250 research outputs found
Development and Validation of the Chinese Attitudes to Starting Insulin Questionnaire (Ch-ASIQ) for Primary Care Patients with Type 2 Diabetes
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2013
- Field of study
Objectives: To develop and evaluate the psychometric properties of a Chinese questionnaire which assesses the barriers and enablers to commencing insulin in primary care patients with poorly controlled Type 2 diabetes. Research Design and Method: Questionnaire items were identified using literature review. Content validation was performed and items were further refined using an expert panel. Following translation, back translation and cognitive debriefing, the translated Chinese questionnaire was piloted on target patients. Exploratory factor analysis and item-scale correlations were performed to test the construct validity of the subscales and items. Internal reliability was tested by Cronbach's alpha. Results: Twenty-seven identified items underwent content validation, translation and cognitive debriefing. The translated questionnaire was piloted on 303 insulin naĂŻve (never taken insulin) Type 2 diabetes patients recruited from 10 government-funded primary care clinics across Hong Kong. Sufficient variability in the dataset for factor analysis was confirmed by Bartlett's Test of Sphericity (P 0.4 and Eigenvalues >1. Total variance for the 10 factors was 66.22%. Kaiser-Meyer-Olkin measure was 0.725. Cronbach's alpha coefficients for the first four factors were â„0.6 identifying four subscales to which 13 items correlated. Remaining sub-scales and items with poor internal reliability were deleted. The final 13-item instrument had a four scale structure addressing: 'Self-image and stigmatization'; 'Factors promoting self-efficacy; 'Fear of pain or needles'; and 'Time and family support'. Conclusion: The Chinese Attitudes to Starting Insulin Questionnaire (Ch-ASIQ) appears to be a reliable and valid measure for assessing barriers to starting insulin. This short instrument is easy to administer and may be used by healthcare providers and researchers as an assessment tool for Chinese diabetic primary care patients, including the elderly, who are unwilling to start insulin. © 2013 Fu et al.published_or_final_versio
The Correlation of Retinal Nerve Fiber Layer Thickness With Blood Pressure in a Chinese Hypertensive Population
- Publication venue
- 'Ovid Technologies (Wolters Kluwer Health)'
- Publication date
- 01/01/2015
- Field of study
To investigate the association between retinal nerve fiber layer (RNFL) thickness and blood pressure (BP) in subjects with systemic hypertension. Subjects with systemic hypertension on anti-hypertensive medications were screened by fundus photography and referred for glaucoma work-up if there was enlarged vertical cup-to-disc (VCDR) ratio â„0.6, VCDR asymmetry â„0.2, or optic disc hemorrhage. Workup included a complete ophthalmological examination, Humphrey visual field test, and RNFL thickness measurement by optical coherence tomography. The intraocular pressure (IOP) and RNFL thicknesses (global and quadrant) were averaged from both eyes and the means were correlated with: the systolic BP (SBP), diastolic BP (DBP), and mean arterial pressure (MAP) using Pearson correlation. Among 4000 screened hypertensive subjects, 133 were referred for glaucoma workup and 110 completed