224 research outputs found
Effect of working characteristics and taught ergonomics on the prevalence of musculoskeletal disorders amongst dental students
- Author
- A Garbin
- AJ Diaz-Caballero
- B Adegoke
- B Valachi
- B Valachi
- BL Finkbeiner
- BP McCauley
- C Graham
- CC Norkin
- D Shehab
- DJ Ahearn
- DW Rising
- FE Biller
- G Waddell
- H Dong
- HI Andersson
- J Lake
- J Newton
- K AlâAli
- K Kanteshwari
- Kwai Yee Chew
- M Asmui
- M Hayes
- M Hayes
- MP Maggio
- MVD De Carvalho
- N Pargali
- OO Hokwerda
- P Dajpratham
- P Lindfors
- PA Leggat
- PA Leggat
- RW Marklin
- S Chowanadisai
- S Gupta
- S Kumar
- Saad A Khan
- T James
- T Morse
- T Morse
- W Karwowski
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Jet energy measurement with the ATLAS detector in proton-proton collisions at root s=7 TeV
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdelalim AA
- Abdesselam A
- Abdinov O
- Abi B
- Abolins M
- Abramowicz H
- Abreu H
- Acerbi E
- Acharya BS
- Adams DL
- Addy TN
- Adelman J
- Aderholz M
- Adomeit S
- Adragna P
- Adye T
- Aefsky S
- Aguilar-Saavedra JA
- Aharrouche M
- Ahlen SP
- Ahles F
- Ahmad A
- Ahsan M
- Aielli G
- Akdogana T
- Akesson TPA
- Akimoto G
- Akimov AV
- Akiyama A
- Aktas A
- Alam MA
- Alam MS
- Albert J
- Albrand S
- Aleksa M
- Aleksandrov IN
- Alessandria F
- Alexa C
- Alexander G
- Alexandre G
- Alexopoulos T
- Alhroob M
- Aliev M
- Alimonti G
- Alison J
- Aliyev M
- Allport PP
- Allwood-Spiers SE
- Almenar CC
- Almond J
- Aloisio A
- Alon R
- Alonso A
- Alviggi MG
- Amako K
- Amaral P
- Amelung C
- Ammosov VV
- Amorim A
- Amoros G
- Amram N
- Anastopoulos C
- Ancu LS
- Andari N
- Andeen T
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- Anders G
- Anderson KJ
- Andreazza A
- Andrei V
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- Anh TV
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- Arguin J-F
- Arik E
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- Yilmaz M
- Yoosootiniya R
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- Yurkewicz A
- Zaets VG
- Zaidan R
- Zaitsev AM
- Zajacova Z
- Zalite YK
- Zanello L
- Zarzhitsky P
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- Zenz S
- Zerwas D
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- Zhang D
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- Zhao Z
- Zhemchugov A
- Zheng S
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- Zhu CG
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- Zhu Y
- Zhuang X
- Zhuravlov V
- Zieminska D
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Zinonos Z
- Ziolkowski M
- Zitoun R
- Zivkovic L
- Zmouchko VV
- Zobernig G
- Zoccoli A
- Zolnierowski Y
- Zsenei A
- Zutshi V
- Zwalinski L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/03/2013
- Field of study
The jet energy scale and its systematic uncertainty are determined for jets measured with the ATLAS detector at the LHC in proton-proton collision data at a centre-of-mass energy of âs = 7TeV corresponding to an integrated luminosity of 38 pb-1. Jets are reconstructed with the anti-kt algorithm with distance parameters R=0. 4 or R=0. 6. Jet energy and angle corrections are determined from Monte Carlo simulations to calibrate jets with transverse momenta pTâ„20 GeV and pseudorapidities {pipe}η{pipe}<4. 