79 research outputs found
Global expression profiling of theophylline response genes in macrophages: evidence of airway anti-inflammatory regulation
- Author
- A Hancock
- A Hancock
- A Lorentz
- A McKay
- B Arnoux
- C Laprise
- CH Wang
- DM Essayan
- ER McFadden Jr
- G Grunig
- GK Hershey
- HJ Patel
- HW Chen
- HY Huh
- J de Rooij
- J Hiscott
- JH Lee
- JJ Chen
- JK Shute
- K Chibana
- K Ito
- K Ohta
- K Tomita
- LM Yesner
- M Joseph
- M Kimura
- M Peters-Golden
- M Wills-Karp
- MC Shepherd
- ML Lohmann-Matthes
- N Wang
- N Yoshida
- PC Carre
- PH Hart
- PJ Barnes
- PM O'Byrne
- Q Hamid
- R Lu
- RA Heller
- RD Ye
- RW Fuller
- RW Janson
- SL Yu
- TC Kotsimbos
- TR Myers
- WJ Calhoun
- Z Zhu
- Publication venue
- BioMed Central
- Publication date
- 01/01/2005
- Field of study
BACKGROUND: Theophylline has been used widely as a bronchodilator for the treatment of bronchial asthma and has been suggested to modulate immune response. While the importance of macrophages in asthma has been reappraised and emphasized, their significance has not been well investigated. We conducted a genome-wide profiling of the gene expressions of macrophages in response to theophylline. METHODS: Microarray technology was used to profile the gene expression patterns of macrophages modulated by theophylline. Northern blot and real-time quantitative RT-PCR were also used to validate the microarray data, while Western blot and ELISA were used to measure the levels of IL-13 and LTC4. RESULTS: We identified dozens of genes in macrophages that were dose-dependently down- or up-regulated by theophylline. These included genes related to inflammation, cytokines, signaling transduction, cell adhesion and motility, cell cycle regulators, and metabolism. We observed that IL-13, a central mediator of airway inflammation, was dramatically suppressed by theophylline. Real-time quantitative RT-PCR and ELISA analyses also confirmed these results, without respect to PMA-treated THP-1 cells or isolated human alveolar macrophages. Theophylline, rolipram, etazolate, db-cAMP and forskolin suppressed both IL-13 mRNA expression (~25%, 2.73%, 8.12%, 5.28%, and 18.41%, respectively) and protein secretion (<10% production) in macrophages. These agents also effectively suppressed LTC4 expression. CONCLUSION: Our results suggest that the suppression of IL-13 by theophylline may be through cAMP mediation and may decrease LTC4 production. This study supports the role of theophylline as a signal regulator of inflammation, and that down regulation of IL-13 by theophylline may have beneficial effects in inflammatory airway diseases
New studies, technology, and the progress of epidemiology
- Author
- A Alpérovitch
- A Hofman
- A Hofman
- A Moayyeri
- A Oliveira
- A Schmassmann
- A Stang
- A Thompson
- ACJW Janssens
- AG Pires de Sousa
- AH Merry
- AK Gulsvik
- Albert Hofman
- AM Asfeldt
- AS Khashan
- BM Kim
- BM Psaty
- C Ahlgren
- C Bexelius
- C Heidemann
- C Luise de
- C Prugger
- D Jacobi
- D Raoult
- D Saleheen
- DA Lawlor
- DB Wieren-de Wijer van
- DH Jaffe
- DS Thelle
- DS Thelle
- E Corpeleijn
- E Hedlund
- E McFadden
- E McFadden
- E Olafsdottir
- E Regidor
- EA Spencer
- F Bloch
- F Wiesbauer
- FE Pisa
- G Andreotti
- G Berg-Beckhoff
- G Tasevska-Dinevska
- H Sylliaas
- H Watanabe
- I Kompauer
- J Danesh
- J Little
- J Pekkanen
- JF Ludvigsson
- JP Loannidis
- K Gemes
- K Schlaefer
- KD Laszlo
- KH Greiser
- L Balk
- L Duijts
- L Forsen
- L Lei
- L Ruan
- LA Ahmed
- M Dörr
- M Osler
- M Reuser
- MS Pearce
- MS Setia
- N Amin
- N Dragano
- N Emaus
- N Fallah
- O Bruyere
- O Ganry
- O Mayer Jr
- OS Miettinen
- P Rzehak
- P Rzehak
- QM Nguyen
- RF Mao
- RP Stolk
- RP Stolk
- S Aarts
- S Graff-Iversen
