431 research outputs found
Environmental and Climatic Determinants of Molecular Diversity and Genetic Population Structure in a Coenagrionid Damselfly
- Author
- A Cordero
- A Cordero Rivera
- A Cordero-Rivera
- A Lammi
- Adolfo Cordero-Rivera
- B Charlesworth
- B Hansson
- Bengt Hansson
- BON Hinnekint
- C Hassall
- C Parmesan
- C Riginos
- C Stettmer
- C-H Kuo
- CG Eckert
- CN Parmesan
- CN Parmesan
- D Bekkevold
- D Falush
- D Keller
- D Smallshire
- Daniel Ortiz-Barrientos
- E Crispo
- E Svensson
- EI Svensson
- EI Svensson
- Erik I. Svensson
- F Rousset
- G Evanno
- G García-Ramos
- G Gerlach
- G Guillot
- G Guillot
- G Hewitt
- G Luikart
- GA Hoelzer
- GM Hewitt
- GM Hewitt
- J Abbott
- J Goudet
- J Sambrook
- JK Abbott
- JK Pritchard
- JR Bridle
- KF Conrad
- L Excoffier
- L Monetti
- LOU Jost
- M Foll
- M Kirkpatrick
- M Mimura
- M Slatkin
- M Slatkin
- M Slatkin
- M Wellenreuther
- M Wellenreuther
- MA Beaumont
- MA Palmer
- MA Peterson
- Maren Wellenreuther
- ME Hellberg
- MJ Genner
- MJ Kittlein
- N Balkenhol
- NG Crawford
- OE Gaggiotti
- PC Brunner
- PC Watts
- PC Watts
- PC Watts
- PS Corbet
- R Hickling
- R Ihaka
- R Sánchez-Guillén
- RA Sánchez-Guillén
- RA Sánchez-Guillén
- RA Sánchez-Guillén
- RL Eckstein
- Rosa A. Sánchez-Guillén
- RR Askew
- S Mopper
- S Piry
- S Wright
- SD Gribbin
- SW Dunkle
- TWJ Garner
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
Identifying environmental factors that structure intraspecific genetic diversity
is of interest for both habitat preservation and biodiversity conservation.
Recent advances in statistical and geographical genetics make it possible to
investigate how environmental factors affect geographic organisation and
population structure of molecular genetic diversity within species. Here we
present a study on a common and wide ranging insect, the blue tailed damselfly
Ischnuraelegans, which has been the target of many
ecological and evolutionary studies. We addressed the following questions: (i)
Is the population structure affected by longitudinal or latitudinal gradients?;
(ii) Do geographic boundaries limit gene flow?; (iii) Does geographic distance
affect connectivity and is there a signature of past bottlenecks?; (iv) Is there
evidence of a recent range expansion and (vi) what is the effect of geography
and climatic factors on population structure? We found low to moderate genetic
sub-structuring between populations (mean
FST = 0.06,
Dest = 0.12), and an effect of longitude, but
not latitude, on genetic diversity. No significant effects of geographic
boundaries (e.g. water bodies) were found. FST-and
Dest-values increased with geographic distance; however, there was no
evidence for recent bottlenecks. Finally, we did not detect any molecular
signatures of range expansions or an effect of geographic suitability, although
local precipitation had a strong effect on genetic differentiation. The
population structure of this small insect has probably been shaped by ecological
factors that are correlated with longitudinal gradients, geographic distances,
and local precipitation. The relatively weak global population structure and
high degree of genetic variation within populations suggest that I.
