127 research outputs found
Widespread Gene Conversion of Alpha-2-Fucosyltransferase Genes in Mammals
- Author
- A Stapleton
- B Walsh
- BN Borges
- C Breton
- C Breton
- D Posada
- David Posada
- DL Swofford
- F Abascal
- FF Wagner
- GM Ruiz-Palacios
- H Shimodaira
- H Uchida
- J Pendu Le
- J Thompson
- J Walsh
- J Walsh
- JA St John
- Jacques Le Pendu
- JJ Garcia-Vallejo
- Joana Abrantes
- JP Barreaud
- K Saunier
- KM Teshima
- M Azevedo
- M Iwamori
- M Soejima
- MA Amin
- MM Halloran
- P Guillon
- PA Apoil
- Patrice Guillon
- Pedro J. Esteves
- R Oriol
- S Guindon
- S Marionneau
- S Ohno
- SA Sawyer
- SL Kosakovsky-Pond
- SL Kosakovsky-Pond
- T Boren
- TM Moehler
- V Bureau
- V Ravn
- Y Koda
- Publication venue
- Springer-Verlag
- Publication date
- 01/01/2009
- Field of study
The alpha-2-fucosyltransferases (α2FTs) are enzymes involved in the biosynthesis of α2fucosylated glycan structures. In mammalian genomes, there are three α2FT genes located in tandem—FUT1, FUT2, and Sec1—each contained within a single exon. It has been suggested that these genes originated from two successive duplications, with FUT1 being generated first and FUT2 and Sec1 second. Despite gene conversion being considered the main mechanism of concerted evolution in gene families, previous studies of primates α2FTs failed to detect it, although the occurrence of gene conversion between FUT2 and Sec1 was recently reported in a human allele. The primary aim of our work was to initiate a broader study on the molecular evolution of mammalian α2FTs. Sequence comparison leads us to confirm that the three genes appeared by two rounds of duplication. In addition, we were able to detect multiple gene-conversion events at the base of primates and within several nonprimate species involving FUT2 and Sec1. Gene conversion involving FUT1 and either FUT2 or Sec1 was also detected in rabbit. The extent of gene conversion between the α2FTs genes appears to be species-specific, possibly related to functional differentiation of these genes. With the exception of rabbits, gene conversion was not observed in the region coding the C-terminal part of the catalytic domain. In this region, the number of amino acids that are identical between FUT1 and FUT2, but different in Sec1, is higher than in other parts of the protein. The biologic meaning of this observation may be related to functional constraints
Relationship between cardiovascular risk factors and the echogenicity and pattern of the carotid intima-media complex in men
- Author
- Andersson J
- Andrea Scaciota
- Arnlöv J
- Bard RL
- Belcaro G
- Bernard S
- Chambless LE
- Feig DI
- Frida Liane Plavnik
- Graf IM
- Grant EG
- Joab Oliveira Lima
- Kablak-Ziembicka A
- Labropoulos N
- Lind L
- Lind L
- Loizou CP
- Lorenz MW
- Mackinnon AD
- Pignoli P
- Priscilla Lopes da Fonseca Abrantes Sarmento
- Ribeiro FF
- Riccioni G
- Robson Barbosa Miranda
- Ross R
- Sergio Aron Ajzen
- Sims EA
- Stary HC
- Strong JP
- Sánchez-Castillo CP
- Tosetto A
- Wohlin M
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- 01/01/2014
- Field of study
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
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- Aish B
- Aiub F
- Aiub J
- Ajax K
- Ajioka M
- Akai Y
- Akatova E
- Akrap B
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- Al-Khalili F
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- Yaoqing H
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- Yilmaz Mb
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- Yokoyama M
- Yong H
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- Youssef G
- Yuan Z
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- Yupanqui H
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- Z Zilahi
- Zadionchenko V
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- Zdrenghea D
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- Zhou H
- Zidova M
- Zielinski M
- Zieve F
- Zineldine A.
