211 research outputs found
Measurement of the Bottom-Strange Meson Mixing Phase in the Full CDF Data Set
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- Tooze SA
- Torre
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- Totaro
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- Travassos LH
- Trovato
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- Uozumi
- V.
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- V.E.
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- Velev
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- Vázquez
- W.
- W.
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- Warburton
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- Wester
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- Wicklund
- Wicklund
- Wilbur
- Williams
- Wilson
- Wilson
- Winer
- Wittich
- Wolbers
- Wolfe
- Wright
- Wu
- Wu
- X.
- Y.
- Y.
- Y.
- Y.
- Y.
- Y.
- Y.
- Y.
- Y.C.
- Y.C.
- Y.D.
- Y.J.
- Y.K.
- Y.S.
- Yamamoto
- Yamato
- Yang
- Yang
- Yang
- Yao
- Yeh
- Yi
- Yoh
- Yorita
- Yoshida
- Yu
- Yu
- Yu
- Yun
- Z.
- Zanetti
- Zeng
- Zhou
- Zucchelli
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2012
- Field of study
We report a measurement of the bottom-strange meson mixing phase \beta_s
using the time evolution of B0_s -> J/\psi (->\mu+\mu-) \phi (-> K+ K-) decays
in which the quark-flavor content of the bottom-strange meson is identified at
production. This measurement uses the full data set of proton-antiproton
collisions at sqrt(s)= 1.96 TeV collected by the Collider Detector experiment
at the Fermilab Tevatron, corresponding to 9.6 fb-1 of integrated luminosity.
We report confidence regions in the two-dimensional space of \beta_s and the
B0_s decay-width difference \Delta\Gamma_s, and measure \beta_s in [-\pi/2,
-1.51] U [-0.06, 0.30] U [1.26, \pi/2] at the 68% confidence level, in
agreement with the standard model expectation. Assuming the standard model
value of \beta_s, we also determine \Delta\Gamma_s = 0.068 +- 0.026 (stat) +-
0.009 (syst) ps-1 and the mean B0_s lifetime, \tau_s = 1.528 +- 0.019 (stat) +-
0.009 (syst) ps, which are consistent and competitive with determinations by
other experiments.Comment: 8 pages, 2 figures, Phys. Rev. Lett 109, 171802 (2012
Performance of CMS muon reconstruction in pp collision events at sqrt(s) = 7 TeV
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Acosta D
- Acosta JG
- Acosta MV
- Adair A
- Adam N
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- Romeo F
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- Sfiligoi I
- Sguazzoni G
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- Sharma A
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- Sharp P
- Sheldon P
- Shepherd-Themistocleous CH
- Shi X
- Shipkowski SP
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- Tsang KV
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- Yilmaz Y
- Yohay R
- Yoo HD
- Yoo J
- Yoon AS
- York A
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- Yumiceva F
- Yun JC
- Zabel J
- Zabi A
- Zablocki J
- Zaganidis N
- Zakaria M
- Zalewski P
- Zanetti M
- Zang J
- Zang SL
- Zarubin A
- Zatserklyaniy A
- Zeinali M
- Zeise M
- Zeuner WD
- Zeyrek M
- Zhang J
- Zhang Z
- Zheng Y
- Zhokin A
- Zhu B
- Zhu RY
- Zhukov V
- Zhukova V
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- Zoeller MH
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- Zumerle G
- Zuranski A
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2012
- Field of study
The performance of muon reconstruction, identification, and triggering in CMS
has been studied using 40 inverse picobarns of data collected in pp collisions
at sqrt(s) = 7 TeV at the LHC in 2010. A few benchmark sets of selection
criteria covering a wide range of physics analysis needs have been examined.
For all considered selections, the efficiency to reconstruct and identify a
muon with a transverse momentum pT larger than a few GeV is above 95% over the
whole region of pseudorapidity covered by the CMS muon system, abs(eta) < 2.4,
while the probability to misidentify a hadron as a muon is well below 1%. The
efficiency to trigger on single muons with pT above a few GeV is higher than
90% over the full eta range, and typically substantially better. The overall
momentum scale is measured to a precision of 0.2% with muons from Z decays. The
transverse momentum resolution varies from 1% to 6% depending on pseudorapidity
for muons with pT below 100 GeV and, using cosmic rays, it is shown to be
better than 10% in the central region up to pT = 1 TeV. Observed distributions
of all quantities are well reproduced by the Monte Carlo simulation.Comment: Replaced with published version. Added journal reference and DO
Performance of CMS muon reconstruction in pp collision events at sqrt(s) = 7 TeV
- Author
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- Wissing C
- Wittich P
- Wittmer B
- Woehri HK
- Wolf M
- Wolf R
- Womersley WJ
- Won S
- Wood D
- Wood J
- Wood JS
- Worm SD
- Wright D
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- Wuerthwein F
- Wulz C-E
- Wyslouch B
- Xiao H
- Xie S
- Xu M
- Yagil A
- Yalvac M
- Yang F
- Yang M
- Yang Y
- Yang ZC
- Yazgan E
- Yelton J
- Yetkin T
- Yi K
- Yildirim E
- Yilmaz Y
- Yohay R
- Yoo HD
- Yoo J
- Yoon AS
- York A
- Yu I
- Yu SS
- Yumiceva F
- Yun JC
- Zabel J
- Zabi A
- Zablocki J
- Zaganidis N
- Zakaria M
- Zalewski P
- Zanetti M
- Zang J
- Zang SL
- Zarubin A
- Zatserklyaniy A
- Zeinali M
- Zeise M
- Zeuner WD
- Zeyrek M
- Zhang J
- Zhang Z
- Zheng Y
- Zhokin A
- Zhu B
- Zhu RY
- Zhukov V
- Zhukova V
- Ziebarth EB
- Ziegler J
- Zielinski M
- Zito G
- Zoeller MH
- Zotto P
- Zou W
- Zumerle G
- Zuranski A
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2012
- Field of study
The performance of muon reconstruction, identification, and triggering in CMS
has been studied using 40 inverse picobarns of data collected in pp collisions
at sqrt(s) = 7 TeV at the LHC in 2010. A few benchmark sets of selection
criteria covering a wide range of physics analysis needs have been examined.
