80 research outputs found
Towards detection of early response in neoadjuvant chemotherapy of breast cancer using Bayesian intravoxel incoherent motion
- Publication venue
- Frontiers Media SA
- Publication date
- 01/01/2023
- Field of study
Copyright \ua9 2023 Cheung, Wu, Senn, Sharma, McGoldrick, Gagliardi, Husain, Masannat and He. Introduction: The early identification of good responders to neoadjuvant chemotherapy (NACT) holds a significant potential in the optimal treatment of breast cancer. A recent Bayesian approach has been postulated to improve the accuracy of the intravoxel incoherent motion (IVIM) model for clinical translation. This study examined the prediction and early sensitivity of Bayesian IVIM to NACT response. Materials and methods: Seventeen female patients with breast cancer were scanned at baseline and 16 patients were scanned after Cycle 1. Tissue diffusion and perfusion from Bayesian IVIM were calculated at baseline with percentage change at Cycle 1 computed with reference to baseline. Cellular proliferative activity marker Ki-67 was obtained semi-quantitatively with percentage change at excision computed with reference to core biopsy. Results: The perfusion fraction showed a significant difference (p = 0.042) in percentage change between responder groups at Cycle 1, with a decrease in good responders [−7.98% (−19.47–1.73), n = 7] and an increase in poor responders [10.04% (5.09–28.93), n = 9]. There was a significant correlation between percentage change in perfusion fraction and percentage change in Ki-67 (p = 0.042). Tissue diffusion and pseudodiffusion showed no significant difference in percentage change between groups at Cycle 1, nor was there a significant correlation against percentage change in Ki-67. Perfusion fraction, tissue diffusion, and pseudodiffusion showed no significant difference between groups at baseline, nor was there a significant correlation against Ki-67 from core biopsy. Conclusion: The alteration in tumour perfusion fraction from the Bayesian IVIM model, in association with cellular proliferation, showed early sensitivity to good responders in NACT. Clinical trial registration: https://clinicaltrials.gov/ct2/show/NCT03501394, identifier NCT03501394
The relation between media promotions and service volume for a statewide tobacco quitline and a web-based cessation program
- Author
- Andrea Mowery
- Andrew Zieffler
- B Erbas
- Barbara A Schillo
- C Miller
- DE McGoldrick
- DM Vallone
- DP Hopkins
- E Lichtenstein
- F Te Poel
- J Saul
- L Biener
- L Stead
- Lija O Greenseid
- M Farrelly
- M Fiore
- M Siahpush
- MA Sheffer
- Matthew Christenson
- MC Farrelly
- Michael G Luxenberg
- ML Lustria
- N Cobb
- N Wilson
- P Keller
- R Muñoz
- Raymond G Boyle
- S Myung
- SM Noar
- T Carroll
- Publication venue
- BioMed Central
- Publication date
- 01/01/2011
- Field of study
<p>Abstract</p> <p>Background</p> <p>This observational study assessed the relation between mass media campaigns and service volume for a statewide tobacco cessation quitline and stand-alone web-based cessation program.</p> <p>Methods</p> <p>Multivariate regression analysis was used to identify how weekly calls to a cessation quitline and weekly registrations to a web-based cessation program are related to levels of broadcast media, media campaigns, and media types, controlling for the impact of external and earned media events.</p> <p>Results</p> <p>There was a positive relation between weekly broadcast targeted rating points and the number of weekly calls to a cessation quitline and the number of weekly registrations to a web-based cessation program. Additionally, print secondhand smoke ads and online cessation ads were positively related to weekly quitline calls. Television and radio cessation ads and radio smoke-free law ads were positively related to web program registration levels. There was a positive relation between the number of web registrations and the number of calls to the cessation quitline, with increases in registrations to the web in 1 week corresponding to increases in calls to the quitline in the subsequent week. Web program registration levels were more highly influenced by earned media and other external events than were quitline call volumes.</p> <p>Conclusion</p> <p>Overall, broadcast advertising had a greater impact on registrations for the web program than calls to the quitline. Furthermore, registrations for the web program influenced calls to the quitline. These two findings suggest the evolving roles of web-based cessation programs and Internet-use practices should be considered when creating cessation programs and media campaigns to promote them. Additionally, because different types of media and campaigns were positively associated with calls to the quitline and web registrations, developing mass media campaigns that offer a variety of messages and communicate through different types of media to motivate tobacco users to seek services appears important to reach tobacco users. Further research is needed to better understand the complexities and opportunities involved in simultaneous promotion of quitline and web-based cessation services.</p
Bookselling online: an examination of consumer behaviour patterns.