- Zirlik A
- Zucchetti C
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
Background: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. Methods: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1β, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P = 0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P = 0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P = 0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P = 0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P = 0.31). Conclusions: Antiinflammatory therapy targeting the interleukin-1β innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. (Funded by Novartis; CANTOS ClinicalTrials.gov number, NCT01327846.
Observation of Two New Excited Ξb0 States Decaying to Λb0 K-π+
- Author
- Aaij R
- Abdelmotteleb ASW
- Abrantes FG
- Ackernley T
- Adeva B
- Adinolfi M
- Afsharnia H
- Agapopoulou C
- Aidala CA
- Aiola S
- Ajaltouni Z
- Akar S
- Akiba KC
- Albero AA
- Albrecht J
- Alepuz CR
- Alessio F
- Alexander M
- Aliouche Z
- Alkhazov G
- Altarelli MP
- Amato S
- Amey JL
- Amhis Y
- An L
- Anderlini L
- Andreianov A
- Andreotti M
- Archilli F
- Artamonov A
- Artuso M
- Arzymatov K
- Aslanides E
- Atzeni M
- Audurier B
- Bachmann S
- Bachmayer M
- Back JJ
- Balagura V
- Baldini W
- Barajas CAC
- Barbetti M
- Barlow RJ
- Barsuk S
- Barter W
- Bartolini M
- Baryshnikov F
- Basels JM
- Bashir S
- Bassi G
- Batsukh B
- Battig A
- Bay A
- Beck A
- Becker M
- Bedeschi F
- Bediaga I
- Beiter A
- Belavin V
- Belin S
- Bellee V
- Belous K
- Belov I
- Belyaev I
- Ben-Haim E
- Bencivenni G
- Benito CM
- Berezhnoy A
- Bernet R
- Berninghoff D
- Bernstein HC
- Bertella C
- Bertolin A
- Betancourt C
- Beteta CA
- Betti F
- Bezshyiko I
- Bhasin S
- Bhom J
- Bian L
- Bieker MS
- Bifani S
- Billoir P
- Birch M
- Bishop FCR
- Bitadze A
- Bizzeti A
- Bjorn M
- Blago MP
- Blake T
- Blanc F
- Blusk S
- Bobulska D
- Boelhauve JA
- Boettcher T
- Boldyrev A
- Bondar A
- Bondar N
- Borghi S
- Borisyak M
- Borsato M
- Borsuk JT
- Bouchiba SA
- Bowcock TJV
- Boyer A
- Bozzi C
- Bradley MJ
- Braun S
- Brodski M
- Brodzicka J
- Brundu D
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- Wyllie K
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- Yao Y
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- Yin H
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- Yuan X
- Yushchenko O
- Zaffaroni E
- Zavertyaev M
- Zdybal M
- Zenaiev O
- Zeng M
- Zhang D
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- Zharkova A
- Zhelezov A
- Zheng Y
- Zhou T
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- Zhou Y
- Zhovkovska V
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- Zhukov V
- Zonneveld JB
- Zou Q
- Zucchelli S
- Zuliani D
- Zunica G
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2022
- Field of study
Two narrow resonant states are observed in the Λb0K-π+ mass spectrum using a data sample of proton-proton collisions at a center-of-mass energy of 13 TeV, collected by the LHCb experiment and corresponding to an integrated luminosity of 6 fb-1. The minimal quark content of the Λb0K-π+ system indicates that these are excited Ξb0 baryons. The masses of the Ξb(6327)0 and Ξb(6333)0 states are m[Ξb(6327)0]=6327.28-0.21+0.23±0.12±0.24 and m[Ξb(6333)0]=6332.69-0.18+0.17±0.03±0.22 MeV, respectively, with a mass splitting of Δm=5.41-0.27+0.26±0.12 MeV, where the uncertainties are statistical, systematic, and due to the Λb0 mass measurement. The measured natural widths of these states are consistent with zero, with upper limits of Γ[Ξb(6327)0]<2.20(2.56) and Γ[Ξb(6333)0]<1.60(1.92) MeV at a 90% (95%) credibility level. The significance of the two-peak hypothesis is larger than nine (five) Gaussian standard deviations compared to the no-peak (one-peak) hypothesis. The masses, widths, and resonant structure of the new states are in good agreement with the expectations for a doublet of 1D Ξb0 resonances