For all considered selections, the efficiency to reconstruct and identify a
muon with a transverse momentum pT larger than a few GeV is above 95% over the
whole region of pseudorapidity covered by the CMS muon system, abs(eta) < 2.4,
while the probability to misidentify a hadron as a muon is well below 1%. The
efficiency to trigger on single muons with pT above a few GeV is higher than
90% over the full eta range, and typically substantially better. The overall
momentum scale is measured to a precision of 0.2% with muons from Z decays. The
transverse momentum resolution varies from 1% to 6% depending on pseudorapidity
for muons with pT below 100 GeV and, using cosmic rays, it is shown to be
better than 10% in the central region up to pT = 1 TeV. Observed distributions
of all quantities are well reproduced by the Monte Carlo simulation.Comment: Replaced with published version. Added journal reference and DO
X-ray emission from the Sombrero galaxy: discrete sources
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Acosta D
- Acosta JG
- Acosta MV
- Adam N
- Adam W
- Adams MR
- Adams T
- Adiguzel A
- Adler V
- Adzic P
- Agostino L
- Agram JL
- Aguilar-Benitez M
- Aguilo E
- Ahmad M
- Ahmad WH
- Ahmed I
- Ahuja S
- Akchurin N
- Akgun B
- Akgun U
- Akin IV
- Alagoz E
- Albajar C
- Albayrak EA
- Albergo S
- Albrow M
- Alexander J
- Aliev T
- Allfrey P
- Almeida N
- Alver B
- Alverson G
- Alves GA
- Amapane N
- Amsler C
- Anagnostou G
- Anastassov A
- Anderson J
- Anderson M
- Andrea J
- Andreev V
- Andreev V
- Andreev Y
- Andrews W
- Anghel IM
- Antonelli L
- Antunes JR
- Antunovic Z
- Apanasevich L
- Apollinari G
- Appelt E
- Aranyi A
- Arce P
- Arcidiacono R
- Arenton MW
- Arfaei H
- Argiro S
- Arisaka K
- Arneodo M
- Asaadi J
- Asghar MI
- Askew A
- Ata M
- Atac M
- Atramentov O
- Attikis A
- Auffray E
- Autermann C
- Auzinger G
- Avery P
- Avetisyan A
- Awad A
- Azarkin M
- Azhgirey I
- Aziz T
- Azzi P
- Azzolini V
- Azzurri P
- Baarmand MM
- Babb J
- Bacchetta N
- Bachtis M
- Baden A
- Baesso P
- Baffioni S
- Bagliesi G
- Bai Y
- Baillon P
- Bainbridge R
- Bakhshiansohi H
- Bakirci MN
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- Yilmaz Y
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- Ziebarth EB
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- Zorbilmez C
- Zotto P
- Zou W
- Zumerle G
- Zuranski A
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2010
- Field of study
We present a study of discrete X-ray sources in and around the
bulge-dominated, massive Sa galaxy, Sombrero (M104), based on new and archival
Chandra observations with a total exposure of ~200 ks. With a detection limit
of L_X = 1E37 erg/s and a field of view covering a galactocentric radius of ~30
kpc (11.5 arcminute), 383 sources are detected. Cross-correlation with Spitler
et al.'s catalogue of Sombrero globular clusters (GCs) identified from HST/ACS
observations reveals 41 X-rays sources in GCs, presumably low-mass X-ray
binaries (LMXBs). We quantify the differential luminosity functions (LFs) for
both the detected GC and field LMXBs, whose power-low indices (~1.1 for the
GC-LF and ~1.6 for field-LF) are consistent with previous studies for
elliptical galaxies. With precise sky positions of the GCs without a detected
X-ray source, we further quantify, through a fluctuation analysis, the GC LF at
fainter luminosities down to 1E35 erg/s. The derived index rules out a
faint-end slope flatter than 1.1 at a 2 sigma significance, contrary to recent
findings in several elliptical galaxies and the bulge of M31. On the other
hand, the 2-6 keV unresolved emission places a tight constraint on the field
LF, implying a flattened index of ~1.0 below 1E37 erg/s. We also detect 101
sources in the halo of Sombrero. The presence of these sources cannot be
interpreted as galactic LMXBs whose spatial distribution empirically follows
the starlight. Their number is also higher than the expected number of cosmic
AGNs (52+/-11 [1 sigma]) whose surface density is constrained by deep X-ray
surveys. We suggest that either the cosmic X-ray background is unusually high
in the direction of Sombrero, or a distinct population of X-ray sources is
present in the halo of Sombrero.Comment: 11 figures, 5 tables, ApJ in pres
Performance of the CMS Cathode Strip Chambers with Cosmic Rays
- Author
- Abadjiev K
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abelev B
- Acosta D
- Acosta JG
- Acosta MV
- Actis O
- Adam N
- Adam W
- Adams MR
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- Adiguzel A
- Adler V
- Adolphi R
- Adzic P
- Afaq MA
- Agostino L
- Agram JL
- Aguilar-Benitez M
- Ahmad M
- Ahmad WH
- Ahmed I
- Ahmed W
- Ahuja S
- Aisa D
- Aisa S
- Akchurin N
- Akgun B
- Akgun U
- Akimenko S
- Akin IV
- Alagoz E
- Alampi G
- Albajar C
- Albayrak EA
- Alberdi J
- Albergo S
- Albert E
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- Alexander J
- Alidra M
- Aliev T
- Allfrey P
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- Altenhofer G
- Altsybeev I
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- Alves GA
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- Ambroglini F
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- Ananthan B
- Anastassov A
- Andelin D
- Anderson M
- Andrea J
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- Andreev Y
- Anghel IM
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- Yaselli I
- Yazgan E
- Yelton J
- Yetkin T
- Yi K
- Yilmaz Y
- Yohay R
- Yoo HD
- Yoon AS
- York A
- Yumiceva F
- Yun JC
- Yuste C
- Zabi A
- Zabolotny W
- Zachariadou A
- Zalewski P
- Zampieri A
- Zanetti M
- Zang SL
- Zarubin A
- Zatzerklyany A
- Zeidler C
- Zeinali M
- Zeise M
- Zelepoukine S
- Zeuner WD
- Zeyrek M
- Zhang J
- Zhang L
- Zhang Y
- Zhang Z
- Zheng Y
- Zhiltsov V
- Zhokin A
- Zhu B
- Zhu K
- Zhu RY
- Zhukov V
- Zhukova V
- Ziebarth EB
- Zielinski M
- Zilizi G
- Zinonos Z
- Zito G
- Zoeller MH
- Zotto P
- Zub S
- Zumerle G
- Zuranski A
- Zuyeuski R
- Zych P
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2009
- Field of study
The Cathode Strip Chambers (CSCs) constitute the primary muon tracking device
in the CMS endcaps. Their performance has been evaluated using data taken
during a cosmic ray run in fall 2008. Measured noise levels are low, with the
number of noisy channels well below 1%. Coordinate resolution was measured for
all types of chambers, and fall in the range 47 microns to 243 microns. The
efficiencies for local charged track triggers, for hit and for segments
reconstruction were measured, and are above 99%. The timing resolution per
layer is approximately 5 ns
Nodal-Dependent Mesendoderm Specification Requires the Combinatorial Activities of FoxH1 and Eomesodermin
- Author
- A Kispert
- AE Bruce
- AF Schier
- AF Schier
- AP Russ
- B Feldman
- B Feldman
- BJ Graves
- BW Bisgrove
- BW Bisgrove
- C Grande
- C Larroux
- C Thisse
- C Wasylyk
- CE Erter
- Christopher E. Slagle
- CR Bjornson
- DP Norris
- DY Stainier
- E Labbe
- EC Liao
- F Lapraz
- F Lim
- F Mazet
- G Zhu
- HI Sirotkin
- HK Chea
- HM Pogoda
- I von Both
- J Alexander
- J Alexander
- J Hagman
- JC Baker
- JE Kugler
- JK Yu
- JN Chen
- K Baetz
- K Gritsman
- K Ryan
- KJ Griffin
- L Izzi
- L Solnica-Krezel
- LA Trinh
- M Brand
- M Fukuda
- M Hammerschmidt
- M Howell
- M Kofron
- M Whitman
- M Yamamoto
- Mary C. Mullins
- ME Halpern
- MM Shen
- MR Rebagliati
- P Haffter
- P Herbomel
- P Picozzi
- PA Hoodless
- PS Kunwar
- Q Tu
- RA Randall
- Rebecca D. Burdine
- S Karlen
- S Krauss
- S Krauss
- S Long
- S Schulte-Merker
- S Sokol
- SE Stachel
- SI Osada
- SJ Arnold
- T Adell
- T Aoki
- Tsutomu Aoki
- U Strahle
- W Driever
- W Pei
- W Pei
- W Weng
- WS Talbot
- X Chen
- X Fan
- Y Kikuchi
- Y Kikuchi
- Y Saijoh
- Y Zhang
- YL Yan
- Publication venue
- Public Library of Science
- Publication date
- 01/05/2011
- Field of study
Vertebrate mesendoderm specification requires the Nodal signaling pathway and its transcriptional effector FoxH1. However, loss of FoxH1 in several species does not reliably cause the full range of loss-of-Nodal phenotypes, indicating that Nodal signals through additional transcription factors during early development. We investigated the FoxH1-dependent and -independent roles of Nodal signaling during mesendoderm patterning using a novel recessive zebrafish FoxH1 mutation called midway, which produces a C-terminally truncated FoxH1 protein lacking the Smad-interaction domain but retaining DNA–binding capability. Using a combination of gel shift assays, Nodal overexpression experiments, and genetic epistasis analyses, we demonstrate that midway more accurately represents a complete loss of FoxH1-dependent Nodal signaling than the existing zebrafish FoxH1 mutant schmalspur. Maternal-zygotic midway mutants lack notochords, in agreement with FoxH1 loss in other organisms, but retain near wild-type expression of markers of endoderm and various nonaxial mesoderm fates, including paraxial and intermediate mesoderm and blood precursors. We found that the activity of the T-box transcription factor Eomesodermin accounts for specification of these tissues in midway embryos. Inhibition of Eomesodermin in midway mutants severely reduces the specification of these tissues and effectively phenocopies the defects seen upon complete loss of Nodal signaling. Our results indicate that the specific combinations of transcription factors available for signal transduction play critical and separable roles in determining Nodal pathway output during mesendoderm patterning. Our findings also offer novel insights into the co-evolution of the Nodal signaling pathway, the notochord specification program, and the chordate branch of the deuterostome family of animals
Genetic Diversity and Protective Efficacy of the RTS,S/AS01 Malaria Vaccine.
