Calculating pesticide residue levels in feed items for terrestrial species requires accounting for the application rate of the pesticide, the frequency and interval of application, the half-life of the pesticide on the food item, and the residue unit dose. Microsoft Excel™-based applications such as the US Environmental Protection Agency's Terrestrial Residue Exposure model (T-REX) and Terrestrial Herpetofaunal Exposure Residue Program (T-HERPS) calculate the residue levels in feed items using a recursive sequence. A recursive sequence is an unwieldy calculation method that presents a barrier to creating a software-based tool capable of conducting flexible assessments. Therefore, we determined the closed form of the recursive mathematical equation used by both T-REX and T-HERPS. With this formula, we can both duplicate screening-level assessments (T-REX, T-HERPS) as well as incrementally refine the assessment with data-driven inputs. Integr Environ Assess Manag 2018;14:703-709. © 2018 SETAC.
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http://dx.doi.org/10.1002/ieam.4082 | DOI Listing |
Nat Commun
December 2024
Department of Theory and Bio-Systems, Max Planck Institute of Colloids and Interfaces, 14476, Potsdam, Germany.
Neurodegeneration in Huntington's disease (HD) is accompanied by the aggregation of fragments of the mutant huntingtin protein, a biomarker of disease progression. A particular pathogenic role has been attributed to the aggregation-prone huntingtin exon 1 (HTTex1), generated by aberrant splicing or proteolysis, and containing the expanded polyglutamine (polyQ) segment. Unlike amyloid fibrils from Parkinson's and Alzheimer's diseases, the atomic-level structure of HTTex1 fibrils has remained unknown, limiting diagnostic and treatment efforts.
View Article and Find Full Text PDFJ Chem Inf Model
December 2024
Xuzhou College of Industrial Technology, Xuzhou 221140, Jiangsu Province, China.
The β-1,4 galactosylation catalyzed by β-1,4 galactosyltransferases (β4Gal-Ts) is not only closely associated with diverse physiological and pathological processes in humans but also widely applied in the -glycan modification of protein glycoengineering. The loop-closing process of β4Gal-Ts is an essential intermediate step intervening in the binding events of donor substrate (UDP-Gal/Mn) and acceptor substrate during its catalytic cycle, with a significant impact on the galactosylation activities. However, the molecular mechanisms in regulating loop-closing dynamics are not entirely clear.
View Article and Find Full Text PDFHealth Inf Sci Syst
December 2025
School of Nursing, National Taipei University of Nursing and Health Sciences, No. 365, Ming-Te Road, Peitou District, Taipei, 112 Taiwan.
Background: Health risks associated with phthalate esters depend on exposure level, individual sensitivities, and other contributing factors.
Purpose: This study employed artificial intelligence algorithms while applying data mining techniques to identify correlations between phthalate esters [di(2-ethylhexyl) phthalate, DEHP], lifestyle factors, and disease outcomes.
Methods: We conducted exploratory analysis using demographic and laboratory data collected from the Taiwan Biobank.
Fish Shellfish Immunol
December 2024
Department of Marine Life Sciences & Center for Genomic Selection in Korean Aquaculture, Jeju National University, Jeju 63243, Republic of Korea; Marine Life Research Institute, Jeju National University, Jeju 63333, Republic of Korea. Electronic address:
Nucleoredoxin (NXN) is a prominent oxidoreductase enzyme, classified under the thioredoxin family, and plays a pivotal role in regulating cellular redox homeostasis. Although the functional characterization of NXN has been extensively studied in mammals, its role in fish remains relatively unexplored. In this study, the NXN gene from Planiliza haematocheilus (PhNXN) was molecularly and functionally characterized using in silico tools, expression analyses, and in vitro assays.
View Article and Find Full Text PDFFront Physiol
December 2024
National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Introduction: Adrenergic activation of protein kinase A (PKA) in cardiac muscle targets the sarcolemma, sarcoplasmic reticulum, and contractile apparatus to increase contractile force and heart rate. In the thin filaments of the contractile apparatus, cardiac troponin I (cTnI) Ser22 and Ser23 in the cardiac-specific N-terminal peptide (NcTnI: residues 1 to 32) are the targets for PKA phosphorylation. Phosphorylation causes a 2-3 fold decrease of affinity of cTn for Ca associated with a higher rate of Ca dissociation from cTnC leading to a faster relaxation rate of the cardiac muscle (lusitropy).
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