5. The jet energy systematic uncertainty is estimated using the single isolated hadron response measured in situ and in test-beams, exploiting the transverse momentum balance between central and forward jets in events with dijet topologies and studying systematic variations in Monte Carlo simulations. The jet energy uncertainty is less than 2. 5 % in the central calorimeter region ({pipe}η{pipe}<0. 8) for jets with 60â€pT<800 GeV, and is maximally 14 % for pT<30 GeV in the most forward region 3. 2â€{pipe}η{pipe}<4. 5. The jet energy is validated for jet transverse momenta up to 1 TeV to the level of a few percent using several in situ techniques by comparing a well-known reference such as the recoiling photon pT, the sum of the transverse momenta of tracks associated to the jet, or a system of low-pT jets recoiling against a high-pT jet. More sophisticated jet calibration schemes are presented based on calorimeter cell energy density weighting or hadronic properties of jets, aiming for an improved jet energy resolution and a reduced flavour dependence of the jet response. The systematic uncertainty of the jet energy determined from a combination of in situ techniques is consistent with the one derived from single hadron response measurements over a wide kinematic range. The nominal corrections and uncertainties are derived for isolated jets in an inclusive sample of high-pT jets. Special cases such as event topologies with close-by jets, or selections of samples with an enhanced content of jets originating from light quarks, heavy quarks or gluons are also discussed and the corresponding uncertainties are determined. © 2013 CERN for the benefit of the ATLAS collaboration
Novel Escape Mutants Suggest an Extensive TRIM5α Binding Site Spanning the Entire Outer Surface of the Murine Leukemia Virus Capsid Protein
- Author
- A Kuroishi
- A Reymond
- A Stevens
- AJ McCoy
- B Pacheco
- B Song
- CA Kozak
- D Perez-Caballero
- David C. Goldstone
- DC Goldstone
- DV Faller
- EY Park
- F Diaz-Griffero
- F Lilly
- G Towers
- GB Mortuza
- GB Mortuza
- GB Mortuza
- H Song
- Ian A. Taylor
- J Painter
- Jonathan P. Stoye
- K Kono
- Kate Holden-Dye
- KM Short
- L DesGroseillers
- LC James
- LMJ Ylinen
- LR Boone
- M Bock
- M Sardiello
- M Stremlau
- M Stremlau
- Melvyn W. Yap
- Michael Emerman
- MW Yap
- MW Yap
- MW Yap
- MW Yap
- NA Kootstra
- P Emsley
- P Jolicoeur
- PH Zwart
- PM Pryciak
- PV Maillard
- RM Newman
- S Nisole
- S Ohkura
- Sadayuki Ohkura
- SL Sawyer
- T Hatziioannou
- T Pincus
- T Pincus
- TR Gamble
- W Herr
- W Hofmann
- WE Diehl
- X Wu
- Z Keckesova
- Z Otwinowski
- Publication venue
- Public Library of Science
- Publication date
- 01/03/2011
- Field of study
After entry into target cells, retroviruses encounter the host restriction
factors such as Fv1 and TRIM5α. While it is clear that these factors target
retrovirus capsid proteins (CA), recognition remains poorly defined in the
absence of structural information. To better understand the binding interaction
between TRIM5α and CA, we selected a panel of novel N-tropic murine
leukaemia virus (N-MLV) escape mutants by a serial passage of replication
competent N-MLV in rhesus macaque TRIM5α (rhTRIM5α)-positive cells using
a small percentage of unrestricted cells to allow multiple rounds of virus
replication. The newly identified mutations, many of which involve changes in
charge, are distributed over the outer âtopâ surface of N-MLV CA,
including the N-terminal ÎČ-hairpin, and map up to 29 Ao apart.
