Relevant bibliographies by topics / L929 cell line

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  2. Dissertations / Theses
  3. Conference papers

Academic literature on the topic 'L929 cell line'

Author: Grafiati
Published: 7 June 2025
Last updated: 17 July 2025

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Journal articles on the topic "L929 cell line"

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You, Jae-Seek, HyangI Lim, Jeong-Yeon Seo, et al. "25-Hydroxycholesterol-Induced Oxiapoptophagy in L929 Mouse Fibroblast Cell Line." Molecules 27, no. 1 (2021): 199. http://dx.doi.org/10.3390/molecules27010199.

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25-hydroxycholesterol (25-HC) is an oxysterol synthesized from cholesterol by cholesterol-25-hydroxylase during cholesterol metabolism. The aim of this study was to verify whether 25-HC induces oxiapoptophagy in fibroblasts. 25-HC not only decreased the survival of L929 cells, but also increased the number of cells with condensed chromatin and altered morphology. Fluorescence-activated cell sorting results showed that there was a dose-dependent increase in the apoptotic populations of L929 cells upon treatment with 25-HC. 25-HC-induced apoptotic cell death was mediated by the death receptor-de
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Tiskratok, Watcharaphol, Masahiro Yamada, Jun Watanabe, Qu Pengyu, Tsuyoshi Kimura, and Hiroshi Egusa. "Mechanoregulation of Osteoclastogenesis-Inducing Potentials of Fibrosarcoma Cell Line by Substrate Stiffness." International Journal of Molecular Sciences 24, no. 10 (2023): 8959. http://dx.doi.org/10.3390/ijms24108959.

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A micro-physiological system is generally fabricated using soft materials, such as polydimethylsiloxane silicone (PDMS), and seeks an inflammatory osteolysis model for osteoimmunological research as one of the development needs. Microenvironmental stiffness regulates various cellular functions via mechanotransduction. Controlling culture substrate stiffness may help spatially coordinate the supply of osteoclastogenesis-inducing factors from immortalized cell lines, such as mouse fibrosarcoma L929 cells, within the system. Herein, we aimed to determine the effects of substrate stiffness on the
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Cannella, Vincenza, Roberta Altomare, Gabriele Chiaramonte, et al. "Cytotoxicity Evaluation of Endodontic Pins on L929 Cell Line." BioMed Research International 2019 (October 30, 2019): 1–5. http://dx.doi.org/10.1155/2019/3469525.

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Objective. The aim of this study was to evaluate the cytotoxic potential of a type of endodontic pin on L929 cell line according to the UNI EN ISO 10993/2009 rule. Methods. L929 cells were used for the assays; extracts were prepared from three different-diameter endodontic pins, made of epoxy resin and fiberglass matrix and from Reference Materials (ZDEC, ZDBC, and HDP films). MTS assay was performed after 24 h, 48 h, and 72 h of exposure of L929 cells to pin and Reference Material extracts, 5% phenol solution, and control reagent. Cells cultured with different media containing extracts were m
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Falciani, F., M. Terao, S. Goldwurm, et al. "Molybdenum(VI) salts convert the xanthine oxidoreductase apoprotein into the active enzyme in mouse L929 fibroblastic cells*." Biochemical Journal 298, no. 1 (1994): 69–77. http://dx.doi.org/10.1042/bj2980069.

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The mouse L929 fibroblastic cell line presents low, but detectable, levels of the mRNA encoding xanthine oxidoreductase under basal conditions, and it responds to type I and type II interferons by inducing the expression of the transcript [Falciani, Ghezzi, Terao, Cazzaniga, and Garattini (1992) Biochem. J. 285, 1001-1008]. This cell line, however, does not show any detectable amount of xanthine oxidoreductase enzymic activity, either before or after treatment with the cytokines. Molybdenum(VI) salts, in the millimolar range, are capable of activating xanthine oxidoreductase in L929 cells both
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Pizzo, P., M. Murgia, A. Zambon, et al. "Role of P2z purinergic receptors in ATP-mediated killing of tumor necrosis factor (TNF)-sensitive and TNF-resistant L929 fibroblasts." Journal of Immunology 149, no. 10 (1992): 3372–78. http://dx.doi.org/10.4049/jimmunol.149.10.3372.