the workup. Of the 4000 screened subjects, 1.3% had glaucoma (0.9% had normal tension glaucoma [NTG], 0.2% had primary open angle glaucoma, and 0.2% had primary angle closure glaucoma), whereas 0.3% were NTG suspects. The SBP was negatively correlated with the mean superior RNFL thickness (P=0.01). The DBP was negatively correlated with the mean global (P=0.03), superior (P=0.02), and nasal (P=0.003) RNFL thickness. The MAP was negatively correlated with the mean global (P=0.01), superior (P=0.002), and nasal (P=0.004) RNFL thickness while positively correlated with the mean IOP (P=0.02). In medically treated hypertensive subjects, glaucoma was present in 1.3%, with NTG being most prevalent. MAP control may help with IOP lowering and RNFL preservation, although future prospective studies will be needed. Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved.published_or_final_versio
Virtual versus Physical Channel for Sex Networking in Men Having Sex with Men of Sauna Customers in the City of Hong Kong
- Author
- Publication venue
- Public Library of Science
- Publication date
- 10/02/2012
- Field of study
BACKGROUND: Advances in communication technology may affect networking pattern, thereby influencing the dynamics of sex partnership. The aim of the study is to explore the impacts of partner sourcing through internet and related channels on exposure risk to sexually transmitted infections (STI) including HIV. METHODS: Using venue-based sampling, a cross-sectional questionnaire survey was conducted at saunas frequented by men having sex with men (MSM) in Hong Kong. Comparison was made between MSM sourcing partners through physical venues alone versus concomitant users of physical and virtual channels, the latter referring to internet and smart-phone applications, using bivariate logistic regression. RESULTS: Over a 7-week study period, 299 MSM were recruited from 9 saunas. Three main types of sex partners were distinguished: steady (46.8%), regular (26.4%) and casual (96.0%) partners. Users of sauna (n = 78) were compared with concomitant users of saunas and virtual channels (n = 179) for partner sourcing. Sauna-visiting virtual channel users were younger and inclined to use selected physical venues for sourcing partners. Smart-phone users (n = 90) were not different from other internet-users in terms of age, education level and single/mixed self-identified body appearance. Classifying respondents into high risk and low risk MSM by their frequency of condom use, concomitant use of both sauna and virtual channels accounted for a higher proportion in the high risk category (71.6% vs. 58.2%, OR = 1.81, p<0.05). In virtual channel users, partner sourcing through smart-phone was not associated with a higher practice of unprotected sex. CONCLUSION: MSM sauna customers commonly use virtual channels for sex partner sourcing. Unprotected sex is more prevalent in sauna customers who use virtual channel for sex partner sourcing. While the popularity of smart-phone is rising, its use is not associated with increased behavioural risk for HIV/STI transmission
An Integrated Approach for Finding Overlooked Genes in Shigella
- Author
- A Huttenhofer
- A Kumar
- A Matsuyama
- A Sittka
- A Toledo-Arana
- AG Oglesby
- AL Delcher
- AR Gruber
- AV Lukashin
- B Tjaden
- BE Suzek
- C Mathe
- C Pichon
- C Wei
- C Ye
- CL Kingsford
- CP Ponting
- E Rivas
- EC Hobbs
