392 research outputs found
Two-loop Anomalous Dimensions of Heavy Baryon Currents in Heavy Quark Effective Theory
We present results on the two-loop anomalous dimensions of the heavy baryon
HQET currents with arbitrary Dirac matrices
and . From our general result we obtain the two-loop
anomalous dimensions for currents with quantum numbers of the ground state
heavy baryons , and . As a by-product of our
calculation and as an additional check we rederive the known two-loop anomalous
dimensions of mesonic scalar, pseudoscalar, vector, axial vector and tensor
currents in massless QCD as well as in HQET.Comment: 21 pages, LaTeX, 2 figures are included in PostScript forma
Helicity Analysis of Semileptonic Hyperon Decays Including Lepton Mass Effects
Using the helicity method we derive complete formulas for the joint angular
decay distributions occurring in semileptonic hyperon decays including lepton
mass and polarization effects. Compared to the traditional covariant
calculation the helicity method allows one to organize the calculation of the
angular decay distributions in a very compact and efficient way. In the
helicity method the angular analysis is of cascade type, i.e. each decay in the
decay chain is analyzed in the respective rest system of that particle. Such an
approach is ideally suited as input for a Monte Carlo event generation program.
As a specific example we take the decay () followed by the nonleptonic decay for which we show a few examples of decay distributions which are
generated from a Monte Carlo program based on the formulas presented in this
paper. All the results of this paper are also applicable to the semileptonic
and nonleptonic decays of ground state charm and bottom baryons, and to the
decays of the top quark.Comment: Published version. 40 pages, 11 figures included in the text. Typos
corrected, comments added, references added and update
Second Order Power Corrections in the Heavy Quark Effective Theory I. Formalism and Meson Form Factors
In the heavy quark effective theory, hadronic matrix elements of currents
between two hadrons containing a heavy quark are expanded in inverse powers of
the heavy quark masses, with coefficients that are functions of the kinematic
variable . For the ground state pseudoscalar and vector mesons, this
expansion is constructed at order . A minimal set of universal form
factors is defined in terms of matrix elements of higher dimension operators in
the effective theory. The zero recoil normalization conditions following from
vector current conservation are derived. Several phenomenological applications
of the general results are discussed in detail. It is argued that at zero
recoil the semileptonic decay rates for and receive only small second order corrections, which are unlikely
to exceed the level of a few percent. This supports the usefulness of the heavy
quark expansion for a reliable determination of .Comment: (34 pages, REVTEX, two postscript figures available upon request),
SLAC-PUB-589
Synthesis and in silico study of 2-furyl(4-{4-[(substituted)sulfonyl]benzyl}-1-piperazinyl)methanone derivatives as suitable therapeutic agents
Abstract In the study presented here, a new series of 2-furyl(4-{4-[(substituted)sulfonyl]benzyl}-1-piperazinyl)methanone derivatives was targeted. The synthesis was initiated by the treatment of different secondary amines (1a-h) with 4-bromomethylbenzenesulfonyl chloride (2) to obtain various 1-{[4-(bromomethyl)phenyl]sulfonyl}amines (3a-h). 2-Furyl(1-piperazinyl)methanone (2-furoyl-1-piperazine; 4) was then dissolved in acetonitrile, with the addition of K2CO3, and the mixture was refluxed for activation. This activated molecule was further treated with equi-molar amounts of 3a-h to form targeted 2-furyl(4-{4-[(substituted)sulfonyl]benzyl}-1-piperazinyl)methanone derivatives (5a-h) in the same reaction set up. The structure confirmation of all the synthesized compounds was carried out by EI-MS, IR and 1H-NMR spectral analysis. The compounds showed good enzyme inhibitory activity. Compound 5h showed excellent inhibitory effect against acetyl- and butyrylcholinesterase with respective IC50 values of 2.91±0.001 and 4.35±0.004 μM, compared to eserine, a reference standard with IC50 values of 0.04±0.0001 and 0.85±0.001 μM, respectively, against these enzymes. All synthesized molecules were active against almost all Gram-positive and Gram-negative bacterial strains tested. The cytotoxicity of the molecules was also checked to determine their utility as possible therapeutic agents
Critical behavior at m-axial Lifshitz points: field-theory analysis and -expansion results
The critical behavior of d-dimensional systems with an n-component order
parameter is reconsidered at (m,d,n)-Lifshitz points, where a wave-vector
instability occurs in an m-dimensional subspace of . Our aim is
to sort out which ones of the previously published partly contradictory
-expansion results to second order in are
correct. To this end, a field-theory calculation is performed directly in the
position space of dimensions, using dimensional
regularization and minimal subtraction of ultraviolet poles. The residua of the
dimensionally regularized integrals that are required to determine the series
expansions of the correlation exponents and and of the
wave-vector exponent to order are reduced to single
integrals, which for general m=1,...,d-1 can be computed numerically, and for
special values of m, analytically. Our results are at variance with the
original predictions for general m. For m=2 and m=6, we confirm the results of
Sak and Grest [Phys. Rev. B {\bf 17}, 3602 (1978)] and Mergulh{\~a}o and