- Author
- Abdulla S
- Adjei S
- Agbenyega T
- Agnandji ST
- Aide P
- Anderson S
- Ansong D
- Aponte JJ
- Asante KP
- Bedford T
- Bejon P
- Benkeser D
- Birkett AJ
- Birren BW
- Bruls M
- Connolly KM
- D'Alessandro U
- Dobaño C
- Gesase S
- Gilbert PB
- Greenwood B
- Griggs A
- Grimsby J
- Hamel MJ
- Hoffman I
- Juraska M
- Kamthunzi P
- Kariuki S
- Kremsner PG
- Lapierre D
- Leach A
- Lell B
- Lennon NJ
- Lievens M
- Lusingu J
- Marsh K
- Martinson F
- Molel JT
- Moss EL
- Neafsey DE
- Njuguna P
- Ockenhouse CF
- Ogutu B Ragama
- Otieno K
- Otieno L
- Otieno W
- Owusu-Agyei S
- Park DJ
- Pellé K
- Robbins D
- Russ C
- Ryan EM
- Sacarlal J
- Sogoloff B
- Sorgho H
- Tanner M
- Theander T
- Tinto H
- Valea I
- Valim C
- Volkman SK
- Wirth DF
- Yu Q
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 19/11/2015
- Field of study
BACKGROUND: The RTS,S/AS01 vaccine targets the circumsporozoite protein of Plasmodium falciparum and has partial protective efficacy against clinical and severe malaria disease in infants and children. We investigated whether the vaccine efficacy was specific to certain parasite genotypes at the circumsporozoite protein locus. METHODS: We used polymerase chain reaction-based next-generation sequencing of DNA extracted from samples from 4985 participants to survey circumsporozoite protein polymorphisms. We evaluated the effect that polymorphic positions and haplotypic regions within the circumsporozoite protein had on vaccine efficacy against first episodes of clinical malaria within 1 year after vaccination. RESULTS: In the per-protocol group of 4577 RTS,S/AS01-vaccinated participants and 2335 control-vaccinated participants who were 5 to 17 months of age, the 1-year cumulative vaccine efficacy was 50.3% (95% confidence interval [CI], 34.6 to 62.3) against clinical malaria in which parasites matched the vaccine in the entire circumsporozoite protein C-terminal (139 infections), as compared with 33.4% (95% CI, 29.3 to 37.2) against mismatched malaria (1951 infections) (P=0.04 for differential vaccine efficacy). The vaccine efficacy based on the hazard ratio was 62.7% (95% CI, 51.6 to 71.3) against matched infections versus 54.2% (95% CI, 49.9 to 58.1) against mismatched infections (P=0.06). In the group of infants 6 to 12 weeks of age, there was no evidence of differential allele-specific vaccine efficacy. CONCLUSIONS: These results suggest that among children 5 to 17 months of age, the RTS,S vaccine has greater activity against malaria parasites with the matched circumsporozoite protein allele than against mismatched malaria. The overall vaccine efficacy in this age category will depend on the proportion of matched alleles in the local parasite population; in this trial, less than 10% of parasites had matched alleles. (Funded by the National Institutes of Health and others.)
A well-kept treasure at depth: precious red coral rediscovered in Atlantic deep coral gardens (SW Portugal) after 300 years
- Author
- A Castric-Fey
- A Drummond
- A Gori
- A Sáenz-Arroyo
- A Tursi
- AA Baldaque da Silva
- AT Tozzeti
- AW Bruckner
- B Horta e Costa
- B Winnepenninckx
- BW Brook
- C Carpine
- C Cerrano
- C Cerrano
- C Linares
- C Marschal
- C Priori
- CG Jones
- Christian Marschal
- CL Doughty
- D Al-Abdulrazzak
- D Aurelle
- D Pauly
- D Vielzeuf
- DA Brazeau
- Didier Aurelle
- Diogo Paulo
- Ester A. Serrão
- F Costantini
- F Costantini
- F Mineur
- F Oliveira
- G Bavestrello
- G Reverdin
- G Russ
- G Santangelo
- G Santangelo
- G Santangelo
- G Tsounis
- G Tsounis
- G Tsounis
- G Tsounis
- H Zibrowius
- H Zibrowius
- HJ Bandelt
- HK Alleway
- HR Lasker
- HR Lasker
- I Gallmetzer
- I Montero-Serra
- J Garrabou
- J Garrabou
- J Hall-Spencer
- J Movilla
- J Sambrook
- JB Andrada e Silva
- JB Boavida
- JBS Lopes
- JF Assis
- JK Reed
- JK Reed
- JMS Gonçalves
- Joana Boavida
- John Reed
- Jorge M. S. Gonçalves
- JT Allen
- K Robert
- L Bramanti
- L Bramanti
- L De Lobo CB
- L McClenachan
- L Watling
- L-A Henry
- L-A Henry
- M Angiolillo
- M García-Rodríguez
- M Slattery
- M Vázquez-Rodríguez
- N Gotelli
- N Gotelli
- N Pinardi
- O Torrents
- P Cárdenas
- P Morais
- P Relvas
- PK Dayton
- PN Boury-Esnault
- R Haynes
- R Nemeth
- Roberto Pronzato
- S Rossi
- S Sartoretto
- Sophie Arnaud-Haond
- T Patarnello
- TC Borges
- V Rau
- V Rau
- Á Peliz
- Í Sampaio
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- 01/01/2016
- Field of study
The highly valuable red coral Corallium rubrum is listed in several Mediterranean Conventions for species protection and management since the 1980s. Yet, the lack of data about its Atlantic distribution has hindered its protection there. This culminated in the recent discovery of poaching activities harvesting tens of kg of coral per day from deep rocky reefs off SW Portugal. Red coral was irregularly exploited in Portugal between the 1200s and 1700s, until the fishery collapsed. Its occurrence has not been reported for the last 300 years.info:eu-repo/semantics/publishedVersio
Genomic Targets of Brachyury (T) in Differentiating Mouse Embryonic Stem Cells
- Author
- A Aulehla
- A Evans
- A Kispert
- A Kispert
- A Kispert
- A Nagy
- A Suzuki
- A Van Eynde
- AA Rana
- AE Popsueva
- AM Faisst
- Amanda L. Evans
- AP Russ
- AS Bernardo
- AT Garnett
- B Valamehr
- BD Shur
- BG Herrmann
- BG Herrmann
- BL Martin
- BW Draper
- C Bernemann
- D Clements
- D Lin
