132 research outputs found
Clinical application of magnetic resonance in acute traumatic brain injury
- Author
- Almir F. Andrade
- Andrade AF
- Andrade AF
- Antonio R. Spotti
- Braga FT
- Dionei F. Morais
- Ducreux D
- Felipe F.P. Gaia
- Gean AD
- Gennarelli TA
- Gentry LR
- Gentry LR
- Gentry RL
- Gentry RL
- Gentry RL
- Gentry RL
- Gusmão SN
- Huisman TAGM
- Kampfl A
- Kelly AB
- Kraus JF
- Lee B
- Liu AY
- Macpherson BC
- Marshall LF
- Mittl RL
- Osborn AG
- Osborn AG
- Parizel PM
- Paterakis K
- Rocha AJ
- Stein SC
- Teasdale G
- Tokutomi T
- Tong KA
- Toyama Y
- Waldir A. Tognola
- Yanagawa Y
- Zar JH
- Zimmerman RA
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
“The Even-Lavie valve as a source for high intensity supersonic beam”
- Author
- A Amirav
- A Bergeat
- A Osterwalder
- AB Bailey
- AB Henson
- B Yan
- CJ Rennick
- D Irimia
- D Pentlehner
- DC Jordan
- E Lavert-Ofir
- F Massines
- G Scoles
- GA Bird
- GR Woestenenk
- H Ashkenas
- H Haberland
- H Stapelfeldt
- HV Tafreshi
- IC Lu
- J Braun
- J Jankunas
- JP Toennies
- K Luria
- L Holmegaard
- L Pedemonte
- M Belan
- M Hillenkamp
- M Mudrich
- MJ Verheien
- N Bednar
- NL Kazanskiya
- OF Hagena
- R Campargue
- R Campargue
- RE Smalley
- S Semushin
- SN Vogels
- T Halfmann
- U Even
- U Even
- U Even
- U Even
- U Even
- U Kogelschatz
- W Christen
- WR Gentry
- WR Gentry
- X He
- Y Shagam
- Z Ren
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Magnetic resonance imaging after most common form of concussion
- Author
- A Pfefferbaum
- A Raine
- B Voller
- CE Coffey
- D Arnone
- D Doezema
- Dalia Mickevičiene
- Danguole Surkiene
- Diana Obelieniene
- EA Wilde
- GJ Harris
- GV Poole
- Harald Schrader
- HQ Jin
- JJ Bazarian
- K Arfanakis
- L Miles
- Lars Jacob Stovner
- LR Gentry
- M Kiraly
- MD De Bellis
- MF Kraus
- MP Laakso
- NA Shaw
- NB Topal
- P Nilsen
- PA Hofman
- R Ferrari
- R Schmidt
- RL Mittl
- RM Dupont
- RM Dupont
- RR Benson
- RR Lewine
- RW Evans
- Rymante Gleizniene
- Silvija Jakstiene
- SM Rao
- SN Niogi
- W Mittenberg
- Publication venue
- BioMed Central
- Publication date
- 01/01/2009
- Field of study
<p>Abstract</p> <p>Background</p> <p>Until now there is a lack of carefully controlled studies with conventional MR imaging performed exclusively in concussion with short lasting loss of consciousness (LOC).</p> <p>Methods</p> <p>A MR investigation was performed within 24 hours and after 3 months in 20 patients who had suffered a concussion with a verified loss of consciousness of maximally 5 minutes. As a control group, 20 age- and gender matched patients with minor orthopaedic injuries had a MR investigation using the same protocol.</p> <p>Results</p> <p>In a concussion population with an average LOC duration of 1. 4 minutes no case with unequivocal intracranial traumatic pathology was detected.</p> <p>Conclusion</p> <p>An ordinary concussion with short lasting LOC does not or only seldom result in a degree of diffuse axonal injury (DAI) that is visualized by conventional MR with field strength of 1.0 Tesla (T). Analysis of earlier MR studies in concussion using field strength of 1.5 T as well as of studies with diffusion tensor MR imaging (MR DTI) reveal methodological shortcomings, in particular use of inadequate control groups. There is, therefore, a need for carefully controlled studies using MR of higher field strength and/or studies with MR DTI exclusively in common concussion with LOC of maximally 5 minutes.</p
Evaluation of Candidate Stromal Epithelial Cross-Talk Genes Identifies Association between Risk of Serous Ovarian Cancer and TERT, a Cancer Susceptibility “Hot-Spot”
