457 research outputs found
EQ-5D-3L Derived Population Norms for Health Related Quality of Life in Sri Lanka
- Author
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2014
- Field of study
Background Health Related Quality of Life (HRQoL) is an important outcome measure in health economic evaluation that guides health resource allocations. Population norms for HRQoL are an essential ingredient in health economics and in the evaluation of population health. The aim of this study was to produce EQ-5D-3L-derived population norms for Sri Lanka. Method A population sample (nâ=â 780) was selected from four districts of Sri Lanka. A stratified cluster sampling approach with probability proportionate to size was employed. Twenty six clusters of 30 participants each were selected; each participant completed the EQ-5D-3L in a face-to-face interview. Utility weights for their EQ-5D-3L health states were assigned using the Sri Lankan EQ-5D-3L algorithm. The population norms are reported by age and socio-economic variables. Results The EQ-5D-3L was completed by 736 people, representing a 94% response rate. Sixty per cent of the sample reported being in full health. The percentage of people responding to any problems in the five EQ-5D-3L dimensions increased with age. The mean EQ-5D-3L weight was 0.85 (SD 0.008; 95%CI 0.84-0.87). The mean EQ-5D-3L weight was significantly associated with age, housing type, disease experience and religiosity. People above 70 years of age were 7.5 times more likely to report mobility problems and 3.7 times more likely to report pain/discomfort than those aged 18-29 years. Those with a tertiary education were five times less likely to report any HRQoL problems than those without a tertiary education. A person living in a shanty was 4.3 more likely to have problems in usual activities than a person living in a single house. Conclusion The population norms in Sri Lanka vary with socio-demographic characteristics. The socioeconomically disadvantaged have a lower HRQoL. The trends of population norms observed in this lower middle income country were generally similar to those previously reported in high income countries
Omacetaxine may have a role in chronic myeloid leukaemia eradication through downregulation of Mcl-1 and induction of apoptosis in stem/progenitor cells
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2011
- Field of study
Chronic myeloid leukaemia (CML) is maintained by a rare population of tyrosine kinase inhibitor (TKI)-insensitive malignant stem cells. Our long-term aim is to find a BcrAbl-independent drug that can be combined with a TKI to improve overall disease response in chronic-phase CML. Omacetaxine mepesuccinate, a first in class cetaxine, has been evaluated by clinical trials in TKI-insensitive/resistant CML. Omacetaxine inhibits synthesis of anti-apoptotic proteins of the Bcl-2 family, including (myeloid cell leukaemia) Mcl-1, leading to cell death. Omacetaxine effectively induced apoptosis in primary CML stem cells (CD34<sup>+</sup>38<sup>lo</sup>) by downregulation of Mcl-1 protein. In contrast to our previous findings with TKIs, omacetaxine did not accumulate undivided cells <i>in vitro</i>. Furthermore, the functionality of surviving stem cells following omacetaxine exposure was significantly reduced in a dose-dependant manner, as determined by colony forming cell and the more stringent long-term culture initiating cell colony assays. This stem cell-directed activity was not limited to CML stem cells as both normal and non-CML CD34<sup>+</sup> cells were sensitive to inhibition. Thus, although omacetaxine is not leukaemia stem cell specific, its ability to induce apoptosis of leukaemic stem cells distinguishes it from TKIs and creates the potential for a curative strategy for persistent disease