- D Martin
- D Schmidt
- David S. Milstone
- DC Weinstein
- DG Wilkinson
- DG Wilkinson
- ES Casey
- ES Casey
- Fiona C. Wardle
- FL Conlon
- FL Conlon
- G Badis
- GE Crooks
- H O'Geen
- HV Isaacs
- J Armstrong
- J Galceran
- James C. Smith
- JC Smith
- JJ Essner
- JJ Pearce
- JY Leung
- KA Lawson
- KA Lawson
- KJ Griffin
- KO Yanagisawa
- L Wittler
- LA Naiche
- Ludovic Vallier
- M Ginsburg
- M Nakaya
- M Niimi
- M Saitou
- M Tada
- M Tada
- M Thomas-Chollier
- M Thomson
- M Wartenberg
- M Zariwala
- MD Wilson
- Michael J. Gilchrist
- N Dobrovolskaïa-Zavadskaïa
- O Nentwich
- O Tamplin
- P Elms
- P Rashbass
- PH Crossley
- PJ Farnham
- R Anderson
- R Sousa-Nunes
- RH Morley
- RJ Jacobs-Cohen
- RL Williams
- Roger A. Pedersen
- S Brown
- S Istrail
- S Schulte-Merker
- S Schulte-Merker
- S Schulte-Merker
- SM White
- T King
- T Kurisaki
- T Kusch
- TA Down
- TE Tsang
- Thomas Down
- Tiago Faial
- TP Yamaguchi
- V Cunliffe
- V Wilson
- Y Ohinata
- YJ Passamaneck
- Publication venue
- Public Library of Science
- Publication date
- 30/03/2012
- Field of study
The T-box transcription factor Brachyury (T) is essential for formation of the posterior mesoderm and the notochord in vertebrate embryos. Work in the frog and the zebrafish has identified some direct genomic targets of Brachyury, but little is known about Brachyury targets in the mouse.Here we use chromatin immunoprecipitation and mouse promoter microarrays to identify targets of Brachyury in embryoid bodies formed from differentiating mouse ES cells. The targets we identify are enriched for sequence-specific DNA binding proteins and include components of signal transduction pathways that direct cell fate in the primitive streak and tailbud of the early embryo. Expression of some of these targets, such as Axin2, Fgf8 and Wnt3a, is down regulated in Brachyury mutant embryos and we demonstrate that they are also Brachyury targets in the human. Surprisingly, we do not observe enrichment of the canonical T-domain DNA binding sequence 5'-TCACACCT-3' in the vicinity of most Brachyury target genes. Rather, we have identified an (AC)(n) repeat sequence, which is conserved in the rat but not in human, zebrafish or Xenopus. We do not understand the significance of this sequence, but speculate that it enhances transcription factor binding in the regulatory regions of Brachyury target genes in rodents.Our work identifies the genomic targets of a key regulator of mesoderm formation in the early mouse embryo, thereby providing insights into the Brachyury-driven genetic regulatory network and allowing us to compare the function of Brachyury in different species
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Search for neutral MSSM Higgs bosons decaying to a pair of tau leptons in pp collisions
- Author
- Abbaneo D. Cv
- Abbiendi G. Bc
- Abbrescia M. Bb
- Abdullin S. Dz
- Abdulsalam A. Ax
- Acosta D. Ea
- Acosta J. G. En
- Adair A. Ey
- Adam W. B
- Adams M. R. Ee
- Adams T. Ec
- Adiguzel A. Dc
- Adler V. G
- Adzic P. Cq
- Afanasiev S. Ci
- Agapitos A. Ao
- Agram J. L. ad
- Ahmad A. Cf
- Ahmad M. Cf
- Ahuja S. Av
- Akchurin N. Fe
- Akgun B. Ey
- Akin I. V. Dd
- Albajar C. Cs
- Albayrak E. A. Ef
- Albergo S. Bd
- Albrow M. Dz
- Alcaraz Maestre J. Cr
- Aldaya Martin M. Al
- Alderweireldt S. D
- Aleksandrov A. M
- Alexander J. Dx
- Alimena J. Do
- Alverson G. Eq
- Alves G. A. J
- Amapane N. Bo
- Amsler C. Cy
- Anagnostou G. An
- Anastassov A. Er
- Anderson J. Dz
- Andrea J. Ad
- Andreev V. Cn
- Andreev Y. Cl
- Andrews W. Ds
- Androsov K. Bm
- Antonelli L. Et
- Antunovic Z. S
- Apanasevich L. Ee
- Apollinari G. Dz
- Appelt E. Ff
- Apresyan A. Du
- Apyan A. El
- Arcidiacono R. Bo
- Arenton M. W. Fg
- Argiro S. Bo
- Arneodo M. Bo
- Arora S. Fb
- Asavapibhop B. Db
- Asawatangtrakuldee C. P
- Asin I. Ak
- Askew A. Ec
- Aslanoglou X. Ap
- Assran Y. W
- Ata M. Ai
- Attikis A. U
- Aubin A. Ad
- Auffray E. Cv
- Autermann C. Ah
- Auzinger G. Cv
- Avdeeva E. Eo
- Avery P. Ea
- Avetisyan A. Dn
- Avila C. Q
- Azarkin M. Cn
- Azhgirey I. Cp
- Aziz T. Ay
- Azzi P. Bj
- Azzolini V. Dv
- Azzurri P. Bm
- Baarmand M. M. Ed
- Babb J. Dr
- Baber M. Dj
- Bacchetta N. Bj
- Bachmair F. Cx
- Bachtis M. Cv
- Baden A. Ek
- Baffioni S. Ac
- Bagliesi G. Bm
- Baillon P. Cv
- Bainbridge R. Dj
- Bakhshiansohi H. Az
- Bakirci M. N. Dc
- Ball A. H. Cv
- Ban Y. P
- Banerjee S. Aw
- Banerjee S. Ay
- Bansal M. D
- Bansal S. D
- Barbagli G. Be
- Barberis E. Eq
- Barbieri R. El
- Barbone L. Bb
- Barfuss A. F. Ei
- Bargassa P. Ci
- Barge D. Dt
- Baringer P. Eh
- Barker A. Fb
- Barnes V. E. Ew
- Barnett B. A. Eg
- Barney D. Cv
- Barone L. Bn
- Barth C. Am
- Bartosik N. Ak
- Basegmez S. H
- Battilana C. Cr
- Bauer G. El
- Bauerdick L. A. T. Dz
- Baumgartel D. Eq
- Baus C. Am
- Bayshev I. Cp
- Bazterra V. E. Ee
- Bean A. Eh
- Beauceron S. Af
- Beaudette F. Ac
- Beaupere N. Af
- Beernaert K. G
- Behnamian H. Az
- Behr J. Ak
- Behrenhoff W. Ak
- Behrens U. Ak
- Beirão Da Cruz E. Silva C. Ci
- Belforte S. Bp
- Beliy N. I
- Belknap D. A. Fi
- Bell A. J. Ak
- Bell K. W. Di
- Bellan R. Bo
- Bellato M. Bj
- Belloni A. Ek
- Beluffi C. H
- Belyaev A. Co
- Belyaev A. Di
- Benaglia A. Cv
- Bencze G. Aq
- Bendavid J. Cv
- Benedetti D. Ew
- Benelli G. Eh
- Benhabib L. Cv
- Beni N. Ar
- Benitez J. F. Cv
- Benucci L. G
- Benussi L. Bf
- Benvenuti A. C. Bc
- Beranek S. Ah
- Beretvas A. Dz
- Bergauer T. B
