antonelli M
- Antrim DJA
- Anulli F
- Aoki M
- Aperio Bella L
- Arabidze G
- Arai Y
- Araque JP
- Araujo Ferraz V
- Araujo Pereira R
- Arce ATH
- Ardell RE
- Arduh FA
- Arguin J-F
- Argyropoulos S
- Armbruster AJ
- Armitage LJ
- Armstrong A
- Arnaez O
- Arnold H
- Arratia M
- Arslan O
- Artamonov A
- Artoni G
- Artz S
- Asai S
- Asbah N
- Ashkenazi A
- Asimakopoulou EM
- Asquith L
- Assamagan K
- Astalos R
- Atkin RJ
- Atkinson M
- Atlas Collaboration
- Atlay NB
- Augsten K
- Avolio G
- Avramidou R
- Axen B
- Ayoub MK
- Azuelos G
- Baas AE
- Baca MJ
- Bachacou H
- Bachas K
- Backes M
- Bagnaia P
- Bahmani M
- Bahrasemani H
- Bailey AJ
- Baines JT
- Bajic M
- Bakalis C
- Baker OK
- Bakker PJ
- Bakshi Gupta D
- Baldin EM
- Balek P
- Balli F
- Balunas WK
- Balz J
- Banas E
- Bandyopadhyay A
- Banerjee S
- Bannoura AAE
- Barak L
- Barbe WM
- Barberio EL
- Barberis D
- Barbero M
- Barillari T
- Barisits M-S
- Barkeloo J
- Barklow T
- Barlow N
- Barnea R
- Barnes SL
- Barnett BM
- Barnett RM
- Barnovska-Blenessy Z
- Baroncelli A
- Barone G
- Barr AJ
- Barranco Navarro L
- Barreiro Guimarães Da Costa J
- Barreiro F
- Bartoldus R
- Barton AE
- Bartos P
- Basalaev A
- Bassalat A
- Bates RL
- Batista SJ
- Batlamous S
- Batley JR
- Battaglia M
- Bauce M
- Bauer F
- Bauer KT
- Bawa HS
- Beacham JB
- Beattie MD
- Beau T
- Beauchemin PH
- Bechtle P
- Beck HC
- Beck HP
- Becker K
- Becker M
- Becot C
- Beddall A
- Beddall AJ
- Bednyakov VA
- Bedognetti M
- Bee CP
- Beermann TA
- Begalli M
- Begel M
- Behera A
- Behr JK
- Bell AS
- Bella G
- Bellagamba L
- Bellerive A
- Bellomo M
- Bellos P
- Belotskiy K
- Belyaev NL
- Benary O
- Benchekroun D
- Bender M
- Benekos N
- Benhammou Y
- Benhar Noccioli E
- Benitez J
- Benjamin DP
- Benoit M
- Bensinger JR
- Bentvelsen S
- Beresford L
- Beretta M
- Berge D
- Bergeaas Kuutmann E
- Berger N
- Bergsten LJ
- Beringer J
- Berlendis S
- Bernard NR
- Bernardi G
- Bernius C
- Bernlochner FU
- Berry T
- Berta P
- Bertella C
- Bertoli G
- Bertram IA
- Besjes GJ
- Bessidskaia Bylund O
- Bessner M
- Besson N
- Bethani A
- Bethke S
- Betti A
- Bevan AJ
- Beyer J
- Bianchi RM
- Biebel O
- Biedermann D
- Bielski R
- Bierwagen K
- Biesuz NV
- Biglietti M
- Billoud TRV
- Bindi M
- Bingul A
- Bini C
- Biondi S
- Bisanz T
- Biswal JP
- Bittrich C
- Bjergaard DM
- Black JE
- Black KM
- Blair RE
- Blazek T
- Bloch I
- Blocker C
- Blue A
- Blumenschein U
- Blunier D
- Bobbink GJ
- Bobrovnikov VS
- Bocchetta SS
- Bocci A
- Boerner D
- Bogavac D
- Bogdanchikov AG
- Bohm C
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- Zhemchugov A
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- Zhulanov V
- Zibell A
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- Zimine NI
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zobernig G
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- Zorbas TG
- Zou R
- Zur Nedden M
- Zwalinski L
- Álvarez Piqueras D
- Åkesson TPA
- Šfiligoj T
- Ženiš T
- Živković L
- Publication venue
- Elsevier
- Publication date
- 01/01/2018
- Field of study
A combined measurement of differential and inclusive total cross sections of Higgs boson production is performed using 36.1 fb−1 of 13 TeV proton–proton collision data produced by the LHC and recorded by the ATLAS detector in 2015 and 2016. Cross sections are obtained from measured H→γγ and H→ZZ*(→4ℓ event yields, which are combined taking into account detector efficiencies, resolution, acceptances and branching fractions. The total Higgs boson production cross section is measured to be 57.0−5.9 +6.0 (stat.) −3.3 +4.0 (syst.) pb, in agreement with the Standard Model prediction. Differential cross-section measurements are presented for the Higgs boson transverse momentum distribution, Higgs boson rapidity, number of jets produced together with the Higgs boson, and the transverse momentum of the leading jet. The results from the two decay channels are found to be compatible, and their combination agrees with the Standard Model predictions
Search for High-Mass Resonances Decaying to τν in pp Collisions at √s=13 TeV with the ATLAS Detector
- Author
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- Aad G
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- Zhemchugov A
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- Zhulanov V
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zu Theenhausen H Meyer
- zur Nedden M
- Zwalinski L
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2018
- Field of study
A search for high-mass resonances decaying to τν using proton-proton collisions at √s=13 TeV produced by the Large Hadron Collider is presented. Only τ-lepton decays with hadrons in the final state are considered. The data were recorded with the ATLAS detector and correspond to an integrated luminosity of 36.1 fb−1. No statistically significant excess above the standard model expectation is observed; model-independent upper limits are set on the visible τν production cross section. Heavy W′ bosons with masses less than 3.7 TeV in the sequential standard model and masses less than 2.2–3.8 TeV depending on the coupling in the nonuniversal G(221) model are excluded at the 95% credibility level