Engineering pyruvate decarboxylase-mediated ethanol production in the thermophilic host Geobacillus thermoglucosidasius
- Author
- A Correa
- A Gupta
- AA Kotze
- AH Thompson
- AJ Shaw
- B Peters
- C Bi
- C Gustafsson
- C Prust
- D Gocke
- D Meyer
- D. A. Cowan
- E Angov
- E Angov
- E Angov
- G Lu
- GL Rosano
- HG Lawford
- J Sambrook
- JF Kane
- JS Tolan
- K Ohta
- K. Eley
- KC Raj
- KC Raj
- L. J. Van Zyl
- LA Talarico
- LA Talarico
- LO Ingram
- M Orencio-Trejo
- M Pohl
- M Pohl
- M. P. Taylor
- M. Tuffin
- MP Taylor
- MP Taylor
- P Siegert
- RE Cripps
- RS Bongers
- RS Gold
- S Feldmann
- S Kim
- S Konig
- S Konig
- S Liu
- S Liu
- S Liu
- SA Underwood
- SA Underwood
- SE Lowe
- SJ Kaczowka
- T Conway
- TA Thanaraj
- TE King
- TF Clarke IV
- UK Laemmli
- Z Vuralhan
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2013
- Field of study
This study reports the expression, purification, and kinetic characterization of a pyruvate decarboxylase (PDC) from Gluconobacter oxydans . Kinetic analyses showed the enzyme to have high affinity for pyruvate (120 ÎŒM at pH 5), high catalytic efficiency (4.75Ă105 Mâ1 sâ1 at pH 5), a pHopt of approximately 4.5 and an in vitro temperature optimum at approximately 55 °C. Due to in vitro thermostablity (approximately 40 % enzyme activity retained after 30 min at 65 °C), this PDC was considered to be a suitable candidate for heterologous expression in the thermophile Geobacillus thermoglucosidasius for ethanol production. Initial studies using a variety of methods failed to detect activity at any growth temperature (45â55 °C). However, the application of codon harmonization (i.e., mimicry of the heterogeneous hostâs transcription and translational rhythm) yielded a protein that was fully functional in the thermophilic strain at 45 °C (as determined by enzyme activity, Western blot, mRNA detection, and ethanol productivity). Here, we describe the first successful expression of PDC in a true thermophile. Yields as high as 0.35±0.04 g/g ethanol per gram of glucose consumed were detected, highly competitive to those reported in ethanologenic thermophilic mutants. Although activities could not be detected at temperatures approaching the growth optimum for the strain, this study highlights the possibility that previously unsuccessful expression of pdcs in Geobacillus spp. may be the result of ineffective transcription/translation coupling.Web of Scienc
Search for the standard model Higgs boson at LEP
- Author
- Abbaneo D
- Abbaneo D
- Abbiendi G
- Abbiendi G
- Abdallah J
- Abreu P
- Achard P
- Adam W
- Adriani O
- Adzic P
- Affholderbach K
- Aguilar-Benitez M
- Ainsley C
- Akesson PF
- Albrecht T
- Alcaraz J
- Alderweireld T
- Alemanni G
- Alemany-Fernandez R
- Alexander G
- Allaby J
- Allison J
- Allmendinger T
- Allport PP
- Aloisio A
- Alviggi MG
- Amaldi U
- Amapane N
- Amaral P
- Amato S
- Anagnostou G
- Anashkin E
- Anderhub H
- Anderson KJ
- Andreazza A
- Andreev VP
- Andringa S
- Anjos N
- Anselmo F
- Antilogus P
- Antonelli A
- Antonelli M
- Apel WD
- Arcelli S
- Arefiev A
- Armstrong SR
- Arnoud Y
- Asai S
- Ask S
- Asman B
- Augustin JE
- Augustinus A
- Awunor O
- Axen D
- Azemoon T
- Aziz T
- Azuelos G
- Azzurri P
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- Bagliesi G
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- Bardin D
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- Baroncelli A
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- Batley RJ
- Battaglia M
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- Becker U
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- Begalli M
- Behner F
- Behnke T
- Behrmann A
- Bell KW
- Bell PJ
- Bella G
- Bellerive A
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- Ben-Haim E
- Bencivenni G
- Benekos N
- Benelli G
- Benvenuti A
- Berat C
- Berbeco R
- Berdugo J
- Berges P
