87 research outputs found
A Research Agenda to Underpin Malaria Eradication
- Author
- A Enayati
- AC Ghani
- AM Dondorp
- B Greenwood
- B. Fenton Hall
- Brian Greenwood
- C Drakeley
- Chetan Chitnis
- Christopher V. Plowe
- CV Plowe
- D Bell
- D de Savigny
- DH Paris
- DL Smith
- FE McKenzie
- Frank Collins
- Fred Binka
- Graham Brown
- H Ranson
- J Nájera
- JA Nájera
- JG Breman
- K Mendis
- Kamini Mendis
- Laurence Slutsker
- M Tanner
- Marcel Tanner
- Mario Henry Rodríguez
- MM Nyunt
- MS Alilio
- Myriam Arevalo-Herrera
- Myron M. Levine
- O Terenius
- Ogobara K. Doumbo
- Pedro L. Alonso
- Robert D. Newman
- Robert Sinden
- SI Hay
- SP Sinkins
- T Bousema
- T Smith
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
Pedro Alonso and colleagues introduce the Malaria Eradication Research Agenda (malERA) initiative and the set of articles published in this PLoS Medicine Supplement that distill the research questions key to malaria eradication
Determination of the Molecular Basis for a Limited Dimorphism, N417K, in the Plasmodium vivax Duffy-Binding Protein
- Author
- A Ranjan
- AM Coley
- Amy M. McHenry
- BT Grimberg
- Christopher L. King
- CL King
- D Hans
- DJ Smith
- DK Kochar
- E Ampudia
- E Tjitra
- Francis B. Ntumngia
- H Choe
- Ivo Mueller
- J Cole-Tobian
- J Healer
- J Xainli
- JC Pizarro
- JH Adams
- JH Adams
- JK Baird
- JL Cole-Tobian
- John H. Adams
- K Arnold
- K Mendis
- KM VanBuskirk
- KM VanBuskirk
- LH Miller
- MJ Betts
- P Michon
- P Michon
- PE Crewther
- Samantha J. Barnes
- SK Singh
- SK Singh
- SP Wertheimer
- T Bai
- T Schwede
- T Tsuboi
- TK Ruebush 2nd
- WG Kho
- Y Nakamura
- Publication venue
- Public Library of Science
- Publication date
- 24/05/2011
- Field of study
Invasion of human red blood cells by Plasmodium merozoites is vital for replication and survival of the parasite and, as such, is an attractive target for therapeutic intervention. Merozoite invasion is mediated by specific interactions between parasite ligands and host erythrocyte receptors. The P. vivax Duffy-binding protein (PvDBP) is heavily dependent on the interaction with the human Duffy blood group antigen/receptor for chemokines (DARC) for invasion. Region II of PvDBP contains many allelic polymorphisms likely to have arisen by host immune selection. Successful vaccine development necessitates a deeper understanding of the role of these polymorphisms in both parasite function and evasion of host immunity. A 3D structure of the homologous P. knowlesi DBP predicts that most variant residues are surface-exposed, including N417K, which is a dimorphic residue change that has previously been shown to be part of a linked haplotype that alters DBP sensitivity to inhibitory antibody. In natural isolates only two residues are found at this site, asparagine (N) and lysine (K). Site-directed mutagenesis of residue 417 was used to create a panel of 20 amino acid variants that were then examined for their binding phenotype and response to immune sera. Our results suggest that the observed dimorphism likely arose due to both structural requirements and immune selection pressure. To our knowledge, this is the first exhaustive examination of this kind of the role of a single amino acid residue in antigenic character and binding ability. Our results demonstrate that a single amino acid substitution can dramatically alter both the ability of the PvDBP to bind to human erythrocytes and its antigenic character
Differential effects of glucagon-like peptide-1 receptor agonists on heart rate
- Author
- A Asmar
- A Asmar
- A Ceriello
- A Gill
- A Jorsal
- A Jorsal
- A Plamboeck
