1,060 research outputs found
Insecticidal, brine shrimp cytotoxicity, antifungal and nitric oxide free radical scavenging activities of the aerial parts of Myrsine africana L.
- Publication venue
- 'African Journals Online (AJOL)'
- Publication date
- 22/08/2013
- Field of study
The crude methanolic extract and various fractions derived from the aerial parts of Myrsine africana were screened in vitro for possible insecticidal, antifungal, brine shrimp lethality and nitric oxide free radical scavenging activities. Low insecticidal activity (20 %) was shown by chloroform (CHCl3) and aqueous fractions against Tribolium castaneum and Rhizopertha dominica, respectively. Good cytotoxic activity (66.66 %) was shown by the n-hexane fraction of the plant at 1000 μg/ml. The rest of the fractions showed low lethality at higher doses. No antifungal activity was observed for the crude extract and fractions screened against various fungal strains. The plant crude extract and fractions showed a concentration dependent nitric oxide free radical scavenging activity.Key words: Myrsine africana, insecticidal, brine shrimp lethality, antifungal and nitric oxide free radical scavenging assay
Unsupervised Multi-Omic Data Fusion: the Neural Graph Learning Network
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2020
- Field of study
In recent years, due to the high availability of omic data, data-driven biology has greatly expanded. However, the analysis of different data sources is still an open challenge. A few multi-omics approaches have been proposed in the literature, none of which takes into consideration the intrinsic topology of each omic, though. In this work, an unsupervised learning method based on a deep neural network is proposed. Foreach omic, a separate network is trained, whose outputs are fused into a single graph; at this purpose, an innovative loss function has been designed to better represent the data cluster manifolds. The graph adjacency matrix is exploited to determine similarities among samples. With this approach, omics having a different number of features are merged into a unique representation. Quantitative and qualitative analyses show that the proposed method has comparable results to the state of the art. The method has great intrinsic flexibility as it can be customized according to the complexity of the tasks and it has a lot of room for future improvements compared to more fine-tuned methods, opening the way for future research
Study protocol of cost-effectiveness and cost-utility of a biopsychosocial multidisciplinary intervention in the evolution of non-specific sub-acute low back pain in the working population: cluster randomised trial.
- Author
- A Brooks
- A Humbría Mendiola
- A Maetzel
- AK Burton
- Anna Berenguera
- C Bombardier
- C Monton
- CB Terwee
- CL Craig
- Concepció Violan
- CV Asche
- CW Lin
- D Wonderling
- Enriqueta Pujol-Ribera
- F Catala-Lopez
- F Kovacs
- FM Kovacs
- FM Kovacs
- FM Kovacs
- FM Kovacs
- FM Kovacs
- Fundació Kovacs
- Grupo Español de Trabajo del Programa Europeo COST B13
- H Breivik
- H Breivik
- HS Picavet
- I Lindstrom
- Instituto Nacional de Estadistica (INE)
- J Fox-Rushby
- J Lahuerta
- J Lopez-Bastida
- JM Bordas
- L Andronis
- LE Kazis
- LR Ruiz
- M Grotle
- M Krismer
- M Krismer
- M Roland
- MA Chaudhary
- MA Gonzalez Viejo