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- Berkelman K
- Berntzon L
- Bertrand D
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- Besancon M
- Besson N
- Betev BL
- Bethke S
- Beuselinck R
- Biasini M
- Biebell O
- Biglietti M
- Biland A
- Binnie DM
- Blair GA
- Blaising JJ
- Bloch D
- Bloch-Devaux B
- Blom M
- Blondel A
- Bloodworth IJ
- Bluj M
- Blumenschein U
- Blyth SC
- Bobbink GJ
- Boccali T
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- Bowcock TJV
- Bowdery CK
- Boyko I
- Braccini S
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- Brandt S
- Branson JG
- Bravo S
- Brenner R
- Brient JC
- Brigliadori L
- Brochu F
- Brodet E
- Brown RM
- Bruckman P
- Bruneliere R
- Brunet JM
- Buchmuller O
- Buesser K
- Bugge L
- Buijs A
- Burckhart HJ
- Burger JD
- Burger WJ
- Buschmann P
- Cai XD
- Callot O
- Calvi M
- Cameron W
- Campana R
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- Camporesi T
- Canale V
- Capell M
- Capon G
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- Carlino G
- Carnegie RK
- Caron B
- Carr J
- Cartacci A
- Carter AA
- Carter JR
- Cartwright S
- Casado MP
- Casaus J
- Castro N
- Cattaneo A
- Cavallari F
- Cavallo F
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- Cavanaugh R
- Cecchi C
- Cerrada M
- Cerutti F
- Chamizo M
- Chang CY
- Chang YH
- Chapkin M
- Charlton DG
- Charpentier P
- Checchia P
- Chemarin M
- Chen A
- Chen G
- Chen GM
- Chen HF
- Chen HS
- Chiarella V
- Chiefari G
- Chierici R
- Chiliapnikov P
- Chmeissani M
- Chudoba J
- Chung SU
- Cieslik K
- Cifarelli L
- Cindolo F
- Ciulli V
- Clare I
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- Clarke DP
- Clerbaux B
- Clifft RW
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- Creanza D
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- Csilling A
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- Curtil C
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- da Silva T
- Da Silva W
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- Dallavalle GM
- Dallison S
- Dalmau J
- David A
- Davier M
- Davies G
- De Angelis A
- de Asmundis R
- De Boer W
- De Bonis I
- De Clercq C
- De Filippis N
- de Guevara PL
- de Jong R
- de la Cruz B
- De Lotto B
- De Maria N
- De Min A
- de Palma M
- de Paula L
- De Roeck A
- De Salvo A
- De Vivie de Regie JB
- De Wolf EA
- Debreczeni J
- Decamp D
- Deglon P
- Degre A
- Deiters K
- Della Ricca G
- della Volpe D
- Delmeire E
- Denes P
- DeNotaristefani F
- Desch K
- Dessagne S
- Dhamotharan S
- Di Ciaccio L
- Di Simone A
- Diemoz M
- Dienes B
- Dierckxsens M
- Dietl H
- Dionisi C
- Dissertori G
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- Drevermann H
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- Duchesneau D
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- Duerdoth IP
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- Edgecock TR
- Eigen G
- Ekelof T
- El Mamouni H
- Elfgren E
- Eline A
- Ellert M
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- Elsing M
- Engler A
- Eppling FJ
- Etzion E
- Ewers A
- Extermann P
- Fabbri F
- Fabbro B
- Falagan MA
- Falciano S
- Falvard A
- Fanourakis G
- Fassouliotis D
- Favara A
- Fay J
- Fayolle D
- Fedin O
- Feindt M
- Felcini M
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- Ferguson DPS
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- Fernandez E
- Fernandez J
- Fernandez-Bosman M
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- Ferrer A
- Ferro F
- Fesefeldt H
- Fiandrini E
- Fiedler F
- Field JH
- Filthaut F
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- Fisher PH
- Fisher W
- Fisk I
- Flagmeyer U
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- Gruenewald MW
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- Sakharov A
- Salicio J
- Salmi L
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- Sander HG
- Sanders MP