- S Holzhauer
- S Larrieu
- S Vaux
- SO Manda
- T Hugg
- T Vikan
- TC Turin
- U Nur
- VWV Jaddoe
- W Zatonski
- YT Lagerros
- Publication venue
- Springer Netherlands
- Publication date
- 01/12/2010
- Field of study
Gene expression profiling of monkeypox virus-infected cells reveals novel interfaces for host-virus interactions
- Author
- A Kumagai
- A Lindqvist
- A Vanderplasschen
- Abdulnaser Alkhalil
- AM Likos
- AS Manoukian
- CE Canman
- CE Lilley
- CJ Sherr
- CL Afonso
- CL Lin
- CS Chung
- CY Peng
- DB Bowe
- DJ Lockhart
- E Assarsson
- E Bales
- E Bossy-Wetzel
- E Fanning
- E Oda
- EK Hui
- EV Pavlov
- F Da Fonseca
- F Puvion-Dutilleul
- F Re
- FG Giancotti
- FL Schuster
- G McFadden
- G Melino
- G Pawlak
- GC Carter
- H Everett
- H Everett
- H Zhao
- J Falck
- J He
- J Lew
- J McGlade
- J Parrino
- JA Armstrong
- JC Donovan
- JC Hsiao
- JG Breman
- JL Shisler
- JL Siegert
- JR Kates
- Justin Hardick
- K Sakamoto
- KH Rubins
- KH Rubins
- KL King
- KM Debatin
- KW Kohn
- L Latella
- LG Martin
- LG Payne
- LM Brum
- LT Quan
- M Bahassi el
- M Dobbelstein
- M Hrimech
- M Nakamoto
- M Thome
- Marti Jett
- MF Lavin
- MF Roussel
- MJ Edick
- MJ Soloski
- MO Hengartner
- Mohamed Ait Ichou
- MV Davies
- N Chen
- N Mailand
- N Mailand
- NG Deane
- O Pochynyuk
- Rasha Hammamieh
- RM Ewing
- RM Scaife
- RY Zhao
- RZ Orlowski
- S Dales
- S Goldstone
- S Guerra
- S Shimizu
- SA Desai
- SJ Werden
- SN Shchelkunov
- SN Willis
- Sofi Ibrahim
- ST Wasilenko
- T Komiyama
- TC Hallstrom
- U Schubert
- V Janssens
- W Munyon
- W Nakajima
- WA Cliby
- WC Earnshaw
- Y Sanchez
- Y Tsuchiya
- Publication venue
- BioMed Central
- Publication date
- 01/01/2010
- Field of study
Monkeypox virus (MPV) is a zoonotic Orthopoxvirus and a potential biothreat agent that causes human disease with varying morbidity and mortality. Members of the Orthopoxvirus genus have been shown to suppress antiviral cell defenses, exploit host cell machinery, and delay infection-induced cell death. However, a comprehensive study of all host genes and virus-targeted host networks during infection is lacking. To better understand viral strategies adopted in manipulating routine host biology on global scale, we investigated the effect of MPV infection on Macaca mulatta kidney epithelial cells (MK2) using GeneChip rhesus macaque genome microarrays. Functional analysis of genes differentially expressed at 3 and 7 hours post infection showed distinctive regulation of canonical pathways and networks. While the majority of modulated histone-encoding genes exhibited sharp copy number increases, many of its transcription regulators were substantially suppressed; suggesting involvement of unknown viral factors in host histone expression. In agreement with known viral dependence on actin in motility, egress, and infection of adjacent cells, our results showed extensive regulation of genes usually involved in controlling actin expression dynamics. Similarly, a substantial ratio of genes contributing to cell cycle checkpoints exhibited concerted regulation that favors cell cycle progression in G1, S, G2 phases, but arrest cells in G2 phase and inhibits entry into mitosis. Moreover, the data showed that large number of infection-regulated genes is involved in molecular mechanisms characteristic of cancer canonical pathways. Interestingly, ten ion channels and transporters showed progressive suppression during the course of infection. Although the outcome of this unusual channel expression on cell osmotic homeostasis remains unknown, instability of cell osmotic balance and membrane potential has been implicated in intracellular pathogens egress. Our results highlight the role of histones, actin, cell cycle regulators, and ion channels in MPV infection, and propose these host functions as attractive research focal points in identifying novel drug intervention sites
