262 research outputs found
Sex differences in risk factors for coronary heart disease: a study in a Brazilian population
- Author
- AC Guimarães
- AJ Hsia
- BT Harris
- D Crook
- D Crook
- DL Wingard
- DR Judelson
- DS Freedman
- Eliana C de Faria
- GA Colditz
- Helena CF Oliveira
- Hildete P Pinheiro
- I Lessa
- J Lima Jr
- JK Fetters
- JL Fleiss
- K. Schenck-Gustafsson
- KM Bass
- KV Bloch
- Letícia S Oliveira
- LJ Franco
- ML Brochier
- NK Wenger
- PA Lotufo
- PA Lotufo
- SN Blair
- TL Bush
- Vera S Castanho
- WB Kannel
- WC Willett
- WP Castelli
- Publication venue
- BioMed Central
- Publication date
- 01/04/2001
- Field of study
BACKGROUND: In Brazil coronary heart disease (CHD) constitutes the most important cause of death in both sexes in all the regions of the country and interestingly, the difference between the sexes in the CHD mortality rates is one of the smallest in the world because of high rates among women. Since a question has been raised about whether or how the incidence of several CHD risk factors differs between the sexes in Brazil the prevalence of various risk factors for CHD such as high blood cholesterol, diabetes mellitus, hypertension, obesity, sedentary lifestyle and cigarette smoking was compared between the sexes in a Brazilian population; also the relationships between blood cholesterol and the other risk factors were evaluated. RESULTS: The population presented high frequencies of all the risk factors evaluated. High blood cholesterol (CHOL) and hypertension were more prevalent among women as compared to men. Hypertension, diabetes and smoking showed equal or higher prevalence in women in pre-menopausal ages as compared to men. Obesity and physical inactivity were equally prevalent in both sexes respectively in the postmenopausal age group and at all ages. CHOL was associated with BMI, sex, age, hypertension and physical inactivity. CONCLUSIONS: In this population the high prevalence of the CHD risk factors indicated that there is an urgent need for its control; the higher or equal prevalences of several risk factors in women could in part explain the high rates of mortality from CHD in females as compared to males
Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers.
- Author
- Ausems Margreet GEM
- Bardram Linda
- Benusiglio Patrick R
- Bisseling Tanya M
- Blair Vanessa
- Bleiker Eveline
- Boussioutas Alex
- Caldas Carlos
- Carneiro Fátima
- Cats Annemieke
- Coit Daniel
- DeGregorio Lynn
- Figueiredo Joana
- Fitzgerald Rebecca C
- Ford James M
- Guilford Parry
- Hardwick Richard H
- Heijkoop Esther
- Hermens Rosella
- Hoogerbrugge Nicoline
- Humar Bostjan
- Huntsman David
- Joe Sheena Tjon A
- Kaurah Pardeep
- Keller Gisella
- Lai Jennifer
- Ligtenberg Marjolijn JL
- O'Donovan Maria
- Oliveira Carla
- Pinheiro Hugo
- Ragunath Krish
- Rasenberg Esther
- Richardson Susan
- Roviello Franco
- Schackert Hans
- Schreiber Karen E Chelcun
- Seruca Raquel
- Taylor Amy
- Ter Huurne Anouk
- Tischkowitz Marc
- van der Post Rachel S
- van Dijck Benjamin
- van Grieken Nicole CT
- van Hillegersberg Richard
- van Krieken J Han
- van Sandick Johanna W
- Vehof Rianne
- Vogelaar Ingrid P
- Publication venue
- J Med Genet
- Publication date
- 01/01/2015
- Field of study