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- Sarkar S
- Sarkisyan EKG
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- Schotanus DJ
- Schroder M
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- Schwering G
- Schwick C
- Schwickerath U
- Sciaba A
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- Scott WG
- Seager P
- Sedgbeer JK
- Segar A
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- Shears TG
- Shen BC
- Shepherd-Themistocleous CH
- Sherwood P
- Shevchenko S
- Shivarov N
- Shoutko V
- Shumilov E
- Shvorob A
- Siebel M
- Siedenburg T
- Sieler U
- Silvestris L
- Simopoulou E
- Siroli G
- Sisakian A
- Skuja A
- Smadja G
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- Smith AM
- Smith D
- Smizanska M
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- Spagnolo S
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- Spillantini P
- Stah A
- Stanitzki M
- Stenzel H
- Stephens K
- Steuer M
- Stickland DP
- Stocchi A
- Stoyanov B
- Straessner A
- Strauss J
- Strohmer R
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- Strong JA
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- Sultanov G
- Sun LZ
- Sushkov S
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- Swain JD
- Swynghedauw M
- Szczekowski M
- Szeptycka M
- Szillasi Z
- Szumlak T
- Tabarelli T
- Taffard AC
- Tanaka R
- Tang XW
- Tarem S
- Tarjan P
- Tasevsky M
- Tauscher L
- Taylor G
- Taylor L
- Taylor RJ
- Tegenfeldt F
- Teixeira-Dias P
- Tejessy W
- Tellili B
- Tempesta P
- Tenchini R
- Teuscher R
- Teyssier D
- Thompson AS
- Thompson JC
- Thompson LF
- Thomson MA
- Tilquin A
- Timmermans C
- Timmermans J
- Ting SCC
- Ting SM
- Tittel K
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- Tobin M
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- Tomalin IR
- Tome B
- Tonazzo A
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- Torrence E
- Tortosa P
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- Toya D
- Trabelsi A
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- Trefzger T
- Treille D
- Tricoli A
- Tricomi A
- Trigger I
- Tristram G
- Trochimczuk M
- Trocme B
- Trocsanyi Z
- Troncon C
- Tsur E
- Tuchming B
- Tully C
- Tung KL
- Turluer ML
- Turner-Watson MF
- Tyapkin IA
- Tyapkin P
- Tzamarias S
- Uchida Y
- Ueda I
- Ujvari B
- Ulbricht J
- Uvarov V
- Vachon B
- Valassi A
- Valente E
- Valenti G
- Vallage B
- van Dalen JA
- Van Dam P
- van de Walle RT
- van Dierendonck D
- Van Eldik J
- van Gulik R
- Van Lysebetten A
- van Remortel N
- Van Vulpen I
- Vannerem P
- Vayaki A
- Vegni G
- Veillet JJ
- Veloso F
- Venturi A
- Venus W
- Verbeure F
- Verdier P
- Verdini PG
- Verzi V
- Verzocchi M
- Veszpremi V
- Vesztergombi G
- Vetlitsky I
- Vicinanza D
- Videau H
- Videau I
- Viertel G
- Vilanova D
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- Vitale L
- Vivargent M
- Vlachos S
- Vodopianov I
- Vogel H
- Vogt H
- Vollmer CF
- von Krogh J
- von Wimmersperg-Toeller JH
- Vorobiev I
- Vorobyov AA
- Voss H
- Vossebeld J
- Vrba V
- Waananen A
- Wachsmuth H
- Wadhwa M
- Wahlen H
- Waller D
- Wallraff W
- Wang M
- Wang T
- Wang XL
- Wang ZM
- Ward CP
- Ward DR
- Ward JJ
- Washbrook AJ
- Wasserbacch S
- Watkins PM
- Watson AT
- Watson NK
- Weber M
- Weiser C
- Well PS
- Wengler T
- Wermes N
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- Wetterling D
- White R
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- Wienemann P
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- Wyatt TR
- Wynhoff S
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- Xu R
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- Xue S
- Yamamoto J
- Yamashita S
- Yang BZ
- Yang CG
- Yang HJ
- Yang M
- Yeh SC
- Yuan C
- Yushchenko O
- Zachariadou K
- Zalewska A
- Zalewski P
- Zalite A
- Zalite Y
- Zavrtanik D
- Zeitnitz C
- Zer-Zion D
- Zhang J
- Zhang L
- Zhang ZP