Contact dermatitis and other skin conditions in instrumental musicians
- Author
- A Inoue
- A Inoue
- A Oga
- AA Fisher
- AA Fisher
- AA Fisher
- AA Fisher
- AA Fisher
- AA Fisher
- AA Fisher
- AH Bryan
- AH O'Hagan
- AJ Kanwar
- AM Zina
- BH Kaufman
- BM Hausen
- BM Hausen
- BM Hausen
- BM Hausen
- BM Hausen
- BM Hausen
- C Lerner
- C Lombardi
- C Pincelli
- CE Dettmann
- D Tennstedt
- DA Basketter
- DA Buckley
- DG Ross
- E Altenmüller
- E Carabias
- E Landeck
- E Rajna
- G Angelini
- G Färm
- G Kick
- G Marshman
- G Sebastian
- H Fruhstorfer
- HA Bird
- HD Lieberman
- HN Mandell
- J Blum
- J James
- J Machácková
- J Machácková
- J Murphy
- J Planas
- JB Stern
- JC Moreno
- JD Jago
- JE Wahlberg
- JM Destouet
- JM Lachappelle
- JM Murphy
- JM Thomas
- JP McFadden
- JR Nethercott
- JS Koransky
- K Bork
- K Bork
- L Peltonen
- LD Gardner
- LH Calabrese
- LJ Goldstein
- M Fishbein
- M Monti
- M Nakamura
- M Önder
- M Önder
- MA Ramirez
- Marcus Freitag
- MG Dahl
- MH Van der Wegen-Keijser
- NJ Reina
- NP Melia
- P Barkvoll
- P Barkvoll
- P Brun
- P Curtis
- P Thomas
- PA Piletta
- PE Shapiro
- R Baran
- R Semple
- RA Hoppmann
- RDG Peachey
- RJ Signore
- RM Adams
- S Freeman
- S Liu
- S Rimmer
- SJ Friedman
- Stefanie Boms
- T Burr
- TC Hindson
- Thilo Gambichler
- TN Helm
- UF Haustein
- Publication venue
- BioMed Central
- Publication date
- 01/04/2004
- Field of study
BACKGROUND: The skin is important in the positioning and playing of a musical instrument. During practicing and performing there is a permanent more or less intense contact between the instrument and the musician's skin. Apart from aggravation of predisposed skin diseases (e.g., atopic eczema or psoriasis) due to music-making, specific dermatologic conditions may develop that are directly caused by playing a musical instrument. METHODS: To perform a systematic review on instrument-related skin diseases in musicians we searched the PubMed database without time limits. Furthermore we studied the online bibliography "Occupational diseases of performing artist. A performing arts medicine bibliography. October, 2003" and checked references of all selected articles for relevant papers. RESULTS: The most prevalent skin disorders of instrumental musicians, in particular string instrumentalists (e.g., violinists, cellists, guitarists), woodwind players (e.g., flautists, clarinetists), and brass instrumentalists (e.g., trumpeters), include a variety of allergic contact sensitizations (e.g., colophony, nickel, and exotic woods) and irritant (physical-chemical noxae) skin conditions whose clinical presentation and localization are usually specific for the instrument used (e.g., "fiddler's neck", "cellist's chest", "guitar nipple", "flautist's chin"). Apart from common callosities and "occupational marks" (e.g., "Garrod's pads") more or less severe skin injuries may occur in musical instrumentalists, in particular acute and chronic wounds including their complications. Skin infections such as herpes labialis seem to be a more common skin problem in woodwind and brass instrumentalists. CONCLUSIONS: Skin conditions may be a significant problem not only in professional instrumentalists, but also in musicians of all ages and ability. Although not life threatening they may lead to impaired performance and occupational hazard. Unfortunately, epidemiological investigations have exclusively been performed on orchestra musicians, though the prevalence of instrument-related skin conditions in other musician groups (e.g., jazz and rock musicians) is also of interest. The practicing clinician should be aware of the special dermatologic problems unique to the musical instrumentalist. Moreover awareness among musicians needs to be raised, as proper technique and conditioning may help to prevent affection of performance and occupational impairment
