284 research outputs found
Fabrication of Porous TiO2 Hollow Spheres and Their Application in Gas Sensing
- Author
- Publication venue
- Springer
- Publication date
- 01/01/2010
- Field of study
In this work, porous TiO2 hollow spheres with an average diameter of 100 nm and shell thickness of 20 nm were synthesized by a facile hydrothermal method with NH4HCO3 as the structure-directing agent, and the formation mechanism for this porous hollow structure was proved to be the Ostwald ripening process by tracking the morphology of the products at different reaction stages. The product was characterized by SEM, TEM, XRD and BET analyses, and the results show that the as-synthesized products are anatase phase with a high surface area up to 132.5 m2/g. Gas-sensing investigation reveals that the product possesses sensitive response to methanal gas at 200°C due to its high surface area
Interactome and Gene Ontology provide congruent yet subtly different views of a eukaryotic cell
- Author
- A Barabási
- A Marco
- Antonio Marco
- AW Rives
- BR Zeeberg
- C von Mering
- CM Deane
- E Hirsh
- F Luo
- GD Bader
- GD Bader
- GT Hart
- H Yu
- I Marín
- Ignacio Marín
- JI Lucas
- K Dolinski
- LJ Lu
- M Burset
- M Deng
- M Tompa
- ME Cusick
- P Bork
- P Uetz
- R Albert
- R Mrowka
- RR Sokal
- S Brohée
- S Kumar
- S Letovsky
- The Gene Ontology Consortium
- TZ Sen
- U Karaoz
- U Stelzl
- V Arnau
- V Arnau
- V Spirin
- X Wu
- Y Xia
- Publication venue
- BioMed Central
- Publication date
- 01/01/2009
- Field of study
15 pages, 6 figures.-- 19604360 [PubMed]BACKGROUND: The characterization of the global functional structure of a cell is a major goal in bioinformatics and systems biology. Gene Ontology (GO) and the protein-protein interaction network offer alternative views of that structure. RESULTS: This study presents a comparison of the global structures of the Gene Ontology and the interactome of Saccharomyces cerevisiae. Sensitive, unsupervised methods of clustering applied to a large fraction of the proteome led to establish a GO-interactome correlation value of +0.47 for a general dataset that contains both high and low-confidence interactions and +0.58 for a smaller, high-confidence dataset. CONCLUSION: The structures of the yeast cell deduced from GO and interactome are substantially congruent. However, some significant differences were also detected, which may contribute to a better understanding of cell function and also to a refinement of the current ontologiesResearch supported by grant BIO2008-05067 (Programa Nacional de Biotecnología;
Ministerio de Ciencia e Innovación. Spain), awarded to IM. AM was a FPI fellow from Ministerio de Educación y Ciencia (Spain).Peer reviewe
A Combined Approach of High-Throughput Sequencing and Degradome Analysis Reveals Tissue Specific Expression of MicroRNAs and Their Targets in Cucumber
- Author
- A Adai
- AC Mallory
- Baohong Zhang
- BC Meyers
- BH Zhang
- BH Zhang
- C Addo-Quaye
- C Addo-Quaye
- C Arenas-Huertero
- C Lelandais-Briere
- C Llave
- C Lu
- C Schommer
- DP Bartel
- E Allen
- E Bonnet
- EK Yoon
- FL Xie
- G Chuck
- G Jagadeeswaran
- G Martínez
- G Szittya
- H Fujii
- HS Guo
- JH Jung
- Jingquan Yu
- K Chaudhuri
- KJ Livak
- L Wang
- L Williams
- LI Shukla
- M Ashburner
- M Kantar
- MA German
- MA German
- MW Jones-Rhoades
- MW Jones-Rhoades
- MW Rhoades
- MZ Li
- N Fahlgren
- P Brodersen
- QX Song
- R Rajagopalan
- R Sunkar
