284 research outputs found
Can we Rationally Learn to Coordinate?
In this paper we examine the issue whether individual rationality considerations are sufficient to guarantee that individuals will learn to coordinate. This question is central in any discussion of whether social phenomena (read: conventions) can be explained in terms of a purely individualistic approach. We argue that the positive answers to this general question that have been obtained in some recent work require assumptions which incorporate some convention. This conclusion may be seen as supporting the viewpoint of institutional individualism in contrast to psychological individualism
Measurement of the branching fraction for
We have studied the leptonic decay of the resonance into tau
pairs using the CLEO II detector. A clean sample of tau pair events is
identified via events containing two charged particles where exactly one of the
particles is an identified electron. We find . The result is consistent with
expectations from lepton universality.Comment: 9 pages, RevTeX, two Postscript figures available upon request, CLNS
94/1297, CLEO 94-20 (submitted to Physics Letters B
Production and Decay of D_1(2420)^0 and D_2^*(2460)^0
We have investigated and final states and
observed the two established charmed mesons, the with mass
MeV/c and width MeV/c and
the with mass MeV/c and width
MeV/c. Properties of these final states, including
their decay angular distributions and spin-parity assignments, have been
studied. We identify these two mesons as the doublet predicted
by HQET. We also obtain constraints on {\footnotesize } as a function of the cosine of the relative phase of the two
amplitudes in the decay.Comment: 15 pages in REVTEX format. hardcopies with figures can be obtained by
sending mail to: [email protected]
Measurement of the Decay Asymmetry Parameters in and
We have measured the weak decay asymmetry parameters (\aLC ) for two \LC\
decay modes. Our measurements are \aLC = -0.94^{+0.21+0.12}_{-0.06-0.06} for
the decay mode and \aLC = -0.45\pm 0.31 \pm
0.06 for the decay mode . By combining these
measurements with the previously measured decay rates, we have extracted the
parity-violating and parity-conserving amplitudes. These amplitudes are used to
test models of nonleptonic charmed baryon decay.Comment: 11 pages including the figures. Uses REVTEX and psfig macros. Figures
as uuencoded postscript. Also available as
http://w4.lns.cornell.edu/public/CLNS/1995/CLNS95-1319.p
Observation of the Charmed Baryon Decays to , , and
We have observed two new decay modes of the charmed baryon into
and using data collected with the
CLEO II detector. We also present the first measurement of the branching
fraction for the previously observed decay mode . The branching fractions for these three modes relative to
are measured to be , , and , respectively.Comment: 12 page uuencoded postscript file, postscript file also available
through http://w4.lns.cornell.edu/public/CLN
Properties of baryon resonances from a multichannel partial wave analysis
Properties of nucleon and resonances are derived from a multichannel
partial wave analysis. The statistical significance of pion and photo-induced
inelastic reactions off protons are studied in a multichannel partial-wave
analysis.Comment: 12 pages, 8 Table
Nucleon resonances in the fourth resonance region
Nucleon and resonances in the fourth resonance region are studied in
a multichannel partial-wave analysis which includes nearly all available data
on pion- and photo-induced reactions off protons. In the high-mass range, above
1850\,MeV, several alternative solutions yield a good description of the data.