- Zhao J
- Zhao W
- Zhu GY
- Zhu RY
- Zhuang HL
- Zhuravlov V
- Zichichi A
- Ziegler T
- Zilizi G
- Zimin NI
- Zimmermann B
- Zintchenko A
- Zito G
- Zivkovic L
- Zobernig G
- Zoller M
- Zupan M
- Publication venue
- ELSEVIER SCIENCE BV
- Publication date
- 17/07/2003
- Field of study
Psip1/Ledgf p52 Binds Methylated Histone H3K36 and Splicing Factors and Contributes to the Regulation of Alternative Splicing
- Author
- A Dhayalan
- A Engelman
- A Hanamura
- A Hombrouck
- A Vezzoli
- A Yokoyama
- AM Zahler
- AR Kornblihtt
- B Efron
- C Englert
- D Cazalla
- D Cazalla
- DJ Hussey
- DP Singh
- DS Johnson
- E Martinez
- ER Yassin
- FH Grand
- FQ Gunderson
- G Hon
- G Maertens
- GG Wang
- GN Maertens
- Graeme R. Grimes
- H Ge
- H Ge
- H Ge
- Heidi G. Sutherland
- HG Ahuja
- HG Sutherland
- HG Sutherland
- HM Marshall
- I Listerman
- IE Schor
- J Han
- J Konig
- J Toedling
- J Ule
- JC Long
- Jernej Ule
- JF Flanagan
- K Bartholomeeusen
- KJ Wright
- M de la Mata
- M de la Mata
- M Llano
- M Llano
- M Vanegas
- M Vermeulen
- Madapura M. Pradeepa
- MC Shun
- MC Shun
- N Spies
- P Cherepanov
- P Cherepanov
- P Cherepanov
- P Cramer
- P Cramer
- P Dhami
- P Kolasinska-Zwierz
- P Zhang
- R Andersson
- RC Davies
- RF Luco
- RF Luco
- RJ Loomis
- RJ Sims III
- RJ Sims III
- S Briers
- S Huang
- S Kadener
- S Kim
- S Maurer-Stroh
- S Peng
- S Schwartz
- S Stamm
- S Xu
- SF de Almeida
- SH Larsson
- T Misteli
- V Saint-Andre
- VG Tusher
- Wendy A. Bickmore
- Wolf Reik
- Z Wang
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
Increasing evidence suggests that chromatin modifications have important roles in modulating constitutive or alternative splicing. Here we demonstrate that the PWWP domain of the chromatin-associated protein Psip1/Ledgf can specifically recognize tri-methylated H3K36 and that, like this histone modification, the Psip1 short (p52) isoform is enriched at active genes. We show that the p52, but not the long (p75), isoform of Psip1 co-localizes and interacts with Srsf1 and other proteins involved in mRNA processing. The level of H3K36me3 associated Srsf1 is reduced in Psip1 mutant cells and alternative splicing of specific genes is affected. Moreover, we show altered Srsf1 distribution around the alternatively spliced exons of these genes in Psip1 null cells. We propose that Psip1/p52, through its binding to both chromatin and splicing factors, might act to modulate splicing
Targeting pathogen metabolism without collateral damage to the host
- Author
- A Montel-Hagen
- A Seyfang
- AL Rampal
- B Vanhollebeke
- BM Bakker
- BM Bakker
- CY Jung
- D Deng
- D Hanahan
- DD van Niekerk
- E Ruppin
- E Tetaud
- E Urcan
- EJ Kerkhoven
- H Yang
- HG Holzhutter
- I Kola
- I Kola
- IA Lewis
- II Concha
- JR Franco
- JR Haanstra
- JR Haanstra
- L Conde de la Rosa
- M Konig
- M Richter
- M-A Albert
- MJ Waring
- ML Jennings
- MP Barrett
- N Lang-Unnasch
- O Folger
- PC De Jonge
- PJ Mulquiney
- PW Kuchel
- R Eisenthal
- R Schuster
- R van Wijk
- RA Norman
- S Biebinger
- S Fujii
- S Hoops
- T Joet
- V Chelliah
- X Barros-Alvarez
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2017
- Field of study
The development of drugs that can inactivate disease-causing cells (e.g. cancer cells or parasites) without causing collateral damage to healthy or to host cells is complicated by the fact that many proteins are very similar between organisms. Nevertheless, due to subtle, quantitative differences between the biochemical reaction networks of target cell and host, a drug can limit the flux of the same essential process in one organism more than in another. We identified precise criteria for this Ăą âŹnetwork-based' drug selectivity, which can serve as an alternative or additive to structural differences. We combined computational and experimental approaches to compare energy metabolism in the causative agent of sleeping sickness, Trypanosoma brucei, with that of human erythrocytes, and identified glucose transport and glyceraldehyde-3-phosphate dehydrogenase as the most selective antiparasitic targets. Computational predictions were validated experimentally in a novel parasite-erythrocytes co-culture system. Glucose-transport inhibitors killed trypanosomes without killing erythrocytes, neurons or liver cells
