Monte Carlo Shower Counter Studies

Activities and accomplishments related to the Monte Carlo shower counter studies are summarized. A tape of the VMS version of the GEANT software was obtained and installed on the central computer at Gallaudet University. Due to difficulties encountered in updating this VMS version, a decision was made to switch to the UNIX version of the package. This version was installed and used to generate the set of data files currently accessed by various analysis programs. The GEANT software was used to write files of data for positron and proton showers. Showers were simulated for a detector consisting of 50 alternating layers of lead and scintillator. Each file consisted of 1000 events at each of the following energies: 0.1, 0.5, 2.0, 10, 44, and 200 GeV. Data analysis activities related to clustering, chi square, and likelihood analyses are summarized. Source code for the GEANT user subprograms and data analysis programs are provided along with example data plots

Multimodal Representation of Space in the Posterior Parietal Cortex and its use in Planning Movements

Recent experiments are reviewed that indicate that sensory signals from many modalities, as well as efference copy signals from motor structures, converge in the posterior parietal cortex in order to code the spatial locations of goals for movement. These signals are combined using a specific gain mechanism that enables the different coordinate frames of the various input signals to be combined into common, distributed spatial representations. These distributed representations can be used to convert the sensory locations of stimuli into the appropriate motor coordinates required for making directed movements. Within these spatial representations of the posterior parietal cortex are neural activities related to higher cognitive functions, including attention. We review recent studies showing that the encoding of intentions to make movements is also among the cognitive functions of this area

The Need for Speed: Eye-Position Signal Dynamics in the Parietal Cortex

Accurate eye-position signals are critically important for localizing targets in space when the eyes move. In this issue of Neuron, Xu et al. (2012) provide evidence that eye-position gain fields in area LIP remain spatially inaccurate for some time after a saccade, indicating they are not updated rapidly enough to play a role in the computation of target locations for upcoming saccades

Theoretical calculation of magnetic structure variation in Pr5Ni2Si3

The variation of magnetization with temperature of the Pr5Ni2Si3 compound was calculated using a nearest neighbor exchange interaction approximation. Pr atoms, which are the only element in this compound with a net magnetic moment, were classified into three types based on the number of nearest neighbor exchange interactions. The expected magnetization versus temperature curve for each type of Pr atom was calculated using the Brillouin function, as well as the average magnetization versus temperature curve for the entire unit cell. The results show that the “corner” atoms exhibit very different behavior from that of the other types of Pr atoms on the “center” or “edge” sites. This is due to the broken symmetry in exchange interaction at the corner site due to interactions with atoms from outside the unit cell that are in closer proximity than atoms within the unit cell. This is considered to be the cause of a second magnetic phase transition observed at a lower temperature than the Curie temperature

Rigid E-Unification: NP-Completeness and Applications to Equational Matings

Rigid E-unification is a restricted kind of unification modulo equational theories, or E-unification, that arises naturally in extending Andrews\u27s theorem proving method of matings to first-order languages with equality. This extension was first presented in Gallier, Raatz, and Snyder, where it was conjectured that rigid E-unification is decidable. In this paper, it is shown that rigid E-unification is NP-complete and that finite complete sets of rigid E-unifiers always exist. As a consequence, deciding whether a family of mated sets is an equational mating is an NP-complete problem. Some implications of this result regarding the complexity of theorem proving in first-order logic with equality are also discussed

Incidence, outcomes, and risk factors of pleural effusion in patients receiving dasatinib therapy for Philadelphia chromosome-positive leukemia.

Dasatinib, a second-generation BCR-ABL1 tyrosine kinase inhibitor, is approved for the treatment of chronic myeloid leukemia and Philadelphia chromosome-positive acute lymphoblastic leukemia, both as first-line therapy and after imatinib intolerance or resistance. While generally well tolerated, dasatinib has been associated with a higher risk for pleural effusions. Frequency, risk factors, and outcomes associated with pleural effusion were assessed in two phase 3 trials (DASISION and 034/Dose-optimization) and a pooled population of 11 trials that evaluated patients with chronic myeloid leukemia and Philadelphia chromosome-positive acute lymphoblastic leukemia treated with dasatinib (including DASISION and 034/Dose-optimization). In this largest assessment of patients across the dasatinib clinical trial program (N=2712), pleural effusion developed in 6-9% of patients at risk annually in DASISION, and in 5-15% of patients at risk annually in 034/Dose-optimization. With a minimum follow up of 5 and 7 years, drug-related pleural effusion occurred in 28% of patients in DASISION and in 33% of patients in 034/Dose-optimization, respectively. A significant risk factor identified for developing pleural effusion by a multivariate analysis was age. We found that overall responses to dasatinib, progression-free survival, and overall survival were similar in patients who developed pleural effusion and in patients who did not. clinicaltrials.gov identifier 00481247; 00123474

Overweight and sudden death increased ventricular ectopy in cardiopathy of obesity

besity has been documented to be an independent risk factor for sudden death and other cardiovascular mortality. The present study was designed to monitor and quantify cardiac arrhythmias in obese subjects with and without eccentric left ventricular hypertrophy, who were matched with regard to arterial pressure, age, sex, and height with lean subjects. Prevalence of premature ventricular (but not atrial) contractions was 30 times higher in obese patients with eccentric left ventricular hypertrophy compared with lean subjects. Similarly, obese patients with left ventricular hypertrophy scored higher with regard to the classification of Lown and Wolf than those without left ventricular hypertrophy and lean subjects having the same level of arterial pressure. Patients' class in the Lown and Wolf system correlated with ventricular diastolic diameter and left ventricular mass. Thus, heart enlargement of the eccentric type as a consequence of obesity predisposes to excessive ventricular ectopy. Echocardiographic assessment and electrocardiographic monitoring allow us to identify the patients who are at highest risk of more serious arrhythmias or possibly sudden death and to subject them to the most specific preventive and therapeutic measures

