349 research outputs found
Search for squarks and gluinos in events with isolated leptons, jets and missing transverse momentum at s√=8 TeV with the ATLAS detector
- Author
- A Djouadi
- A Kulesza
- A Kulesza
- A Lazopoulos
- A Neveu
- A Neveu
- A Sherstnev
- A. A. E. Bannoura
- A. A. Elliot
- A. A. Grillo
- A. A. Komar
- A. A. Korol
- A. A. Maier
- A. A. Minaenko
- A. A. Nepomuceno
- A. A. Snesarev
- A. A. Solodkov
- A. A. Talyshev
- A. Aloisio
- A. Alonso
- A. Altheimer
- A. Amorim
- A. Andreazza
- A. Angerami
- A. Annovi
- A. Antonov
- A. Artamonov
- A. Ashkenazi
- A. B. Fenyuk
- A. Baroncelli
- A. Bassalat
- A. Basye
- A. Beddall
- A. Bellerive
- A. Bingul
- A. Bocci
- A. Bogouch
- A. Borisov
- A. Boveia
- A. Brandt
- A. Bruni
- A. Buzatu
- A. C. Bundock
- A. C. Daniells
- A. C. König
- A. C. Martyniuk
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- A. Castelli
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- A. Cattai
- A. Cerri
- A. Cervelli
- A. Chafaq
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- A. Cheplakov
- A. Chilingarov
- A. Chitan
- A. Ciocio
- A. Clark
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- A. Cortes-Gonzalez
- A. D. Hawkins
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- A. De Santo
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- A. Demilly
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- A. Di Domenico
- A. Di Girolamo
- A. Di Mattia
- A. Di Simone
- A. Dimitrievska
- A. Doria
- A. Dudarev
- A. Durglishvili
- A. E. Baas
- A. E. Barton
- A. E. Kiryunin
- A. E. Loevschall-Jensen
- A. Ereditato
- A. Ezhilov
- A. F. Saavedra
- A. Farbin
- A. Farilla
- A. Favareto
- A. Ferrari
- A. Ferrer
- A. Ferretto Parodi
- A. Filipčič
- A. Firan
- A. Fischer
- A. Floderus
- A. Formica
- A. Forti
- A. G. Bogdanchikov
- A. G. Buckley
- A. G. Goussiou
- A. G. Leister
- A. G. Myagkov
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- A. Irles Quiles
- A. J. Armbruster
- A. J. Barr
- A. J. Beddall
- A. J. Bevan
- A. J. Brennan
- A. J. Horton
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- A. J. Lowe
- A. J. Tanasijczuk
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- A. K. Kopp
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- S. V. Chekulaev
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- T. Hayashi
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- T. Hryn’ova
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- T. Masubuchi
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- Th. D. Papadopoulou
- U. Blumenschein
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- V. A. Bednyakov
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- W Beenakker
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- Y Grossman
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- Y. Chen
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- Y. Coadou
- Y. Davygora
- Y. Enari
- Y. F. Ryabov
- Y. Fang
- Y. Hasegawa
- Y. Heng
- Y. Hernández Jiménez
- Y. Horii
- Y. Huang
- Y. Ikegami
- Y. Ilchenko
- Y. Inamaru
- Y. J. Schnellbach
- Y. Jiang
- Y. Kataoka
- Y. Komori
- Y. Kulchitsky
- Y. Li
- Y. Liu
- Y. Makida
- Y. Minami
- Y. Ming
- Y. Munwes
- Y. Nagai
- Y. Nagasaka
- Y. Nakahama
- Y. Ninomiya
- Y. Okumura
- Y. Oren
- Y. Qin
- Y. Rozen
- Y. S. Gao
- Y. Sakurai
- Y. Sasaki
- Y. Silver
- Y. Smirnov
- Y. Sugaya
- Y. Suzuki
- Y. Takubo
- Y. Tayalati
- Y. Unno
- Y. V. Grishkevich
- Y. Wu
- Y. Yamaguchi
- Y. Yamazaki
- Y. Yang
- Y. Yasu
- Y. Zhao
- Y. Zhu
- Yu. A. Tikhonov
- Z. Barnovska
- Z. D. Greenwood
- Z. Dolezal
- Z. Gecse
- Z. H. Citron
- Z. Hajduk
- Z. Hubacek
- Z. Idrissi
- Z. J. Grout
- Z. Kohout
- Z. L. Ren
- Z. Liang
- Z. M. Karpova
- Z. Marshall
- Z. Rurikova
- Z. V. Krumshteyn
- Z. Vykydal
- Z. Weng
- Z. Yan
- Z. Zhang
- Z. Zhao
- Z. Zinonos
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
The results of a search for supersymmetry in final states containing at least one isolated lepton (electron or muon), jets and large missing transverse momentum with the ATLAS detector at the Large Hadron Collider are reported. The search is based on proton-proton collision data at a centre-of-mass energy s√=8 TeV collected in 2012, corresponding to an integrated luminosity of 20 fb−1. No significant excess above the Standard Model expectation is observed. Limits are set on supersymmetric particle masses for various supersymmetric models. Depending on the model, the search excludes gluino masses up to 1.32 TeV and squark masses up to 840 GeV. Limits are also set on the parameters of a minimal universal extra dimension model, excluding a compactification radius of 1/R c = 950 GeV for a cut-off scale times radius (ΛR c) of approximately 30
Ru(II)-diimine complexes and cytochrome P450 working hand-in-hand
- Author
- Aalbers
- Agudo
- Al-Afyouni
- Andralojc
- Arnold
- Bakkes
- Berepiki
- Berepiki
- Bisterfeld
- Bormann
- Bowen
- Brandenberg
- Campagna
- Celine Eidenschenk
- Chen
- Churchfield
- Cirino
- Contakes
- Denard
- Denard
- Denisov
- Denisov
- Di Nardo
- Do
- Dunn
- Ener
- Ener
- Faiza
- Fessner
- Fruk
- Gandomkar
- Girhard
- Grant
- Greule
- Gulder
- Gumulya
- Han
- Hannemann
- Havrylyuk
- Heinemann
- Hofrichter
- Holtmann
- Howerton
- Hsieh
- Ilie
- Jung
- Kalyanasundaram
- Kato
- Kato
- Kato
- King-Smith
- Klingenberg
- Lam
- Lam
- Le-Huu
- Li
- Li
- Li
- Li
- Li
- Liang
- Lionel Cheruzel
- Liou
- Loida
- Lu
- Manning
- Mellor
- Mellor
- Mital
- Morlock
- Munro
- Nakano
- Nazor
- Omura
- Ortiz De Montellano
- Panneerselvam
- Park
- Perret
- Qu
- Reetz
- Rentmeister
- Rittle
- Robert
- Roiban
- Rudroff
- Russo
- Sadeghi
- Sadeghi
- Salazar
- Savateev
- Schmermund
- Schrittwieser
- Schwaneberg
- Sevrioukova
- Shalan
- Shalan
- Sheldon
- Sheldon
- Shoji
- Shoji
- Sorensen
- Sosa
- Spradlin
- Stephenson
- Sun
- Teply
- Thompson
- Thota
- Tran
- Tran
- Tran
- Tripathi
- Twilton
- Urlacher
- van Schie
- Verma
- Wang
- Wei
- Wenger
- Whitehouse
- Willot
- Winkler
- Winkler
- Wise
- Xu
- Yang
- Yasuda
- Yu
- Zamora
- Zangar
- Zayat
- Zhang
- Zhang
- Zhao
- Zilly
- Publication venue
- SJSU ScholarWorks
- Publication date
- 12/09/2020
- Field of study
