756 research outputs found
Entanglement induced by a single-mode heat environment
A thermal field, which frequently appears in problems of decoherence,
provides us with minimal information about the field. We study the interaction
of the thermal field and a quantum system composed of two qubits and find that
such a chaotic field with minimal information can nevertheless entangle the
qubits which are prepared initially in a separable state. This simple model of
a quantum register interacting with a noisy environment allows us to understand
how memory of the environment affects the state of a quantum register.Comment: 13pages, 3 figure
Dynamical modelling of the elliptical galaxy NGC 2974
In this paper we analyse the relations between a previously described oblate
Jaffe model for an ellipsoidal galaxy and the observed quantities for NGC 2974,
and obtain the length and velocity scales for a relevant elliptical galaxy
model. We then derive the finite total mass of the model from these scales, and
finally find a good fit of an isotropic oblate Jaffe model by using the
Gauss-Hermite fit parameters and the observed ellipticity of the galaxy NGC
2974. The model is also used to predict the total luminous mass of NGC 2974,
assuming that the influence of dark matter in this galaxy on the image,
ellipticity and Gauss-Hermite fit parameters of this galaxy is negligible
within the central region, of radius Comment: 7 figure
Can residuals of the Solar system foreground explain low multipole anomalies of the CMB ?
The low multipole anomalies of the Cosmic Microwave Background has received
much attention during the last few years. It is still not ascertained whether
these anomalies are indeed primordial or the result of systematics or
foregrounds. An example of a foreground, which could generate some non-Gaussian
and statistically anisotropic features at low multipole range, is the very
symmetric Kuiper Belt in the outer solar system. In this paper, expanding upon
the methods presented by Maris et al. (2011), we investigate the contributions
from the Kuiper Belt objects (KBO) to the WMAP ILC 7 map, whereby we can
minimize the contrast in power between even and odd multipoles in the CMB,
discussed discussed by Kim & Naselsky (2010). We submit our KBO de-correlated
CMB signal to several tests, to analyze its validity, and find that
incorporation of the KBO emission can decrease the quadrupole-octupole
alignment and parity asymmetry problems, provided that the KBO signals has a
non-cosmological dipole modulation, associated with the statistical anisotropy
of the ILC 7 map. Additionally, we show that the amplitude of the dipole
modulation, within a 2 sigma interval, is in agreement with the corresponding
amplitudes, discussed by Lew (2008).Comment: 24 pages, 9 figures, 5 tables. Matches version in JCA
Defense gene expression and phenotypic changes of rice (Oryza sativa L.) at the reproductive stage in response to whitebacked planthopper (Sogatella furcifera Horvath) infestation
This study was to determine the gene expression pattern and phenotypic change of Cheongcheong, Nagdong, TN1, and 8 different pedigrees of the CNDH population when WBPH infestation initiated at the reproductive stage of the crop. WBPH infested plants generally showed higher expression level of defense genes compared with the uninfected plants. LOX transcriptional levels in Nagdong and CNDH42-1 did not increase after WBPH feeding at all-time course. Chlorophyll content declined in infested plants compared to their controls, but still CNDH3, CNDH14-2, and CNDH65 were healthier. Heavy and extensive WBPH feeding affected rice yield and grain quality although the infestation started at the reproductive stage
Targeting the YAP/TAZ pathway in uveal and conjunctival melanoma with verteporfin