Measurement of the inclusive and dijet cross-sections of b-jets in pp collisions at sqrt(s) = 7 TeV with the ATLAS detector
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdelalim AA
- Abdesselam A
- Abdinov O
- Abi B
- Abolins M
- Abramowicz H
- Abreu H
- Acerbi E
- Acharya BS
- Ackers M
- Adams DL
- Addy TN
- Adelman J
- Aderholz M
- Adomeit S
- Adragna P
- Adye T
- Aefsky S
- Aguilar-Saavedra JA
- Aharrouche M
- Ahlen SP
- Ahles F
- Ahmad A
- Ahsan M
- Aielli G
- Akdogan T
- Akesson TPA
- Akimoto G
- Akimov AV
- Alam MA
- Alam MS
- Albrand S
- Aleksa M
- Aleksandrov IN
- Aleppo M
- Alessandria F
- Alexa C
- Alexander G
- Alexandre G
- Alexopoulos T
- Alhroob M
- Aliev M
- Alimonti G
- Alison J
- Aliyev M
- Allport PP
- Allwood-Spiers SE
- Almenar CC
- Almond J
- Aloisio A
- Alon R
- Alonso A
- Alonso J
- Alviggi MG
- Amako K
- Amaral P
- Amelung C
- Ammosov VV
- Amorim A
- Amoros G
- Amram N
- Anastopoulos C
- Andari N
- Andeen T
- Anders CF
- Anderson KJ
- Andreazza A
- Andrei V
- Andrieux M-L
- Anduaga XS
- Angerami A
- Anghinolfi F
- Anh TV
- Anjos N
- Annovi A
- Antonaki A
- Antonelli M
- Antonelli S
- Antos J
- Anulli F
- Aoun S
- Apolle R
- Arabidze G
- Aracena I
- Arai Y
- Arce ATH
- Archambault JP
- Arfaoui S
- Arguin J-F
- Arik E
- Arik M
- Armbruster AJ
- Arms KE
- Armstrong SR
- Arnaez O
- Arnault C
- Artamonov A
- Artoni G
- Arutinov D
- Asai S
- Asfandiyarov R
- Ask S
- Asman B
- Asquith L
- Assamagan K
- Astbury A
- Astvatsatourov A
- Atoian G
- Aubert B
- Auerbach B
- Auge E
- Augsten K
- Aurousseau M
- Austin N
- Avramidou R
- Axen D
- Ay C
- Azuelos G
- Azuma Y
- Baak MA
- Baccaglioni G
- Bacci C
- Bach AM
- Bachacou H
- Bachas K
- Bachy G
- Backes M
- Badescu E
- Bagnaia P
- Bahinipati S
- Bai Y
- Bailey DC
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- Baker OK
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- Bansal V
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- Barashkou A
- Barber T
- Barberio EL
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- Barbero M
- Bardin DY
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- Barklow T
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- Battaglia A
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- Castanheira MTD
- Castillo Gimenez V
- Castillo LRF
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- Cataldi G
- Cataneo F
- Catinaccio A
- Catmore JR
- Cattai A
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- Cerri A
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- Chapleau B
- Chapman JD
- Chapman JW
- Chareyre E
- Charlton DG
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- Cheatham S
- Chekanov S
- Chekulaev SV
- Chelkov GA
- Chen H
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- Chen S
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- Chen X
- Cheng S
- Cheong ALF
- Cheplakov A
- Chepurnov VF
- Cherkaoui El Moursli R
- Chernyatin V
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- Christov A
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- Diblen F
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 31/12/2010
- Field of study
The inclusive and dijet production cross-sections have been measured for jets
containing b-hadrons (b-jets) in proton-proton collisions at a centre-of-mass
energy of sqrt(s) = 7 TeV, using the ATLAS detector at the LHC. The
measurements use data corresponding to an integrated luminosity of 34 pb^-1.