elegans has high dispersal ability, which is consistent with this
species being an effective and early coloniser of new habitats
Quercetin and Allopurinol Ameliorate Kidney Injury in STZ-Treated Rats with Regulation of Renal NLRP3 Inflammasome Activation and Lipid Accumulation
- Author
- A Hiukka
- A Momeni
- A Tone
- A Vilaysane
- AA Shigeoka
- AR Kraynak
- B Vandanmagsar
- C Keembiyehetty
- CA Dinarello
- CC Chuang
- CH Wu
- Chuang Wang
- CSL Arlehamn
- CW Park
- EC Estevez
- F Frigerio
- Fu-Meng Wang
- GH Tesch
- H Poeck
- HA Hostetler
- HG Eskandari
- I Tamai
- IT Abdel-Raheem
- J Kerner
- J Park
- JF Navarro-Gonzalez
- JF Navarro-González
- JW Griffith
- K Rajamäki
- KE Wellen
- KJ Livak
- L Rivera
- L Sun
- LA Joosten
- Ling-Dong Kong
- M Anjaneyulu
- M Kobori
- M Krzystanek
- M Minami
- M Murea
- MA Hediger
- MY Donath
- O Ergun
- O Poulain-Godefroy
- OE Ayodele
- P Duewell
- P Gasse
- P Hovind
- P Hovind
- QH Hu
- Qing-Yu Zhang
- QQ Cheng
- R Stienstra
- RA Power
- RA Zager
- RA Zager
- RL Edwards
- S Farfari
- S Reungjui
- Samithamby Jeyaseelan
- SJ Wakil
- SL Fink
- SL Masters
- SO Olusi
- SS Iyer
- T Fernandes-Alnemri
- T Kosugi
- T Mahesh
- Y Guan
- Ying Pan
- YT Moriwaki
- Z Wang
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
Hyperuricemia, hyperlipidemia and inflammation are associated with diabetic nephropathy. The NLRP3 inflammasome-mediated inflammation is recently recognized in the development of kidney injury. Urate and lipid are considered as danger signals in the NLRP3 inflammasome activation. Although dietary flavonoid quercetin and allopurinol alleviate hyperuricemia, dyslipidmia and inflammation, their nephroprotective effects are currently unknown. In this study, we used streptozotocin (STZ)-induced diabetic nephropathy model with hyperuricemia and dyslipidemia in rats, and found over-expression of renal inflammasome components NLRP3, apoptosis-associated speck-like protein and Caspase-1, resulting in elevation of IL-1β and IL-18, with subsequently deteriorated renal injury. These findings demonstrated the possible association between renal NLRP3 inflammasome activation and lipid accumulation to superimpose causes of nephrotoxicity in STZ-treated rats. The treatment of quercetin and allopurinol regulated renal urate transport-related proteins to reduce hyperuricemia, and lipid metabolism-related genes to alleviate kidney lipid accumulation in STZ-treated rats. Furthermore, quercetin and allopurinol were found to suppress renal NLRP3 inflammasome activation, at least partly, via their anti-hyperuricemic and anti-dyslipidemic effects, resulting in the amelioration of STZ-induced the superimposed nephrotoxicity in rats. These results may provide a basis for the prevention of diabetes-associated nephrotoxicity with urate-lowering agents such as quercetin and allopurinol
Evidence for rangewide panmixia despite multiple barriers to dispersal in a marine mussel
- Author
- A Folkard
- A Jueterbock
- A Liaw
- A Makaoui
- A Villamor
- A Zhan
- AB Dennis
- AF Rozenfeld
- AH Fielding
- ALF Lacerda
- AM Bowcock
- AP Diz
- AR Robinson
- B Bayne
- B Emanuel
- B Martínez
- BP Kinlan
- BS Weir
- C Griffiths
- C Millot
- C Oosterhout van
- CD Harley
- CE Rivera de
- CR Lourenço
- D Posada
- DA Earl
- DW Hicks
- DW Hicks
- E Sanford
- E Vidal-Fernández
- F Alberto
- FP Lima
- FP Lima
- FP Lima
- G Evanno
- G Zardi
- G Zardi
- GI Zardi
- H Demarcq
- H Jaziri
- H Reiss
- HJ Bandelt
- I Calderón
- I Munwes
- J Arístegui
- J Assis
- J Assis
- J Eiríksson
- J Erlandsson
- J Goudet
- J Marcello
- J Neiva
- J Provan
- J Sunday
- J Tintore
- JB Sigurdsson
- JD Storey
- JK Pritchard
- JM Harris
- K Keenan
- K Nicastro
- K Tamura
- KR Nicastro
- L Excoffier
- L Jin
- L Tyberghein
- LOU Jost
- M Chlaida
- M Chlaida
- M Coll
- M Jakobsson
- M Neethling
- M Rubal
- M Shafee
- M Tagliarolo
- ME Mann
- ME Newman
- MJ Anderson
- MM Lal
- N Coelho
- N Mieszkowska
- O Allouche
- OE Diekmann
- P Librado
- P Villesen
- PAR Hockey
- PB Fenberg
- PM Callapez
- PR Teske
- R Buonomo
- R Engler
- R Fernández
- R Pérez-Portela
- RA Oomen
- RL Cunha
- RL Varney
- RM Chefaoui
- RM Chefaoui
- RP Kelly
- S Fratini
- S Leidenberger
- SG Pereira
- SJ Bownes
- SJ Jones
- T Jombart
- T Jombart
- T Pastor
- T Patarnello
- Y-M Abada-Boudjema
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2017
- Field of study