PURPOSE. The purpose of this study was to determine whether YAP/TAZ activation in uveal melanoma (UM) and the susceptibility of melanoma cell lines to YAP/TAZ inhibition by verteporfin (VP) is related to the tumor's genetic background.METHODS. Characteristics of 144 patients with enucleated UM were analyzed together with mRNA expression levels of YAP/TAZ-related genes (80 patients from the The Cancer Genome Atlas [TCGA] project and 64 patients from Leiden, The Netherlands). VP was administered to cell lines 92.1, OMM1, Mel270, XMP46, and MM28 (UM), CRMM1 and CRMM2 (conjunctival melanoma), and OCM3 (cutaneous melanoma). Viability, growth speed, and expression of YAP1-related proteins were assessed.RESULTS. In TCGA data, high expression of YAP1 and WWTR1 correlated with the presence of monosomy 3 (P = 0.009 and P < 0.001, respectively) and BAP1-loss (P = 0.003 and P = 0.001, respectively) in the primary UM; metastasis development correlated with higher expression of YAP1 (P = 0.05) and WWTR1 (P = 0.003). In Leiden data, downstream transcription factor TEAD4 was increased in cases with M3/BAP1-loss (P = 0.002 and P = 0.006) and related to metastasis (P = 0.004). UM cell lines 92.1, OMM1, and Mel270 (GNAQ/11-mutation, BAP1-positive) and the fast-growing cell line OCM3 (BRAF-mutation) showed decreased proliferation after exposure to VP. Two slow-growing UM cell lines XMP46 and MM28 (GNAQ/11-mutation, BAP1-negative) were not sensitive to VP, and neither were the two conjunctival melanoma cell lines (BRAF/NRAS-mutation).CONCLUSIONS. High risk UM showed an increased expression of YAP/TAZ-related genes. Although most UM cell lines responded in vitro to VP, BAP1-negative and conjunctival melanoma cell lines did not. Not only the mutational background, but also cell growth rate is an important predictor of response to YAP/TAZ inhibition by VP.Ophthalmic researc
Mechanical Responses and Stress Fluctuations of a Supercooled Liquid in a Sheared Non-Equilibrium State
A steady shear flow can drive supercooled liquids into a non-equilibrium
state. Using molecular dynamics simulations under steady shear flow
superimposed with oscillatory shear strain for a probe, non-equilibrium
mechanical responses are studied for a model supercooled liquid composed of
binary soft spheres. We found that even in the strongly sheared situation, the
supercooled liquid exhibits surprisingly isotropic responses to oscillating
shear strains applied in three different components of the strain tensor. Based
on this isotropic feature, we successfully constructed a simple two-mode
Maxwell model that can capture the key features of the storage and loss moduli,
even for highly non-equilibrium state. Furthermore, we examined the correlation
functions of the shear stress fluctuations, which also exhibit isotropic
relaxation behaviors in the sheared non-equilibrium situation. In contrast to
the isotropic features, the supercooled liquid additionally demonstrates
anisotropies in both its responses and its correlations to the shear stress
fluctuations. Using the constitutive equation (a two-mode Maxwell model), we
demonstrated that the anisotropic responses are caused by the coupling between
the oscillating strain and the driving shear flow. We measured the magnitude of
this violation in terms of the effective temperature. It was demonstrated that
the effective temperature is notably different between different components,
which indicates that a simple scalar mapping, such as the concept of an
effective temperature, oversimplifies the true nature of supercooled liquids
under shear flow. An understanding of the mechanism of isotropies and
anisotropies in the responses and fluctuations will lead to a better
appreciation of these violations of the FDT, as well as certain consequent
modifications to the concept of an effective temperature.Comment: 15pages, 17figure
Novel loss-of-function variants in CDC14A are associated with recessive sensorineural hearing loss in Iranian and Pakistani patients
CDC14A encodes the Cell Division Cycle 14A protein and has been associated with autosomal recessive non-syndromic hearing loss (DFNB32), as well as hearing impairment and infertile male syndrome (HIIMS) since 2016. To date, only nine variants have been associated in patients whose initial symptoms included moderate-to-profound hearing impairment. Exome analysis of Iranian and Pakistani probands who both showed bilateral, sensorineural hearing loss revealed a novel splice site variant (c.1421+2T>C, p.?) that disrupts the splice donor site and a novel frameshift variant (c.1041dup, p.Ser348Glnfs*2) in the gene CDC14A, respectively. To evaluate the pathogenicity of both loss-of-function variants, we analyzed the effects of both variants on the RNA-level. The splice variant was characterized using a minigene assay. Altered expression levels due to the c.1041dup variant were assessed using RT-qPCR. In summary, cDNA analysis confirmed that the c.1421+2T>C variant activates a cryptic splice site, resulting in a truncated transcript (c.1414_1421del, p.Val472Leufs*20) and the c.1041dup variant results in a defective transcript that is likely degraded by nonsense-mediated mRNA decay. The present study functionally characterizes two variants and provides further confirmatory evidence that CDC14A is associated with a rare form of hereditary hearing loss