Search for the direct production of charginos and neutralinos in final states with tau leptons in √s=13 TeV collisions with the ATLAS detector
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdinov O
- Abeloos B
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abreu R
- Abulaiti Y
- Acharya BS
- Adachi S
- Adamczyk L
- Adelman J
- Adersberger M
- Adye T
- Affolder AA
- Afik Y
- Agatonovic-Jovin T
- Agheorghiesei C
- Aguilar-Saavedra JA
- Ahlen SP
- Ahmadov F
- Aielli G
- Akatsuka S
- Akerstedt H
- Akesson TPA
- Akilli E
- Akimov AV
- Albergh GL
- Albert J
- Albicocco P
- Alconada Verzini MJ
- Alderweireldt SC
- 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
- Alshehri AA
- Alstaty MI
- Alvarez Piqueras D
- Alviggi MG
- Amadio BT
- Amelung C
- Amidei D
- Amoroso S
- Amundsen G
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders JK
- Anderson KJ
- Andreazza A
- Andrei V
- Angelidakis S
- Angelozzi I
- Angerami A
- Anisenkov AV
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- Annovi A
- Antel C
- Antonelli M
- Antonov A
- Antrim DJ
- Anulli F
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- Arabidze G
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- Araque JP
- Arce ATH
- Ardell RE
- Arduh FA
- Arguin J-F
- Argyropoulos S
- Arik M
- Armadans R Caminal
- Armbruster AJ
- Armitage LJ
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- Artz S
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- Castillo I Santoyo
- Castillo LR Flores
- Castro NF
- Catinaccio A
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- Cavaliere V
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- Cervelli A
- Cetin SA
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- Chapman JD
- Charlton DG
- Chau CC
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- Chekulaev SV
- Chelkov GA
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- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann C
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zou R
- zur Nedden M
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2017
- Field of study
A search for the direct production of charginos and neutralinos in final states with at least two hadronically decaying tau leptons is presented. The analysis uses a dataset of pp collisions corresponding to an integrated luminosity of 36.1 fb−1, recorded with the ATLAS detector at the Large Hadron Collider at a centre-of-mass energy of 13TeV.Nosignificant deviation from the expected Standard Model background is observed. Limits are derived in scenarios of ˜χ+1 ˜χ−1 pair production and of ˜χ±1 ˜χ02 and ˜χ+1 ˜χ−1 production in simplified models where the neutralinos and charginos decay solely via intermediate left-handed staus and tau sneutrinos, and the mass of the ˜ τL state is set to be halfway between the masses of the ˜χ±1 and the ˜χ01. Chargino masses up to 630 GeV are excluded at 95% confidence level in the scenario of direct production of ˜χ+1 ˜χ−1 for a massless ˜χ01. Common ˜χ±1 and ˜χ02 masses up to 760 GeV are excluded in the case of production of ˜χ±1 ˜χ02 and ˜χ+1 ˜χ−1 assuming a massless ˜χ01. Exclusion limits for additional benchmark scenarios with large and small mass-splitting between the ˜χ±1 and the ˜χ01 are also studied by varying the ˜ τL mass between the masses of the ˜χ±1 and the ˜χ01
Measurement of differential cross sections and W + /W − cross-section ratios for W boson production in association with jets at √s =8 TeV with the ATLAS detector
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdinov O
- Abeloos B
- Abidi SH
- AbouZeid OS
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
This paper presents a measurement of the W boson production cross section and the W + /W − cross-section ratio, both in association with jets, in proton--proton collisions at s √ =8 TeV with the ATLAS experiment at the Large Hadron Collider. The measurement is performed in final states containing one electron and missing transverse momentum using data corresponding to an integrated luminosity of 20.2 fb −1 . Differential cross sections for events with one or two jets are presented for a range of observables, including jet transverse momenta and rapidities, the scalar sum of transverse momenta of the visible particles and the missing transverse momentum in the event, and the transverse momentum of the W boson. For a subset of the observables, the differential cross sections of positively and negatively charged W bosons are measured separately. In the cross-section ratio of W + /W − the dominant systematic uncertainties cancel out, improving the measurement precision by up to a factor of nine. The observables and ratios selected for this paper provide valuable input for the up quark, down quark, and gluon parton distribution functions of the proto
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