ERP Correlates of Recognition Memory in Autism Spectrum Disorder

Recognition memory in autism spectrum disorder (ASD) tends to be undiminished compared to that of typically developing (TD) individuals (Bowler et al. 2007), but it is still unknown whether memory in ASD relies on qualitatively similar or different neurophysiology. We sought to explore the neural activity underlying recognition by employing the old/new word repetition event-related potential effect. Behavioural recognition performance was comparable across both groups, and demonstrated superior recognition for low frequency over high frequency words. However, the ASD group showed a parietal rather than anterior onset (300–500 ms), and diminished right frontal old/new effects (800–1500 ms) relative to TD individuals. This study shows that undiminished recognition performance results from a pattern of differing functional neurophysiology in ASD

Statistical properties of a localization-delocalization transition induced by correlated disorder

The exact probability distributions of the resistance, the conductance and the transmission are calculated for the one-dimensional Anderson model with long-range correlated off-diagonal disorder at E=0. It is proved that despite of the Anderson transition in 3D, the functional form of the resistance (and its related variables) distribution function does not change when there exists a Metal-Insulator transition induced by correlation between disorders. Furthermore, we derive analytically all statistical moments of the resistance, the transmission and the Lyapunov Exponent. The growth rate of the average and typical resistance decreases when the Hurst exponent $H$ tends to its critical value ($H_{cr}=1/2$) from the insulating regime. In the metallic regime $H\geq1/2$, the distributions become independent of size. Therefore, the resistance and the transmission fluctuations do not diverge with system size in the thermodynamic limit

Effects of the alcoholic extract of white mulberry leaves on behavioral performance of rats

White mulberry tree is a genus of Morus in the family Moraceae. The leaves and root of this tree have been traditionally medical applications as a laxative, analgesic, diuretic, antitussive, and sedative agent as well as for reducing blood pressure. The present study aimed to investigate the effects of the alcoholic extract of the leaves of white mulberry tree on the behavioral performance of rats. In this study, 24 male Wistar rats were kept under the condition of normal 12-12 h light-dark cycle for adaptation with the animal house environment and experiments location (23-27C0). All animals have access to food and water ad libitum and were weighed weekly to control their natural growth. These rats were divided into four groups of six rats. First, the open field behavioral test was performed on all rats and after 35 days the gavage feeding of the alcoholic extract of white mulberry leaves was performed. Group one received distilled water and groups two to four respectively received concentrations of 150, 300, and 600 mg per unit body weight of the alcoholic extract white mulberry leaves. Then, open field behavioral test was performed again. Results showed that regarding the number of visited zones there is a significant difference between the control group and the groups receiving the extract. Up to the sixth week that the condition of all rats was identical the rate of weight increase was the same and from the seventh week on that the gavage of the hydro-alcoholic extract of white mulberry leaves began, the trend of the weight increase of the control group was different than that of the other groups. due to the effect of the alcoholic extract of white mulberry leaves on the weight of the rats at concentrations above, it can be concluded that the extract is effective for weight loss. Findings of open field test showed that this extract has anti-anxiety effects while imposing no toxic effects

Bi-Level Decomposition Approach for Coordinated Planning of an Energy Hub With Gas-Electricity Integrated Systems

Integrationof multiple energy systemsand the presence of smart energy hubs have provided increased flexibility and improved efficiency for the system. In this article, a bi-level decomposition approach (BLDA) is presented for coplanning of electricity and gas networks as well as the energy hub in distribution networks. The proposed multistage planning determines the investment candidates with optimum capacity for the components of integrated systems. Due to the complexity and nonlinearity of the models and energy subsystems interactions, the expansion planning problem is a difficult task with many limitations, especially for large-scale systems. To overcome these obstacles, achieve an optimum response and reduce computation time, a mixed integer linear programming model and a new BLDA methodology are developed in this article. Moreover, to evaluate the effectiveness and superiority of the proposed approach, the interactions among the energy systems are simulated in a large-scale distribution system and the results are compared.© 2022 IEEE. Personal use of this material is permitted. Permission from IEEE must be obtained for all other uses, in any current or future media, including reprinting/republishing this material for advertising or promotional purposes, creating new collective works, for resale or redistribution to servers or lists, or reuse of any copyrighted component of this work in other works.fi=vertaisarvioitu|en=peerReviewed

Ruppeiner Geometry of Anyon Gas

We derive the thermodynamic curvature of a two dimensional ideal anyon gas of particles obeying fractional statistics. The statistical interactions of anyon gas can be attractive or repulsive. For attractive statistical interactions, thermodynamic curvature is positive and for repulsive statistical interactions, it is negative, which indicates a more stable anyon gas. There is a special case between the two where the thermodynamic curvature is zero. Small deviations from the classical limit will also be explored.Comment: 12 page