Biological characterisation with a number of restriction factors revealed that
only one of the new mutations affects restriction by human TRIM5α,
indicating significant differences in the binding interaction between N-MLV and
the two TRIM5αs, whereas three of the mutations result in dual sensitivity
to Fv1n and Fv1b. Structural studies of two mutants show
that no major changes in the overall CA conformation are associated with escape
from restriction. We conclude that interactions involving much, if not all, of
the surface of CA are vital for TRIM5α binding
Electrochemically synthesized polymers in molecular imprinting for chemical sensing
- Author
- A Aghaei
- A Cutivet
- A Gomez-Caballero
- A GĂłmez-Caballero
- A GĂłmez-Caballero
- A GĂłmez-Caballero
- A Hulanicki
- A Jaramillo
- A McCluskey
- A Menaker
- A Namvar
- A Pietrzyk
- A Pietrzyk
- A Pietrzyk
- A Pietrzyk
- A Pizzariello
- A Ramanaviciene
- A Ramanavicienea
- A Ramanavicius
- A Witkowski
- A Ăpik
- AF Diaz
- AF Diaz
- Agnieszka Pietrzyk-Le
- AJ Heeger
- B Deore
- B Deore
- B Deore
- B Krische
- C Malitesta
- C Malitesta
- C Malitesta
- C Weidlich
- C Xie
- C Xie
- C-H Weng
- C-L Choong
- CK Baker
- CK Chiang
- D Cai
- D Centonze
- D Du
- D Kriz
- D Lakshmi
- DC Apodaca
- DR Albano
- DR Theavenot
- E Granot
- E Hedborg
- E Mazzotta
- E Mazzotta
- E Mazzotta
- E Pardieu
- E Turiel
- E Turiel
- EL Holthoff
- ES Benilda
- ETA Vork
- EV Hauff
- F Huang
- FG Tamayo
- Francis DâSouza
- FTC Moreira
- G Gupta
- G Hagen
- G Heywang
- G Inzelt
- G Inzelt
- G Schopf
- G Tourillon
- G Wegner
- GE Wnek
- GO Buica
- H Liao
- H Okuno
- H Peng
- H Peng
- H Peng
- H Shiigi
- H Shiigi
- H Shiigi
- H Shirakawa
- H Sirringhaus
- HH Weetall
- HH Weetall
- HL Wang
- HL Wang
- HP Welzel
- I Losito
- J Heinze
- J Huang
- J Janata
- J Li
- J Li
- J Li
- J Migdalshi
- J Mostany
- J Rick
- J Zhang
- J Zhang
- J-L Gong
- J-L Gong
- JCC Yu
- JH Burroughes
- JH Schön
- K Kontturi
- K Mosbach
- K-C Ho
- KD Shimizu
- L Feng
- L Ozcan
- L Xia
- L Yang
- L Ăzcan
- LD Spurlock
- LM Kindschy
- M Avila
- M Delamar
- M Dietrich
- M Frasconi
- M Frasconi
- M Riskin
- M Riskin
- M Riskin
- M Trojanowicz
- MC Blanco-Lopez
- MC Blanco-LĂłpez
- N Alizadeh
- N Gupta
- N Luo
- N Sallacan
- NF Atta
- NS Sariciftci
- P Novak
- PAG Cormack
- Piyush S. Sharma
- PM Narula
- PR Teasdale
- Q Ei
- Q Xiao
- R John
- R Noufi
- R Ouyang
- R Pernites
- R Suedee
- RB Pernites
- RJ Ansell
- S Cosnier
- S Huan
- S Kröger
- S Sadki
- S Vidyasankar
- S-W Choi
- SA Hashmi
- SA Piletsky
- SM Richardson-Burns
- SP Ăzkorucuklu
- T Panasyuk
- TA Kerr
- TA Skotheim
- TL Panasyuk
- U Lange
- V Suryanarayanan
- V Syritski
- W Song
- W Wen
- W Zhang
- W Zhaoyang
- W-M Yeh
- Wlodzimierz Kutner
- X FeĂĄs
- X Kan
- X Liu
- Y Kong
- Y Liu
- Y Yasuo
- YT Liu
- YV Meteleva-Fischer
- YV Ulyanova
- Z Chen
- Z Cheng
- Z Gao
- Z Gao
- Z Wang
- Publication venue
- Springer-Verlag
- Publication date
- 01/01/2012
- Field of study
This critical review describes a class of polymers prepared by electrochemical polymerization that employs the concept of molecular imprinting for chemical sensing. The principal focus is on both conducting and nonconducting polymers prepared by electropolymerization of electroactive functional monomers, such as pristine and derivatized pyrrole, aminophenylboronic acid, thiophene, porphyrin, aniline, phenylenediamine, phenol, and thiophenol. A critical evaluation of the literature on electrosynthesized molecularly imprinted polymers (MIPs) applied as recognition elements of chemical sensors is presented. The aim of this review is to highlight recent achievements in analytical applications of these MIPs, including present strategies of determination of different analytes as well as identification and solutions for problems encountered
Amyloid Plaques Beyond AÎČ: A Survey of the Diverse Modulators of Amyloid Aggregation
- Author
- A Abelein
- A Alzheimer
- A Clements
- A Oohira
- A Rhie
- AA Belaidi
- AB Caballero
- AD Cardin
- AD Ellington
- AD Snow
- AD Snow
- AE Roher
- AG Woods
- AI Bush
- AJ Borysik