- Author
- A Oliphant
- A Orimo
- A Sadlonova
- AD Skol
- Aleksandra Gentry-Maharaj
- Alice S. Whitemore
- Amanda B. Spurdle
- Andrew Berchuck
- Anna deFazio
- Anna H. Wu
- Argyrios Ziogas
- AS Whittemore
- Catherine M. Phelan
- Celeste L. Pearce
- CL Pearce
- Claus Hogdall
- CS Carlson
- D Spentzos
- DA Hinds
- Daniel O. Stram
- Daniel W. Cramer
- David L. Duffy
- David N. Rider
- DF Easton
- DM Feldser
- DM Parkin
- Edwin S. Iversen
- EK Amankwah
- Ellen L. Goode
- Emmanouil T. Dermitzakis
- Estrid Hogdall
- F Yang
- Galina Lurie
- Georgia Chenevix-Trench
- GM Petersen
- GR Cunha
- H Donninger
- H Song
- H Song
- HA Risch
- Hannah Yang
- Hoda Anton-Culver
- Honglin Song
- Izhak Haviv
- J Boyd
- J Campisi
- J Gudmundsson
- J Wang
- JB Fan
- JC Barrett
- JD McKay
- Jennifer Anne Doherty
- Jenny Chang-Claude
- JM Cunningham
- Joellen M. Schildkraut
- Jolanta Lissowska
- Jonathan Beesley
- JS Fleming
- Julie M. Cunningham
- Kathryn L. Terry
- Kirsten B. Moysich
- KJ Wu
- KS Frazier
- L Zhang
- Lynne R. Wilkens
- Malcolm C. Pike
- Marc T. Goodman
- Mary Anne Rossing
- MF Fathalla
- MM Pomerantz
- Montserrat Garcia-Closas
- MT Landi
- N Gava
- Natalie Gava
- Pamela J. Thompson
- Patricia G. Moorman
- Paul D. Pharoah
- PD Pharoah
- Penelope M. Webb
- PI de Bakker
- RM Wenham
- Robert A. Vierkant
- Roberta B. Ness
- RW Tothill
- S Purcell
- S Shete
- S Tuupanen
- S Wacholder
- SA Gayther
- SB Gabriel
- SE Johnatty
- Shan Wang-Gohrke
- Sharon E. Johnatty
- Shelley S. Tworoger
- Simon A. Gayther
- SJ Ramus
- SN Stacey
- Stephen J. Chanock
- Stuart Macgregor
- Susan E. Hankinson
- Susan J. Ramus
- Susanne K. Kjaer
- T Bonome
- T Jacks
- T Rafnar
- T Riman
- Thomas A. Sellers
- Usha Menon
- Xiaoqing Chen
- Publication venue
- Public Library of Science
- Publication date
- 01/07/2010
- Field of study
We hypothesized that variants in genes expressed as a consequence of interactions between ovarian cancer cells and the host micro-environment could contribute to cancer susceptibility. We therefore used a two-stage approach to evaluate common single nucleotide polymorphisms (SNPs) in 173 genes involved in stromal epithelial interactions in the Ovarian Cancer Association Consortium (OCAC). In the discovery stage, cases with epithelial ovarian cancer (n = 675) and controls (n = 1,162) were genotyped at 1,536 SNPs using an Illumina GoldenGate assay. Based on Positive Predictive Value estimates, three SNPs—PODXL rs1013368, ITGA6 rs13027811, and MMP3 rs522616—were selected for replication using TaqMan genotyping in up to 3,059 serous invasive cases and 8,905 controls from 16 OCAC case-control studies. An additional 18 SNPs with Pper-allele<0.05 in the discovery stage were selected for replication in a subset of five OCAC studies (n = 1,233 serous invasive cases; n = 3,364 controls). The discovery stage associations in PODXL, ITGA6, and MMP3 were attenuated in the larger replication set (adj. Pper-allele≥0.5). However genotypes at TERT rs7726159 were associated with ovarian cancer risk in the smaller, five-study replication study (Pper-allele = 0.03). Combined analysis of the discovery and replication sets for this TERT SNP showed an increased risk of serous ovarian cancer among non-Hispanic whites [adj. ORper-allele 1.14 (1.04–1.24) p = 0.003]. Our study adds to the growing evidence that, like the 8q24 locus, the telomerase reverse transcriptase locus at 5p15.33, is a general cancer susceptibility locus
Prognostic gene expression signature for high-grade serous ovarian cancer.
