16 research outputs found
Implications of the Top Quark Mass Measurement for the CKM Parameters, and CP Asymmetries
Motivated by the recent determination of the top quark mass by the CDF
collaboration, \mt =174 \pm 10 ^{+13}_{-12} GeV, we review and update the
constraints on the parameters of the quark flavour mixing matrix in
the standard model. In performing our fits, we use inputs from the measurements
of the following quantities: (i) \abseps, the CP-violating parameter in
decays, (ii) \delmd, the mass difference due to the \bdbdbar\ mixing, (iii)
the matrix elements \absvcb and \absvub, and (iv) -hadron lifetimes. We
find that the allowed region of the unitarity triangle is very large, mostly
due to theoretical uncertainties. (This emphasizes the importance of
measurements of CP-violating rate asymmetries in the system.) Nevertheless,
the present data do somewhat restrict the allowed values of the coupling
constant product and the renormalization-scale
invariant bag constant . With the updated CKM matrix we present the
currently-allowed range of the ratio , as well as
the standard model predictions for the \bsbsbar\ mixing parameter \xs and the
quantities , and , which characterize
the CP-asymmetries in -decays. The ALEPH collaboration has recently reported
a significant improvement on the lower limit on the \bs-\bsb mass
difference, (95\% C.L.). This has interesting
consequences for the CKM parameters which are also worked out.
NOTE: this is a revised and updated version of our previous paper.Comment: LaTeX, 27 pages, 16 uuencoded figures (enclosed), CERN-TH.7398/94,
UdeM-GPP-TH-94-0
Fractal dimension and degree of order in sequential deposition of mixture
We present a number models describing the sequential deposition of a mixture
of particles whose size distribution is determined by the power-law , . We explicitly obtain the scaling function in
the case of random sequential adsorption (RSA) and show that the pattern
created in the long time limit becomes scale invariant. This pattern can be
described by an unique exponent, the fractal dimension. In addition, we
introduce an external tuning parameter beta to describe the correlated
sequential deposition of a mixture of particles where the degree of correlation
is determined by beta, while beta=0 corresponds to random sequential deposition
of mixture. We show that the fractal dimension of the resulting pattern
increases as beta increases and reaches a constant non-zero value in the limit
when the pattern becomes perfectly ordered or non-random
fractals.Comment: 16 pages Latex, Submitted to Phys. Rev.
Leptonic and Semileptonic Decays of Charm and Bottom Hadrons
We review the experimental measurements and theoretical descriptions of
leptonic and semileptonic decays of particles containing a single heavy quark,
either charm or bottom. Measurements of bottom semileptonic decays are used to
determine the magnitudes of two fundamental parameters of the standard model,
the Cabibbo-Kobayashi-Maskawa matrix elements and . These
parameters are connected with the physics of quark flavor and mass, and they
have important implications for the breakdown of CP symmetry. To extract
precise values of and from measurements, however,
requires a good understanding of the decay dynamics. Measurements of both charm
and bottom decay distributions provide information on the interactions
governing these processes. The underlying weak transition in each case is
relatively simple, but the strong interactions that bind the quarks into
hadrons introduce complications. We also discuss new theoretical approaches,
especially heavy-quark effective theory and lattice QCD, which are providing
insights and predictions now being tested by experiment. An international
effort at many laboratories will rapidly advance knowledge of this physics
during the next decade.Comment: This review article will be published in Reviews of Modern Physics in
the fall, 1995. This file contains only the abstract and the table of
contents. The full 168-page document including 47 figures is available at
http://charm.physics.ucsb.edu/papers/slrevtex.p
from the Hadron Energy Spectrum in Inclusive Semileptonic B Decays
A measurement of the hadron energy spectrum in inclusive semileptonic
decays is proposed as a viable method for extracting . Compared to
the traditional energy spectrum of the charged lepton, the hadron energy
spectrum exhibits kinematical advantages such as a wider energy window and a
larger signal branching fraction. It is emphasized that the hadron energy
spectrum method is most suited for symmetric factories, such as CLEO. The
hadron energy distribution is calculated in the approach of the Altarelli et
al. model and of the heavy-quark effective field theory. In both methods,
perturbative QCD corrections, the Fermi motion of the -quark in the
-meson, and the recoil momentum of the -meson (stemming from the
resonance) are taken into account. We have found excellent
agreement between the spectra calculated in both methods, especially in the
relevant kinematical region below the charmed meson threshold. The theoretical
error to , which is dominated by the uncertainty of the -quark
mass, is estimated to be at the level.Comment: 16 pages, 4 Figures included in the text (uses epsfig.sty), 1 tabl
Determination of |Vcb| using the semileptonic decay \bar{B}^0 --> D^{*+}e^-\bar{\nu}
We present a measurement of the Cabibbo-Kobayashi-Maskawa (CKM) matrix
element |Vcb| using a 10.2 fb^{-1} data sample recorded at the \Upsilon(4S)
resonance with the Belle detector at the KEKB asymmetric e^+e^- storage ring.