- Berger J. Am
- Bergholz M. Ak
- Beri S. B. Au
- Bernardes C. A. L
- Bernardini J. Bm
- Bernet C. Cv
- Berry D. Ee
- Berry E. Do
- Berryhill J. Dz
- Bertl W. Cw
- Besancon M. Ab
- Betchart B. Ez
- Bethani A. Ak
- Betts R. R. Ee
- Bhardwaj A. Av
- Bhat P. C. Dz
- Bhatnagar V. Au
- Bhattacharya S. Aw
- Bhattacharya S. Do
- Bhawandeep U. Au
- Bhowmik S. Ay
- Bialkowska H. Cg
- Bian J. G. O
- Bianchi G. Cv
- Bianchini L. Cx
- Bianco S. Bf
- Biasini M. Bl
- Biasotto M. Bj
- Biino C. Bo
- Bilei G. M. Bl
- Bilin B. Dd
- Bilki B. Ef
- Bilmis S. Dd
- Bitioukov S. Cp
- Blekman F. E
- Blobel V. Al
- Bloch D. Ad
- Bloch P. Cv
- Bloom K. Eo
- Bluj M. Cg
- Blumenfeld B. Eg
- Blyweert S. E
- Boccali T. Bm
- Bocci A. Cv
- Bochenek J. Ec
- Bodek A. Ez
- Bodlak M. V
- Boimska B. Cg
- Bolla G. Ew
- Bolognesi S. Eg
- Bonacorsi D. Bc
- Bonato A. Cv
- Bondu O. Cv
- Bontenackels M. Ah
- Boos E. Co
- Bornheim A. Du
- Borras K. Ak
- Bortignon P. Cx
- Bortoletto D. Ew
- Bose S. Eo
- Bose T. Dn
- Botta C. Cv
- Boudoul G. Af
- Bouhali O. Fd
- Bourilkov D. Ea
- Boutle S. Fg
- Bouvier E. Af
- Bradmiller Feld J. Dt
- Braibant Giacomelli S. Bc
- Branca A. Bj
- Branson J. G. Ds
- Breedon R. Dp
- Breto G. Dp
- Breuker H. Cv
- Brew C. Di
- Brigliadori L. Bc
- Brigljevic V. T
- Brinkerhoff A. Es
- Brinson J. Et
- Brito L. J
- Broccolo G. Bm
- Brochero Cifuentes J. A. Cu
- Brochet S. Af
- Brodski M. Ai
- Brom J. M. ad
- Brona G. Ch
- Brooke J. J. Dh
- Brown R. M. Di
- Brownson E. Ev
- Brun H. Ct
- Bruner C. Eh
- Bruno G. H
- Buchmann M. A. Cx
- Buchmuller O. Dj
- Bucinskaite I. Ee
- Bunin P. Cj
- Bunkowski K. Ch
- Bunn J. Du
- Buontempo S. Bi
- Burgmeier A. Ak
- Burkett K. Dz
- Burt K. Dr
- Burton D. Dj
- Busson P. Ac
- Busza W. El
- Butler J. N. Dz
- Butler P. H. Ce
- Butz E. Am
- Bylsma B. Et
- Bäni L. Cx
- Böser C. Am
- Cabrillo I. J. Cu
- Caebergs T. I
- Caillol C. F
- Caiulo D. Bm
- Cakir A. Ak
- Calabria C. Bb
- Calamba A. Dv
- Calderon De La Barca Sanchez M. Dp
- Calderon A. Cu
- Cali I. A. El
- Calligaris L. Ak
- Calvert B. Ek
- Calvo E. Cr
- Campagnari C. Dt
- Campanini R. Bc
- Campbell A. Ak
- Camporesi T. Cv
- Candelise V. Bp
- Canelli M. F. Cy
- Cankocak K. Df
- Capiluppi P. Bc
- Cappello G. Bd
- Cardaci M. Cz
- Carlsmith D. Fi
- Carlson B. Dv
- Carrillo Montoya C. A. Af
- Carrillo Moreno S. Ca
- Cartiglia N. Bo
- Carvalho W. K
- Carver M. Ea
- Casal B. Cx
- Casarsa M. Bp
- Casasso S. Bo
- Casimiro Linares E. Cc
- Castaldi R. Bm
- Castello R. H
- Castilla Valdez H. Bz
- Castro A. Bc
- Caudron A. H
- Cavallari F. Bn
- Cavallo F. R. Bc
- Cavallo N. Bi
- Cavanaugh R. Ee
- Ceard L. H
- Centis Vignali M. Al
- Cepeda M. Fi
- Cerati G. B. Ds
- Cerci S. Dc
- Cerminara G. Cv
- Cerrada M. Cr
- Chabert E. C. Ad
- Chakaberia I. Ei
- Chamizo Llatas M. Cr
- Chan K. M. Es
- Chan M. El
- Chang P. Da
- Chang S. Bq
- Chang Y. H. Da
- Chang Y. W. Da
- Chanon N. Cx
- Chao Y. Da
- Chaparro Sierra L. F. Q
- Charaf O. Dm
- Charlot C. Ac
- Chasco M. Eq
- Chasserat J. Af
- Chatterjee A. Dx
- Chatterjee K. Aw
- Chatterjee R. M. Ay
- Chauhan S. Dp
- Chen G. M. O
- Chen H. S. O
- Chen K. F. Da
- Chen K. H. Cz
- Chen M. O
- Chen P. H. Da
- Chen Y. Du
- Cheng T. Ea
- Cherepanov V. Aj
- Chertok M. Dp
- Cheung H. W. K. Dz
- Chhibra S. S. Bb
- Chierici R. Af
- Chinellato J. K
- Chiochia V. Cy
- Chiorboli M. Bd
- Chlebana F. Dz
- Choi M. Bv
- Choi S. Bu
- Choi Y. Bw
- Choi Y. K. Bw
- Chou J. P. Fb
- Choudhary B. C. Av
- Choudhury S. Ak
- Christopher G. Do
- Chu J. Dx
- Chwalek T. Am
- Ciangottini D. Bl
- Ciesielski R. Fa
- Cihangir S. Dz
- Cimmino A. G
- Ciocci M. A. Bm
- Cittolin S. Ds
- Ciulli V. Be
- Civinini C. Be
- Claes D. R. Eo
- Clare R. Dr
- Clarida W. Ef
- Clarke C. Fg
- Clement E. Dh
- Clerbaux B. F
- Cockerill D. J. A. Di
- Codispoti G. Bc
- Colafranceschi S. Cv
- Colaleo A. Bb
- Cole J. E. Dk
- Colino N. Cr
- Collard C. Ad
- Colling D. Dj
- Contardo D. Af
- Conte E. Ad
- Contreras Campana C. Fb
- Contreras Campana E. Fb
- Conway J. Dp
- Conway R. Dp
- Cooper S. I. Dm
- Cornelis T. D
- Correa Martins Junior M. J
- Cossutti F. Bp
- Costa M. Bo
- Costa S. Bd
- Costantini S. G
- Costanza F. Ak
- Couderc F. Ab
- Coughlan J. A. Di
- Cousins R. Dq
- Covarelli R. Ez
- Cowden C. Fe
- Cox B. Fg
- Cox P. T. Dp
- Creanza D. Bb
- Cremaldi L. M. En
- Cripps N. Dj
- Crucy S. G
- Cuevas J. Ct
- Cuffiani M. Bc
- Cumalat J. P. Dw
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- Cussans D. Dh
- Custódio A. K
- Cutajar M. Dj
- Cutts D. Do
- Cwiok M. Ch
- Czellar S. Ar
- Da Costa E. M. K
- Da Silveira G. G. H
- Dabrowski A. Cv
- Daci N. E
- Dahmes B. Em
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- Damgov J. Fe
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- Das S. Ea
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- Daubie E. I
- Dauncey P. Dj
- David A. Cv
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- de Barbaro P. Ez
- De Benedetti A. Em
- De Boer W. Am
- De Cosa A. Cy
- De Filippis N. Bb
- De Gruttola M. Ea
- De Guio F. Cv
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- De Lentdecker G. F
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- De Roeck A. Cv
- de Trocóniz J. F. Cs
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- Degano A. Bo
- Deisher A. Cx
- Deiters K. Cw
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- Delannoy A. G. Ff
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- Della Negra M. Dj