- AJ Geddes
- AK Buell
- AK Paravastu
- AR Coker
- Assoc. A.s
- AT Alexandrescu
- B Lindahl
- B Liu
- B Regland
- C Haass
- C Scala Di
- C Scala Di
- C Tuerk
- C Ullrich
- CB Jendresen
- CC Liu
- CJ Maynard
- CJ Sarell
- CJ Sarell
- CJ Thalhauser
- CL Masters
- CM Cremers
- CS Atwood
- CW Ritchie
- D Ozawa
- D Proske
- DA Dewitt
- DB Carter
- DHJ Bunka
- DJ Hare
- DJ Selkoe
- DJ Selkoe
- DL Robertson
- DM Holtzman
- DS Yang
- EC Williams
- F Rahimi
- F Ylera
- FL Heppner
- FL Meng
- G Bitan
- G Casadesus
- G Cenini
- G Meisl
- G Perry
- G Szumanska
- GA Tennent
- GM Castillo
- GW Preston
- H Akiyama
- H Cui
- H Jick
- HN Yassine
- HY Shao
- I Bjork
- J Colin
- J Diaz-Nido
- J Fantini
- J Horssen van
- J Kiskis
- J Madine
- J Madine
- J Mayes
- J McLaurin
- J McLaurin
- J McLaurin
- J Shearer
- J Wiltfang
- JA Hardy
- JB Ancsin
- JD Sipe
- JD Sipe
- JJ Valle-Delgado
- JN Rao
- JP Solomon
- JT Pedersen
- JT Pedersen
- JW Karr
- JW Karr
- JW Karr
- JX Lu
- K Annamalai
- K Ikeda
- K Matsuzaki
- K Matsuzaki
- K Simons
- K Steenland
- Katie L. Stewart
- KL Stewart
- L Bergamaschini
- L Bergamaschini
- L Bonar
- L Liao
- L Puglielli
- LA Farrer
- M Calamai
- M Goedert
- M Loef
- M Mold
- M Serra-Batiste
- M So
- M Sobel
- M Wakabayashi
- MB Pepys
- MC Meneghetti
- MC Morris
- MP Burns
- MP Cuajungco
- N Arispe
- N Motamedi-Shad
- N Motamedi-Shad
- N Rezaei-Ghaleh
- NE Shepardson
- NG Faux
- NL Komarova
- P Faller
- P Goloubinoff
- P Wang
- PB Verghese
- PD Dinkel
- PD Gorevic
- PE Fraser
- PK Nandi
- PS Aisen
- PT Wong
- R Bravo
- R Kisilevsky
- R Kisilevsky
- R Kisilevsky
- R Mayeux
- R Tycko
- RA Cherny
- RG Warner
- RLK Virchow
- S Ayton
- S Bourgault
- S Camero
- S Inoue
- S Jha
- SA Khmeleva
- SD Ginsberg
- SD Ginsberg
- SD Jayasena
- Sheena E. Radford
- SI Kim
- SM Butterfield
- T Bitter
- T Eichner
- T Okada
- TCRG Vieira
- TE Audas
- TE Audas
- TG Fletcher
- TPJ Knowles
- TR Rudd
- V Tougu
- VM Perreau
- W Kim
- W Li
- WA Gunderson
- WJ Huang
- WJ Strittmatter
- XD Huang
- Y Shafrir
- YWA Huang
- ZS Khachaturian
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 19/06/2017
- Field of study
Aggregation of the amyloid-ÎČ (AÎČ) peptide is strongly correlated with Alzheimerâs disease (AD). Recent research has improved our understanding of the kinetics of amyloid fibril assembly and revealed new details regarding different stages in plaque formation. Presently, interest is turning toward studying this process in a holistic context, focusing on cellular components which interact with the AÎČ peptide at various junctures during aggregation, from monomer to cross-ÎČ amyloid fibrils. However, even in isolation, a multitude of factors including protein purity, pH, salt content, and agitation affect AÎČ fibril formation and deposition, often producing complicated and conflicting results. The failure of numerous inhibitors in clinical trials for AD suggests that a detailed examination of the complex interactions that occur during plaque formation, including binding of carbohydrates, lipids, nucleic acids, and metal ions, is important for understanding the diversity of manifestations of the disease. Unraveling how a variety of key macromolecular modulators interact with the AÎČ peptide and change its aggregation properties may provide opportunities for developing therapies. Since no protein acts in isolation, the interplay of these diverse molecules may differentiate disease onset, progression, and severity, and thus are worth careful consideration
Multi-messenger observations of a binary neutron star merger
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- Zhang B-B
- Zhang C
- Zhang CL
- Zhang CM
- Zhang F
- Zhang H
- Zhang HM
- Zhang J
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- Zhang Y
- Zhang Y
- Zhang Y-H
- Zhang YF
- Zhang YJ
- Zhang Z
- Zhang ZL
- Zhao C
- Zhao HS
- Zhao JL
- Zhao W
- Zhao XF
- Zheng SJ
- Zhou H
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- Zhou M
- Zhou Z
- Zhu SJ
- Zhu XJ
- Zhu Y
- Zhu YX
- Zhu Z
- Ziegler A
- Zimmerman AB
- Zimmermann B
- Zimnukhov DS
- Ziolkowski M
- Zoll M
