336 research outputs found
Dzyaloshinskii-Moriya interaction in transport through single molecule transistors
The Dzyaloshinskii-Moriya interaction is shown to result in a canting of
spins in a single molecule transistor. We predict non-linear transport
signatures of this effect induced by spin-orbit coupling for the generic case
of a molecular dimer. The conductance is calculated using a master equation and
is found to exhibit a non-trivial dependence on the magnitude and direction of
an external magnetic field. We show how three-terminal transport measurements
allow for a determination of the coupling-vector characterizing the
Dzyaloshinskii-Moriya interaction. In particular, we show how its orientation,
defining the intramolecular spin chirality, can be probed with ferromagnetic
electrodes
Longitude : a privacy-preserving location sharing protocol for mobile applications
Location sharing services are becoming increasingly popular. Although many location sharing services allow users to set up privacy policies to control who can access their location, the use made by service providers remains a source of concern. Ideally, location sharing providers and middleware should not be able to access usersâ location data without their consent. In this paper, we propose a new location sharing protocol called Longitude that eases privacy concerns by making it possible to share a userâs location data blindly and allowing the user to control who can access her location, when and to what degree of precision. The underlying cryptographic algorithms are designed for GPS-enabled mobile phones. We describe and evaluate our implementation for the Nexus One Android mobile phone
On the nature of tunable hole g-factors in quantum dots
Electrically tunable g-factors in quantum dots are highly desirable for
applications in quantum computing and spintronics. We report giant modulation
of the hole g-factor in a SiGe nanocrystal when an electric field is applied to
the nanocrystal along its growth direction. We derive a contribution to the
g-factor that stems from an orbital effect of the magnetic field, which lifts
the Kramers degeneracy in the nanocrystal by altering the mixing between the
heavy and the light holes. We show that the relative displacement between the
heavy- and light-hole wave functions, occurring upon application of the
electric field, has an effect on the mixing strength and leads to a strong
non-monotonic modulation of the g-factor. Despite intensive studies of the
g-factor since the late 50's, this mechanism of g-factor control has been
largely overlooked in the literature.Comment: 9 pages, 6 figure
Observation of spin-selective tunneling in SiGe nanocrystals
Spin-selective tunneling of holes in SiGe nanocrystals contacted by
normal-metal leads is reported. The spin selectivity arises from an interplay
of the orbital effect of the magnetic field with the strong spin-orbit
interaction present in the valence band of the semiconductor. We demonstrate
both experimentally and theoretically that spin-selective tunneling in
semiconductor nanostructures can be achieved without the use of ferromagnetic
contacts. The reported effect, which relies on mixing the light and heavy
holes, should be observable in a broad class of quantum-dot systems formed in
semiconductors with a degenerate valence band.Comment: 8 pages, 5 figure
On the origin of the A and B electronic Raman scattering peaks in the superconducting state of YBaCuO
The electronic Raman scattering has been investigated in optimally oxygen
doped YBaCuO single crystals as well as in crystals
with non-magnetic, Zn, and magnetic, Ni, impurities. We found that the
intensity of the A peak is impurity independent and their energy to
ratio is almost constant (). Moreover, the
signal at the B channel is completely smeared out when non-magnetic Zn
impurities are present. These results are qualitatively interpreted in terms of
the Zeyher and Greco's theory that relates the electronic Raman scattering in
the A and B channels to \textit{d}-CDW and superconducting order
parameters fluctuations, respectively.Comment: Submited to Phys. Rev. Let
Assessing Environmental Control Strategies in Cage-Free Egg Production Systems: Effect on Spatial Occupancy and Natural Behaviors.
Animal welfare concerns have been a challenging issue for producers and international marketing. In laying hen production, cage-free systems (CFS) have been identified as an alternative to ensure the laying hensâ well-being. Nevertheless, in CFS, important environmental issues have been reported, decreasing indoor air quality. Environmental control strategies (ECS) have been designed to enhance indoor air quality in CFSs. However, little information exists about the effect of these ECSs on natural animal behaviors. Four strategies and one control were tested in an experimental CFS, previously designed to track behavioral variables using video recordings over seven time-lapses of 1 hour per day. Spatial occupancy (SO) and laying hen behaviors (LHB) were registered. One statistical analysis was applied to evaluate the effect of ECS on SO and LHB using a multinomial response model. Results show lower chances to use litter area within the reduction of litter allowance treatment (T17) (p < 0.05). Neither the four ECSs nor the control implemented in this experiment affected the natural behaviors of the hens. However, stress patterns and high activity were reported in the T17 treatment. This study shows that it is possible to use these ECSs without disrupting laying hensâ natural behaviors
The "Strange Metal" is a Projected Fermi Liquid with Edge Singularities
The puzzling "strange metal" phase of the high Tc cuprate phase diagram
reveals itself as closer to a Fermi liquid than previously supposed: it is a
consequence of Gutzwiller projection and does not necessarily require exotica
such as an RVB or mysterious quantum critical points. There is a Fermi
liquid-like excitation spectrum but the excitations are asymmetric between
electrons and holes, show anomalous forward scattering and have Z equal to 0.