- MA Koopmanschap
- Marc Casajuana
- Marta Trapero-Bertran
- MF Drummond
- MF Drummond
- MI Meltzer
- MK Campbell
- Nelleke de Kort
- O Airaksinen
- OC Ukoumunne
- P Savigny
- PF Bejarano
- R Melzack
- R Ruiz López
- RN van der
- S Dagenais
- S Dagenais
- S Ramsey
- S Wieser
- SE Lamb
- SJ Linton
- SJ Linton
- T Pincus
- T Rodriguez-Blanco
- T Rodriguez-Blanco
- Teresa Rodriguez-Blanco
- TM van
- WJ Meerding
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2011
- Field of study
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.Background: Low back pain (LBP), with high incidence and prevalence rate, is one of the most common reasons to consult the health system and is responsible for a significant amount of sick leave, leading to high health and social costs. The objective of the study is to assess the cost-effectiveness and cost-utility analysis of a multidisciplinary biopsychosocial educational group intervention (MBEGI) of non-specific sub-acute LBP in comparison with the usual care in the working population recruited in primary healthcare centres. Methods/design:
The study design is a cost-effectiveness and cost-utility analysis of a MBEGI in comparison with the usual care of non-specific sub-acute LBP.Measures on effectiveness and costs of both interventions will be obtained from a cluster randomised controlled clinical trial carried out in 38 Catalan primary health care centres, enrolling 932 patients between 18 and 65 years old with a diagnosis of non-specific sub-acute LBP. Effectiveness measures are: pharmaceutical treatments, work sick leave (% and duration in days), Roland Morris disability, McGill pain intensity, Fear Avoidance Beliefs (FAB) and Golberg Questionnaires. Utility measures will be calculated from the SF-12. The analysis will be performed from a social perspective. The temporal horizon is at 3 months (change to chronic LBP) and 12 months (evaluate the outcomes at long term. Assessment of outcomes will be blinded and will follow the intention-to-treat principle. Discussion: We hope to demonstrate the cost-effectiveness and cost-utility of MBEGI, see an improvement in the patients' quality of life, achieve a reduction in the duration of episodes and the chronicity of non-specific low back pain, and be able to report a decrease in the social costs. If the intervention is cost-effectiveness and cost-utility, it could be applied to Primary Health Care Centres. Trial registration:
ISRCTN: ISRCTN5871969
Status, challenges and pathways to the sustainable use of wild species
- Author
- Publication venue
- Elsevier
- Publication date
- 01/07/2023
- Field of study
DATA AVAILABILITY : Data will be made available on request.The use of wild species is extensive in both high- and low-income countries. At least 50,000 wild species are used by billions of people around the world for food, energy, medicine, material, education or recreation, contributing significantly to efforts to achieve the United Nations Sustainable Development Goals. However, overexploitation remains a major threat to many wild species. Ensuring and enhancing the sustainability of use of wild species is thus essential for human well-being and biodiversity conservation. Globally, the use of wild species is increasing due to growing human demand and efficiency, but its sustainability varies and depends on the