Littérature scientifique sur le sujet « Colon fibroblasts »
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Articles de revues sur le sujet "Colon fibroblasts"
Laudadio, Ilaria, Alex Bastianelli, Valerio Fulci, Claudia Carissimi, Eleonora Colantoni, Francesca Palone, Roberta Vitali et al. « ZNF281 Promotes Colon Fibroblast Activation in TGFβ1-Induced Gut Fibrosis ». International Journal of Molecular Sciences 23, no 18 (6 septembre 2022) : 10261. http://dx.doi.org/10.3390/ijms231810261.
Texte intégralBruckner, R. S., M. C. Barnhoorn, H. Mei, S. M. Kiełbasa, T. J. Harrijvan, S. K. Hakuno, J. J. van der Reijden, A. E. van der Meulen-de Jong et L. J. A. C. Hawinkels. « DOP85 The role of fibroblasts in the pathogenesis of Crohn’s disease-associated fistulas and in mesenchymal stem cell therapy ». Journal of Crohn's and Colitis 14, Supplement_1 (janvier 2020) : S125. http://dx.doi.org/10.1093/ecco-jcc/jjz203.124.
Texte intégralJasso, Guadalupe J., Alok Jaiswal, Mukund Varma, Tyler Laszewski, Angelo Grauel, Abdifatah Omar, Nilsa Silva et al. « Colon stroma mediates an inflammation-driven fibroblastic response controlling matrix remodeling and healing ». PLOS Biology 20, no 1 (27 janvier 2022) : e3001532. http://dx.doi.org/10.1371/journal.pbio.3001532.
Texte intégralFuhr, Abreu, Carbone, El-Athman, Bianchi, Laukkanen, Mazzoccoli et Relógio. « The Interplay between Colon Cancer Cells and Tumour-Associated Stromal Cells Impacts the Biological Clock and Enhances Malignant Phenotypes ». Cancers 11, no 7 (15 juillet 2019) : 988. http://dx.doi.org/10.3390/cancers11070988.
Texte intégralHerrera, Mercedes, Artur Mezheyeuski, Lisa Villabona, Sara Corvigno, Carina Strell, Christian Klein, Gabriele Hölzlwimmer et al. « Prognostic Interactions between FAP+ Fibroblasts and CD8a+ T Cells in Colon Cancer ». Cancers 12, no 11 (3 novembre 2020) : 3238. http://dx.doi.org/10.3390/cancers12113238.
Texte intégralHeichler, Christina, Kristina Scheibe, Anabel Schmied, Carol I. Geppert, Benjamin Schmid, Stefan Wirtz, Oana-Maria Thoma et al. « STAT3 activation through IL-6/IL-11 in cancer-associated fibroblasts promotes colorectal tumour development and correlates with poor prognosis ». Gut 69, no 7 (4 novembre 2019) : 1269–82. http://dx.doi.org/10.1136/gutjnl-2019-319200.
Texte intégralKnowles, Jonathan P., Xu Shi-Wen, Samer-ul Haque, Ashish Bhalla, Michael R. Dashwood, Shiyu Yang, Irving Taylor, Marc C. Winslet, David J. Abraham et Marilena Loizidou. « Endothelin-1 stimulates colon cancer adjacent fibroblasts ». International Journal of Cancer 130, no 6 (9 juin 2011) : 1264–72. http://dx.doi.org/10.1002/ijc.26090.
Texte intégralBrügger, Michael David, Tomas Valenta, Hassan Fazilaty, George Hausmann et Konrad Basler. « Distinct populations of crypt-associated fibroblasts act as signaling hubs to control colon homeostasis ». PLOS Biology 18, no 12 (11 décembre 2020) : e3001032. http://dx.doi.org/10.1371/journal.pbio.3001032.
Texte intégralKikuchi, Yoshinao, Takeshi G. Kashima, Takashi Nishiyama, Kazuhiro Shimazu, Yasuyuki Morishita, Masashi Shimazaki, Isao Kii et al. « Periostin Is Expressed in Pericryptal Fibroblasts and Cancer-associated Fibroblasts in the Colon ». Journal of Histochemistry & ; Cytochemistry 56, no 8 (14 avril 2008) : 753–64. http://dx.doi.org/10.1369/jhc.2008.951061.
Texte intégralAgrawal, Khushboo, Viswanath Das, Natálie Táborská, Ján Gurský, Petr Džubák et Marián Hajdúch. « Differential Regulation of Methylation-Regulating Enzymes by Senescent Stromal Cells Drives Colorectal Cancer Cell Response to DNA-Demethylating Epi-Drugs ». Stem Cells International 2018 (12 août 2018) : 1–11. http://dx.doi.org/10.1155/2018/6013728.
Texte intégralThèses sur le sujet "Colon fibroblasts"
Davies, Paul Andrew. « Studies on the regulation of marrow fibroblast colony formation and differentiation ». Thesis, University of Sheffield, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.364241.