Germline CDH1 mutations confer a high lifetime risk of developing diffuse gastric (DGC) and lobular breast cancer (LBC). A multidisciplinary workshop was organised to discuss genetic testing, surgery, surveillance strategies, pathology reporting and the patient's perspective on multiple aspects, including diet post gastrectomy. The updated guidelines include revised CDH1 testing criteria (taking into account first-degree and second-degree relatives): (1) families with two or more patients with gastric cancer at any age, one confirmed DGC; (2) individuals with DGC before the age of 40 and (3) families with diagnoses of both DGC and LBC (one diagnosis before the age of 50). Additionally, CDH1 testing could be considered in patients with bilateral or familial LBC before the age of 50, patients with DGC and cleft lip/palate, and those with precursor lesions for signet ring cell carcinoma. Given the high mortality associated with invasive disease, prophylactic total gastrectomy at a centre of expertise is advised for individuals with pathogenic CDH1 mutations. Breast cancer surveillance with annual breast MRI starting at age 30 for women with a CDH1 mutation is recommended. Standardised endoscopic surveillance in experienced centres is recommended for those opting not to have gastrectomy at the current time, those with CDH1 variants of uncertain significance and those that fulfil hereditary DGC criteria without germline CDH1 mutations. Expert histopathological confirmation of (early) signet ring cell carcinoma is recommended. The impact of gastrectomy and mastectomy should not be underestimated; these can have severe consequences on a psychological, physiological and metabolic level. Nutritional problems should be carefully monitored
Bebida à base de flocos de abóbora com inulina: características prebióticas e aceitabilidade
- Author
- Alda Verônica de Souza Livera
- Ambrósio CLB
- Barry JL
- Boone DR
- Bosscher D
- Cambrodon IG
- Cummings JH
- Dutcosky SD
- Faro ZP
- Franco BDGM
- Freitas DGC
- Fuchs RHB
- Greger JL
- Hauly MCO
- Jacira Antonia Brasil
- Karina Correia da Silveira
- Nonete Barbosa Guerra
- Rao VA
- Reid G
- Rodriguez-Amaya DB
- Rycroft CE
- Salgado SM
- Schlegel HG
- Seo JS
- Silva RML
- Silvana Magalhães Salgado
- Thamer LG
- Thamer LG
- Vanderzant C
- Wiele TV
- Zelyta Pinheiro de Faro
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Evidence for Reductive Genome Evolution and Lateral Acquisition of Virulence Functions in Two Corynebacterium pseudotuberculosis Strains
- Author
- A Alvarez-Ordóñez
- A Barinov
- A Kabus
- A Khamis
- A Khamis
- A Silva
- A Tauch
- Adhemar Zerlotini
- AL Hodgson
- Amjad Ali
- Ana Flávia Costa
- Anderson Dominitini
- Anderson Miyoshi
- Anderson R. Santos
- Andreas Tauch
- André L. Pedrosa
- Anne C. Pinto
- Artur Silva
- Aryanne A. M. C. Rocha
- AS Guimarães
- AS Moomaw
- B Blombach
- B Ewing
- B Saïd-Salim
- BG Hall
- C Song
- C Wittmann
- C Wittmann
- CA Kunkle
- Carlos U. Vieira
- CC Brown
- CE Zhou
- Cláudia T. Guimarães
- CY Soto
- D Aguilar
- D Böltner
- D Rittmann
- DA Rasko
- Daniela C. Bartholomeu
- Daniela M. Resende
- DG Eggleton
- DG Vassylyev
- Diana M. Oliveira
- DK Karaolis
- Débora O. Lopes
- E Pérez
- E Trost
- Elisângela M. Coser
- EM Zdobnov
- Eva Trost
- F Veyrier
- FA Dorella
- FA Dorella
- Fabrício R. Santos
- Fernanda A. Dorella
- Francisco P. Lobo
- G Enkavi
- Glória R. Franco
- Guilherme C. Oliveira
- H Shiotani
- H Yamamoto
- I Smith
- IA Merchant
- Ieso M. Castro
- Igor Mokrousov
- J Arsenault
- J Gonzalo-Asensio
- Jan Baumbach
- Jerônimo C. Ruiz
- Jesus A. Ferro
- JL Ayers
- John McCulloch
- José Miguel Ortega
- Juliana Franco Almeida
- K Lagesen
- K O'Connor
- K Rumbold
- K Rutherford
- KM Connor
- L Wooldridge
- L Zhang
- Louise T. Cerdeira
- Luciana M. Oliveira
- Luciano V. Paiva
- Luis G. C. Pacheco
- Luiz R. Goulart
- M Casalino
- M Krauthammer
- Marcília P. Costa
- Maria Inês T. Ferro
- Maria Paula C. Schneider
- MD Piontkowski
- Meritxell Z. Turk
- MG Ribeiro
- MS Ben Saïd
- MW Paton
- N Seyffert
- Newton P. Carneiro
- Núbia Seyffert
- OF Join-Lambert
- P Kiefer
- P Rice
- P Urbina
- Pablo M. R. O. Moraes
- Paula R. K. Falcão
- PD Karp
- PEJ Carlson
- PJ McNamara
- Priscila Grynberg
- R Caspi
- R Caspi
- R Rübenhagen
- RA Burne
- Robert J. Moore
- Roberto Meyer
- Rommel T. J. Ramos