social-ecological contexts in which the use occurs. Multiple environmental and social (including economic) drivers affect the sustainability of use of wild species, posing major current and future challenges. In particular, climate change has already increased the vulnerability of many uses and is expected to increase it further in the coming decades, while global and illegal trades are, in many cases, key drivers of unsustainability. There is no single “silver bullet” policy to address these and other major challenges in the sustainable use of wild species. Rather, effective policies need to integrate inclusive actions at multiple scales that adopt right-based approaches, pay attention to equitable distribution of access and costs and benefits, employ participatory processes, strengthen monitoring programs, build robust customary or government institutions and support context-specific policies, as well as adaptive management.http://www.elsevier.com/locate/gloenvchahj2023Plant Production and Soil Scienc
Toxin-Based Therapeutic Approaches
- Author
- Abdul-Ghani
- Abi-Habib
- Abi-Habib
- Abi-Habib
- Abi-Habib
- Abrami
- Abrami
- Abrami
- Adams
- Agrawal
- Alfano
- Alfano
- Alfano
- Altaner
- Amlot
- Amlot
- Anderson
- Andreasen
- Andronicos
- Ariel
- Ariel
- Arora
- Arora
- Ascenzi
- Assaf Shapira
- Aumuller
- Azemar
- Baenziger
- Bagel
- Bagga
- Baluna
- Baluna
- Bantel
- Barbieri
- Barbieri
- Barbieri
- Barbieri
- Barbieri
- Barbieri
- Bass
- Bass
- Beauregard
- Bergamaschi
- Berube
- Blackburn
- Blakey
- Blakey
- Blaustein
- Bolognesi
- Bolognesi
- Bolognesi
- Bosch
- Bourrie
- Bradley
- Brigotti
- Brigotti
- Brigotti
- Brumlik
- Byers
- Byers
- Campana
- Cao
- Cao
- Carroll
- Castillo
- Cathomen
- Cavallaro
- Cavallaro
- Chakraborty
- Chan
- Chaudhary
- Chaudhry
- Chiron
- Cho
- Choe
- Chopra
- Chuang
- Clark
- Clark
- Cola
- Collier
- Collier
- Conry
- Cross
- Cunningham
- Curiel
- da Silva
- Dang
- Dang
- Dass
- Davies
- Dean
- Debinski
- Deeks
- Demirtas
- Deng
- Di Nezza
- Diaw
- Dinges
- Dishart
- Donovan
- Dorer
- Douc-Rasy
- Drum
- Drum
- Duesbery
- Duesbery
- Duffy
- Durrant
- Eagle
- Endo
- Endo
- Engert
- Epstein
- Erbguth
- Erdmann
- Falini
- Falnes
- Falnes
- Falnes
- Fanales-Belasio
- Fathman
- Filpula
- Fingleton
- Finkelstein
- Finkelstein
- Fishwild
- Fogar
- Fong
- Foxwell
- Fracasso
- Fracasso
- Frankel
- Frankel
- Frankel
- Frankel
- Frankel
- Frankel
- Frankel
- Frankel
- Freed
- Frierson
- Froese
- Fryling
- Fuchs
- Fujimoto
- Fulton
- Garland
- Gasperi-Campani
- Geden
- Gelber
- Girbes
- Girbes
- Goldberg
- Gonzalez
- Gordon
- Gould
- Greenfield
- Griffiths
- Grossbard
- Grossbard
- Grossbard
- Gudowius
- Gump
- Harrison
- Harrison
- Harrison
- Hartley
- Haviv
- Hazes
- Heilbronn
- Helmy
- Herceg
- Herrera
- Hertler
- Hertler
- Hertler
- Hessler
- Hibi
- Hine
- Hough
- Houston
- Hsu
- Hu
- Huang
- Hudak
- Hughes
- Hwang
- Iglesias
- Iglewski
- Iglewski
- Ilana
- Itai Benhar
- Itaka
- Jackson
- Jacobs
- Jenkins
- Jirtle
- Johnson
- Kagan
- Kaplan
- Kawashiri
- Kedzierska
- Kelleher
- Kernan
- Kilpatrick
- Klimpel
- Kodaka
- Kondo
- Konjević
- Konopka
- Konvalinka
- Koo
- Koopmann
- Kostrzewa
- Kounnas
- Kouraklis
- Krantz
- Krantz
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kreitman
- Kuan
- Kunitomi
- Kunwar
- Kunwar
- Kunwar
- Kurizaki
- Kuzel
- Laske
- Laske