With a growing interest in utilizing visible light to drive biocatalytic processes, several light-harvesting units and approaches have been employed to harness the synthetic potential of heme monooxygenases and carry out selective oxyfunctionalization of a wide range of substrates. While the fields of cytochrome P450 and Ru(II) photochemistry have separately been prolific, it is not until the turn of the 21st century that they converged. Non-covalent and subsequently covalently attached Ru(II) complexes were used to promote rapid intramolecular electron transfer in bacterial P450 enzymes. Photocatalytic activity with Ru(II)-modified P450 enzymes was achieved under reductive conditions with a judicious choice of a sacrificial electron donor. The initial concept of Ru(II)-modified P450 enzymes was further improved using protein engineering, photosensitizer functionalization and was successfully applied to other P450 enzymes. In this review, we wish to present the recent contributions from our group and others in utilizing Ru(II) complexes coupled with P450 enzymes in the broad context of photobiocatalysis, protein assemblies and chemoenzymatic reactions. The merging of chemical catalysts with the synthetic potential of P450 enzymes has led to the development of several chemoenzymatic approaches. Moreover, strained Ru(II) compounds have been shown to selectively inhibit P450 enzymes by releasing aromatic heterocycle containing molecules upon visible light excitation taking advantage of the rapid ligand loss feature in those complexes
Insect pathogens as biological control agents: back to the future
- Author
- Abdel-Razek
- Abolins
- Abot
- Acevedo
- Adams
- Adhikari
- Adjei
- Adler
- Adler
- Akello
- Akhurst
- Al-mazra’awi
- Al-mazra’awi
- Al-Mazra’awi
- Alcázar
- Ali
- Alm
- Alston
- Alves
- Alves
- An
- Anbesse
- Anderson
- Ansari
- Ansari
- Ansari
- Ansari
- Ansari
- Ansari
- Ansari
- Ansell
- Aranda
- Arthurs
- Arthurs
- Arthurs
- Arthurs
- Arthurs
- Arthurs
- Asano
- Asser-Kaiser
- Asser-Kaiser
- Athanassiou
- Backman
- Bai
- Bai
- Bai
- Bai
- Bailey
- Ballard
- Ballard
- Barbara
- Bateman
- Bauce
- Bauer
- Baur
- Baverstock
- Bedding
- Beegle
- Beegle
- Behie
- Behle
- Behle
- Behle
- Belloncik
- Bellotti
- Belur
- Berger
- Bergoin
- Bernstein
- Bidochka
- Bidochka
- Bielza
- Bilgrami
- Birch
- Bird
- Bischoff
- Bixby
- Bixby-Brosi
- Black
- Blackwell
- Blanford
- Blanford
- Blommers
- Bonning
- Boonserm
- Boonserm
- Bravo
- Bravo
- Bravo
- Brinkman
- Brookes
- Brown
- Brownbridge
- Brownbridge
- Brownbridge
- Brownbridge
- Brownbridge
- Broza
- Bruck
- Bruck
- Bruck
- Bruck
- Brusselman
- Bucchini
- Buerger
- Buitenhuis
- Burdan
- Burges
- Burges
- Burnell
- Bussaman
- Butt
- Butt
- Böszörmènyi
- Cadogan
- Campbell
- Campbell
- Campbell
- Campos-Herrera
- Caprio
- Carneiro
- Castillejos
- Castrillo
- Castrillo
- Chambers
- Chandler
- Chandler
- Chandler
- Chandler
- Charles
- Charles
- Charmillot
- Charnley
- Charnley
- Chaston
- Chavarria-Hernandez
- Chavarria-Hernandez
- Chavarria-Hernandez
- Chen
- Chen
- Chen
- Cherry
- Cherry
- Cherry
- Choudhary
- Christen
- Christian
- Ciche
- Cisneros
- Clarke
- Cliquet
- Cloyd
- Copping
- Copping
- Cory
- Cory
- Cory
- Cory
- Cottrell
- Couch
- Couch
- Cowles
- Cross
- Cross
- Cunningham
- Cuthbertson
- Cuthbertson
- D. Grzywacz
- D.I. Shapiro-Ilan
- Da Silva
- Davidson
- Davidson
- Davidson
- De Carvalho Barbosa Negrisoli
- de la Rosa
- de la Torre
- de Morães Lessa
- Del Valle
- Del Valle
- Dempsey
- Denno
- Dillman
- Dillon
- Dimbi
- Dively
- Dolci
- Dolinski
- Douches
- Douches
- Dowd
- Dowds
- Down
- Dransfield
- Driver
- Dromph
- Duchaud
- Duncan
- Duncan
- Duncan
- Duncan
- Easom
- Eberle
- Eberle
- Eberle
- Eberle
- Edwards
- Efron
- Ehlers
- Ehlers
- Ehlers
- Ekesi
- El-Borai
- Elliot
- Ellis
- Engler
- Enkerli
- Enkerli
- Enkerli
- Enkerli
- Ennis
- Entz
- European Commission
- Fallon
- Fallon
- Faria
- Farrar
- Farrar
- Farrar
- Farrar
- Federici
- Federici
- Fenton
- ffrench-Constant
- Fife
- Fife
- Fife
- Foster
- Fransen
- Franzmann
- Freimoser
- Fritsch
- Frutos
- Fujimoto
- Furlong
- Fushing
- Fuxa
- Galitsky
- Gan-Mor
- Gassmann
- Gaugler
- Gaugler
- Gaugler
- Gelernter
- Genissel
- Georgis
- Georgis
- Gil
- Girard
- Glare
- Glare
- Glare
- Goettel
- Goettel
- Goettel
- Goettel
- Goodrich-Blair
- Graham
- Granados
- Grewal
- Grewal
- Griffitts
- Grochulski
- Gross
- Grzywacz
- Grzywacz
- Grzywacz
- Grzywacz
- Gómez-Bonilla
- Hajek
- Hajek
- Hajek
- Hajek
- Hajek
- Hajek
- Hajek
- Hajek
- Han
- Hao
- Hao
- Harrison
- Hartmann
- Hauxwell
- Head
- Heckel
- Hellmich
- Herniou
- Hibbett
- Hillocks
- Hiltpold
- Hirao
- Hirao
- Hodson
- Hoover
- Hoover
- Hoy
- Hoy
- Hoy
- Hu
- Huanga
- Huger
- Hummel
- Hussa
- Hyde
- Ignoffo
- Ignoffo
- Ilan
- Inceoglu
- Inglis
- Inglis
- Inglis
- Inglis
- Inyang
- Isaacson
- Islas-López
- Jabbour
- Jaber
- Jackson
- Jackson
- Jackson
- Jackson
- Jackson
- Jackson
- Jackson
- Jackson
- Jackson
- Jackson
- Jackson
- Jagdale
- Jagdale
- Jagdale
- Jagdale
- Jagdale
- James
- Jaramillo
- Jaronski
- Jaronski
- Jaronski
- Jaronski
- Jehle
- Jenkins
- Jenkins
- Ji
- Johnigk
- Johnson
- Jones
- Jung
- Jurat-Fuentes
- Jurat-Fuentes
- Kabaluk
- Kambrekar
- Kang
- Kaplan
- Kapongo
- Kapongo
- Kariuki
- Kaya
- Kaya
- Kaya
- Keller
- Keller
- Keller
- Kennedy
- Kepler
- Kerwin
- Kevan
- Khan
- Khan
- Kiewnick
- Kikankie
- Kim
- Klein
- Klein
- Klein
- Klingen
- Klingen
- Klingen
- Knight
- Knowles
- Koike
- Kolodny-Hirsch
- Koppenhöfer
- Koppenhöfer
- Koppenhöfer
- Koppenhöfer
- Koppenhöfer
- Koppenhöfer
- Koppenhöfer
- Koppenhöfer
- Koppenhöfer
- Koppenhöfer
- Kouassi
- Kreig
- Kreutz
- Krishna
- Krishna
- Kumar
- Kunimi
- Kunkel
- L.A. Lacey
- Labbé
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Lacey
- Langenbruch
- Lapointe
- Lasa
- Lasa
- Lebel
- Leland
- Leland
- Leuschner
- Lewis
- Lewis
- Li
- Li
- Li
- Lisansky
- Liu
- Liu
- Llàcer
- Lomer
- Lomer
- Lorang
- Lord
- Losey
- Loya
- Lucarotti
- Längle
- M. Brownbridge
- M.S. Goettel
- Maniania
- Maniania
- Martignoni
- Martin
- Martin
- Martin
- Martinez
- Martinez del Altube
- Marvier
- Marx-Stoelting
- Mashtoly
- Mashtoly
- Masson
- Mbata
- McCoy
- McCrevy
- McDougall
- McGaughey
- McGaughey
- McGuire
- McGuire
- Meekers
- Meeussen
- Mensah
- Meyling
- Meyling
- Meyling
- Meyling
- Meyling
- Meyling
- Meyling
- Migiro
- Millar
- Milner
- Minorsky
- Moar