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- Di Giovanni G. P. Ea
- Di Guida S. Bi
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- Dildick S. G
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- Dordevic M. Cv
- Dorigo T. Bj
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- Dosselli U. Bj
- Dozen C. Dc
- Draeger A. R. Al
- Dragicevic M. B
- Dragoiu C. Fe
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- Dutta D. Ax
- Dutta S. Aw
- Dutta V. El
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- D’Agnolo R. T. Ds
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- Edelhoff M. Ah
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- Ekmedzic M. Cq
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- Eskut E. Dc
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- Eugster J. Cv
- Eusebi R. Fd
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- Filipovic N. Ac
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- Giubilato P. Bj
- Givernaud A. Ab
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- Gribushin A. Co
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- Grunewald M. Ba
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- Guchait M. Ay
- Gude A. Em
- Guida R. Cv
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- Gunnellini P. Ak
- Guo Y. P
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- Guthoff M. Cv
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- Haas J. Ec
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- Hildreth M. Es
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- Hindrichs O. Ah
- Hinzmann A. Cy
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- Hoepfner K. Ai
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- Hugon J. Ea
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- Kalogeropoulos A. Ak
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- Meng Z. Dh
- Menichelli M. Bl
- Meola S. Bi
- Mercadante P. G. L
- Meridiani P. Bn
- Merino G. Cr
- Merkel P. Ew
- Merlo J. P. ef
- Mermerkaya H. Ef
- Merola M. Bi
- Merschmeyer M. Ai
- Mersi S. Cv
- Meschi E. Cv
- Meschini M. Be
- Mesropian C. Fa
- Messineo A. Bm
- Mestvirishvili A. Ef
- Mesyats G. Cn
- Meyer A. Ai
- Meyer A. B. Ak
- Miceli T. Dp
- Micheli F. Bn
- Michlin B. Ey
- Migliore E. Bo
- Mignerey A. C. Ek
- Mikulec I. B
- Milenovic P. Ea
- Millan Mejias B. Cy
- Miller D. H. Ew
- Millet P. Ai
- Milosevic J. Cq
- Miné P. Ac
- Mirabito L. Af
- Mirman N. Dx
- Mironov C. Ac
- Mishra K. Dz
- Misiura M. Ch
- Missiroli M. Cs
- Mitselmakher G. Ea
- Mitta G. Ak
- Mittal M. Au
- Mnich J. Ak
- Modak A. Aw
- Moeller A. Ef
- Mohammadi Najafabadi M. Az
- Mohammadi A. F
- Mohanty A. K. Ax
- Mohanty G. B. Ay
- Mohapatra A. Fi
- Mohr N. Cx
- Moisenz P. Cj
- Molnar J. Ar
- Monaco V. Bo
- Montalvo R. Fd
- Montanari A. Bc
- Montanino D. Bp
- Moon C. S. Bm
- Moon D. H. Ee
- Mooney M. Eu
- Moortgat F. Cv
- Moran D. Cs
- Morelos Pineda A. Cc
- Moroni L. Bh
- Morovic S. Cv
- Mossolov V. C
- Mott A. Du
- Mousa J. U
- Mozer M. U. Am
- Mrenna S. Dz
- Mucia N. Er
- Mukherjee S. Aw
- Mulders M. Cv
- Mulhearn M. Dp
- Mundim L. K
- Muniz L. Ea
- Munoz Sanchez F. J. Cu
- Murray M. Eh
- Murumaa M. X
- Murzin V. Ck
- Musella P. Cv
- Musich M. Bo
- Musienko Y. Dz
- Mussgiller A. Ak
- My S. Bb
- Mäenpää T. Z
- Müller T. Am
- Nachtman J. Ef
- Nahn S. Dz
- Naimuddin M. Av
- Nam S. K. Bq
- Narain M. Do
- Naranjo I. N. Ac
- Naseri M. Az
- Nash D. Eq
- Nash J. Dj
- Nauenberg U. Dw
- Naumann Emme S. Ak
- Navarria F. L. Bc
- Navarro De Martino E. Cr
- Nawrocki K. Cg
- Nayak A. Ak
- Negrete M. O. Dr
- Nessi Tedaldi F. Cx
- Neu C. Fg
- Neumeister N. Ew
- Newbold D. M. Dh
- Newman Holmes C. Dz
- Newman H. B. Du
- Ngadiuba J. Cy
- Nguyen F. Ci
- Nguyen H. Dr
- Nguyen M. Ac
- Nicolaou C. U
- Nicolas Kaufman G. Dx
- Nikitenko A. Dj
- Nishu N. Au
- Nogima H. K
- Noonan D. Eh
- Nourbakhsh S. Bn
- Novaes S. F. L
- Novgorodova O. Ak
- Nowack A. Aj
- Nowak F. Ak
- Ntomari E. Ak
- Nugent I. M. Aj
- Nuttens C. H
- Nuzzo S. Bb
- Nägeli C. Cx
- Nürnberg A. Am
- Obertino M. M. Bo
- Obraztsov S. Co
- Ocalan K. Dd
- Ocampo Rios A. A. G
- Ochando C. Ac
- Ochesanu S. D
- Odell N. Er
- Ogul H. Ef
- Oh Y. D. Br
- Ojalvo I. Fi
- Olaiya E. Di
- Olbrechts A. E
- Oliveros S. En
- Olivito D. Ds
- Olschewski M. Ai
- Olsen J. Eu
- Olszewski M. Ch
- Onel Y. Ef
- Onengut G. Dc
- Oreshkin V. Ck
- Organtini G. Bn
- Orimoto T. Eq
- Orsini L. Cv
- Ortona G. Bo
- Osipenkov I. Fd
- Ostapchuk A. Ah
- Ott J. Al
- Ozdemir K. Dc
- Ozok F. Ef
- Ozturk S. Dc
- O’Brien C. Ee
- O’Dell V. Dz
- Pacher L. Bo
- Padeken K. Ai
- Padhi S. Ds
- Padley B. P. Ey
- Padula S. S. L
- Paganini P. Ac
- Pagano D. H
- Paganoni M. Bh
- Pakhotin Y. Fd
- Paktinat Mehdiabadi S. Az
- Palichik V. Cj
- Palinkas J. Ar
- Palla F. Bm
- Palmer C. Ds
- Panagiotou A. Ao
- Pandolfi F. Cx
- Pant L. M. Ax
- Panwalkar S. Fb
- Paoletti S. Be
- Paolucci P. Bi
- Papacz P. Ai
- Papadopoulos I. Ap
- Pape L. Cv
- Paradas E. Ap
- Paramatti R. Bn
- Paramesvaran S. Dh
- Parashar N. Ex
- Parida B. Ay
- Park H. Br
- Park I. C. Bv
- Park M. Fb
- Park S. Bv
- Park S. K. Bu
- Pashenkov A. Cl
- Pastika N. Em
- Pastrone N. Bo
- Patel R. Fb
- Patterson J. R. Dx
- Paulini M. Dv
- Paus C. El
- Pauss F. Cx
- Pavlov B. N
- Pazzini J. Bj
- Pearson T. Es
- Pedraza I. Cb
- Pedrini D. Bh
- Pedro K. Ek
- Peiffer T. Al
- Pela J. Dj
- Pellett D. Dp
- Pelliccioni M. Bo
