2,325 research outputs found
Transport dynamics of ultracold atoms in a triple-well transistor-like potential
The transport of atoms is experimentally studied in a transistor-like
triple-well potential consisting of a narrow gate well surrounded by source and
drain wells. Atoms are initially loaded into the source well with
pre-determined temperature and chemical potential. Energetic atoms flow from
the source, across the gate, and into the drain where they are removed using a
resonant light beam. The manifestation of atom-atom interactions and
dissipation is evidenced by a rapid population growth in the initially vacant
gate well. The transport dynamics are shown to depend strongly on a feedback
parameter determined by the relative heights of the two barriers forming the
gate region. For a range of feedback parameter values, experiments establish
that the gate atoms develop a larger chemical potential and lower temperature
than those in the source.Comment: 13 pages, 5 figures, accepted for publication in NJ
Observation of eta_b(2S) in Upsilon(2S) -> gamma eta_b(2S), eta_b(2S) -> hadrons, and Confirmation of eta_b(1S)
The data for 9.3 million Upsilon(2S) and 20.9 million Upsilon(1S) taken with
the CLEO III detector has been used to study the radiative population of states
identified by their decay into twenty six different exclusive hadronic final
states. In the Upsilon(2S) decays an enhancement is observed at a ~5 sigma
level at a mass of 9974.6+-2.3(stat)+-2.1(syst) MeV. It is attributed to
eta_b(2S), and corresponds to the Upsilon(2S) hyperfine splitting of
48.7+-2.3(stat)+-2.1(syst) MeV. In the Upsilon(1S) decays, the identification
of eta_b(1S) is confirmed at a ~3 sigma level with M(eta_b(1S)) in agreement
with its known value.Comment: 5 pages, 2 figure
High-Resolution Imaging and Optical Control of Bose-Einstein Condensates in an Atom Chip Magnetic Trap
A high-resolution projection and imaging system for ultracold atoms is
implemented using a compound silicon and glass atom chip. The atom chip is
metalized to enable magnetic trapping while glass regions enable high numerical
aperture optical access to atoms residing in the magnetic trap about 100
microns below the chip surface. The atom chip serves as a wall of the vacuum
system, which enables the use of commercial microscope components for
projection and imaging. Holographically generated light patterns are used to
optically slice a cigar-shaped magnetic trap into separate regions; this has
been used to simultaneously generate up to four Bose-condensates. Using
fluorescence techniques we have demonstrated in-trap imaging resolution down to
2.5 micronsComment: 4 pages, 5 figures, 12 reference
Light Quark Resonances in pbar p Annihilations at 5.2 GeV/c
Data from the Fermilab E835 experiment have been used to study the reaction
pbar p -> eta eta pi0 at 5.2 GeV/c. A sample of 22 million six photons events
has been analyzed to construct the Dalitz plot containing ~80k eta eta pi0
events. A partial wave analysis of the data has been done. Six f_J-states
decaying into eta eta and five a_J-states decaying into eta pi0 are identified
in the mass region ~1.3 and 2.4 GeV, and their masses, widths and spins are
determined by maximum likelihood analysis of the data. Two f_0 states are
identified with the popular candidates for the lightest scalar glueball,
f_0(1500) and f_0(1710).Comment: 7 pages, 6 figure
The cell cycle regulatory DREAM complex is disrupted by high expression of oncogenic B-Myb.
Overexpression of the oncogene MYBL2 (B-Myb) is associated with increased cell proliferation and serves as a marker of poor prognosis in cancer. However, the mechanism by which B-Myb alters the cell cycle is not fully understood. In proliferating cells, B-Myb interacts with the MuvB core complex including LIN9, LIN37, LIN52, RBBP4, and LIN54, forming the MMB (Myb-MuvB) complex, and promotes transcription of genes required for mitosis. Alternatively, the MuvB core interacts with Rb-like protein p130 and E2F4-DP1 to form the DREAM complex that mediates global repression of cell cycle genes in G0/G1, including a subset of MMB target genes. Here, we show that overexpression of B-Myb disrupts the DREAM complex in human cells, and this activity depends on the intact MuvB-binding domain in B-Myb. Furthermore, we found that B-Myb regulates the protein expression levels of the MuvB core subunit LIN52, a key adapter for assembly of both the DREAM and MMB complexes, by a mechanism that requires S28 phosphorylation site in LIN52. Given that high expression of B-Myb correlates with global loss of repression of DREAM target genes in breast and ovarian cancer, our findings offer mechanistic insights for aggressiveness of cancers with MYBL2 amplification, and establish the rationale for targeting B-Myb to restore cell cycle control
Enhancing GAN-Based Vocoders with Contrastive Learning Under Data-limited Condition
Vocoder models have recently achieved substantial progress in generating
authentic audio comparable to human quality while significantly reducing memory
requirement and inference time. However, these data-hungry generative models
require large-scale audio data for learning good representations. In this
paper, we apply contrastive learning methods in training the vocoder to improve
the perceptual quality of the vocoder without modifying its architecture or
adding more data. We design an auxiliary task with mel-spectrogram contrastive
learning to enhance the utterance-level quality of the vocoder model under
data-limited conditions. We also extend the task to include waveforms to
improve the multi-modality comprehension of the model and address the
discriminator overfitting problem. We optimize the additional task
simultaneously with GAN training objectives. Our result shows that the tasks
improve model performance substantially in data-limited settings. Our analysis
based on the result indicates that the proposed design successfully alleviates
discriminator overfitting and produces audio of higher fidelity
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