- R Sunkar
- R Sunkar
- R Sunkar
- R Sunkar
- RD Morin
- RLR Pilcher
- S Subramanian
- SW Huang
- T Unver
- T Unver
- TZ Wang
- V Pantaleo
- Weihua Mao
- WZ Yang
- Xiaojian Xia
- Yadan Li
- YF Li
- Zeyun Li
- ZJ Yin
- Publication venue
- Public Library of Science
- Publication date
- 30/03/2012
- Field of study
MicroRNAs (miRNAs) are endogenous small RNAs playing an important regulatory function in plant development and stress responses. Among them, some are evolutionally conserved in plant and others are only expressed in certain species, tissue or developmental stages. Cucumber is among the most important greenhouse species in the world, but only a limited number of miRNAs from cucumber have been identified and the experimental validation of the related miRNA targets is still lacking. In this study, two independent small RNA libraries from cucumber leaves and roots were constructed, respectively, and sequenced with the high-throughput Illumina Solexa system. Based on sequence similarity and hairpin structure prediction, a total of 29 known miRNA families and 2 novel miRNA families containing a total of 64 miRNA were identified. QRT-PCR analysis revealed that some of the cucumber miRNAs were preferentially expressed in certain tissues. With the recently developed ‘high throughput degradome sequencing’ approach, 21 target mRNAs of known miRNAs were identified for the first time in cucumber. These targets were associated with development, reactive oxygen species scavenging, signaling transduction and transcriptional regulation. Our study provides an overview of miRNA expression profile and interaction between miRNA and target, which will help further understanding of the important roles of miRNAs in cucumber plants
Investigating the validity of current network analysis on static conglomerate networks by protein network stratification
- Author
- A Bossi
- A Ma'ayan
- AC Gavin
- AH Tong
- AK Ramani
- AL Barabasi
- AL Hopkins
- B Zybailov
- C Alfarano
- C von Mering
- D Eisenberg
- D Greenbaum
- D Swarbreck
- G Balazsi
- G Joshi-Tope
- G Palla
- H Huang
- H Jeong
- H Ma
- H Rutschow
- H Yu
- H Yu
- H Yu
- H Zhang
- HW Ma
- HY Chuang
- IW Taylor
- J Cui
- JD Han
- JF Rual
- K Baerenfaller
- K Yang
- KY Yip
- LH Hartwell
- Long J Lu
- M Arita
- M Ashburner
- M Girvan
- M Hamacher
- M Miyamoto
- M Zhang
- ME Newman
- Minlu Zhang
- MJ Herrgard
- MP Samanta
- N Bertin
- N Guelzim
- N Lemke
- NM Luscombe
- NN Batada
- NN Batada
- P Braun
- P Qiu
- PV Missiuro
- R Guimera
- R Kelley
- R Milo
- R Sharan
- RJ Prill
- S Li
- S Peri
- S Wuchty
- SA Teichmann
- SE Calvano
- T Ideker
- T Kislinger
- TZ Berardini
- U de Lichtenberg
- U Stelzl
- WH Lin
- Y Xia
- YR Cho
- Z Wang
- Z Zhang
- Publication venue
- BioMed Central
- Publication date
- 01/01/2010
- Field of study
<p>Abstract</p> <p>Background</p> <p>A molecular network perspective forms the foundation of systems biology. A common practice in analyzing protein-protein interaction (PPI) networks is to perform network analysis on a conglomerate network that is an assembly of all available binary interactions in a given organism from diverse data sources. Recent studies on network dynamics suggested that this approach might have ignored the dynamic nature of context-dependent molecular systems.