The Generation R Study: design and cohort update 2010
- Author
- A Alonso
- A Britton
- A Ekman
- A Gasparrini
- A Ghasemi
- A Goodman
- A Heraclides
- A Hofman
- A Hofman
- A Isaacs
- A Julihn
- A Lebon
- A Lebon
- A Lebon
- A Leclerc
- A Moayyeri
- A Oliveira
- A Stang
- A Thompson
- AC Janssens
- AD Mohangoo
- AF Seabra
- AG Pires de Sousa
- AH Merry
- AJLL Brock De
- Albert Hofman
- Albert J. van der Heijden
- AM Asfeldt
- AM Fraga
- Andre G. Uitterlinden
- AS Khashan
- B Clarisse
- B Dierckx
- B Durmus
- BM Kim
- BO Verburg
- BO Verburg
- BO Verburg
- BO Verburg
- C Bexelius
- C Gabriele
- C Heidemann
- C Hublin
- C Luise de
- C Nabet
- C Sabanayagam
- C Thomas
- CCG Collaboration
- Cock M. van Duijn
- CP Barakat-Haddad
- CU Rask
- D Jacobi
- D Raoult
- D Saleheen
- DA Lawlor
- DA Lawlor
- DB Bartels
- DB Wieren-de Wijer van
- DC Greenwood
- DJ Carver
- DM Hafeman
- DO Mook-Kanamori
- DO Mook-Kanamori
- DO Mook-Kanamori
- DO Mook-Kanamori
- DO Mook-Kanamori
- DS Thelle
- E Abatih
- E Cardis
- E Casiglia
- E Corpeleijn
- E Hedlund
- E McFadden
- E McFadden
- E McFadden
- E McFadden
- E Olafsdottir
- E Regidor
- EA Spencer
- EH Hooven van den
- EJ Troe
- EJ Troe
- Eric A. P. Steegers
- F Banhidy
- F Bloch
- F Muller-Riemenschneider
- F Wiesbauer
- Frank C. Verhulst
- G Andreotti
- G Berg-Beckhoff
- GI Rours
- H El Marroun
- H El Marroun
- H Ireton
- H Raat
- Henning Tiemeier
- Henriëtte A. Moll
- I Kompauer
- I Pitrou
- I Romon
- I Sandven
- I St James-Roberts
- I St James-Roberts
- I St James-Roberts
- J Henrichs
- J Henrichs
- J Henrichs
- J Klenk
- J Little
- J Matthiessen
- J Pekkanen
- J Wardle
- JA Delaney
- JA Labout
- JA Maas
- JC Kiefte-de Jong
- JC Taylor
- JE Ware Jr
- JF Ludvigsson
- JJ Geelhoed
- JJ Geelhoed
- JJ Geelhoed
- JJ Geelhoed
- JJ Geelhoed
- JJ Geelhoed
- JL Cox
- JL Zhu
- Johan P. Mackenbach
- JR Gerris
- K Gemes
- K Schlaefer
- K Strandberg-Larsen
- K Tunon
- KD Laszlo
- KH Greiser
- KJ Saudino
- L Ay
- L Ay
- L Ay
- L Balk
- L Duijts
- L Duijts
- L Duijts
- L Duijts
- L Duijts
- L Fenson
- L Forsen
- L Huang
- L Richiardi
- L Rossem van
- L Ruan
- L Silva
- LA Ahmed
- LC See
- LM Silva
- LM Silva
- LR Derogatis
- LS Walker
- M Coolman
- M Dorr
- M Heys
- M Osler
- M Reuser
- M Touvier
- MA Gartstein
- MA Jenkins
- MF Faramawi
- MJ Geelhoed
- MJ Geelhoed
- MP Berg van den
- MP Luijk
- MS Pearce
- MS Setia
- N Amin
- N Dragano
- N Emaus
- N Fallah
- N Orsini
- N Wolff
- NA Abdullah
- NJ Verkaik
- NJ Wolff
- NR Bindraban
- NS Saridjan
- O Bruyere
- O Mayer Jr
- OS Miettinen
- OS Miettinen
- P Astolfi
- P Niemiec
- P Rzehak
- P Rzehak
- P Troude
- PI Pfefferle
- PK Isquith
- PW Jansen
- PW Jansen
- PW Jansen
- PW Jansen
- Q Tan
- QM Nguyen
- R Bakker
- R Bakker
- R Foraita
- R Quansah
- RJF Burgmeijer
- RM Freathy
- RP Stolk
- S Aarts
- S Alatupa
- S Graff-Iversen
- S Hernandez-Diaz
- S Holzhauer
- S Holzhauer
- S Lundbye-Christensen
- S Timmermans
- S Timmermans
- S Walter
- SJ Roza
- SJ Roza
- SJ Roza
- SJ Roza
- SJ Roza
- SJ Roza
- SJ Roza
- SO Manda
- Statistics Netherlands
- Statistics Netherlands
- T Batenburg-Eddes van
- T Batenburg-Eddes van
- T Batenburg-Eddes van
- T Behrens
- T Chimonas
- T Hugg
- T Lallukka
- T Rodrigues
- T Vikan
- TC Turin
- TJ VanderWeele
- TM Achenbach
- TN Jacobsen
- U Nur
- U Stromberg
- V Baste
- VA Houten van
- VA Houten van
- Vincent W. V. Jaddoe
- VW Jaddoe
- VW Jaddoe
- VW Jaddoe
- VW Jaddoe
- VW Jaddoe