- AA Voors
- AG Bertoni
- Anne Lehmann
- B Darpo
- B Darpo
- B Mendis
- BM Scirica
- C Perret-Guillaume
- C Pyke
- Christine Roy-Duval
- David Owens
- Denis Raccah
- DJ Drucker
- Francesca Lawson
- GS Hillis
- GS Hillis
- H Linnebjerg
- J Can van
- J Skov
- J Tillner
- JA Lovshin
- JJ Meier
- JJ Meier
- JR Ussher
- K Swedberg
- KB Margulies
- KB Margulies
- KC Ferdinand
- KJ Griffioen
- L Blonde
- L Ryden
- Lawrence Blonde
- LE Robinson
- LG Trahair
- M Kim
- M Komajda
- M Lorenz
- MA Nauck
- MA Pfeffer
- Martin Lorenz
- MT Cooney
- P Kumarathurai
- P Sager
- R Simo
- Riccardo Perfetti
- RR Holman
- SE Inzucchi
- SP Marso
- T Vilsboll
- X Zhou
- Y Nakatani
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2017
- Field of study
Abstract
While glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are known to increase heart rate (HR), it is insufficiently recognized that the extent varies greatly between the various agonists and is affected by the assessment methods employed. Here we review published data from 24-h time-averaged HR monitoring in healthy individuals and subjects with type 2 diabetes mellitus (T2DM) treated with either short-acting GLP-1 RAs, lixisenatide or exenatide, or long-acting GLP-1 RAs, exenatide LAR, liraglutide, albiglutide, or dulaglutide (N\ua0=\ua01112; active-treatment arms). HR effects observed in two independent head-to-head trials of lixisenatide and liraglutide (N\ua0=\ua0202; active-treatment arms) are also reviewed. Short-acting GLP-1 RAs, exenatide and lixisenatide, are associated with a transient (1\u201312\ua0h) mean placebo- and baseline-adjusted 24-h HR increase of 1\u20133\ua0beats per minute (bpm). Conversely, long-acting GLP-1 RAs are associated with more pronounced increases in mean 24-h HR; the highest seen with liraglutide and albiglutide at 6\u201310\ua0bpm compared with dulaglutide and exenatide LAR at 3\u20134\ua0bpm. For both liraglutide and dulaglutide, HR increases were recorded during both the day and at night. In two head-to-head comparisons, a small, transient mean increase in HR from baseline was observed with lixisenatide; liraglutide induced a substantially greater increase that remained significantly elevated over 24\ua0h. The underlying mechanism for increased HR remains to be elucidated; however, it could be related to a direct effect at the sinus node and/or stimulation of the sympathetic nervous system, with this effect related to the duration of action of the respective GLP-1 RAs. In conclusion, this review indicates that the effects on HR differ within the class of GLP-1 RAs: short-acting GLP-1 RAs are associated with a modest and transient HR increase before returning to baseline levels, while some long-acting GLP-1 RAs are associated with a more pronounced and sustained increase during the day and night. Findings from recently completed trials indicate that a GLP-1 RA-induced increase in HR, regardless of magnitude, does not present an increased cardiovascular risk for subjects with T2DM, although a pronounced increase in HR may be associated with adverse clinical outcomes in those with advanced heart failure
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The integration of lipid-sensing and anti-inflammatory effects: how the PPARs play a role in metabolic balance
- Author
- A Fredenrich
- A Hirasawa
- A Ledesma
- A Planavila
- A Sahu
- AH Berg
- Alistair VW Nunn
- AM Bodles
- AM Carroll
- AP Russell
- AP Russell
- B Lu
- B Sung
- B Vozarova
- BA Mizock
- BB Duncan
- BE Wisse
- BJ Goldstein
- BJ Morris
- BR Troen
- C Sachot
- CH Lee
- CT De Souza
- D Tripathy
- DM Tham
- DP Pearlstein
