Auswahl der wissenschaftlichen Literatur zum Thema „Fibroblastes gingivaux“
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Zeitschriftenartikel zum Thema "Fibroblastes gingivaux"
Lauritano, Dorina, Alberta Lucchese, Dario Di Stasio, Fedora Della Vella, Francesca Cura, Annalisa Palmieri und Francesco Carinci. „Molecular Aspects of Drug-Induced Gingival Overgrowth: An In Vitro Study on Amlodipine and Gingival Fibroblasts“. International Journal of Molecular Sciences 20, Nr. 8 (25.04.2019): 2047. http://dx.doi.org/10.3390/ijms20082047.
Der volle Inhalt der QuelleLiu, Kaining, Bing Han, Jianxia Hou, Jianyun Zhang, Jing Su und Huanxin Meng. „Expression of vitamin D 1α-hydroxylase in human gingival fibroblasts in vivo“. PeerJ 9 (04.01.2021): e10279. http://dx.doi.org/10.7717/peerj.10279.
Der volle Inhalt der QuelleSmith, Q. T., und J. E. Hinrichs. „Phenytoin and 5-(p-hydroxyphenyl)-5-phenylhydantoin do not Alter the Effects of Bacterial and Amplified Plaque Extracts on Cultures of Fibroblasts from Normal and Overgrown Gingivae“. Journal of Dental Research 66, Nr. 8 (August 1987): 1393–98. http://dx.doi.org/10.1177/00220345870660082201.
Der volle Inhalt der QuelleFrancetti, Luca, Claudia Dellavia, Stefano Corbella, Nicolò Cavalli, Claudia Moscheni, Elena Canciani und Nicoletta Gagliano. „Morphological and Molecular Characterization of Human Gingival Tissue Overlying Multiple Oral Exostoses“. Case Reports in Dentistry 2019 (22.05.2019): 1–10. http://dx.doi.org/10.1155/2019/3231759.
Der volle Inhalt der QuelleDanastri, Arifia Anindita, Suryono Suryono und Kwartarini Murdiastuti. „THE INFLUENCE BETWEEN INJECTABLE PLATELET-RICH FIBRIN AND PLATELET-RICH PLASMA TOWARDS GINGIVAL FIBROBLAST CELL PROLIFERATION“. ODONTO : Dental Journal 8, Nr. 2 (22.12.2021): 25. http://dx.doi.org/10.30659/odj.8.2.25-31.
Der volle Inhalt der QuelleLauritano, Dorina, Marcella Martinelli, Alessandro Baj, Giada Beltramini, Valentina Candotto, Francesco Ruggiero und Annalisa Palmieri. „Drug-induced gingival hyperplasia: An in vitro study using amlodipine and human gingival fibroblasts“. International Journal of Immunopathology and Pharmacology 33 (Januar 2019): 205873841982774. http://dx.doi.org/10.1177/2058738419827746.
Der volle Inhalt der QuelleWalters, J. D., R. J. Nakkula und P. Maney. „Modulation of Gingival Fibroblast Minocycline Accumulation by Biological Mediators“. Journal of Dental Research 84, Nr. 4 (April 2005): 320–23. http://dx.doi.org/10.1177/154405910508400405.
Der volle Inhalt der QuelleRuggeri, A., L. Montebugnoli, A. Matteucci, N. Zini, L. Solimando, D. Servidio, P. Suppa, M. Cadenaro, L. Cocco und L. Breschi. „Cyclosporin A Specifically Affects Nuclear PLCβ1 in Immunodepressed Heart Transplant Patients with Gingival Overgrowth“. Journal of Dental Research 84, Nr. 8 (August 2005): 747–51. http://dx.doi.org/10.1177/154405910508400812.
Der volle Inhalt der QuelleDamanaki, Anna, Marjan Nokhbehsaim, Sigrun Eick, Werner Götz, Jochen Winter, Gerhard Wahl, Andreas Jäger, Søren Jepsen und James Deschner. „Regulation of NAMPT in Human Gingival Fibroblasts and Biopsies“. Mediators of Inflammation 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/912821.