- RP Huntley
- RR Pinheiro
- S Klaffl
- S Parche
- S Schönert
- S Waack
- Santuza M. R. Teixeira
- SAR Webb
- SD Carson
- SF Altschul
- SG Stoops
- SH Binns
- Sintia S. Almeida
- Siomar C. Soares
- ST Cole
- Sérgio Brommonschenkel
- Sérgio C. Oliveira
- Sílvia Regina Costa Dias
- T May
- T Selby
- T Shimizu
- Thiago L. P. Castro
- TJ Carver
- TM Lowe
- U Dobrindt
- U Dobrindt
- U Hentschel
- V D'Afonseca
- V Merhej
- Vasco Azevedo
- Vinicius A. C. Abreu
- Vívian D'Afonseca
- W Schumann
- Y Nakamura
- Élida Mara Rabelo
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
Ruiz JC, D'Afonseca V, Silva A, et al. Evidence for Reductive Genome Evolution and Lateral Acquisition of Virulence Functions in Two Corynebacterium pseudotuberculosis Strains. PLoS ONE. 2011;6(4): e18551.Background: Corynebacterium pseudotuberculosis, a Gram-positive, facultative intracellular pathogen, is the etiologic agent of the disease known as caseous lymphadenitis (CL). CL mainly affects small ruminants, such as goats and sheep; it also causes infections in humans, though rarely. This species is distributed worldwide, but it has the most serious economic impact in Oceania, Africa and South America. Although C. pseudotuberculosis causes major health and productivity problems for livestock, little is known about the molecular basis of its pathogenicity. Methodology and Findings: We characterized two C. pseudotuberculosis genomes (Cp1002, isolated from goats; and CpC231, isolated from sheep). Analysis of the predicted genomes showed high similarity in genomic architecture, gene content and genetic order. When C. pseudotuberculosis was compared with other Corynebacterium species, it became evident that this pathogenic species has lost numerous genes, resulting in one of the smallest genomes in the genus. Other differences that could be part of the adaptation to pathogenicity include a lower GC content, of about 52%, and a reduced gene repertoire. The C. pseudotuberculosis genome also includes seven putative pathogenicity islands, which contain several classical virulence factors, including genes for fimbrial subunits, adhesion factors, iron uptake and secreted toxins. Additionally, all of the virulence factors in the islands have characteristics that indicate horizontal transfer. Conclusions: These particular genome characteristics of C. pseudotuberculosis, as well as its acquired virulence factors in pathogenicity islands, provide evidence of its lifestyle and of the pathogenicity pathways used by this pathogen in the infection process. All genomes cited in this study are available in the NCBI Genbank database (http://www.ncbi.nlm.nih.gov/genbank/) under accession numbers CP001809 and CP001829
Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease
- Author
- A Abbate
- A Abhyankar
- A Adams
- A Agafina
- A Akyea-Djamson
- A Alan
- A Alfieri
- A Alfrey
- A Alvarisqueta
- A Amos
- A Anadiotis
- A Anneveldt
- A Antolick
- A Arthur
- A Aslam
- Abaci F
- Abdullakutty J
- Abhaichand R
- Abib E Jr
- Aboufakher R
- Abrantes J
- Abreu M
- Abulencia K
- Acampora D
- Acampora M
- Accini Mendoza Jl
- Aceto L
- Acevedo B
- Acevedo L
- Acheatel R
- Actis Mv
- Adams M
- Adjic Nc
- Affaki Gs
- Agarwal Dk
- Aggarwal Rk
- Agosta Gf
- Aguilar M
- Aguilar M
- Ahire N
- Ahmad I
- Ahmed Sh
- Ahn Y
- Aish B
- Aiub F
- Aiub J
- Ajax K
- Ajioka M
- Akai Y
- Akatova E
- Akrap B
- Al Joundi T
- Al-Khalili F
- Albisu J
- Alcalde Jm
- Alcide P
- Alfonso T
- Allen J
- Alllison Dc
- Almaliky T
- Amerena J
- Andersen K
- Andor M
- Angelova I
- Angiolillo D
- Anita S
- Anker Sd
- Antalik L
- Antonicelli R
- Aparicio Cv
- Apel T
- Apostolovic S
- Ara M
- Aragorn L
- Arango Jl
- Araujo Fonseca M
- Ardissino D
- Arenas Leon Jl
- Arevalo S
- Argiolas G
- Arif I
- Armas E
- Aron G
- Arora S