- DT Stein
- E Ito
- E Ruiz-Narvaez
- F Balkwill
- F Duska
- FB Hu
- G Boden
- G Boden
- GD Barish
- GE Demas
- H Xiao
- HY Chung
- HY Yoo
- I Inoue
- I Issemann
- IB Sears
- J Aubert
- J Lindstrom
- J Pandhare
- J Youssef
- JA Simon
- JC Corton
- JC Corton
- JC Pickup
- JE Blundell
- Jimmy Bell
- JM Fernandez-Real
- JM Fernandez-Real
- JM Reilly
- JM Ye
- JP Cosgrove
- JV NEEL
- K Tsintzas
- KM Ajuwon
- L Michalik
- L Michalik
- LJ Kelly
- M Diamant
- M Elisaf
- M Jamaluddin
- M Koffler
- M Pignatelli
- M Yamamoto
- M Zackova
- M Zhu
- MB Armstrong
- MC Sugden
- ME Poynter
- MI Phillips
- MM Haluzik
- MP Thompson
- MS Kim
- MW Schwartz
- N Finnberg
- N Houstis
- NA Johnson
- NF Spencer
- NS Chandel
- P Becuwe
- P Cettour-Rose
- P Delerive
- P Dowell
- P Escher
- P Froment
- P Jezek
- P Puigserver
- P Puigserver
- P Puigserver
- P Schrauwen
- PG Sullivan
- Philip Barter
- PQ Bessey
- R Cancello
- R Stienstra
- RB Vega
- S Gremlich
- S Luquet
- S Mendis
- S Narravula
- SA Goldstein
- SA Jebb
- SA Kliewer
- SB Eaton
- SE Nissen
- SP Campos
- SR Stannard
- ST Metel'skii
- T Cramer
- T Kitamura
- U Riserus
- V Laudet
- Y Kamei
- Y Lavrovsky
- Y Rival
- YC Chen
- YG Figueroa
- YJ Jung
- Z Yun
- Publication venue
- BioMed Central
- Publication date
- 01/01/2007
- Field of study
The peroxisomal proliferating-activated receptors (PPARs) are lipid-sensing transcription factors that have a role in embryonic development, but are primarily known for modulating energy metabolism, lipid storage, and transport, as well as inflammation and wound healing. Currently, there is no consensus as to the overall combined function of PPARs and why they evolved. We hypothesize that the PPARs had to evolve to integrate lipid storage and burning with the ability to reduce oxidative stress, as energy storage is essential for survival and resistance to injury/infection, but the latter increases oxidative stress and may reduce median survival (functional longevity). In a sense, PPARs may be an evolutionary solution to something we call the 'hypoxia-lipid' conundrum, where the ability to store and burn fat is essential for survival, but is a 'double-edged sword', as fats are potentially highly toxic. Ways in which PPARs may reduce oxidative stress involve modulation of mitochondrial uncoupling protein (UCP) expression (thus reducing reactive oxygen species, ROS), optimising forkhead box class O factor (FOXO) activity (by improving whole body insulin sensitivity) and suppressing NFkB (at the transcriptional level). In light of this, we therefore postulate that inflammation-induced PPAR downregulation engenders many of the signs and symptoms of the metabolic syndrome, which shares many features with the acute phase response (APR) and is the opposite of the phenotype associated with calorie restriction and high FOXO activity. In genetically susceptible individuals (displaying the naturally mildly insulin resistant 'thrifty genotype'), suboptimal PPAR activity may follow an exaggerated but natural adipose tissue-related inflammatory signal induced by excessive calories and reduced physical activity, which normally couples energy storage with the ability to mount an immune response. This is further worsened when pancreatic decompensation occurs, resulting in gluco-oxidative stress and lipotoxicity, increased inflammatory insulin resistance and oxidative stress. Reactivating PPARs may restore a metabolic balance and help to adapt the phenotype to a modern lifestyle
"I think my body has become addicted to those tablets" Chronic heart failure patients' understanding of and beliefs about their illness and its treatment: a qualitative longitudinal study from Uganda