Der volle Inhalt der QuelleKujundzic, Bojan, Zlatibor Andjelkovic, Radmila Maric, Ruzica Lukic, Veljko Maric, Helena Maric, Miroslav Obrenovic und Sinisa Kojic. „Periodontal Disease: Correlation with Histological and Immunological Parameters“. Experimental and Applied Biomedical Research (EABR) 24, Nr. 1 (01.03.2023): 57–62. http://dx.doi.org/10.2478/sjecr-2020-0024.
Der volle Inhalt der QuelleDissertationen zum Thema "Fibroblastes gingivaux"
Lorimier, Sandrine. „L'influence de l'environnement cellulaire sur le phenotype des fibroblastes gingivaux et dermiques“. Paris 5, 1996. http://www.theses.fr/1996PA05M091.
Der volle Inhalt der QuelleSenni, Karim. „Effets de polysaccharides d'origine marine sur le remodelage des tissus gingivaux et dermiques“. Paris 13, 2000. http://www.theses.fr/2000PA132031.
Der volle Inhalt der QuelleNaveau, Adrien. „Traitement de l'anévrysme abdominal aortique par transplantation de fibroblastes gingivaux autologues : études in vitro“. Paris 5, 2007. http://www.theses.fr/2007PA05M006.
Der volle Inhalt der QuelleAbdominal aortic aneurysm (AAA) formation is associated with matrix degradation an metalloproteinases activity increase. We aimed to test the embryo-like healing propertie attributed to the gingival fibroblast (GF) on these arteries ex vivo. In order to identify the GF in coculture, we first established a labeling method from anioni nanoparticles. We have then analyzed the secretion of metalloproteinases (MMP)-9, MMP- and MMP-3, and their tissue inhibitor (TIMP)-1 in rabbit aortic rings cultured in presence o GF, and in smooth muscle cells cultured gingival, dermal and adventitial fibroblasts. These in vitro resuits do show an increase of TIMP-1 associated with GF presence, whic inhibits these enzymes and protects as well the arterial elastic network. The GF transplantation seems to us of crucial interest to treat AAA
Letzelter, Corinne. „Cytotoxicite activites proteolytiques des produits metaboliques de bacteries buccales vis-a-vis de fibroblastes gingivaux in vitro“. Toulouse 3, 1999. http://www.theses.fr/1999TOU30092.
Der volle Inhalt der QuelleGiraud, Andréas. „Développement d’une approche de thérapie cellulaire de l’anévrisme de l’aorte abdominale utilisant les fibroblastes gingivaux chez la souris“. Thesis, Sorbonne Paris Cité, 2016. http://www.theses.fr/2016USPCB029/document.
Der volle Inhalt der QuelleAbdominal aortic aneurysm (AAA), frequently diagnosed in old patients, is characterized by chronic inflammation, vascular cell apoptosis and metalloproteinases-mediated extracellular matrix destruction. Depiste improvement in the understanding of the pathophysiology of the aortic aneurysm disease, no pharmacological treatment is available to limit dilatation and/or rupture. In the study reported here, we tested whether periadventitial allograft of GF prevented abdominal aortic aneurysmal growth and rupture in mice and investigated the mechanisms of vascular protection. In vitro, mouse GF proliferated and produced large amounts of anti-inflammatory cytokines and Timp-1, an inhibitor of metalloproteinases. When layed down in the periadventitial abdominal aorta, we documented that GF survived in vivo, proliferated and organized as a thick layer. Furthermore, GF locally produced Il-10, TGF-β and Timp-1. In an elastase-induced AAA, GF prevented both macrophage and lymphocyte infiltration, elastin degradation and aneurysm growth. Specific invalidation of Timp-1 in GF abolished the beneficial effect of cell therapy. In an Angiotensin II/anti-TGF-β model of AAA, GF cell therapy limited AAA development and prevented abdominal rupture. Gingival fibroblast is a promising cell therapy approach to inhibit aneurysmal progression and rupture through the local production of Timp-1
Soheili-Majd, Esmat. „Etudes des mécanismes de la cytotoxicité des biomatériaux dentaires sur les fibroblastes pulpaires et gingivaux humains : effets des anti-oxydants“. Paris 5, 2004. http://www.theses.fr/2004PA05M122.
