391 research outputs found
Gender Differences in Carbohydrate Metabolism and Carbohydrate Loading
- Author
- AC Hackney
- AE Hardman
- AL Friedlander
- AP James
- B Kiens
- B Mittendorfer
- BC Ruby
- BC Ruby
- BJ Nicklas
- C Roepstorff
- CA Tate
- Darryn Willoughby
- EA Galliven
- EJ Schaefer
- EV Lambert
- GA Brooks
- GS Ellis
- J Bergstrom
- J Karlsson
- JA Driskell
- JA Hawley
- JA Romijn
- JA Romijn
- Jennifer Wismann
- JL Andrews
- JL Walker
- KT Borer
- L Millet
- LJ Tarnopolsky
- LM Burke
- LM Burke
- LS Lamont
- M Tarnopolsky
- MA Tarnopolsky
- MA Tarnopolsky
- MAES Tarnopolsky
- PA Hansen
- S Carter
- SE Campbell
- SL Carter
- TJ Horton
- TP Rooney
- WM Sherman
- ZV Kendrick
- ZV Kendrick
- Publication venue
- BioMed Central
- Publication date
- 01/01/2006
- Field of study
Prior to endurance competition, many endurance athletes participate in a carbohydrate loading regimen in order to help delay the onset of fatigue. The "classic" regimen generally includes an intense glycogen depleting training period of approximately two days followed by a glycogen loading period for 3–4 days, ingesting approximately 60–70% of total energy intake as carbohydrates, while the newer method does not consist of an intense glycogen depletion protocol. However, recent evidence has indicated that glycogen loading does not occur in the same manner for males and females, thus affecting performance. The scope of this literature review will include a brief description of the role of estradiol in relation to metabolism and gender differences seen in carbohydrate metabolism and loading
Women Have Higher Protein Content of β-Oxidation Enzymes in Skeletal Muscle than Men
- Author
- A Fredenrich
- AC Maher
- AL Friedlander
- AL Friedlander
- AL Hevener
- Amy C. Maher
- B Kiens
- B Knechtle
- B Mittendorfer
- BC Ruby
- BF Hurley
- BZ Yang
- C Binnert
- C Roepstorff
- C Roepstorff
- C Roepstorff
- C Roepstorff
- C Roepstorff
- DJ Mahoney
- E Ingelsson
- EE Spangenburg
- F Peronnet
- G Perseghin
- GP Holloway
- GP Holloway
- H Hatta
- JA Romijn
- Jerry Vockley
- K Izai
- KJ Livak
- LJ Tarnopolsky
- MA Tarnopolsky
- MA Tarnopolsky
- MA Tarnopolsky
- MA Tarnopolsky
- MA Tarnopolsky
- Mahmood Akhtar
- Mark A. Tarnopolsky
- MC Devries
- MC Devries
- MC Riddell
- MH Fu
- Michael Polymenis
- MJ Hamadeh
- MJ Yoon
- PM Berthon
- RB Vega
- RH Amin
- RJ Havel
- RJ Havel
- RJ Wanders
- S Carter
- S Luquet
- S Mandard
- S McKenzie
- S Welle
- SL Carter
- SL Carter
- SM Phillips
- SM Phillips
- SM Roth
- TJ Horton
- U Dressel
- V Bezaire
- V Bourdeau
- Y Uchida
- ZV Kendrick
- ZV Kendrick
- Publication venue
- Public Library of Science
- Publication date
- 01/08/2010
- Field of study
It is well recognized that compared with men, women have better ultra-endurance capacity, oxidize more fat during endurance exercise, and are more resistant to fat oxidation defects i.e. diet-induced insulin resistance. Several groups have shown that the mRNA and protein transcribed and translated from genes related to transport of fatty acids into the muscle are greater in women than men; however, the mechanism(s) for the observed sex differences in fat oxidation remains to be determined. Muscle biopsies from the vastus lateralis were obtained from moderately active men (N = 12) and women (N = 11) at rest to examine mRNA and protein content of genes involved in lipid oxidation. Our results show that women have significantly