- Zong Z
- Zorn J
- Zornoza JD
- Zou CL
- Zuccarello F
- Zucker ME
- Zuniga J
- Zweizig J
- Zywucka N
- Publication venue
- 'American Astronomical Society'
- Publication date
- 01/01/2017
- Field of study
On 2017 August 17 a binary neutron star coalescence candidate (later designated GW170817) with merger time 12:41:04 UTC was observed through gravitational waves by the Advanced LIGO and Advanced Virgo detectors. The Fermi Gamma-ray Burst Monitor independently detected a gamma-ray burst (GRB 170817A) with a time delay of ~1.7 s with respect to the merger time. From the gravitational-wave signal, the source was initially localized to a sky region of 31 deg2 at a luminosity distance of 40+8-8 Mpc and with component masses consistent with neutron stars. The component masses were later measured to be in the range 0.86 to 2.26 Mo. An extensive observing campaign was launched across the electromagnetic spectrum leading to the discovery of a bright optical transient (SSS17a, now with the IAU identification of AT 2017gfo) in NGC 4993 (at ~40 Mpc) less than 11 hours after the merger by the One- Meter, Two Hemisphere (1M2H) team using the 1 m Swope Telescope. The optical transient was independently detected by multiple teams within an hour. Subsequent observations targeted the object and its environment. Early ultraviolet observations revealed a blue transient that faded within 48 hours. Optical and infrared observations showed a redward evolution over ~10 days. Following early non-detections, X-ray and radio emission were discovered at the transientâs position ~9 and ~16 days, respectively, after the merger. Both the X-ray and radio emission likely arise from a physical process that is distinct from the one that generates the UV/optical/near-infrared emission. No ultra-high-energy gamma-rays and no neutrino candidates consistent with the source were found in follow-up searches. These observations support the hypothesis that GW170817 was produced by the merger of two neutron stars in NGC4993 followed by a short gamma-ray burst (GRB 170817A) and a kilonova/macronova powered by the radioactive decay of r-process nuclei synthesized in the ejecta
Localization and broadband follow-up of the gravitational-wave transient GW150914
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- Zweizig J
- Publication venue
- Astrophysical Journal Letters
- Publication date
- 01/01/2016
- Field of study
A gravitational-wave (GW) transient was identified in data recorded by the Advanced Laser Interferometer Gravitational-wave Observatory (LIGO) detectors on 2015 September 14. The event, initially designated G184098 and later given the name GW150914, is described in detail elsewhere. By prior arrangement, preliminary estimates of the time, significance, and sky location of the event were shared with 63 teams of observers covering radio, optical, near-infrared, X-ray, and gamma-ray wavelengths with ground- and space-based facilities. In this Letter we describe the low-latency analysis of the GW data and present the sky localization of the first observed compact binary merger. We summarize the follow-up observations reported by 25 teams via private Gamma-ray Coordinates Network circulars, giving an overview of the participating facilities, the GW sky localization coverage, the timeline, and depth of the observations. As this event turned out to be a binary black hole merger, there is little expectation of a detectable electromagnetic (EM) signature. Nevertheless, this first broadband campaign to search for a counterpart of an Advanced LIGO source represents a milestone and highlights the broad capabilities of the transient astronomy community and the observing strategies that have been developed to pursue neutron star binary merger events. Detailed investigations of the EM data and results of the EM follow-up campaign are being disseminated in papers by the individual teams
A922 Sequential measurement of 1 hour creatinine clearance (1-CRCL) in critically ill patients at risk of acute kidney injury (AKI)
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- Filipe E
