461 research outputs found
HIP2: An online database of human plasma proteins from healthy individuals
- Author
- Publication venue
- BioMed Central
- Publication date
- Field of study
The Drosophila melanogaster PeptideAtlas facilitates the use of peptide data for improved fly proteomics and genome annotation
- Author
- A Keller
- A Stark
- AG Clark
- AI Nesvizhskii
- AI Nesvizhskii
- AJ Lynn
- B Domon
- B Kuster
- C Ahrens
- D Fermin
- DH Lundgren
- E Brunner
- Eric W Deutsch
- Erich Brunner
- Ernst Hafen
- EW Deutsch
- EW Myers
- F Desiere
- F Desiere
- FlyBaseConsortium
- FlyBaseConsortium
- FlyBaseConsortium
- FlyBaseConsortium
- FlyBaseConsortium
- FlyBaseConsortium
- H Lam
- H Lam
- J Colinge
- J Kyte
- J Stahl-Zeng
- JK Eng
- JS Choudhary
- JS Choudhary
- L Anderson
- LM de Godoy
- LY Geer
- M Stapleton
- M Stapleton
- MD Adams
- MF Lin
- NE Castellana
- NH Lee
- Nichole L King
- NL King
- R Craig
- RA Hoskins
- RD Fleischmann
- Ruedi Aebersold
- S Tanner
- Sandra N Loevenich
- SE Celniker
- SE Stein
- SF Altschul
- Stephen E Stein
- WM Gelbart
- Publication venue
- BioMed Central
- Publication date
- 01/01/2009
- Field of study
<p>Abstract</p> <p>Background</p> <p>Crucial foundations of any quantitative systems biology experiment are correct genome and proteome annotations. Protein databases compiled from high quality empirical protein identifications that are in turn based on correct gene models increase the correctness, sensitivity, and quantitative accuracy of systems biology genome-scale experiments.</p> <p>Results</p> <p>In this manuscript, we present the <it>Drosophila melanogaster </it>PeptideAtlas, a fly proteomics and genomics resource of unsurpassed depth. Based on peptide mass spectrometry data collected in our laboratory the portal <url>http://www.drosophila-peptideatlas.org</url> allows querying fly protein data observed with respect to gene model confirmation and splice site verification as well as for the identification of proteotypic peptides suited for targeted proteomics studies. Additionally, the database provides consensus mass spectra for observed peptides along with qualitative and quantitative information about the number of observations of a particular peptide and the sample(s) in which it was observed.</p> <p>Conclusion</p> <p>PeptideAtlas is an open access database for the <it>Drosophila </it>community that has several features and applications that support (1) reduction of the complexity inherently associated with performing targeted proteomic studies, (2) designing and accelerating shotgun proteomics experiments, (3) confirming or questioning gene models, and (4) adjusting gene models such that they are in line with observed <it>Drosophila </it>peptides. While the database consists of proteomic data it is not required that the user is a proteomics expert.</p
Expression-Dependent Folding of Interphase Chromatin
- Author
- A Bolzer
- A Khalil
- AI Grosberg
- CM Clemson
- D Marenduzzo
- DA Jackson
- Dieter W. Heermann
- DW Heermann
- E Jones
- E Lieberman-Aiden
- H Schiessel
- Hansjoerg Jerabek
- HP Deutsch
- I Carmesin
- J Dekker
- J Dorier
- J Langowski
- J Mateos-Langerak
- J Rudnick
- K Maeshima
- L Valenzuela
- LA Mirny
- M Bohn
- M Bohn
- M Bohn
- M Doi
- M Simonis
- M Simonis
- MO Scheuermann
- MR Branco
- NL Mahy
- NL Mahy
- PJ Verschure
- PR Cook
- PR Cook
- R Abranches
- R Eils
- RK Sachs
- S de Nooijer
- S Dietzel
- S Goetze
- S Kurukuti
- S Schoenfelder
- Simon Keith Whitehall
- SM Gasser
- ST Kosak
- T Cremer
- T Cremer
- T Sexton
- T Takizawa
- Y Vassetzky
- Z Zhao
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