- Asafu-Adjaye N
- Ashcom T
- Ashford M
- Ashino K
- Asim Oktay Ao
- Assarsson E
- Ata B
- Ather N
- Atieh M
- Aull L
- Avalos V
- Avdonina N
- Awasthi Ak
- Axthelm C
- Ayala M
- Ayasse D
- Ayasse M
- Azizad M
- Azize Gm
- B Becker
- Baar M
- Babu R
- Backer T
- Badea C
- Baden M
- Baehl S
- Baek C
- Baeumer A
- Bagi Es
- Bai A
- Bailey K
- Bailey S
- Bair S
- Baker A
- Baker C
- Bakhai A
- Bakker H
- Baksi A
- Baldin Mg
- Bali Hk
- Ballantyne C
- Ballmajo M
- Balode A
- Balukova E
- Bang Sa
- Banker D
- Banker K
- Baquero A
- Barbarash Ol
- Barbato E
- Barbosa E
- Barnett S
- Baron S
- Barreto M
- Barroso A
- Barroso W
- Bartkowiak A
- Bartosh L
- Bartuseviciene S
- Bashir K
- Baszak J
- Bata Ir
- Bayram E
- Beall K
- Beaudry M
- Beauregard La
- Beckett L
- Belejchak P
- Belle Isle J
- Belohlavek J
- Bendelow T
- Bender D
- Benedetti G
- Benjamin S
- Benton J
- Berdoff R
- Berger V
- Bergeron P
- Bergholtz T
- Bergler-Klein J
- Berk M
- Berli Ma
- Bernstein M
- Berra Fc
- Berti S
- Berulfsen A
- Bevilacqua Mt
- Bhadade S
- Bilazarian S
- Bilodeau N
- Binder A
- Binns Y
- Birdane A
- Bisne V
- Bitzer V
- Blagdon M
- Blahey M
- Blankenberg S
- Blazsek Z
- Bloch S
- Blom Kb
- Bluemel J
- Blumberg C
- Blumenthal R
- Bocanera M
- Bodanese L
- Boffetti P
- Bohra P
- Bohula E
- Boivin Mc
- Bolduc H
- Boley K
- Bolognesi Mg
- Bolsmann C
- Boman K
- Bonner J
- Borrayo Na
- Boström På
- Botelho R
- Botta C
- Boudreaux R
- Boulanger K
- Bourgeois S
- Bouvy C
- Bowen L
- Boyarkin M
- Bradley A
- Brady L
- Bramlet D
- Brath H
- Braun P
- Bredlau C
- Brickman T
- Briggs S
- Briké C
- Brodmann M
- Brons S
- Brousalis L
- Brouwer M
- Brown C
- Brown N
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- Buchannan C
- Budaj A
- Budassi N
- Budkova J
- Bugan V
- Buhlman S
- Bulashova O
- Bunschoten P
- Burke W
- Burley T
- Burova N
- Burris H
- Burton C
- Burton J
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- Burtt D
- Busak L
- Busic N
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- Bøen Rh
- C Clavier-Firmin
- C Conradie
- C Contzen
- C Cotes
- C Covert
- C Cuneo
- Caballero-Valiente B
- Cabau Jr
- Calabrese A
- Campanale Eg
- Candusso R
- Cantor W
- CANTOS Trial Group. Krum H
- Capova L
- Carabajal T
- Carr K
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- Cech V
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- Chambers J
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- Chang K
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- Chang Wh
- Charlier F
- Charmarthi B
- Chattin W
- Chauhan D
- Chauhan H
- Chaussé I
- Chavada J
- Chaverra I
- Chaware G
- Chee L
- Chella S
- Chen Cp
- Chen J
- Chen Mh
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- Chhabra A
- Chintala P
- Chiodi L
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- Chouinard G
- Christensen L
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- Cislowski D
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- Crocamo A
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- Cuentas I
- Cuervo A
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- D'Amours Dg
- D Dash
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- D Denham
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- Da Silva A
- Da Silva D Jr
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- Dahlen G
- Dalseg Am
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- Danik J
- Davalos C
- Dave B
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- Dawkins-Hughes S
- Dawood Sy
- Dayer M
- De Boer P
- De Caterina R
- De Jong C
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- Defosse C
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- Delfonso F
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- Dellborg M