</p> <p>Results</p> <p>In this study, we employed a network stratification strategy to investigate the validity of the current network analysis on conglomerate PPI networks. Using the genome-scale tissue- and condition-specific proteomics data in <it>Arabidopsis thaliana</it>, we present here the first systematic investigation into this question. We stratified a conglomerate <it>A. thaliana </it>PPI network into three levels of context-dependent subnetworks. We then focused on three types of most commonly conducted network analyses, i.e., topological, functional and modular analyses, and compared the results from these network analyses on the conglomerate network and five stratified context-dependent subnetworks corresponding to specific tissues.</p> <p>Conclusions</p> <p>We found that the results based on the conglomerate PPI network are often significantly different from those of context-dependent subnetworks corresponding to specific tissues or conditions. This conclusion depends neither on relatively arbitrary cutoffs (such as those defining network hubs or bottlenecks), nor on specific network clustering algorithms for module extraction, nor on the possible high false positive rates of binary interactions in PPI networks. We also found that our conclusions are likely to be valid in human PPI networks. Furthermore, network stratification may help resolve many controversies in current research of systems biology.</p
Models of chronic obstructive pulmonary disease
- Author
- A Adler
- A Churg
- A Churg
- A Churg
- A Farone
- A Kauffmann-Zeh
- A Sydbom
- AG Agusti
- AJ Sandford
- AM Schols
- AM Vignola
- B Jany
- B Meshi
- BG Cosio
- BR Celli
- C Albrecht
- C Fletcher
- C Kuhn
- C Kuhn
- C Martin
- CJL Murray
- D Stanescu
- DA Groneberg
- DA Groneberg
- DA Groneberg
- DA Groneberg
- DA Groneberg
- DA Groneberg
- DA Groneberg
- DA Groneberg
- DA Groneberg
- DA Lomas
- DE Niewoehner
- DG Morris
- DP Wendel
- DR Parkinson
- E Azoulay-Dupuis
- E Cano
- E Ogawa
- E Pizzichini
- EB Haddad
- EB Haddad
- EB Haddad
- EC Lucey
- EH Wittels
- EK Silverman
- ER Sutherland
- F Chung
- F Vai
- FM Moodie
- GA Finlay
- GD Massaro
- GD Massaro
- GL Snider
- GL Snider
- GL Snider
- GL Snider
- GW Hunninghake
- GW Hunninghake
- H Bostrom
- H Ernst
- H Parfrey
- H Tsukagoshi
- HJ Colebatch
- HP Gerber
- I Ito
- I Retamales
- I Rubio-Aliaga
- IS Mudway
- J D'Armiento
- J Kleinerman
- J Majo
- J Springer
- J Springer
- J Springer
- J Springer
- J Springer
- J Sun
- JA Marwick
- JC Hogg
- JC Kips
- JL Wright
- JL Wright
- JM Drazen
- JN Clark
- JR Foster
- JR Harkema
- JT Mao
- JY Ma
- K Donaldson
- K Donaldson
- K Fujimoto
- K Ito
- K Kostikas
- KF Chung
- KF Chung
- KF Chung
- KJ Holroyd
- KJ Leco
- L Wu
- LM Fabbri
- LM Reid
- M Corradi
- M Cosio
- M Fujita
- M Hind
- M Nishikawa
- M Saetta
- M Saetta
- M Saetta
- M Saetta
- M Saetta
- M Saetta
- M Wegmann
- M Weinstein
- M Wills-Karp
- M Yoshida
- ML Miller
- N Keicho
- N Minematsu
- NC Long
- NC Long
- NH Al-Humadi
- NM Lightowler
- P Chanez
- P Lindahl
- P Montuschi
- P Paredi
- PA Martorana
- PA Martorana
- PJ Barnes
- PJ Barnes
- PJ Barth
- PJ Rombout
- PM O'Byrne
- PR Eynott
- PR Eynott
- PR Eynott
- R Corteling
- R Dhami
- R Mahadeva
- RA Pauwels
- RA Pauwels
- RA Stockley
- RD Hautamaki
- RM Senior
- RW Penman
- S Baraldo
- S Kerzel
- S Lim
- S Nicosia
- S Shore
- SA Kharitonov
- SAM Lim
- SC McCloskey
- SD Shapiro
- SD Shapiro
- SD Shapiro
- SD Shapiro
- SD Shapiro
- SF Man
- STEVEND Shapiro
- SV Culpitt
- T Matsuse
- T Nakamura
- T Zheng
- TC O'Shaughnessy