- ER Murphy
- F Yang
- G Padalon-Brauch
- G Padalon-Brauch
- G Storz
- GM Pupo
- GM Pupo
- H He
- H Nie
- HC Tsui
- HF Oliver
- HY Huang
- J Livny
- J Livny
- J Livny
- J Peng
- J Peng
- J Wei
- J Yang
- Jian Yang
- JM Liu
- JM Silvaggi
- JP Kastenmayer
- Junping Peng
- K Ohtani
- KB Arnvig
- KM Wassarman
- L Argaman
- L David
- L Wang
- LS Waters
- M Giangrossi
- ML Bernardini
- MR Hemm
- N Majdalani
- N Perez
- NA Grieshaber
- P Dam
- P Mandin
- P Romby
- Paul J. Planet
- PJ Sansonetti
- PJ Wilderman
- PP Gardner
- Q Jin
- Qi Jin
- R Kumar
- R Sorek
- RJ Carter
- S Chen
- S Saito
- S Washietl
- T Akama
- T Shimizu
- T Song
- V Pfeiffer
- X Wang
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2010
- Field of study
Background: The completion of numerous genome sequences introduced an era of whole-genome study. However, many genes are missed during genome annotation, including small RNAs (sRNAs) and small open reading frames (sORFs). In order to improve genome annotation, we aimed to identify novel sRNAs and sORFs in Shigella, the principal etiologic agents of bacillary dysentery. Methodology/Principal Findings: We identified 64 sRNAs in Shigella, which were experimentally validated in other bacteria based on sequence conservation. We employed computer-based and tiling array-based methods to search for sRNAs, followed by RT-PCR and northern blots, to identify nine sRNAs in Shigella flexneri strain 301 (Sf301) and 256 regions containing possible sRNA genes. We found 29 candidate sORFs using bioinformatic prediction, array hybridization and RT-PCR verification. We experimentally validated 557 (57.9%) DOOR operon predictions in the chromosomes of Sf301 and 46 (76.7%) in virulence plasmid.We found 40 additional co-expressed gene pairs that were not predicted by DOOR. Conclusions/Significance: We provide an updated and comprehensive annotation of the Shigella genome. Our study increased the expected numbers of sORFs and sRNAs, which will impact on future functional genomics and proteomics studies. Our method can be used for large scale reannotation of sRNAs and sORFs in any microbe with a known genom
Analysis of Thyroid Response Element Activity during Retinal Development
- Author
- A Baniahmad
- A Guadaño-Ferraz
- A Rusch
- A Sechman
- AC Bianco
- AJ Cooney
- AJ Hörlein
- AM Zavacki
- AM Zavacki
- B Desvergne
- B Gereben
- B Gereben
- B Morte
- BCG Freitas
- C Ehrhardt
- C Weinberger
- CK Glass
- CL Cheng
- CM Wilson
- CN PessĂŽa
- Constance L. Cepko
- D Forrest
- D Forrest
- DJ Mangelsdorf
- DS Kim
- DS Kim
- E Prost
- EA Nillni
- FR Crantz
- GA Brent
- GA Brent
- H Heuer
- HY Park
- I Jones
- IJ McEwan
- J Bernal
- J Bernal
- J Bernal
- J Mey
- JC Raine
- JC Raine
- JD Chen
- JH Dussault
- JH Oppenheimer
- JM Trimarchi
- JR de Wet
- JT Dunn
- K Umesono
- K Umesono
- KH Tsui
- KJ Petty
- KR Yamamoto
- L Ng
- L Ng
- L Ng
- L Ng
- L Ng
- LA Desouza
- M Beato
- M Dentice
- M Dentice
- M Inoue
- M Prati
- Mark M. Emerson
- MHI Dodd
- Mike Klymkowsky
- ML Applebury
- ML Applebury
- MM Mader
- MR Roberts
- MW Kelley
- N Hitoshi
- N Marsh-Armstrong
- Nathan A. Billings
- P McCaffery
- P Tran
- RJ Koenig
- RM Das
- RM Evans
- SA Kliewer
- SG Sprecher
- SL Bruhn
- SR Hilfer
- T Matsuda
- T Nagaya
- VA Galton
- WE Visser
- WS Simonides
- WT Allison
- XK Zhang
- Y Sakai
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2010
- Field of study