Der volle Inhalt der QuelleKut-Lasserre, Christelle. „Effet protecteur des insaponifiables d'huile d'avocat et de soja sur la matrice conjonctive gingivale et sur leur capacite a remodeler cette matrice par les fibroblastes gingivaux humains en culture : etude ex vivo et in vitro“. Paris 5, 1999. http://www.theses.fr/1999PA05M083.
Der volle Inhalt der QuellePapa, Steve. „Evaluation de l'adhérence gingivale et du potentiel antibactérien de surfaces structurées par laser femtoseconde pour l'implantologie orale“. Electronic Thesis or Diss., Saint-Etienne, 2023. http://www.theses.fr/2023STET0063.
Der volle Inhalt der QuelleThis thesis addresses issues related to infections of dental implants, such as peri-implantitis, caused by the adhesion of periodontopathogenic bacteria. It explores the use of femtosecond laser (fs-L) texturing to enhance the properties of titanium alloy (Ti6Al4V) implant surfaces.The project, funded by the ANR and conducted in collaboration with various laboratories, employed advanced characterization techniques to analyze textured surfaces and evaluate their effectiveness under biological conditions. The results demonstrate that fs-L texturing can create micro and nanometric periodic surface structures (LIPSS), altering the contact surface and thus cellular and bacterial adhesion. Textured surfaces showed a significant reduction in the adhesion of periodontopathogenic bacteria, such as Porphyromonas gingivalis, potentially reducing the risks of peri-implantitis.In vitro studies also confirmed better adhesion of gingival fibroblasts to textured surfaces, which could reduce the risk of bacterial infiltration and thus improve implant stability and integration.In conclusion, femtosecond laser texturing of dental implant surfaces holds promise for creating more durable and dual-functionalized implants, enhancing cellular adhesion, and possessing increased antibacterial properties. These advancements pave the way for implants better suited to current clinical challenges while contributing to the fight against antibiotic resistance. Further studies closer to clinical settings are planned to validate these results and explore the interactions between fs-L topographies and the biological responses of surrounding tissues
Azevedo, Fabiola Pontes. „Avaliação comparativa do comportamento adaptativo de fibroblastos humanos cultivados de mucosa palatina não marginal e de enxerto gengival em área marginal“. Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/25/25146/tde-05062013-093746/.
Der volle Inhalt der QuelleFree gingival grafts are important to ensure conditions for the establishment of homeostasis of the periodontal soft tissues. The process of inflammation does not occur the same way in all connective tissues and fibroblasts have the ability to respond to aggressive stimuli through the release of various cytokines, which play an important role in the inflammatory infiltrate formation. In literature, there are no studies comparing the behavior of fibroblasts from palatal mucosa (not marginal) and fibroblasts from marginal free gingival graft (FGG) regarding their resistance towards periodontal disease aggressive stimuli. Thus, the purpose of this study was to investigate whether fibroblasts from the palatal mucosa behave differently when grafted to the gingival margin considering their mechanism of cytokine secretion. Biopsies from the palatal mucosa were collected at the time of FGG surgery (initial period) and after 4 months (final period) when surgery for root coverage was performed. The fibroblasts were cultured and stimulated with LPS of Porphyromonas gingivalis (Pg) and Escherichia coli (Ec) for 24 and 48 hours in order to make a comparative evaluation of cytokines and mediators of tissue repair expression, such as IL-6, IL-8/CXCL8, MIP-1α/CCL3, TGF-β, VEGF and CXCL16. Cytokines were measured in the cell supernatant by enzyme immunoassay (ELISA). For cytokine IL- 6, fibroblasts from palatal mucosa maintained the same secretion pattern when grafted to the gingival margin; for MIP-1α the secretion was significantly increased by fibroblasts from the marginal gingival graft after 48 hours of stimulation with Pg when compared to palatal mucosa fibroblasts; IL-8 secretion by palatal mucosa fibroblasts did not increase in response to Pg LPS challenge and fibroblasts from marginal gingival graft showed secretion even without the stimulus of LPS; only fibroblasts from marginal gingival graft showed secretion of TGF-β, even in the absence of LPS stimulation; VEGF and CXCL16 secretion by fibroblasts was not detected. It was concluded that fibroblasts from palatal mucosa seem to adapt to local conditions when grafted to the gingival margin area, providing evidence of its effective participation in the homeostasis of marginal periodontium through the production of important inflammatory mediators.