Texte intégral胡, 興柏. « ACTIVATION OF FIBROBLAST-DERIVED MATRIX METALLOPROTEINASE-2 BY COLON CANCER CELLS IN NON-CONTACT CO-CULTURES ». Doctoral thesis, Kyoto University, 2000. http://hdl.handle.net/2433/151419.
Texte intégral0048
新制・課程博士
博士(医学)
甲第8550号
医博第2272号
新制||医||747(附属図書館)
UT51-2000-M14
京都大学大学院医学研究科内科系専攻
(主査)教授 鍋島 陽一, 教授 月田 承一郎, 教授 千葉 勉
学位規則第4条第1項該当
Doctor of Medical Science
Kyoto University
DAM
Bellomo, Alicia. « Contrôle de l’homéostasie des macrophages de la pulpe rouge splénique par une niche fibroblastique ». Thesis, Aix-Marseille, 2020. http://www.theses.fr/2020AIXM0197.
Texte intégralLocated within red pulp cords, splenic red pulp macrophages (RPM) are constantly exposed tothe blood flow, clearing senescent red blood cells (RBC) and recycling iron from hemoglobin.Here, we studied the mechanisms underlying RPM homeostasis, focusing on the involvement ofstromal cells as these cells perform anchoring and nurturing macrophage niche functions inlymph nodes and liver. Microscopy revealed that RPM are embedded in a reticular meshwork ofred pulp fibroblasts characterized by the expression of Wilm’s Tumor 1 (WT1) and colonystimulating factor 1 (CSF1). Conditional deletion of Csf1 in WT1+ red pulp fibroblasts, but notwhite pulp fibroblasts, drastically altered the RPM network without altering circulating CSF1levels. Upon RPM depletion, red pulp fibroblasts transiently produced the monocytechemoattractants CCL2 and CCL7, thereby contributing to the replenishment of the RPMnetwork. Thus, red pulp fibroblasts anchor and nurture RPM, a function likely conserved inhumans
Yu, Bei. « Basic fibroblast growth factor as a therapeutic target for chemosensitization in colorectal cancer ». Columbus, Ohio : Ohio State University, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1142882177.
Texte intégralDumortier, Jérôme. « Interactions épithélio-mésenchymateuses au cours du développement des tumeurs malignes digestives : étude expérimentale in vivo et in vitro ». Lyon 1, 2000. http://www.theses.fr/2000LYO1T152.
Texte intégralManka, Margareta [Verfasser], et Florian [Akademischer Betreuer] Obermeier. « Modulation der Immunantwort von Colon Lamina Propria Fibroblasten bei Morbus Crohn durch Interleukin-33 / Margareta Manka. Betreuer : Florian Obermeier ». Regensburg : Universitätsbibliothek Regensburg, 2013. http://d-nb.info/1037021347/34.
Texte intégralJordan, Grant R. « Regulation of the proliferation and osteogenic differentiation of colony forming units-fibroblastic derived from human bone marrow ». Thesis, University of Bath, 1999. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323593.
Texte intégralMayr, Rebecca Anna [Verfasser], et Florian [Akademischer Betreuer] Obermeier. « GSK3-β – ein Modulator proinflammatorischer Prozesse in primären humanen Colon Lamina Propria Fibroblasten und in Kolonepithelzellen / Rebecca Anna Mayr. Betreuer : Florian Obermeier ». Regensburg : Universitätsbibliothek Regensburg, 2013. http://d-nb.info/1037021282/34.
Texte intégralSilva, David Ramos da [UNESP]. « Efeito do etanol na cicatrização do cólon distal do rato : estudo da força de ruptura, avaliação histológica, quantificação de fibroblastos e análise morfométrica sa área da cicatriz ». Universidade Estadual Paulista (UNESP), 2001. http://hdl.handle.net/11449/88909.
Texte intégralEste trabalho investigou o processo de reparação de uma ferida cirúrgica do cólon distal de ratos tratados com etanol. Foi utilizado o estudo da força de ruptura, avaliação histológica, quantificação de fibroblastos e análise morfométrica da área da cicatriz. Foram utilizados 126 ratos distribuídos por sorteio em 02 grupos: Grupo A1-controle e Grupo A2- etanol. Os animais do grupo A1 receberam ração e água “ad libitum” por 60 dias, após este período 12 animais foram sacrificados e submetidos ao estudo da força de ruptura. Os demais foram operados e submetidos a uma anastomose do cólon distal e estudados no 7o, 14o e 21o dias pósoperatório. Os animais do grupo A2 receberam ração e solução hidroalcoólica a 30% por 60 dias. Após este período foram submetidos ao mesmo procedimento do grupo controle; receberam ração e água no período pósoperatório, até o final do experimento. Verificou-se que a força de ruptura do segmento intestinal estudado foi menor em animais não operados tratados com etanol (A2M0) e, também foi menor nos animais tratados com etanol, operados e estudados no 14o dia pós-operatório (A2M2) quando comparados ao controle. A análise morfométrica da área da cicatriz demonstrou valores significantemente maiores nos animais tratados com etanol e estudados no 7o dia pós-operatório (A2M1) quando comparados ao controle...