- Mohan
- Monobrullah
- Montesinos
- Moore
- Moore
- Moore
- Morales
- Moreau
- Morse
- Morton
- Moscardi
- Moscardi
- Moscardi
- Moscardi
- Moshayov
- Mudgal
- Mumm
- Murillo
- Murray
- Nahar
- Nair
- Nakai
- Nakai
- Nakai
- Neves
- Nguyen
- Nielsen
- Nielsen
- Nielsen
- Nimkingrat
- Nyczepir
- Oestergaard
- Olleka
- Ortiz-Urquiza
- Ownley
- Ownley
- O’Callaghan
- O’Callaghan
- Panazzi
- Papierok
- Parsa
- Pava-Ripoll
- Pedrini
- Pell
- Pell
- Peng
- Pereault
- Perez
- Perez
- Phipps
- Pigott
- Pleasants
- Podgewaite
- Poinar
- Poinar
- Polavarapu
- Porcar
- Poulin
- Poulin
- Prater
- Preisser
- Premachandra
- Pszczolkowski
- Pszczolkowski
- Qazi
- Quesada-Moraga
- Queseda-Moraga
- Queseda-Moraga
- Quintela
- R. Frutos
- Rabindra
- Rahman
- Ram
- Ramle
- Ramos-Rodríguez
- Ramos-Rodríguez
- Ranjard
- Rasmann
- Ravensberg
- Reay
- Rehner
- Rehner
- Rehner
- Reid
- Reis-Menini
- Ricroch
- Riga
- Roberts
- Roh
- Rohles
- Rohner-Thielen
- Romeis
- Rowley
- Roy
- Roy
- Ryder
- Sajap
- San-Blas
- Sanchis
- Sandhu
- Sauphanor
- Saxena
- Scheepmaker
- Schmidt
- Schmitz
- Schnepf
- Scholte
- Scholte
- Scholte
- Schroer
- Schroer
- Schwartz
- Schwartz
- Schwarzenbach
- Schwarzenbach
- Sears
- Shah
- Shah
- Shah
- Shah
- Shah
- Shah
- Shapiro
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shapiro-Ilan
- Shelton
- Shelton
- Shelton
- Shimazu
- Siegel
- Singh
- Singhal
- Skadsen
- Skovmand
- Skovmand
- Slavicek
- Solter
- Somasekhar
- Somvanshi
- Sosa-Gómez
- Spiridonov
- Sporleder
- Sporleder
- Sporleder
- Sporleder
- St. Leger
- St. Leger
- Stanley-Horn
- Steinkraus
- Steinkraus
- Steinkraus
- Steinkraus
- Stevenson
- Stock
- Stock
- Storer
- Strauch
- Stuart
- Stuart
- Sun
- Sundh
- Sundh
- Sung
- Sung
- Suzuki
- Szewcyk
- Tabashnik
- Tabashnik
- Tabashnik
- Tabashnik
- Tabashnik
- Tabashnik
- Tabashnik
- Tamez-Guerra
- Tamez-Guerra
- Tanada
- Tarocco
- Teulon
- Teulon
- Thakore
- Thakre
- Thaochan
- Theilmann
- Thompson
- Thornström
- Thurston
- Thurston
- Toepfer
- Toprak
- Torr
- Torzilli
- Townsend
- Townsend
- Traugott
- Tsao
- Tschenn
- Tyson
- Ugine
- Ugine
- Unruh
- Vachon
- Vachon
- Vachon
- Vail
- Vail
- Vail
- Van Beek
- Van Beek
- van Frankenhuyzen
- van Frankenhuyzen
- van Frankenhuyzen
- van Tol
- Van Tol
- Van Tol
- van Tol
- Vega
- Vega
- Vega
- Vega
- Vega
- Vey
- Vidal
- Vidal
- Villani
- Villani
- Vincent
- Vié
- Wang
- Wang
- Wang
- Wang
- Wei
- Wekesa
- Whalon
- Williams
- Williams
- Williams
- Wolfenbarger
- Wraight
- Wraight
- Wraight
- Wraight
- Wraight
- Wraight
- Wraight
- Wright
- Wu
- Wu
- Yang
- Zamora-Avilés
- Zangerl
- Zeddam
- Zenner
- Zhang
- Zhou
- Zhu
- Zichová
- Zimmermann
- Zimmermann
- Zimmermann
- Zimmermann
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/11/2015
- Field of study
The development and use of entomopathogens as classical, conservation and augmentative biological control agents have included a number of successes and some setbacks in the past 15 years. In this forum paper we present current information on development, use and future directions of insect-specific viruses, bacteria, fungi and nematodes as components of integrated pest management strategies for control of arthropod pests of crops, forests, urban habitats, and insects of medical and veterinary importance.
Insect pathogenic viruses are a fruitful source of MCAs, particularly for the control of lepidopteran pests. Most research is focused on the baculoviruses, important pathogens of some globally important pests for which control has become difficult due to either pesticide resistance or pressure to reduce pesticide residues. Baculoviruses are accepted as safe, readily mass produced, highly pathogenic and easily formulated and applied control agents. New baculovirus products are appearing in many countries and gaining an increased market share. However, the absence of a practical in vitro mass production system, generally higher production costs, limited post application persistence, slow rate of kill and high host specificity currently contribute to restricted use in pest control. Overcoming these limitations are key research areas for which progress could open up use of insect viruses to much larger markets.
A small number of entomopathogenic bacteria have been commercially developed for control of insect pests. These include several Bacillus thuringiensis sub-species, Lysinibacillus (Bacillus) sphaericus, Paenibacillus spp. and Serratia entomophila. B. thuringiensis sub-species kurstaki is the most widely used for control of pest insects of crops and forests, and B. thuringiensis sub-species israelensis and L. sphaericus are the primary pathogens used for medically important pests including dipteran vectors,. These pathogens combine the advantages of chemical pesticides and microbial control agents (MCAs): they are fast acting, easy to produce at a relatively low cost, easy to formulate, have a long shelf life and allow delivery using conventional application equipment and systemics (i.e. in transgenic plants). Unlike broad spectrum chemical pesticides, B. thuringiensis toxins are selective and negative environmental impact is very limited. Of the several commercially produced MCAs, B. thuringiensis (Bt) has more than 50% of market share. Extensive research, particularly on the molecular mode of action of Bt toxins, has been conducted over the past two decades. The Bt genes used in insect-resistant transgenic crops belong to the Cry and vegetative insecticidal protein families of toxins. Bt has been highly efficacious in pest management of corn and cotton, drastically reducing the amount of broad spectrum chemical insecticides used while being safe for consumers and non-target organisms. Despite successes, the adoption of Bt crops has not been without controversy. Although there is a lack of scientific evidence regarding their detrimental effects, this controversy has created the widespread perception in some quarters that Bt crops are dangerous for the environment. In addition to discovery of more efficacious isolates and toxins, an increase in the use of Bt products and transgenes will rely on innovations in formulation, better delivery systems and ultimately, wider public acceptance of transgenic plants expressing insect-specific Bt toxins.