Thyroid hormone (TH) signaling components are expressed during retinal development in dynamic spatial and temporal patterns. To probe the competence of retinal cells to mount a transcriptional response to TH, reporters that included thyroid response elements (TREs) were introduced into developing retinal tissue. The TREs were placed upstream of a minimal TATA-box and two reporter genes, green fluorescent protein (GFP) and human placental alkaline phosphatase (PLAP). Six of the seven tested TREs were first tested in vitro where they were shown to drive TH-dependent expression. However, when introduced into the developing retina, the TREs reported in different cell types in both a TH-dependent and TH-independent manner, as well as revealed specific spatial patterns in their expression. The role of the known thyroid receptors (TR), TRα and TRÎČ, was probed using shRNAs, which were co-electroporated into the retina with the TREs. Some TREs were positively activated by TR+TH in the developing outer nuclear layer (ONL), where photoreceptors reside, as well as in the outer neuroblastic layer (ONBL) where cycling progenitor cells are located. Other TREs were actively repressed by TR+TH in cells of the ONBL. These data demonstrate that non-TRs can activate some TREs in a spatially regulated manner, whereas other TREs respond only to the known TRs, which also read out activity in a spatially regulated manner. The transcriptional response to even simple TREs provides a starting point for understanding the regulation of genes by TH, and highlights the complexity of transcriptional regulation within developing tissue
Trends in template/fragment-free protein structure prediction
- Author
- A BenNaim
- A Cavalli
- A Elofsson
- A Grossfield
- A Jagielska
- A Liwo
- A Liwo
- A Pillardy
- A Warshel
- A Warshel
- A Warshel
- AE Roitberg
- AF Voter
- AP Lyubartsev
- AR Ortiz
- AR Panchenko
- AV Morozov
- B Fain
- B Roux
- B Xue
- B Zagrovic
- BR Brooks
- C Alsenoy Van
- C Bystroff
- C Hardin
- C Hoppe
- C Simmerling
- C Simmerling
- C Zhang
- C Zhang
- C Zhang
- C Zhang
- C Zhang
- CL Brooks
- CM Deane
- CM Summa
- D Chivian
- D Eramian
- D Gilis
- D Hamelberg
- D Jiao
- D Katagiri
- D Kihara
- D Kim
- DE Kim
- DE Shaw
- DS Wishart
- DT Jones
- E Faraggi
- E Faraggi
- E Ferrada
- E Ferrada
- E Haber
- E Krieger
- E Marinari
- E Pettersson
- Eshel Faraggi
- F Wagner
- F Zhao
- F Zhao
- F Zhao
- FG Wang
- G Chopra
- G Cornilescu
- G Pollastri
- G Yona
- GA Kaminski
- GA Papoian
- GM Torrie
- GR Bowman
- H Fan
- H Kamberaj
- H Kamisetty
- H Lu
- H Zhou
- H Zhou
- Hongxing Lei
- HP Gong
- HS Kang
- HX Lei
- HX Lei
- HX Lei
- HX Lei
- HX Lei
- HY Liu
- HY Zhou
- HZ Li
- J Cheng
- J DeBartolo
- J DeBartolo
- J Lundstrom
- J Meiler
- J Moult
- J Pei
- J Shi
- J Skolnick
- J Vreede
- J Wang
- J Xu
- J Zhu
- J Zhu
- JA Hegler
- JA McCammon
- JA McCammon
- JA Vila
- JE Stone
- JF Gibrat
- JL Gao
- JL Knight
- JM Bujnicki
- JM Bujnicki
- JP Ma
- JP Piquemal
- JW Pitera
- K Karplus
- KT Simons
- LA Kelley
- LC Song
- LJ Yang
- LJ Yang
- LJ Yang
- LQ Zheng
- M Ben-David
- M Challacombe
- M Christen
- M Lu
- M Lu
- M Masella
- M Mirzaie
- M Nanias
- M Stork
- M Vieth
- MJ Rooman
- MJ Sippl
- MM Seibert
- MR Betancourt
- MR Lee
- MS Friedrichs
- MS Lin
- MS Shell
- MY Shen
- N Todorova
- N Yu
- N Yu
- NV Buchete
- O Dor
- O Dor
- O Zimmermann
- P Bradley
- P Robustelli
- P Sherwood