higher protein content for tri-functional protein alpha (TFPα), very long chain acyl-CoA dehydrogenase (VLCAD), and medium chain acyl-CoA dehydrogenase (MCAD) (P<0.05). There was no significant sex difference in the expression of short-chain hydroxyacyl-CoA dehydrogenase (SCHAD), or peroxisome proliferator activated receptor alpha (PPARα), or PPARγ, genes potentially involved in the transcriptional regulation of lipid metabolism. In conclusion, women have more protein content of the major enzymes involved in long and medium chain fatty acid oxidation which could account for the observed differences in fat oxidation during exercise
Genome-Wide Analysis of Small RNA and Novel MicroRNA Discovery in Human Acute Lymphoblastic Leukemia Based on Extensive Sequencing Approach
- Author
- A Esquela-Kerscher
- AI Saeed
- AM Cheng
- AS O'Toole
- B Zhang
- Baohong Zhang
- BC Bostrom
- BJ Lange
- BP Lewis
- BP Lewis
- C Chen
- CH Pui
- CH Pui
- CH Pui
- CI Castillo-Davis
- CZ Chen
- D Schotte
- DL Zanette
- DP Bartel
- E Berezikov
- E Bonnet
- EA Glazov
- F Kuchenbauer
- FW Hofacker IL
- GA Calin
- GA Calin
- H Seitz
- Hua Zhang
- Hui Zhou
- I Wojcik
- J Lu
- JE Babiarz
- JG Ruby
- Jian-Hua Yang
- Jun Wu
- K Okamura
- KJ Livak
- Liang-Hu Qu
- Ling Xu
- LP Lim
- M Ashburner
- M Bergsland
- MR Friedlander
- P Clote
- P Landgraf
- P Steffen
- Peng Zhang
- RD Morin
- RJ Hutchinson
- S Audic
- S Faderl
- S Lall
- S Marton
- S Mi
- S Narayan
- S Ro
- S Takada
- S Washietl
- SF Altschul
- V Del Gaizo Moore
- WO Lui
- X Wang
- Xiao Chen
- Xue-Qun Luo
- Yu-Sheng Zheng
- Yue-Qin Chen
- Zhi-Yong Ke
- Publication venue
- Public Library of Science
- Publication date
- 01/09/2009
- Field of study
BACKGROUND:MicroRNAs (miRNAs) have been proved to play an important role in various cellular processes and function as tumor suppressors or oncogenes in cancers including leukemia. The identification of a large number of novel miRNAs and other small regulatory RNAs will provide valuable insights into the roles they play in tumorgenesis. METHODOLOGY/PRINCIPAL FINDINGS:To gain further understanding of the role of miRNAs relevant to acute lymphoblastic leukemia (ALL), we employed the sequencing-by-synthesis (SBS) strategy to sequence small RNA libraries prepared from ALL patients and normal donors. In total we identified 159 novel miRNAs and 116 novel miRNA*s from both libraries. Among the 159 novel miRNAs, 42 were identified with high stringency in our data set. Furthermore, we demonstrated the different expression patterns of 20 newly identified and several known miRNAs between ALL patients and normal donors, suggesting these miRNAs may be associated with ALL and could constitute an ALL-specific miRNA signature. Interestingly, GO "biological process" classifications revealed that a set of significantly abnormally expressed miRNAs are associated with disease relapse, which implies that these dysregulated miRNAs might promote the progression of ALL by regulating genes involved in the pathway of the disease development. CONCLUSION/SIGNIFICANCE:The study presents a comprehensive picture of the expression of small RNAs in human acute lymphoblastic leukemia and highlights novel and known miRNAs differentially expressed between ALL patients and normal donors. To our knowledge, this is the first study to look at genome-wide known and novel miRNA expression patterns in in human acute lymphoblastic leukemia. Our data revealed that these deregulated miRNAs may be associated with ALL or the onset of relapse