By extrapolating the differential decay width of the \bar{B}^0 -->
D^{*+}e^-\bar{\nu} decay to the kinematic limit at which the D^{*+} is at rest
with respect to the \bar{B}^0, we extract the product of |Vcb| with the
normalization of the decay form factor F(1), |Vcb |F(1)=
(3.54+/-0.19+/-0.18)x10^{-2}, where the first error is statistical and the
second is systematic. A value of |Vcb| = (3.88+/-0.21+/-0.20+/-0.19)x10^{-2} is
obtained using a theoretical calculation of F(1), where the third error is due
to the theoretical uncertainty in the value of F(1). The branching fraction
B(\bar{B}^0 --> D^{*+}e^-\bar{\nu}) is measured to be
(4.59+/-0.23+/-0.40)x10^{-2}.Comment: 20 pages, 6 figures, elsart.cls, submitted to PL
Dislocation multi-junctions and strain hardening
At the microscopic scale, the strength of a crystal derives from the motion, multiplication and interaction of distinctive line defects--dislocations. First theorized in 1934 to explain low magnitudes of crystal strength observed experimentally, the existence of dislocations was confirmed only two decades later. Much of the research in dislocation physics has since focused on dislocation interactions and their role in strain hardening: a common phenomenon in which continued deformation increases a crystal's strength. The existing theory relates strain hardening to pair-wise dislocation reactions in which two intersecting dislocations form junctions tying dislocations together. Here we report that interactions among three dislocations result in the formation of unusual elements of dislocation network topology, termed hereafter multi-junctions. The existence of multi-junctions is first predicted by Dislocation Dynamics (DD) and atomistic simulations and then confirmed by the transmission electron microscopy (TEM) experiments in single crystal molybdenum. In large-scale Dislocation Dynamics simulations, multi-junctions present very strong, nearly indestructible, obstacles to dislocation motion and furnish new sources for dislocation multiplication thereby playing an essential role in the evolution of dislocation microstructure and strength of deforming crystals. Simulation analyses conclude that multi-junctions are responsible for the strong orientation dependence of strain hardening in BCC crystals
Semileptonic Meson Decays in the Quark Model: An Update
We present the predictions of ISGW2, an update of the ISGW quark model for
semileptonic meson decays. The updated model incorporates a number of features
which should make it more reliable, including the constraints imposed by Heavy
Quark Symmetry, hyperfine distortions of wavefunctions, and form factors with
more realistic high recoil behaviors.Comment: All text and tables contained in the ".latex" file and all figures
(14) contained in the ".uu" file
Measurement of the B -> D^* l nu Branching Fractions and |Vcb|
We study the exclusive semileptonic B meson decays B- -> D*0 l- nu and B0 ->
D*+ l- nu using data collected with the CLEO II detector at CESR. We present
measurements of the branching fractions B(B0 -> D*+ l-nu) = 0.5/f00*
[4.49+/-0.32+/-0.39]% and B(B- -> D*0 l-nu) = 0.5/f+-*[5.13+/-0.54+/-0.64]%,
where f00 and f+- are the neutral and charged B meson production fractions at
the Upsilon(4s) resonance. Assuming isospion invariance and taking the charged
to neutral B meson lifetimes measured at higher energy machines, we determine
the ratio f+-/f00=1.04+/-0.14+/-0.13+-/-0.10; further assuming f+- + f00 = 1 we
also determine the partial width G(B->D* l nu) = 29.9+/-1.9+/-2.7+/-2.0 ns-1
(independent of f+-/f00). From this partial width we calculate B -> D* l nu
branching fractions that do not depend on f+-/f00, nor the individual B
lifetimes, but only on the charged to neutral lifetime ratio. The product of
the CKM matrix element |Vcb| times the normalization of the decay form factor
at the point of zero recoil of the D* meson, F(y=1), is determined from a
linear fit to the combined differential decay rate of the exclusive B->D* l nu
decays: |Vcb|F(y) = 0.0351 +/- 0.0019 +/- 0.0018 +/- 0.0008. Using theoretical
calculations of the form factor normalization we extract a value for |Vcb|.