- TH March
- TZ Vitalis
- UP Kodavanti
- V Lagente
- V Ranga
- W Klein
- WA Biernacki
- WM Elliott
- X Xu
- Y Kasahara
- Y Zhang
- YASUNORI Kasahara
- Z Xia
- Z Zhu
- Publication venue
- BioMed Central
- Publication date
- 01/01/2004
- Field of study
Chronic obstructive pulmonary disease (COPD) is a major global health problem and is predicted to become the third most common cause of death by 2020. Apart from the important preventive steps of smoking cessation, there are no other specific treatments for COPD that are as effective in reversing the condition, and therefore there is a need to understand the pathophysiological mechanisms that could lead to new therapeutic strategies. The development of experimental models will help to dissect these mechanisms at the cellular and molecular level. COPD is a disease characterized by progressive airflow obstruction of the peripheral airways, associated with lung inflammation, emphysema and mucus hypersecretion. Different approaches to mimic COPD have been developed but are limited in comparison to models of allergic asthma. COPD models usually do not mimic the major features of human COPD and are commonly based on the induction of COPD-like lesions in the lungs and airways using noxious inhalants such as tobacco smoke, nitrogen dioxide, or sulfur dioxide. Depending on the duration and intensity of exposure, these noxious stimuli induce signs of chronic inflammation and airway remodelling. Emphysema can be achieved by combining such exposure with instillation of tissue-degrading enzymes. Other approaches are based on genetically-targeted mice which develop COPD-like lesions with emphysema, and such mice provide deep insights into pathophysiological mechanisms. Future approaches should aim to mimic irreversible airflow obstruction, associated with cough and sputum production, with the possibility of inducing exacerbations
The Current State of Proteomics in GI Oncology
- Author
- A Emadali
- A Gorg
- A Schmidt
- AC Polley
- AL Feldman
- AM Rodriguez-Pineiro
- AM Salzano
- AR Shekouh
- B Chen
- B Quaresima
- B Sitek
- B Tomaino
- C Gulmann
- C Huang
- C Li
- C Li
- C Li
- C Melle
- C Melle
- C Melle
- C Melle
- C Rosty
- C Yoo
- CD Chen
- CJ Scarlett
- CJ Scarlett
- CP Paweletz
- CY Chen
- D Lykidis
- D Zhang
- DA Wolters
- DB Friedman
- DF Ransohoff
- DG Ward
- DG Ward
- DG Ward
- E Orvisky
- EB Chang
- EE Schwegler
- EH Seeley
- EP Diamandis
- FM Smith
- G Ernst
- G Stanta
- G Zhao
- GC Bloom
- GI Murray
- GX Zheng
- H Hatakeyama
- H Hu
- H Pei
- H Ren
- H Roelofsen
- HJ Kang
- HJ Lee
- HY Song
- IC Guerrera
- IN Lee
- IN Lee
- International Human Genome Sequencing Consortium
- J Ai
- J Cui
- J Ingvarsson
- J Kim
- J Koopmann
- J Madoz-Gurpide
- J Shaw
- J Shen
- J Zhao
- JC Chung
- JD Wulfkuhle
- Jeffrey R. Lee
- JF Blanc
- JF Cui
- JM Luk
- JQ Li
- JS Jang
- JW Ryu
- JX Wang
- JY An
- JY Engwegen
- JY Lim
- K Lee
- KE Wilson
- KG Kenrick
- KH Yu
- KM Sheehan
- KR Calvo
- KS Park
- L Fu
- L Li
- L Zhou
- LD Wang
- LY Zhang
- M Bloomston
- M Gronborg
- M Karas
- M Seimiya
- M Stoeckli
- M Tian
- MA Meuwis
- MC Hagenstein
- MH Yang
- MJ MacCoss
- MP Ebert
- MP Ebert
- MP Washburn
- NS Azad
- NT Zinkin
- O Greengauz-Roberts
- P Alfonso
- PI Hsu
- PL Ross
- PM Harrison
- Q Huang
- QY He
- QY He
- R Aebersold
- R Chen
- R Chen
- R Chen
- R Chen
- R Lemaire
- R Marouga
- R Mazzanti
- R Teramoto
- R Tian
- Robert R. Schade
- S Din