- Peltola T. Z
- Pena C. Du
- Penzo A. Ef
- Perchalla L. Aj
- Perelygin V. Cj
- Perera L. En
- Perez E. Cv
- Perieanu A. Ah
- Perloff A. Fd
- Perniè L. F
- Perrey H. Ak
- Perries S. Af
- Perrini L. H
- Perrotta A. Bc
- Perrozzi L. Cv
- Perry T. Fi
- Peruzzi M. Cx
- Pesaresi M. Dj
- Petkov P. N
- Petrakou E. Da
- Petridis K. Dj
- Petrilli A. Cv
- Petrillo G. Ez
- Petrov V. Cp
- Petrucciani G. Cv
- Petrushanko S. Co
- Petyt D. Di
- Pfeiffer A. Cv
- Piccolo D. Bf
- Piedra Gomez J. Cu
- Pieri M. Ds
- Pierini M. Cv
- Pierro G. A. Fi
- Pietsch N. Al
- Pilot J. Dp
- Pimiä M. Cv
- Pin A. H
- Pinna Angioni G. L. Bo
- Piotrzkowski K. H
- Piparo D. Cv
- Piperov S. M
- Piroué P. Eu
- Pitzl D. Ak
- Placakyte R. Ak
- Plagge M. Cv
- Planer M. Es
- Plestina R. O
- Poehlsen J. Al
- Poehlsen T. Al
- Pol M. E. J
- Polatoz A. Dc
- Polese G. Fi
- Polic D. R
- Poll A. Dh
- Pollack B. Er
- Pompili A. Bb
- Pooth O. Aj
- Popov A. H
- Popov V. Cm
- Potenza A. Bo
- Potenza R. Bd
- Pozdnyakov A. Er
- Pozzobon N. Bj
- Prado Da Silva W. L. K
- Primavera F. Bc
- Prokofyev O. Dz
- Prosper H. Ec
- Psallidas A. An
- Ptochos F. U
- Puerta Pelayo J. Cr
- Pugliese G. Bb
- Puigh D. Et
- Puljak I. R
- Python Q. E
- Pérez Calero Yzquierdo A. Cr
- Qian S. J. P
- Quan X. Eu
- Quast G. Am
- Quertenmont L. H
- Quintario Olmeda A. Cr
- Quittnat M. Cx
- Rabady D. B
- Rabbertz K. Am
- Racz A. Cv
- Radburn Smith B. C. Ew
- Radi A. W
- Radogna R. Bb
- Ragazzi S. Bh
- Rahatlou S. Bn
- Rahbaran B. B
- Rahmat R. Ef
- Raics P. As
- Raidal M. X
- Rakness G. Dq
- Ralph D. El
- Ramirez Vargas J. E. Ev
- Rander J. Ab
- Ranjan K. Av
- Rappoccio S. Ep
- Raspereza A. Ak
- Rathjens D. Al
- Ratnikov F. Am
- Ratti S. P. Bk
- Raupach F. Ah
- Raymond D. M. Dj
- Razis P. A. U
- Rebane L. Cx
- Rebassoo F. Ej
- Redaelli N. Bh
- Redjimi R. Ey
- Redondo I. Cr
- Regnard S. Ac
- Reid I. D. Dk
- Reis T. F
- Reithler H. Ai
- Rekovic V. Cq
- Renker D. Cw
- Reucroft S. Ce
- Rezaei Hosseinabadi F. Az
- Ribeiro Cipriano P. M. Ak
- Riccardi C. Bk
- Ricci Tam F. Dp
- Richardson C. Dn
- Richman J. Dt
- Rinkevicius A. Ea
- Rizzi A. Bm
- Roberts J. Ey
- Robmann P. Cy
- Robutti E. Bg
- Rodenburg M. Et
- Rodozov M. M
- Rodrigo T. Cu
- Rodrigues Antunes J. Ci
- Rodriguez J. L. Eb
- Rodríguez Marrero A. Y. Cu
- Roe J. Fd
- Rogan C. Du
- Rogerson S. Dj
- Roh Y. Bu
- Rohe T. Cw
- Rohlf J. Dn
- Rohringer H. B
- Roland B. D
- Roland C. El
- Roland G. El
- Rolandi G. Cv
- Romanowska Rybinska K. Cg
- Romeo F. Bl
- Romero A. Bo
- Romero L. Cr
- Ron E. Ak
- Ronchese P. Bj
- Ronga F. J. Cy
- Rose A. Dj
- Rose A. Fd
- Rose K. Fc
- Rosowsky A. Ab
- Ross I. Fi
- Rossi A. M. Bc
- Rossini M. Cx
- Rougny R. D
- Rovelli C. Bn
- Rovelli T. Bc
- Rovere M. Cv
- Roy D. Aw
- Ruchti R. Es
- Ruiz Alvarez J. D. Af
- Ruiz Jimeno A. Cu
- Rumerio P. Dm
- Rusack R. Em
- Rusakov S. V. Cn
- Ruspa M. Bo
- Russ J. Dv
- Ryckbosch D. G
- Ryd A. Dx
- Ryu G. Bv
- Ryu M. S. Bv
- Ryutin R. Cp
- Röcker S. Am
- Sabes D. Af
- Sacchi R. Bo
- Safarzadeh B. Az
- Safonov A. Fd
- Safronov G. Cm
- Saha A. Bl
- Sahin M. Ö. Ak
- Saini L. K. Ei
- Saka H. Eu
- Sakharov A. Br
- Sakulin H. Cv
- Sakuma T. Fd
- Salazar Ibarguen H. A. Cb
- Salerno R. Ac
- Salfeld Nebgen J. Ak
- Salur S. Fb
- Salva Diblen S. G
- Salvati E. Dx
- Salvini P. Bk
- Sammet J. Ah
- Sanabria J. C. Q
- Sanchez Hernandez A. Bz
- Sander C. Al
- Sanders D. A. En
- Sanders S. Eh
- Sani M. Ds
- Santanastasio F. Bn
- Santaolalla J. K
- Santocchia A. Bl
- Santoro A. K
- Saoulidou N. Ao
- Sarangi T. Fi
- Sarkar S. Aw
- Sauvan J. B. Ac
- Savin A. Fi
- Savoy Navarro A. Bm
- Savrin V. Co
- Saxena P. Ak
- Scarborough T. Dl
- Schael S. Ah
- Schettler H. Al
- Schizzi A. Bp
- Schleper P. Al
- Schlieckau E. Al
- Schmidt A. Al
- Schmidt R. Ak
- Schmitt M. Er
- Schmitz S. A. Ai
- Schnetzer S. Fb
- Schoerner Sadenius T. Ak
- Schröder M. Ak
- Schwick C. Cv
- Schäfer C. Cv
- Schöfbeck R. B
- Scodellaro L. Cu
- Searle M. Dp
- Seez C. Dj
- Segala M. Do
- Seidel M. Al
- Seitz C. Ak
- Seixas J. Ci
- Sekaric J. Eh
- Sekmen S. Dd
- Selvaggi G. Bb
- Selvaggi M. H
- Semenov S. Cm
- Sen S. Ef
- Senkin S. Dh
- Seo H. Bw
- Serban A. T. Bm
- Seva T. F
- Sexton Kennedy E. Dz
- Sgandurra L. Af
- Sguazzoni G. Be
- Shah M. A. Cf
- Shalhout S. Dp
- Sharan M. Aw
- Sharma A. Cv
- Sharma M. Ff
- Sharma S. Dz
- Sharma V. Av
- Sharma V. Ds
- Sharp P. Dj
- Shchutska L. Ea
- Sheldon P. Ff
- Shepherd Themistocleous C. H. Di
- Shi X. Ew
- Shipsey I. Ew
- Shmatov S. Cj
- Shoaib M. Cf
- Shrestha S. Ei
- Shrinivas A. Dr
- Shukla P. Ax
- Shumeiko N. C
- Siegrist P. Cv
- Sigamani M. G
- Sikler F. Aq
- Silkworth C. Ee
- Silva P. Cv
- Silvers D. Ew
- Silvestris L. Bb
- Simon M. Cv
- Simon S. Ds
- Simonetto F. Bj
- Simonis H. J. Am
- Singh G. Bb
- Singh J. B. Au
- Singovsky A. Em
- Sinthuprasith T. Do
- Sirois Y. Ac
- Siroli G. P. Bc
- Sirunyan A. M. A
- Skatchkov N. Cj
- Skhirtladze N. Ei
- Skinnari L. Dx
- Skuja A. Ek
- Smirnov I. Ck
- Smirnov V. Cj
- Smith G. Et
- Smith J. Dp
- Smith J. G. Dw
- Smith V. J. Dh
- Smith W. H. Fi
- Snigirev A. Co
- Snook B. Ff
- Snow G. R. Eo
- Snowball M. Ea
- Soares M. S. Cr
- Sobol A. Cp
- Soffi L. Bn
- Sogut K. Dc
- Soha A. Dz
- Sola V. Al
- Solano A. Bo
- Somalwar S. Fb
- Son D. C. Br
- Song S. Bt
- Sonnenschein L. Ai
- Sordini V. Af
- Sorokin P. Dg
- Spagnolo P. Bm
- Spalding W. J. Dz
- Spanier S. Fc
- Spannagel S. Ak
- Speer T. Do
- Sperka D. Dn
- Sphicas P. Cv