Oceanographic features shape the distributional and genetic patterns of marine species by interrupting or promoting connections among populations. Although general patterns commonly arise, distributional ranges and genetic structure are species-specific and do not always comply with the expected trends. By applying a multimarker genetic approach combined with Lagrangian particle simulations (LPS) we tested the hypothesis that oceanographic features along northeastern Atlantic and Mediterranean shores influence dispersal potential and genetic structure of the intertidal mussel Perna perna. Additionally, by performing environmental niche modelling we assessed the potential and realized niche of P. perna along its entire native distributional range and the environmental factors that best explain its realized distribution. Perna perna showed evidence of panmixia across > 4,000 km despite several oceanographic breaking points detected by LPS. This is probably the result of a combination of life history traits, continuous habitat availability and stepping-stone dynamics. Moreover, the niche modelling framework depicted minimum sea surface temperatures (SST) as the major factor shaping P. perna distributional range limits along its native areas. Forthcoming warming SST is expected to further change these limits and allow the species to expand its range polewards though this may be accompanied by retreat from warmer areas.Fundacao para a Ciencia e Tecnologia (FCT-MEC, Portugal) [UID/Multi/04326/2013, IF/01413/2014/CP1217/CT0004]; South African Research Chairs Initiative (SARChI) of the Department of Science and Technology; National Research Foundation; South African National Research Foundation (NRF); Portuguese Fundacao para a Ciencia e Tecnologia (FCT) [SFRH/BPD/85040/2012, SFRH/BPD/111003/2015]info:eu-repo/semantics/publishedVersio
Edible bio-based nanostructures: delivery, absorption and potential toxicity
- Author
- A des Rieux
- A Guri
- A Hafner
- A Lakshmanan
- A Manke
- A Poma
- A Shpigelman
- A Totosaus
- A Zattoni
- AC Hunter
- AC Pinheiro
- AH Sneharani
- AJ Genot
- AJ Vander
- AL Neal
- Ana C. Pinheiro
- Ana I. Bourbon
- António A. Vicente
- AO Elzoghby
- AS Karakoti
- AV Kabanov
- B Díaz
- B He
- B Kowalczyk
- B Loretz
- B Sarmento
- B Semete
- BD Chithrani
- BJ Aungst
- BS Zolnik
- C Blasco
- C Chang
- C Feng
- C Feng
- C Giese
- C Pinto Reis
- C Prego
- C Szakal
- C Zhu
- CB Woitiski
- CC Berton-Carabin
- CE Mora-Huertas
- D Dell’Orco
- D Guzey
- D Rosenblum
- D-W Tang
- DJ McClements
- DJ McClements
- DJ McClements
- DV Tatiraju
- DY Lai
- E Acosta
- E Dickinson
- E Roger
- E Troncoso
- EC
- EC
- EFSA
- EFSA
- F Kong
- F Leonard
- F Liu
- F Lu
- F Wang
- F. Xavier Malcata
- FE Alemdaroglu
- G Joshi
- G Sahay
- GB Sukhorukov
- GK Agrawal
- H Bouwmeester
- H Kettiger
- H Ruh
- H Salminen
- H Zhang
- H-J Doh
- HC Fischer
- HD Silva
- Hélder D. Silva
- IJ Joye
- IJ Joye
- IL Bergin
- J Cui
- J Lee
- J Ma
- J Wolfram
- J Zhao
- J-E Kim
- JE Wong
- JJ Powell
- JK Oh
- Joana T. Martins
- JP Rao
- JPK Tan
- JW Loh
- K Kesarwani
- K Ofokansi
- K Sonaje
- K Thanki
- KB Chalasani
- KE Fischer
- KL Aillon
- KR Vega-Villa
- KS Soppimath
- L Chen
- L Chen
- L Donato-Capel
- L Hu
- L Plapied
- L Sagalowicz
- L Salvia-Trujillo
- L Yan
- LL Mercato del
- LM Ensign
- Lorenzo Pastrana
- M Cerqueira
- M Delcea
- M Desai
- M Elsabahy
- M Grassi
- M Mahmoudi
- M Moros
- M Motornov
- M Rajaonarivony
- M Rubinstein
- M Sessa
- M Subirade
- M Torres-Lugo
- M Zhaojie
- M-C Chen
- MA Azevedo
- MA Dobrovolskaia
- MA Lopes
- Melissa C. Rivera
- Miguel A. Cerqueira
- MJ Buehler
- MR Papasani
- N Atal
- N Khalid
- NM Molino
- O Akbulut
- OE Pérez
- P Couvreur
- P Kovatcheva-Datchary
- P M-M
- P Sanguansri
- P Zimet
- PP Dandekar
- Q Peng
- R Lima De
- R Peters
- R Simón-Vázquez
- R Wang
- RK Das
- S Arora
- S Drusch
- S Dufort
- S Patil
- S Sharifi
- S Vicente
- S Xu
- SJ Torne
- SK Lai
- SK Mwilu
- SM Krug
- SV Vinogradov
- T David-Birman
- T Jung
- T Lozano
- T Miller
- TPJ Linsinger
- W Somchue
- WE Hennink
- X Li
- X Zhang
- Y Jin
- Y Li
- Y Li
- Y Liu
- Y Luo
- Y Sheng
- Y Ting
- Y Wang
- Y Yin
- Y-H Lin
- Z Liu
- Z Teng
- Z Teng
- Z-H Zhang
- África González-Fernández
- Óscar L. Ramos
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
The development of bio-based nanostructures as nanocarriers of bioactive compounds to specific body sites has been presented as a hot topic in food, pharmaceutical and nanotechnology fields. Food and pharmaceutical industries seek to explore the huge potential of these nanostructures, once they can be entirely composed of biocompatible and non-toxic materials. At the same time, they allow the incorporation of lipophilic and hydrophilic bioactive compounds protecting them against degradation, maintaining its active and functional performance. Nevertheless, the physicochemical properties of such structures (e.g., size and charge) could change significantly their behavior in the gastrointestinal (GI) tract. The main challenges in the development of these nanostructures are the proper characterization and understanding of the processes occurring at their surface, when in contact with living systems. This is crucial to understand their delivery and absorption behavior as well as to recognize potential toxicological effects. This review will provide an insight into the recent innovations and challenges in the field of delivery via GI tract using bio-based