Test of lepton universality in b→sℓ+ℓ− decays
- Author
- Aaij R
- Abdelmotteleb ASW
- Abellan Beteta C
- Abudinén F
- Ackernley T
- Adeva B
- Adinolfi M
- Adlarson P
- Afsharnia H
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- Aidala CA
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- Amey JL
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- Craik DC
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- d'Argent P
- Da Silva CL
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- Publication venue
- Publication date
- 18/12/2022
- Field of study
The first simultaneous test of muon-electron universality using
B+→K+ℓ+ℓ− and B0→K∗0ℓ+ℓ− decays is performed, in two ranges of the dilepton
invariant-mass squared, q2. The analysis uses beauty mesons produced in
proton-proton collisions collected with the LHCb detector between 2011 and
2018, corresponding to an integrated luminosity of 9 fb−1. Each
of the four lepton universality measurements reported is either the first in
the given q2 interval or supersedes previous LHCb measurements. The
results are compatible with the predictions of the Standard Model.Comment: All figures and tables, along with any supplementary material and
additional information, are available at
https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2022-046.html (LHCb
public pages
Observation and branching fraction measurement of the decay Ξb- → Λ0 bπ -
- Author
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- Abdelmotteleb ASW
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- Abudinen F
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- Grecu AT
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- Grieser NA
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- Zunica G
- Publication venue
- Publication date
- 01/01/2023
- Field of study
Precision measurement of CP violation in the penguin-mediated decay Bs0→ϕϕ
- Author
- Aaij R
- Abdelmotteleb ASW
- Abellan Beteta C
- Abudinén F
- Ackernley T
- Adeva B
- Adinolfi M
- Adlarson P
- Afsharnia H
- Agapopoulou C
- Aidala CA
- Ajaltouni Z
- Akar S
- Akiba K
- Albicocco P
- Albrecht J
- Alessio F
- Alexander M
- Alfonso Albero A
- Aliouche Z
- Alvarez Cartelle P
- Amalric R
- Amato S
- Amey JL
- Amhis Y
- An L
- Anderlini L
- Andersson M
- Andreianov A
- Andreotti M
- Andreou D
- Ao D
- Archilli F
- Artamonov A
- Artuso M
- Aslanides E
- Atzeni M
- Audurier B
- Bachiller Perea IB
- Bachmann S
- Bachmayer M
- Back JJ
- Bailly-Reyre A
- Baladron Rodriguez P
- Balagura V
- Baldini W
- Baptista de Souza Leite J
- Barbetti M
- Barlow RJ
- Barsuk S
- Barter W
- Bartolini M
- Baryshnikov F
- Basels JM
- Bassi G
- Batozskaya V
- Batsukh B
- Battig A
- Bay A
- Beck A
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- Bedeschi F
- Bediaga IB
- Beiter A
- Belin S
- Bellee V
- Belous K
- Belov I
- Belyaev I
- Ben-Haim E
- Benane G
- Bencivenni G
- Berezhnoy A
- Bernet Andres S
- Bernet R
- Berninghoff D
- Bernstein HC
- Bertella C
- Bertolin A
- Betancourt C
- Betti F
- Bezshyiko Ia
- Bhom J
- Bian L
- Bieker MS
- Biesuz NV
- Billoir P
- Biolchini A
- Birch M
- Bishop FCR
- Bitadze A
- Bizzeti A
- Blago MP
- Blake T
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- Blusk S
- Bobulska D
- Bocharnikov VB
- Boelhauve JA
- Boente Garcia O
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- Bolognani CS
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- Hushchyn M
- Hutchcroft D
- Ibis P
- Idzik M
- Ilin D
- Ilten P
- Inglessi A
- Iniukhin A
- Ishteev A
- Ivshin K
- Jacobsson R
- Jage H
- Jaimes Elles SJ
- Jakobsen S
- Jans E
- Jashal BK
- Jawahery A
- Jevtic V