Multiple studies suggest that chromatin looping might play a crucial role in organizing eukaryotic genomes. To investigate the interplay between the conformation of interphase chromatin and its transcriptional activity, we include information from gene expression profiles into a polymer model for chromatin that incorporates genomic loops. By relating loop formation to transcriptional activity, we are able to generate chromosome conformations whose structural and topological properties are consistent with experimental data. The model particularly allows to reproduce the conformational variations that are known to occur between highly and lowly expressed chromatin regions. As previously observed in experiments, lowly expressed regions of the simulated polymers are much more compact. Due to the changes in loop formation, the distributions of chromatin loops are also expression-dependent and exhibit a steeper decay in highly active regions. As a results of entropic interaction between differently looped parts of the chromosome, we observe topological alterations leading to a preferential positioning of highly transcribed loci closer to the surface of the chromosome territory. Considering the diffusional behavior of the chromatin fibre, the simulations furthermore show that the higher the expression level of specific parts of the chromatin fibre is, the more dynamic they are. The results exhibit that variations of loop formation along the chromatin fibre, and the entropic changes that come along with it, do not only influence the structural parameters on the local scale, but also effect the global chromosome conformation and topology
Search for new phenomena in final states with an energetic jet and large missing transverse momentum in pp collisions at √ s = 8 TeV with 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
- Adachi S
- 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
- 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
- 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
- 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
- Araque JP
- 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
- Bandyopadhyay A
- Banerjee S
- Bannoura AAE
- Barak L
- Barbe WM
- Barberio EL
- Barberis D
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- Barillari T
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- Barkeloo J
- Barklow T
- Barnea R
- Barnett BM
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- Baroncelli A
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- Barr AJ
- Barreiro F
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- Bassalat A
- Basso MJ
- Bates RL
- Batlamous S
- Batley JR
- Batool B
- Battaglia M
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- Bauer F
- Bauer KT
- Bawa HS
- Beacham JB
- Beau T
- Beauchemin PH
- Becherer F
- Bechtle P
- Beck HC
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- Becot C
- Beddall A
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- Bednyakov VA
- Bedognetti M
- Beermann TA
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- Behera A
- Behr JK
- Beisiegel F
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- Beloborodov K
- Belotskiy K
- Belyaev NL
- Benchekroun D
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- Benjamin DP
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- Bensinger JR
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- Bergmann B
- Bergsten LJ
- Beringer J
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- Berlingen JM
- Bernardi G
- Bernius C
- Bernlochner FU
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- Chisholm AS
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- De Regie JBDV
- de Renstrom PAB
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- Deviveiros PO
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- Schroeder TV
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- Tsukerman II
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- Vaniachine A
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- Varnes EW
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- Vuillermet R
- Vukotic I
- Wagner P
- Wagner W
- Wagner-Kuhr J
- Wahdan S
- Wahlberg H
- Walbrecht VM
- Walder J