- VW Jaddoe
- W Thomas
- WY Wang
- X Ye
- Y Qi
- Y Yaegashi
- YK Tu
- YT Lagerros
- YT Lagerros
- Publication venue
- Springer Netherlands
- Publication date
- 01/01/2010
- Field of study
The Generation R Study is a population-based prospective cohort study from fetal life until young adulthood. The study is designed to identify early environmental and genetic causes of normal and abnormal growth, development and health during fetal life, childhood and adulthood. The study focuses on four primary areas of research: (1) growth and physical development; (2) behavioural and cognitive development; (3) diseases in childhood; and (4) health and healthcare for pregnant women and children. In total, 9,778 mothers with a delivery date from April 2002 until January 2006 were enrolled in the study. General follow-up rates until the age of 4 years exceed 75%. Data collection in mothers, fathers and preschool children included questionnaires, detailed physical and ultrasound examinations, behavioural observations, and biological samples. A genome wide association screen is available in the participating children. Regular detailed hands on assessment are performed from the age of 5 years onwards. Eventually, results forthcoming from the Generation R Study have to contribute to the development of strategies for optimizing health and healthcare for pregnant women and children
Early influences on cardiovascular and renal development
- Author
- A Bree de
- A Britton
- A Gasparrini
- A Oliveira
- A Stang
- A Toprak
- A Trichopoulou
- A Wong
- AA Baschat
- AA Brooks
- AA Mamun
- AA Montgomery
- AC Hokken-Koelega
- AD Goldberg
- AD Stein
- AH Merry
- AJ Bennett
- AL Fowden
- AL Fowden
- AM Di Blasio
- AM Siega-Riz
- AT Hattersley
- B Buemann
- B Jiang
- BM Brenner
- BM Brenner
- BO Verburg
- BO Verburg
- BT Heijmans
- C Heidemann
- C Merlet-Benichou
- C Osmond
- C Prugger
- C Schneider
- C Weikert
- CG Victora
- CN Martyn
- CP Leeson
- D Levy
- D Levy
- D Saleheen
- DA Lawlor
- DA Lawlor
- DA Lawlor
- DJ Barker
- DJ Barker
- DJ Barker
- DJ Barker
- DM Jensen
- DO Mook-Kanamori
- DO Mook-Kanamori
- DS Thelle
- DT Lackland
- E Casiglia
- E Hedlund
- E Hotoura
- E McFadden
- E McFadden
- E Regidor
- E Strandhagen
- EA Spencer
- EF Rossum van
- EF Rossum van
- EL Akker van den
- EM Urbina
- F Mzayek
- F Wiesbauer
- FM Severi
- G Andreotti
- G Celsi
- G Guron
- G Keller
- G Rizzo
- G Tasevska-Dinevska
- GC Smith
- GC Watt
- H Bassan
- H Gardiner
- H Martin
- H Martin
- H Schulman
- H Yliharsila
- H Zheng
- HM Gardiner
- HM Inskip
- I Kardys
- IM Hooft van
- IM Schmidt
- J Eriksson
- J Golding
- J Klenk
- J Matthiessen
- J Olsen
- J Pekkanen
- J. J. Miranda Geelhoed
- JA Delaney
- JA Wijngaard van den
- JC King
- JC Konje
- JC Veille
- JG Eriksson
- JG Eriksson
- JJ Geelhoed
- JJ Geelhoed
- JJ Geelhoed
- JJ Geelhoed
- JJ Geelhoed
- JJ Walker
- JM Belizan
- JM Kerver
- JP Halcox
- JR Nyengaard
- JW Rich-Edwards
- K Gemes
- KD Laszlo
- KD Sinclair
- KF Janz
- KH Greiser
- KK Ong
- KM Godfrey
- KV Blake
- L Ay
- L Zeng
- LA Mierlo van
- LD Jacobs
- LG Larsen
- LK Callaway
- LS Webber
- LT Mahoney
- LT Mahoney
- M Dramé
- M Hughson
- M Lampl
- M Lelievre-Pegorier
- M Osler
- M Reuser
- M Vijayakumar
- M Vujkovic
- M Zureik
- MCP Silva
- MD Hughson
- MJ Brion
- MJ Brion
- MJ Finken
- MJ Geelhoed
- MJ Geelhoed
- MJ Jarvisalo
- MK Ikram
- MM Bergmann
- MR Hammerman
- MS Pearce
- MW Gillman
- MW Lorenz
- N Dragano
- N Fallah
- N Orsini
- NA Huizenga
- O Mayer Jr
- P Bateson
- P Magnus
- P Niemiec
- P Sparen
- PD Gluckman
- PD Gluckman
- PD Gluckman
- PH Davis
- PH Whincup
- R Bakker
- R Benediktsson
- R Huxley
- R Huxley
- R Jacobsen
- R Manalich
- R Morley
- R Rosmond
- R Rosmond