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Abstract Two closely related cell lines were characterized in their responses to extracellular ATP (ATPo): the fibroblast cell line L929 and a TNF-resistant variant L929/R. Both lines showed ATPo-activated increases in intracellular Ca2+, inward current, and sustained depolarization of the plasma membrane, cell responses compatible with activation of purinergic receptors of the P2y, P2x, or P2z subtype; however, only the L929/R variant was susceptible to ATPo-dependent early permeabilization of the plasma membrane to hydrophilic solutes of M(r) below 900, a response uniquely caused by the acti
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Mat Salleh, Noor Fadilatul Akmal, Ahmad Azlina, Masitah Hayati Harun, et al. "Cytotoxicity and Morphological Effects of Aqueous Areca Nut Crude Extract on L929 Fibroblast Cell Line." Asian Journal of Medicine and Biomedicine 4, no. 1 (2020): 34–41. http://dx.doi.org/10.37231/ajmb.2020.4.1.328.

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Betel quid chewing is a detrimental recreational habit amongst Asians and a risk factor for oral cancer. Arecoline, a component of areca nut (a major constituent of betel quid) is a known carcinogen. However, the effect of areca nut crude extract is not much studied. To evaluate the cytotoxicity and morphologic effects of areca nut aqueous extract on mouse fibroblast cell line (L929). Dried raw areca nut obtained from a local market in Kota Bharu, Kelantan was prepared and suspended in DMEM (Dulbecco’s Modified Eagle’s medium), prior to serial dilution of 1.56, 0.781, 0.39, 0.195, 0.0976, 0.04
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Melekoglu, Abdullah, Yasin Özkabadayı, Mustafa Türk, and Siyami Karahan. "CYTOTOXIC, APOPTOTIC AND NECROTIC EFFECTS OF INULA VISCOSA: AN IN VITRO STUDY ON DIFFERENT CELL LINES." Journal of Applied Biological Sciences 17, no. 1 (2023): 184–99. https://doi.org/10.71336/jabs.1127.

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This study aimed to evaluate the cytotoxic, apoptotic and necrotic effects of Inula viscosa on mouse fibroblast cell line (L929), human breast cancer cell line (MCF7) and human lung adenocarcinoma cell line (A549). The WST-1 (4-[3-(4-Iodophenyl) -2-(4-nitrophenyl)-2H-5-tetrazolio]-1,3-benzene disulfonate, BioVision) test was used to determine cytotoxicity. Apoptotic and necrotic rates were determined by double staining technique, Propidium iodide and Hoechst 33342.The water extract of Inula viscosa extract caused cytotoxicity in a dose dependent manner on L929, MCF7, and A549 cell lines with I
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Neagu, Georgeta, Amalia Stefaniu, Bujor Albu, Iulian Terchescu, Lucia Pintilie, and Lucia Camelia Pirvu. "Stokesia laevis Ethanolic Extract Activity on the Normal and Malignant Murine Cell Line Viability L969 and B16." Chemistry Proceedings 3, no. 1 (2020): 42. http://dx.doi.org/10.3390/ecsoc-24-08318.