- Author
- A Damasceno
- A Kleinman
- AK Uskul
- BC Atulomah
- BG Glaser
- Christophe Leroyer
- DA DeWalt
- E Okello
- Elizabeth Namukwaya
- G Oyoo
- G.Y.H. Lip
- H Arksey
- J Breckenridge
- J Saldaña
- JA Astin
- JK Kuule
- JR Tabuti
- Julia Downing
- JW Creswell
- K Charmaz
- K Morgan
- K Sørensen
- K. Klindtworth
- K.N. Kimani
- KN Denzin
- L Selman
- Liz Grant
- LP Sabuni
- M Bury
- M Calnan
- M Crotty
- M Metra
- MH Liu
- Mhoira Leng
- PN Peterson
- R Horne
- R Thomson
- S Dixit
- S Mendis
- Scott A. Murray
- SP Hirani
- V Braun
- VA Thurmond
- W Gareth
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 28/09/2017
- Field of study
Patients with heart failure in Uganda present for health care with advanced structural heart disease, have repeated hospitalizations and poorly controlled disease symptoms. The reasons for these are unclear. Literature from other settings shows that patients' understanding of their illness and their beliefs influence their health related behaviour. The study aimed to explore the beliefs of patients with heart failure, their understanding of their illness and its treatment, and how this influenced their health related behaviour to inform future health education programs, information and palliative care services.Serial qualitative in-depth interviews were conducted with Heart Failure patients who were purposively sampled and recruited in Mulago National Referral Hospital until thematic saturation was reached. In-depth interviews were conducted at three time points over the course of their illness with intervals of 3 months between interviews. A grounded theory approach was used in data analysis. The University of Edinburgh ethics committee, Mulago Hospital Research Ethics committee and the Uganda National Council of Science and Technology (Reference numbers D/GC/178; MREC 33, SS 3083 respectively) approved the research.A total of 40 face to face qualitative longitudinal interviews (36-patient alone, 4 paired-patient and family carer), were conducted with 21 patients. The findings revealed that heart failure patients were unaware of the symptoms of the illness and their definition of illness differed from that of health professionals. Patients understood their diagnosis, cause of illness, prognosis and the importance of the medicines differently from health professionals, and had insufficient information on self-care. Lay beliefs were used to explain many aspects of the illness and treatments. All these influenced where patients sought care and their adherence to treatment, self-care and follow up leading to uncontrolled disease.There is a high level of health illiteracy among heart failure patients in Uganda. Patients rely on lay beliefs to make health decisions and medical information is often miscomprehended. There is an urgent need for health education using culturally appropriate information
Search for the pair production of light top squarks in the e(+/-)mu(-/+) final state in proton-proton collisions at root s=13 TeV
- Author
- Aarrestad TK
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullah WAT Wan
- Abdullin S
- Abdulsalam A
- Abercrombie D
- Abu Zeid S
- Ackert A
- Acosta D
- Acosta G
- Adam W
- Adams MR
- Adams T
- Adzic P
- Afanasiev S
- Agapitos A
- Agaras MN
- Aggleton R
- Agram J-L
- Ahmad A
- Ahmad M
- Ahmad M
- Ahmed I
- Ahuja S
- Akbiyik M
- Akchurin N
- Akgun B
- Al-Bataineh A
- Albajar C
- Albergo S
- Albert A
- Albrow M
- Alcaraz Maestre J
- Aleksandrov A
- Alexakhin V
- Alexander J
- Alhusseini M
- Ali MAB Md
- Alimena J
- Allen B