- R Rosmond
- R Ross
- R Ross
- RA Waterland
- RA Waterland
- RA Waterland
- RC Lin
- RF Mao
- RJ Morrow
- RM Freathy
- S Frankel
- S Graff-Iversen
- S Hawkesworth
- S Higgins
- S Kinra
- S Lundbye-Christensen
- S Masud
- S Tenhola
- SA Hinchliffe
- SA Hinchliffe
- SC Langley-Evans
- SE Lipshultz
- SJ Moat
- SJ Pinto-Sietsma
- SK Nigram
- SP Ramirez
- SY Huh
- T Chimonas
- T Pfab
- T Vikan
- TC Turin
- TJ Roseboom
- TM Nafee
- V Giapros
- Vincent W. V. Jaddoe
- VW Jaddoe
- VW Jaddoe
- VW Jaddoe
- W Kabiru
- W Zatonski
- WC Winkelmayer
- WE Hoy
- Y Wang
- YF Cheung
- YS Cho
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2010
- Field of study
The hypothesis that a developmental component plays a role in subsequent disease initially arose from epidemiological studies relating birth size to both risk factors for cardiovascular disease and actual cardiovascular disease prevalence in later life. The findings that small size at birth is associated with an increased risk of cardiovascular disease have led to concerns about the effect size and the causality of the associations. However, recent studies have overcome most methodological flaws and suggested small effect sizes for these associations for the individual, but an potential important effect size on a population level. Various mechanisms underlying these associations have been hypothesized, including fetal undernutrition, genetic susceptibility and postnatal accelerated growth. The specific adverse exposures in fetal and early postnatal life leading to cardiovascular disease in adult life are not yet fully understood. Current studies suggest that both environmental and genetic factors in various periods of life may underlie the complex associations of fetal growth retardation and low birth weight with cardiovascular disease in later life. To estimate the population effect size and to identify the underlying mechanisms, well-designed epidemiological studies are needed. This review is focused on specific adverse fetal exposures, cardiovascular adaptations and perspectives for new studies. Copyrigh
Early influences on cardiovascular and renal development
- Author
- A Bree de
- A Britton
- A Gasparrini
- A Oliveira
- A Stang
- A Toprak
- A Trichopoulou
- A Wong
- AA Baschat
- AA Brooks
- AA Mamun
- AA Montgomery
- AC Hokken-Koelega
- AD Goldberg
- AD Stein
- AH Merry
- AJ Bennett
- AL Fowden
- AL Fowden
- AM Di Blasio
- AM Siega-Riz
- AT Hattersley
- B Buemann
- B Jiang
- BM Brenner
- BM Brenner
- BO Verburg
- BO Verburg
- BT Heijmans
- C Heidemann
- C Merlet-Benichou
- C Osmond
- C Prugger
- C Schneider
- C Weikert
- CG Victora
- CN Martyn
- CP Leeson
- D Levy
- D Levy
- D Saleheen
- DA Lawlor
- DA Lawlor
- DA Lawlor
- DJ Barker
- DJ Barker
- DJ Barker
- DJ Barker
- DM Jensen
- DO Mook-Kanamori
- DO Mook-Kanamori
- DS Thelle
- DT Lackland
- E Casiglia
- E Hedlund
- E Hotoura
- E McFadden
- E McFadden
- E Regidor
- E Strandhagen
- EA Spencer
- EF Rossum van
- EF Rossum van
- EL Akker van den
- EM Urbina
- F Mzayek
- F Wiesbauer
- FM Severi
- G Andreotti
- G Celsi
- G Guron
- G Keller
- G Rizzo
- G Tasevska-Dinevska
- GC Smith
- GC Watt
- H Bassan
- H Gardiner
- H Martin
- H Martin
- H Schulman
- H Yliharsila
- H Zheng
- HM Gardiner
- HM Inskip
- I Kardys
- IM Hooft van
- IM Schmidt
- J Eriksson
- J Golding
- J Klenk
- J Matthiessen
- J Olsen
- J Pekkanen
- J. J. Miranda Geelhoed
- JA Delaney
- JA Wijngaard van den
- JC King
- JC Konje
- JC Veille
- JG Eriksson
- JG Eriksson
- JJ Geelhoed
- JJ Geelhoed
- JJ Geelhoed
- JJ Geelhoed
- JJ Geelhoed
- JJ Walker
- JM Belizan
- JM Kerver
- JP Halcox
- JR Nyengaard
- JW Rich-Edwards
- K Gemes
- KD Laszlo
- KD Sinclair
- KF Janz
- KH Greiser
- KK Ong
- KM Godfrey