- S Kanmura
- S Shimma
- SH Xia
- SI Hwang
- SJ Wang
- SP Gygi
- T Gobel
- T Grote
- T Guo
- T Kawakami
- T Nishimori
- T Qi
- TZ Kristiansen
- UB Nielsen
- UJ Roblick
- V Paradis
- VC Wasinger
- W Sun
- WH Xu
- William S. Dynan
- WX Guo
- X Geng
- X Jiang
- X Yi
- X Zheng
- XD Zhu
- XL Du
- XP Liu
- Y Fujita
- Y Fujita
- Y Hao
- Y Hayashida
- Y Kuramitsu
- Y Liang
- Y Lin
- Y Qi
- Y Su
- Y Suehara
- Y Wang
- Y Yu
- YD Chen
- Ying Lin
- Z Lu
- Zhao-Hua Zhu
- ZL Sun
- ZT Hammoud
- ZY Huang
- Publication venue
- Springer US
- Publication date
- 01/01/2008
- Field of study
Proteomics refers to the study of the entire set of proteins in a given cell or tissue. With the extensive development of protein separation, mass spectrometry, and bioinformatics technologies, clinical proteomics has shown its potential as a powerful approach for biomarker discovery, particularly in the area of oncology. More than 130 exploratory studies have defined candidate markers in serum, gastrointestinal (GI) fluids, or cancer tissue. In this article, we introduce the commonly adopted proteomic technologies and describe results of a comprehensive review of studies that have applied these technologies to GI oncology, with a particular emphasis on developments in the last 3 years. We discuss reasons why the more than 130 studies to date have had little discernible clinical impact, and we outline steps that may allow proteomics to realize its promise for early detection of disease, monitoring of disease recurrence, and identification of targets for individualized therapy
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
- Boisvert V
- Bokan P
- Bold T
- Boldyrev AS
- Bolz AE
- Bomben M
- Bona M
- Bonilla JS
- Boonekamp M
- Borisov A
- Borissov G
- Bortfeldt J
- Bortoletto D
- Bortolotto V
- Boscherini D
- Bosman M
- Bossio Sola JD
- Bouaouda K
- Boudreau J
- Bouhova-Thacker EV
- Boumediene D
- Bourdarios C
- Boutle SK
- Boveia A
- Boyd J
- Boyko IR
- Bozson AJ
- Bracinik J
- Brahimi N
- Brandt A
- Brandt G
- Brandt O
- Braren F
- Bratzler U
- Brau B
- Brau JE
- Breaden Madden WD
- Brendlinger K
- Brennan AJ
- Brenner L
- Brenner R
- Bressler S
- Brickwedde B
- Briglin DL
- Britton D
- Britzger D
- Brock I
- Brock R
- Brooijmans G
- Brooks T
- Brooks WK
- Brost E
- Broughton JH
- Bruckman De Renstrom PA
- Bruncko D
- Bruni A
- Bruni G
- Bruni LS
- Bruno S
- Brunt BH
- Bruschi M
- Bruscino N
- Bryant P
- Bryngemark L
- Buanes T
- Buat Q
- Buchholz P
- Buckley AG
- Budagov IA
- Buehrer F
- Bugge MK
- Bulekov O
- Bullock D
- Burch TJ
- Burdin S
- Burgard CD
- Burger AM
- Burghgrave B
- Burka K
- Burke S
- Burmeister I
- Burr JTP
- Buschmann E
- Bussey P
- Butler JM
- Buttar CM
- Butterworth JM
- Butti P
- Buttinger W
- Buzatu A
- Buzykaev AR
- Büscher D
- Büscher V
- Cabras G
- Cabrera Urbán S
- Caforio D
- Cai H
- Cairo VMM
- Cakir O
- Calace N
- Calafiura P
- Calandri A
- Calderini G
- Calfayan P
- Callea G
- Caloba LP
- Calvente Lopez S
- Calvet D
- Calvet S
- Calvet TP
- Calvetti M
- Camacho Toro R
- Camarda S
- Camarri P
- Cameron D
- Caminal Armadans R
- Camincher C
- Campana S
- Campanelli M
- Camplani A
- Campoverde A
- Canale V
- Cano Bret M
- Cantero J
- Cao T
- Cao Y
- Capeans Garrido MDM
- Caprini I
- Caprini M
- Capua M
- Carbone RM
- Cardarelli R
- Cardillo FC
- Carli I
- Carli T
- Carlino G
- Carlson BT
- Carminati L
- Carney RMD
- Caron S
- Carquin E
- Carrillo-Montoya GD