- Author
- A Atalay
- A Citrin
- A Clements
- A Coley
- A Laing
- A Rohm
- AP Vrechopoulos
- Audrey Laing
- B Page
- B Soars
- C Anderson
- C Mathwick
- C McMahan
- D Hoffman
- D Horner
- D Miller
- D Teather
- DM Szymanski
- E Brynjolfsson
- E Brynjolfsson
- E Howard
- J Peck
- J Rowley
- JA Chevalier
- Jo Royle
- K Backstrom
- L Bury
- M Adjei
- M Chen
- M Denscombe
- MF Cramphorn
- NF Doherty
- P Kotler
- P McGoldrick
- P Underhill
- Publishers Weekly
- PW Ballantine
- S Burt
- S Jones
- S Kim
- S Lee
- SM Mudambi
- T Tivnan
- TJ Gaiser
- Y Chen
- Y Shih
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 20/04/2013
- Field of study
Based upon empirical research, and using a range of methods, this paper examines the behaviour and experiences of consumers in online bookselling settings and offers comparison between online and offline (traditional) bookselling. The research finds that while the convenience of online bookshops is important, the key factors enticing consumers online are a combination of breadth of range, ease of access to obscure titles, as well as personalised recommendations and customer reviews. The research is of value to the book trade, highlighting consumer responses to widely adopted online marketing approaches. The research also contributes to scholarly knowledge in the fields of consumer behaviour, e-marketing and e-commerce in online bookselling, as well as providing findings which can be tested in other online settings, informing future theoretical research
Selective estrogen receptor modulators inhibit growth and progression of premalignant lesions in a mouse model of ductal carcinoma in situ
- Author
- A Howell
- A Rosner
- Alexander D Borowsky
- C Dabrosin
- Carol L MacLeod
- D Medina
- D Medina
- DJ Slamon
- EM Rutanen
- Erik T McGoldrick
- EY Lin
- Gregory T Wurz
- J Cuzick
- JE Maglione
- JE Maglione
- Jeannie E Maglione
- Jeffrey P Gregg
- JM Harvey
- KC Morello
- KV Desai
- Lawrence JT Young
- M Crump
- M Dowsett
- M Kalidas
- MC Gutierrez
- MD Althuis
- Michael W DeGregorio
- P Carthew
- P Nanni
- Q Qu
- R Namba
- RB Buchanan
- RD Cardiff
- Robert D Cardiff
- Ruria Namba
- S Menard
- SC Hewitt
- SK Voipio
- SM Dilworth
- Stephenie Liu
- TL Taras
- TL Taras
- X Yang
- X Zhang
- Publication venue
- BioMed Central
- Publication date
- 01/01/2005
- Field of study
INTRODUCTION: Ductal carcinoma in situ (DCIS) is a noninvasive premalignant lesion and is considered a precursor to invasive carcinoma. DCIS accounts for nearly 20% of newly diagnosed breast cancer, but the lack of experimentally amenable in vivo DCIS models hinders the development of treatment strategies. Here, we demonstrate the utility of a mouse transplantation model of DCIS for chemoprevention studies using selective estrogen receptor modulators (SERMs). This model consists of a set of serially transplanted lines of genetically engineered mouse mammary intraepithelial neoplasia (MIN) outgrowth (MIN-O) tissue that have stable characteristics. We studied the ovarian-hormone-responsiveness of one of the lines with a particular focus on the effects of two related SERMs, tamoxifen and ospemifene. METHODS: The estrogen receptor (ER) status and ovarian-hormone-dependence of the mouse MIN outgrowth tissue were determined by immunohistochemistry and ovarian ablation. The effects of tamoxifen and ospemifene on the growth and tumorigenesis of MIN outgrowth were assessed at 3 and 10 weeks after transplantation. The effects on ER status, cell proliferation, and apoptosis were studied with immunohistochemistry. RESULTS: The MIN-O was ER-positive and ovarian ablation resulted in