- Almond J
- Alvarez Fernandez A
- Alvarez JD Ruiz
- Alverson G
- Alves FL
- Alves GA
- Alyari M
- Amapane N
- Ambrogi F
- Amendola C
- Amin N
- Amsler C
- Anagnostou G
- Anampa K Hurtado
- Anderson D
- Andrea J
- Andreev V
- Andreev Yu
- Andrews MB
- Androsov K
- Angioni GL Pinna
- Antonelli L
- Antropov I
- Antunovic Z
- Apanasevich L
- Apollinari G
- Apresyan A
- Apyan A
- Araujo M
- Arcaro D
- Arcidiacono R
- Arenton MW
- Argiro S
- Arndt T
- Arneodo M
- Asavapibhop B
- Asawatangtrakuldee C
- Asghar MI
- Asilar E
- Askew A
- Assran Y
- Atakisi IO
- Atay S
- Ather MW
- Attikis A
- Auffray E
- Aushev T
- Autermann C
- Auzinger G
- Avdeeva E
- Avery P
- Avila C
- Ayala E
- Azarkin M
- Azhgirey I
- Aziz T
- Azzi P
- Azzolini V
- Azzurri P
- Baarmand MM
- Babaev A
- Babounikau I
- Bacchetta N
- Bachiller I
- Bachtis M
- Backhaus M
- Baden A
- Bagliesi G
- Bahinipati S
- Baidali S
- Baillon P
- Bainbridge R
- Bakhshiansohi H
- Ball AH
- Ball F
- Ban Y
- Band R
- Banerjee S
- Banerjee S
- Bani L
- Bansal S
- Barbagli G
- Barberis E
- Bargassa P
- Baringer P
- Barker A
- Barnes VE
- Barney D
- Baron O
- Barone L
- Barrera C Oropeza
- Barria P
- Barrio Luna M
- Bartek R
- Barth C
- Bartok M
- Bartosik N
- Baselga M
- Baskakov A
- Bat A
- Battilana C
- Baty A
- Bauer G
- Bauerdick LAT
- Baur S
- Bayshev I
- Bean A
- Beauceron S
- Beaudette F
- Becerra DA Sanz
- Beck L
- Beernaert K
- Beghin D
- Behera PK
- Behnke O
- Behrens U
- Bein S
- Beirao Da Cruz E Silva C
- Belchior Batista Das Chagas E
- Belforte S
- Bell KW
- Bellan R
- Belloni A
- Belyaev A
- Belyaev A
- Benaglia A
- Benato L
- Bencze G
- Bendavid J
- Benecke A
- Benelli G
- Beni N
- Benussi L
- Benvenuti AC
- Beretvas A
- Bergauer T
- Berger P
- Beri SB
- Bernardes CA
- Bernet C
- Berry D
- Berryhill J
- Bertsche D
- Besancon M
- Beschi A
- Betts RR
- Bhandari R
- Bhardwaj A
- Bhardwaj R
- Bharti M
- Bhat MA
- Bhat PC
- Bhatnagar V
- Bhattacharya R
- Bhattacharya S
- Bhattacharya S
- Bhattacharya S
- Bhawandeep U
- Bheesette S
- Bhopatkar V
- Bhowmik D
- Bhowmik S
- Bi R
- Bialkowska H
- Bian JG
- Bianchini L
- Bianco M
- Bianco S
- Biasini M
- Biino C
- Bilei GM
- Bilin B
- Bilki B
- Bin Anuar AA
- Bitioukov S
- Blanco J Martin
- Blekman F
- Blinov V
- Blobel V
- Bloch D
- Bloch P
- Bloom K
- Bluj M
- Blumenfeld B
- Boccali T
- Bocci A
- Bodek A
- Boimska B
- Boletti A
- Bolla G
- Bonacorsi D
- Bondu O
- Boos E
- Boran F
- Boren S
- Borg J
- Borgonovi L
- Bornheim A
- Borras K
- Borrello L
- Bortignon P
- Bose T
- Botta C
- Botta V
- Boudoul G
- Bouhali O
- Bourilkov D
- Bouvier E
- Bowen J
- Bradmiller-Feld J
- Bragagnolo A
- Braghieri A
- Braibant-Giacomelli S
- Brainerd C
- Brandstetter J
- Brandt S
- Branson JG
- Bravo C
- Breedon R
- Breeze S
- Brew C
- Brianza L
- Brigljevic V
- Brinkerhoff A
- Brivio F
- Brochero Cifuentes JA
- Brochet S
- Brodski M
- Brom J-M
- Brondolin E
- Brooke JJ
- Brown RM
- Brun H
- Bruno G
- Brzhechko D
- Bucci R
- Buccilli A
- Buchanan J
- Buchmuller O
- Bundock A
- Bunin P
- Bunkowski K
- Buontempo S
- Burkett K
- Burns D
- Burns D
- Burt K
- Busson P
- Busza W
- Butler JN
- Butler PH
- Butz E
- Bylinkin A
- Bylsma B
- Byszuk A
- Cabrera A
- Cabrillo IJ
- Cadamuro L
- Caillol C
- Cakir A
- Calabria C
- Calderon A
- Cali IA
- Call K
- Calligaris L
- Caminada L
- Campagnari C
- Campanini R
- Campbell A
- Camporesi T
- Candelise V
- Canelli MF
- Canepa A
- Cankocak K
- Capiluppi P
- Caputo C
- Carlin R
- Carlsmith D
- Carnes A
- Carrillo Montoya CA
- Cartiglia N
- Carvalho W
- Carver M
- Casarsa M
- Casasso S
- Caspart R
- Castaldi R
- Castilla-Valdez H
- Castle J
- Castro A