Origin and Evolution of TRIM Proteins: New Insights from the Complete TRIM Repertoire of Zebrafish and Pufferfish
- Author
- A Baranova
- A Orimo
- A Reymond
- Abdenour Benmansour
- AH Keeble
- AT McCurley
- BA Reddy
- BC Viertlboeck
- C Furnes
- C O'Farrell
- C Simons
- C Stein
- C Vilches
- CA Virgen
- CJ Rold
- D Steinke
- DA Rhodes
- DA Yergeau
- DL Mallery
- DM Sayah
- E Danchin
- E Darbo
- EL Sonnhammer
- F Diaz-Griffero
- F Diaz-Griffero
- G Aguileta
- G Brennan
- G Lutfalla
- H Javanbakht
- H Roest Crollius
- HJ Kong
- I Lassot
- J Henry
- J Perry
- J Zha
- JA Spencer
- Jean-Pierre Levraud
- JG Sambrook
- JL Stafford
- JM Dijkstra
- JN Volff
- JP Bielawski
- JS Woo
- JS Woo
- K Ozato
- K Scheffler
- KM Short
- KP Yan
- L Carthagena
- L Du Pasquier
- L Du Pasquier
- L Du Pasquier
- LC James
- Lieke M. van der Aa
- LM van der Aa
- Louis Du Pasquier
- Luc Jouneau
- M Kasahara
- M Kasahara
- M Meyer
- M Muffato
- M Sardiello
- M Stremlau
- M Stremlau
- MF Flajnik
- MU Gack
- MY Matsuo
- Nikolas Nikolaidis
- O Jaillon
- Pierre Boudinot
- Pierre Pontarotti
- R Chang
- R Higgs
- R Higgs
- R Rajsbaum
- R Sakuma
- RB Mehta
- RM Newman
- S Nisole
- S Nisole
- S Ohkura
- S Yokoyama
- SJ Wilson
- SL Kosakovsky Pond
- SL Sawyer
- SL Sawyer
- SP Georgescu
- T Hibino
- T Ruby
- TC Tuoc
- Valérie Briolat
- X Li
- Y Ohta
- Z Yang
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
Tripartite motif proteins (TRIM) constitute a large family of proteins containing a RING-Bbox-Coiled Coil motif followed by different C-terminal domains. Involved in ubiquitination, TRIM proteins participate in many cellular processes including antiviral immunity. The TRIM family is ancient and has been greatly diversified in vertebrates and especially in fish. We analyzed the complete sets of trim genes of the large zebrafish genome and of the compact pufferfish genome. Both contain three large multigene subsets - adding the hsl5/trim35-like genes (hltr) to the ftr and the btr that we previously described - all containing a B30.2 domain that evolved under positive selection. These subsets are conserved among teleosts. By contrast, most human trim genes of the other classes have only one or two orthologues in fish. Loss or gain of C-terminal exons generated proteins with different domain organizations; either by the deletion of the ancestral domain or, remarkably, by the acquisition of a new C-terminal domain. Our survey of fish trim genes in fish identifies subsets with different evolutionary dynamics. trims encoding RBCC-B30.2 proteins show the same evolutionary trends in fish and tetrapods: they evolve fast, often under positive selection, and they duplicate to create multigenic families. We could identify new combinations of domains, which epitomize how new trim classes appear by domain insertion or exon shuffling. Notably, we found that a cyclophilin-A domain replaces the B30.2 domain of a zebrafish fintrim gene, as reported in the macaque and owl monkey antiretroviral TRIM5α. Finally, trim genes encoding RBCC-B30.2 proteins are preferentially located in the vicinity of MHC or MHC gene paralogues, which suggests that such trim genes may have been part of the ancestral MHC
Beetroot supplementation improves the physiological responses to incline walking
- Author
- A Hernández
- A Vanhatalo
- AA Kenjale
- Adrian Gray