reduced MIN-O growth and tumor development. Likewise, tamoxifen and ospemifene treatments decreased the MIN growth and tumor incidence in comparison with the control (P < 0.01). Both SERMs significantly decreased cell proliferation. Between the two SERM treatment groups, there were no statistically significant differences in MIN-O size, tumor latency, or proliferation rate. In contrast, the ospemifene treatment significantly increased ER levels while tamoxifen significantly decreased them. CONCLUSION: Tamoxifen and ospemifene inhibit the growth of premalignant mammary lesions and the progression to invasive carcinoma in a transplantable mouse model of DCIS. The inhibitory effects of these two SERMs are similar except for their effects on ER modulation. These differences in ER modulation may suggest different mechanisms of action between the two related SERMs and may portend different long-term outcomes. These data demonstrate the value of this model system for preclinical testing of antiestrogen or other therapies designed to prevent or delay the malignant transformation of premalignant mammary lesions in chemoprevention
Molecular analysis of metastasis in a polyomavirus middle T mouse model: the role of osteopontin
- Author
- A Merzak
- AB Tuck
- AB Tuck
- AD Borowsky
- AJ Oates
- Alexander D Borowsky
- Andrea Rosner
- ATW Cheung
- BA Oostra
- Clifford G Tepper
- CP Sodhi
- CT Guy
- CT Guy
- D Sliva
- DM Barnes
- EA Clark
- EI Behrend
- Erik T McGoldrick
- FM Ausubel
- G Zhang
- GP Yang
- H Singhal
- HA Gardner
- J Hutchinson
- J Wang-Rodriguez
- J You
- JA Sharp
- JE Maglione
- Jeffrey P Gregg
- JN Hutchinson
- Juliana Karrim
- K Paigen
- KA Jessen
- Katayoun Alavi Jessen
- KB DeOme
- KV Desai
- L Diatchenko
- Lawrence JT Young
- LJT Young
- LJT Young
- LM Shaw
- LY Bourguignon
- M Nemir
- M Schena
- M Whitman
- MA Webster
- MG Baik
- N Soga
- P Chomczynski
- PM Siegel
- PS Rudland
- R Mazzieri
- R Zohar
- RD Cardiff
- RD Cardiff
- RD Cardiff
- Robert D Cardiff
- Robert J Munn
- SA Courtneidge
- SM Welford
- SR Rittling
- Stephenie Y Liu
- T Maniatis
- V Kansra
- V Urquidi
- WH Baricos
- WJ Muller
- WJ Muller
- Publication venue
- BioMed Central
- Publication date
- 01/01/2004
- Field of study
INTRODUCTION: In order to study metastatic disease, we employed the use of two related polyomavirus middle T transgenic mouse tumor transplant models of mammary carcinoma (termed Met and Db) that display significant differences in metastatic potential. METHODS: Through suppression subtractive hybridization coupled to the microarray, we found osteopontin (OPN) to be a highly expressed gene in the tumors of the metastatic mouse model, and a lowly expressed gene in the tumors of the lowly metastatic mouse model. We further analyzed the role of OPN in this model by examining sense and antisense constructs using in vitro and in vivo methods. RESULTS: With in vivo metastasis assays, the antisense Met cells showed no metastatic tumor formation to the lungs of recipient mice, while wild-type Met cells, with higher levels of OPN, showed significant amounts of metastasis. The Db cells showed a significantly reduced metastasis rate in the in vivo metastasis assay as compared with the Met cells. Db cells with enforced overexpression of OPN showed elevated levels of OPN but did not demonstrate an increase in the rate of metastasis compared with the wild-type Db cells. CONCLUSIONS: We conclude that OPN is an essential regulator of the metastatic phenotype seen in polyomavirus middle T-induced mammary tumors. Yet OPN expression alone is not sufficient to cause metastasis. These data suggest a link between metastasis and phosphatidylinositol-3-kinase-mediated transcriptional upregulation of OPN, but additional phosphatidylinositol-3-kinase-regulated genes may be essential in precipitating the metastasis phenotype in the polyomavirus middle T model