- PA Bash
- PD Renfrew
- PD Thomas
- PEM Lopes
- PH Maccallum
- PH Maccallum
- PI Bakker de
- R Kuang
- R Paulini
- R Samudrala
- R Srinivasan
- RW Montalvao
- S Brown
- S Chowdhury
- S Kannan
- S Liu
- S Miyazawa
- S Miyazawa
- S Neal
- S Oldziej
- S Patel
- S Piana
- S Piana
- S Roy
- S Tanaka
- SB Ozkan
- SF Altschul
- SJ Weiner
- T Hamelryck
- T Kortemme
- T Lazaridis
- T Yoshidome
- TC Terwilliger
- TJ Brunette
- U Ryde
- UHE Hansmann
- V Leone
- V Tozzini
- V Tozzini
- V Tsui
- VA Eyrich
- W Blokzijl
- W Boomsma
- W Xie
- W Zhang
- WS Xie
- WW Chen
- X Zhu
- XF Li
- XP Xu
- Y Duan
- Y Duan
- Y Shan
- Y Shen
- Y Shen
- Y Sugita
- Y Zhang
- Y Zhang
- Y Zhou
- Yaoqi Zhou
- YD Yang
- YD Yang
- YD Yang
- YG Mu
- YH Tan
- YH Wu
- Yong Duan
- YQ Gao
- YQ Gao
- Yuedong Yang
- YX Liu
- Z Wang
- ZX Wang
- Publication venue
- Springer-Verlag
- Publication date
- 01/01/2010
- Field of study
Predicting the structure of a protein from its amino acid sequence is a long-standing unsolved problem in computational biology. Its solution would be of both fundamental and practical importance as the gap between the number of known sequences and the number of experimentally solved structures widens rapidly. Currently, the most successful approaches are based on fragment/template reassembly. Lacking progress in template-free structure prediction calls for novel ideas and approaches. This article reviews trends in the development of physical and specific knowledge-based energy functions as well as sampling techniques for fragment-free structure prediction. Recent physical- and knowledge-based studies demonstrated that it is possible to sample and predict highly accurate protein structures without borrowing native fragments from known protein structures. These emerging approaches with fully flexible sampling have the potential to move the field forward
Measurement of the W±Z boson pair-production cross section in pp collisions at âs=13TeV with the ATLAS detector
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Abeloos B
- Aben R
- AbouZeid OS
- Abraham NL
- Abramowicz H
- Abreu H
- Abreu R
- Abulaiti Y
- Acharya BS
- Adamczyk L
- Adams DL
- Adelman J
- Adomeit S
- Adye T
- Affolder AA
- Agatonovic-Jovin T
- Agricola J
- Aguilar-Saavedra JA
- Ahlen SP
- Ahmadov F
- Aielli G
- Akerstedt H
- Akesson TPA
- Akimov AV
- Alberghi GL
- Albert J
- Albrand S
- AlconadaVerzini MJ
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexander G
- Alexopoulos T
- Alhroob M
- Ali B
- Aliev M
- Alimonti G
- Alison J
- Alkire SP
- Allbrooke BMM
- Allen BW
- Allport PP
- Aloisio A
- Alonso A
- Alonso F
- Alpigiani C
- Alstaty M
- Alvarez Piqueras D
- Alviggi MG
- Amadio BT
- Amako K
- Amaral Coutinho Y
- Amelung C
- Amidei D
- Amor Dos Santos SP
- Amorim A
- Amoroso S
- Amundsen G
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
- Anders G
- Anders JK
- Anderson KJ
- Andreazza A
- Andrei V
- Angelidakis S
- Angelozzi I
- Anger P
- Angerami A
- Anghinolfi F
- Anisenkov AV
- Anjos CN
- Annovi A
- Antel C
- Antonelli M
- Antonov A
- Anulli F
- Aoki M
- Arabidze G
- Arai Y
- Araque JP
- Arce ATH
- Arduh FA
- Arguin J-F
- Argyropoulos S
- Arik M
- Armadans RC
- Armbruster AJ
- Armitage LJ
- Arnaez O
- Arnold H
- Arratia M
- Arslan O
- Artamonov A
- Artoni G
- Artz S
- Asai S
- Asbah N
- Ashkenazi A
- Asman B
- Asquith L
- Assamagan K
- Astalos R
- Astigarraga MEP
- Atkinson M