- Spiegel L. Dz
- Spiezia A. Bl
- Spiga D. Cv
- Spiridonov A. Cm
- Spiropulu M. Du
- Squillacioti P. Bm
- Squires M. Dp
- Srimanobhas N. Db
- Stadie H. Al
- Stahl A. Aj
- Staiano A. Bo
- Starodumov A. Cx
- Steggemann J. Cv
- Steinbrück G. Al
- Stenson K. Dw
- Stephans G. S. F. El
- Stickland D. Eu
- Stieger B. Cv
- Stiliaris E. Ao
- Stober F. M. Am
- Stolin V. Cm
- Stolp D. Dp
- Stone R. Fb
- Stoye M. Cv
- Stoykova S. M
- Stoynev S. Er
- Strauss J. B
- Stringer R. Eh
- Strobbe N. G
- Strom D. E
- Stuart D. Dt
- Stupak J. Ex
- Sturdy J. Fh
- Stöckli F. El
- Suarez Gonzalez J. C
- Suarez I. Fd
- Sudano E. Ds
- Sudhakar K. Ay
- Sudic L. T
- Sulak L. Dn
- Sulimov V. Ck
- Sultanov G. M
- Summers D. En
- Sumorok K. El
- Sumowidagdo S. Dr
- Sun W. Dx
- Sunar Cerci D. Dc
- Sung K. Er
- Surat U. E. Dd
- Suwonjandee N. Db
- Svintradze I. Ei
- Svyatkovskiy A. Ew
- Swain S. K. At
- Swanson J. Do
- Swartz M. Eg
- Symonds P. Dk
- Szillasi Z. Ar
- Szleper M. Cg
- Sznajder A. K
- Tabarelli de Fatis T. Bh
- Tadel M. Ds
- Takahashi M. Cx
- Takahashi Y. Cv
- Takasugi E. Dq
- Tali B. Dc
- Talvitie J. Aa
- Tambe N. Em
- Tamponi U. Bo
- Tan P. Ef
- Tao J. O
- Tapper A. Dj
- Taroni S. Cy
- Tatarinov A. Fd
- Taurok A. B
- Tavernier S. E
- Taylor L. Dz
- Tcholakov V. M
- Tenchini R. Bm
- Teo W. D. Dx
- Teodorescu L. Dk
- Teyssier D. Ai
- Thea A. Di
- Theofilatos K. Cx
- Thom J. Dx
- Thomas L. F
- Thomas S. Fb
- Thomassen P. Fb
- Thompson J. Dx
- Thyssen F. G
- Thüer S. Ai
- Tiko A. X
- Timciuc V. Du
- Tiras E. Ef
- Titov M. Ab
- Tkaczyk S. Dz
- Tlisov D. Cl
- To W. Dt
- Tomalin I. R. Di
- Tonelli Manganote E. J. K
- Tonelli G. Bm
- Tonjes M. B. Ek
- Tonwar S. C. Ek
- Topakli H. Dc
- Topkar A. Ax
- Topsis Giotis I. An
- Torassa E. Bj
- Toropin A. Cl
- Tosi M. Bj
- Tosi N. Bc
- Tosi S. Bg
- Tourtchanovitch L. Cp
- Traczyk P. Bn
- Tran N. V. Dz
- Travaglini R. Bc
- Treberer Treberspurg W. B
- Treille D. Cv
- Tricomi A. Bd
- Trioss A. Bj
- Tripathi M. Dp
- Trocino D. Eq
- Trocsanyi Z. L. As
- Troendle D. Al
- Tropiano A. Be
- Troshin S. Cp
- Tsamalaidze Z. Ag
- Tsirou A. Cv
- Tu Y. Ds
- Tucker J. Dx
- Tully C. Eu
- Tumasyan A. A
- Tuo S. Ff
- Tuominen E. Z
- Tuominiemi J. Z
- Tuovinen E. Z
- Turkewitz J. Em
- Turner M. Dk
- Turner P. Ee
- Tuuva T. Aa
- Tuve C. Bd
- Tytgat M. G
- Tyurin N. Cp
- Tzeng Y. M. Da
- Ujvari B. As
- Ulmer K. A. Dw
- Ulrich R. Am
- Umer T. Bp
- Uplegger L. Dz
- Usai E. Al
- Uvarov L. Ck
- Uzunian A. Cp
- Vaandering E. W. Dz
- Valls N. Es
- Valuev V. Dq
- Van De Klundert M. D
- Van Doninck W. E
- Van Haevermaet H. D
- Van Hove P. Ad
- Van Mechelen P. D
- Van Mulders P. E
- Van Onsem G. P. E
- Van Remortel N. D
- Van Spilbeeck A. D
- Vander Donckt M. Af
- Vander Velde C. F
- Vanelderen L. Al
- Vanini S. Bj
- Vanlaer P. F
- Vardarlı F. I. Df
- Varela J. Ci
- Varelas N. Ee
- Vargas Trevino A. D. R. Ak
- Vartak A. Ds
- Vavilov S. Ck
- Vazquez Acosta M. Dj
- Vazquez Valencia F. Ca
- Veelken C. Ac
- Veeraraghavan V. Ec
- Velasco M. Er
- Velicanu D. El
- Velkovska J. Ff
- Venditti R. Bb
- Ventura S. Bj
- Venturi A. Bm
- Verdier P. Af
- Verdini P. G. Bm
- Veres G. I. Cv
- Vergili M. Dc
- Vernieri C. Bm
- Verwilligen P. Bb
- Verzetti M. Cy
- Veszpremi V. Aq
- Vesztergombi G. Aq
- Veverka J. El
- Vidal Marono M. H
- Vidal R. Dz
- Vila I. Cu
- Vilar Cortabitarte R. Cu
- Vilela Pereira A. K
- Villella I. E
- Vinogradov A. Cn
- Virdee T. Dj
- Viret S. Af
- Vischia P. Ci
- Vishnevskiy D. Ez
- Vitulo P. Bk
- Vizan Garcia J. M. H
- Vlasov E. Cm
- Vlimant J. R. Cv
- Vogel H. Dv
- Volkov A. Cp
- Volobouev I. Fe
- Volpe R. Cz
- Vorobiev I. Dv
- Vorobyev A. Ck
- Vorobyev A. Ck
- Voutilainen M. Y
- Vuosalo C. Fi
- Vutova M. M
- Wagner Kuhr J. Am
- Wagner S. R. Dw
- Walker M. Fb
- Wallny R. Cx
- Walsh R. Ak
- Waltenberger W. B
- Wang D. P
- Wang F. Ew
- Wang J. F
- Wang Q. Eh
- Wang R. J. eq
- Wang X. O
- Wang Z. O
- Wardle N. Cv
- Wayand S. Am
- Wayne M. Es
- Weber H. A. Cx
- Weber H. Ah
- Weber M. Ai
- Weber M. Dq
- Weiler T. Am
- Weinberg M. Ec
- Welke C. Ds
- Wendland L. Z
- Weng Y. Dx
- Werner J. S. Eu
- West C. Dt
- Wetzel J. Ef
- Whitbeck A. Dz
- Whitmore J. Dz
- Wickramage N. Ay
- Wilbur S. Dp
- Wilken R. Da
- Wilkinson R. Du
- Williams T. Dh
- Wimpenny S. Dr
- Winer B. L. Et
- Winn D. Dy
- Winstrom L. Dx
- Wissing C. Ak
- Wittich P. Dx
- Wittmer B. Ah
- Wolf M. Es
- Wolf R. Am
- Wolfe H. Et
- Wollny H. Cv
- Wolszczak W. Ch
- Womersley W. J. Di
- Won S. Er
- Wood D. Eq
- Wood J. Fg
- Wood J. S. Eh
- Woodard A. Es
- Woods N. Fi
- Worm S. D. Di
- Wright D. Ej
- Wulsin H. W. Et
- Wulz C. E. b
- Wyslouch B. El
- Wöhri H. K. Cv
- Würthwein F. Ds
- Xiao H. Af
- Xie S. Du
- Xie W. Ew
- Xu L. Ew
- Yagil A. Ds
- Yalvac M. Dd
- Yang F. Dz
- Yang M. El
- Yang Y. Cy
- Yazgan E. G
- Yelton J. Ea
- Yetkin T. Ef
- Yi K. Ef
- Yilmaz Y. Ac
- Yohay R. Dp
- Yoo H. D. Ew
- Yoo J. Ds
- Yoon A. S. El
- York A. Fc
- Yu I. Bw
- Yu S. S. Cz
- Yumiceva F. Ed
- Zabel J. Ey
- Zabi A. Ac
- Zablocki J. Ew
- Zaganidis N. G
- Zakaria M. Ea
- Zalewski P. Cg
- Zanetti A. Bp
- Zanetti M. El
- Zarubin A. Cj
- Zeinali M. Az
- Zenz S. C. Dj
- Zeuner W. D. Cv
- Zeyrek M. Dd
- Zhang J. Eq
- Zhang L. P
- Zheng Y. Ew
- Zhokin A. Cm
- Zhu R. Y. Du
- Zhukov V. Ah
- Zhukova V. El
- Zito G. Bb
- Zotto P. Bj
- Zou W. P
- Zsigmond A. J. Aq
- Zucchetta A. Bj
- Zuranski A. Eu
- Publication venue
- Publication date
- 01/01/2014
- Field of study
Peer reviewe
- …