3,132 research outputs found
The teaching profession in Europe : historical and sociological analysis
A possible effect of direct CP violation in D -> K-S(0)pi(+)pi(-) decay on the gamma measurement from B-+/- -> DK +/-, D -> K-S(0)pi(+)pi(-) Dalitz plot analysis is considered. Systematic uncertainty of gamma coming from the current limits on direct CP violation in D -> K-S(0)pi(+)pi(-) is estimated, and a modified model-independent procedure of B-+/- -> DK +/-, D -> K-S(0)pi(+)pi(-) Dalitz plot analysis is proposed that gives an unbiased gamma measurement even in presence of direct CP violation in charm decays. The technique is applicable to other threebody D decays such as D-0 -> (KSK+K-)-K-0, D-0 -> pi(+)pi(-)pi(0), etc
Copper Inhibits the Water and Glycerol Permeability of Aquaporin-3
Aquaporin-3 (AQP3) is an aquaglyceroporin expressed in erythrocytes and several other tissues. Erythrocytes are, together with kidney and liver, the main targets for copper toxicity. Here we report that both water and glycerol permeability of human AQP3 is inhibited by copper. Inhibition is fast, dose-dependent, and reversible. If copper is dissolved in carbonic acid-bicarbonate buffer, the natural buffer system in our body, doses in the range of those observed in Wilson disease and in copper poisoning caused significant inhibition. AQP7, another aquaglyceroporin, was insensitive to copper. Three extracellular amino acid residues, Trp128, Ser152, and His241, were identified as responsible for the effect of copper on AQP3. We have previously shown that Ser152 is involved in regulation of AQP3 by pH. The fact that Ser152 mediates regulation of AQP3 by copper may explain the phenomenon of exquisite sensitivity of human erythrocytes to copper at acidic pH. When AQP3 was co-expressed with another AQP, only glycerol but not water permeability was inhibited by copper. Our results provide a better understanding of processes that occur in severe copper metabolism defects such as Wilson disease and in copper poisoning
Genetic variability and population structure of endangered Panax ginseng in the Russian Primorye
<p>Abstract</p> <p>Background</p> <p>The natural habitat of wild <it>P. ginseng </it>is currently found only in the Russian Primorye and the populations are extremely exhausted and require restoration. Analysis of the genetic diversity and population structure of an endangered species is a prerequisite for conservation. The present study aims to investigate the patterns and levels of genetic polymorphism and population structures of wild <it>P. ginseng </it>with the AFLP method to (1) estimate the level of genetic diversity in the <it>P. ginseng </it>populations in the Russian Primorsky Krai, (2) calculate the distribution of variability within a population and among populations and (3) examine the genetic relationship between the populations.</p> <p>Methods</p> <p>Genetic variability and population structure of ten <it>P. ginseng </it>populations were investigated with Amplified Fragment Length Polymorphism (AFLP) markers. The genetic relationships among <it>P. ginseng </it>plants and populations were delineated.</p> <p>Results</p> <p>The mean genetic variability within populations was high. The mean level of polymorphisms was 55.68% at the population level and 99.65% at the species level. The Shannon's index ranged between 0.1602 and 0.3222 with an average of 0.2626 at the population level and 0.3967 at the species level. The analysis of molecular variances (AMOVA) showed a significant population structure in <it>P. ginseng</it>. The partition of genetic diversity with AMOVA suggested that the majority of the genetic variation (64.5%) was within populations of <it>P. ginseng</it>. The inter-population variability was approximately 36% of the total variability. The genetic relationships among <it>P. ginseng </it>plants and populations were reconstructed by Minimum Spanning tree (MS-tree) on the basis of Euclidean distances with ARLEQUIN and NTSYS, respectively. The MS-trees suggest that the southern <it>Uss</it>, <it>Part </it>and <it>Nad </it>populations may have promoted <it>P. ginseng </it>distribution throughout the Russian Primorye.</p> <p>Conclusion</p> <p>The <it>P. ginseng </it>populations in the Russian Primorye are significant in genetic diversity. The high variability demonstrates that the current genetic resources of <it>P. ginseng </it>populations have not been exposed to depletion.</p
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Search for lepton-flavour-violating decays of Higgs-like bosons.