Temperature dependence of magnetic anisotropy of Ga-substituted cobalt ferrite

The temperature dependence of magnetization, magnetic anisotropy, and coercive field of gallium-substituted cobaltferrite was investigated for a series of compositions of CoGaxFe2−xO4 (0⩽x⩽0.8). Hysteresis loops were measured for each sample over the range of −5T⩽μ0H⩽5T for selected temperatures between 10 and 400K. The magnetization at 5T and low temperatures was found to increase for the lower Ga contents (x=0.2 and 0.4) compared to pure CoFe2O4, indicating that at least initially, Ga3+substitutes predominantly into the tetrahedral sites of the spinel structure. The high field regions of these loops were modeled using the law of approach to saturation, which represents the rotational process, together with an additional linear forced magnetization term. The first order cubic magnetocrystalline anisotropy coefficient K1 was calculated from curve fitting to these data. It was found that K1 decreased with increasing Ga content at all temperatures. Both anisotropy and coercivity increased substantially as temperature decreased. Below 150K, for certain compositions (x=0, 0.2, 0.4), the maximum applied field of μ0H=5T was less than the anisotropy field and, therefore, insufficient to saturate the magnetization. In these cases, the use of the law of approach method can lead to calculated values of K1 which are lower than the correct value

Variation of magnetostriction with temperature in Tb5Si2.2Ge1.8 single crystal

The Tb5(SixGe4−x) alloy system is similar to the better known Gd5(SixGe4−x), except it has a more complex magnetic and structural phase diagram. Gd5(SixGe1−x)4 has received much attention recently due to its giant magnetocaloric effect, colossal magnetostriction and giant magnetoresistance in the vicinity of a first order combined magnetic-structural phase transition. The magnetostriction changes that accompany the phase transitions of single crystal Tb5(Si2.2Ge1.8) have been investigated at temperatures between 20 and150 K by measurements of magnetostriction along the a axis. Over this temperature range the shape and slope of the magnetostriction curves change, indicative of changes in the magnetic state, crystal structure, and magnetic anisotropy. The results appear to indicate a phase transition that occurs near 106 K (onset-completion range of 116–100 K). The steepness of the strain transition, its unusual hysteresis, and its temperature dependence appear to indicate a first order phase transition which is activated by applied magnetic field in addition to temperature (see Fig. 1). Magnetostriction measurements at temperature below the transition region appear to indicate a magnetostriction of small overall magnitude (about 30×10−6) but high anisotropy, with anistropy showing considerable temperature dependence

Efficient Derivation of Human Cardiac Precursors and Cardiomyocytes from Pluripotent Human Embryonic Stem Cells with Small Molecule Induction

To date, the lack of a suitable human cardiac cell source has been the major setback in regenerating the human myocardium, either by cell-based transplantation or by cardiac tissue engineering. Cardiomyocytes become terminally-differentiated soon after birth and lose their ability to proliferate. There is no evidence that stem/progenitor cells derived from other sources, such as the bone marrow or the cord blood, are able to give rise to the contractile heart muscle cells following transplantation into the heart. The need to regenerate or repair the damaged heart muscle has not been met by adult stem cell therapy, either endogenous or via cell delivery. The genetically stable human embryonic stem cells (hESCs) have unlimited expansion ability and unrestricted plasticity, proffering a pluripotent reservoir for in vitro derivation of large supplies of human somatic cells that are restricted to the lineage in need of repair and regeneration. Due to the prevalence of cardiovascular disease worldwide and acute shortage of donor organs, there is intense interest in developing hESC-based therapies as an alternative approach. However, how to channel the wide differentiation potential of pluripotent hESCs efficiently and predictably to a desired phenotype has been a major challenge for both developmental study and clinical translation. Conventional approaches rely on multi-lineage inclination of pluripotent cells through spontaneous germ layer differentiation, resulting in inefficient and uncontrollable lineage-commitment that is often followed by phenotypic heterogeneity and instability, hence, a high risk of tumorigenicity (see a schematic in Fig. 1A). In addition, undefined foreign/animal biological supplements and/or feeders that have typically been used for the isolation, expansion, and differentiation of hESCs may make direct use of such cell-specialized grafts in patients problematic. To overcome these obstacles, we have resolved the elements of a defined culture system necessary and sufficient for sustaining the epiblast pluripotence of hESCs, serving as a platform for de novo derivation of clinically-suitable hESCs and effectively directing such hESCs uniformly towards clinically-relevant lineages by small molecules (see a schematic in Fig. 1B). After screening a variety of small molecules and growth factors, we found that such defined conditions rendered nicotinamide (NAM) sufficient to induce the specification of cardiomesoderm direct from pluripotent hESCs that further progressed to cardioblasts that generated human beating cardiomyocytes with high efficiency (Fig. 2). We defined conditions for induction of cardioblasts direct from pluripotent hESCs without an intervening multi-lineage embryoid body stage, enabling well-controlled efficient derivation of a large supply of human cardiac cells across the spectrum of developmental stages for cell-based therapeutics