Fungi are ubiquitous natural entomopathogens that often cause epizootics in host insects and possess many desirable traits that favor their development as MCAs. Presently, commercialized microbial pesticides based on entomopathogenic fungi largely occupy niche markets. A variety of molecular tools and technologies have recently allowed reclassification of numerous species based on phylogeny, as well as matching anamorphs (asexual forms) and teleomorphs (sexual forms) of several entomopathogenic taxa in the Phylum Ascomycota. Although these fungi have been traditionally regarded exclusively as pathogens of arthropods, recent studies have demonstrated that they occupy a great diversity of ecological niches. Entomopathogenic fungi are now known to be plant endophytes, plant disease antagonists, rhizosphere colonizers, and plant growth promoters. These newly understood attributes provide possibilities to use fungi in multiple roles. In addition to arthropod pest control, some fungal species could simultaneously suppress plant pathogens and plant parasitic nematodes as well as promote plant growth. A greater understanding of fungal ecology is needed to define their roles in nature and evaluate their limitations in biological control. More efficient mass production, formulation and delivery systems must be devised to supply an ever increasing market. More testing under field conditions is required to identify effects of biotic and abiotic factors on efficacy and persistence. Lastly, greater attention must be paid to their use within integrated pest management programs; in particular, strategies that incorporate fungi in combination with arthropod predators and parasitoids need to be defined to ensure compatibility and maximize efficacy.
Entomopathogenic nematodes (EPNs) in the genera Steinernema and Heterorhabditis are potent MCAs. Substantial progress in research and application of EPNs has been made in the past decade. The number of target pests shown to be susceptible to EPNs has continued to increase. Advancements in this regard primarily have been made in soil habitats where EPNs are shielded from environmental extremes, but progress has also been made in use of nematodes in above-ground habitats owing to the development of improved protective formulations. Progress has also resulted from advancements in nematode production technology using both in vivo and in vitro systems; novel application methods such as distribution of infected host cadavers; and nematode strain improvement via enhancement and stabilization of beneficial traits. Innovative research has also yielded insights into the fundamentals of EPN biology including major advances in genomics, nematode-bacterial symbiont interactions, ecological relationships, and foraging behavior. Additional research is needed to leverage these basic findings toward direct improvements in microbial control
Evolving trends in the management of acute appendicitis during COVID-19 waves. The ACIE appy II study
- Author
- Agresta Ferdinando
- Ajawin Pawel
- Al Amri Nadiah
- al-Najami Issam
- AlAamer Ohood
- Alconchel Felipe
- Alghamdi Abdulrahman
- Alharthi Qasem
- Alhazmi Ahmad
- Ali Mazin
- Ali Mujahid
- Almalki Abdulrahman
- Alselaim Nahar
- Alshamrani Abdullah
- Alsherif Omar
- Alsofyani Fahad
- Alsufyani Ahmed
- Althobaiti Shabab
- AlThomali Musab
- Altinel Yuksel
- Alturkistani Abdullah
- Andriola Valeria
- André Ana
- Angelico Roberta
- Angrisani Marco
- Anoldo Pietro
- Anselmo Alessandro
- Antonacci Nicola
- Argenio Giulio
- Arredondo Gerardo
- Avila Mercado Octavio
- Awad Selmy
- Azfar Mohammad
- Bacchiocchi Giulia
- Bagaglini Giulia
- Baili Efstratia
- Balciscueta Izaskun
- Balciscueta Zutoia
- Bandin Alfonso
- Barcenas Francisco Javier Quezada
- Baroffio Paolo
- Bavikatte Akshay
- Bechstein Wolf
- Bekele Kebebe
- Bellanova Giovanni
- Bellato Vittoria
- Bellido Juan
- Bellini Maria Irene
- Benli Sami
- Benzoni Enrico
- Blanco-Antona Francisco
- Bonavina Luigi
- Bondurri Andrea
- Bouhuwaish Ahmad
- Bozbiyik Osman
- Brady Richard
- Brillantino Antonio
- Brisinda Giuseppe
- Buonomi Oreste Claudio
- Cabrera Vargas Luis Felipe
- Calderón Duque Teresa
- Calini Giacomo
- Calussi Marco
- Campagnaro Tommaso
- Campanelli Michela
- Cardamone Eugenia
- Caruso Riccardo
- Castaldi Antonio
- Catarci Marco
- Celentano Valerio
- Cerdán Carlos
- Chacón Carlos Petrola
- Charalabopoulos Alexandros
- Chessa Antonella
- Chiappetta Sonja
- Chiarello Maria Michela
- Cillara Nicola
- Colombo Francesco
- Colucci Gianluca
- Colás-Ruiz Enrique
- Conti Luigi
- Cordera Fernando
- Cornejo Isabel
- Costanzi Andrea
- Creavin Ben
- Curella Luciano
- Das Andre
- Daskalakis Theodoros
- Davies Justin
- de Andrés-Asenjo Beatriz
- De Campos Tercio
- de Guzmán Aragón Sara Ortiz
- de las Casas Sara Gortázar
- De Luca Alessandro
- De Luca Giuseppe Massimiliano
- De Lucia Chiara
- De Nobili Giovanni
- De Rosa Michele
- de San Ildefonso Pereira Alberto
- De Simone Belinda
- Delis Spiros
- Delko Tarik
- Delogu Daniele
- Di Giovanni Silvia
- Di Martino Marcello
- Di Marzo Francesco
- Di Saverio Salomone
- Diaz-Elizondo Jose Antonio
- Dominguez Casandra
- Dorovinis Panagiotis
- Douka Eleftheria
- Dudi-Venkata Nagendra
- Dziakova Jana
- Díaz Carlos Javier Gómez
- D’Antonio Dario
- Elhadi Muhammed
- Elia Rossella
- Erdas Enrico
- Esposito Giuseppe
- Faisal Alsulaimani
- Fajardo Roosevelt
- Falco Nicolò
- Faro Carmelo Lo
- Feituri Nura
- Ferrara Francesco
- Ferrario Luca
- Ferronetti Antonio
- Fidoshev Iliya
- Foianini Esteban
- Folliero Cristina
- Formisano Giampaolo
- Francone Elisa
- Frazzetta Giuseppe
- Frontali Alice
- Fuentes Sara
- Fung Chia Chi
- Fung Tak Lit Derek
- Galiffa Giampaolo
- Gallo Gaetano
- García Domínguez Melody
- García Orozco Víctor Hugo
- Gazia Carlo
- Gentilli Sergio
- Ghedan Soliman
- Gica Corina
- Gica Nicolae
- Giordano Luca
- Giordano Marco
- Giuliani Antonio
- Goh Brian
- González Tomás Elosua
- Graham Victoria
- Gravante Gianpiero
- Grossi Ugo
- Guaitoli Eleonora
- Guerci Claudio
- Hamid Amal
- Hernández Palmas Oscar Isaac
- Herrera-Almario Gabriel
- Iacobone Maurizio
- Ielpo Benedetto
- Ioannidis Argyrios
- Ioannidis Orestis
- Iossa Angelo
- Iqbal Atif
- Irkorucu Oktay
- Isernia Roberta Maria
- Izzo Giuliano
- Jamiri Al-Radjid
- Jennifer Chiu Hiu Fung
- Jiménez Carneros Virginia
- Jovanovic Branislav
- Jovanovic Jelena Pejanovic
- Julio Abba
- Junaid Sofi
- Kampouroglou Georgios
- Katta Venkateswara Rao
- Keller Deborah
- Kenington Cleo
- Khalid Ahmad
- Khan Farhan
- Khan Mansoor
- Koh Peng Soon
- Koëter Tijmen
- Krivan Sylvia
- Kumar Akshay
- Kuvvetli Adnan
- Kykalos Stylianos
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- Parreira Jose Gustavo
- Pata Francesco
- Pattacini Gianmaria Casoni
- Pecchini Francesca
- Pecorelli Nicolò
- Pedraza Ciro Mauricio
- Pellicciaro Marco
- Pellino Gianluca
- Peltrini Roberto
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- Smith-Singares Eduardo
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- Spampinato Marcello Giuseppe
- Sretenovic Aleksandar
- Stavrou Habil Gregor
- Stubbs Ben
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- Treviño Figueroa Adriana Michelle
- Tromba Antonella
- Tropeano Francesca Paola
- Turrado-Rodriguez Victor
- Tutino Roberta
- Tzivanakis Alexios
- Ugon Gustavo Armand
- Valles-Guerra Orestes
- van Ramshorst Gabrielle
- Vanni Gianluca
- Varela Cristopher
- Vaterlini Elisa Maria
- Veroux Massimiliano
- Vertaldi Sara
- Vicente Rodríguez Irune
- Vigorita Vincenzo
- Vinci Danilo
- Viola Marcelo
- Visag-Castillo Victor
- Voglino Valerio
- Voon Kelvin
- Weckmann Lujan Sergio Alberto
- Weerasekera Mihiri
- Younis Muhammad Umar
- Yánez Carlos
- Zalla Tiku
- Zigiotto Daniele
- Zuchini Andres Mendoza
- Zuluaga Mauricio
- Zuolo Michele
- Çetinkünar Süleyman
- Publication venue
- Publication date
- 01/01/2022
- Field of study
Background: In 2020, ACIE Appy study showed that COVID-19 pandemic heavily affected the management of patients with acute appendicitis (AA) worldwide, with an increased rate of non-operative management (NOM) strategies and a trend toward open surgery due to concern of virus transmission by laparoscopy and controversial recommendations on this issue. The aim of this study was to survey again the same group of surgeons to assess if any difference in management attitudes of AA had occurred in the later stages of the outbreak.