- Author
- Alsop J
- Anglesio MS
- AOCS Group
- Banerjee SN
- Beeghly-Fadiel A
- Behrens S
- Benitez J
- Bentley RC
- Berchuck A
- Bodelon C
- Boros J
- Bowtell DD
- Brenton JD
- Brinton L
- Brown R
- Budden T
- Carney ME
- Chang-Claude J
- Chen S
- Chenevix-Trench G
- Chiu DS
- Chow V
- Cushing-Haugen KL
- Cybulski C
- deFazio A
- Doherty JA
- Elatre W
- Ennis D
- Fasching PA
- Fereday S
- Fortner RT
- Gao B
- García MJ
- García-Donas J
- Gayther SA
- Gentry-Maharaj A
- George J
- Gilks B
- Glasspool R
- Goode EL
- Goodman MT
- Goranova T
- Greene CS
- Gronwald J
- Haluska P
- Harnett PR
- Harris HR
- Henderson MJ
- Hendley J
- Hernandez BY
- Hernando Polo S
- Herpel E
- Hinsley S
- Huntsman DG
- Intermaggio MP
- Jimenez-Linan M
- Johnatty SE
- Karlan BY
- Karpinskyj C
- Kaufmann SH
- Keeney GL
- Kelemen LE
- Kennedy CJ
- Kommoss S
- Konecny GE
- Koziak JM
- Köbel M
- Larson MC
- Leong HS
- Lester J
- Leung SCY
- Levine DA
- Lewsley LA
- Lissowska J
- Lubiński J
- Luk H
- Lum A
- Macintyre G
- Mackenzie R
- Mahner S
- McNeish IA
- Menkiszak J
- Menon U
- Millstein J
- Nazeran T
- Orsulic S
- Oszurek O
- Pearce CL
- Pharoah PDP
- Pike MC
- Piskorz AM
- Ramus SJ
- Ramón Y Cajal T
- Ray-Coquard I
- Rhenius V
- Rodriguez GC
- Rossing MA
- Sayer R
- Schildkraut JM
- Senz J
- Sharma R
- Sherman ME
- Silva De Silva D
- Singh N
- Sinn P
- Slamon D
- Song H
- Steed H
- Stronach EA
- Sudderuddin H
- Talhouk A
- Thompson PJ
- Tołoczko A
- Trabert B
- Traficante N
- Tseng C
- Volchek M
- Wang C
- Wentzensen N
- Widschwendter M
- Wilkens LR
- Winham SJ
- Winterhoff B
- Wu AH
- Zelaya RA
- Publication venue
- Ann Oncol
- Publication date
- 01/01/2020
- Field of study
BACKGROUND: Median overall survival (OS) for women with high-grade serous ovarian cancer (HGSOC) is ∼4 years, yet survival varies widely between patients. There are no well-established, gene expression signatures associated with prognosis. The aim of this study was to develop a robust prognostic signature for OS in patients with HGSOC. PATIENTS AND METHODS: Expression of 513 genes, selected from a meta-analysis of 1455 tumours and other candidates, was measured using NanoString technology from formalin-fixed paraffin-embedded tumour tissue collected from 3769 women with HGSOC from multiple studies. Elastic net regularization for survival analysis was applied to develop a prognostic model for 5-year OS, trained on 2702 tumours from 15 studies and evaluated on an independent set of 1067 tumours from six studies. RESULTS: Expression levels of 276 genes were associated with OS (false discovery rate < 0.05) in covariate-adjusted single-gene analyses. The top five genes were TAP1, ZFHX4, CXCL9, FBN1 and PTGER3 (P < 0.001). The best performing prognostic signature included 101 genes enriched in pathways with treatment implications. Each gain of one standard deviation in the gene expression score conferred a greater than twofold increase in risk of death [hazard ratio (HR) 2.35, 95% confidence interval (CI) 2.02-2.71; P < 0.001]. Median survival [HR (95% CI)] by gene expression score quintile was 9.5 (8.3 to -), 5.4 (4.6-7.0), 3.8 (3.3-4.6), 3.2 (2.9-3.7) and 2.3 (2.1-2.6) years. CONCLUSION: The OTTA-SPOT (Ovarian Tumor Tissue Analysis consortium - Stratified Prognosis of Ovarian Tumours) gene expression signature may improve risk stratification in clinical trials by identifying patients who are least likely to achieve 5-year survival. The identified novel genes associated with the outcome may also yield opportunities for the development of targeted therapeutic approaches