- Atlay NB
- Augsten K
- Avolio G
- Axen B
- Ayoub MK
- Azuelos G
- Baak MA
- Baas AE
- Baca MJ
- Bachacou H
- Bachas K
- Backes M
- Backhaus M
- Bagiacchi P
- Bagnaia P
- Bai Y
- Baines JT
- Baker OK
- Baldin EM
- Balek P
- Balestri T
- Balli F
- Balunas WK
- Banas E
- Banerjee S
- Bannoura AAE
- Barajas CAC
- Barak L
- Barberio EL
- Barberis D
- Barbero M
- Barillari T
- Barisits M-S
- Barklow T
- Barlow N
- Barnes SL
- Barnett BM
- Barnett RM
- Barnovska Z
- Baroncelli A
- Barone G
- Barr AJ
- Barranco Navarro L
- Barreiro F
- Bartoldus R
- Barton AE
- Bartos P
- Basalaev A
- Bassalat A
- Bates RL
- Batista SJ
- Batley JR
- Battaglia M
- Bauce M
- Bauer F
- Baw HS
- Beacham JB
- Beattie MD
- Beau T
- Beauchemin PH
- Bechtle P
- Beck HP
- Becker K
- Becker M
- Beckingham M
- Becot C
- Beddall A
- Beddall AJ
- Bednyakov VA
- Bedognetti M
- Bee CP
- Beemster LJ
- Beermann TA
- Begel M
- Behr JK
- Belanger-Champagne C
- Bell AS
- Bella G
- Bella LA
- Bellagamba L
- Bellerive A
- Bellomo M
- Belotskiy K
- Beltramello O
- Belyaev NL
- Benary O
- Benchekroun D
- Bender M
- Bendtz K
- Benekos N
- Benhammou Y
- Benitez J
- Benjamin DP
- Bensinger JR
- Bentvelsen S
- Beresford L
- Beretta M
- Berge D
- Berger N
- Beringer J
- Berlendis S
- Berlingen JM
- Bernard NR
- Bernius C
- Bernlochner FU
- Berry T
- Berta P
- Bertella C
- Bertoli G
- Bertolucci F
- Bertram IA
- Bertsche C
- Bertsche D
- Besjes GJ
- Bessner M
- Besson N
- Betancourt C
- Bethke S
- Bevan AJ
- Bianchi RM
- Bianchini L
- Bianco M
- Biebel O
- Biedermann D
- Bielski R
- Biesuz NV
- Biglietti M
- Billoud TRV
- Bilokon H
- Bindi M
- Binet S
- Bingul A
- Bini C
- Biondi S
- Bjergaard DM
- Black CW
- Black JE
- Black KM
- Blackburn D
- Blair RE
- Blanchard J-B
- Blanco JE
- Blazek T
- Bloch I
- Blocker C
- Blum W
- Blumenschein U
- Blunier S
- Bobbink GJ
- Bobrovnikov VS
- Bocchetta SS
- Bocci A
- Bock C
- Boehler M
- Boeriu OEV
- Boerner D
- Bogaerts JA
- Bogavac D
- Bogdanchikov AG
- Bohm C
- Boisvert V
- Bokan P
- Bold T
- Boldyrev AS
- Bomben M
- Bona M
- Boonekamp M
- Borisov A
- Borissov G
- Bortfeldt J
- Bortoletto D
- Bortolotto V
- Bos K
- Boscherini D
- Bosman M
- Bossio Sola JD
- Boudreau J
- Bouffard J
- Bouhova-Thacker EV
- Boumediene D
- Bourdarios C
- Boutle SK
- Boveia A
- Boyd J
- Boyko IR
- Bracinik J
- Brandt A
- Brandt G
- Brandt O
- Bratzler U
- Brau B
- Brau JE
- Braun HM
- Bravo AG
- Brendlinger K
- Brennan AJ
- Brenner L
- Brenner R
- Bressler S
- Bret MC
- Bristow TM
- Britton D
- Britzger D
- Brochu FM
- Brock I
- Brock R
- Brooijmans G
- Brooks T
- Brooks WK
- Brosamer J
- Brost E
- Broughton JH
- Bruncko D
- Bruneliere R
- Bruni A
- Bruni G
- Bruni LS
- 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
- Burckhart H
- Burdin S
- Burgard CD
- Burghgrave B
- Burka K
- Burke S
- Burmeister I
- Burr JTP
- Busato E
- Bussey P
- Butler JM
- Buttar CM
- Butterworth JM
- Butti P
- Buttinger W
- Buzatu A
- Buzykaev AR
- Bylund OB
- Cabrera Urban S
- Caforio D
- Cairoa VM
- 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
- Camarda S
- Camarri P
- Cameron D
- Camincher C
- Campana S
- Campanelli M
- Camplani A
- Campoverde A
- Canale V
- Canepa A
- Cantero J
- Cantrill R
- Cao T
- Caprini I
- Caprini M
- Capua M
- Caputo R
- Carbone RM
- Cardarelli R
- Cardillo F
- Carli I
- Carli T
- Carlino G
- Carminati L
- Caron S
- Carquin E
- Carrillo-Montoya GD