- Laurent
- Law
- Lee
- Lee
- LeMaistre
- LeMaistre
- LeMaistre
- LeMaistre
- Lemichez
- Leppla
- Leppla
- Li
- Li
- Li
- Li
- Li
- Liang
- Lidor
- Lilja
- Lilja
- Ling
- Liu
- Liu
- Liu
- Liu
- Liu
- Liu
- Logie
- Lombardi
- Lord
- LoRusso
- Lynch
- Mabjeesh
- Magnusson
- Magnusson
- Mahajan
- Makarov
- Mansfield
- Mark
- Martin
- Martin
- Martin
- Mason
- Massuda
- Maxwell
- Maxwell
- Maxwell
- McGinnis
- McKee
- McMahon
- Meacock
- Menestrina
- Messmann
- Mi
- Milne
- Milne
- Milne
- Mischak
- Miyake
- Mizrahi
- Mizrahi
- Moayeri
- Mock
- Mogk
- Mogridge
- Montanaro
- Moolten
- Moolten
- Moolten
- Moran
- Morimoto
- Multani
- Murayama
- Mussai
- Narayanan
- Nettelbeck
- Nicolas
- Nicolas
- Nicolas
- Nicolson
- Nicolson
- Nicolson
- Nie
- Nielsen
- Nilsson
- Ogata
- Ogata
- Ohana
- Ohana
- Olejniczak
- Olsen
- Olsen
- Onda
- Onda
- Onda
- Onda
- Oratz
- Ordonez
- Ozawa
- Pai
- Pai
- Pai
- Pai-Scherf
- Parikh
- Park
- Parney
- Pastan
- Pastan
- Pathak
- Patick
- Pellizzari
- Peng
- Peng
- Peng
- Peng
- Petersen
- Peumans
- Pezzutto
- Picard
- Platanias
- Poe
- Polito
- Posey
- Posey
- Potala
- Pow-Sang
- Powell
- Prince
- Pugliese
- Qin
- Rao
- Rapak
- Ratts
- Ravid
- Rawstron
- Re
- Recht
- Reinbothe
- Riccobono
- Rippmann
- Riviere
- Robbins
- Robbins
- Roberts
- Robson
- Roncuzzi
- Rono
- Roomi
- Rothfels
- Roy
- Rundhaug
- Rundhaug
- Sakamoto
- Sampson
- Sandvig
- Sato
- Sausville
- Schnell
- Schnell
- Schnell
- Schnell
- Scholler
- Schummer
- Scobie
- Sebolt-Leopold
- Selkirk
- Selvaggi
- Sestili
- Sharma
- Shaughnessy
- Shay
- Shen
- Shen
- Showalter
- Sidi
- Siegall
- Siegall
- Sikriwal
- Simmons
- Simpson
- Skilleter
- Skilleter
- Skyler
- Smallshaw
- Smith
- Song
- Spencer
- Spitler
- Spooner
- Spooner
- Stafford
- Stamenkovic
- Steenman
- Stein
- Stirpe
- Stirpe
- Stirpe
- Stirpe
- Stirpe
- Stish
- Stone
- Strand
- Strauchen
- Strauchen
- Strebhardt
- Strickland
- Su
- Suhasini
- Syrovets
- Tamayo
- Tana
- Tanos
- Tcherniuk
- Tedder
- Tepler
- Testa
- Theuer
- Theuer
- Thorburn
- Thorburn
- Tonello
- Tong
- Trown
- Trujillo
- Trujillo
- Truong
- Tsampalas
- Tsuneoka
- Tsutsumi
- Turpeenniemi-Hujanen
- Uchiyama
- Uchiyama
- Uckun
- Uckun
- Ulmer
- Vago
- Van Damme
- Van der Goot
- van Oosterhout
- Varshavsky
- Varshavsky
- Varshavsky
- Varshavsky
- Vitale
- Vitale
- Vitetta
- Vivanco
- von Minckwitz
- Wadhwa
- Waldmann
- Walsh
- Walther
- Wang
- Wang
- Wang
- Wang
- Wayne
- Weaver
- Weber
- Weber
- Weiner
- Wesche
- Wesche
- Wesche
- Westermarck
- Williams
- Williams
- Winau
- Wolf
- Woo
- Wu
- Wu
- Xu
- Yagura
- Yamaizumi
- Yang
- Yin
- Young
- Yu
- Zalcberg
- Zhang
- Zheng
- Publication venue
- MDPI
- Publication date
- 01/10/2010
- Field of study
Protein toxins confer a defense against predation/grazing or a superior pathogenic competence upon the producing organism. Such toxins have been perfected through evolution in poisonous animals/plants and pathogenic bacteria. Over the past five decades, a lot of effort has been invested in studying their mechanism of action, the way they contribute to pathogenicity and in the development of antidotes that neutralize their action. In parallel, many research groups turned to explore the pharmaceutical potential of such toxins when they are used to efficiently impair essential cellular processes and/or damage the integrity of their target cells. The following review summarizes major advances in the field of toxin based therapeutics and offers a comprehensive description of the mode of action of each applied toxin
