607 research outputs found
Magnetization and Level Statistics at Quantum Hall Liquid-Insulator Transition in the Lattice Model
Statistics of level spacing and magnetization are studied for the phase
diagram of the integer quantum Hall effect in a 2D finite lattice model with
Anderson disorder.Comment: 4 pages, 6 figure
Lentiviral Vector-Mediated Correction of a Mouse Model of Leukocyte Adhesion Deficiency Type I
Leukocyte adhesion deficiency type I (LAD-I) is a primary immunodeficiency caused by mutations in the ITGB2 gene and is characterized by recurrent and life-threatening bacterial infections. These mutations lead to defective or absent expression of β2 integrins on the leukocyte surface, compromising adhesion and extravasation at sites of infection. Three different lentiviral vectors (LVs) conferring ubiquitous or preferential expression of CD18 in myeloid cells were constructed and tested in human and mouse LAD-I cells. All three hCD18-LVs restored CD18 and CD11a membrane expression in LAD-I patient-derived lymphoblastoid cells. Corrected cells recovered the ability to aggregate and bind to sICAM-1 after stimulation. All vectors induced stable hCD18 expression in hematopoietic cells from mice with a hypomorphic Itgb2 mutation (CD18(HYP)), both in vitro and in vivo after transplantation of corrected cells into primary and secondary CD18(HYP) recipients. hCD18(+) hematopoietic cells from transplanted CD18(HYP) mice also showed restoration of mCD11a surface co-expression. The analysis of in vivo neutrophil migration in CD18(HYP) mice subjected to two different inflammation models demonstrated that the LV-mediated gene therapy completely restored neutrophil extravasation in response to inflammatory stimuli. Finally, these vectors were able to correct the phenotype of human myeloid cells derived from CD34(+) progenitors defective in ITGB2 expression. These results support for the first time the use of hCD18-LVs for the treatment of LAD-I patients in clinical trials
Angle-dependence of quantum oscillations in YBa2Cu3O6.59 shows free spin behaviour of quasiparticles
Measurements of quantum oscillations in the cuprate superconductors afford a
new opportunity to assess the extent to which the electronic properties of
these materials yield to a description rooted in Fermi liquid theory. However,
such an analysis is hampered by the small number of oscillatory periods
observed. Here we employ a genetic algorithm to globally model the field,
angular, and temperature dependence of the quantum oscillations observed in the
resistivity of YBa2Cu3O6.59. This approach successfully fits an entire data set
to a Fermi surface comprised of two small, quasi-2-dimensional cylinders. A key
feature of the data is the first identification of the effect of Zeeman
splitting, which separates spin-up and spin-down contributions, indicating that
the quasiparticles in the cuprates behave as nearly free spins, constraining
the source of the Fermi surface reconstruction to something other than a
conventional spin density wave with moments parallel to the CuO2 planes.Comment: 8 pages, 4 figure
Spin magnetization of strongly correlated electron gas confined in a two-dimensional finite lattice
The influence of disorder and interaction on the ground state polarization of
the two-dimensional (2D) correlated electron gas is studied by numerical
investigations of unrestricted Hartree-Fock equations. The ferromagnetic ground
state is found to be plausible when the electron number is lowered and the
interaction and disorder parameters are suitably chosen. For a finite system at
constant electronic density the disorder induced spin polarization is cut off
when the electron orbitals become strongly localized to the individual network
sites. The fluctuations of the interaction matrix elements are calculated and
brought out as favoring the ferromagnetic instability in the extended and weak
localization regime. The localization effect of the Hubbard interaction term is
discussed.Comment: 7 pages, 9 figure
Expression, regulation and clinical relevance of the ATPase Inhibitory Factor 1 (IF1) in human cancers
Recent findings in colon cancer cells indicate that inhibition of the mitochondrial H(+)-adenosine triphosphate (ATP) synthase by the ATPase inhibitory factor 1 (IF1) promotes aerobic glycolysis and a reactive oxygen species (ROS)-mediated signal that enhances proliferation and cell survival. Herein, we have studied the expression, biological relevance, mechanism of regulation and potential clinical impact of IF1 in some prevalent human carcinomas. We show that IF1 is highly overexpressed in most (>90%) of the colon (n=64), lung (n=30), breast (n=129) and ovarian (n=10) carcinomas studied as assessed by different approaches in independent cohorts of cancer patients. The expression of IF1 in the corresponding normal tissues is negligible. By contrast, the endometrium, stomach and kidney show high expression of IF1 in the normal tissue revealing subtle differences by carcinogenesis. The overexpression of IF1 also promotes the activation of aerobic glycolysis and a concurrent ROS signal in mitochondria of the lung, breast and ovarian cancer cells mimicking the activity of oligomycin. IF1-mediated ROS signaling activates cell-type specific adaptive responses aimed at preventing death in these cell lines. Remarkably, regulation of IF1 expression in the colon, lung, breast and ovarian carcinomas is exerted at post-transcriptional levels. We demonstrate that IF1 is a short-lived protein (t(1/2) ∼100 min) strongly implicating translation and/or protein stabilization as main drivers of metabolic reprogramming and cell survival in these human cancers. Analysis of tumor expression of IF1 in cohorts of breast and colon cancer patients revealed its relevance as a predictive marker for clinical outcome, emphasizing the high potential of IF1 as therapeutic target
Survival and residence times in disordered chains with bias
We present a unified framework for first-passage time and residence time of
random walks in finite one-dimensional disordered biased systems. The
derivation is based on exact expansion of the backward master equation in
cumulants. The dependence on initial condition, system size, and bias strength
is explicitly studied for models with weak and strong disorder. Application to
thermally activated processes is also developed.Comment: 13 pages with 2 figures, RevTeX4; v2:minor grammatical changes, typos
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Partial Volume Correction in Quantitative Amyloid Imaging.