Mathematical Modelling as a Proof of Concept for MPNs as a Human Inflammation Model for Cancer Development
- Author
- A Enblom
- A Lindholm Sørensen
- A Mantovani
- A Pardanani
- A Parihar
- A Tefferi
- A Tefferi
- AG Fleischman
- AL Jackson
- AL Sørensen
- AS Christensen
- AV Jones
- C Desterke
- C James
- C Nielsen
- C Nielsen
- C Rank
- CH Riley
- CH Riley
- CH Riley
- Christina Ellervik
- CL Andersen
- CS Attolini
- D Dingli
- D Hanahan
- D Olcaydu
- DC Rockey
- E Pikarsky
- E Pourcelot
- EJ Baxter
- F Ciaffoni
- F Michor
- F Michor
- F Michor
- F Michor
- G Barosi
- G Barosi
- G Brevetti
- GJ Titmarsh
- H Frederiksen
- H Frederiksen
- H Haeno
- H Pettersson
- H Takizawa
- Hans Carl Hasselbalch
- HC Hasselbalch
- HC Hasselbalch
- HC Hasselbalch
- HC Hasselbalch
- HC Hasselbalch
- HC Hasselbalch
- HC Hasselbalch
- HC Hasselbalch
- HC Hasselbalch
- HC Hasselbalch
- HF Dvorak
- HF Dvorak
- HL Geyer
- J Danesh
- J Nangalia
- J Wehrle
- JA Jacquez
- JB Nikas
- JC Barrett
- Jesper Troelsen
- JH Goldie
- JH Goldie
- JJ Kiladjian
- JL Dunster
- Johanne Gudmand-Hoeyer
- Johnny T. Ottesen
- JS Jutzi
- JS Jutzi
- KB Kaufmann
- KE Panteli
- KH Nielsen
- KH Nielsen
- KY King
- Lasse Kjær
- LG De Pillis
- LG De Pillis
- LR Ferguson
- LR Ferguson
- M Bak
- M Baker
- M Bjorkholm
- M Cazzola
- M Karin
- M Kleppe
- M Lu
- M Saleem
- Mads Thomassen
- MC Herald
- MC Martyre
- ME Bjørn
- ME Bjørn
- MJ Pittet
- Morten Andersen
- MS Cooke
- NC Cross
- Niels Pallisgaard
- O Kilpivaara
- O Kiraly
- P Lundberg
- Pal Bela Szecsi
- PJ Campbell
- PM Ridker
- Q Zhang
- R Kralovics
- R Leblanc
- R Marchioli
- R Roelz
- R Vaidya
- Rasmus K. Pedersen
- RL Levine
- RT Silver
- S Hermouet
- S Hermouet
- S Hermouet
- S Koschmieder
- S Verstovsek
- SN Gentry
- SY Kristinsson
- T Barbui
- T Barbui
- T Klampfl
- T Stiehl
- T Stiehl
- T Stiehl
- T Stiehl
- T Walenda
- Torben A. Kruse
- TS Larsen
- V Skov
- V Skov
- V Skov
- V Skov
- V Skov
- Vibe Skov
- VP Čokić
- W Tapper
- WC Lo
- Y Zhang
- Zamra Sajid
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2017
- Field of study
<p><b>Left:</b> Typical development in stem cells (top panel A) and mature cells (bottom panel B). Healthy hematopoietic cells (full blue curves) dominate in the early phase where the number of malignant cells (stipulated red curves) are few. The total number of cells is also shown (dotted green curves). When a stem cell mutates without repairing mechanisms, a slowly increasing exponential growth starts. At a certain stage, the malignant cells become dominant, and the healthy hematopoietic cells begin to show a visible decline. Finally, the composition between the cell types results in a takeover by the malignant cells, leading to an exponential decline in hematopoietic cells and ultimately their extinction. The development is driven by an approximately exponential increase in the MPN stem cells, and the development is closely followed by the mature MPN cells. <b>Right:</b> B)The corresponding allele burden (7%, 33% and 67% corresponding to ET, PV, and PMF, respectively) defined as the ratio of MPN mature cells to the total number of mature cells.</p
