Measurement of the B Semileptonic Branching Fraction with Lepton Tags

We have used the CLEO II detector and 2.06fb^(-1) of ϒ(4S) data to measure the B-meson semileptonic branching fraction. The B→Xeν momentum spectrum was obtained over nearly the full momentum range by using charge and kinematic correlations in events with a high-momentum lepton tag and an additional electron. We find B(B→Xeν) = (10.49±0.17±0.43)%, with overall systematic uncertainties less than those of untagged single-lepton measurements. We use this result to calculate the magnitude of the Cabibbo-Kobayashi-Maskawa matrix element V_(cb) and to set an upper limit on the fraction of ϒ(4S) decays to final states other than BB̅

Measurement of B(D^0 → K^-π^+) Using Partial Reconstruction of B̅ → D^(*+)Xℓ^-ν̅

We present a measurement of the absolute branching fraction for D^0→K^-π^+ using the reconstruction of the decay chain B̅ →D^(*+)Xℓ^-ν̅ , D^(*+)→D^0π^+ where only the lepton and the low-momentum pion from the D^(*+) are detected. With data collected by the CLEO II detector at the Cornell Electron Storage Ring, we have determined B(D^0→K^-π^+) = [3.81±0.15(stat)±0.16(syst)]%

Two-Body B Meson Decays to η and η': Observation of B → η'K

In a sample of 6.6×10^6 produced B mesons we have observed decays B→η′K, with branching fractions B(B^+→η′K^+) = (6.5_(-1.4)^(+1.5)±0.9)×10^(-5) and B(B^0→η′K^0) = (4.7_(-2.0)^(+2.7)±0.9)×10^(-5). We have searched with comparable sensitivity for 17 related decays to final states containing an η or η′ meson accompanied by a single particle or low-lying resonance. Our upper limits for these constrain theoretical interpretations of the B→η′K signal

Bioelectronic DNA detection of human papillomaviruses using eSensor™: a model system for detection of multiple pathogens

BACKGROUND: We used human papillomaviruses (HPV) as a model system to evaluate the utility of a nucleic acid, hybridization-based bioelectronic DNA detection platform (eSensor™) in identifying multiple pathogens. METHODS: Two chips were spotted with capture probes consisting of DNA oligonucleotide sequences specific for HPV types. Electrically conductive signal probes were synthesized to be complementary to a distinct region of the amplified HPV target DNA. A portion of the HPV L1 region that was amplified by using consensus primers served as target DNA. The amplified target was mixed with a cocktail of signal probes and added to a cartridge containing a DNA chip to allow for hybridization with complementary capture probes. RESULTS: Two bioelectric chips were designed and successfully detected 86% of the HPV types contained in clinical samples. CONCLUSIONS: This model system demonstrates the potential of the eSensor platform for rapid and integrated detection of multiple pathogens

Observation of the Radiative Decay D^(*+) → D^+y

We have observed a signal for the decay D^(*+)→D^+γ at a significance of 4 standard deviations. From the measured branching ratio B(D^(*+)→D^+γ)/B(D^(*+)→D^+π^0) = 0.055±0.014±0.010 we find B(D^(*+)→D^+γ) = 0.017±0.004±0.003, where the first uncertainty is statistical and the second is systematic. We also report the highest precision determination of the remaining D^(*+) branching fractions

Search for the decay B→D_(s1)^+ (2536)X

We have searched for the decay B⃗D_(s1)^+(2536)X and measured an upper limit for the inclusive branching fraction of B(B⃗D_(s1)^+X)<0.96% at the 90% confidence level. This limit is small compared with the total expected B⃗D^((*))D^((*))KX rate. Assuming factorization, the D_(s1)^+ decay constant is constrained to be fD_(s1)^+<114 MeV at the 90% confidence level, at least 2.5 times smaller than that of D_s^+