N′-(2-Hydr­oxy-4-methoxy­benzyl­idene)-4-methoxy­benzohydrazide

In the title compound, C16H16N2O4, the dihedral angle between the two benzene rings is 8.7 (2)°. The mol­ecule adopts an E configuration about the C=N bond, with an intra­molecular O—H⋯N hydrogen bond involving the hydr­oxy substituent and the hydrazide N atom. In the crystal structure, adjacent mol­ecules are linked through inter­molecular N—H⋯O hydrogen bonds, forming chains propagating in the b-axis direction

4-Meth­oxy-N′-(2-methoxy­benzyl­idene)benzohydrazide

In the title compound, C16H16N2O3, the two benzene rings are inclined to one another by 75.4 (2)°, and the mol­ecule adopts an E configuration about the C=N bond. In the crystal structure, symmetry-related mol­ecules are linked via inter­molecular N—H⋯O hydrogen bonds, forming chains running parallel to the c axis

Complex Dynamics in a Singular Delayed Bioeconomic Model with and without Stochastic Fluctuation

A singular delayed biological economic predator-prey system with and without stochastic fluctuation is proposed. The conditions of singularity induced bifurcation are gained, and a state feedback controller is designed to eliminate such bifurcation. Furthermore, saddle-node bifurcation is also showed. Next, the local stability of the positive equilibrium and the existence of Hopf bifurcation are obtained by analyzing the distribution of roots of the corresponding characteristic equation, and the hybrid control strategy is used to control the occurrence of Hopf bifurcation. In addition, some explicit formulas determining the spectral densities of the populations and harvest effort are given when the system is considered with stochastic fluctuation. Finally, numerical simulations are illustrated to verify the theoretical results

Peak in the critical current density in (Cax_{x}Sr1−x_{1-x})3_3Rh4_4Sn13_{13} tuned towards the structural quantum critical point

(Ca$_{x}$Sr$_{1-x}$)$_3$Rh$_4$Sn$_{13}$ is a rare system that has been shown to display an interesting interplay between structural quantum criticality and superconductivity. A putative structural quantum critical point, which is hidden beneath a broad superconducting dome, is believed to give rise to optimized superconducting properties in (Ca$_{x}$Sr$_{1-x}$)$_3$Rh$_4$Sn$_{13}$. However, the presence of the superconducting dome itself hinders the examination of the quantum critical point through electrical transport, as the transport coefficients vanish in the superconducting state. Here, we use critical current density to explore within the superconducting dome. Our measurements reveal a large enhancement of the critical current density at the zero-temperature limit when the system is tuned towards the structural quantum critical point.Comment: 7 pages, 4 figure

Proteomics analysis reveals differentially activated pathways that operate in peanut gynophores at different developmental stages

Specific proteins identified in S3 gynophores. (XLS 91 kb

Peanut (Arachis hypogaea) Expressed Sequence Tag Project: Progress and Application

Many plant ESTs have been sequenced as an alternative to whole genome sequences, including peanut because of the genome size and complexity. The US peanut research community had the historic 2004 Atlanta Genomics Workshop and named the EST project as a main priority. As of August 2011, the peanut research community had deposited 252,832 ESTs in the public NCBI EST database, and this resource has been providing the community valuable tools and core foundations for various genome-scale experiments before the whole genome sequencing project. These EST resources have been used for marker development, gene cloning, microarray gene expression and genetic map construction. Certainly, the peanut EST sequence resources have been shown to have a wide range of applications and accomplished its essential role at the time of need. Then the EST project contributes to the second historic event, the Peanut Genome Project 2010 Inaugural Meeting also held in Atlanta where it was decided to sequence the entire peanut genome. After the completion of peanut whole genome sequencing, ESTs or transcriptome will continue to play an important role to fill in knowledge gaps, to identify particular genes and to explore gene function

Causal association of genetically determined plasma metabolites with osteoarthritis: a two-sample Mendelian randomization study

BackgroundWe aimed to elucidate the causal relationship between plasma metabolites and the vulnerability to Osteoarthritis (OA), encompassing both hip OA and knee OA.MethodsWe conducted a two-way two-sample Mendelian randomization (MR) analysis to investigate the association of 1,400 plasma metabolites with OA. The Inverse Variance Weighted (IVW) model served as the primary two-sample MR Analysis method, with supplementary analysis using the Weighted Median (WM) and MR Egger methods. To ensure the robustness of our findings, sensitivity analyses were performed, incorporating Cochran’s Q test, MR-Egger intercept test, MR-PRESSO, and Leave-One-Out analyses. To validate the identified metabolites, we utilized the Steiger test and linkage disequilibrium score regression.ResultsA total of 94 plasma metabolites were associated with osteoarthritis, with 60 associated with hip OA and 106 associated with knee OA. IVW analysis revealed that tryptophan levels showed the strongest positive association with hip OA (OR [95% CI]: 1.119 [1.024, 1.223]), while X-24757 levels exhibited the highest positive association with knee osteoarthritis (OR [95% CI]: 1.095 [1.032, 1.162]). Ethylparaben sulfate levels were found to have the greatest positive association with hip OA (OR [95% CI]: 1.118 [1.015, 1.231]). Notably, the plasma metabolite X-2475 showed a strong robust random effect across all three types of osteoarthritis. Metabolic pathway analysis revealed that the pathogenesis of osteoarthritis in the hip was mediated by acetylarginine, specifically in four important metabolic pathways: ethanol degradation (p = 0.044), amino sugar metabolism (p = 0.090), fatty acid biosynthesis (p = 0.095), and aspartate metabolism (p = 0.097816).ConclusionThere is a significant association between tryptophan levels and the risk of hip OA, as well as X-24757 levels and the risk of knee osteoarthritis. Additionally, X-24757 levels are also linked to the risk of hip OA. Moreover, this study has identified four crucial metabolic pathways in hip osteoarthritis, which are all regulated by acetylarginine. These findings provide valuable insights into potential biomarkers for OA and highlight potential pathways for its prevention and clinical intervention

High expression of DOCK2 indicates good prognosis in acute myeloid leukemia

DOCK family proteins are evolutionarily conserved guanine nucleotide exchange factors for Rho GTPase with different cellular functions. It has been demonstrated that DOCK1 had adverse prognostic effect in acute myeloid leukemia (AML). We first analyzed data of 85 AML patients who were treated with chemotherapy and had available DOCK1 to DOCK11 expression information and found that DOCK1 and DOCK2 had prognostic significance in AML. In view of the known prognosis of DOCK1 in AML, we then explored the prognostic role of DOCK2. One hundred fifty-six AML patients with DOCK2 expression data were extracted from The Cancer Genome Atlas (TCGA) database and enrolled in this study. Patients were divided based on treatment modality into the chemotherapy group and the allogeneic hematopoietic stem cell transplant (allo-HSCT) group. Each group was divided into two groups by the median expression levels of DOCK2. In the chemotherapy group, high DOCK2 expression was associated with longer event-free survival (EFS, P=0.001) and overall survival (OS, P=0.007). In the allo-HSCT group, EFS and OS were not significantly different between high and low DOCK2 expression groups. Multivariate analysis showed that high DOCK2 expression was an independent favorable prognostic factor for both EFS and OS in all patients (all