Search for strongly interacting massive particles generating trackless jets in proton-proton collisions at s = 13 TeV
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abercrombie D
- Acharya H
- Acosta D
- Acosta JG
- Adam W
- Adams E
- Adams MR
- Adams T
- Adloff C
- Adzic P
- Agapitos A
- Agarwal G
- Aggleton R
- Agram J-L
- Aguilar-Benitez M
- Ahmad A
- Ahmad M
- Ahmed A
- Ahuja S
- Aime C
- Akchurin N
- Akgun B
- Akpinar A
- Albajar C
- Albergo S
- Albert A
- Albrow M
- Alcaraz Maestre J
- Aldaya Martin M
- Aldá Júnior WL
- Aleksandrov A
- Alexander J
- Alhusseini M
- Alimena J
- Alison J
- Allen B
- Almond J
- Alvarez Gonzalez B
- Alverson G
- Alves GA
- Aly R
- Alyari M
- Amapane N
- Amendola C
- Amin N
- Amram O
- Amsler C
- Anagnostou G
- Andrea J
- Andreev V
- Andreev Y
- Andrews MB
- Androsov K
- Antchev G
- Antunovic Z
- Apanasevich L
- Apollinari G
- Appelt E
- Apresyan A
- Apyan A
- Araujo M
- Arcaro D
- Arcidiacono R
- Arenton MW
- Argiro S
- Arneodo M
- Aruta C
- Asavapibhop B
- Asawatangtrakuldee C
- Asenov P
- Asghar MI
- Asilar E
- Askew A
- Asmuss P
- Aspell P
- Atakisi IO
- Atanassov I
- Ather MW
- Attikis A
- Auffray E
- Aushev T
- Auzinger G
- Avati V
- Avery P
- Avila C
- Awais A
- Awan MIM
- Ayala E
- Ayala G
- Aydogmus Sen F
- Azarkin M
- Azhgirey I
- Aziz T
- Azzi P
- Azzurri P
- Baarmand MM
- Babaev A
- Babounikau I
- Bacchetta N
- Bachiller I
- Bachtis M
- Backhaus M
- Baden A
- Baechler J
- Baginyan A
- Bagliesi G
- Bahinipati S
- Baillon P
- Bainbridge R
- Bakas G
- Bakhshiansohi H
- Bakirci MN
- Baldenegro Barrera C
- Ball AH
- Ban Y
- Band R
- Bandyopadhyay H
- Banerjee S
- Banerjee S
- Bansal S
- Barbagli G
- Barberis E
- Bargassa P
- Baringer P
- Barnes VE
- Barney D
- Baron O
- Barrio Luna M
- Bartek R
- Bartosik N
- Bartók M
- Bastos D
- Battilana C
- Baty A
- Bauer G
- Bauerdick LAT
- Baxter S
- Bayshev I
- Bean A
- Beauceron S
- Beaudette F
- Becerril Gonzalez H
- Bechtel J
- Bedoya CF
- Beghin D
- Behera PK
- Behera SC
- Behnke O
- Bein S
- Belchior Batista Das Chagas E
- Belforte S
- Bell KW
- Bellan R
- Belloni A
- Bellora A
- Belyaev A
- Belyaev A
- Benaglia A
- Benato L
- Bencze G
- Bendavid J
- Benecke A
- Benelli G
- Beni N
- Benitez JF
- Benussi L
- Berardi V
- Berenguer Antequera J
- Beretvas A
- Bergauer T
- Berger P
- Berger T
- Beri SB
- Bermúdez Martínez A
- Bernardes CA
- Bernet C
- Berretti M
- Berry D
- Berryhill J
- Bertacchi V
- Besancon M
- Beschi A
- Bhal E
- Bhardwaj A
- Bharti M
- Bhat MA
- Bhat PC
- Bhatnagar V
- Bhattacharya R
- Bhattacharya S
- Bhattacharya S
- Bhattacharya S
- Bheesette S
- Bhowmik D
- Bhowmik S
- Bhyun JH
- Bi R
- Bialkowska H
- Bianchini L
- Bianco M
- Bianco S
- Biasini M
- Biino C
- Bilei GM
- Bilin B
- Bin Anuar AA
- Bisello D
- Black K
- Blekman F
- Blinov V
- Bloch D
- Bloch P
- Bloom K
- Bluj M
- Blumenfeld B
- Boccali T
- Bocci A
- Bodek A
- Boimska B
- Boletti A
- Bologna S
- Bols ES
- Bonacorsi D
- Bonanomi M
- Bonham B
- Bonomally S
- Boos E
- Boran F
- Borchsh V
- Borg J
- Borgonovi L
- Bornheim A
- Borras K
- Bortignon P
- Bose T
- Bossini E
- Botta C
- Botta V
- Bottigli U
- Boudoul G
- Bouhali O
- Bourgatte G
- Bourilkov D