Long-term outcome of patients undergoing liver transplantation for mixed hepatocellular carcinoma and cholangiocarcinoma: an analysis of the UNOS database

AbstractBackgroundMixed hepatocellular and cholangiocarcinoma (HCC-CC) have been associated with a poor prognosis after liver transplantation (LT). We aimed to evaluate long-term outcomes in patients undergoing LT for HCC-CC versus patients with hepatocellular carcinoma (HCC) or cholangiocarcinoma (CC).MethodsRetrospective analysis of the United Network for Organ Sharing (UNOS) database from 1994–2013. Overall survival (OS) in patients with HCC-CC, HCC, and CC, were compared.ResultsWe identified 4049 patients transplanted for primary malignancy (94 HCC-CC; 3515 HCC; 440 CC). Mean age of patients with HCC-CC was 57 ± 10 years, and 77% were male. MELD score did not differ among the groups (p = 0.637). Hepatitis C virus was the most common secondary diagnosis within the HCC-CC (44%) and HCC (36%) cohorts, with primary sclerosing cholangitis in the CC (16%) cohort. OS rates at 1, 3 and 5 years for HCC-CC (82%, 47%, 40%) were similar to CC (79%, 58%, 47%), but significantly worse than HCC (86%, 72%, and 62% p = 0.002).DiscussionPatients undergoing LT for HCC had significantly better survival compared to those transplanted for HCC-CC and CC. LT for mixed HCC-CC confers a survival rate similar to selected patients with CC. Efforts should be made to identify HCC-CC patients preoperatively

Comprehensive Genomic Profiling in Routine Clinical Practice Leads to a Low Rate of Benefit from Genotype-Directed Therapy

Background: Describe a single-center real-world experience with comprehensive genomic profiling (CGP) to identify genotype directed therapy (GDT) options for patients with malignancies refractory to standard treatment options. Methods: Patients who had CGP by a CLIA-certified laboratory between November 2012 and December 2015 were included. The medical records were analyzed retrospectively after Institutional Review Board (IRB) approval. The treating oncologist made the decision to obtain the assay to provide potential therapeutic options. The objectives of this study were to determine the proportion of patients who benefited from GDT, and to identify barriers to receiving GDT. Results: A total of 125 pediatric and adult patients with a histologically confirmed diagnosis of malignancy were included. Among these, 106 samples were from adult patients, and 19 samples were from pediatric patients. The median age was 54 years for adults. The majority had stage IV malignancy (53%) and were pretreated with 2–3 lines of therapy (45%). The median age was 8 years for pediatric patients. The majority had brain tumors (47%) and had received none or 1 line of therapy (58%) when the profiling was requested. A total of 111 (92%) patients had genomic alterations and were candidates for GDT either via on/off-label use or a clinical trial (phase 1 through 3). Fifteen patients (12%) received GDT based on these results including two patients who were referred for genomically matched phase 1 clinical trials. Three patients (2%) derived benefit from their GDT that ranged from 2 to 6 months of stable disease. Conclusions: CGP revealed potential treatment options in the majority of patients profiled. However, multiple barriers to therapy were identified, and only a small minority of the patients derived benefit from GDT

Differences in signaling properties of the cytoplasmic domains of the insulin receptor and insulin-like growth factor receptor in 3T3-L1 adipocytes

Insulin and insulin-like growth factors (IGFs) elicit distinct but overlapping biological effects in vivo. To investigate whether differences in intrinsic signaling capacity of receptors contribute to biological specificity, we constructed chimeric receptors containing the extracellular portion of the neurotrophin receptor TrkC fused to the intracellular portion of the insulin or IGF-I receptors, Chimeras were stably expressed in 3T3-L1 adipocytes at levels comparable to endogenous insulin receptors and were efficiently activated by neurotrophin-3. The wild-type insulin receptor chimera mediated approximately 2-fold greater phosphorylation of insulin receptor substrate 1 (IRS-1), association of IRS-1 with phosphoinositide 3-kinase, stimulation of glucose uptake, and GLUT4 translocation, compared with the IGF-I receptor chimera. In contrast, the IGF-I receptor chimera mediated more effective Shc phosphorylation, association of Shc with Grb2, and activation of mitogen-activated protein kinase compared with the insulin receptor chimera. The two receptors elicited similar activation of protein kinase B, p70S6 kinase, and glycogen synthesis. We conclude that the insulin receptor mediates some aspects of metabolic signaling in adipocytes more effectively than the IGF-I receptor, as a consequence of more efficient phosphorylation of IRS-1 and greater recruitment/activation of phosphoinositide 3-kinase