The b-jets are identified using either a lifetime-based method, where secondary
decay vertices of b-hadrons in jets are reconstructed using information from
the tracking detectors, or a muon-based method where the presence of a muon is
used to identify semileptonic decays of b-hadrons inside jets. The inclusive
b-jet cross-section is measured as a function of transverse momentum in the
range 20 < pT < 400 GeV and rapidity in the range |y| < 2.1. The bbbar-dijet
cross-section is measured as a function of the dijet invariant mass in the
range 110 < m_jj < 760 GeV, the azimuthal angle difference between the two jets
and the angular variable chi in two dijet mass regions. The results are
compared with next-to-leading-order QCD predictions. Good agreement is observed
between the measured cross-sections and the predictions obtained using POWHEG +
Pythia. MC@NLO + Herwig shows good agreement with the measured bbbar-dijet
cross-section. However, it does not reproduce the measured inclusive
cross-section well, particularly for central b-jets with large transverse
momenta.Comment: 10 pages plus author list (21 pages total), 8 figures, 1 table, final
version published in European Physical Journal
Search for direct pair production of the top squark in all-hadronic final states in proton-proton collisions at sâ=8 TeV with the ATLAS detector
- Author
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- Zhemchugov A
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- Zurzolo G
- Zutshi V
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2014
- Field of study
The results of a search for direct pair production of the scalar partner to the top quark using an integrated luminosity of 20.1fbâ1 of protonâproton collision data at âs = 8 TeV recorded with the ATLAS detector at the LHC are reported. The top squark is assumed to decay via tËâtÏË01 or tËâ bÏ˱1 âbW(â)ÏË01 , where ÏË01 (Ï˱1 ) denotes the lightest neutralino (chargino) in supersymmetric models. The search targets a fully-hadronic final state in events with four or more jets and large missing transverse momentum. No significant excess over the Standard Model background prediction is observed, and exclusion limits are reported in terms of the top squark and neutralino masses and as a function of the branching fraction of tË â tÏË01 . For a branching fraction of 100%, top squark masses in the range 270â645 GeV are excluded for ÏË01 masses below 30 GeV. For a branching fraction of 50% to either tË â tÏË01 or tË â bÏ˱1 , and assuming the Ï˱1 mass to be twice the ÏË01 mass, top squark masses in the range 250â550 GeV are excluded for ÏË01 masses below 60 GeV
Search for R-parity-violating supersymmetry in events with four or more leptons in sqrt(s) =7 TeV pp collisions with the ATLAS detector
- Author
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- Winkelmann S
- Winklmeier F
- Wittgen M
- Wollstadt SJ
- Wolter MW
- Wolters H
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- Wooden G
- Wosiek BK
- Wotschack J
- Woudstra MJ
- Wozniak KW
- Wraight K
- Wright M
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- Wu SL
- Wu X
- Wu Y
- Wulf E
- Wynne BM
- Xella S
- Xiao M
- Xie S
- Xu C
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- Xu L
- Yabsley B
- Yacoob S
- Yamada M
- Yamaguchi H
- Yamamoto A
- Yamamoto K
- Yamamoto S
- Yamamura T
- Yamanaka T
- Yamazaki T
- Yamazaki Y
- Yan Z
- Yang H
- Yang UK
- Yang Y
- Yang Z
- Yanush S
- Yao L
- Yao Y
- Yasu Y
- Smit GVY
- Ye J
- Ye S
- Yilmaz M
- Yoosoofmiya R
- Yorita K
- Yoshida R
- Yoshihara K
- Young C
- Young CJ
- Youssef S
- Yu D
- Yu DR
- Yu J
- Yu J
- Yuan L
- Yurkewicz A
- Zabinski B
- Zaidan R
- Zaitsev AM
- Zajacova Z
- Zanello L
- Zanzi D
- Zaytsev A
- Zeitnitz C
- Zeman M
- Zemla A
- Zendler C
- Zenin O
- Zenis T
- Zinonos Z
- Zerwas D
- della Porta GZ
- Zhang D
- Zhang H
- Zhang J
- Zhang X
- Zhang Z
- Zhao L
- Zhao Z
- Zhemchugov A
- Zhong J
- Zhou B
- Zhou N
- Zhou Y
- Zhu CG
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhuravlov V
- Zibell A
- Zieminska D
- Zimin NI
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Ziolkowski M
- Zitoun R
- Zivkovic L
- Zmouchko VV
- Zobernig G
- Zoccoli A
- zur Nedden M
- Zutshi V
- Zwalinski L
- Collaboration ATLAS
- Publication venue
- Springer Verlag
- Publication date
- 01/01/2008
- Field of study
A search for new phenomena in final states with four or more leptons (electrons or muons) is presented. The analysis is based on 4.7 fbâ1 of sâ=7TeV proton-proton collisions delivered by the Large Hadron Collider and recorded with the ATLAS detector. Observations are consistent with Standard Model expectations in two signal regions: one that requires moderate values of missing transverse momentum and another that requires large effective mass. The results are interpreted in a simplified model of R-parity-violating supersymmetry in which a 95% CL exclusion region is set for charged wino masses up to 540 GeV. In an R-parity-violating MSUGRA/CMSSM model, values of m 1/2 up to 820 GeV are excluded for 10 < tan ÎČ < 40
- âŠ