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- Walker SD
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- Wallangen V
- Wang AM
- Wang AZ
- Wang C
- Wang F
- Wang H
- Wang J
- Wang P
- Wang Q
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- Wang R-J
- Wang SM
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- Wang WT
- Wang WX
- Wang Y
- Wang Z
- Wanotayaroj C
- Warburton A
- Ward CP
- Wardrope DR
- Warrack N
- Washbrook A
- Watson AT
- Watson MF
- Watts G
- Waugh BM
- Webb AF
- Webb S
- Weber C
- Weber MS
- Weber SA
- Weber SM
- Weidberg AR
- Weingarten J
- Weirich M
- Weiser C
- Wells PS
- Wenaus T
- Wengler T
- Wenig S
- Wermes N
- Werner MD
- Wessels M
- Weston TD
- Whalen K
- Whallon NL
- 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 HH
- Williams S
- Willis C
- Willocq S
- Wingerter-Seez I
- Winkels E
- Winklmeier F
- Winston OJ
- Winter BT
- Wittgen M
- Wobisch M
- Wolf A
- Wolf TMH
- Wolff R
- Wolker R
- Wollrath J
- Wolter MW
- Wolters H
- Wong VWS
- Woods NL
- Worm SD
- Wosiek BK
- Wozniak KW
- Wraight K
- Wu SL
- Wu X
- Wu Y
- Wyatt TR
- Wynne BM
- Xella S
- Xi Z
- Xia L
- Xiao X
- Xiotidis I
- Xu D
- Xu H
- Xu L
- Xu T
- Xu W
- Xu Z
- Yabsley B
- Yacoob S
- Yajima K
- Yallup DP
- Yamaguchi N
- Yamaguchi Y
- Yamamoto A
- Yamatani M
- Yamazaki T
- Yamazaki Y
- Yan Z
- Yang HJ
- Yang HT
- Yang S
- Yang T
- Yang X
- Yang Y
- Yao W-M
- Yap YC
- Yasu Y
- Yatsenko E
- Ye H
- Ye J
- Ye S
- Yeletskikh I
- Yexley MR
- Yigitbasi E
- Yildiz HD
- 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
- Zaripovas DR
- Zeissner S
- Zeitnitz C
- Zemaityte G
- Zeng JC
- Zenin O
- Zenis T
- Zerwas D
- Zgubic M
- Zhang B
- Zhang DF
- Zhang G
- Zhang H
- Zhang J
- Zhang L
- Zhang M
- Zhang R
- Zhang S
- Zhang X
- Zhang Y
- Zhang Z
- Zhao P
- Zhao Z
- Zhemchugov A
- Zheng Z
- Zhong D
- Zhou B
- Zhou C
- Zhou M
- Zhou MS
- 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 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
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Results of a search for new phenomena in final states with an energetic jet and large missing transverse momentum are reported. The search uses 20.3 fb−1 of √ s = 8 TeV data collected in 2012 with the ATLAS detector at the LHC. Events are required to have at least one jet with pT > 120 GeV and no leptons. Nine signal regions are considered with increasing missing transverse momentum requirements between Emiss T > 150 GeV and Emiss T > 700 GeV. Good agreement is observed between the number of events in data and Standard Model expectations. The results are translated into exclusion limits on models with either large extra spatial dimensions, pair production of weakly interacting dark matter candidates, or production of very light gravitinos in a gauge-mediated supersymmetric model. In addition, limits on the production of an invisibly decaying Higgs-like boson leading to similar topologies in the final state are presente
Counter-Gradient Variation in Respiratory Performance of Coral Reef Fishes at Elevated Temperatures
- Author
- AL Perry
- AP Farrell
- AS Brierley
- C Parmesan
- CA Deutsch
- DO Conover
- DO Conover
- EM Goolish
- ES Poloczanska
- G Gerlach
- G-R Walther
- GA Meehl
- GE Nilsson
- GE Nilsson
- GE Nilsson
- GE Nilsson
- GR Allen
- GR Allen
- Göran E. Nilsson
- HO Pörtner
- HO Pörtner
- HO Pörtner
- HO Pörtner
- HO Pörtner
- J Sollid
- JC Lai
- JE Randall
- JJ Tewksbury
- JL Gardner
- JM Grebmeier
- JM Lough
- LJ Chapman
- LK Bay
- M Schroer
- MJ Angilletta
- NA Fangue
- Naomi M. Gardiner
- NL Bindoff
- NM Gardiner
- Philip L. Munday
- PJ Doherty
- PL Munday
- PM Schulte
- R Levins
- RJ Gonzalez
- S Schaak
- S Östlund-Nilsson
- SB Munch
- Tamara Natasha Romanuk
- TL Root
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2010
- Field of study