A search is presented for a Higgs-like boson with mass in the range 45 to 195 GeV/c2 decaying into a muon and a tau lepton. The dataset consists of proton-proton interactions at a centre-of-mass energy of 8 TeV , collected by the LHCb experiment, corresponding to an integrated luminosity of 2 fb-1 . The tau leptons are reconstructed in both leptonic and hadronic decay channels. An upper limit on the production cross-section multiplied by the branching fraction at 95% confidence level is set and ranges from 22 pb for a boson mass of 45 GeV/c2 to 4 pb for a mass of 195 GeV/c2
Study of the Process e+ e- --> omega pi0 --> pi0 pi0 gamma in c.m. Energy Range 920--1380 MeV at CMD-2
The cross section of the process e+ e- --> omega pi0 --> pi0 pi0 gamma has
been measured in the c.m. energy range 920-1380 MeV with the CMD-2 detector.
Its energy dependence is well described by the interference of the rho(770) and
rho'(1450) mesons decaying to omega pi0. Upper limits for the cross sections of
the direct processes e+ e- --> pi0 pi0 gamma, eta pi0 gamma have been set.Comment: Accepted for publication in PL
Observation of the Cabibbo-suppressed decay Xi_c+ -> p K- pi+
We report the first observation of the Cabibbo-suppressed charm baryon decay
Xi_c+ -> p K- pi+. We observe 150 +- 22 events for the signal. The data were
accumulated using the SELEX spectrometer during the 1996-1997 fixed target run
at Fermilab, chiefly from a 600 GeV/c Sigma- beam. The branching fractions of
the decay relative to the Cabibbo-favored Xi_c+ -> Sigma+ K- pi+ and Xi_c+ ->
X- pi+ pi+ are measured to be B(Xi_c+ -> p K- pi+)/B(Xi_c+ -> Sigma+ K- pi+) =
0.22 +- 0.06 +- 0.03 and B(Xi_c+ -> p K- pi+)/B(Xi_c+ -> X- pi+ pi+) = 0.20 +-
0.04 +- 0.02, respectively.Comment: 5 pages, RevTeX, 3 figures (postscript), Submitted to Phys. Rev. Let
Differential branching fraction and angular analysis of the decay B0âKâ0ÎŒ+ÎŒâ
The angular distribution and differential branching fraction of the decay B 0â K â0 ÎŒ + ÎŒ â are studied using a data sample, collected by the LHCb experiment in pp collisions at sâ=7 TeV, corresponding to an integrated luminosity of 1.0 fbâ1. Several angular observables are measured in bins of the dimuon invariant mass squared, q 2. A first measurement of the zero-crossing point of the forward-backward asymmetry of the dimuon system is also presented. The zero-crossing point is measured to be q20=4.9±0.9GeV2/c4 , where the uncertainty is the sum of statistical and systematic uncertainties. The results are consistent with the Standard Model predictions
Measurement of the ratio of branching fractions BR(B0 -> K*0 gamma)/BR(Bs0 -> phi gamma)
The ratio of branching fractions of the radiative B decays B0 -> K*0 gamma
and Bs0 -> phi gamma has been measured using 0.37 fb-1 of pp collisions at a
centre of mass energy of sqrt(s) = 7 TeV, collected by the LHCb experiment. The
value obtained is BR(B0 -> K*0 gamma)/BR(Bs0 -> phi gamma) = 1.12 +/- 0.08
^{+0.06}_{-0.04} ^{+0.09}_{-0.08}, where the first uncertainty is statistical,
the second systematic and the third is associated to the ratio of fragmentation
fractions fs/fd. Using the world average for BR(B0 -> K*0 gamma) = (4.33 +/-
0.15) x 10^{-5}, the branching fraction BR(Bs0 -> phi gamma) is measured to be
(3.9 +/- 0.5) x 10^{-5}, which is the most precise measurement to date.Comment: 15 pages, 1 figure, 2 table
Opposite-side flavour tagging of B mesons at the LHCb experiment
The calibration and performance of the oppositeside
flavour tagging algorithms used for the measurements
of time-dependent asymmetries at the LHCb experiment
are described. The algorithms have been developed using
simulated events and optimized and calibrated with
B
+ âJ/ÏK
+, B0 âJ/ÏK
â0 and B0 âD
ââ
Ό
+
ΜΌ decay
modes with 0.37 fbâ1 of data collected in pp collisions
at
â
s = 7 TeV during the 2011 physics run. The oppositeside
tagging power is determined in the B
+ â J/ÏK
+
channel to be (2.10 ± 0.08 ± 0.24) %, where the first uncertainty
is statistical and the second is systematic
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