Carneiro's recent field-theory analysis [Phys. Rev. B {\bf 59},13954 (1999)].Comment: Latex file with one figure (eps-file). Latex file uses texdraw to
generate figures that are included in the tex
1/m_Q Corrections to the Bethe-Salpeter Equation for \Lambda_{Q} in the Diquark Picture
Corrections of order 1/m_Q (Q=b or c) to the Bethe-Salpeter (B-S) equation
for \Lambda_Q are analyzed on the assumption that the heavy baryon \Lambda_Q is
composed of a heavy quark and a scalar, light diquark. It is found that in
addition to the one B-S scalar function in the limit m_Q -> \infty, two more
scalar functions are needed at the order 1/m_Q. These can be related to the B-S
scalar function in the leading order. The six form factors for the weak
transition \Lambda_b -> \Lambda_c are expressed in terms of these wave
functions and the results are consistent with heavy quark effective theory to
order 1/m_Q. Assuming the kernel for the B-S equation in the limit m_Q ->
\infty to consist of a scalar confinement term and a one-gluon-exchange term we
obtain numerical solutions for the B-S wave functions, and hence for the
form factors to order 1/m_Q. Predictions are given
for the differential and total decay widths for \Lambda_b -> \Lambda_c l
\bar{\nu}, and also for the nonleptonic decay widths for \Lambda_b -> \Lambda_c
plus a pseudoscalar or vector meson, with QCD corrections being also included.Comment: Latex, 24 pages, two figure
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
Measurement of the Bottom-Strange Meson Mixing Phase in the Full CDF Data Set
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
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements
DATA AVAILABILITY :
All non-clinical data analyzed during this study are included in this article (and its Supplementary Information). The 20p11.2 variants reported in this study were uploaded to ClinVar (SUB14235415). Clinical and genotype data can be used to identify individuals and are therefore available only through collaboration to experienced teams working on approved studies examining the mechanisms, cause, diagnosis and treatment of diabetes and other beta cell disorders. Requests for collaboration will be considered by a steering committee following an application to the Genetic Beta Cell Research Bank (https://www.diabetesgenes.org/current-research/genetic-beta-cell-research-bank/). Contact by email should be directed to S. Flanagan ([email protected]). All requests for access to data will be responded to within 14 d. Accession codes and DOI numbers for all ChIP-seq, ATAC-seq, RNA-seq and scRNA-seq datasets are provided in Supplementary Table 2. We used the Genome Reference Consortium Human Build 37 (GRCh37) to annotate genetic data (accession number GCF_000001405.13). Details of this assembly are provided at https://www.ncbi.nlm.nih.gov/assembly/GCF_000001405.13/.Persistent congenital hyperinsulinism (HI) is a rare genetically heterogeneous condition characterised by dysregulated insulin secretion leading to life-threatening hypoglycaemia. For up to 50% of affected individuals screening of the known HI genes does not identify a disease-causing variant. Large deletions have previously been used to identify novel regulatory regions causing HI. Here, we used genome sequencing to search for novel large (>1 Mb) deletions in 180 probands with HI of unknown cause and replicated our findings in a large cohort of 883 genetically unsolved individuals with HI using off-target copy number variant calling from targeted gene panels. We identified overlapping heterozygous deletions in five individuals (range 3–8 Mb) spanning chromosome 20p11.2. The pancreatic beta-cell transcription factor gene, FOXA2, a known cause of HI was deleted in two of the five individuals. In the remaining three, we found a minimal deleted region of 2.4 Mb adjacent to FOXA2 that encompasses multiple non-coding regulatory elements that are in conformational contact with FOXA2. Our data suggests that the deletions in these three children may cause disease through the dysregulation of FOXA2 expression. These findings provide new insights into the regulation of FOXA2 in the beta-cell and confirm an aetiological role for chromosome 20p11.2 deletions in syndromic HI.Funded in whole, or in part, by Wellcome.http://www.nature.come/jhghj2024Biochemistry, Genetics and Microbiology (BGM)SDG-03:Good heatlh and well-bein
Evaluation of sesamum gum as an excipient in matrix tablets
In developing countries modern medicines are often beyond the affordability of the majority of the population. This is due to the reliance on expensive imported raw materials despite the abundance of natural resources which could provide an equivalent or even an improved function. The aim of this study was to investigate the potential of sesamum gum (SG) extracted from the leaves of Sesamum radiatum (readily cultivated in sub-Saharan Africa) as a matrix former. Directly compressed matrix tablets were prepared from the extract and compared with similar matrices of HPMC (K4M) using theophylline as a model water soluble drug. The compaction, swelling, erosion and drug release from the matrices were studied in deionized water, 0.1 N HCl (pH 1.2) and phosphate buffer (pH 6.8) using USP apparatus II. The data from the swelling, erosion and drug release studies were also fitted into the respective mathematical models. Results showed that the matrices underwent a combination of swelling and erosion, with the swelling action being controlled by the rate of hydration in the medium. SG also controlled the release of theophylline similar to the HPMC and therefore may have use as an alternative excipient in regions where Sesamum radiatum can be easily cultivated
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