- Bozzo M
- Bragagnolo A
- Braghieri A
- Braibant-Giacomelli S
- Brainerd C
- Brandao Malbouisson H
- Brandt S
- Branson JG
- Breedon R
- Breeze S
- Brew C
- Brigljevic V
- Brinkerhoff A
- Brivio F
- Brochero Cifuentes JA
- Brom J-M
- Brondolin E
- Brooke JJ
- Brown RM
- Brunner D
- Bruno G
- Brzhechko D
- Brücken E
- Bucci R
- Buccilli A
- Buchanan J
- Buchmuller O
- Buchot Perraguin A
- Bueghly J
- Bundock A
- Bunkowski K
- Buontempo S
- Burkett K
- Burkhardt H
- Burkle B
- Burt K
- Bury F
- Busson P
- Busza W
- Butalla S
- Butler JN
- Butler PH
- Butz E
- Bylinkin A
- Bylsma B
- Cabrera A
- Cabrillo IJ
- Cadamuro L
- Cafagna FS
- Caillol C
- Cakir A
- Calandri A
- Calderon De La Barca Sanchez M
- Calderon A
- Cali IA
- Call K
- Calligaris L
- Calzaferri S
- Camen C
- Caminada L
- Campagnari C
- Campanini R
- Campbell A
- Camporesi T
- Candelise V
- Canelli MF
- Canepa A
- Cankocak K
- Capeans Garrido M
- Capiluppi P
- Cappati A
- Caputo C
- Caraway B
- Cardini A
- Cardwell B
- Carle A
- Carlin R
- Carrera Jarrin E
- Carrillo Montoya CA
- Carrillo Moreno S
- Cartiglia N
- Carvalho Antunes De Oliveira A
- Carvalho W
- Casarsa M
- Caspart R
- Cassese A
- Castaldi R
- Castaneda Hernandez A
- Castilla-Valdez H
- Castro A
- Catanesi MG
- Cavallari F
- Cavallo FR
- Cavallo N
- Cavanaugh R
- Ceard L
- Ceccarelli R
- Cepaitis V
- Cepeda M
- Cerati GB
- Cerci S
- Cerminara G
- Cerrada M
- Cerri O
- Cetorelli F
- Chabert EC
- Chahal GS
- Chang P
- Chang P
- Chanon N
- Chao Y
- Chapon E
- Charaf O
- Charlot C
- Chatterjee RM
- Chatterjee S
- Chaudhary G
- Chauhan S
- Chauhan S
- Chawla R
- Chazin Quero B
- Checchia P
- Chekhovsky V
- Chen C
- Chen GM
- Chen HS
- Chen KF
- Chen M
- Chen PH
- Chen X
- Chen Y
- Chen Y
- Chen Z
- Chenarani S
- Cheng T
- Cheng Y
- Cherepanov V
- Chernyavskaya N
- Chertok M
- Cheung HWK
- Chhibra SS
- Chiarito B
- Chinellato J
- Chistov R
- Chlebana F
- Cho S
- Choi J
- Choi S
- Choi Y
- Chou JP
- Choudhary BC
- Choudhury S
- Chu J
- Chudasama R
- Chwalek T
- Ciangottini D
- Ciocca C
- Ciocci MA
- Cipriani M
- Ciriolo V
- Cirkovic P
- Citron M
- Cittolin S
- Ciulli V
- Civinini C
- Claes DR
- Clare R
- Clement E
- Clerbaux B
- CMS Collaboration<sup>†</sup>
- Cockerill DJA
- Coelho E
- Colaleo A
- Cole JE
- Colino N
- Collard C
- Colling D
- Cometti S
- Connor P
- Consuegra Rodríguez S
- Contardo D
- Conway J
- Conway R
- Cooper SI
- Cooperstein S
- Corcodilos L
- Cornelis T
- Cosby C
- Cossutti F
- Costa M
- Costa S
- Coubez X
- Couderc F
- Cousins R
- Covarelli R
- Cox B
- Cox PT
- Cranshaw DJ
- Creanza D
- Cremonesi M
- Cristella L
- Csanád M
- Csörgő T
- Cuevas J
- Cuffiani M
- Cumalat JP
- Cummings G
- Cussans D
- Cutts D
- Czellar S
- D'Alessandro R
- D'Alfonso M
- D'Enterria D
- D'Hondt J
- Da Costa EM
- Da Rold A
- Da Silveira GG
- Dabrowski A
- Daci N
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- Zorbilmez C
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- Álvarez Fernández A
- Österberg K
- Özçelik Ö
- Široký J
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