nanostructures. Also, an overview of the approaches followed to ensure an effective deliver (e.g., avoiding physiological barriers) and to enhance stability and absorptive intestinal uptake of bioactive compounds will be provided. Information about nanostructures potential toxicity and a concise description of the in vitro and in vivo toxicity studies will also be given.Joana T. Martins, Oscar L. Ramos, Ana C. Pinheiro, Ana I. Bourbon, Helder D. Silva and Miguel A. Cerqueira (SFRH/BPD/89992/2012, SFRH/BPD/80766/2011, SFRH/BPD/101181/2014, SFRH/BD/73178/2010, SFRH/BD/81288/2011, and SFRH/BPD/72753/2010, respectively) are the recipients of a fellowship from the Fundacao para a Ciencia e Tecnologia (FCT, POPH-QREN and FSE, Portugal). The authors thank the FCT Strategic Project PEst-OE/EQB/LA0023/2013 and the project "BioInd-Biotechnology and Bioengineering for improved Industrial and Agro-Food processes," REF.NORTE-07-0124-FEDER-000028, co-funded by the Programa Operacional Regional do Norte (ON.2-O Novo Norte), QREN, FEDER. We also thank to the European Commission: BIOCAPS (316265, FP7/REGPOT-2012-2013.1) and Xunta de Galicia: Agrupamento INBIOMED (2012/273) and Grupo con potencial de crecimiento. The support of EU Cost Action FA1001 is gratefully acknowledged
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
Microwave-induced resistance oscillations and zero resistance states in 2D bilayer systems
- Author
- 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
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- 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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- Yildiz H Duran
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- Yuen SPY
- Yusuff I
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- Zalieckas J
- Zambito S
- Zanzi D
- Zeitnitz C
- Zemaityte G
- Zeng JC
- Zeng Q
- Zenin O
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- Zerwas D
- Zgubic M
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- Zhang Z
- Zhao X
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zhou B
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- Zhou L
- Zhou M
- Zhou M
- Zhou N
- Zhou Y
- Zhu CG
- Zhu H
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- 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
Operation and performance of the ATLAS Tile Calorimeter in Run 1
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Abeloos B
- Abhayasinghe DK
- Abidi SH
- Abouelfadl 
- 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
- Akerstedt H
- Akilli E
- Akimov AV
- Alberghi GL
- Albert J
- Albicocco P
- Alconada Verzini MJ
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexander G
- 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 
- Alviggi MG
- Amadio BT
- Amaral Coutinho Y
- Ambroz L
- Amelung C
- Amidei D
- Amor 
- 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
- Arce ATH
- Ardell RE
- Arduh FA
- Argos FC
- Arguin J-
- Argyropoulos S
- Armadans R
- 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
- Astigarraga ME
- Atkin RJ
- Atkinson M
- Atlay NB
- Auerbach B
- Augsten K
- Avolio G
- Avramidou R
- Axen B
- Ayoub MK
- Azuelos G
- Álvarez Piqueras D
- Åkesson TPA
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- Baca MJ
- Bachacou H
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- Backes M
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- Bahilo JJL
- Bahmani M
- Bahrasemani H
- Bailey AJ
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- Baldin EM
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- Balunas WK
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- Banerjee S
- Bannoura AAE
- Barak L
- Barbe WM
- Barberio EL
- Barberis D
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- Barisits M
- Barkeloo J
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- Barnovska-Blenessy Z
- Baroncelli A
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- Barranco Navarro L
- Barreiro Guimarães da Costa J
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- Batista SJ
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- Batley JR
- Battaglia M
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- Bauer F
- Bauer KT
- Bawa HS
- Beacham JB
- Beattie MD
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- Biesuz NV
- Biglietti M
- Billoud TRV
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- Black JE
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- Blair RE
- Blazek T
- Bloch I
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- Blumenschein U
- Blunier D
- Bobbink GJ
- Bobrovnikov VS
- Bocchetta SS
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- Bogavac D
- Bogdanchikov AG
- Bohm C
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- Bossio Sola JD
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- Bruckman de Renstrom PA
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- Buzatu A