- Cavallari F
- Cavallo FR
- Cavallo N
- Cavanaugh R
- Ceballos G Gomez
- Cecchi C
- Celik A
- Cenna F
- Cepeda M
- Cerati GB
- Cerci S
- Cerminara G
- Cerrada M
- Chabert EC
- Chang P
- Chang YH
- Chanon N
- Chao Y
- Chaparro Sierra LF
- Chapon E
- Charaf O
- Charlot C
- Chatterjee K
- Chatterjee RM
- Chatterjee S
- Chauhan S
- Chauhan S
- Chaves J
- Chawla R
- Chazin Quero B
- Checchia P
- Chekhovsky V
- Chen G
- Chen GM
- Chen HS
- Chen KF
- Chen M
- Chen PH
- Chen X
- Chen Y
- Chen Y
- Chen Z
- Chenarani S
- Cheng KY
- Cheng T
- Cheng Y
- Cherepanov V
- Chernyavskaya N
- Chertok M
- Cheung HWK
- Chhibra SS
- Chierici R
- Chinellato J
- Chistov R
- Chlebana F
- Cho S
- Choi S
- Choi Y
- Chou JP
- Choudhary BC
- Choudhury S
- Chowdhury S Roy
- Chu J
- Chudasama R
- Chwalek T
- Ciangottini D
- Cieri D
- Ciocca C
- Ciocci MA
- Cipriani M
- Ciriolo V
- Cirkovic P
- Citron M
- Cittolin S
- Ciulli V
- Civinini C
- Claes DR
- Clare R
- Clarida W
- Clement E
- Clerbaux B
- Cockerill DJA
- Cocoros A
- Codispoti G
- Coelho E
- Colafranceschi S
- Colaleo A
- Cole JE
- Colino N
- Collaboration CMS
- Collard C
- Colling D
- Colombo F
- Cometti S
- Connor P
- Contardo D
- Conte E
- Contreras-Campana C
- Conway J
- Conway R
- Cooper SI
- Cooperstein S
- Cornelis T
- Corpe L
- Correia Silva G
- Cossutti F
- Costa M
- Costanza F
- Coubez X
- Couderc F
- Coughlan JA
- Courbon B
- Cousins R
- Covarelli R
- Cox B
- Cox PT
- Creanza D
- Cremonesi M
- Cristella L
- Csanad M
- Cucciati G
- Cuevas J
- Cuffiani M
- Cumalat JP
- Curry D
- Cussans D
- Cutts D
- Czellar S
- D'Alessandro R
- D'Alfonso M
- d'Enterria D
- D'Hondt J
- Da Costa EM
- Da Silveira GG
- Dabrowski A
- Daci N
- Dalchenko M
- Dallavalle GM
- Damarseckin S
- Damgov J
- Damiani D Dominguez
- Danilov M
- Danilov V
- Daponte V
- Das P
- Das S
- Dasgupta A
- Daskalakis G
- Dasu S
- Datta A
- Dauncey P
- David A
- David P
- Davies G
- Davignon O
- de Barbaro P
- De Boer W
- De Bruyn I
- de Cassagnac R Granier
- De Clercq J
- De Cosa A
- de Fatis T Tabarelli
- De Filippis N
- De Guio F
- De Jesus Damiao D
- De La Cruz B
- De La Cruz-Burelo E
- De Lentdecker G
- De Lima R Teixeira
- De Mattia M
- de Monchenault G Hamel
- De Oliveira Martins C
- De Oliveira A Carvalho Antunes
- De Palma M
- De Roeck A
- de Troconiz JF
- De Wit A
- De Wolf EA
- Deelen N
- Defranchis MM
- Deiters K
- Dejardin M
- Del Burgo R
- Del Re D
- Del Valle A Escalante
- Delaere C
- Delannoy AG
- Delannoy H
- Delcourt M
- Delgado Peris A
- Delgado A
- Dell'Orso R
- Della Negra M
- Della Porta G Zevi
- Della Ricca G
- Demaria N
- Demina R
- Demiragli Z
- Demiroglu ZS
- Denegri D
- Depasse P
- Derdzinski M
- Dermenev A
- Deroover K
- Dev N
- Devetak D
- Dewanjee RK
- Dey S
- Dhingra N
- Di Crescenzo A
- Di Croce D
- Di Florio A
- Di Francesco A
- Di Guida S
- Di Maria R
- Di Mattia A
- Diemoz M
- Dierlamm A
- Dildick S
- Dilsiz K
- Dimitrov A
- Dimova T
- Dinardo ME
- Dishaw A
- Dissertori G
- Dittmann J
- Dittmar M
- Dittmer S
- Doan TH
- Dobson M
- Dobur D
- Dodd L
- Dolek F
- Dolen J
- Dominguez A
- Donato S
- Donega M
- Dordevic M
- Dorfer C
- Dorigo T
- Dorney B
- Doroba K
- Dosselli U
- Dozen C
- Dragicevic M
- Dremin I
- Dreyer T
- Duarte Campderros J
- Duarte J
- Dube S
- Dubinin M
- Duchardt D
- Dudenas V
- Dudero PR
- Dudko L
- Dugad S
- Duh YT
- Dulemba JL
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- Publication venue
- Publication date
- 01/01/2019
- Field of study