- AE Minetti
- AJ Webb
- AM Jones
- BC Breese
- BC Ruby
- C Oggioni
- Craig Lawlor
- FJ Larsen
- FW Kolkhorst
- G Vernillo
- H-M Choi
- J Kelly
- J Whitfield
- Jamie Highton
- JS Gottschall
- JS Staab
- KE Lansley
- KE Lansley
- KH Wesseling
- LJ Wylie
- Luke Waldron
- M Amman
- M Gilchrist
- M Gilchrist
- M Horiuchi
- MA Sloniger
- Mark Waldron
- NS Bryan
- O Peacock
- OM Shannon
- P Porcelli
- PM Christensen
- PN Ainslie
- PN Ainslie
- R Margaria
- RK Boorsma
- SJ Bailey
- SJ Bailey
- SJ Bailey
- SJ Bailey
- SK Ferguson
- V Bond
- V Bond
- V Kapil
- V Kapil
- WG Hopkins
- 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/s00421-018-3843-xPurpose: We investigated the effects of an acute 24-h nitrate-rich beetroot juice supplement (BR) on the energy cost, exercise efficiency and blood pressure responses to intermittent walking at different gradients. Methods: In a double-blind, cross-over design, eight participants were provided with a total of 350 ml of nitrate-rich (~20.5 mmol nitrate) BR or placebo (PLA) across 24-h before completing intermittent walking at 3 km/h on treadmill at gradients of 1%, 5%, 10%, 15% and 20%. Results: Resting mean arterial pressure (MAP) was ~4.1% lower after BR (93 vs. 89 mmHg; P = 0.001), as well as during exercise (102 vs. 99 mmHg; P = 0.011) and recovery (97 vs. 94 mmHg; P = 0.001). Exercising (1227 vs. 1129 ml/min P < 0.001) and end-stage (1404 vs. 1249 ml/min; P = 0.002) oxygen uptake (O2) was lower in BR compared to PLA, which was accompanied by an average reduction in phase II ̇O2 amplitude (1067 vs. 940 ml/min; P = 0.025). Similarly, recovery O2 (509 vs. 458 ml/min; P = 0.001) was lower in BR. Whole-blood potassium concentration increased from pre-post exercise in PLA (4.1 ± 0.3 vs. 4.5 ± 0.3 mmol/L; P = 0.013) but not BR (4.1 ± 0.31 vs. 4.3 ± 0.2 mmol/L; P = 0.188). Conclusions: Energy cost of exercise, recovery of O2, MAP and blood markers were ameliorated after BR. Previously reported mechanisms explain these findings, which are more noticeable during less efficient walking at steep gradients (15-20%). These findings have practical implications for hill-walkers
Present state and future perspectives of using pluripotent stem cells in toxicology research
- Author
- A Abuin
- A Albini
- A Beqqali
- A Bradley
- A Colman
- A Dolci
- A Fraichard
- A Hansen
- A Krtolica
- A Lesman
- A Lombardo
- A Lorico
- A Mehta
- A Moretti
- A Nagy
- A Nagy
- A Norstrom
- A Schnerch
- A Seifinejad
- A Seiler
- A Seiler
- A Soto-Gutierrez
- A Suzuki
- A Urbach
- AA Filipczyk
- AB McLean
- AD Ebert
- AD Ebert
- AG Hendrickx
- AG Smith
- AH Piersma
- AI Di Domenico
- AK Peters
- AM Newman
- AM Wobus
- AM Wobus
- AM Wobus
- AM Wobus
- AM Wobus
- AM Wobus
- Anna M. Wobus
- Anon
- B Ekwall
- B Thyagarajan
- BA Schwetz
- BC Heng
- BE Petersen
- BE Reubinoff
- BP Schmidt
- BW Kahan
- BW Phillips
- BY Hu
- C Buecker
- C Dani
- C Denning
- C Denning
- C Freund
- C Kim
- C Mummery
- C Strubing
- C Xu
- C Xu
- CE Murry
- CK Lim
- CL Stewart
- D Anderson
- D Hockemeyer
- D Hoof Van
- D Huangfu
- D Kim
- D Laustriat
- D Zhao
- DA Eastmond
- DA Kerr
- DC Hay
- DC Hay
- DC Hay
- DE Kehoe
- DJ Tester
- DL Cockroft
- E Chiao
- E Dolgin
- E Genschow
- E Kolossov
- E Schmelzer
- E Sonoda
- EJ Topol
- EM Jones-Villeneuve
- F Hattori
- F Soldner
- FJ Müller
- G Amabile
- G Brolen
- G Laschinski
- G Lee
- G Pless
- G Tzimas
- GJ Sullivan
- GL Kimmel
- GR Martin
