4,128 research outputs found

    The X-ray luminosity of solar-mass stars in the intermediate age open cluster NGC 752

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    AIMS. While observational evidence shows that most of the decline in a star's X-ray activity occurs between the age of the Hyades (~8 x 10^8 yrs) and that of the Sun, very little is known about the evolution of stellar activity between these ages. To gain information on the typical level of coronal activity at a star's intermediate age, we studied the X-ray emission from stars in the 1.9 Gyr old open cluster NGC 752. METHODS. We analysed a ~140 ks Chandra observation of NGC 752 and a ~50 ks XMM-Newton observation of the same cluster. We detected 262 X-ray sources in the Chandra data and 145 sources in the XMM-Newton observation. Around 90% of the catalogued cluster members within Chandra's field-of-view are detected in the X-ray. The X-ray luminosity of all observed cluster members (28 stars) and of 11 cluster member candidates was derived. RESULTS. Our data indicate that, at an age of 1.9 Gyr, the typical X-ray luminosity of the cluster members with M=0.8-1.2 Msun is Lx = 1.3 x 10^28 erg s^-1, so approximately a factor of 6 less intense than that observed in the younger Hyades. Given that Lx is proportional to the square of a star's rotational rate, the median Lx of NGC 752 is consistent, for t > 1 Gyr, to a decaying rate in rotational velocities v_rot ~ t^-alpha with alpha ~ 0.75, steeper than the Skumanich relation (alpha ~ 0.5) and significantly steeper than observed between the Pleiades and the Hyades (where alpha < 0.3), suggesting that a change in the rotational regimes of the stellar interiors is taking place at t ~ 1 Gyr.Comment: Accepted for publication in A&A (13 pages, 8 figures

    Spintronic transport and Kondo effect in quantum dots

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    We investigate the spin-dependent transport properties of quantum-dot based structures where Kondo correlations dominate the electronic dynamics. The coupling to ferromagnetic leads with parallel magnetizations is known to give rise to nontrivial effects in the local density of states of a single quantum dot. We show that this influence strongly depends on whether charge fluctuations are present or absent in the dot. This result is confirmed with numerical renormalization group calculations and perturbation theory in the on-site interaction. In the Fermi-liquid fixed point, we determine the correlations of the electric current at zero temperature (shot noise) and demonstrate that the Fano factor is suppressed below the Poissonian limit for the symmetric point of the Anderson Hamiltonian even for nonzero lead magnetizations. We discuss possible avenues of future research in this field: coupling to the low energy excitations of the ferromagnets (magnons), extension to double quantum dot systems with interdot antiferromagnetic interaction and effect of spin-polarized currents on higher symmetry Kondo states such as SU(4).Comment: 11 pages, 5 figures. Proceedings of the 3rd Intl. Conf. on Physics and Applications of Spin-Related Phenomena in Semiconductors, Santa Barbara, 200

    Applications of scalar attractor solutions to Cosmology

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    We develop a framework to study the phase space of a system consisting of a scalar field rolling down an arbitrary potential with varying slope and a background fluid, in a cosmological setting. We give analytical approximate solutions of the field evolution and discuss applications of its features to the issues of quintessence, moduli stabilisation and quintessential inflation.Comment: 9 pages, 7 figures. Accepted for publication in PR

    Numerical Renormalization Group Approach to a Quantum Dot Coupled to Normal and Superconducting Leads

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    We study transport through a quantum dot coupled to normal and superconducting leads using the numerical renormalization group method. We show that the low-energy properties of the system are described by the local Fermi liquid theory despite of the superconducting correlations penetrated into the dot due to a proximity effect. We calculate the linear conductance due to the Andreev reflection in the presence of the Coulomb interaction. It is demonstrated that the maximum structure appearing in the conductance clearly characterizes a crossover between two distinct spin-singlet ground states, i.e. the superconducting singlet state and the Kondo singlet state. It is further elucidated that the gate-voltage dependence of the conductance shows different behavior in the superconducting singlet region from that in the Kondo singlet region.Comment: 10 pages, 6 figures; a typo in eq. (B.5) corrected, which does not affect any other results of the pape

    The actin-myosin regulatory MRCK kinases: regulation, biological functions and associations with human cancer

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    The contractile actin-myosin cytoskeleton provides much of the force required for numerous cellular activities such as motility, adhesion, cytokinesis and changes in morphology. Key elements that respond to various signal pathways are the myosin II regulatory light chains (MLC), which participate in actin-myosin contraction by modulating the ATPase activity and consequent contractile force generation mediated by myosin heavy chain heads. Considerable effort has focussed on the role of MLC kinases, and yet the contributions of the myotonic dystrophy-related Cdc42-binding kinases (MRCK) proteins in MLC phosphorylation and cytoskeleton regulation have not been well characterized. In contrast to the closely related ROCK1 and ROCK2 kinases that are regulated by the RhoA and RhoC GTPases, there is relatively little information about the CDC42-regulated MRCKα, MRCKβ and MRCKγ members of the AGC (PKA, PKG and PKC) kinase family. As well as differences in upstream activation pathways, MRCK and ROCK kinases apparently differ in the way that they spatially regulate MLC phosphorylation, which ultimately affects their influence on the organization and dynamics of the actin-myosin cytoskeleton. In this review, we will summarize the MRCK protein structures, expression patterns, small molecule inhibitors, biological functions and associations with human diseases such as cancer