- KV Blake
- L Ay
- L Zeng
- LA Mierlo van
- LD Jacobs
- LG Larsen
- LK Callaway
- LS Webber
- LT Mahoney
- LT Mahoney
- M Dramé
- M Hughson
- M Lampl
- M Lelievre-Pegorier
- M Osler
- M Reuser
- M Vijayakumar
- M Vujkovic
- M Zureik
- MCP Silva
- MD Hughson
- MJ Brion
- MJ Brion
- MJ Finken
- MJ Geelhoed
- MJ Geelhoed
- MJ Jarvisalo
- MK Ikram
- MM Bergmann
- MR Hammerman
- MS Pearce
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- N Dragano
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- N Orsini
- NA Huizenga
- O Mayer Jr
- P Bateson
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- P Sparen
- PD Gluckman
- PD Gluckman
- PD Gluckman
- PH Davis
- PH Whincup
- R Bakker
- R Benediktsson
- R Huxley
- R Huxley
- R Jacobsen
- R Manalich
- R Morley
- R Rosmond
- R Rosmond
- R Rosmond
- R Ross
- R Ross
- RA Waterland
- RA Waterland
- RA Waterland
- RC Lin
- RF Mao
- RJ Morrow
- RM Freathy
- S Frankel
- S Graff-Iversen
- S Hawkesworth
- S Higgins
- S Kinra
- S Lundbye-Christensen
- S Masud
- S Tenhola
- SA Hinchliffe
- SA Hinchliffe
- SC Langley-Evans
- SE Lipshultz
- SJ Moat
- SJ Pinto-Sietsma
- SK Nigram
- SP Ramirez
- SY Huh
- T Chimonas
- T Pfab
- T Vikan
- TC Turin
- TJ Roseboom
- TM Nafee
- V Giapros
- Vincent W. V. Jaddoe
- VW Jaddoe
- VW Jaddoe
- VW Jaddoe
- W Kabiru
- W Zatonski
- WC Winkelmayer
- WE Hoy
- Y Wang
- YF Cheung
- YS Cho
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Measurement of W+W− production in association with one jet in proton–proton collisions at sqrt(s) = 8TeV with the ATLAS detector
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Abeloos B
- Aben R
- Abraham NL
- Abramowicz H
- Abreu H
- Abreu R
- Abulaiti Y
- Acharya BS
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- Zhemchugov A
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- Zimmermann C
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- Zinonos Z
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- Zu Theenhausen HM
- zur Nedden M
- Zwalinski L
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2016
- Field of study
The production of W boson pairs in association with one jet in pp collisions at View the MathML sources=8 TeV is studied using data corresponding to an integrated luminosity of 20.3 fb−1 collected by the ATLAS detector during 2012 at the CERN Large Hadron Collider. The cross section is measured in a fiducial phase-space region defined by the presence of exactly one electron and one muon, missing transverse momentum and exactly one jet with a transverse momentum above 25 GeV and a pseudorapidity of |η|<4.5|η|<4.5. The leptons are required to have opposite electric charge and to pass transverse momentum and pseudorapidity requirements. The fiducial cross section is found to be View the MathML sourceσWWfid,1-jet=136±6(stat)±14(syst)±3(lumi) fb. In combination with a previous measurement restricted to leptonic final states with no associated jets, the fiducial cross section of WW production with zero or one jet is measured to be View the MathML sourceσWWfid,≤1-jet=511±9(stat)±26(syst)±10(lumi) fb. The ratio of fiducial cross sections in final states with one and zero jets is determined to be 0.36±0.050.36±0.05. Finally, a total cross section extrapolated from the fiducial measurement of WW production with zero or one associated jet is reported. The measurements are compared to theoretical predictions and found in good agreement
Search for squarks and gluinos in final states with jets and missing transverse momentum using 139 fb−1 of s√ = 13 TeV pp collision data with the ATLAS detector
- Author
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- Aad G
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- Abdinov O