- H Baharvand
- H Baharvand
- H Basma
- H Gai
- H Green
- H Guenou
- H Jakob
- H Liang
- H Liu
- H Nau
- H Pei
- H Reinecke
- H Shirahashi
- H Song
- H Spielmann
- H Spielmann
- H Spielmann
- H Spielmann
- H Vaziri
- H Xie
- H Xue
- H Zaehres
- H Zhou
- I Huber
- I Kehat
- I Kola
- IF Ben-Nun
- IF Khan
- IG Brons
- IH Park
- J Cai
- J Czyz
- J Czyz
- J Favor
- J Fletcher
- J Hanna
- J Jensen
- J Liu
- J Rohwedel
- J Rohwedel
- J Rohwedel
- J Rohwedel
- J Satin
- J Synnergren
- J Yu
- J Yu
- J Zhang
- J Zou
- JA Bantle
- JA Thomson
- JC Mohr
- JC Moore
- JE Trosko
- JG Hengstler
- JL Resnick
- JM Polo
- JQ He
- JT Dimos
- K Abe
- K Chen
- K Dolnikov
- K Eggan
- K Guan
- K Hübner
- K Kaji
- K Kim
- K Ko
- K Mitsui
- K Narwani
- K Okita
- K Prelle
- K Saha
- K Sakurai
- K Sasaki
- K Si-Tayeb
- K Si-Tayeb
- K Suzuki
- K Takahashi
- K Takahashi
- K Vojnits
- K Woltjen
- KA Atkinson
- KA D’Amour
- KD Wilson
- KM Ruby
- KR Boheler
- KR Chien
- KR Thomas
- L Bu
- L Hareng
- L Kang
- L Rambhatla
- L Sartiani
- L Yang
- L Zwi
- LA Donehower
- LB Russell
- LB Russell
- LC Stevens
- LC Stevens
- LC Stevens
- LM Hondeghem
- LT Lock
- M Baker
- M Balls
- M Brito-Martins
- M Drab
- M Ek
- M Ieda
- M Jalving
- M Kessel
- M Klemm
- M Klemm
- M Krishnamoorthy
- M Leist
- M Mikkola
- M Nakayama
- M Pekkanen-Mattila
- M Pekkanen-Mattila
- M Puceat
- M Reppel
- M Skrzypiec-Spring
- M Snir
- M Stadtfeld
- M Stadtfeld
- M Stojkovic
- M Verwei
- M Wernig
- M Zalzman
- MA Baxter
- MA Laflamme
- MG Guenther
- MG Perino
- MH Chin
- MJ Boland
- MJ Evans
- MJ Evans
- MJ Shamblott
- MK Edwards
- MK Jonsson
- MM Schmidt
- MT Donato
- MW McBurney
- N Chalasani
- N Gilbert
- N Lavon
- N Lavon
- N Lee
- N Maherali
- N Shiraki
- N Terada
- N Yokoo
- NA Brown
- NI zur Nieden
- NJ Hewitt
- O Bluteau
- O Caspi
- O Caspi
- O Sedan
- P Blyszczuk
- P Löser
- P Marx-Stoelting
- P Sancho-Bru
- P Sarkar
- P Sartipy
- Peter Löser
- PJ Tesar
- PP Sloun Van
- PR West
- PS Knoepfler
- PW Andrews
- PW Burridge
- Q Feng
- Q Zhou
- QL Ying
- R Buesen
- R Fassler
- R Graichen
- R Jelinek
- R Meamar
- R Pal
- R Passier
- R Passier
- RB Cervantes
- RE Horton
- RE Schwartz
- RK Li
- RK Rowntree
- RL Brinster
- RL Davis
- RL Williams
- RM Marion
- RN Moore
- RN Moore
- RP Davis
- S Adler
- S Adler
- S Agarwal
- S Boehn
- S Bremer
- S Bremer
- S Bremer
- S Conrad
- S Ehnert
- S Irion
- S Lin
- S Niebruegge
- S Nishikawa
- S Peng
- S Russmann
- S Snykers
- S Strickland
- S Yao
- SJ Flora
- SJ Gwak
- SR Braam
- SR Khetani
- ST Rashid
- T Cao
- T Ishii
- T Ishii
- T Mosmann
- T Ochiya
- T Peura
- T Shimizu
- T Söderdahl
- T Tenzen
- T Touboul
- T Vierbuchen
- T Zdravkovic
- TC Doetschman
- TC Stummann
- TC Stummann
- TC Stummann
- TG Otsuji
- TP Zwaka
- TT Peura
- TW Sadler
- U Sehlmeyer
- U Sehlmeyer
- U Sehlmeyer
- U Sehlmeyer
- UH Ehling
- UH Ehling
- V Krizhanovsky
- VA Maltsev
- VE Papaioannou
- W Rust
- W Zhou
- WH Zimmermann
- WM Westerink
- WZ Zhu
- X Carvajal-Vergara
- X Zeng
- X Zeng
- X Zhang
- XQ Xu
- XQ Xu
- XQ Xu
- XY Zhao
- Y Chung
- Y Duan
- Y Duan
- Y Matsui
- Y Mayshar
- Y Shi
- Y Toyooka
- Z Song
- Publication venue
- Springer-Verlag
- Publication date
- 01/01/2011
- Field of study
