217 research outputs found
A search for the decay modes B+/- to h+/- tau l
We present a search for the lepton flavor violating decay modes B+/- to h+/-
tau l (h= K,pi; l= e,mu) using the BaBar data sample, which corresponds to 472
million BBbar pairs. The search uses events where one B meson is fully
reconstructed in one of several hadronic final states. Using the momenta of the
reconstructed B, h, and l candidates, we are able to fully determine the tau
four-momentum. The resulting tau candidate mass is our main discriminant
against combinatorial background. We see no evidence for B+/- to h+/- tau l
decays and set a 90% confidence level upper limit on each branching fraction at
the level of a few times 10^-5.Comment: 15 pages, 7 figures, submitted to Phys. Rev.
Observation and study of baryonic B decays: B -> D(*) p pbar, D(*) p pbar pi, and D(*) p pbar pi pi
We present a study of ten B-meson decays to a D(*), a proton-antiproton pair,
and a system of up to two pions using BaBar's data set of 455x10^6 BBbar pairs.
Four of the modes (B0bar -> D0 p anti-p, B0bar -> D*0 p anti-p, B0bar -> D+ p
anti-p pi-, B0bar -> D*+ p anti-p pi-) are studied with improved statistics
compared to previous measurements; six of the modes (B- -> D0 p anti-p pi-, B-
-> D*0 p anti-p pi-, B0bar -> D0 p anti-p pi- pi+, B0bar -> D*0 p anti-p pi-
pi+, B- -> D+ p anti-p pi- pi-, B- -> D*+ p anti-p pi- pi-) are first
observations. The branching fractions for 3- and 5-body decays are suppressed
compared to 4-body decays. Kinematic distributions for 3-body decays show
non-overlapping threshold enhancements in m(p anti-p) and m(D(*)0 p) in the
Dalitz plots. For 4-body decays, m(p pi-) mass projections show a narrow peak
with mass and full width of (1497.4 +- 3.0 +- 0.9) MeV/c2, and (47 +- 12 +- 4)
MeV/c2, respectively, where the first (second) errors are statistical
(systematic). For 5-body decays, mass projections are similar to phase space
expectations. All results are preliminary.Comment: 28 pages, 90 postscript figures, submitted to LP0
Study of Bbar --> Xu l nubar decays in BBbar events tagged by a fully reconstructed B-meson decay and determination of |V_{ub}|
We report measurements of partial branching fractions for inclusive charmless
semileptonic B decays Bbar --> Xu l nubar, and the determination of the CKM
matrix element |V_{ub}|. The analysis is based on a sample of 467 million
Upsilon(4S) --> BBar decays recorded with the BaBar detector at the PEP-II e^+
e^- storage rings. We select events in which the decay of one of the B mesons
is fully reconstructed and an electron or a muon signals the semileptonic decay
of the other B meson. We measure partial branching fractions DeltaB in several
restricted regions of phase space and determine the CKM element |V_{ub}| based
on four different QCD predictions. For decays with a charged lepton momentum
p_l^* > 1.0 GeV in the B meson rest frame, we obtain DeltaB = (1.80 \pm 0.13
(stat.) \pm 0.15 (sys.) \pm 0.02 (theo.)) \times 10^{-3} from a fit to the
two-dimensional mX-q^2 distribution. Here, mX refers to the invariant mass of
the final state hadron X and q^2 is the invariant mass squared of the charged
lepton and neutrino. From this measurement we extract |V_{ub}| = (4.33\pm 0.24
(exp.) \pm 0.15 (theo.)) \times 10^{-3} as the arithmetic average of four
results obtained from four different QCD predictions of the partial rate. We
separately determine partial branching fractions for B^0 and B^- decays and
derive a limit on the isospin breaking in Bbar --> Xu l nubar decays.Comment: 26 pages, 9 postscript figures, 9 tables, accepted for publication in
PR
Search for the and states in and
We search for the and states, reported by the
Belle Collaboration, decaying to in the decays and where \chi_{c1} \to
\jpsi \gamma. The data were collected with the BaBar detector at the SLAC
PEP-II asymmetric-energy collider operating at center-of-mass energy
10.58 GeV, and correspond to an integrated luminosity of 429 fb. In this
analysis, we model the background-subtracted, efficiency-corrected
mass distribution using the mass distribution and the
corresponding normalized Legendre polynomial moments, and then test the
need for the inclusion of resonant structures in the description of the
mass distribution. No evidence is found for the
and resonances, and 90% confidence level upper limits on the
branching fractions are reported for the corresponding -meson decay modes.Comment: 15 pages, 12 postscript figures, to be published in Phys. Rev.
