0000000000549117
AUTHOR
Chen W
showing 8 related works from this author
Production of Charmed Mesons In Z Decays
1994
The production of charmed mesons $$\mathop {D^0 }\limits^{( - )} $$ ,D ± , andD *± is studied in a sample of 478,000 hadronicZ decays. The production rates are measured to be $$\begin{gathered} \frac{{\Gamma ({\rm Z} \to D^{* \pm } X)}}{{\Gamma _{had} }} = 0.187 \pm 0.015(\exp .) \pm 0.013(BR), \hfill \\ \frac{{\Gamma ({\rm Z} \to D^ \pm X)}}{{\Gamma _{had} }} = 0.251 \pm 0.026(\exp .) \pm 0.025(BR), \hfill \\ \frac{{\Gamma ({\rm Z} \to \mathop {D^0 }\limits^{( - )} X)}}{{\Gamma _{had} }} = 0.518 \pm 0.052(\exp .) \pm 0.035(BR), \hfill \\ \end{gathered} $$ where the errors from this analysis are separated from those coming from theD branching ratios (BR). TheD *± momentum distribution is ex…
Measurements of mean lifetime and branching fractions of b hadrons decaying to J/ψ
1992
From a data sample of 450 000 hadronic events recorded with the ALEPH detector at LEP, 92 +/- 10 events are observed containing a J/psi meson decaying to mu+mu- or e+e-. From these data the measured inclusive branching fraction for a b flavoured hadron to decay to a J/psi is BR(b --> J/psiX) = (1.21 +/- 0.13 (stat.) +/- 0.08 (syst.))%, and the average b hadron lifetime in the events tagged with a J/psi is tau(b) = 1.35(-0.17)+0.19 +/- 0.05 ps. Five events are observed consistent with the exclusive decay B+/- --> J/psiK+/- and from these events the exclusive branching fraction is measured to be BR(B+/- --> J/psiK+/-) = (0.22 +/- 0.10 +/- 0.02)%. Upper limits for other exclusive branching rat…
Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity
2013
The pubertal height growth spurt is a distinctive feature of childhood growth reflecting both the central onset of puberty and local growth factors. Although little is known about the underlying genetics, growth variability during puberty correlates with adult risks for hormone-dependent cancer and adverse cardiometabolic health. The only gene so far associated with pubertal height growth, LIN28B, pleiotropically influences childhood growth, puberty and cancer progression, pointing to shared underlying mechanisms. To discover genetic loci influencing pubertal height and growth and to place them in context of overall growth and maturation, we performed genome-wide association meta-analyses i…
A measurement of the b baryon lifetime
1992
In 451 000 hadronic Z0 decays, recorded with the ALEPH detector at LEP, the yields of lambdal- and lambdal+ combinations are measured. Semileptonic decays of b baryons result in a signal of 122 +/- 18(stat.)+22/-23(syst.) lambdal- combinations. From a fit to the impact parameter distribution of the leptons in the lambdal- sample, the lifetime of b baryons is measured to be 1.12+0.32/-0.29(stat.) +/- 0.16(syst.) ps.
Heavy Flavor Production and Decay With Prompt Leptons In the Aleph Detector
1994
In 431 000 hadronicZ decays recorded with the ALEPH detector at LEP, the yields of electrons and muons in events with one or more prompt leptons have been analysed to give information on the production and decay of heavy quarks. The fractions of $$b\bar b$$ and $$c\bar c$$ events are measured to be 0.219±0.006±0.005 and 0.165±0.005±0.020, and the corresponding forward-backward asymmetries at theZ mass are measured to be 0.090±0.013±0.003 and 0.111±0.021±0.018, after QED and QCD corrections. Measurements for the semileptonic branching ratios BR $$(b \to \ell ^ - \bar vX)$$ and BR (b→cl+ vX) yield 0.114±0.003±0.004 and 0.082±0.003±0.012, respectively. The dilepton events enable measurement of…
Search for CP violation in ZmF ττ
1992
Abstract Using the 18.8 pb−1 of data accumulated at LEP in 1990 and 1991 with the ALEPH detector, a direct test of neutral current CP-invariance is performed by a search for CP-odd correlations in Z decays to τ pairs where both τ decay modes are identified. No evidence for CP-violation is observed. The weak dipole moment of the τ has been measured to be dτ(mZ) = (1.3 ± 1.4 ± 0.1) × 10−17 e·cm which results in an upper limit on the weak dipole moment of |dτ(mZ)| ⩽ 3.7 × 10−17 e·cm with 95% confidence level.
No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder.
2008
Contains fulltext : 71091.pdf (Publisher’s version ) (Closed access) Several independent studies have reported association between serotonin transporter gene (SLC6A4) polymorphisms and attention deficit hyperactivity disorder (ADHD). Five studies found evidence for association between the long-allele of a 44-bp insertion/deletion polymorphism (5-HTTLPR) and ADHD. Another two studies corroborated this finding while a further six studies did not find such an association. For a second polymorphism within the gene, a variable number tandem repeat (VNTR) within intron 2, one study demonstrated that the 12/12 genotype was significantly less frequent in ADHD cases compared to controls, while a sec…
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.
2006
Contains fulltext : 35205.pdf (Publisher’s version ) (Closed access) Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, starting in early childhood and persisting into adulthood in the majority of cases. Family and twin studies have demonstrated the importance of genetic factors and candidate gene association studies have identified several loci that exert small but significant effects on ADHD. To provide further clarification of reported associations and identify novel associated genes, we examined 1,038 single-nucleotide polymorphisms (SNPs) spanning 51 candidate genes involved in the regulation of neurotransmitter pathways, particularly dopamine, nor…