Charged pion form factor between Q^2=0.60 and 2.45 GeV^2. II. Determination of, and results for, the pion form factor
The charged pion form factor, Fpi(Q^2), is an important quantity which can be
used to advance our knowledge of hadronic structure. However, the extraction of
Fpi from data requires a model of the 1H(e,e'pi+)n reaction, and thus is
inherently model dependent. Therefore, a detailed description of the extraction
of the charged pion form factor from electroproduction data obtained recently
at Jefferson Lab is presented, with particular focus given to the dominant
uncertainties in this procedure. Results for Fpi are presented for
Q^2=0.60-2.45 GeV^2. Above Q^2=1.5 GeV^2, the Fpi values are systematically
below the monopole parameterization that describes the low Q^2 data used to
determine the pion charge radius. The pion form factor can be calculated in a
wide variety of theoretical approaches, and the experimental results are
compared to a number of calculations. This comparison is helpful in
understanding the role of soft versus hard contributions to hadronic structure
in the intermediate Q^2 regime.Comment: 18 pages, 11 figure
Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism
BACKGROUND: PHF21A has been associated with intellectual disability and craniofacial anomalies based on its deletion in the Potocki-Shaffer syndrome region at 11p11.2 and its disruption in three patients with balanced translocations. In addition, three patients with de novo truncating mutations in PHF21A were reported recently. Here, we analyze genomic data from seven unrelated individuals with mutations in PHF21A and provide detailed clinical descriptions, further expanding the phenotype associated with PHF21A haploinsufficiency. METHODS: Diagnostic trio whole exome sequencing, Sanger sequencing, use of GeneMatcher, targeted gene panel sequencing, and MiSeq sequencing techniques were used to identify and confirm variants. RT-qPCR was used to measure the normal expression pattern of PHF21A in multiple human tissues including 13 different brain tissues. Protein-DNA modeling was performed to substantiate the pathogenicity of the missense mutation. RESULTS: We have identified seven heterozygous coding mutations, among which six are de novo (not maternal in one). Mutations include four frameshifts, one nonsense mutation in two patients, and one heterozygous missense mutation in the AT Hook domain, predicted to be deleterious and likely to cause loss of PHF21A function. We also found a new C-terminal domain composed of an intrinsically disordered region. This domain is truncated in six patients and thus likely to play an important role in the function of PHF21A, suggesting that haploinsufficiency is the likely underlying mechanism in the phenotype of seven patients. Our results extend the phenotypic spectrum of PHF21A mutations by adding autism spectrum disorder, epilepsy, hypotonia, and neurobehavioral problems. Furthermore, PHF21A is highly expressed in the human fetal brain, which is consistent with the neurodevelopmental phenotype. CONCLUSION: Deleterious nonsense, frameshift, and missense mutations disrupting the AT Hook domain and/or an intrinsically disordered region in PHF21A were found to be associated with autism spectrum disorder, epilepsy, hypotonia, neurobehavioral problems, tapering fingers, clinodactyly, and syndactyly, in addition to intellectual disability and craniofacial anomalies. This suggests that PHF21A is involved in autism spectrum disorder and intellectual disability, and its haploinsufficiency causes a diverse neurological phenotype
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