The response of species to global warming depends on how different populations are affected by increasing temperature throughout the species' geographic range. Local adaptation to thermal gradients could cause populations in different parts of the range to respond differently. In aquatic systems, keeping pace with increased oxygen demand is the key parameter affecting species' response to higher temperatures. Therefore, respiratory performance is expected to vary between populations at different latitudes because they experience different thermal environments. We tested for geographical variation in respiratory performance of tropical marine fishes by comparing thermal effects on resting and maximum rates of oxygen uptake for six species of coral reef fish at two locations on the Great Barrier Reef (GBR), Australia. The two locations, Heron Island and Lizard Island, are separated by approximately 1200 km along a latitudinal gradient. We found strong counter-gradient variation in aerobic scope between locations in four species from two families (Pomacentridae and Apogonidae). High-latitude populations (Heron Island, southern GBR) performed significantly better than low-latitude populations (Lizard Island, northern GBR) at temperatures up to 5°C above average summer surface-water temperature. The other two species showed no difference in aerobic scope between locations. Latitudinal variation in aerobic scope was primarily driven by up to 80% higher maximum rates of oxygen uptake in the higher latitude populations. Our findings suggest that compensatory mechanisms in high-latitude populations enhance their performance at extreme temperatures, and consequently, that high-latitude populations of reef fishes will be less impacted by ocean warming than will low-latitude populations
A Crucial Role for Infected-Cell/Antibody Immune Complexes in the Enhancement of Endogenous Antiviral Immunity by Short Passive Immunotherapy
- Author
- A Bergthaler
- A Corbin
- A Gallimore
- A Regnault
- A Takada
- A Trkola
- B Heyman
- C Ohlen
- CA Guyre
- Chantal Jacquet
- CJ Pitcher
- CP Simmons
- D Lavillette
- D Valmori
- DD Pinschewer
- DH Schuurhuis
- DH Schuurhuis
- E Galun
- F Aiuti
- F Villinger
- FJ McAtee
- GM Lee
- H Dreja
- H Song
- H Wu
- Henri-Alexandre Michaud
- HJ Hong
- IM Stromnes
- J Sui
- Javier Hernandez
- JL Portis
- JM Pestka
- JM Reichert
- K Akiyama
- K Rafiq
- K Schepers
- Kevin Thiolon
- KM Dhodapkar
- L Gros
- L Gros
- L Gros
- L Hangartner
- Laurent Gros
- LJ Brady
- LV Vasovic
- M Deutsch
- M Elrefaei
- M Pelegrin
- M Sitbon
- M Sitbon
- Marc Piechaczyk
- MB Lutz
- MF Bachmann
- Mireia Pelegrin
- N Selenko
- NL Haigwood
- R Weiss
- RH Carter
- Richard A. Koup
- RJ Kurlander
- RM Zinkernagel
- Roudaina Nasser
- S Balkow
- SH Pincus
- SM Hammer
- SN Franki
- T Oliphant
- Tiphanie Gomard
- V Groh
- W Chen
- WA Marasco
- WP Lynch
- X Yao
- Y Hamano
- Y Wu
- Z Zhu
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2010
- Field of study
Antiviral monoclonal antibodies (mAbs) represent promising therapeutics. However, most mAbs-based immunotherapies conducted so far have only considered the blunting of viral propagation and not other possible therapeutic effects independent of virus neutralization, namely the modulation of the endogenous immune response. As induction of long-term antiviral immunity still remains a paramount challenge for treating chronic infections, we have asked here whether neutralizing mAbs can, in addition to blunting viral propagation, exert immunomodulatory effects with protective outcomes. Supporting this idea, we report here that mice infected with the FrCasE murine retrovirus on day 8 after birth die of leukemia within 4–5 months and mount a non-protective immune response, whereas those rapidly subjected to short immunotherapy with a neutralizing mAb survive healthy and mount a long-lasting protective antiviral immunity with strong humoral and cellular immune responses. Interestingly, the administered mAb mediates lysis of infected cells through an antibody-dependent cell