The use of novel drugs and chemicals requires reliable data on their potential toxic effects on humans. Current test systems are mainly based on animals or in vitro–cultured animal-derived cells and do not or not sufficiently mirror the situation in humans. Therefore, in vitro models based on human pluripotent stem cells (hPSCs) have become an attractive alternative. The article summarizes the characteristics of pluripotent stem cells, including embryonic carcinoma and embryonic germ cells, and discusses the potential of pluripotent stem cells for safety pharmacology and toxicology. Special attention is directed to the potential application of embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) for the assessment of developmental toxicology as well as cardio- and hepatotoxicology. With respect to embryotoxicology, recent achievements of the embryonic stem cell test (EST) are described and current limitations as well as prospects of embryotoxicity studies using pluripotent stem cells are discussed. Furthermore, recent efforts to establish hPSC-based cell models for testing cardio- and hepatotoxicity are presented. In this context, methods for differentiation and selection of cardiac and hepatic cells from hPSCs are summarized, requirements and implications with respect to the use of these cells in safety pharmacology and toxicology are presented, and future challenges and perspectives of using hPSCs are discussed
Measurement and interpretation of same-sign W boson pair production in association with two jets in pp collisions at s = 13 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abeling K
- Abicht NJ
- Abidi SH
- Aboulhorma A
- Abramowicz H
- Abreu H
- Abulaiti Y
- Abusleme Hoffman AC
- Acharya BS
- Adam Bourdarios C
- Adamczyk L
- Adamek L
- Addepalli SV
- Addison MJ
- Adelman J
- Adiguzel A
- Adye T
- Affolder AA
- Afik Y
- Agaras MN
- Agarwala J
- Aggarwal A
- Agheorghiesei C
- Ahmad A
- Ahmadov F
- Ahmed WS
- Ahuja S
- Ai X
- Aielli G
- Aikot A
- Ait Tamlihat M
- Aitbenchikh B
- Aizenberg I
- Akbiyik M
- Akimov AV
- Akiyama D
- Akolkar NN
- Al Khoury K
- Alberghi GL
- Albert J
- Albicocco P
- Albouy GL
- Alderweireldt S
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexopoulos T
- Alfonsi F
- Algren M
- Alhroob M
- Ali B
- Ali HMJ
- Ali S
- Alibocus SW
- Aliev M
- Alimonti G
- Alkakhi W
- Allaire C
- Allbrooke BMM
- Allen JF
- Allendes Flores CA
- Allport PP
- Aloisio A
- Alonso F
- Alpigiani C
- Alvarez Estevez M
- Alvarez Fernandez A
- Alves Cardoso M
- Alviggi MG
- Aly M
- Amaral Coutinho Y
- Ambler A
- Amelung C
- Amerl M
- Ames CG
- Amidei D
- Amor Dos Santos SP
- Amos KR
- Ananiev V
- Anastopoulos C
- Andeen T
- Anders JK
- Andrean SY
- Andreazza A
- Angelidakis S
- Angerami A
- Anisenkov AV
- Annovi A
- Antel C
- Anthony MT
- Antipov E
- Antonelli M
- Anulli F
- Aoki M
- Aoki T
- Aparisi Pozo JA
- Aparo MA
- Aperio Bella L
- Appelt C
- Apyan A
- Aranzabal N
- Arcangeletti C
- Arce ATH
- Arena E
- Arguin J-F
- Argyropoulos S
- Arling J-H
- Arnaez O
- Arnold H
- Artoni G
- Asada H
- Asai K
- Asai S
- Asbah NA
- Assamagan K
- Astalos R
- Atashi S
- Atkin RJ
- Atkinson M
- Atmani H
- Atmasiddha PA
- Augsten K
- Auricchio S
- Auriol AD
- Austrup VA
- Avolio G
- Axiotis K
- Azuelos G
- Babal D
- Bachacou H
- Bachas K
- Bachiu A
- Backman F
- Badea A
- Bagnaia P
- Bahmani M
- Bailey AJ
- Bailey VR
- Baines JT
- Baines L
- Bakalis C
- Baker OK
- Bakos E
- Bakshi Gupta D
- Balakrishnan V
- Balasubramanian R
- Baldin EM
- Balek P
- Ballabene E
- Balli F
- Baltes LM
- Balunas WK
- Balz J
- Banas E
- Bandieramonte M
- Bandyopadhyay A
- Bansal S
- Barak L
- Barakat M
- Barberio EL