A search for dark matter in the form of strongly interacting massive particles (SIMPs) using the CMS detector at the LHC is presented. The SIMPs would be produced in pairs that manifest themselves as pairs of jets without tracks. The energy fraction of jets carried by charged particles is used as a key discriminator to suppress efficiently the large multijet background, and the remaining background is estimated directly from data. The search is performed using proton-proton collision data corresponding to an integrated luminosity of 16.1 fb - 1 , collected with the CMS detector in 2016. No significant excess of events is observed above the expected background. For the simplified dark matter model under consideration, SIMPs with masses up to 100 GeV are excluded and further sensitivity is explored towards higher masses
Effects of alirocumab on types of myocardial infarction: insights from the ODYSSEY OUTCOMES trial
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- Zrazhevsky K
- Zuniga JDH
- Zurakowski A
- Zuran I
- Zweiker R
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2019
- Field of study
Aims The third Universal Definition of Myocardial Infarction (MI) Task Force classified MIs into five types: Type 1, spontaneous; Type 2, related to oxygen supply/demand imbalance; Type 3, fatal without ascertainment of cardiac biomarkers; Type 4, related to percutaneous coronary intervention; and Type 5, related to coronary artery bypass surgery. Low-density lipoprotein cholesterol (LDL-C) reduction with statins and proprotein convertase subtilisin–kexin Type 9 (PCSK9) inhibitors reduces risk of MI, but less is known about effects on types of MI. ODYSSEY OUTCOMES compared the PCSK9 inhibitor alirocumab with placebo in 18 924 patients with recent acute coronary syndrome (ACS) and elevated LDL-C (≥1.8 mmol/L) despite intensive statin therapy. In a pre-specified analysis, we assessed the effects of alirocumab on types of MI. Methods and results Median follow-up was 2.8 years. Myocardial infarction types were prospectively adjudicated and classified. Of 1860 total MIs, 1223 (65.8%) were adjudicated as Type 1, 386 (20.8%) as Type 2, and 244 (13.1%) as Type 4. Few events were Type 3 (n = 2) or Type 5 (n = 5). Alirocumab reduced first MIs [hazard ratio (HR) 0.85, 95% confidence interval (CI) 0.77–0.95; P = 0.003], with reductions in both Type 1 (HR 0.87, 95% CI 0.77–0.99; P = 0.032) and Type 2 (0.77, 0.61–0.97; P = 0.025), but not Type 4 MI. Conclusion After ACS, alirocumab added to intensive statin therapy favourably impacted on Type 1 and 2 MIs. The data indicate for the first time that a lipid-lowering therapy can attenuate the risk of Type 2 MI. Low-density lipoprotein cholesterol reduction below levels achievable with statins is an effective preventive strategy for both MI types.For complete list of authors see http://dx.doi.org/10.1093/eurheartj/ehz299</p
Observation of a New Excited Beauty Strange Baryon Decaying to Ξb- π+π-
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- Aarup Petersen H
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- Yohay R
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- Yu PR
- Yu SS
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- Yumiceva F
- Yusli MN
- Zabi A
- Zacharopoulou A
- Zahid S
- Zaleski S
- Zalewski P
- Zanetti M
- Zarubin A
- Zarucki M
- Zecchinelli AG
- Zeinali M
- Zeuner WD
- Zghiche A
- Zhang F
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- Zhizhin I
- Zhokin A
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- Ziemons T
- Zientek M
- Zlebcik R
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- Zolkapli Z
