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14341por Abdullah Issa, Mohammed, Z. Abidin, Zurina, Sobri, Shafreeza, Rashid, Suraya, Adzir Mahdi, Mohd, Azowa Ibrahim, Nor, Y. Pudza, Musa“…The mechanism could be attributed to the particularly high thermodynamic affinity of Cu(2+) for the N-chelate groups over the surface of N–CDs and the fast metal-to-ligand binding kinetics. …”
Publicado 2019
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14342por de J. Parra, Yonathan, Andueza L, Felix D., Ferrer M, Rosa E., Bruno Colmenarez, Julia, Acosta, María E., Charris, Jaime, Rosenthal, Philip J., Gut, Jiri“…The spectral results suggested that the ligand acted as chelating species coordinating the metal through the endocyclic nitrogen of the quinoline ring in both complexes, with general formulae expressed in two ways, according to the phase in which they are: [Cu(L)(2)Cl(2)] for solid phase and [Cu(L)(2)][2Cl] for liquid phase. …”
Publicado 2019
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14343por Ulhassan, Zaid, Huang, Qian, Gill, Rafaqat Ali, Ali, Skhawat, Mwamba, Theodore Mulembo, Ali, Basharat, Hina, Faiza, Zhou, Weijun“…MT promotes the accumulation of chelating agents in the roots, detoxifies Se there, and impedes its further translocation to the leaves. …”
Publicado 2019
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14344por ter Meulen, Karlien J., Dekker, Marijke J. E., Pasch, Andreas, Broers, Natascha J. H., van der Sande, Frank M., van der Net, Jeroen B., Konings, Constantijn J. A. M., Gsponer, Isabelle M., Bachtler, Matthias D. N., Gauly, Adelheid, Canaud, Bernard, Kooman, Jeroen P.“…The use of citric-acid dialysate may have a beneficial effect on the calcification propensity due to the chelating effect on calcium and magnesium. The aim of this study was to compare the intradialytic and short-term effects of haemodialysis with either standard acetic-acid dialysate with dCa1.50 (A1.5) or dCa1.25 (A1.25), as well as citric-acid dialysate with dCa1.50 (C1.5) in bicarbonate dialysis on the calcification propensity of serum. …”
Publicado 2019
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14345por Lv, Panpan, Liu, Zeyuan, Xu, Bin, Tang, Chuanhao, Li, Xiaoyan, Qin, Haifeng, Yang, Shaoxing, Gao, Hongjun, He, Kun, Liu, Xiaoqing“…Serum and urine peptides were extracted using copper ion-chelating nanomagnetic beads, and mass spectra were obtained using MALDI-TOF-MS. …”
Publicado 2020
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14346por Lin, Jian-Hong, Ting, Pei-Ching, Lee, Wen-Sen, Chiu, Hung-Wen, Chien, Chun-An, Liu, Chin-Hung, Sun, Li-Yi, Yang, Kun-Ta“…Cotreatment with PAME and a calcium chelator together inhibited the PAME-increased intracellular Ca(2+) levels but did not affect the PAME-induced cell proliferation inhibition and G(2)/M cell cycle arrest. …”
Publicado 2019
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14347por Noskova, Yulia, Likhatskaya, Galina, Terentieva, Natalia, Son, Oksana, Tekutyeva, Liudmila, Balabanova, Larissa“…The exogenous ions, such as Zn(2+), Cu(2+), and Mn(2+), as well as chelating agents EDTA and EGTA, do not have an appreciable effect on the CamPhoD activity. …”
Publicado 2019
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14348por Wang, Tongtong, Ye, Xin, Bian, Wei, Chen, Zhichi, Du, Juanjuan, Li, Mengyi, Zhou, Peng, Cui, Huairui, Ding, Yu-Qiang, Qi, Shuangshuang, Liao, Min, Sun, Chenyou“…In order to investigate the neuroprotective effect of APα, as well as to clarify its possible molecular mechanisms, SH-SY5Y neuronal cell lines were incubated with 6-hydroxydopamine (6-OHDA), which has been widely used as an in vitro model for PD, along with APα alone or in combination with GABAAR antagonist (bicuculline, Bic), intracellular Ca(2+) chelator (EGTA) and voltage-gated L-type Ca(2+) channel blocker (Nifedipine). …”
Publicado 2020
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14349por Chastel, Adrien, Worm, Dennis J., Alves, Isabel D., Vimont, Delphine, Petrel, Melina, Fernandez, Samantha, Garrigue, Philippe, Fernandez, Philippe, Hindié, Elif, Beck-Sickinger, Annette G., Morgat, Clément“…By using solid-phase peptide synthesis, the hY(1)R-preferring [F(7),P(34)]-NPY was modified with a fatty acid, a cathepsin B-cleavable linker, followed by a nuclear localization sequence (NLS), and a DOTA chelator (compound pb12). In this proof-of-concept study, labeling was performed with either native terbium-159 ((nat)Tb), as surrogate for (161)Tb, or with indium-111 ((111)In). …”
Publicado 2020