- Barberis D
- Barbero M
- Barel MZ
- Barends KN
- Barillari T
- Barisits M-S
- Barklow T
- Baron Moreno DA
- Baron P
- Baroncelli A
- Barone G
- Barr AJ
- Barr JD
- Barranco Navarro L
- Barreiro Guimarães da Costa J
- Barreiro F
- Barron U
- Barros Teixeira MG
- Barsov S
- Bartels F
- Bartoldus R
- Barton AE
- Bartos P
- Basan A
- Baselga M
- Bassalat A
- Basso MJ
- Basson CR
- Bates RL
- Batlamous S
- Batley JR
- Batool B
- Battaglia M
- Battulga D
- Bauce M
- Bauer M
- Bauer P
- Bazzano Hurrell LT
- Beacham JB
- Beau T
- Beauchemin PH
- Becherer F
- Bechtle P
- Beck HP
- Becker K
- Becot C
- Beddall AJ
- Bednyakov VA
- Bee CP
- Beemster LJ
- Beermann TA
- Begalli M
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- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Springer Nature
- Publication date
- 01/04/2024
- Field of study
This paper presents the measurement of fducial and diferential cross sections for both the inclusive and electroweak production of a same-sign W-boson pair in association with two jets (W±W±jj) using 139 fb−1 of proton-proton collision data recorded at a centre-of-mass energy of √s = 13 TeV by the ATLAS detector at the Large Hadron Collider. The analysis is performed by selecting two same-charge leptons, electron or muon, and at least two jets with large invariant mass and a large rapidity diference. The measured fducial cross sections for electroweak and inclusive W±W±jj production are 2.92 ± 0.22 (stat.) ± 0.19 (syst.)fb and 3.38±0.22 (stat.)±0.19 (syst.)fb, respectively, in agreement with Standard Model predictions. The measurements are used to constrain anomalous quartic gauge couplings by extracting 95% confdence level intervals on dimension-8 operators. A search for doubly charged Higgs bosons H±± that are produced in vector-boson fusion processes and decay into a same-sign W boson pair is performed. The largest deviation from the Standard Model occurs for an H±± mass near 450 GeV, with a global signifcance of 2.5 standard deviations
Measurement of the tt¯tt¯ production cross section in pp collisions at √s=13 TeV with the ATLAS detector
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- Zeißner SV
- Zemaityte G
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- Zhemchugov A
- Zheng Z
- Zhong D
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- Zhu Y
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- Zhukov K
- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
- Ziolkowski M
- Zoccoli A
- Zoch K
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- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 16/11/2021
- Field of study
A measurement of four-top-quark production using proton-proton collision data at a centre-of-mass energy of 13 TeV collected by the ATLAS detector at the Large Hadron Collider corresponding to an integrated luminosity of 139 fb−1 is presented. Events are selected if they contain a single lepton (electron or muon) or an opposite-sign lepton pair, in association with multiple jets. The events are categorised according to the number of jets and how likely these are to contain b-hadrons. A multivariate technique is then used to discriminate between signal and background events. The measured four-top-quark production cross section is found to be 26+17−15 fb, with a corresponding observed (expected) significance of 1.9 (1.0) standard deviations over the background-only hypothesis. The result is combined with the previous measurement performed by the ATLAS Collaboration in the multilepton final state. The combined four-top-quark production cross section is measured to be 24+7−6 fb, with a corresponding observed (expected) signal significance of 4.7 (2.6) standard deviations over the background-only predictions. It is consistent within 2.0 standard deviations with the Standard Model expectation of 12.0 ± 2.4 fb