Behavioral genetics and taste
- Author
- A Hajnal
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AA Bachmanov
- AB Kampov-Polevoy
- AB Kampov-Polevoy
- AB Kampov-Polevoy
- AB Kampov-Polevoy
- AB Kampov-Polevoy
- AC Spector
- AC Spector
- AD Salbe
- AF Blakeslee
- AH McDaniel
- AI Spielman
- AJ Drewnowski
- AL Fox
- AL Fox
- AL Huang
- Alexander A Bachmanov
- AS Levine
- B Bufe
- BA Gosnell
- BA McMillen
- BG Green
- BK Formaker
- BK Formaker
- BK Smith
- BM Reddy
- BS Kotlus
- C Conte
- C Conte
- C Kuhn
- CD Dotson
- CG Capeless
- CG Capeless
- CH Lemon
- CL Hubell
- CP Richter
- D Denton
- D Drayna
- D Drayna
- DA Blizard
- DA Blizard
- DA Blizard
- DA Blizard
- DA Rodgers
- DA Rodgers
- DA Rodgers
- DB Harder
- DB Harder
- DB Harder
- DB Harder
- DG Mook
- DH Overstreet
- DH Overstreet
- DP Atchley
- DR Reed
- DR Reed
- DR Reed
- DR Reed
- DS Cannon
- E Adler
- E Sainz
- E Terenina-Rigaldie
- E Terenina-Rigaldie
- EE Midkiff
- EE Midkiff
- EE Midkiff
- EX Freed
- FA Caputo
- G Hellekant
- G Nelson
- G Nelson
- G Whitney
- G Whitney
- G Whitney
- GA Falciglia
- GE McClearn
- GJ Lawrence
- GK Beauchamp
- GK Beauchamp
- GK Beauchamp
- GQ Zhao
- GT Wong
- H Harris
- H Harris
- H Looy
- H Looy
- H Matsunami
- H Xu
- HJ Grill
- I Le Roy
- I Ramirez
- IE Lush
- IE Lush
- IE Lush
- IE Lush
- IE Lush
- IE Lush
- IE Lush
- IE Lush
- IL Bernstein
- J Brand
- J Chandrashekar
- J Chandrashekar
- J Liao
- J-X Guinard
- JA Desor
- JC Molina
- JC Smith
- JD Boughter Jr
- JD Boughter Jr
- JF Gent
- JI Glendinning
- JI Glendinning
- JI Glendinning
- JK Belknap
- JK Belknap
- JK Belknap
- JL Fuller
- JL Fuller
- JL Hansen
- JM Olson
- John D Boughter
- JP Montmayeur
- JT Fitzsimons
- K Hoshishima
- K Hoshishima
- K Lu
- K Scott
- K Scott
- KL Mueller
- KS Curtis
- KS Gannon
- LH Snyder
- LM Bartoshuk
- LM Bartoshuk
- LM Bartoshuk
- LR Intranuovo
- LS Greene
- M Behrens
- M Inoue
- M Inoue
- M Inoue
- M Inoue
- M Kitagawa
- M Max
- M Nachman
- M Nachman
- MA Austin
- MA Enoch
- MA Hoon
- MD Basson
- MD Stockton
- ME Dinehart
- ME Frank
- ME Frank
- ME Yamamoto
- MG Tordoff
- ML Pelchat
- MM Minear
- N Chaudhari
- N Sako
- N Shigemura
- N Shigemura
- N Soranzo
- NE Rowland
- NK Dess
- NK Dess
- O Lugaz
- O Pucilowski
- P Mombaerts
- P Shi
- PM Conneally
- PM Di Lorenzo
- R Di Nicolantonio
- R DiNicolantonio
- R DiNicolantonio
- RB Stewart
- RB Stewart
- RD Mattes
- RP Warren
- RT Gentry
- S Damak
- S Eylam
- S Eylam
- S Eylam
- S Manita
- S Marella
- SA Lanier
- SA Simon
- SB Harrap
- SI Sollars
- SI Sollars
- SI Sollars
- SJ St John
- SN Clarke
- SR George
- SR Lewis
- ST DiCarlo
- SW Kiefer
- SW Kiefer
- SW Kiefer
- T Foroud
- TA Gilbertson
- TA Richter
- TJ Phillips
- TM Nelson
- TM Nelson
- TR Scott
- TW Klein
- UK Kim
- UK Kim
- VB Duffy
- WE Pelz
- X Li
- X Li
- X Li
- X Li
- X Li
- X Wang
- Y Go
- Y Go
- Y Ishimaru
- Y Maruyama
- Y Nie
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- Y Ninomiya
- YA Blednov
- YK Cho
- Publication venue
- BioMed Central