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- Dessalvi Cc
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- Dhanak R
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- Diago M
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- Diederich C
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- Dimitrov G
- Diodati J
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- Dodds G
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- Donaubauer T
- Dong X
- Dormidontova G
- Dorogova I
- Dos Santos A
- Dos Santos F
- Dos Santos P
- Doughty A
- Doughty L
- Dovgalevskiy Y
- Dovgolis S
- Dragutksy B
- Dreese M
- Drost I
- Drouin K
- Duchesne L
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- Edillo C
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- Eki Y
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- Espinosa V
- Everett Bm
- F Fedele
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- Facello A
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- Fail P
- Falcon D
- Fang C
- Fang Cy
- Farias E
- Fattal P
- Fawson A
- Feitosa G
- Felario Junior Ga
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- Ferdinand K
- Ferkl R
- Fernandez Aa
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- Ferrario M
- Ferraz R
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- Ferreira-Jardim A
- Fien E
- Filardi Pp
- Filho P
- Fintel D
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- Fitz-Patrick D
- Fitzpatrick L
- Flaksa I
- Flather M
- Flezar M
- Fliesser-Goerzer E
- Flores E
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- Flores Gs
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- Floro T
- Foerster A
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- Fonseca A
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- Frankenstein L
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- Genova D
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- Gervais B
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- Godoy Sanchez M
- Goette A
- Goff R
- Goffinet C
- Gohel P
- Goldberg N
- Gomez Sanchez J
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- Gonzales D
- Gonzales V
- Gonzalez E
- Gordeev I
- Gorges R
- Gospodinov K
- Gotcheva N
- Goudev A
- Gould R
- Govindaraj D
- Goyal B
- Goyal S
- Grabeau R
- Grable M
- Graham J
- Graham Ja
- Graif J
- Gralow J
- Gravellone M
- Gravenhorst-Muenter U
- Green E
- Greener R
- Greenway F
- Grieshaber V
- Griffin S
- Grigaraviciene I
- Grigorova V
- Gros C
- Grosse A
- Grover A
- Grundtvig M
- Gudipati Rvc
- Guerrero A
- Guillinta P
- Gundala Ak
- Gupta A
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- Gupta M
- Gupta V
- Gutmann J
- Guzman I
- Guzman P
- Gwyn M
- Gyorgyova E
- H Haldane
- H Hansen
- H Haught
- H Hill
- Haase F
- Haege R
- Haenel T
- Hage F
- Hageman T
- Hagemann D
- Hagenow A
- Hagiwara Y
- Haidar A
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- Hakas J
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- Hamer Bjb
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- Han B
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- Hanefeld M
- Hangyal T
- Hansson A
- Hanustiakova A
- Hao Y
- Hardas S
- Hardee L
- Harrell W
- Harrington A
- Harris B
- Hartleib M
- Hartwell J
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- Hasbani E
- Hasegawa K
- Hattler B
- Haughton G
- Haynes E
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- Hernandez E
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- Zdrenghea D
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- Zielinski M
- Zieve F
- Zineldine A.
- Zirlik A
- Zucchetti C
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