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14350“…Inflammatory responses triggered by α-syn were not affected by iron overload. The iron chelator desferrioxamine (DFO, 100 μmol/L) exerted suppressive effects on TNF-α mRNA levels, although no change was observed for TNF-α release. …”
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14351por Feng, Jiankang, Li, Cuiping, Xu, Ruifang, Li, Yongli, Hou, Qi, Feng, Rui, Wang, Senye, Zhang, Lei, Li, Changzheng“…In addition, some studies have shown that ROS participates in EMT process, but the effect of ROS stemmed from ferritin degradation on EMT has not been fully established. A novel iron chelator, DpdtC (2,2′-di-pyridylketone dithiocarbamate), which could induce ferritinophagy in HepG2 cell in our previous study, was used to investigate its effect on EMT in gastric cancer cells. …”
Publicado 2020
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14352“…For 38 medications the mechanism of interaction with ARAs was identified as gastric pH dependent, and for 83 medications the interaction was found to be not gastric pH mediated, with mechanisms involving metabolic enzymes, transporters, chelation, and urine alkalization. Additionally, 109 medications were studied and did not have a clinically meaningful interaction with ARAs. …”
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14353por Yang, Kun, Wu, Yi, Zhou, Yali, Long, Binbin, Lu, Qian, Zhou, Tianhong, Wang, Li, Geng, Zhili, Yin, Xiaolin“…METHODS: Patients with non-transfusion-dependent thalassemia (NTDT) or transfusion-dependent thalassemia (TDT), who were unable to pursue conventional therapy with transfusion and chelation, were recruited over 3 years in three centers in southern China. …”
Publicado 2020
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14354por Sinan, Kouadio Ibrahime, Zengin, Gokhan, Zheleva-Dimitrova, Dimitrina, Etienne, Ouattara Katinan, Fawzi Mahomoodally, Mohamad, Bouyahya, Abdelhakim, Lobine, Devina, Chiavaroli, Annalisa, Ferrante, Claudio, Menghini, Luigi, Recinella, Lucia, Brunetti, Luigi, Leone, Sheila, Orlando, Giustino“…Among tested extracts, the infused extract displayed the highest free radical quenching, reducing and metal-chelating ability. The extracts (except infusion) were effective as enzyme inhibitors against AChE, while only methanolic and infused extracts showed noteworthy anti-BChE effects. …”
Publicado 2020
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14355“…Pulmonary disease (31.1%, n=369) was the most frequent complication; blood transfusions (mean: 8.4 [SD:7.0]) and iron-chelating therapies (mean: 8.6 [SD:10]) were the most common interventions and medications, respectively. …”
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14356por Zhu, Yuan, Plaza, Nayomi, Kojima, Yuka, Yoshida, Makoto, Zhang, Jiwei, Jellison, Jody, Pingali, Sai Venkatesh, O’Neill, Hugh, Goodell, Barry“…Brown rot (BR) decay mechanisms employ carbohydrate-active enzymes (CAZymes) as well as a unique non-enzymatic chelator-mediated Fenton (CMF) chemistry to deconstruct lignocellulosic materials. …”
Publicado 2020
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14357“…The pre-treatments of a specific ferroptosis inhibitor Ferrostatin-1 (Fer-1) and an iron chelater Deferoxamine mesylate (DFO) not only inhibited cell death, but also alleviated iron overload, LPO and alternations in ferroptosis biomarkers in microglia, which were caused by N-GQDs. …”
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14358por Saiyarsarai, Parisa, Khorasani, Elahe, Photogeraphy, Hasti, Ghaffari Darab, Mohsen, Seyedifar, Meysam“…A systematic review was conducted in order to evaluate the clinical effectiveness of comparators. Because of chelating therapy is weight-dependent, patients were assumed to be 2 years-old at initiation in first and 18 years-old in second scenario, and model was estimated lifetime costs and utilities. …”
Publicado 2020
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14359por Barwiolek, Magdalena, Kaczmarek-Kędziera, Anna, Muziol, Tadeusz M., Jankowska, Dominika, Jezierska, Julia, Bieńko, Alina“…Despite the fact that the chelate formed by the NNO ligand donors (C26-C25H(2)-C24H(2)-N23=C23H-C22-C19Ph(O1)-C2(Ph)-C3H=N3-C4H(2)-C5H(2)-C6 fragment) are identical, as well as the synthesis of Cu(II) complexes (Cu:L = 2:1 molar ratio) was performed in the same manner, the structures of the complexes differ significantly. …”
Publicado 2020
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14360“…The application of TPEN, a Zn(2+) chelator, in control, HP He and HBOTox conditions, revealed that the increase in GluN1 + GluN2A current is associated with the removal of the high-affinity voltage-independent Zn(2+) inhibition of the receptor. …”
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