A search for the production of a pair of top squarks at the LHC is presented. This search targets a region of parameter space where the kinematics of top squark pair production and top quark pair production are very similar, because of the mass difference between the top squark and the neutralino being close to the top quark mass. The search is performed with 35.9 fb(-1) of proton-proton collisions at a centre-of-mass energy of root s = 13 TeV, collected by the CMS detector in 2016, using events containing one electron-muon pair with opposite charge. The search is based on a precise estimate of the top quark pair background, and the use of the M-T2 variable, which combines the transverse mass of each lepton and the missing transverse momentum. No excess of events is found over the standard model predictions. Exclusion limits are placed at 95% confidence level on the production of top squarks up to masses of 208 GeV for models with a mass difference between the top squark and the lightest neutralino close to that of the top quark.Peer reviewe
Measurement of B_{s}^{0} meson production in pp and PbPb collisions at \sqrt{SNN}
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- Xu Q
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- Yang UK
- Yang YC
- Yates BR
- Yazgan E
- Yetkin EA
- Yohay R
- Yoo HD
- Yoo J
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- Yu D
- Yu GB
- Yu I
- Yu SS
- Yuan L
- Yumiceva F
- Yusli MN
- Zabi A
- Zaganidis N
- Zahid S
- Zaleski S
- Zalewski P
- Zanetti A
- Zanetti M
- Zarubin A
- Zarucki M
- Zeinali M
- Zenaiev O
- Zenz SC
- Zeuner WD
- Zeyrek M
- Zghiche A
- Zhang A
- Zhang F
- Zhang H
- Zhang J
- Zhang S
- Zhang Z
- Zhao J
- Zhokin A
- Zhu DH
- Zhu RY
- Zientek M
- Zito G
- Zobec J
- Zoi I
- Zolkapli Z
- Zorbakir IS
- Zorbilmez C
- Zotto P
- Zou D
- Zucchetta A
- Zumerle G
- Zuo X
- Zuolo D
- Publication venue
- 'Elsevier BV'
- Publication date
- 10/09/2019
- Field of study
The production cross sections of B_{s}^{0} mesons and charge conjugates are measured in proton-proton (pp) and PbPb collisions via the exclusive decay channel B_{s}^{0}→J/ψϕ→μ^{+}μ^{−}K^{+}K^{−} at a center-of-mass energy of 5.02 TeV per nucleon pair and within the rapidity range |y|<2.4 using the CMS detector at the LHC. The pp measurement is performed as a function of transverse momentum (p_{T}) of the B_{s}^{0} mesons in the range of 7 to 50 GeV/c and is compared to the predictions of perturbative QCD calculations. The B_{s}^{0} production yield in PbPb collisions is measured in two p_{T} intervals, 7 to 15 and 15 to 50 GeV/c, and compared to the yield in pp collisions in the same kinematic region. The nuclear modification factor (R_{AA}) is found to be 1.5±0.6(stat)±0.5(syst) for 7–15 GeV/c, and 0.87±0.30(stat)±0.17(syst) for 15–50 GeV/c, respectively. Within current uncertainties, the B_{s}^{0} results are consistent with models of strangeness enhancement, and suppression by parton energy loss, as observed for the B+ mesons
Measurement of the tt¯ production cross section, the top quark mass, and the strong coupling constant using dilepton events in pp collisions at √s = 13 TeV
- Author
- Aarrestad TK
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdalla H
- Abdullah WATW
- Abdullin S
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- Zabi A
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- Zientek M
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- Zuolo D
- Publication venue
- 'Springer Fachmedien Wiesbaden GmbH'
- Publication date
- 29/04/2019
- Field of study