Methods: From August 15 to September 30, 2021, an online questionnaire was sent to all 709 participants of the ACIE Appy study. The questionnaire included questions on personal protective equipment (PPE), local policies and screening for SARS-CoV-2 infection, NOM, surgical approach and disease presentations in 2021. The results were compared with the results from the previous study.
Results: A total of 476 answers were collected (response rate 67.1%). Screening policies were significatively improved with most patients screened regardless of symptoms (89.5% vs. 37.4%) with PCR and antigenic test as the preferred test (74.1% vs. 26.3%). More patients tested positive before surgery and commercial systems were the preferred ones to filter smoke plumes during laparoscopy. Laparoscopic appendicectomy was the first option in the treatment of AA, with a declined use of NOM.
Conclusion: Management of AA has improved in the last waves of pandemic. Increased evidence regarding SARS-COV-2 infection along with a timely healthcare systems response has been translated into tailored attitudes and a better care for patients with AA worldwide
Charged-particle distributions at low transverse momentum in √s=13 13 TeV pp interactions measured with the ATLAS detector at the LHC
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- Zhemchugov A
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- Zibell A
- Zieminska D
- Zimine NI
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- Zivkovic L
- Zobernig G
- Zoccoli A
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Measurements of distributions of charged particles produced in proton–proton collisions with a centre-of-mass energy of 13 TeV are presented. The data were recorded by the ATLAS detector at the LHC and correspond to an integrated luminosity of 151 μb −1 μb−1 . The particles are required to have a transverse momentum greater than 100 MeV and an absolute pseudorapidity less than 2.5. The charged-particle multiplicity, its dependence on transverse momentum and pseudorapidity and the dependence of the mean transverse momentum on multiplicity are measured in events containing at least two charged particles satisfying the above kinematic criteria. The results are corrected for detector effects and compared to the predictions from several Monte Carlo event generators
Measurement of the inelastic proton-proton cross section at √s=13 TeV with the ATLAS detector at the LHC
- Author
- Aaboud M
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Abeloos B
- Aben R
- AbouZeid OS
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- Agricola J
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- Zhemchugov A
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- Zobernig G
- Zoccoli A
- Zwalinski L
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2015
- Field of study
This Letter presents a measurement of the inelastic proton-proton cross section using 60 μb −1 of pp collisions at a center-of-mass energy √s of 13 TeV with the ATLAS detector at the LHC. Inelastic interactions are selected using rings of plastic scintillators in the forward region (2.0710 −6 , where M X is the larger invariant mass of the two hadronic systems separated by the largest rapidity gap in the event. In this ξ range the scintillators are highly efficient. For diffractive events this corresponds to cases where at least one proton dissociates to a system with M X >13 GeV . The measured cross section is compared with a range of theoretical predictions. When extrapolated to the full phase space, a cross section of 78.1±2.9 mb is measured, consistent with the inelastic cross section increasing with center-of-mass energy
Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease
- Author
- A Abbate
- A Abhyankar
- A Adams
- A Agafina
- A Akyea-Djamson
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- A Alfieri
- A Alfrey
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- A Amos
- A Anadiotis
- A Anneveldt
- A Antolick
- A Arthur
- A Aslam
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- Abdullakutty J
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- Abib E Jr
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- Aguilar M
- Ahire N
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- Ahmed Sh
- Ahn Y
- Aish B
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- Aiub J
- Ajax K
- Ajioka M
- Akai Y
- Akatova E
- Akrap B
- Al Joundi T
- Al-Khalili F
- Albisu J
- Alcalde Jm
- Alcide P
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- Alllison Dc
- Almaliky T
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- Andor M
- Angelova I
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- Anker Sd
- Antalik L
- Antonicelli R
- Aparicio Cv
- Apel T
- Apostolovic S
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- Arango Jl
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- 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
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- Baden M
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- Baek C
- Baeumer A
- Bagi Es
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- Bailey K
- Bailey S
- Bair S
- Baker A
- Baker C
- Bakhai A
- Bakker H
- Baksi A
- Baldin Mg
- Bali Hk
- Ballantyne C
- Ballmajo M
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- Banker K
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- Barbarash Ol
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- Barbosa E
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- Barreto M
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- Barroso W
- Bartkowiak A
- Bartosh L
- Bartuseviciene S
- Bashir K
- Baszak J
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- Bayram E
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- Beaudry M
- Beauregard La
- Beckett L
- Belejchak P
- Belle Isle J
- Belohlavek J
- Bendelow T
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- Benedetti G
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- 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
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- Bilazarian S
- Bilodeau N
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- Birdane A
- Bisne V
- Bitzer V
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- Blahey M
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- Blazsek Z
- Bloch S
- Blom Kb
- Bluemel J
- Blumberg C
- Blumenthal R
- Bocanera M
- Bodanese L
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- 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
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- Briké C
- Brodmann M
- Brons S
- Brousalis L
- Brouwer M
- Brown C
- Brown N
- Brown S
- Buchannan C
- Budaj A
- Budassi N
- Budkova J
- Bugan V
- Buhlman S
- Bulashova O
- Bunschoten P
- Burke W
- Burley T
- Burova N
- Burris H
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- Burton J
- Burton M
- Burtt D
- Busak L
- Busic N
- Byars W
- 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
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- Carr K
- Carrillo J
- Caruso G
- Casala J
- Caso P
- Casoinic F
- Castillo J
- Castillo T
- Cech V
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- Cendali G
- Cepinskiene L
- Cerda L
- Cermak O
- Chachalis G
- Chaggar S
- Chambers J
- Chamblee T
- Chang K
- Chang Kc
- Chang Wh
- Charlier F
- Charmarthi B
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- Chauhan D
- Chauhan H
- Chaussé I
- Chavada J
- Chaverra I
- Chaware G
- Chee L
- Chella S
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- Chen J
- Chen Mh
- Chen Y
- Chen Yc
- Chen Zc
- Cheng Jj
- Cheng S
- Cheng Sm
- Cherlin R
- Cheung D
- Chhabra A
- Chintala P
- Chiodi L
- Choi Aj
- Chou S
- Chouinard G
- Christensen L
- Christenson S
- Chung A
- Churina S
- Cifkova R
- Ciglenecki N
- Cioffi A
- Cislowski D
- Cleveland T
- Clocotan M
- Cmrecnjak J
- Colfer H
- Colhoun H
- Collier D
- Collins R
- Coloma G
- Colquhoun D
- Colvin T
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- Commerford P
- Commerford P
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- Cools F
- Cornel Jh
- Corona V