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- Jones TP
- Joshi SJ
- Jost B
- Jurik N
- Juszczak I
- Kandybei S
- Kang Y
- Karacson M
- Karpenkov D
- Karpov M
- Kautz JW
- Keizer F
- Keller DM
- Kenzie M
- Ketel T
- Khanji B
- Kharisova A
- Kholodenko S
- Khreich G
- Kirn T
- Kirsebom VS
- Kitouni O
- Klaver S
- Kleijne N
- Klimaszewski K
- Kmiec MR
- Koliiev S
- Kolk L
- Kondybayeva A
- Konoplyannikov A
- Kopciewicz P
- Kopecna R
- Koppenburg P
- Korolev M
- Kostiuk I
- Kot O
- Kotriakhova S
- Kozachuk A
- Kravchenko P
- Kravchuk L
- Kreps M
- Kretzschmar S
- Krokovny P
- Krupa W
- Krzemien W
- Kubat J
- Kubis S
- Kucewicz W
- Kucharczyk M
- Kudryavtsev V
- Kulikova EK
- Kupsc A
- Lacarrere D
- Lafferty G
- Lai A
- Lampis A
- Lancierini D
- Landesa Gomez C
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- Lane R
- Langenbruch C
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- Latham T
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- Leverington B
- LHCb Collaboration
- Li A
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- Publication venue
- Publication date
- 01/01/2023
- Field of study
A flavor-tagged time-dependent angular analysis of the decay
Bs0→ϕϕ is performed using pp collision data collected
by the LHCb experiment at % at s=13 TeV, the center-of-mass energy of
13 TeV, corresponding to an integrated luminosity of 6 fb^{-1}. The
CP-violating phase and direct CP-violation parameter are measured
to be ϕssˉs=−0.042±0.075±0.009 rad and
∣λ∣=1.004±0.030±0.009, respectively, assuming the same values
for all polarization states of the ϕϕ system. In these results, the
first uncertainties are statistical and the second systematic. These parameters
are also determined separately for each polarization state, showing no evidence
for polarization dependence. The results are combined with previous LHCb
measurements using pp collisions at center-of-mass energies of 7 and 8 TeV,
yielding ϕssˉs=−0.074±0.069 rad and ∣lambda∣=1.009±0.030. This is the most precise study of time-dependent CP violation
in a penguin-dominated B meson decay. The results are consistent with
CP symmetry and with the Standard Model predictions.Comment: All figures and tables, along with any supplementary material and
additional information, are available at
https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2023-001.html (LHCb
public pages
Observation of a resonant structure near the Ds+Ds− threshold in the B+→Ds+Ds−K+ decay
- Author
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- Abdelmotteleb ASW
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- Abudinén F
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- Zunica G
- Publication venue
- Publication date
- 26/10/2022
- Field of study
An amplitude analysis of the B+→Ds+Ds−K+ decay is carried out to
study for the first time its intermediate resonant contributions, using
proton-proton collision data collected with the LHCb detector at centre-of-mass
energies of 7, 8 and 13 TeV. A near-threshold peaking structure, referred to as
X(3960), is observed in the Ds+Ds− invariant-mass spectrum with
significance greater than 12 standard deviations. The mass, width and the
quantum numbers of the structure are measured to be 3956±5±10 MeV,
43±13±8 MeV and JPC=0++, respectively, where the first
uncertainties are statistical and the second systematic. The properties of the
new structure are consistent with recent theoretical predictions for a state
composed of ccˉssˉ quarks. Evidence for an additional structure is
found around 4140 MeV in the Ds+Ds− invariant mass, which might be
caused either by a new resonance with the 0++ assignment or by a J/ψϕ↔Ds+Ds− coupled-channel effect.Comment: All figures and tables, along with any supplementary material and