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- Frithiof R
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- Gainnier M
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- Gajic O
- Galache JA
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- Garnacho-Montero J
- Garrido BB
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- Garrouste M
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- Gattinoni L
- Gaudard P
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- Hatakeyama J
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- Jardim JJ
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- JSEPTIC (Japanese Society of Education for Physicians and Trainees in Intensive Care) Clinical Trial Group
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- Karanjia N
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- Kokkini S
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- Lebiedz P
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- Lebut J
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- Maggiorini M
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- PĂ©rez LP
- Qiu H
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- Quintana S
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- Rapid Diagnosis of Infections in the Critically Ill Team
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- Runge I
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- Rutherford WB
- Rutten AM
- Rydingsward JE
- Saadat F
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- Sadamoto Y
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- Sandiumenge A
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- Santiago AI
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- Sanui M
- Sanz ER
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- Sanz NM
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- Sawamura A
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- Scales DC
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- Sciurti R
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- Spadaro S
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- Spronk PE
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- Sprung CL
- St Georgeâs University of London
- Stamm J
- Stamouli M
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- Starczewska M
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- Stretti F
- Struijs A
- Stubbs C
- Stubbs C
- Student Research Committee - Shiraz University of Medical Sciences
- StĂŒmpfle R
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- Su F
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- Suchomel P
- Suh GJ
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- SĂĄnchez MJ
- SĂĄnchez MJ
- SĂĄnchez MJ
- SĂĄnchez MJ
- SĂĄnchez MJ
- SĂĄnchez PC
- SĂĄnchez PC
- SĂĄnchez-Elvira LA
- Tabatabaei HR
- Tabei SH
- Taccone F
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- Tokyo Womens Medical University
- Tomas E
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- Tsukahara K
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- van der Hoeven JG
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- van Wijk A
- Vandijck D
- Vaneker I
- Vanhuyse F
- Vaporidi K
- Vaquerizo C
- Varas GM
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- Varea MM
- Vargiolu A
- Varma A
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- Vatsik MV
- Vazquez D
- Vedage D
- Vega LM
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- Venn R
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- Vincent JL
- Vincent JL
- Vincent JL
- Vincent JL
- Vinje LJ
- Vinsonneau C
- Vitaller S
- Vittone F
- Vogelaers D
- Voiriot G
- Volker T
- Volta CA
- Volta CA
- Vondrakova D
- Vondrakova D
- Vondrakova D
- Vong LV
- Vourli S
- Vrettou C
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- VĂĄzquez CF
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- Wada T
- Wada T
- Wada T
- Wada T
- Waldauf P
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- Wang CH
- Wang H