- Coronel J
- Cosgrove N
- Cosgrove S
- Cosmi F
- Costa Amorim R
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- Covell W
- Cox B
- Cox R
- Craig W
- Crandall L
- Crawford G
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- Crepps K
- Crocamo A
- Cromer M
- Cruz H
- Cruz H
- Cruz M
- Csala L
- Cucher F
- Cuentas I
- Cuervo A
- Curiac D
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- Cyprian R
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- D'Amours Dg
- D Dash
- D Dattani
- D Denham
- D Desai
- D Desalle
- D Digangi
- D Dunn
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- Da Silva D Jr
- Da Silva O Jr
- Dahlen G
- Dalseg Am
- Damron M
- Danik J
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- Dave B
- Dave K
- Davidsson K
- Davies M
- Davies N
- Davis B
- Davis M
- Dawkins-Hughes S
- Dawood Sy
- Dayer M
- De Boer P
- De Caterina R
- De Jong C
- De Knijf K
- De Krumbach L
- De Los Milagros Had M
- De Los Rios M
- De Rosa S
- De Vos A
- De Wolf L
- Dean J
- Debnam S
- Decsi K
- Decsi Kl
- Dedek V
- Dedkova S
- Defosse C
- Degennaro N
- Dehning M
- Dela Llana A
- Delfonso F
- Delforge M
- Delgadillo T
- Dellasa M
- Dellborg M
- Dellorso M
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- Dengler T
- Dermitzakis A
- Deslongchamps F
- Dessalvi Cc
- Destro M
- Dettmer M
- Devasia T
- Deweerdt N
- Dhanak R
- Dhawan M
- Di Biase M
- Diago M
- Diaz M
- Dicken T
- Dickstein K
- Diederich C
- Diederich M
- Diehl R
- Diller P
- Dimattia M
- Dimitrov G
- Diodati J
- Dobariya H
- Dobilas V
- Dodds G
- Doesborg L
- Doggett J
- Dognini Gp
- Doi M
- Dokupilova A
- Dommerholt R
- Donahue K
- Donath M
- 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
- Duckert A
- Duda N
- Dudarev M
- Dudhatra N
- Duff J
- Duhan S
- Dunhurst F
- Dussan Ma
- Dutka C
- Dwenger E
- Dzupina A
- Dékány Jn
- E Eleuteri
- E Englmann
- Earl J
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- Eaton C
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- Ebeling K
- Ebrahim I
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- Edgerton L
- Edillo C
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- Eichinger G
- Einhorn D
- Eki Y
- El Hachem M
- El Hafi S
- Ellenbroek D
- Ellis M
- Emil B
- Endo T
- Engelen W
- Erhard M
- Erickson B
- Ervin W
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- Espinosa V
- Everett Bm
- F Fedele
- F Fonseca
- F Fucci
- Facello A
- Facello M
- Faghih M
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- Fang Cy
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- Fattal P
- Fawson A
- Feitosa G
- Felario Junior Ga
- Felix L
- Feng Y
- Feng Z
- Ferdinand K
- Ferkl R
- Fernandez Aa
- Ferrari V
- Ferrario M
- Ferraz R
- Ferreira Dos Santos T
- Ferreira-Jardim A
- Fien E
- Filardi Pp
- Filho P
- Fintel D
- Firek C
- Fischer Sm
- Fisher J
- Fitilev S
- Fitz-Patrick D
- Fitzpatrick L
- Flaksa I
- Flather M
- Flezar M
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- Flores E
- Flores Gs
- Flores H
- Floro T
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- Folkeringa Rj
- Fonseca A
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- Forgon T
- Forgosh L
- Forker A
- Forster T
- Foster M
- Foucauld J
- Fowler V
- Fox B
- Franco M
- Francoeur L
- Frandsen B
- Frandsen B
- Frankenstein L
- Fratczak M
- Freitas E
- French J
- Frivold G
- Fruchter G
- Fu G
- Fucak E
- Fuchs R
- Fucili A
- Fukuike C
- Fullerton D
- Fulop P
- Fulop T
- Fulwani M
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- Furuseth B
- G Gacioch
- G Gosselin
- Gabito A
- Gabor M
- Gabriel J
- Gabrielli D
- Gaeb-Strasas B
- Gamba C
- Ganau A
- Gapon L
- Garas S
- Garcia Duran R
- Garcia Pinna J
- Garcia Rinaldi R
- Garcia F
- Garcia N
- Garcia-Fragoso V
- Garcia-Portela M
- Garner K
- Gazizianova V
- Gelb R
- Genest J
- Genova D
- George F
- Germann H
- Gersh B
- Gervais B
- Ghali J
- Ghondale N
- Ghosh N
- Ghosh S
- Giese C
- Gilbert J
- Gilley J
- Gits F
- Glancy R
- Glenny J
- Glover J
- Glynn Rj
- Godoy Sanchez M
- Goette A
- Goff R
- Goffinet C
- Gohel P
- Goldberg N
- Gomez Sanchez J
- Gonsorcik J
- Gonzales D
- Gonzales V
- Gonzalez E
- Gordeev I
- Gorges R
- Gospodinov K
- Gotcheva N
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- Gould R
- Govindaraj D
- Goyal B
- Goyal S
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- Grable M
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- Graham Ja
- Graif J
- Gralow J
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- Greener R
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- Grundtvig M
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- Gupta M
- Gupta V
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- Guzman P
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- H Hansen
- H Haught
- H Hill
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- Hanustiakova A
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- Hardee L
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- Hartleib M
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- He Z
- Heaney L
- Hecht J
- Heeren G
- Hegedus V
- Heider J
- Heisters J
- Henley L
- Hennig D
- Henriksson A
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- Hernandez I
- Hernandez M
- Hernández N
- Herrman Jp
- Herzog W
- Hess E
- Hettwer Magedanz E
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- Hielscher S
- Higuchi T
- Higuchi Y
- Hilkert R
- Hilton T
- Himpel-Boenninghoff A
- Hinderaker P
- Hioki M
- Hirayama A
- Hiroma J
- Ho Cj
- Hodnett P
- Hoffman M
- Hofsoey K
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- Hollanders G
- Holmes Z
- Holoubek D
- Holscher A
- Hominal M
- Homza M
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- Hong T
- Hoogslag Pam
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- Horak A
- Hornig M
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- Hotchkiss D
- Houra M
- Hristova K
- Hsieh Ic
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- Huang P
- Huang Ph
- Humbert J
- Hurtig U
- Hutchens E
- Huynh T
- Hwang Jj
- Hwang Jj
- Hyun K
- Härstedt N
- Høivik Ho
- I Ilic
- I Ivanov
- Iachini K
- Iannopollo G
- Ibarra J
- Ibarra M
- Ibañez J
- Iby M
- Ichisawa M
- Igbokidi O
- Iijima T
- Ilahi T
- Ilic S
- Ilsley M
- Imbrognio M
- Imre Bs
- Inada T
- Inagaki M
- Indolfi C
- Infusino F
- Invitti C
- Ipp E
- Isaza D
- Istratoaie O
- Istvan Kp
- Iteld B
- Ito K
- Ivan P
- Iveta H
- Izmozherova N
- J Jiang
- J Johnson
- J Johnston
- J Jose
- Jacques G
- Jafri A
- Jafry B
- Jagtap P
- Jaguszewska G
- Jain A
- Jansen M
- Jardula M
- Jayasinghe R
- Jefferson D
- Jenkins R
- Jensen Ed
- Jeric M
- Jerzewski A
- Jeserich M
- Jia Z
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- Jiang X
- Jimenez D
- Jirvankar P
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- Johansen E
- Johansson K
- Johnson E
- Jones S
- Jonsson Je
- Joosten C
- Joshi U
- Julien Ve
- Julião K
- Jure D
- Jure H
- Jutrisa N
- K Kaigawa
- K Katahira
- K Kiroglu
- K Kordic
- K Kostov
- Kabakchieva Vm
- Kaczmarek N
- Kafarakis P
- Kaiserova L
- Kajihara S
- Kala P
- Kaldara E
- Kalina A
- Kalkman C
- Kam J
- Kamensky G
- Kamiya H
- Kamiya J
- Kan G
- Kaneno Y
- Kanitz S
- Kapp I
- Kara Yd
- Karakai H
- Karel I
- Karpuram M
- Karsai Xz
- Kastelein Jjp
- Kataoka M
- Katona A
- Katova T
- Kaur H
- Kawahara M
- Kawai M
- Kawasaki T
- Kawka-Urbanek T
- Kazanskay E
- Ke Y
- Keba E
- Keenan S
- Kelehan S
- Kellnerova I
- Kelly R
- Kelt T
- Kendall T
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- Khan M
- Khan R
- Khan S
- Khariouzov A
- Khirmanov V
- Khromtsova O
- Kick J
- Kiefer R
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- Kim B
- Kim Ks
- Kim M
- Kimmel M
- King A
- King T
- Kirkland S
- Kiss Rg
- Kissel S
- Kitchens D
- Klamm M
- Klein C
- Klein P
- Klemsdal To
- Kleve R
- Klugherz B
- Knight J
- Knutsson A
- Koba M
- Kobalava Z
- Kodem Dr
- Koeitti P
- Koenig W
- Kojima E
- Kok M
- Koldas N
- Koleckar P
- Kolikova V
- Kolleroy C
- Kolokathis F
- Komati S
- Komura Y
- Kondagunta V
- Konradi A
- Kooiman E
- Kopaczewski J
- Kopczyńska M
- Korban E
- Koren M
- Kormann A
- Korte M
- Korth-Wiemann B