- Carter JR
- Carvalho J
- Casadei D
- Casado MP
- Casolino M
- Casper DW
- Castaneda-Miranda E
- Castelijn R
- Castelli A
- Castillo Gimenez V
- 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
- Ceradini F
- Cerda Alberich L
- Cerio BC
- Cerqueira AS
- Cerri A
- Cerrito L
- Cerutti F
- Cerv M
- Cervelli A
- Cetin SA
- Chafaq A
- Chakraborty D
- Chan SK
- Chan YL
- Chang P
- Chapman JD
- Charlton DG
- Chatterjee A
- Chau CC
- Che S
- Cheatham S
- Chegwidden A
- Chekanov S
- Chekulaev SV
- Chelkov GA
- Chelstowska MA
- Chen C
- Chen H
- Chen K
- Chen S
- Chen S
- Chen X
- Chen Y
- Cheng HC
- Cheng HJ
- Cheng Y
- Cheplakov A
- Cheremushkina E
- Chernyatin V
- Cheu E
- Chevalier L
- Chiarella V
- Chiarelli G
- Chiodini G
- Chisholm AS
- Chitan A
- Chizhov MV
- Choi K
- Chomont AR
- Chouridou S
- Chow BKB
- Christodoulou V
- Chromek-Burckhart D
- Chudoba J
- Chuinard AJ
- Chwastowski JJ
- Chytka L
- Ciapetti G
- Ciftci AK
- Cinca D
- Cindro V
- Cioara IA
- Ciocca C
- Ciocio A
- Cirotto F
- Citron ZH
- Citterio M
- Ciubancan M
- Clark A
- Clark BL
- Clark MR
- Clark PJ
- Clarke RN
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- Youssef S
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- Yusuff I
- Zabinski B
- Zaidan R
- Zaitsev AM
- Zakharchuk N
- Zalieckas J
- Zaman A
- Zambito S
- Zanello L
- Zanzi D
- Zeitnitz C
- Zeman M
- Zemla A
- Zeng JC
- Zeng Q
- Zengel K
- Zenin O
- Zenis T
- Zerwas D
- Zhang D
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- Zhang H
- Zhang J
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- Zhang Z
- Zhao X
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zhong J
- Zhou B
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- Zhou M
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- Zhu CG
- Zhu H
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- Zhuang X
- Zhukov K
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann C
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zu Theenhausen HM
- zur Nedden M
- Zwalinski L
- Publication venue
- Netherlands
- Publication date
- 01/01/2016
- Field of study
published_or_final_versio
Search for anomalous couplings in the W tb vertex from the measurement of double differential angular decay rates of single top quarks produced in the t-channel with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Aben R
- Abolins M
- AbouZeid OS
- Abramowicz H
- Abreu H
- Abreu R
- Abulaiti Y
- Acharya BS
- Adamczyk L
- Adams DL
- Adelman J
- Adomeit S
- Adye T
- Affolder AA
- Agatonovic-Jovin T
- Agricola J
- Aguilar-Saavedra JA
- Ahlen SP
- Ahmadov F
- Aielli G
- Akerstedt H
- Akesson TPA
- Akimov AV
- Alberghi GL
- Albert J
- Albrand S
- Alconada Verzini MJ
- Aleksa M
- Aleksandrov IN
- Alexa C
- Alexander G
- Alexopoulos T
- Alhroob M
- Alimonti G
- Alio L
- Alison J
- Alkire SP
- Allbrooke BMM
- Allport PP
- Aloisio A
- Alonso A
- Alonso F
- Alpigiani C
- Altheimer A
- Alvarez Piqueras D
- Alviggi MG
- Amadio BT
- Amako K
- Amaral Coutinho Y
- Amelung C
- Amidei D
- Amor Dos Santos SP
- Amorim A
- Amoroso S
- Amram N
- Amundsen G
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
- Anders CF
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 13/10/2015
- Field of study