We explain the power law dependence of conductivity on frequency and predict
anomalies in the tunneling and photoemission spectra.Comment: replaced tocorrect a math error in a later section, to clarify
exposition, and to add references to more experiment
The heparan sulfate sulfotransferase 3-OST3A (HS3ST3A) is a novel tumor regulator and a prognostic marker in breast cancer
International audienceHeparan sulfate (HS) proteoglycan chains are key components of the breast tumor microenvironment that critically influence the behavior of cancer cells. It is established that abnormal synthesis and processing of HS play a prominent role in tumorigenesis, albeit mechanisms remain mostly obscure. HS function is mainly controlled by sulfotransferases, and here we report a novel cellular and pathophysiological significance for the 3-O-sulfotransferase 3-OST3A (HS3ST3A), catalyzing the final maturation step of HS, in breast cancer. We show that 3-OST3A is epigenetically repressed in all breast cancer cell lines of a panel representative of distinct molecular subgroups, except in human epidermal growth factor receptor 2-positive (HER2+) sloan-kettering breast cancer (SKBR3) cells. Epigenetic mechanisms involved both DNA methylation and histone modifications, producing different repressive chromatin environments depending on the cell molecular signature. Gain and loss of function experiments by cDNA and siRNA transfection revealed profound effects of 3-OST3A expression on cell behavior including apoptosis, proliferation, response to trastuzumab in vitro and tumor growth in xenografted mice. 3-OST3A exerted dual activities acting as tumor-suppressor in lumA-michigan cancer foundation (MCF)-7 and triple negative-MD Anderson (MDA) metastatic breast (MB)-231 cells, or as an oncogenic factor in HER2+-SKBR3 cells. Mechanistically, fluorescence-resonance energy transfer-fluorescence-lifetime imaging microscopy experiments indicated that the effects of 3-OST3A in MCF-7 cells were mediated by altered interactions between HS and fibroblast growth factor-7 (FGF-7). Further, this interplay between HS and FGF-7 modulated downstream ERK, AKT and p38 cascades, suggesting that altering 3-O-sulfation affects FGFR2IIIb-mediated signaling. Corroborating our cellular data, a clinical study conducted in a cohort of breast cancer patients uncovered that, in HER2+ patients, high level expression of 3-OST3A in tumors was associated with reduced relapse-free survival. Our findings define 3-OST3A as a novel regulator of breast cancer pathogenicity, displaying tumor-suppressive or oncogenic activities in a cell-and tumor-dependent context, and demonstrate the clinical value of the HS-O-sulfotransferase 3-OST3A as a prognostic marker in HER2+ patients
Toll-Like Receptor Agonists Synergize with CD40L to Induce Either Proliferation or Plasma Cell Differentiation of Mouse B Cells
In a classical dogma, pathogens are sensed (via recognition of Pathogen Associated Molecular Patterns (PAMPs)) by innate immune cells that in turn activate adaptive immune cells. However, recent data showed that TLRs (Toll Like Receptors), the most characterized class of Pattern Recognition Receptors, are also expressed by adaptive immune B cells. B cells play an important role in protective immunity essentially by differentiating into antibody-secreting cells (ASC). This differentiation requires at least two signals: the recognition of an antigen by the B cell specific receptor (BCR) and a T cell co-stimulatory signal provided mainly by CD154/CD40L acting on CD40. In order to better understand interactions of innate and adaptive B cell stimulatory signals, we evaluated the outcome of combinations of TLRs, BCR and/or CD40 stimulation. For this purpose, mouse spleen B cells were activated with synthetic TLR agonists, recombinant mouse CD40L and agonist anti-BCR antibodies. As expected, TLR agonists induced mouse B cell proliferation and activation or differentiation into ASC. Interestingly, addition of CD40 signal to TLR agonists stimulated either B cell proliferation and activation (TLR3, TLR4, and TLR9) or differentiation into ASC (TLR1/2, TLR2/6, TLR4 and TLR7). Addition of a BCR signal to CD40L and either TLR3 or TLR9 agonists did not induce differentiation into ASC, which could be interpreted as an entrance into the memory pathway. In conclusion, our results suggest that PAMPs synergize with signals from adaptive immunity to regulate B lymphocyte fate during humoral immune response
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