    Spin-Polarized Transprot through Double Quantum Dots

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    We investigate spin-polarized transport phenomena through double quantum dots coupled to ferromagnetic leads in series. By means of the slave-boson mean-field approximation, we calculate the conductance in the Kondo regime for two different configurations of the leads: spin-polarization of two ferromagnetic leads is parallel or anti-parallel. It is found that transport shows some remarkable properties depending on the tunneling strength between two dots. These properties are explained in terms of the Kondo resonances in the local density of states.Comment: 8 pages, 11 figure

    Transcatheter closure of small ductus arteriosus with amplatzer vascular plug

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    PurposeThe purpose of this study was to share our experience of transcatheter closure of small patent ductus arteriosus (PDA) by using an Amplatzer vascular plug (AVP).MethodsWe reviewed the medical records of 20 patients who underwent transcatheter closure at Samsung Medical Center and Sejong General Hospital from January 2008 to August 2012. The size and shape of the PDAs were evaluated by performing angiograms, and the PDA size and the AVP devices size were compared.ResultsThe mean age of the patients was 54.9±45.7 months old. The PDAs were of type C (n=5), type D (n=12), and type E (n=3). The mean pulmonary end diameter of the PDA was 1.7±0.6 mm, and the aortic end diameter was 3.6±1.4 mm. The mean length was 7.3±1.8 mm. We used 3 types of AVP devices: AVP I (n=5), AVP II (n=7), and AVP IV (n=8). The ratio of AVP size to the pulmonary end diameter was 3.37±1.64, and AVP size/aortic end ratio was 1.72±0.97. The aortic end diameter was significantly larger in those cases repaired with AVP II than in the others (P=0.002). The AVP size did not significantly correlate with the PDA size, but did correlate with smaller ratio of AVP size to aortic end diameter (1.10±0.31, P=0.032).ConclusionTranscatheter closure of small PDA with AVP devices yielded satisfactory outcome. AVP II was equally effective with smaller size of device, compared to others

    FAS-dependent cell death in α-synuclein transgenic oligodendrocyte models of multiple system atrophy

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    Multiple system atrophy is a parkinsonian neurodegenerative disorder. It is cytopathologically characterized by accumulation of the protein p25α in cell bodies of oligodendrocytes followed by accumulation of aggregated α-synuclein in so-called glial cytoplasmic inclusions. p25α is a stimulator of α-synuclein aggregation, and coexpression of α-synuclein and p25α in the oligodendroglial OLN-t40-AS cell line causes α-synuclein aggregate-dependent toxicity. In this study, we investigated whether the FAS system is involved in α-synuclein aggregate dependent degeneration in oligodendrocytes and may play a role in multiple system atrophy. Using rat oligodendroglial OLN-t40-AS cells we demonstrate that the cytotoxicity caused by coexpressing α-synuclein and p25α relies on stimulation of the death domain receptor FAS and caspase-8 activation. Using primary oligodendrocytes derived from PLP-α-synuclein transgenic mice we demonstrate that they exist in a sensitized state expressing pro-apoptotic FAS receptor, which makes them sensitive to FAS ligand-mediated apoptosis. Immunoblot analysis shows an increase in FAS in brain extracts from multiple system atrophy cases. Immunohistochemical analysis demonstrated enhanced FAS expression in multiple system atrophy brains notably in oligodendrocytes harboring the earliest stages of glial cytoplasmic inclusion formation. Oligodendroglial FAS expression is an early hallmark of oligodendroglial pathology in multiple system atrophy that mechanistically may be coupled to α-synuclein dependent degeneration and thus represent a potential target for protective intervention

    Targeted Genome-Wide Enrichment of Functional Regions

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    Only a small fraction of large genomes such as that of the human contains the functional regions such as the exons, promoters, and polyA sites. A platform technique for selective enrichment of functional genomic regions will enable several next-generation sequencing applications that include the discovery of causal mutations for disease and drug response. Here, we describe a powerful platform technique, termed “functional genomic fingerprinting” (FGF), for the multiplexed genomewide isolation and analysis of targeted regions such as the exome, promoterome, or exon splice enhancers. The technique employs a fixed part of a uniquely designed Fixed-Randomized primer, while the randomized part contains all the possible sequence permutations. The Fixed-Randomized primers bind with full sequence complementarity at multiple sites where the fixed sequence (such as the splice signals) occurs within the genome, and multiplex amplify many regions bounded by the fixed sequences (e.g., exons). Notably, validation of this technique using cardiac myosin binding protein-C (MYBPC3) gene as an example strongly supports the application and efficacy of this method. Further, assisted by genomewide computational analyses of such sequences, the FGF technique may provide a unique platform for high-throughput sample production and analysis of targeted genomic regions by the next-generation sequencing techniques, with powerful applications in discovering disease and drug response genes
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