Kreidly, Mariam. „IL-34 Expression in Gingival Fibroblasts, Gingival Crevicular Fluid and Gingival Tissue“. Thesis, Umeå universitet, Tandläkarutbildning, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-97861.
Der volle Inhalt der QuelleBücher zum Thema "Fibroblastes gingivaux"
Chou, Debra Hsin-I. TNF-r̀egulation of phagocytosis in human gingival fibroblasts. Ottawa: National Library of Canada, 1995.
Den vollen Inhalt der Quelle findenChou, Debra Hsin-I. TNF-[alpha] regulation of phagocytosis in human gingival fibroblasts. [Toronto: Faculty of Dentistry, University of Toronto], 1995.
Den vollen Inhalt der Quelle findenNémeth, Endre. Responses of gingival fibroblast and endothelial cell populations to experimentally-inducedinflammation in monkeys. Ottawa: National Library of Canada, 1993.
Den vollen Inhalt der Quelle findenYang, Po Fong. Filamentous actin disruption and diminished inositol phosphate response in gingival fibroblasts caused by Treponema denticola. [Toronto: University of Toronto, Faculty of Dentistry], 1998.
Den vollen Inhalt der Quelle findenNémeth, Endre. Responses of gingival fibroblast and endothelial cell populations to experimentally-induced inflammation in monkeys. [Toronto: Faculty of Dentistry, University of Toronto], 1993.
Den vollen Inhalt der Quelle findenBattikhi, Tulin. Treponema Denticola outer membrane extract enhances the phagocytosis of collagen coated-beads by human gingival fibroblasts. [Toronto: University of Toronto, Faculty of Dentistry], 1998.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Fibroblastes gingivaux"
Egusa, Hiroshi. „The Impact of Gingival Fibroblast-Derived iPS Cells in Dentistry“. In Interface Oral Health Science 2011, 9–13. Tokyo: Springer Japan, 2012. http://dx.doi.org/10.1007/978-4-431-54070-0_2.
Der volle Inhalt der QuelleChoi, C. H., B. I. Kim, H. K. Kwon und Suck Jin Hong. „Effects of Herbal Extracts on Dental Plaque Formation and Human Gingival Fibroblasts“. In Advanced Biomaterials VII, 773–76. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-436-7.773.
Der volle Inhalt der QuelleChou, Patty, und Trudy J. Milne. „Real-Time PCR Focused-Gene Array Profiling of Gingival and Periodontal Ligament Fibroblasts“. In Methods in Molecular Biology, 373–83. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-820-1_23.
Der volle Inhalt der QuelleKerr, Janet S., George A. Boswell, Neil R. Ackerman und Theresa M. Stevens. „Induction of Superoxide Dismutase Activity by Paraquat or Edu in Human Gingival Fibroblasts“. In Oxygen Radicals in Biology and Medicine, 695–98. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5568-7_109.
Der volle Inhalt der QuelleKhashaba, Rania M. „Calcium Phosphate based Perforation Repair Materials using Human Gingival Fibroblasts: An in vitro Cytotoxicity Evaluation“. In New Horizons in Medicine and Medical Research Vol. 9, 83–91. Book Publisher International (a part of SCIENCEDOMAIN International), 2022. http://dx.doi.org/10.9734/bpi/nhmmr/v9/15713d.
Der volle Inhalt der QuelleEl-Bialy, Tarek, Hagai Hazan Molina, Yuval Aizenbud, Wasif Qayyum, Saleem Ali und Dror Aizenbud. „Effects of Intraligamentary Injection of Osteogenic-Induced Gingival Fibroblasts on Cementum Thickness in the Dog Model of Tooth Root Resorption“. In Advances in Experimental Medicine and Biology. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/5584_2020_551.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Fibroblastes gingivaux"
Vo Quang Costantini, S., S. Petit, A. Nassif, F. Ferre und B. Fournier. „Perspectives thérapeutiques du matrisome gingival dans la cicatrisation pathologique“. In 66ème Congrès de la SFCO. Les Ulis, France: EDP Sciences, 2020. http://dx.doi.org/10.1051/sfco/20206602013.