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- Zorbilmez C
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- Zuolo D
- Zygala L
- Álvarez Fernández A
- Özçelik Ö
- Publication venue
- American Physical Society
- Publication date
- 01/01/2021
- Field of study
The Ξb-π+π- invariant mass spectrum is investigated with an event sample of proton-proton collisions at s=13 TeV, collected by the CMS experiment at the LHC in 2016-2018 and corresponding to an integrated luminosity of 140 fb-1. The ground state Ξb- is reconstructed via its decays to J/ψΞ- and J/ψΛK-. A narrow resonance, labeled Ξb(6100)-, is observed at a Ξb-π+π- invariant mass of 6100.3±0.2(stat)±0.1(syst)±0.6(Ξb-) MeV, where the last uncertainty reflects the precision of the Ξb- baryon mass. The upper limit on the Ξb(6100)- natural width is determined to be 1.9 MeV at 95% confidence level. The low Ξb(6100)- signal yield observed in data does not allow a measurement of the quantum numbers of the new state. However, following analogies with the established excited Ξc baryon states, the new Ξb(6100)- resonance and its decay sequence are consistent with the orbitally excited Ξb- baryon, with spin and parity quantum numbers JP=3/2-
Measurement of the inclusive and differential Higgs boson production cross sections in the decay mode to a pair of τ Leptons in pp collisions at sqrt[s]=13 TeV
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- Xiang Y
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- Yang UK
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- Yao Y
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- Yi K
- Yigitbasi E
- Yohay R
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- Yoo J
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- Yu D
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- Yuldashev BS
- Yumiceva F
- Yusli MN
- Zabi A
- Zacharopoulou A
- Zahid S
- Zaleski S
- Zalewski P
- Zanetti M
- Zarubin A
- Zarucki M
- Zecchinelli AG
- Zeinali M
- Zeuner WD
- Zghiche A
- Zhang F
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- Zhang L
- Zhang W
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- Zhao J
- Zhizhin I
- Zhokin A
- Zhu DH
- Zhu RY
- Ziemons T
- Zoi I
- Zolkapli Z
- Zorbakir IS
- Zorbilmez C
- Zotto P
- Zotz A
- Zou D
- Zou R
- Zucchetta A
- Zumerle G
- Zuo X
- Zuolo D
- Zygala L
- Álvarez Fernández A
- Özçelik Ö
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2022
- Field of study
Measurements of the inclusive and differential fiducial cross sections of the Higgs boson are presented, using the τ lepton decay channel. The differential cross sections are measured as functions of the Higgs boson transverse momentum, jet multiplicity, and transverse momentum of the leading jet in the event, if any. The analysis is performed using proton-proton collision data collected with the CMS detector at the LHC at a center-of-mass energy of 13 TeV and corresponding to an integrated luminosity of 138 fb^{-1}. These are the first differential measurements of the Higgs boson cross section in the final state of two τ leptons. In final states with a large jet multiplicity or with a Lorentz-boosted Higgs boson, these measurements constitute a significant improvement over measurements performed in other final states
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