The oyster genome reveals stress adaptation and complexity of shell formation
- Author
- Andrew Mount
- AS Mount
- B Star
- Baoyu Huang
- Binghang Liu
- Bo Wang
- Bo Wen
- C Sauvage
- CA Lemmon
- CE Bender
- Christian E. W. Steinberg
- Chunfang Peng
- D Hedgecock
- DD Mosser
- DEK Ferrier
- Dennis Hedgecock
- Dingding Fan
- DJ McGoldrick
- E Sauvage
- E Sodergren
- EF Lee
- EK Suk
- ET Walters
- F Marin
- Fei Xu
- Fengji Tan
- Fucun Wu
- Guofan Zhang
- Guojie Zhang
- Guoying Miao
- H Li
- Haigang Qi
- Hailong Yang
- Haiyan Wang
- Huanming Yang
- Huayong Que
- JH Waite
- Jiafeng Wang
- Jian Wang
- Jibiao Zhang
- Jie Meng
- Jinpeng Wang
- JO Kitzman
- Jordi Paps
- Juan Li
- Jun Liu
- Jun Wang
- Junyi Wang
- JV Goldstone
- K Caldeira
- K Nagai
- KS Small
- Lan Yang
- Li Chen
- Li Li
- Linlin Zhang
- Longhai Luo
- Lumin Qian
- LW Hillier
- M Barucca
- M Stark
- Maoshan Chen
- Mei Yang
- N Kourtis
- Na Li
- Na Zhang
- Ning Li
- Patrick M. Gaffney
- PC Hanington
- Peixiang Ni
- Peizhou Cheng
- Pengcheng Yang
- Peter W. H. Holland
- PM Gaffney
- PS Galtsoff
- Qiang Wang
- Qihui Zhu
- Qiumei Zheng
- R Bonasio
- R Li
- R Li
- RA Dalloul
- Ronglian Huang
- Ruibang Luo
- S Keller
- S Mathivanan
- S Weiner
- SC Talmage
- Shan Wang
- Shoudu Zhang
- Shu Zhang
- SM Zhang
- T Furuhashi
- Tao Qu
- TM Carland
- Tomislav Domazet-Lošo
- Tong Wang
- TS Chang
- Wei Wang
- Wen Huang
- Wenjing Fu
- WF Ponder
- X Xu
- Xiao Liu
- Xiaodong Fang
- Xiaoqing Sun
- Xiaorui Song
- Xiaotong Wang
- Ximing Guo
- Xuanting Jiang
- Xuedi Du
- Y Han
- Yabing Zhu
- Yan He
- Yao Ming
- Ye Yin
- Yingrui Li
- Yingxiang Li
- Yinlong Xie
- Yishuai Du
- Yong Zhang
- Yuanxin Chen
- Yue Feng
- Yunjie Liu
- Zhe Xu
- Zhicai She
- Zhiqiang Xiong
- Zhiyong Huang
- Zhiyu Peng
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2012
- Field of study
The Pacific oyster Crassostrea gigas belongs to one of the most species-rich but genomically poorly explored phyla, the Mollusca. Here we report the sequencing and assembly of the oyster genome using short reads and a fosmid-pooling strategy, along with transcriptomes of development and stress response and the proteome of the shell. The oyster genome is highly polymorphic and rich in repetitive sequences, with some transposable elements still actively shaping variation. Transcriptome studies reveal an extensive set of genes responding to environmental stress. The expansion of genes coding for heat shock protein 70 and inhibitors of apoptosis is probably central to the oyster's adaptation to sessile life in the highly stressful intertidal zone. Our analyses also show that shell formation in molluscs is more complex than currently understood and involves extensive participation of cells and their exosomes. The oyster genome sequence fills a void in our understanding of the Lophotrochozoa. © 2012 Macmillan Publishers Limited. All rights reserved
Selection and Prioritization of Candidate Drug Targets for Amyotrophic Lateral Sclerosis Through a Meta-Analysis Approach
- Author
- A Gorio
- A Matilla
- A Neymotin
- Antonio Gianmaria Spampinato
- B Liu
- B Schutz
- C Carlesi
- C Casas
- C Janssen
- C Raoul
- C Sunyach
- CF Chan
- CG Saris
- CS Nicolas
- CW Lederer
- D Maglott
- D Offen
- D Singh
- DJ Graber
- DL Wheeler
- DR Marsh
- E Aronica
- E Nagata
- EW Stommel
- F Achilli
- F Albo
- FF Cox
- FL Conforti
