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BRISC inactivation alleviates alcohol-induced liver injury in mice
Sulfur Lone Pairs Open Avenues for π* → n Orange-to-Red TADF and OLEDs
De novo Transcriptomic analysis to unveil the deltamethrin induced resistance mechanisms in Callosobruchus chinensis (L.)
Photolytic and Thermal Reactions of [C<sub>6</sub>H<sub>4</sub>(PPh<sub>2</sub>)<sub>2</sub>(μ-N<sub>2</sub>)] and Its Lewis Acid Adducts: N–N Bond Cleavage and Liberation of N<sub>2</sub>
Oxidative stress index-based scoring for prediction of long-term prognosis in patients with colorectal cancer with liver metastases
Dimerization of Hexaphyrin with an Appendant Pyrrole Possessing a Reactive Site to Alleviate the Steric Hindrance
Evaluation of the effects on the tensile properties of medical gloves after repeated disinfection
Pd<sub>1</sub>Ni<sub>2</sub> Trimer Sites Drive Efficient and Durable Hydrogen Oxidation in Alkaline Media
Author Correction: Public attitudes towards social media field experiments
Polarization Switching from Valence Trapping in an Oxo-Bridged Trinuclear Iron Complex
Development and validation of a stability-indicating HPLC method for the simultaneous determination of anticoccidial drugs in veterinary formulations: greenness and whiteness assessment
Abstract Intestinal coccidiosis is a significant parasitic disease affecting poultry, resulting in substantial economic losses for the industry. It compromises the nutrition absorption, leading to weight loss and elevated mortality rates. Furthermore, the stress caused by the infection can compromise the immune system, making poultry more susceptible to secondary infections and reducing overall productivity. As a result, simple analytical techniques are critical for determining anticoccidial drugs. A new, sensitive, and environmentally friendly HPLC method was developed for determining amprolium (AMP), sulfaquinoxaline (SUL), diaveridine (DIV), and vitamin K3 (VIT K3) in their formulations for the first time. Stability tests were performed under diverse stress conditions to verify the safety and efficiency of the formulation throughout its designated shelf time. These investigations ascertain the influence of various environmental conditions on a drug’s chemical stability and physical characteristics. A Supelcosil C18 column was used as the stationary phase, and 0.05 M KH2PO4 and acetonitrile were mixed in a ratio of 80:20 (v/v) as the developing system with a flow rate of 2.0 mL min−1. The proposed drugs were quantified at 260 nm. It was tested and found that the novel analytical method was linear for AMP and SUL between 20.0 and 60.0 µg mL−1, 2.0–6.0 µg mL−1 for VIT K3, and 2.1–6.3 µg mL−1 for DIV. The anticipated method was validated according to ICH guidelines. Advanced evaluation tools, such as GAPI, Red Green Blue (RGB 12, whiteness), Blue Applicability Grade Index (BAGI), the Analytical Eco-Scale, and (AGREE) assessed the sustainability profile of the proposed method, illustrating its enhanced environmental friendliness and sustainability.
Activating Redox Chemistry of Quinones for High Energy Density Aqueous Sodium-Ion Batteries
Adherence to combined healthy lifestyle and odds of metabolic syndrome in Iranian adults: the PERSIAN Dena cohort study
Structural Modulation and Enhanced Magnetic Ordering in Incommensurate K<sub>1–<i>x</i></sub>CrSe<sub>2</sub> Crystals
Unveiling a novel model of cell senescence-related genes for prognostic assessment and immunotherapeutic insights in gastric cancer
A Supramolecular Fluorescent Chemosensor Enabling Specific and Rapid Quantification of Norepinephrine Dynamics
Long-term social memory of mate copying in Drosophila melanogaster is localized in mushroom bodies
Abstract Long-term social memory (LTSM) is a key feature to elicit the cultural inheritance of behaviour independently of genetics. However, the neurobiological basis of LTSM remains largely unknown. We previously used the Drosophila animal model, which is known to perform mate copying through observational learning of the mate choice of conspecifics to show that the expression of the rutabaga gene, a calcium/calmodulin-dependent adenylyl cyclase (AC-Rut+) that acts as a coincidence detector enabling associative learning, is necessary and sufficient in the γ-Kenyon cells (KCs) of the mushroom bodies (MBs). Here, we show that the expression of AC-Rut+ in both the γ- and the α/β-KCs is required for LTSM involving de novo protein synthesis in a mate-copying context, whether using demonstrations involving real flies or involving pictures of copulating conspecifics. Thus, pathways of short- and long-term memory show considerable overlap in the MBs across social vs. asocial learning contexts.