cytotoxicity (ADCC) mechanism. In addition, it forms immune complexes (ICs) with infected cells that enhance antiviral CTL responses through FcγR-mediated binding to dendritic cells (DCs). Importantly, the endogenous antiviral antibodies generated in mAb-treated mice also display the same properties, allowing containment of viral propagation and enhancement of memory cellular responses after disappearance of the administered mAb. Thus, our data demonstrate that neutralizing antiviral mAbs can act as immunomodulatory agents capable of stimulating a protective immunity lasting long after the end of the treatment. They also show an important role of infected-cells/antibody complexes in the induction and the maintenance of protective immunity through enhancement of both primary and memory antiviral T-cell responses. They also indicate that targeting infected cells, and not just viruses, by antibodies can be crucial for elicitation of efficient, long-lasting antiviral T-cell responses. This must be considered when designing antiviral mAb-based immunotherapies
Thermal Tolerance of the Coffee Berry Borer Hypothenemus hampei: Predictions of Climate Change Impact on a Tropical Insect Pest
- Author
- A Addo-Bediako
- A Campbell
- A Damon
- A Davidson
- A Jaramillo
- A Jaramillo
- A Maia
- A Teodoro
- Adenirin Chabi-Olaye
- AE Bustillo
- Alvaro Jaramillo
- AP Davis
- BB Lin
- C Alègre
- C Gay
- C Gordon
- C Parmesan
- C Parmesan
- CA Deutsch
- Charles Kamonjo
- Christian Borgemeister
- CR Ruiz
- DA Roff
- DJ Lactin
- DL Musolin
- E Mendesil
- ED Assad
- F Damatta
- FE Vega
- FE Vega
- FE Vega
- FE Vega
- FE Vega
- Fernando E. Vega
- FI Hulting
- FL Wellman
- GC Stevens
- GRID
- Hans-Michael Poehling
- HS Pinto
- I Perfecto
- ID Hodkinson
- ID Hodkinson
- J Arcila
- J Bale
- J Beer
- J Bergamin
- J Jaramillo
- J Jaramillo
- J Pérez
- J Ticheler
- JA Logan
- JA Patz
- JAT Amaral do
- JM Tylianakis
- JS Terblanche
- JS Terblanche
- JT Houghton
- Juliana Jaramillo
- JV Romero
- JV Romero
- K Kiritani
- K Kiritani
- KJ Gaston
- MP Ayres
- MR Salazar
- NJ Dingemanse
- NL Ward
- P Benavides
- P Calosi
- P Vaast
- PS Baker
- PS Baker
- PT De Alvim
- R Coste
- R Karban
- R Menendez
- RE Forkner
- RG Muschler
- RH Le Pelley
- RJC Cannon
- RS Wilson
- S Fernandez
- S Neuvonen
- Sean Rands
- T Gomi
- TW Kirkpatrick
- VL Barradas
- WH van der Putten
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2009
- Field of study
Coffee is predicted to be severely affected by climate change. We determined the thermal tolerance of the coffee berry borer , Hypothenemus hampei, the most devastating pest of coffee worldwide, and make inferences on the possible effects of climate change using climatic data from Colombia, Kenya, Tanzania, and Ethiopia. For this, the effect of eight temperature regimes (15, 20, 23, 25, 27, 30, 33 and 35°C) on the bionomics of H. hampei was studied. Successful egg to adult development occurred between 20–30°C. Using linear regression and a modified Logan model, the lower and upper thresholds for development were estimated at 14.9 and 32°C, respectively. In Kenya and Colombia, the number of pest generations per year was considerably and positively correlated with the warming tolerance. Analysing 32 years of climatic data from Jimma (Ethiopia) revealed that before 1984 it was too cold for H. hampei to complete even one generation per year, but thereafter, because of rising temperatures in the area, 1–2 generations per year/coffee season could be completed. Calculated data on warming tolerance and thermal safety margins of H. hampei for the three East African locations showed considerably high variability compared to the Colombian site. The model indicates that for every 1°C rise in thermal optimum (Topt.), the maximum intrinsic rate of increase (rmax) will increase by an average of 8.5%. The effects of climate change on the further range of H. hampei distribution and possible adaption strategies are discussed. Abstracts in Spanish and French are provided as supplementary material Abstract S1 and Abstract S2