- Francesca Luisa Conforti
- G Morello
- G Morello
- G Yu
- Giovanna Morello
- GP Oliveira de
- H Jarvelainen
- H Takuma
- HJ Habisch
- I Niebroj-Dobosz
- J Aebischer
- J Crespo-Barreto
- J Xin
- JD Mitchell
- JH Ward
- JK Ryu
- JM Scorisa
- JR Maximino
- K Tanaka
- K Xu
- L Ferraiuolo
- L Ferraiuolo
- LA Lampson
- LC Kudo
- LJ Martin
- M Brkic
- M De Paola
- M Kiaei
- M Mizuno
- M Paizs
- M Tateno
- M Tortarolo
- MC Dal Canto
- ME Woodbury
- MR Turner
- MR Vargas
- O Goureau
- OA Shemesh
- P Cassina
- P Heneberg
- P McGoldrick
- P Pasinelli
- P Van Damme
- PA McCombe
- PH Gordon
- PJ Shaw
- PL Vieira
- R Arnon
- R Costa
- RM Pascuzzi
- RS Ignarro
- S Cavallaro
- S Cavallaro
- S Cavallaro
- S Cavallaro
- S Kwak
- S Li
- S Millecamps
- S Paratore
- S Perrin
- S Petri
- S Petri
- Sebastiano Cavallaro
- SM Hearst
- T Bordet
- T Kabuta
- T Lenglet
- T Okuda
- Velia D’Agata
- VN Trieu
- VN Trieu
- W Boston-Howes
- W Dong
- W Huang
- Y Kajiwara
- Y Nikolsky
- Y Ohta
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
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
- 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
- Armadans RC
- 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 MEP
- Atkin RJ
- Atkinson M
- Atlay NB
- Augsten K
- Avolio G
- Avramidou R
- 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
- Baldin EM
- Balek P
- Balli F
- Balunas WK
- Balz J
- Banas E
- Bandyopadhyay A
- Banerjee S
- Bannoura AAE
- Barajas CAC
- Barak L
- Barbe WM
- Barberio EL
- Barberis D
- Barbero M
- Barillari T
- Barisits M-S
- Barkeloo J
- Barklow T
- Barlow N
- Barnea R
- Barnes SL
- Barnett BM
- Barnett RM
- Barnovska-Blenessy Z
- Baroncelli A
- Barone G
- Barr AJ
- Barranco Navarro L
- Barreiro Guimaraes da Costa J
- Barreiro F
- Bartoldus R
- Barton AE
- Bartos P
- Basalaev A
- Bassalat A
- Bates RL
- Batista SJ
- Batlamous S
- Batley JR
- Battaglia M
- Bauce M
- Bauer F
- Bauer KT
- Bawa HS
- Beacham JB
- Beau T
- Beauchemin PH
- Bechtle P
- Beck HC
- Beck HP
- Becker K
- Becker M
- Becot C
- Beddall A
- Beddall AJ
- Bednyakov VA
- Bedognetti M
- Bee CP
- Beermann TA
- Begalli M
- Begel M
- Behera A
- Behr JK
- Bell AS
- Bella G
- Bellagamba L
- Bellerive A
- Bellomo M
- Bellos P
- Belotskiy K
- Belyaev NL
- Benary O
- Benchekroun D
- Bender M
- Benekos N
- Benhammou Y
- Benhar Noccioli E
- Benitez J
- Benjamin DP
- Benoit M
- Bensinger JR
- Bentvelsen S
- Beresford L
- Beretta M
- Berge D
- Bergeaas Kuutmann E
- Berger N
- Bergsten LJ
- Beringer J
- Berlendis S
- Berlingen JM
- Bernard NR
- Bernardi G
- Bernius C
- Bernlochner FU
- Berry T
- Berta P
- Bertella C
- Bertoli G
- Bertram IA
- Besjes GJ
- Bessidskaia Bylund O
- Bessner M
- Besson N
- Bethani A
- Bethke S
- Betti A
- Bevan AJ
- Beyer J
- Bianchi RM
- Biebel O
- Biedermann D
- Bielski R
- Bierwagen K
- Biesuz NV
- Biglietti M
- Billoud TRV
- Bindi M
- Bingul A
- Bini C
- Biondi S
- Birman M
- Bisanz T
- Biswal JP
- Bittrich C
- Bjergaard DM
- Black JE
- Black KM
- Blazek T
- Bloch I
- Blocker C
- Blue A
- Blumenschein U
- Blunier D
- Bobbink GJ
- Bobrovnikov VS
- Bocchetta SS
- Bocci A
- Boeriu OEV
- Boerner D
- Bogavac D
- Bogdanchikov AG
- Bohm C
- Boisvert V
- Bokan P
- Bold T
- Boldyrev AS
- Bolz AE
- Bomben M
- Bona M
- Bonilla JS
- Boonekamp M
- Borisov A
- Borissov G
- Bortfeldt J
- Bortoletto D
- Bortolotto V
- Boscherini D
- Bosman M
- Bossio Sola JD
- Bostanabad MG
- Bouaouda K
- Boudreau J
- Bouhova-Thacker EV
- Boumediene D
- Bourdarios C
- Boutle SK
- Boveia A
- Boyd J
- Boye D
- Boyko IR
- Bozson AJ
- Bracinik J
- Brahimi N
- Brandt A
- Brandt G
- Brandt O
- Braren F
- Bratzler U