LATEX (REVTEX style) file with uuencoded figures attached (uses PSBOX).
Available on WWW http://w4.lns.cornell.edu/public/CLNS/Comment: 42 pages,CLNS 94/1285, CLEO 94-2
Altered H3 histone acetylation impairs high-fidelity DNA repair to promote cerebellar degeneration in spinocerebellar ataxia type 7.
A common mechanism in inherited ataxia is a vulnerability of DNA damage. Spinocerebellar ataxia type 7 (SCA7) is a CAG-polyglutamine-repeat disorder characterized by cerebellar and retinal degeneration. Polyglutamine-expanded ataxin-7 protein incorporates into STAGA co-activator complex and interferes with transcription by altering histone acetylation. We performed chromatic immunoprecipitation sequencing ChIP-seq on cerebellum from SCA7 mice and observed increased H3K9-promoter acetylation in DNA repair genes, resulting in increased expression. After detecting increased DNA damage in SCA7 cells, mouse primary cerebellar neurons, and patient stem-cell-derived neurons, we documented reduced homology-directed repair (HDR) and single-strand annealing (SSA). To evaluate repair at endogenous DNA in native chromosome context, we modified linear amplification-mediated high-throughput genome-wide translocation sequencing and found that DNA translocations are less frequent in SCA7 models, consistent with decreased HDR and SSA. Altered DNA repair function in SCA7 may predispose the subject to excessive DNA damage, leading to neuron demise and highlights DNA repair as a therapy target
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Glucocorticoid receptor recruits to enhancers and drives activation by motif-directed binding
Glucocorticoids are potent steroid hormones that regulate immunity and metabolism by activating the transcription factor (TF) activity of glucocorticoid receptor (GR). Previous models have proposed that DNA binding motifs and sites of chromatin accessibility predetermine GR binding and activity. However, there are vast excesses of both features relative to the number of GR binding sites. Thus, these features alone are unlikely to account for the specificity of GR binding and activity. To identify genomic and epigenetic contributions to GR binding specificity and the downstream changes resultant from GR binding, we performed hundreds of genome-wide measurements of TF binding, epigenetic state, and gene expression across a 12-h time course of glucocorticoid exposure. We found that glucocorticoid treatment induces GR to bind to nearly all pre-established enhancers within minutes. However, GR binds to only a small fraction of the set of accessible sites that lack enhancer marks. Once GR is bound to enhancers, a combination of enhancer motif composition and interactions between enhancers then determines the strength and persistence of GR binding, which consequently correlates with dramatic shifts in enhancer activation. Over the course of several hours, highly coordinated changes in TF binding and histone modification occupancy occur specifically within enhancers, and these changes correlate with changes in the expression of nearby genes. Following GR binding, changes in the binding of other TFs precede changes in chromatin accessibility, suggesting that other TFs are also sensitive to genomic features beyond that of accessibility