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: Stokesia laevis (common name Stokes aster) ethanolic extract (Slae26) containing 5 mg GAE/mL extract was investigated to establish cytotoxicity and anti-proliferative effects. The assays were performed on normal murine fibroblast cell line L929 and malignant murine melanoma cell line B16, respectively; for the first time in literature data, potential cytotoxic and anti-proliferative effects of the ethanolic extract from S. laevis on both, normal murine fibroblast cell line L929, and murine melanoma cell line B16 have been proved. The study is supplemented by molecular docking simulations of
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Xie, Changchuan, Na Zhang, Huamin Zhou, et al. "Distinct Roles of Basal Steady-State and Induced H-Ferritin in Tumor Necrosis Factor-Induced Death in L929 Cells." Molecular and Cellular Biology 25, no. 15 (2005): 6673–81. http://dx.doi.org/10.1128/mcb.25.15.6673-6681.2005.

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ABSTRACT Tumor necrosis factor (TNF) alpha is a cytokine capable of inducing caspase-dependent (apoptotic) cell death in some cells and caspase-independent (necrosis-like) cell death in others. Here, using a mutagenesis screen for genes critical in TNF-induced death in L929 cells, we have found that H-ferritin deficiency is responsible for TNF resistance in a mutant line and that, upon treatment with TNF, this line fails to elevate levels of labile iron pool (LIP), critical for TNF-induced reactive oxygen species (ROS) production and ROS-dependent cell death. Since we found that TNF-induced LI
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Abdullah, Melekoğlu, Özkabadayı Yasin, Türk Mustafa, and Karahan Siyami. "CYTOTOXIC, APOPTOTIC AND NECROTIC EFFECTS OF INULA VISCOSA: AN IN VITRO STUDY ON DIFFERENT CELL LINES." Journal of Applied Biological Sciences 17, no. 1 (2023): 184–99. https://doi.org/10.5281/zenodo.7580015.

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This study aimed to evaluate the cytotoxic, apoptotic and necrotic effects of <em>Inula viscosa</em> on mouse fibroblast cell line (L929), human breast cancer cell line (MCF7) and human lung adenocarcinoma cell line (A549). The WST-1 (4-[3-(4-Iodophenyl) -2-(4-nitrophenyl)-2H-5-tetrazolio]-1,3-benzene disulfonate, BioVision) test was used to determine cytotoxicity. Apoptotic and necrotic rates were determined by double staining technique, Propidium iodide and Hoechst 33342.The water extract of <em>Inula viscosa</em> extract caused cytotoxicity in a dose dependent manner on L929, MCF7, and A549
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Dissertations / Theses on the topic "L929 cell line"

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Chou, Hsien-Yeh, and 周賢曄. "Mechanism of 24p3 Protein, Mouse Uterine Secretory Protein Internalizes to L929 Cell Line." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/22748601908241426394.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>93<br>24p3 protein is a 25.8 kD glycoprotein which belongs to the lipocalin superfamily. It is expressed and secreted from uterine endometrial epithelia during the proestrous phase of female mice, but is constitutively expressed in epididymis. The protein could associate with sperm head and then enhance the sperm motility, but was suggested as a stressor of sperm capacitation and fertility. It was also considered as an apoptotic factor or inflammatory factor in blood cells. The real function is unclear. Our previous studies showed that 24p3 protein could internalize
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Pei-Tzu, Li, and 李倍慈. "Functional study of secreted 24p3 protein via mouse connective tissue cell line L929." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/64233912481255694795.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>92<br>24p3 protein is a secreted glycoprotein, which is estrogen-dependently expressed in mouse uterus, but is constitutively expressed in epididymis. The protein could associate with sperm head and enhance the sperm motility, and was also suggested as a stressor, apoptotic factor or inflammatory factor in blood cells, the function is not clear yet. Using mouse connective tissue cell line L929as a model, we are going to elucidate the reaction mechanism of 24p3 protein on the cells. First of all, dexamethasone could induce the 24p3 gene expression and protein secretio
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Li, Pei-Tzu, and 李倍慈. "Functional study of secreted 24p3 protein via mouse connective tissue cell line L929." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/79869168129470628080.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>92<br>24p3 protein is a secreted glycoprotein, which is estrogen-dependently expressed in mouse uterus, but is constitutively expressed in epididymis. The protein could associate with sperm head and enhance the sperm motility, and was also suggested as a stressor, apoptotic factor or inflammatory factor in blood cells, the function is not clear yet. Using mouse connective tissue cell line L929as a model, we are going to elucidate the reaction mechanism of 24p3 protein on the cells. First of all, dexamethasone could induce the 24p3 gene expression and protein secretio
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Conference papers on the topic "L929 cell line"