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- Abhayasinghe DK
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- Yildirim E
- Yildiz HD
- Yorita K
- Yoshihara K
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- Yue X
- Yuen SPY
- Zabinski B
- Zacharis G
- Zaffaroni E
- Zaidan R
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- Zakareishvili T
- Zakharchuk N
- Zalieckas J
- Zambito S
- Zanzi D
- Zaripovas DR
- Zeissner SV
- Zeitnitz C
- Zemaityte G
- Zeng JC
- Zeng Q
- Zenin O
- Zenis T
- Zerwas D
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- Zhang Y
- Zhang Z
- Zhao P
- Zhao X
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- Zhao Z
- Zhemchugov A
- Zhou B
- Zhou C
- Zhou L
- Zhou M
- Zhou MS
- Zhou N
- Zhou Y
- Zhu CG
- Zhu H
- Zhu HL
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zoch K
- Zorbas TG
- Zou R
- Zwalinski L
- Publication venue
- 'Springer Fachmedien Wiesbaden GmbH'
- Publication date
- 17/02/2021
- Field of study
A search for the supersymmetric partners of quarks and gluons (squarks and gluinos) in final states containing jets and missing transverse momentum, but no electrons or muons, is presented. The data used in this search were recorded by the ATLAS experiment in proton-proton collisions at a centre-of-mass energy of s√ = 13 TeV during Run 2 of the Large Hadron Collider, corresponding to an integrated luminosity of 139 fb−1. The results are interpreted in the context of various R-parity-conserving models where squarks and gluinos are produced in pairs or in association and a neutralino is the lightest supersymmetric particle. An exclusion limit at the 95% confidence level on the mass of the gluino is set at 2.30 TeV for a simplified model containing only a gluino and the lightest neutralino, assuming the latter is massless. For a simplified model involving the strong production of mass-degenerate first- and second-generation squarks, squark masses below 1.85 TeV are excluded if the lightest neutralino is massless. These limits extend substantially beyond the region of supersymmetric parameter space excluded previously by similar searches with the ATLAS detector
Measurement of Azimuthal Anisotropy of Muons from Charm and Bottom Hadrons in pp Collisions 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
- Akesson TPA
- Akilli E
- Akimov AV
- Alberghi GL
- Albert J
- Albicocco P
- 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 Piqueras D
- Alviggi MG
- Amadio BT
- 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
- Aparisi Pozo JA
- Aperio Bella L
- Arabidze G
- Aranda CP
- Araque JP
- Araujo Ferraz V
- Araujo Pereira R
- Araya ST
- Arce ATH
- Ardell RE
- Arduh FA
- Arguin J-F
- Argyropoulos S
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- Publication venue
- AMER PHYSICAL SOC
- Publication date
- 28/02/2020
- Field of study
The elliptic flow of muons from the decay of charm and bottom hadrons is measured in
p
p
collisions at
√
s
=
13
TeV
using a data sample with an integrated luminosity of
150
pb
−
1
recorded by the ATLAS detector at the LHC. The muons from heavy-flavor decay are separated from light-hadron decay muons using momentum imbalance between the tracking and muon spectrometers. The heavy-flavor decay muons are further separated into those from charm decay and those from bottom decay using the distance-of-closest-approach to the collision vertex. The measurement is performed for muons in the transverse momentum range 4–7 GeV and pseudorapidity range
|
η
|
<
2.4
. A significant nonzero elliptic anisotropy coefficient
v
2
is observed for muons from charm decays, while the
v
2
value for muons from bottom decays is consistent with zero within uncertainties
- …