Computational Mass Spectrometry–Based Proteomics
- Author
- A Bell
- A Bertsch
- A Keller
- A Subramanian
- A Thompson
- AC Gavin
- AHP America
- AI Nesvizhskii
- AI Nesvizhskii
- AK Yocum
- AL Boulesteix
- AL Oberg
- AR Joyce
- AW Liew
- B Domon
- B MacLean
- B Schwanhäusser
- C Ansong
- C H
- C Kumar
- CH Ahrens
- D Huang
- DF Ransohoff
- DH Lundgren
- DL Tabb
- DW Huang
- EW Deutsch
- F Emmert-Streib
- Fran Lewitter
- H Choi
- H Lam
- J Cox
- J Cox
- J Hu
- JA Cham Mead
- JD Venable
- JV Olsen
- JV Olsen
- K Jeong
- L Käll
- L Nie
- L Reiter
- L Reiter
- L Valledor
- LMF de Godoy
- LN Mueller
- Lukas Käll
- M Ackermann
- M Beck
- M Gstaiger
- M Mann
- M Sturm
- M Uhlen
- MW Duncan
- MYK Brusniak
- N Bandeira
- N Castellana
- N Gehlenborg
- N Gupta
- N Gupta
- N Rifai
- NL Anderson
- NM Griffin
- NR Kitteringham
- Olga Vitek
- P Mallick
- P Picotti
- P Picotti
- PL Ross
- R Aebersold
- R Clarke
- R de Sousa Abreu
- R Moore
- R Sharan
- R Wu
- RA Irizarry
- RK Nibbe
- S Abbatiello
- S Carr
- S Dasari
- S Hanash
- S Pan
- SE Ong
- SJ Callister
- SS Huang
- T Aittokallio
- T Clough
- T Geiger
- T Maier
- T Nilsson
- TA Addona
- TC Walther
- TH Corzett
- V Granholm
- V Lange
- WX Schulze
- Y Karpievitch
- YF Li
- Publication venue
- Public Library of Science
- Publication date
- 01/12/2011
- Field of study
Search for heavy neutral Higgs bosons produced in association with b-quarks and decaying into b-quarks at root s=13 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abbott DC
- Abdinov O
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
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- Zhemchugov A
- Zheng Z
- Zhong D
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- Zu Theenhausen HM
- Zwalinski L
- Publication venue
- AMER PHYSICAL SOC
- Publication date
- 13/08/2020
- Field of study
A search for heavy neutral Higgs bosons produced in association with one or two
b
-quarks and decaying to
b
-quark pairs is presented using
27.8
fb
−
1
of
√
s
=
13
TeV
proton-proton collision data recorded by the ATLAS detector at the Large Hadron Collider during 2015 and 2016. No evidence of a signal is found. Upper limits on the heavy neutral Higgs boson production cross section times its branching ratio to
b
¯
b
are set, ranging from 4.0 to 0.6 pb at 95% confidence level over a Higgs boson mass range of 450 to 1400 GeV. Results are interpreted within the two-Higgs-doublet model and the minimal supersymmetric Standard Model
Measurement of single top-quark production in association with a W boson in the single-lepton channel at \sqrt{s} = 8\,\text {TeV} with the ATLAS detector
- Author
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- Zimmermann S
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- Publication venue
- 'Springer Fachmedien Wiesbaden GmbH'
- Publication date
- 01/01/2021
- Field of study
The production cross-section of a top quark in association with a W boson is measured using proton–proton collisions at \sqrt{s} = 8\,\text {TeV}. The dataset corresponds to an integrated luminosity of 20.2\,\text {fb}^{-1}, and was collected in 2012 by the ATLAS detector at the Large Hadron Collider at CERN. The analysis is performed in the single-lepton channel. Events are selected by requiring one isolated lepton (electron or muon) and at least three jets. A neural network is trained to separate the tW signal from the dominant t{\bar{t}} background. The cross-section is extracted from a binned profile maximum-likelihood fit to a two-dimensional discriminant built from the neural-network output and the invariant mass of the hadronically decaying W boson. The measured cross-section is \sigma _{tW} = 26 \pm 7\,\text {pb}, in good agreement with the Standard Model expectation
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