1

Düzgören, İpek, Mustafa Kemal Ruhi, and Murat Gülsoy. "Effect of different laser power densities on photobiomodulation of L929 cell line." In European Conferences on Biomedical Optics, edited by Lothar D. Lilge and Ronald Sroka. SPIE, 2017. http://dx.doi.org/10.1117/12.2286190.

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Bakhori, Siti Khadijah Mohd, Shahrom Mahmud, Ling Chuo Ann, et al. "Toxicity evaluation of ZnO nanostructures on L929 fibroblast cell line using MTS assay." In NATIONAL PHYSICS CONFERENCE 2014 (PERFIK 2014). AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4915162.

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"The Effects of Hydroalcoholic Extract of Xanthium Strumarium on L929 Tumor Cell Line." In International Conference on Earth, Environment and Life sciences. International Institute of Chemical, Biological & Environmental Engineering, 2014. http://dx.doi.org/10.15242/iicbe.c1214110.

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Hashimoto, Shigehiro, Kiyoshi Yoshinaka, and Hiroki Yonezawa. "Behavior of Cell Under Wall Shear Stress in Flow Field: Comparison Among Cell Types." In ASME 2021 Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/fedsm2021-65205.

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Abstract Does the hysteresis effect remain in each cell after division? In the present study, the cell activity has been investigated after division under a shear stress field. To apply the constant shear stress field on cells, a Couette type flow device has been manufactured: between parallel walls (a lower stationary culture disk, and an upper rotating disk) with a constant gap. The wall shear stress was controlled by the rotating speed of the upper disk. Four types of cells were used in the test: C2C12 (mouse myoblast cell line), HUVEC (Human Umbilical Vein Endothelial Cells), 3T3-L1 (mouse
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Chippada, Uday, Xue Jiang, Michelle Previtera, et al. "Alteration of Fibroblast Cell Behavior due to Contraction of Substrate." In ASME 2010 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2010. http://dx.doi.org/10.1115/sbc2010-19507.

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Many researchers have utilized hydrogels as substrates for cell attachment. The stiffness of these substrates has been found to influence the cellular behavior such as morphology, proliferation, growth and differentiation. Lo et al. deformed polyacrylamide substrates with a blunted microneedle and observed the movement of NIH 3T3 fibroblasts. In both pulling and pushing, the cells reversed their direction and moved away from the needle. This shows that cellular behavior is also affected by stretching the underlying substrates. In a previous study, Lin et al. have demonstrated the ability to co
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Fomenko, A. N., and M. S. Korovin. "Comparative analysis of the effect of low-dimensional alumina structures on cell lines L929 and Neuro-2a." In PHYSICS OF CANCER: INTERDISCIPLINARY PROBLEMS AND CLINICAL APPLICATIONS (PC’16): Proceedings of the International Conference on Physics of Cancer: Interdisciplinary Problems and Clinical Applications 2016. Author(s), 2016. http://dx.doi.org/10.1063/1.4960234.

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Monteiro, Juliana S. D. C., Katia V. M. de Moura, Cibelle B. Lopes, Cristina P. Soares та Antonio L. B. Pinheiro. "Effects of a polarized light source (λ400-2000nm) on H.Ep.2 and L929 cell lines: a spectroscopic in vitro study". У SPIE BiOS: Biomedical Optics, редактори Michael R. Hamblin, Ronald W. Waynant та Juanita Anders. SPIE, 2009. http://dx.doi.org/10.1117/12.807942.

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