Measurements of Higgs bosons decaying to bottom quarks from vector boson fusion production with the ATLAS experiment at √=13TeV
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- Abbott B
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- Abhayasinghe DK
- Abidi SH
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- Zhou C
- Zhou H
- Zhou M
- Zhou N
- Zhou Y
- Zhu C
- Zhu CG
- Zhu H
- Zhu HL
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 23/06/2021
- Field of study
The paper presents a measurement of the Standard Model Higgs Boson decaying to b-quark pairs in the vector boson fusion (VBF) production mode. A sample corresponding to 126 fb−1 of s√=13TeV proton–proton collision data, collected with the ATLAS experiment at the Large Hadron Collider, is analyzed utilizing an adversarial neural network for event classification. The signal strength, defined as the ratio of the measured signal yield to that predicted by the Standard Model for VBF Higgs production, is measured to be 0.95+0.38−0.36 , corresponding to an observed (expected) significance of 2.6 (2.8) standard deviations from the background only hypothesis. The results are additionally combined with an analysis of Higgs bosons decaying to b-quarks, produced via VBF in association with a photon
Measurements of W+W−+ ≥ 1 jet production cross-sections in pp collisions at s = 13 TeV with the ATLAS detector
- Author
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- Abbott B
- Abbott DC
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- Abeling K
- Abhayasinghe DK
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- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/06/2021
- Field of study
Fiducial and differential cross-section measurements of W+W− production in
association with at least one hadronic jet are presented. These measurements are sensitive
to the properties of electroweak-boson self-interactions and provide a test of perturbative
quantum chromodynamics and the electroweak theory. The analysis is performed using
proton-proton collision data collected at p
s = 13TeV with the ATLAS experiment, corresponding
to an integrated luminosity of 139 fb−1. Events are selected with exactly one oppositely
charged electron-muon pair and at least one hadronic jet with a transverse momentum
of pT > 30 GeV and a pseudorapidity of |�| < 4.5. After subtracting the background
contributions and correcting for detector effects, the jet-inclusive W+W−+ � 1 jet fiducial
cross-section and W+W−+ jets differential cross-sections with respect to several kinematic
variables are measured. These measurements include leptonic quantities, such as the lepton
transverse momenta and the transverse mass of the W+W− system, as well as jet-related
observables such as the leading jet transverse momentum and the jet multiplicity. Limits on
anomalous triple-gauge-boson couplings are obtained in a phase space where interference
between the Standard Model amplitude and the anomalous amplitude is enhanced
- …