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Measurement of the branching fraction ratios and CP asymmetries in B-→ D0 CP K-decays
We present a preliminary study of and decays, with the reconstructed in the CP-odd
eigenstates , , in the CP-even eigenstates ,
, and in the (non-CP) flavor eigenstate . Using a
sample of about 382 million Y(4S) decays into BBbar pairs, collected with the
BABAR detector operating at the PEP-II asymmetric-energy B Factory at SLAC, we
measure the ratios of the branching fractions R_CP+- and the direct CP
asymmetries A_CP+-. The results are:
R_CP- = 0.81 \pm 0.10 (stat) \pm 0.05 (syst)
R_CP+ = 1.07 \pm 0.10 (stat) \pm 0.04 (syst)
A_CP- = -0.19 \pm 0.12 (stat) \pm 0.02 (syst)
A_CP+ = 0.35 \pm 0.09 (stat) \pm 0.05 (syst
Minority quasispecies of drug-resistant HIV-1 that lead to early therapy failure in treatment-naive and -adherent patients
BACKGROUND: Early virological failure of antiretroviral therapy associated with the selection of drug-resistant human immunodeficiency virus type 1 in treatment-naive patients is very critical, because virological failure significantly increases the risk of subsequent failures. Therefore, we evaluated the possible role of minority quasispecies of drug-resistant human immunodeficiency virus type 1, which are undetectable at baseline by population sequencing, with regard to early virological failure. METHODS: We studied 4 patients who experienced early virological failure of a first-line regimen of lamivudine, tenofovir, and either efavirenz or nevirapine and 18 control patients undergoing similar treatment without virological failure. The key mutations K65R, K103N, Y181C, M184V, and M184I in the reverse transcriptase were quantified by allele-specific real-time polymerase chain reaction performed on plasma samples before and during early virological treatment failure. RESULTS: Before treatment, none of the viruses showed any evidence of drug resistance in the standard genotype analysis. Minority quasispecies with either the M184V mutation or the M184I mutation were detected in 3 of 18 control patients. In contrast, all 4 patients whose treatment was failing had harbored drug-resistant viruses at low frequencies before treatment, with a frequency range of 0.07%-2.0%. A range of 1-4 mutations was detected in viruses from each patient. Most of the minority quasispecies were rapidly selected and represented the major virus population within weeks after the patients started antiretroviral therapy. All 4 patients showed good adherence to treatment. Nonnucleoside reverse-transcriptase inhibitor plasma concentrations were in normal ranges for all 4 patients at 2 separate assessment times. CONCLUSIONS: Minority quasispecies of drug-resistant viruses, detected at baseline, can rapidly outgrow and become the major virus population and subsequently lead to early therapy failure in treatment-naive patients who receive antiretroviral therapy regimens with a low genetic resistance barrier
Search for the highly suppressed decays B- -> K+π-π- and B- -> K-K-π+
We report a search for the decays B- -> K+pi(-)pi(-) and B- -> K-K-pi(+), which are highly suppressed in the standard model. Using a sample of (467 +/- 5) x 10(6) B (B) over bar pairs collected with the BABAR detector, we do not see any evidence of these decays and determine 90% confidence level upper limits of B(B- -> K+pi(-)pi(-)) and K-K-pi(+)) and < 1.6 x 10(-7) on the corresponding branching fractions, including systematic uncertainties
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