For these solutions, masses, widths, pole residues and photo-couplings are
given. In particular, we find evidence for nucleon resonances with
spin-parities . For one set of solutions, there are four
resonances forming naturally a spin-quartet of resonances with orbital angular
momentum L=2 and spin S=3/2 coupling to . Just below 1.9\,GeV we
find a spin doublet of resonances with and . Since a spin
partner with is missing at this mass, the two resonances form a
spin doublet which must have a symmetric orbital-angular-momentum wave function
with L=1. For another set of solutions, the four positive-parity resonances are
accompanied by mass-degenerate negative-parity partners -- as suggested by the
conjecture of chiral symmetry restoration. The possibility of a spin doublet at 1900\,MeV belonging to a 20-plet is discussed.Comment: 16 page
Asymptotic stability of solitary waves
We show that the family of solitary waves (1-solitons) of the Korteweg-de Vries equation is asymptotically stable. Our methods also apply for the solitary waves of a class of generalized Korteweg-de Vries equations, In particular, we study the case where f(u)=u p+1 / (p+1) , p =1, 2, 3 (and 30, with f ∈ C 4 ). The same asymptotic stability result for KdV is also proved for the case p =2 (the modified Korteweg-de Vries equation). We also prove asymptotic stability for the family of solitary waves for all but a finite number of values of p between 3 and 4. (The solitary waves are known to undergo a transition from stability to instability as the parameter p increases beyond the critical value p =4.) The solution is decomposed into a modulating solitary wave, with time-varying speed c(t) and phase γ( t ) ( bound state part ), and an infinite dimensional perturbation ( radiating part ). The perturbation is shown to decay exponentially in time, in a local sense relative to a frame moving with the solitary wave. As p →4 − , the local decay or radiation rate decreases due to the presence of a resonance pole associated with the linearized evolution equation for solitary wave perturbations.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/46489/1/220_2005_Article_BF02101705.pd
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Epstein-Barr virus: clinical and epidemiological revisits and genetic basis of oncogenesis
Epstein-Barr virus (EBV) is classified as a member in the order herpesvirales, family herpesviridae, subfamily gammaherpesvirinae and the genus lymphocytovirus. The virus is an exclusively human pathogen and thus also termed as human herpesvirus 4 (HHV4). It was the first oncogenic virus recognized and has been incriminated in the causation of tumors of both lymphatic and epithelial nature. It was reported in some previous studies that 95% of the population worldwide are serologically positive to the virus. Clinically, EBV primary infection is almost silent, persisting as a life-long asymptomatic latent infection in B cells although it may be responsible for a transient clinical syndrome called infectious mononucleosis. Following reactivation of the virus from latency due to immunocompromised status, EBV was found to be associated with several tumors. EBV linked to oncogenesis as detected in lymphoid tumors such as Burkitt's lymphoma (BL), Hodgkin's disease (HD), post-transplant lymphoproliferative disorders (PTLD) and T-cell lymphomas (e.g. Peripheral T-cell lymphomas; PTCL and Anaplastic large cell lymphomas; ALCL). It is also linked to epithelial tumors such as nasopharyngeal carcinoma (NPC), gastric carcinomas and oral hairy leukoplakia (OHL). In vitro, EBV many studies have demonstrated its ability to transform B cells into lymphoblastoid cell lines (LCLs). Despite these malignancies showing different clinical and epidemiological patterns when studied, genetic studies have suggested that these EBV- associated transformations were characterized generally by low level of virus gene expression with only the latent virus proteins (LVPs) upregulated in both tumors and LCLs. In this review, we summarize some clinical and epidemiological features of EBV- associated tumors. We also discuss how EBV latent genes may lead to oncogenesis in the different clinical malignancie
Identification of common genetic risk variants for autism spectrum disorder
Autism spectrum disorder (ASD) is a highly heritable and heterogeneous group of neurodevelopmental phenotypes diagnosed in more than 1% of children. Common genetic variants contribute substantially to ASD susceptibility, but to date no individual variants have been robustly associated with ASD. With a marked sample-size increase from a unique Danish population resource, we report a genome-wide association meta-analysis of 18,381 individuals with ASD and 27,969 controls that identified five genome-wide-significant loci. Leveraging GWAS results from three phenotypes with significantly overlapping genetic architectures (schizophrenia, major depression, and educational attainment), we identified seven additional loci shared with other traits at equally strict significance levels. Dissecting the polygenic architecture, we found both quantitative and qualitative polygenic heterogeneity across ASD subtypes. These results highlight biological insights, particularly relating to neuronal function and corticogenesis, and establish that GWAS performed at scale will be much more productive in the near term in ASD.Peer reviewe
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