Relevant bibliographies by topics / Murine macrophages (RAW 264.7)

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  2. Dissertations / Theses

Academic literature on the topic 'Murine macrophages (RAW 264.7)'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Murine macrophages (RAW 264.7)"

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Trivedi, Mahendra Kumar, Alice Branton, Dahryn Trivedi, Gopal Nayak, Sambhu Charan Mondal, and Snehasis Jana. "Immunomodulatory Effect of the Biofield Energy Treated Cell Growth Medium (DMEM) and FBS in Immune Cells (Murine Macrophage RAW 264.7)." Journal of Cellular Immunology and Serum Biology 3, no. 2 (2018): 1–5. https://doi.org/10.15436/2471-5891.18.1946.

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The objective of the present study was to evaluate the immunomodulatory effect of Biofield Energy Treatment (The Trivedi Effect®) on Dulbecco’s Modified Eagle’s Medium (DMEM) and fetal bovine serum (FBS) in murine macrophage cells (RAW 264.7). The study parameters were evaluated using cell viability by MTT assay and estimation of proinflammatory cytokine like tumor necrosis factor - alpha (TNF-α) on immunomodulation using enzyme linked immune sorbent assay (ELISA). The cell viability using MTT assay data showed that more than 80% cell viability was observed in all the tes
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Tellez, Angela, Milena Corredig, Lubov Y. Brovko, and Mansel W. Griffiths. "Characterization of immune-active peptides obtained from milk fermented byLactobacillus helveticus." Journal of Dairy Research 77, no. 2 (2010): 129–36. http://dx.doi.org/10.1017/s002202990999046x.

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The objectives of this research were to confirm the effect of compounds derived from milk fermented byLactobacillus helveticus(LH-2) on the nonspecific host defence system, and isolate and characterize the active peptides that mediate the immune response. The cell-free supernatant obtained from the fermented milk and its fractions were testedin vitrofor immuno-modulating activity using murine macrophages (RAW 264·7 cell line). Cytokine production (Interleukin-6 (IL-6), Tumor Necrosis Factor-α (TNF-α), and Interleukin-1β (IL1-β)), nitric oxide (NO) production and phagocytosis were used as bioma
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Jofre-Monseny, Laia, Sonia de Pascual-Teresa, Eva Plonka, et al. "Differential effects of apolipoprotein E3 and E4 on markers of oxidative status in macrophages." British Journal of Nutrition 97, no. 5 (2007): 864–71. http://dx.doi.org/10.1017/s0007114507669219.

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ApoE is secreted by macrophages at the lesion site of the atherosclerotic plaque, where it is thought to play a protective role against atherosclerosis independently of its effects on lipid metabolism. Of the three common isoforms for apoE, apoE4 is associated with higher risk of cardiovascular disease (CVD). In vitro studies have shown that recombinant apoE may act as an antioxidant in an isoform-dependent manner (E2>E3>E4). The oxidative status of the macrophages plays a key role in the process of atherosclerosis. In the present study the possible differential actions of apoE3 and apoE
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Tabouret, G., I. Vouldoukis, C. Duranton, et al. "Oestrus ovis (Diptera: Oestridae): effects of larval excretory/secretory products on nitric oxide production by murine RAW 264·7 macrophages." Parasite Immunology 23, no. 3 (2001): 111–19. http://dx.doi.org/10.1046/j.1365-3024.2001.00355.x.

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Chon, H., B. Choi, E. Lee, S. Lee, and G. Jeong. "Immunomodulatory effects of specific bacterial components ofLactobacillus plantarumKFCC11389P on the murine macrophage cell line RAW 264·7." Journal of Applied Microbiology 107, no. 5 (2009): 1588–97. http://dx.doi.org/10.1111/j.1365-2672.2009.04343.x.

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Koc, A., T. Ozkan, A. Z. Karabay, A. Sunguroglu, and F. Aktan. "Effect of L-carnitine on the synthesis of nitric oxide in RAW 264·7 murine macrophage cell line." Cell Biochemistry and Function 29, no. 8 (2011): 679–85. http://dx.doi.org/10.1002/cbf.1807.