Der volle Inhalt der QuelleLafont, J., J. H. Catherine, M. Lejeune, U. Ordioni, R. Lan und F. Campana. „Manifestations buccales de la sclérose tubéreuse de Bourneville“. In 66ème Congrès de la SFCO. Les Ulis, France: EDP Sciences, 2020. http://dx.doi.org/10.1051/sfco/20206603014.
Der volle Inhalt der QuelleThaweboon, Sroisiri, Ratchaporn Srichan, Supaporn Mala und Boonyanit Thaweboon. „The Development of Artificial Saliva with Oral Wound Healing Property“. In 2023 7th International Conference on Nanomaterials and Biomaterials & 2023 5th Asia Conference on Material and Manufacturing Technology. Switzerland: Trans Tech Publications Ltd, 2024. http://dx.doi.org/10.4028/p-wc6acn.
Der volle Inhalt der QuelleAl Sufyani, Noha Moslah, Nahed Ahmed Hussien und Yousef Mohammed Hawsawi. „Cytotoxic effect of synthesized silver nanoparticles on normal human gingival fibroblast GF01 cells“. In 2021 International Conference of Women in Data Science at Taif University (WiDSTaif ). IEEE, 2021. http://dx.doi.org/10.1109/widstaif52235.2021.9430249.
Der volle Inhalt der QuelleAlmeida-Lopes, Luciana, Marcia M. M. Jaeger, Aldo Brugnera, Jr. und Josepa Rigau. „Action of low-power laser irradiation on the proliferation of human gingival fibroblasts in vitro“. In BiOS '98 International Biomedical Optics Symposium, herausgegeben von John D. B. Featherstone, Peter Rechmann und Daniel Fried. SPIE, 1998. http://dx.doi.org/10.1117/12.306022.
Der volle Inhalt der QuelleBakhori, Siti Khadijah Mohd, Shahrom Mahmud, Sam’an Malik Masudi, Azman Seeni, Dasmawati Mohamad, Ling Chuo Ann und Amna Sirelkhatim. „Cytotoxicity evaluation of ZnO-eugenol (ZOE) using different ZnO structure on human gingival fibroblast“. In PROCEEDING OF THE 3RD INTERNATIONAL CONFERENCE OF GLOBAL NETWORK FOR INNOVATIVE TECHNOLOGY 2016 (3RD IGNITE-2016): Advanced Materials for Innovative Technologies. Author(s), 2017. http://dx.doi.org/10.1063/1.4993327.
Der volle Inhalt der QuelleIlleperuma, Rasika P., Young J. Park, Hwa K. Son, Jin M. Kim, Da-Woon Jung, Wanninayake M. Tilakaratne und Jin Kim. „Abstract 5471: Implication of cytokines released from gingival fibroblasts exposed by areca nut extract in carcinogenesis“. In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-5471.
Der volle Inhalt der QuelleKrismariono, A., N. Ulfa, U. N. Wardi und S. C. S. Budijono. „Viability test of water hyacinth leaf extract (Eichornia Crassipes) on human gingival fibroblast cell culture“. In THE 2ND INTERNATIONAL CONFERENCE ON PHYSICAL INSTRUMENTATION AND ADVANCED MATERIALS 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0034976.
Der volle Inhalt der QuelleWasi, S., P. Alles, D. Gauthier, U. Bhargava, J. Farsi, J. E. Aubin und J. Sodeki. „STUDIES ON SMALL MOLECULAR WEIGHT ADHESION PROTEINS (SAPs) FROM CONNECTIVE TISSUES“. In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643556.
Der volle Inhalt der QuelleWasi, S., S. Juodvalkis, P. Alles und J. E. Aubin. „STUDIES ON THE DIRECT PROTEOLYTIC ACTION OF HUMAN TISSUE PLASMINOGEN ACTIVATOR ON HUMAN FIBRONECTIN AND VITRONECTIN“. In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644376.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Fibroblastes gingivaux"
J.P, Babu. Long-term dental adhesive toxicity on human gingival fibroblasts and epithelial cells. Science Repository, Juni 2019. http://dx.doi.org/10.31487/j.dobcr.2019.03.01.
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