- Buzykaev AR
- Bührer F
- Büscher D
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- Cabras G
- Cabrera Urbán S
- Caforio D
- Cai H
- Cairo VMM
- Cakir I
- Cakir O
- Calace N
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- Calandri A
- Calderini G
- Calfayan P
- Callea G
- Caloba LP
- Calvente Lopez S
- Calvet D
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- Camarda S
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- Camincher C
- Campana S
- Campanelli M
- Camplani A
- Campoverde A
- Canale V
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- Cao T
- Cao Y
- Capeans Garrido MDM
- Caprini I
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- Capua M
- Carbone RM
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- Cardillo FC
- Carli I
- Carli T
- Carlino G
- Carlson BT
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- Carrillo-Montoya GD
- Casadei D
- Casado MP
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- Casolino M
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- Castillo Gimenez V
- Castillo FL
- Castro NF
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- Cerqueira AS
- Cerri A
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- Cetin SA
- Chafaq A
- Chakraborty D
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- Chan YL
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- Chapman JD
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- Chau CC
- Chavez Barajas CA
- Che S
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- Chen C
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- Cherkaoui El Moursli R
- Cheu E
- Cheung K
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- Chiarella V
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- Christodoulou V
- Chu MC
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- Ciocio A
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- Cunha 
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- Czodrowski P
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- Fiolhais MCN
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- Lipniacka A
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- Lopez 
- Lopez JA
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- Zwalinski L
- Ženiš T
- Živković L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
The Tile Calorimeter is the hadron calorimeter covering the central region of the ATLAS experiment at the Large Hadron Collider. Approximately 10,000 photomultipliers collect light from scintillating tiles acting as the active material sandwiched between slabs of steel absorber. This paper gives an overview of the calorimeter’s performance during the years 2008–2012 using cosmic-ray muon events and proton–proton collision data at centre-of-mass energies of 7 and 8TeV with a total integrated luminosity of nearly 30 fb−1. The signal reconstruction methods, calibration systems as well as the detector operation status are presented. The energy and time calibration methods performed excellently, resulting in good stability of the calorimeter response under varying conditions during the LHC Run 1. Finally, the Tile Calorimeter response to isolated muons and hadrons as well as to jets from proton–proton collisions is presented. The results demonstrate excellent performance in accord with specifications mentioned in the Technical Design Report
Performance of missing transverse momentum reconstruction with the ATLAS detector using proton–proton collisions at √s = 13 TeV
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
The performance of the missing transverse momentum (EmissT) reconstruction with the ATLAS detector is evaluated using data collected in proton–proton collisions at the LHC at a centre-of-mass energy of 13 TeV in 2015. To reconstruct EmissT, fully calibrated electrons, muons, photons, hadronically decaying τ -leptons, and jets reconstructed from calorimeter energy deposits and charged-particle tracks are used. These are combined with the soft hadronic activity measured by reconstructed charged-particle tracks not associated with the hard objects. Possible double counting of contributions from reconstructed charged-particle tracks from the inner detector, energy deposits in the calorimeter, and reconstructed muons from the muon spectrometer is avoided by applying a signal ambiguity resolution procedure which rejects already used signals when combining the various EmissT contributions. The individual terms as well as the overall reconstructed EmissT are evaluated with various performance metrics for scale (linearity), resolution, and sensitivity to the data-taking conditions. The method developed to determine the systematic uncertainties of the EmissT scale and resolution is discussed. Results are shown based on the full 2015 data sample corresponding to an integrated luminosity of 3.2 fb−1
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