Amyloid imaging is a valuable tool for research and diagnosis in dementing disorders. As positron emission tomography (PET) scanners have limited spatial resolution, measured signals are distorted by partial volume effects. Various techniques have been proposed for correcting partial volume effects, but there is no consensus as to whether these techniques are necessary in amyloid imaging, and, if so, how they should be implemented. We evaluated a two-component partial volume correction technique and a regional spread function technique using both simulated and human Pittsburgh compound B (PiB) PET imaging data. Both correction techniques compensated for partial volume effects and yielded improved detection of subtle changes in PiB retention. However, the regional spread function technique was more accurate in application to simulated data. Because PiB retention estimates depend on the correction technique, standardization is necessary to compare results across groups. Partial volume correction has sometimes been avoided because it increases the sensitivity to inaccuracy in image registration and segmentation. However, our results indicate that appropriate PVC may enhance our ability to detect changes in amyloid deposition
Chaos-Based Bitwise Dynamical Pseudorandom Number Generator on FPGA
In this paper, a new pseudorandom number generator (PRNG) based on the logistic map has been proposed. To prevent the system to fall into short period orbits as well as increasing the randomness of the generated sequences, the proposed algorithm dynamically changes the parameters of the chaotic system. This PRNG has been implemented in a Virtex 7 field-programmable gate array (FPGA) with a 32-bit fixed point precision, using a total of 510 lookup tables (LUTs) and 120 registers. The sequences generated by the proposed algorithm have been subjected to the National Institute of Standards and Technology (NIST) randomness tests, passing all of them. By comparing the randomness with the sequences generated by a raw 32-bit logistic map, it is shown that, by using only an additional 16% of LUTs, the proposed PRNG obtains a much better performance in terms of randomness, increasing the NIST passing rate from 0.252 to 0.989. Finally, the proposed bitwise dynamical PRNG is compared with other chaos-based realizations previously proposed, showing great improvement in terms of resources and randomness
Randomized crossover pharmacokinetic evaluation of subcutaneous versus intravenous granisetron in cancer patients treated with platinum-based chemotherapy
BACKGROUND:
5-HT3-receptor antagonists are one of the mainstays of antiemetic treatment, and they are administered either i.v. or orally. Nevertheless, sometimes neither administration route is feasible, such as in patients unable to admit oral intake managed in an outpatient setting. Our objective was to evaluate the bioavailability of s.c. granisetron.
PATIENTS AND METHODS:
Patients receiving platinum-based chemotherapy were randomized to receive 3 mg of granisetron either s.c. or i.v. in a crossover manner during two cycles. Blood and urine samples were collected after each cycle. Pharmacokinetic parameters observed with each administration route were compared by analysis of variance.
RESULTS:
From May to November 2005, 31 patients were included and 25 were evaluable. Subcutaneous granisetron resulted in a 27% higher area under the concentration-time curve for 0-12 hours (AUC(0-12h)) and higher levels at 12 hours, with similar values for AUC(0-24h). The maximum concentration was lower with the s.c. than with the i.v. route and was observed 30 minutes following s.c. administration.
CONCLUSION:
Granisetron administered s.c. achieves complete bioavailability. This is the first study that shows that s.c. granisetron might be a valid alternative to i.v. delivery. Further trials to confirm clinical equivalence are warranted. This new route of administration might be especially relevant for outpatient management of emesis in cancer patients
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