A measurement of the top quark–antiquark pair production cross section σtt¯ in proton–proton collisions at a centre-of-mass energy of 13TeV is presented. The data correspond to an integrated luminosity of 35.9fb−1, recorded by the CMS experiment at the CERN LHC in 2016. Dilepton events (e ± μ ∓, μ+μ−, e+e−) are selected and the cross section is measured from a likelihood fit. For a top quark mass parameter in the simulation of mMCt=172.5GeV the fit yields a measured cross section σtt¯=803±2(stat)±25(syst)±20(lumi)pb, in agreement with the expectation from the standard model calculation at next-to-next-to-leading order. A simultaneous fit of the cross section and the top quark mass parameter in the POWHEG simulation is performed. The measured value of mMCt=172.33±0.14(stat)+0.66−0.72(syst)GeV is in good agreement with previous measurements. The resulting cross section is used, together with the theoretical prediction, to determine the top quark mass and to extract a value of the strong coupling constant with different sets of parton distribution functions
Evidence for Top Quark Production in Nucleus-Nucleus Collisions
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- Zorbilmez C
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- Zuo X
- Zuolo D
- Zygala L
- Álvarez Fernández A
- Özçelik Ö
- Publication venue
- Publication date
- 01/01/2019
- Field of study
Peer reviewe
Search for an exotic decay of the Higgs boson to a pair of light pseudoscalars in the final state with two bquarks and two tau leptons in proton-proton collisions at root s=13 TeV The CMS Collaboration
- Author
- Aarrestad TK
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdalla H
- Abdelalim AA
- Abdullah Wan WAT
- Abdullin S
- Abdulsalam A
- Abercrombie D
- Abu Zeid S
- Ackert A
- Acosta D
- Acosta JG
- Adam W
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- Xu Q
- Xu Z
- Yagil A
- Yalvac M
- Yang UK
- Yang YC
- Yates BR
- Yazgan E
- Yetkin EA
- Yohay R
- Yoo HD
- Yoo J
- You C
- Yu D
- Yu GB
- Yu I
- Yu SS
- Yuan L
- Yumiceva F
- Yusli MN
- Zabel J
- Zabi A
- Zaganidis N
- Zahid S
- Zaleski S
- Zalewski P
- Zanetti A
- Zanetti M
- Zarubin A
- Zarucki M
- Zeinali M
- Zenaiev O
- Zenz SC
- Zeuner WD
- Zeyrek M
- Zghiche A
- Zhang A
- Zhang F
- Zhang H
- Zhang J
- Zhang S
- Zhang Z
- Zhao J
- Zhaozhong S
- Zhokin A
- Zhu DH
- Zhu RY
- Zhukov V
- Zientek M
- Zito G
- Zobec J
- Zolkapli Z
- Zorbakir IS
- Zorbilmez C
- Zotto P
- Zou D
- Zucchetta A
- Publication venue
- Publication date
- 01/01/2018
- Field of study
A search for an exotic decay of the Higgs boson to a pair of light pseudoscalar bosons is performed for the first time in the final state with two b quarks and two tau leptons. The search is motivated in the context of models of physics beyond the standard model (SM), such as two Higgs doublet models extended with a complex scalar singlet (2HDM + S), which include the next-to-minimal supersymmetric SM (NMSSM). The results are based on a data set of proton-proton collisions corresponding to an integrated luminosity of 35.9 fb(-1), accumulated by the CMS experiment at the LHC in 2016 at a center-of-mass energy of 13 TeV. Masses of the pseudoscalar boson between 15 and 60 GeVare probed, and no excess of events above the SM expectation is observed. Upper limits between 3 and 12% are set on the branching fraction B(h -> aa -> 2 tau 2b) assuming the SM production of the Higgs boson. Upper limits are also set on the branching fraction of the Higgs boson to two light pseudoscalar bosons in different 2HDM + S scenarios. Assuming the SM production cross section for the Higgs boson, the upper limit on this quantity is as low as 20% for a mass of the pseudoscalar of 40 GeV in the NMSSM. (C) 2018 The Author(s). Published by Elsevier B.V.Peer reviewe
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