Background: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. Methods: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1β, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P = 0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P = 0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P = 0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P = 0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P = 0.31). Conclusions: Antiinflammatory therapy targeting the interleukin-1β innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. (Funded by Novartis; CANTOS ClinicalTrials.gov number, NCT01327846.
Combination of searches for heavy spin-1 resonances using 139 fb−1 of proton-proton collision data at s = 13 TeV with the ATLAS detector
- Author
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- Aakvaag E
- Abbott B
- Abeling K
- Abicht NJ
- Abidi SH
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- Aboulhorma A
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- Zhemchugov A
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- Zimine NI
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- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Springer Nature
- Publication date
- 19/04/2024
- Field of study
A combination of searches for new heavy spin-1 resonances decaying into different pairings of W, Z, or Higgs bosons, as well as directly into leptons or quarks, is presented. The data sample used corresponds to 139 fb−1 of proton-proton collisions at
= 13 TeV collected during 2015–2018 with the ATLAS detector at the CERN Large Hadron Collider. Analyses selecting quark pairs (qq, bb,
, and tb) or third-generation leptons (τν and ττ) are included in this kind of combination for the first time. A simplified model predicting a spin-1 heavy vector-boson triplet is used. Cross-section limits are set at the 95% confidence level and are compared with predictions for the benchmark model. These limits are also expressed in terms of constraints on couplings of the heavy vector-boson triplet to quarks, leptons, and the Higgs boson. The complementarity of the various analyses increases the sensitivity to new physics, and the resulting constraints are stronger than those from any individual analysis considered. The data exclude a heavy vector-boson triplet with mass below 5.8 TeV in a weakly coupled scenario, below 4.4 TeV in a strongly coupled scenario, and up to 1.5 TeV in the case of production via vector-boson fusion
Measurement and interpretation of same-sign W boson pair production in association with two jets in pp collisions at s = 13 TeV with the ATLAS detector
- Author
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- Abbott B
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- Abicht NJ
- Abidi SH
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- Zaazoua M
- Zabinski B
- Zaid E
- Zakareishvili T
- Zakharchuk N
- Zambito S
- Zamora Saa JA
- Zang J
- Zanzi D
- Zaplatilek O
- Zeitnitz C
- Zeng H
- Zeng JC
- Zenger DT
- Zenin O
- Zenz S
- Zerradi S
- Zerwas D
- Zhai M
- Zhang B
- Zhang DF
- Zhang J
- Zhang J
- Zhang K
- Zhang L
- Zhang P
- Zhang R
- Zhang S
- Zhang T
- Zhang X
- Zhang X
- Zhang Y
- Zhang Y
- Zhang Z
- Zhang Z
- Zhao H
- Zhao P
- Zhao T
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zheng J
- Zheng K
- Zheng X
- Zheng Z
- Zhong D
- Zhou B
- Zhou H
- Zhou N
- Zhou Y
- Zhu CG
- Zhu J
- Zhu Y
- Zhu Y
- Zhuang X
- Zhukov K
- Zhulanov V
- Zimine NI
- Zinsser J
- Ziolkowski M
- Zoccoli A
- Zoch K
- Zorbas TG
- Zormpa O
- Zou W
- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- Springer Nature
- Publication date
- 01/04/2024
- Field of study