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7

Keen, Imelda, Traian V. Chirila, Zeke Barnard, Z. Zainuddin, and Andrew K. Whittaker. "Degradable Hydrogels for Tissue Engineering - Part II: Responses of Fibroblasts and Macrophages to Linear PHEMA." Journal of Biomimetics, Biomaterials and Tissue Engineering 8 (November 2010): 91–104. http://dx.doi.org/10.4028/www.scientific.net/jbbte.8.91.

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A series of linear poly(2-hydroxyethyl methacrylate) (PHEMA) with defined molecular weights (MW) and narrow molecular distributions were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization using cumyl dithiobenzoate (CDB) as a chain transfer agent. Murine fibroblasts (3T3) were exposed to eluates from various PHEMA samples, washed or unwashed, and with or without dithioester end groups. After 72 hrs in cell culture, no cytotoxic response was elicited by the polymer samples devoid of dithioester end groups, and which also underwent a thorough washing regime. Sp
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8

Tjandrawinata, R. R., L. Hawel, and C. V. Byus. "Regulation of putrescine export in lipopolysaccharide or IFN-gamma-activated murine monocytic-leukemic RAW 264 cells." Journal of Immunology 152, no. 6 (1994): 3039–52. http://dx.doi.org/10.4049/jimmunol.152.6.3039.

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Abstract The regulation of putrescine/polyamine export out of the cell was investigated during activation of monocytic-leukemic RAW 264 cells with LPS and IFN-gamma. The RAW 264 cells exported putrescine constitutively at a significant rate into the culture medium. This export process appeared to be selective for putrescine in that only a small amount of other polyamines (spermidine and N1-acetylspermidine) was found in the culture medium. LPS and IFN-gamma alone and in combination markedly stimulated putrescine export and nitrite production throughout a 24-h period. The efflux of putrescine b
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Homsani, Fortune, Gleyce Moreno, Camila Siqueira, Juliana Grechi, André Luis Santos, and Carla Holandino. "Cellular Alterations Induced by Candida albicans RC Nosodes: an in vitro Study." International Journal of High Dilution Research - ISSN 1982-6206 11, no. 40 (2021): 209–10. http://dx.doi.org/10.51910/ijhdr.v11i40.600.

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Introduction: Candidiasis is an opportunist infection, caused by yeast of the genus Candida, which emerges as one of the main causes of systemic infections in hospitalized patients. Candida albicans is the most common causing agent of these infections. According to the Brazilian Homeopathic Pharmacopeia[1], nosodes are medicines compounded from chemically undefined biological products. Living nosodes are prepared using the etiologic agent of an illness in its infective form, were first developed by Brazilian physician Roberto Costa (RC). Roberto Costa’s research indicated that
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Rao, P., L. A. Falk, S. F. Dougherty, T. Sawada, and D. H. Pluznik. "Colchicine down-regulates lipopolysaccharide-induced granulocyte-macrophage colony-stimulating factor production in murine macrophages." Journal of Immunology 159, no. 7 (1997): 3531–39. http://dx.doi.org/10.4049/jimmunol.159.7.3531.

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Abstract Activation of macrophages by LPS and taxol results in production of IL-1, IL-6, TNF-alpha, and granulocyte-macrophage CSF (GM-CSF), which are involved in regulating hemopoiesis, inflammation, and immune responses. Microtubules are proposed as a target site for LPS interaction(s), based on similarities between the effects of the tubulin-binding drug taxol and LPS. To clarify the role of microtubules in LPS-induced GM-CSF expression in macrophages, we examined whether microtubule depolymerizing agents affect GM-CSF production in macrophages. Pretreatment with colchicine impaired LPS ind
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Dissertations / Theses on the topic "Murine macrophages (RAW 264.7)"

1

Alruwaili, Muhannad Falah. "The Impact of Cytokines and HSV-1 on Rab5 Protein Expression, F-actin Cytoskeleton Rearrangement, and Cell Viability of Uninfected and Virus-Infected M0, M1, and M2 RAW264.7 Murine Macrophages." Wright State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=wright1526015378786658.

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