- Kose V
- Kosmacheva E
- Kostakou P
- Kostis J
- Kotek L
- Kouz Sm
- Kovacic D
- Kovacs A
- Kozak M
- Kozlova S
- Krapivsky A
- Kreckova M
- Kreutter F
- Krupciakova B
- Krupicka J
- Kuenzler J
- Kulibaba E
- Kulkarni L
- Kullal P
- Kultursay H
- Kumar Ks
- Kumbla M
- Kuntzsch A
- Kuo Jy
- Kuramochi T
- Kuruma T
- Kusnick B
- Kuzin A
- Kyo E
- L Levinson
- L Lim
- L Link
- L Liu
- Laane E
- Labovitz R
- Lachance P
- Lai Wt
- Lail J
- Lainscak M
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- Lamance J
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- Lameira A
- Lamontagne C
- Landers B
- Landolfi A
- Landzberg J
- Lang C
- Langdon J
- Laniec M
- Lappo M
- Lardinois R
- Laszlo Z
- Latheef K
- Laube S
- Lauzon C
- Lavoie W
- Lazov P
- Ledger G
- Lee Hn
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- Lee Jh
- Lee K
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- Lee Sh
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- Leggewie S
- Lehman Kf
- Lehman R
- Lehmann D
- Leimbach W
- Lekakis J
- Lembo G
- Lenderink T
- Lennard M
- Lenner E
- Lennerova J
- Leon S
- Lepage S
- Lepor N
- Lepp H
- Lester F
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- Li X
- Li Y
- Li Y
- Li Y
- Li Yh
- Li Z
- Libby P
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- Libov I
- Lierse T
- Ligueros M
- Lillo J
- Lima F
- Limaye Ap
- Lin T
- Lindholm Cj
- Lindner C
- Liniado G
- Lino E
- Lipchenko A
- Liu B
- Liu B
- Liu Hm
- Liu P
- Liu S
- Liu Y
- Liviu C
- Lock E
- Lohkare M
- Lok Dja
- Long C
- Longaker R
- Lopes R
- Lopez P
- Lorch G
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- Lorenzatti A
- Lousberg A
- Lozhkina N
- Lu Z
- Luciardi H
- Lucksinger G
- Luecke-Uzar M
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- Lukac J
- Lundqvist M
- Lupkovics G
- Luquez H
- Luz Serrano H
- Lv Y
- Lynd S
- Lysek R
- Lönnberg I
- M Malek
- M Mallagray
- M Mandati
- M Mandviwala
- M Marsters
- M Mays
- M Mcdonald
- M Medvegy
- M Meinrich
- M Mikus
- M Milanova
- M Moustafa
- Ma C
- Ma G
- Maboyi S
- Macdonald J
- Macfadyen Jg
- Machova V
- Madder R
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- Maheshwari A
- Maheux K
- Maia L
- Majercak I
- Majul C
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- Makhe B
- Makotoko E
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- Maletz L
- Malhotra S
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- Malik J
- Mancikova I
- Mandic L
- Manenti E
- Manfreda S
- Manga P
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- Manning B
- Mannucci E
- Manolis A
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- Mantas I
- Manuel J
- Manukov D
- Manukov I
- Manyari D
- Manzur F
- Marcela Wenetz Lm
- Marchelletta N
- Marchi Al
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- Marinaro S
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- Maron B
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- Maus O
- Mavromatis K
- Maximov D
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- Maynard R
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- Mbulaiteye A
- Mcalister R
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- Mccrary D Jr
- Mccullough-O'Brien H
- Mcgill J
- Mcgrew F
- Mcintosh C
- Mckenzie A
- Mckenzie C
- Mckibbin A
- Mclaurin B
- Mclellan Ba
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- Mcneill R
- Mcpherson C
- Medina F
- Megalou A
- Mehrle A
- Mehta A
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- Mejia I
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- Mercuro G
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- Militaru C
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- 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.
Search for new phenomena in final states with an energetic jet and large missing transverse momentum in pp collisions at root s = 8 TeV with the ATLAS detector (vol 75, 299, 2015)
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Aben R
- Abi B
- Abolins M
- AbouZeid OS
- Abramowicz H
- Abreu H
- Abreu R
- Abulaiti Y
- Acharya BS
- Adam ER
- Adamczyk L
- Adams DL
- Adelman J
- Adomeit S
- Adye T
- Agatonovic-Jovin T
- Aguilar-Saavedra JA
- Agustoni M
- Ahlen SP
- Ahmadov F
- Aielli G
- Akerstedt H
- Akesson TPA
- Akimoto G
- Akimov AV
- Alberghi GL
- Albert J
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- Alconada Verzini MJ
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- Aleksandrov IN
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- Alexandre G
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- Alimonti G
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- Allbrooke BMM
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- Yen AL
- Yildirim E
- Yildiz HD
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- Yoshihara K
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- Youssef S
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- Yurkewicz A
- Yusuff I
- Zabinski B
- Zaidan R
- Zaitsev AM
- Zaman A
- Zambito S
- Zanello L
- Zanzi D
- Zeitnitz C
- Zeman M
- Zemla A
- Zengel K
- Zenin O
- Zenis T
- Zerwas D
- Zhang D
- Zhang F
- Zhang J
- Zhang L
- Zhang R
- Zhang X
- Zhang Z
- Zhao X
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zhong J
- Zhou B
- Zhou C
- Zhou L
- Zhou L
- Zhou N
- Zhu CG
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann C
- Zimmermann R
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- zur Nedden M
- Zurzolo G
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Results of a search for new phenomena in final states with an energetic jet and large missing transverse momentum are reported. The search uses 20.3 fb−1 of √s=8 TeV data collected in 2012 with the ATLAS detector at the LHC. Events are required to have at least one jet with pT>120 GeV and no leptons. Nine signal regions are considered with increasing missing transverse momentum requirements between EmissT>150 GeV and EmissT>700 GeV. Good agreement is observed between the number of events in data and Standard Model expectations. The results are translated into exclusion limits on models with either large extra spatial dimensions, pair production of weakly interacting dark matter candidates, or production of very light gravitinos in a gauge-mediated supersymmetric model. In addition, limits on the production of an invisibly decaying Higgs-like boson leading to similar topologies in the final state are presented
Search for new phenomena in final states with an energetic jet and large missing transverse momentum in pp collisions at root s = 8 TeV with the ATLAS detector (vol 75, 299, 2015)
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdinov O
- Aben R
- Abi B
- Abolins M
- AbouZeid OS
- Abramowicz H
- Abreu H
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- Abulaiti Y
- Acharya BS
- Adam ER
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- Aguilar-Saavedra JA
- Agustoni M
- Ahlen SP
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- Akesson TPA
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- Akimov AV
- Alberghi GL
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- Alconada Verzini MJ
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- Chalupkova I
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- Chapman JD
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- Charlton DG
- Chau CC
- Cheatham S
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- Chekanov S
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- Chelkov GA
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- Zivkovic L
- Zobernig G
- Zoccoli A
- zur Nedden M
- Zurzolo G
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Measurement of the W±Z boson pair-production cross section in pp collisions at √s=13TeV with the ATLAS detector
- Author
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- Aad G
- Abbott B
- Abdallah J
- Abdinov O
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- Ozcan VE
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- P
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- Schaffer AC
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- Schmidt-Sommerfeld KR