- Publication date
- 01/01/2007
- Field of study
This review focuses on behavioral genetic studies of sweet, umami, bitter and salt taste responses in mammals. Studies involving mouse inbred strain comparisons and genetic analyses, and their impact on elucidation of taste receptors and transduction mechanisms are discussed. Finally, the effect of genetic variation in taste responsiveness on complex traits such as drug intake is considered. Recent advances in development of genomic resources make behavioral genetics a powerful approach for understanding mechanisms of taste
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
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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
Combination of searches for heavy spin-1 resonances using 139 fb−1 of proton-proton collision data at s = 13 TeV with the ATLAS detector
- Author
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- Zhemchugov A
- Zheng J
- Zheng K
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- Zimine NI
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- Zorbas TG
- Zormpa O
- Zou W
- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Springer Nature
- Publication date
- 19/04/2024
- Field of study
A combination of searches for new heavy spin-1 resonances decaying into different pairings of W, Z, or Higgs bosons, as well as directly into leptons or quarks, is presented. The data sample used corresponds to 139 fb−1 of proton-proton collisions at
= 13 TeV collected during 2015–2018 with the ATLAS detector at the CERN Large Hadron Collider. Analyses selecting quark pairs (qq, bb,
, and tb) or third-generation leptons (τν and ττ) are included in this kind of combination for the first time. A simplified model predicting a spin-1 heavy vector-boson triplet is used. Cross-section limits are set at the 95% confidence level and are compared with predictions for the benchmark model. These limits are also expressed in terms of constraints on couplings of the heavy vector-boson triplet to quarks, leptons, and the Higgs boson. The complementarity of the various analyses increases the sensitivity to new physics, and the resulting constraints are stronger than those from any individual analysis considered. The data exclude a heavy vector-boson triplet with mass below 5.8 TeV in a weakly coupled scenario, below 4.4 TeV in a strongly coupled scenario, and up to 1.5 TeV in the case of production via vector-boson fusion
Optimal beam sources for Stark decelerators in collision experiments: a tutorial review
- Author
- A Osterwalder
- A Trimeche
- A von Zastrow
- ATJB Eppink
- B Yan
- BC Sawyer
- BK Stuhl
- C Abeysekera
- D Irimia
- E Lavert-Ofir
- E Lavert-Ofir
- E Narevicius
- E Narevicius
- ER Hudson
- HL Bethlem
- HL Bethlem
- HL Bethlem
- HL Bethlem
- J Jankunas
- J Küpper
- J Onvlee
- J van Veldhoven
- JJ Gilijamse
- L Scharfenberg
- L Scharfenberg
- M Brouard
- M Kirste
- M Quintero-Perez
- MT Bell
- N Vanhaecke
- S Jung
- SA Meek
- SA Meek
- SN Vogels
- SYT van de Meerakker
- SYT van de Meerakker
- SYT van de Meerakker
- SYT van de Meerakker
- SYT van de Meerakker
- SYT van de Meerakker
- U Even
- U Even
- WR Gentry
- Y Liu
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
- …