The electroweak production and subsequent decay of single top quarks is determined by the properties of the Wtb vertex. This vertex can be described by the complex parameters of an effective Lagrangian. An analysis of angular distributions of the decay products of single top quarks produced in the t -channel constrains these parameters simultaneously. The analysis described in this paper uses 4.6 fbâ1 of proton-proton collision data at âs =7 TeV collected with the ATLAS detector at the LHC. Two parameters are measured simultaneously in this analysis. The fraction f 1 of decays containing transversely polarised W bosons is measured to be 0.37 ± 0.07 (stat.âsyst.). The phase ÎŽ â between amplitudes for transversely and longitudinally polarised W bosons recoiling against left-handed b-quarks is measured to be â0.014Ï Â± 0.036Ï (stat.âsyst.). The correlation in the measurement of these parameters is 0.15. These values result in two-dimensional limits at the 95% confidence level on the ratio of the complex coupling parameters g R and V L, yielding Re[g R /V L] â [â0.36, 0.10] and Im[g R /V L] â [â0.17, 0.23] with a correlation of 0.11. The results are in good agreement with the predictions of the Standard Model
Anatomy of the sign-problem in heavy-dense QCD
- Author
- Adam E Romero
- Aranda C Padilla
- Arjanovic MM
- Armadans R Caminal
- Astigarraga ME Pozo
- Barajas CA Chavez
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- Beck HP
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
QCD at finite densities of heavy quarks is investigated
using the density-of-states method. The phase factor
expectation value of the quark determinant is calculated to
unprecedented precision as a function of the chemical potential.
Results are validated using those from a reweighting
approach where the latter can produce a significant signalto-noise
ratio. We confirm the particleâhole symmetry at low
temperatures, find a strong sign problem at intermediate values
of the chemical potential, and an inverse Silver Blaze
feature for chemical potentials close to the onset value: here,
the phase-quenched theory underestimates the density of the
full theory
Charged-particle distributions at low transverse momentum in âs=13 13 TeV pp interactions measured with the ATLAS detector at the LHC
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
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- Agricola J
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- Aleksandrov IN
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- Zenis T
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- Zhemchugov A
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- Zibell A
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Measurements of distributions of charged particles produced in protonâproton collisions with a centre-of-mass energy of 13 TeV are presented. The data were recorded by the ATLAS detector at the LHC and correspond to an integrated luminosity of 151 ÎŒb â1 ÎŒbâ1 . The particles are required to have a transverse momentum greater than 100 MeV and an absolute pseudorapidity less than 2.5. The charged-particle multiplicity, its dependence on transverse momentum and pseudorapidity and the dependence of the mean transverse momentum on multiplicity are measured in events containing at least two charged particles satisfying the above kinematic criteria. The results are corrected for detector effects and compared to the predictions from several Monte Carlo event generators
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