This paper presents the measurement of fducial and diferential cross sections for both the inclusive and electroweak production of a same-sign W-boson pair in association with two jets (W±W±jj) using 139 fb−1 of proton-proton collision data recorded at a centre-of-mass energy of √s = 13 TeV by the ATLAS detector at the Large Hadron Collider. The analysis is performed by selecting two same-charge leptons, electron or muon, and at least two jets with large invariant mass and a large rapidity diference. The measured fducial cross sections for electroweak and inclusive W±W±jj production are 2.92 ± 0.22 (stat.) ± 0.19 (syst.)fb and 3.38±0.22 (stat.)±0.19 (syst.)fb, respectively, in agreement with Standard Model predictions. The measurements are used to constrain anomalous quartic gauge couplings by extracting 95% confdence level intervals on dimension-8 operators. A search for doubly charged Higgs bosons H±± that are produced in vector-boson fusion processes and decay into a same-sign W boson pair is performed. The largest deviation from the Standard Model occurs for an H±± mass near 450 GeV, with a global signifcance of 2.5 standard deviations
Search for pair production of squarks or gluinos decaying via sleptons or weak bosons in final states with two same-sign or three leptons with the ATLAS detector
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- Zhemchugov A
- Zheng K
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- Zheng Z
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- Zhulanov V
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- Ziolkowski M
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- Zwalinski L
- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 15/02/2024
- Field of study
A search for pair production of squarks or gluinos decaying via sleptons or weak bosons is reported. The search targets a final state with exactly two leptons with same-sign electric charge or at least three leptons without any charge requirement. The analysed data set corresponds to an integrated luminosity of 139 fb−1 of proton-proton collisions collected at a centre-of-mass energy of 13 TeV with the ATLAS detector at the LHC. Multiple signal regions are defined, targeting several SUSY simplified models yielding the desired final states. A single control region is used to constrain the normalisation of the WZ + jets background. No significant excess of events over the Standard Model expectation is observed. The results are interpreted in the context of several supersymmetric models featuring R-parity conservation or R-parity violation, yielding exclusion limits surpassing those from previous searches. In models considering gluino (squark) pair production, gluino (squark) masses up to 2.2 (1.7) TeV are excluded at 95% confidence level
Software Performance of the ATLAS Track Reconstruction for LHC Run 3
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- Zhemchugov A
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- Åkesson TPA
- Öncel ÖO
- Ženiš T
- Živković L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 02/04/2024
- Field of study
Charged particle reconstruction in the presence
of many simultaneous proton–proton (pp) collisions in the
LHC is a challenging task for the ATLAS experiment’s reconstruction software due to the combinatorial complexity. This
paper describes the major changes made to adapt the software
to reconstruct high-activity collisions with an average of 50 or
more simultaneous pp interactions per bunch crossing (pileup) promptly using the available computing resources. The
performance of the key components of the track reconstruction chain and its dependence on pile-up are evaluated, and
the improvement achieved compared to the previous software
version is quantified. For events with an average of 60 pp collisions per bunch crossing, the updated track reconstruction
is twice as fast as the previous version, without significant
reduction in reconstruction efficiency and while reducing the
rate of combinatorial fake tracks by more than a factor two
- …