- Carrá S
- Casadei D
- Casado MP
- Casha AF
- Casolino M
- Casper DW
- Castelijn R
- Castillo Gimenez V
- Castillo FL
- Castro NF
- Catinaccio A
- Catmore JR
- Cattai A
- Caudron J
- Cavaliere V
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- Yue X
- Yuen SPY
- Yusuff I
- Zabinski B
- Zacharis G
- Zaffaroni E
- Zaidan R
- Zaitsev AM
- Zakharchuk N
- Zalieckas J
- Zambito S
- Zanzi D
- Zaripovas DR
- Zeitnitz C
- Zeißner SV
- Zemaityte G
- Zeng JC
- Zeng Q
- Zenin O
- Zerwas D
- Zgubič M
- Zhang D
- Zhang DF
- Zhang F
- Zhang G
- Zhang H
- Zhang J
- Zhang L
- Zhang L
- Zhang M
- Zhang P
- Zhang R
- Zhang R
- Zhang X
- Zhang Y
- Zhang Z
- Zhao P
- Zhao X
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zhou B
- Zhou C
- Zhou L
- Zhou M
- Zhou MS
- Zhou N
- Zhou Y
- Zhu CG
- Zhu H
- Zhu HL
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zobernig G
- Zoccoli A
- Zoch K
- 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
- Aaboud M
- Aad G
- Abbott B
- Abdinov O
- Abeloos B
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
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- Abulaiti Y
- Acharya BS
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- Adersberger M
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- Alberghi GL
- Albert J
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- Alconada Verzini MJ
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
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- Casadei D
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- Zinonos Z
- Zinser M
- Ziolkowski M
- Zivkovic L
- Zobernig G
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- 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
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- Alshehri AA
- Alstaty MI
- Alvarez Piqueras D
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- Da Costa J Goncalves Pinto Firmino
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- de Andrade Filho L Manhaes
- de Asmundis R
- De Benedetti A
- De Bruin PH Sales
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- De Groot N
- de Jong P
- De la Torre H
- de Lima DE Ferreira
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- Yeletskikh I
- Yigitbasi E
- Yildirim E
- Yildiz H Duran
- Yorita K
- Yoshihara K
- Young C
- Young CJS
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- Yusuff I
- Zabinski B
- Zacharis G
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- Zemaityte G
- Zemla A
- Zeng JC
- Zeng Q
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- Zhao Z
- Zhemchugov A
- Zhou B
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- Zhou N
- Zhu CG
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- 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
- 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
- Agheorghiesei C
- Aguilar-Saavedra JA
- Ahlen SP
- Ahmadov F
- Aielli G
- Akatsuka S
- Akerstedt H
- Akesson TPA
- Akilli E
- Akimov AV
- Alberghi GL
- Alberich L Cerda
- Albert J
- Albicocco P
- 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
- Alviggi MG
- Amadio BT
- Amelung C
- Amidei D
- Amoroso S
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders JK
- Anderson KJ
- Andreazza A
- Andrei V
- Angelidakis S
- Angelozzi I
- Angerami A
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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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