- Schmieden K
- Schmitt C
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- Schmitz S
- Schneider B
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- Schoeffel L
- Schoening A
- Schoenrock BD
- Schopf E
- Schott M
- Schovancova J
- Schramm S
- Schreyer M
- Schroeder TV
- Schuh N
- Schulte A
- Schultens MJ
- Schultz-Coulon H-C
- Schulz H
- Schumacher M
- Schumm BA
- Schune P
- Schwartzman A
- Schwarz TA
- Schwegler P
- Schweiger H
- Schwemling P
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- Schwindling J
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- Sciolla G
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- Seliverstov DM
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- Serfon C
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- Sessa M
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- Sfiligoj T
- Sforza F
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- Shabalina E
- Shaikh NW
- Shan LY
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- Shapiro M
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- Shaw SM
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- Shehu CY
- Sherwood P
- Shi L
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- Shimmin CO
- Shimojima M
- Shiyakova M
- Shmeleva A
- Shochet MJ
- Shojaii S
- Shrestha S
- Shulga E
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- Sicho P
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- Silverstein SB
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- Skottowe HP
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- Slawinska M
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- Smakhtin V
- Smart BH
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- Soloshenko A
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- Stanitzki MM
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- Starchenko EA
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- Stelzer B
- Stelzer HJ
- Stelzer-Chilton O
- Stenzel H
- Stewart GA
- Stillings JA
- Stockton MC
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- Stoicea G
- Stolte P
- Stonjek S
- Stradling AR
- Straessner A
- Stramaglia ME
- Strandberg J
- Strandberg S
- Strandlie A
- Strauss M
- Strizenec P
- Stroehmer R
- Strom DM
- Stroynowski R
- Strubig A
- Stucci SA
- Stugu B
- Styles NA
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- Su J
- Suchek S
- Sugaya Y
- Suk M
- Sulin VV
- Sultansoy S
- Sumida T
- Sun S
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- Sundermann JE
- Suruliz K
- Susinno G
- Sutton MR
- Suzuki S
- Svatos M
- Swiatlowski M
- Sykora I
- Sykora T
- Ta D
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- Taenzer J
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- Takeshita T
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- Talby M
- Talyshev AA
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- Tanaka R
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- Tannenwald BB
- Tapia Araya S
- Tapprogge S
- Tarem S
- Tartarelli GF
- Tas P
- Tasevsky M
- Tashiro T
- Tassi E
- Tavares Delgado A
- Tayalati Y
- Taylor AC
- Taylor GN
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- Tehrani FS
- Teischinger FA
- Teixeira-Dias P
- Temming KK
- Temple D
- Ten Kate H
- Teng PK
- Teoh JJ
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- Testa M
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- Trzebinski M
- Trzupek A
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- Tsiareshka PV
- Tsipolitis G
- Tsirintanis N
- Tsiskaridze S
- Tsiskaridze V
- Tskhadadze EG
- Tsui KM
- Tsukerman II
- Tsulaia V
- Tsuno S
- Tsybychev D
- Tudorache A
- Tudorache V
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- Tupputi SA
- Turchikhin S
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- Turgeman D
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- Tyndel M
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- Ueda I
- Ughetto M
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- Unal G
- Undrus A
- Unel G
- Ungaro FC
- Unno Y
- Unverdorben C
- Urban J
- Urquijo P
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- Usai G
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- Vacek V
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- Valderanis C
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- Valentinetti S
- Valero A
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- Vallecorsa S
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- Van der Deijl PC
- van der Geer R
- van der Graaf H
- van Eldik N
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- Van Nieuwkoop J
- van Vulpen I
- van Woerden MC
- Vanadia M
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- Vanguri R
- Vaniachine A
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- Vardanyan G
- Vari R
- Varnes EW
- Varol T
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- Varvell KE
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- Vazeille F
- Vazquez JGP
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- Veloce LM
- Veloso F
- Veneziano S
- Ventura A
- Venturi M
- Venturi N
- Venturini A
- Vercesi V
- Verducci M
- Verkerke W
- Vermeulen JC
- Vest A
- Vetterli MC
- Viazlo O
- Vichou I
- Vickey T
- Viehhauser GHA
- Viel S
- Vigani L
- Villa M
- Villar DIN
- Vilucchi E
- Vincter MG
- Vinogradov VB
- Vittori C
- Vivarelli I
- Vlachos S
- Vlasak M
- Vogel M
- Vokac P
- Volpi G
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- von der Schmitt H
- von Toerne E
- Vorobel V
- Vorobev K
- Vos M
- Voss R
- Vossebeld JH
- Vranjes N
- Vrba V
- Vreeswijk M
- Vuillermet R
- Vukotic I
- Vykydal Z
- Wagner P
- Wagner W
- Wahlberg H
- Wahrmund S
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- Walder J
- Walker R
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- Wallangen V
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- Warburton A
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- Wardrope DR
- Washbrook A
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- Weber MS
- Weber SW
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- Weidberg AR
- Weinert B
- Weingarten J
- Weiser C
- Weits H
- Wells PS
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- Wengler T
- Wenig S
- Wermes N
- Werner M
- Werner MD
- Werner P
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- Wetter J
- Whalen K
- Whallon NL
- Wharton AM
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- White R
- Whiteson D
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- Wiedenmann W
- Wielers M
- Wienemann P
- Wiglesworth C
- Wiik-Fuchs LAM
- Wildauer A
- Wilk F
- Wilkens HG
- Williams HH
- Williams S
- Willis C
- Willocq S
- Wilson JA
- Wingerter-Seez I
- Winklmeier F
- Winston OJ
- Winter BT
- Wittgen M
- Wittkowski J
- Wolf TMH
- Wolter MW
- Wolters H
- Wong KHY
- Worm SD
- Wosiek BK
- Wotschack J
- Woudstra MJ
- Wozniak KW
- Wu M
- Wu M
- Wu SL
- Wu X
- Wu Y
- Wyatt TR
- Wynne BM
- Xella S
- Xu D
- Xu L
- Yabsley B
- Yacoob S
- Yakabe R
- Yamaguchi D
- Yamaguchi Y
- Yamamoto A
- Yamamoto S
- Yamanaka T
- Yamauchi K
- Yamazaki Y
- Yan Z
- Yang H
- Yang H
- Yang Y
- Yang Z
- Yao W-M
- Yap YC
- Yasu Y
- Yatsenko E
- Ye J
- Ye S
- Yeletskikh I
- Yen AL
- Yildirim E
- Yildiz HD
- Yorita K
- Yoshida R
- Yoshihara K
- Young C
- Young CJS
- Youssef S
- Yu DR
- Yu J
- Yu J
- Yu JM
- Yuan L
- Yuen SPY
- Yusuff I
- Zabinski B
- Zaidan R
- Zaitsev AM
- Zakharchuk N
- Zalieckas J
- Zaman A
- Zambito S
- Zanello L
- Zanzi D
- Zeitnitz C
- Zeman M
- Zemla A
- Zeng JC
- Zeng Q
- Zengel K
- Zenin O
- Zenis T
- Zerwas D
- Zhang D
- Zhang F
- Zhang G
- Zhang H
- Zhang J
- Zhang L
- Zhang R
- Zhang R
- Zhang X
- Zhang Z
- Zhao X
- Zhao Y
- Zhao Z
- Zhemchugov A
- Zhong J
- Zhou B
- Zhou C
- Zhou L
- Zhou L
- Zhou M
- Zhou N
- Zhu CG
- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhukov K
- Zibell A
- Zieminska D
- Zimine NI
- Zimmermann C
- Zimmermann S
- Zinonos Z
- Zinser M
- Ziolkowski M
- Zivkovic L
- Zobernig G
- Zoccoli A
- Zu Theenhausen HM
- zur Nedden M
- Zwalinski L
- Publication venue
- Netherlands
- Publication date
- 01/01/2016
- Field of study
published_or_final_versio
- …