- Brau B
- Brau JE
- Brendlinger K
- Brennan AJ
- Brenner L
- Brenner R
- Bressler S
- Bret MC
- Brickwedde B
- Briglin DL
- Britton D
- Britzger D
- Brock I
- Brock R
- Brooijmans G
- Brooks T
- Brooks WK
- Brost E
- Broughton JH
- Bruckman de Renstrom PA
- Bruncko D
- Bruni A
- Bruni G
- Bruni LS
- Bruno S
- Brunt BH
- Bruschi M
- Bruscino N
- Bryant P
- Bryngemark L
- Buanes T
- Buat Q
- Buchholz P
- Buckley AG
- Budagov IA
- Buehrer F
- Buescher D
- Buescher V
- Bugge MK
- Bulekov O
- Bullock D
- Burch TJ
- Burdin S
- Burgard CD
- Burger AM
- Burghgrave B
- Burka K
- Burke S
- Burmeister I
- Burr JTP
- Buschmann E
- Bussey P
- Butler JM
- Buttar CM
- Butterworth JM
- Butti P
- Buttinger W
- Buzatu A
- Buzykaev AR
- Cabras G
- Cabrera Urban S
- Caforio D
- Cai H
- Cairo VMM
- Cakir IT
- Cakir O
- Calace N
- Calafiura P
- Calandri A
- Calderini G
- Calfayan P
- Callea G
- Caloba LP
- Calvente Lopez S
- Calvet D
- Calvet S
- Calvet TP
- Calvetti M
- Camarda S
- Camarri P
- Cameron D
- Camincher C
- Campana S
- Campanelli M
- Camplani A
- Campoverde A
- Canale V
- Cantero J
- Cao T
- Cao Y
- Capeans Garrido MDM
- Caprini I
- Caprini M
- Capua M
- Carbone RM
- Cardarelli R
- Cardillo FC
- Carli I
- Carli T
- Carlino G
- Carlson BT
- Carminati L
- Carney RMD
- Caron S
- Carquin E
- Carra S
- Carrillo-Montoya GD
- Casadei D
- Casado MP
- Casha AF
- Casper DW
- Castelijn R
- Castillo Gimenez V
- Castillo FL
- Castillo IS
- Castillo LRF
- Castro NF
- Catinaccio A
- Catmore JR
- Cattai A
- Caudron J
- Cavaliere V
- Cavallaro E
- Cavalli D
- Cavalli-Sforza M
- Cavasinni V
- Celebi E
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- Zhang R
- Zhang R
- Zhang X
- Zhang Y
- Zhang Z
- Zhao P
- Zhao X
- Zhao Y
- 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
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- Abramowicz H
- Abreu H
- Abulaiti Y
- Acharya BS
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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
Properties of jet fragmentation using charged particles measured with the ATLAS detector in pp collisions at root s=13 TeV
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdinov O
- Abeloos B
- Abhayasinghe DK
- Abidi SH
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- Zwalinski L
- Publication venue
- AMER PHYSICAL SOC
- Publication date
- 01/09/2019
- Field of study
This paper presents a measurement of quantities related to the formation of jets from high-energy quarks and gluons (fragmentation). Jets with transverse momentum 100 GeV 500 MeV and |η| < 2.5 are used to probe the detailed structure of the jet. The fragmentation properties of the more forward and the more central of the two leading jets from each event are studied. The data are unfolded to correct for detector resolution and acceptance effects. Comparisons with parton shower Monte Carlo generators indicate that existing models provide a reasonable description of the data across a wide range of phase space, but there are also significant differences. Furthermore, the data are interpreted in the context of quark- and gluon-initiated jets by exploiting the rapidity dependence of the jet flavor fraction. A first measurement of the charged-particle multiplicity using model-independent jet labels (topic modeling) provides a promising alternative to traditional quark and gluon extractions using input from simulation. The simulations provide a reasonable description of the quark-like data across the jet
Pt range presented in -this measurement, but the gluon-like data have systematically fewer charged particles than the simulation
- …