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6521por Li, Huihui, Ma, Zhi, Zhai, Yajun, Lv, Chao, Yuan, Peng, Zhu, Feng, Wei, Liping, Li, Qi, Qi, Xin“…To evaluate apoptosis, we used Tunel staining. Metabolic substrate contents of glucose, free fatty acid, ketone bodies, lactic acid, and pyruvate and ATP levels in myocardial tissues were measured with the corresponding kit. …”
Publicado 2020
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6522por Sun, Zhenni, Luan, Shufang, Yao, Yasai, Qin, Tao, Xu, Xiaomei, Shen, Zan, Yao, Ruyong, Yue, Lu“…METHODS: The expression of NHE1 was examined by qPCR in the SGC7901/5-FU cell line and its parental cell line. pcDNA3.1-NHE1 and NHE1-siRNA were transfected to SGC7901/5-FU resistance cells and cell apoptosis was detected via TUNEL assay. The upstream activators in NHE1 mediated 5-Fu resistant gastric cancer cells were detected by Western blot and immunofluorescent. …”
Publicado 2020
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6523por Yuan, Kai, Mei, Jingtian, Shao, Dandan, Zhou, Feng, Qiao, Han, Liang, Yakun, Li, Kai, Tang, Tingting“…The cytotoxic and proapoptotic effects of CeO(2)NPs were detected by cell counting kit (CCK-8) assay, TdT-mediated dUTP nick-end labeling (TUNEL) assay, and flow cytometry. RESULTS: The results of this study demonstrated that although CeO(2)NPs were capable of scavenging ROS in acellular environments, they facilitated the production of ROS in the acidic cellular environment during receptor activator of nuclear factor kappa-Β ligand (RANKL)-dependent osteoclast differentiation of bone marrow-derived macrophages (BMMs). …”
Publicado 2020
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6524por Wang, Kankai, Ru, Junnan, Zhang, Hengli, Chen, Jiayu, Lin, Xiao, Lin, Zhongxiao, Wen, Min, Huang, Lijie, Ni, Haoqi, Zhuge, Qichuan, Yang, Su“…Pyroptosis in the ischemic cortex was detected through dUTP nick-end labeling (TUNEL) assay, lactate dehydrogenase (LDH) release, and gasdermin D (GSDMD) cleavage. …”
Publicado 2020
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6525por Fan, Yameng, Li, Jiaqiao, Yang, Yuxuan, Zhao, Xiaodan, Liu, Yamei, Jiang, Yude, Zhou, Long, Feng, Yang, Yu, Yan, Cheng, Yilong“…Cell viability was determined by MTT assay, and flow cytometry and TUNEL assay were used to evaluate cell apoptosis. …”
Publicado 2020
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6526“…Apoptosis was further inhibited with LIG, as shown with Terminal dUTP nick-end labeling (TUNEL) staining and expression of Caspase-3, Caspase-9, Bax, and Bcl-2. …”
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6527por Zhang, Jinyu, Miller, Zachary, Musich, Phillip R., Thomas, Ashlin E., Yao, Zhi Q., Xie, Qian, Howe, Philip H., Jiang, Yong“…The effects of DSTYK on apoptosis were investigated by MTT assays, flow cytometry assays, and TUNEL assays. The expression of DSTYK in CRC patients and its correlation with EMT markers were determined by bioinformatics analysis. …”
Publicado 2020
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6528por Chen, Maojian, Jiang, Wei, Xiao, Chanchan, Yang, Weiping, Qin, Qinghong, Mao, Anyun, Tan, Qixing, Lian, Bin, Wei, Changyuan“…CCK-8, colony formation assay, Hoechst 33258 staining, flow cytometry and TUNEL assay were employed to detect proliferation, cell cycle and apoptosis. qRT-PCR and Western blot analysis were applied to detect the mRNA and protein expression of Gli1. …”
Publicado 2020
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6529“…Immunohistochemistry and a TUNEL assay were performed to detect the Ki67 levels and the cell apoptotic rate, respectively. …”
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6530“…EdU staining, colony formation, transwell, flow cytometry and TUNEL assays were applied for measuring the impact of FBXL19-AS1 on cervical cancer cell functions. …”
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6531“…CCK-8 and clone formation assays were conducted to detect cell proliferation, TUNEL assay was used to detect apoptosis, and transwell assay was executed to test migration and invasion. …”
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6532“…Hematoxylin and eosin (HE) staining, immunohistochemistry (IHC), Cell Counting Kit-8 (CCK8), flow cytometry, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay, enzyme-linked immunosorbent assay (ELISA), and western blotting were used to evaluate histopathology, proliferation, apoptosis, oxidative stress, and inflammatory response, respectively. …”
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6533“…In addition, serum cTnI levels, MDA content, expression levels of pro-apoptotic proteins, and the number of TUNEL-positive nuclei were remarkably higher in CME group than those in the Sham group. …”
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6534“…TNF-α, IL-1β, and IL-6 concentrations were measured using Elisa assays. HE staining and TUNEL assays were used to evaluate pathology and apoptosis in kidney tissues, respectively. …”
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6535“…The biological properties of cervical cancer cells were evaluated using Transwell, EdU, and TUNEL assays, respectively. Xenograft tumors in nude mice were observed to assess cervical tumorigenesis in vivo. …”
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6536por Ismy, Jufriady, Sugandi, Suwandi, Rachmadi, Dedi, Hardjowijoto, Sunaryo, Mustafa, Akhmad“…Apoptotic index is calculated based on the reaction introduction 3OH end of fragmentation of DNA by the enzyme terminal transferase in preparations with TUNEL staining reagents. A one-way ANOVA test and Pearson correlation test were used to determine the relationship between SOD with expression of caspase-3 and apoptotic index. …”
Publicado 2020
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6537por Oh, Chang-Ki, Choi, Young Ki, Hwang, Ih-Yeon, Ko, Yeon Uk, Chung, In Kwon, Yun, Nuri, Oh, Young J.“…In certain conditions, overexpression of RNF166 accelerates the naturally occurring neuronal death and 6-OHDA–induced MN9D cell death as determined by TUNEL and annexin-V staining, and caspase activation. …”
Publicado 2020
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6538“…The apoptosis of hippocampal neurons was detected by terminal deoxynucleotidyl transferase transfer‑mediated dUTP nick end‑labeling (TUNEL) assay and flow cytometry. The expression of proteins related to apoptosis (Caspase-3, Bax, and Bcl-2) and the PI3K/AKT/mTOR pathway was detected by Western blot. …”
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6539“…After indicated transfection, proliferation, apoptosis and inflammation of these cells were respectively detected by CCK-8 assay, TUNEL assay and certain ELISA kits. Expression of β-catenin pathway-related proteins was analyzed by Western blot analysis. …”
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6540“…The cell counting kit-8 (CCK-8), colony formation and TdT-mediated dUTP Nick-End Labeling (TUNEL) assays, as well as flow cytometry analysis, were employed to evaluate the modulation of DARS-AS1 on the proliferation and apoptosis of CC cells. …”
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