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- Wann SR
- Wathanawatthu T
- Wee S
- Welte T
- Welters I
- Wetz A
- Weyer CM
- White C
- Wiesner O
- Wijayatilake DS
- Wildenberg L
- Wilks M
- Wilson ME
- WIND study group
- WIND study group
- WIND study group
- Winder-Rhodes S
- Witter T
- Wolf M
- Wolff M
- Wong Y
- Wood B
- Wood CA
- Wood D
- Wood M
- Wray J
- Xie Z
- Xini A
- Xini A
- Xiol EA
- Xu M
- Yager T
- Yaguchi A
- Yaguchi A
- Yamaguchi O
- Yamaguchi O
- Yamaguchi Y
- Yamaguchi Y
- Yamamoto H
- Yamamoto N
- Yaman G
- Yamashita K
- Yamazaki A
- Yan WW
- Yan WW
- Yang JH
- Yang JS
- Yang YL
- Yasuda H
- Yatabe T
- Yebenes JC
- Yeh YC
- Yemets H
- Yergaliyeva A
- Yılmaz G
- Yilmazer F
- Yodice P
- Yokoyama M
- Yonis H
- Yonis H
- Yonis H
- Yoon SZ
- Yoruk F
- Yoshida K
- Yoshida T
- Yoshida T
- Yoshida T
- Yoshida T
- Yoshihiro S
- Yoshitake E
- You KM
- Youn AM
- Young A
- Yu KM
- Yumoto T
- Yuzawa J
- Yuzawa J
- Zabaletta WJ
- Zabini D
- Zahorec M
- Zaien I
- Zakynthinos S
- Zanello M
- Zani D
- Zarantonello F
- Zayas B
- Zepeda EM
- Zeroual N
- Zerva L
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- Zhou JC
- Zhou JC
- Zhou JX
- Zhovnir V
- Zibandah N
- Zijlstra F
- Zimmerman J
- Zogheib E
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- Zogheib E
- Zullino V
- Zwaag J
- ZĂœkovĂĄ I
- Ălvarez JT
- Ălvarez-Lerma F
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Meeting abstrac
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 PÄ
- 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
- 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
- Burton C
- Burton J
- Burton M
- Burtt D
- Busak L
- Busic N
- Byars W
- BĂžen 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
- Carrillo J
- Caruso G
- Casala J
- Caso P
- Casoinic F
- Castillo J
- Castillo T
- Cech V
- Cei L
- 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
- Chattin W
- Chauhan D
- Chauhan H
- Chaussé I
- Chavada J
- Chaverra I
- Chaware G
- Chee L
- Chella S
- Chen Cp
- 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
- Coman S
- Commerford P
- Commerford P
- Conrado Y
- Cools F
- Cornel Jh
- Corona V
- Coronel J
- Cosgrove N
- Cosgrove S
- Cosmi F
- Costa Amorim R
- Coufalova Z
- Covell W
- Cox B
- Cox R
- Craig W
- Crandall L
- Crawford G
- Crea F
- Crepps K
- Crocamo A
- Cromer M
- Cruz H
- Cruz H
- Cruz M
- Csala L
- Cucher F
- Cuentas I
- Cuervo A
- Curiac D
- Cymerman K
- Cyprian R
- Czerski T
- D'Amours Dg
- D Dash
- D Dattani
- D Denham
- D Desai
- D Desalle
- D Digangi
- D Dunn
- Da Costa F
- Da Silva A
- Da Silva D Jr
- Da Silva O Jr
- Dahlen G
- Dalseg Am
- Damron M
- Danik J
- Davalos C
- 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
- Demidova M
- Den Hartog F
- Denecke C
- 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
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- Zineldine A.
- Zirlik A
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- 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-1ÎČ, 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-1ÎČ 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.
Observation of a New Excited Beauty Strange Baryon Decaying to Îb- Ï+Ï-
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbrescia M
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- Ăzçelik Ă
- Publication venue
- American Physical Society
- Publication date
- 01/01/2021
- Field of study
The Îb-Ï+Ï- 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 Îb- is reconstructed via its decays to J/ÏÎ- and J/ÏÎK-. A narrow resonance, labeled Îb(6100)-, is observed at a Îb-Ï+Ï- invariant mass of 6100.3±0.2(stat)±0.1(syst)±0.6(Îb-) MeV, where the last uncertainty reflects the precision of the Îb- baryon mass. The upper limit on the Îb(6100)- natural width is determined to be 1.9 MeV at 95% confidence level. The low Îb(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 Îc baryon states, the new Îb(6100)- resonance and its decay sequence are consistent with the orbitally excited Îb- baryon, with spin and parity quantum numbers JP=3/2-
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