المؤلفون: Giorgio Fuiano, Vincenzo Altieri, Vincenzo Bisesti, Bruno Memoli, Pasquale Esposito, Michele Andreucci, Alfredo Procino, Ashour Michael, Teresa Faga, Pierangela Presta, Carmela Tozzo

المساهمون: Andreucci, M, Fuiano, G, Presta, P, Esposito, P, Faga, T, Bisesti, Vincenzo, Procino, A, Altieri, V, Tozzo, C, Memoli, Bruno, Michael, A.

المصدر: Biochemical Pharmacology. 72:1334-1342

مصطلحات موضوعية: Kinase, iopromide, diatrizoate, Contrast Media, Kidney, incubation time, Biochemistry, target variable, Cell survival, Tubular cells, Kidney Tubules, Proximal, contrast medium, iomeprol, mammalian target of rapamycin inhibitor, mitogen activated protein kinase 1, mitogen activated protein kinase 3, protein kinase, protein kinase B, serine, threonine, transcription factor FKHR, transcription factor FKHRL1, article, cell viability, controlled study, downstream processing, drug blood level, genetic transfection, human, human cell, intracellular space, kidney proximal tubule, kidney tubule cell, molecular dynamics, priority journal, protein dephosphorylation, protein family, signal transduction, Cell Line, Cell Survival, Down-Regulation, Epithelial Cells, Humans, Phosphorylation, Proto-Oncogene Proteins c-akt, Signal Transduction, Transfection, Nephrotoxicity, Proximal, Cell biology, Signaling, Kidney Tubules, medicine.anatomical_structure, Signal transduction, medicine.medical_specialty, Biology, Internal medicine, medicine, Protein kinase B, Cell damage, PI3K/AKT/mTOR pathway, Settore MED/14 - Nefrologia, Pharmacology, medicine.disease, Endocrinology

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf94c1296f19e08c5c86b1555f5917eTest
https://doi.org/10.1016/j.bcp.2006.08.008Test

المؤلفون: Nicole H.P. Cnubben, Peter J. van Bladeren, Jelmer J. van Zanden, Ivonne M.C.M. Rietjens, Heleen M. Wortelboer, Liesbeth Geraets

المساهمون: TNO Voeding

المصدر: Biochemical Pharmacology 67 (2004) 8
Biochemical Pharmacology, 67(8), 1607-1617
Biochemical Pharmacology, 8, 67, 1607-1617

مصطلحات موضوعية: family, IC50, animal cell, Pharmacology, Toxicology, Biochemistry, quercetin, taxifolin, multidrug-resistance protein, glutathione transferase, toxicokinetics, S-(2,4-dinitrophenyl)glutathione, Tumor Cells, Cultured, heterocyclic compounds, eriodictyol, Biology Toxicology, multidrug resistance protein 1, multidrug resistance protein 2, flavanoid, chemistry.chemical_classification, food and beverages, Catechin, 1-chloro-2,4-dinitrobenzene, priority journal, Myricetin, plant polyphenols, hydroxyl group, 50% inhibition concentration, Multidrug resistance associated protein, Structure-Activity Relationship, catechin, Membrane Transport Modulators, GSH, Taxifolin, Humans, human, GST, luteolin, Toxicologie, VLAG, human cell, fungi, Membrane Transport Proteins, Eriodictyol, chemistry, Glutathione S-Transferase pi, P-gp, genetic transfection, Carrier Proteins, abc transporters, organic anion transporter, Flavonoid, myricetin, chemistry.chemical_compound, p-glycoprotein, lipophilicity, flavone derivative, chemical bond, enzyme inhibition, Glutathione Transferase, article, drug, 3',4' dihydroxyflavone, Glutathione, inhibition, Drug Resistance, Multiple, Multidrug Resistance-Associated Protein 2, CDNB, unclassified drug, enzyme activity, Galangin, Isoenzymes, GS-X, Multidrug Resistance-Associated Proteins, Quercetin, drug potency, MRP, Breast Neoplasms, Physiological Sciences, breast cancer, drug activity, DNP-SG, controlled study, gene, structure activity relation, Flavonoids, galanin, kaempferol, nonhuman, Glutathione conjugate, carbon, catechol derivative, IC 50, Biological Transport, morin, Glutathione S-transferase, cell strain MCF 7, Drug Resistance, Neoplasm, Luteolin

وصف الملف: application/pdf; application/octet-stream

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c41482dcd4864166f4cb1b5c38ec230Test
https://pubmed.ncbi.nlm.nih.gov/15041478Test