additional information, are available at
https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2022-018.html (LHCb
public pages
Measurement of the Λb0→Λ(1520)μ+μ− differential branching fraction
- Author
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- Pawley CJ
- Pellegrino A
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- Perazzini S
- Pereima D
- Pereiro Castro A
- Perret P
- Petridis K
- Petrolini A
- Petrucci S
- Petruzzo M
- Pham H
- Philippov A
- Piandani R
- Pica L
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- Pietrzyk G
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- Pinci D
- Pisani F
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- Placinta V
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- Plo Casasus M
- Polci F
- Poli Lener M
- Poluektov A
- Polukhina N
- Polyakov I
- Polycarpo E
- Ponce S
- Popov D
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- Publication venue
- Publication date
- 01/01/2023
- Field of study
The branching fraction of the rare decay Λb0→Λ(1520)μ+μ− is measured for the first time, in the squared dimuon mass
intervals, q2, excluding the J/ψ and ψ(2S) regions. The data
sample analyzed was collected by the LHCb experiment at center-of-mass energies
of 7, 8, and 13 TeV, corresponding to a total integrated luminosity of $9\
\mathrm{fb}^{-1}.Theresultinthehighestq^{2}interval,q^{2} >15.0\
\mathrm{GeV}^2/c^4$, where theoretical predictions have the smallest model
dependence, agrees with the predictions.Comment: All figures and tables, along with any supplementary material and
additional information, are available at
https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2022-050.html (LHCb
public pages
Effects of alirocumab on types of myocardial infarction: insights from the ODYSSEY OUTCOMES trial
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- Zweiker R
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2019
- Field of study
Aims The third Universal Definition of Myocardial Infarction (MI) Task Force classified MIs into five types: Type 1, spontaneous; Type 2, related to oxygen supply/demand imbalance; Type 3, fatal without ascertainment of cardiac biomarkers; Type 4, related to percutaneous coronary intervention; and Type 5, related to coronary artery bypass surgery. Low-density lipoprotein cholesterol (LDL-C) reduction with statins and proprotein convertase subtilisin–kexin Type 9 (PCSK9) inhibitors reduces risk of MI, but less is known about effects on types of MI. ODYSSEY OUTCOMES compared the PCSK9 inhibitor alirocumab with placebo in 18 924 patients with recent acute coronary syndrome (ACS) and elevated LDL-C (≥1.8 mmol/L) despite intensive statin therapy. In a pre-specified analysis, we assessed the effects of alirocumab on types of MI. Methods and results Median follow-up was 2.8 years. Myocardial infarction types were prospectively adjudicated and classified. Of 1860 total MIs, 1223 (65.8%) were adjudicated as Type 1, 386 (20.8%) as Type 2, and 244 (13.1%) as Type 4. Few events were Type 3 (n = 2) or Type 5 (n = 5). Alirocumab reduced first MIs [hazard ratio (HR) 0.85, 95% confidence interval (CI) 0.77–0.95; P = 0.003], with reductions in both Type 1 (HR 0.87, 95% CI 0.77–0.99; P = 0.032) and Type 2 (0.77, 0.61–0.97; P = 0.025), but not Type 4 MI. Conclusion After ACS, alirocumab added to intensive statin therapy favourably impacted on Type 1 and 2 MIs. The data indicate for the first time that a lipid-lowering therapy can attenuate the risk of Type 2 MI. Low-density lipoprotein cholesterol reduction below levels achievable with statins is an effective preventive strategy for both MI types.For complete list of authors see http://dx.doi.org/10.1093/eurheartj/ehz299</p
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