This study investigated the healing process of a distal colon surgical wound in rats treated with ethanol. The rupture strength, histological evaluation, fibroblast quantification and morphometric analysis of the healing tissue were performed. One hundred and twenty-six rats were randomized into 2 groups: Group A1 – control group and Group A2 – ethanol group. Group A1 animals received food and water ad libidum for 60 days, after this period, 12 animals were sacrificed and underwent an evaluation of rupture strength. The remaining rats were operated and underwent distal colon anastomosis and were evaluated on the 7th /14th and 21st postoperative days. Group A2 animals received food and hydroalcoholic solution at 30% for 60 days. After this period they underwent the same procedure used for the control group. In the postoperative period they received food and water until the end of the investigation. It was observed that the rupture strength of the studied intestinal segment was lower in the animals which were not operated and treated with ethanol (A2T0). This strength was also lower in the animals which were operated and treated with ethanol evaluated on the 14th postoperative day (A2T2), when compared to the control group... (Complete abstract, click electronic access below)
Silva, David Ramos da. « Efeito do etanol na cicatrização do cólon distal do rato estudo da força de ruptura, avaliação histológica, quantificação de fibroblastos e análise morfométrica sa área da cicatriz / ». Botucatu : [s.n.], 2001. http://hdl.handle.net/11449/88909.
Texte intégralResumo: Este trabalho investigou o processo de reparação de uma ferida cirúrgica do cólon distal de ratos tratados com etanol. Foi utilizado o estudo da força de ruptura, avaliação histológica, quantificação de fibroblastos e análise morfométrica da área da cicatriz. Foram utilizados 126 ratos distribuídos por sorteio em 02 grupos: Grupo A1-controle e Grupo A2- etanol. Os animais do grupo A1 receberam ração e água "ad libitum" por 60 dias, após este período 12 animais foram sacrificados e submetidos ao estudo da força de ruptura. Os demais foram operados e submetidos a uma anastomose do cólon distal e estudados no 7o, 14o e 21o dias pósoperatório. Os animais do grupo A2 receberam ração e solução hidroalcoólica a 30% por 60 dias. Após este período foram submetidos ao mesmo procedimento do grupo controle; receberam ração e água no período pósoperatório, até o final do experimento. Verificou-se que a força de ruptura do segmento intestinal estudado foi menor em animais não operados tratados com etanol (A2M0) e, também foi menor nos animais tratados com etanol, operados e estudados no 14o dia pós-operatório (A2M2) quando comparados ao controle. A análise morfométrica da área da cicatriz demonstrou valores significantemente maiores nos animais tratados com etanol e estudados no 7o dia pós-operatório (A2M1) quando comparados ao controle... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: This study investigated the healing process of a distal colon surgical wound in rats treated with ethanol. The rupture strength, histological evaluation, fibroblast quantification and morphometric analysis of the healing tissue were performed. One hundred and twenty-six rats were randomized into 2 groups: Group A1 - control group and Group A2 - ethanol group. Group A1 animals received food and water ad libidum for 60 days, after this period, 12 animals were sacrificed and underwent an evaluation of rupture strength. The remaining rats were operated and underwent distal colon anastomosis and were evaluated on the 7th /14th and 21st postoperative days. Group A2 animals received food and hydroalcoholic solution at 30% for 60 days. After this period they underwent the same procedure used for the control group. In the postoperative period they received food and water until the end of the investigation. It was observed that the rupture strength of the studied intestinal segment was lower in the animals which were not operated and treated with ethanol (A2T0). This strength was also lower in the animals which were operated and treated with ethanol evaluated on the 14th postoperative day (A2T2), when compared to the control group... (Complete abstract, click electronic access below)
Mestre
Chapitres de livres sur le sujet "Colon fibroblasts"
Hendriks, T., K. M. L. C. Huyben et M. F. W. C. Martens. « Regulatory Aspects of Collagen Synthesis in Fibroblasts from Human Colon and Skin ». Dans Wound Healing and Skin Physiology, 245–54. Berlin, Heidelberg : Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-77882-7_22.
Texte intégralDiecke, Sebastian, Leszek Lisowski, Nigel G. Kooreman et Joseph C. Wu. « Second Generation Codon Optimized Minicircle (CoMiC) for Nonviral Reprogramming of Human Adult Fibroblasts ». Dans Methods in Molecular Biology, 1–13. New York, NY : Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1047-2_1.
Texte intégralValent, P., K. Geissler, P. Kalhs, P. Kier et P. Bettelheim. « Fibroblast Colony Stimulating Activity of GM-CSF and IL-3 in Human Bone Marrow Cell Cultures ». Dans Cytokines in Hemopoiesis, Oncology, and AIDS, 85–89. Berlin, Heidelberg : Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75510-1_12.
Texte intégral« Colony-Forming Fibroblastic Cells ». Dans Encyclopedia of Systems Biology, 440. New York, NY : Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-9863-7_100227.
Texte intégralWernert, Nicolas. « 15 Role of fibroblastic stroma in colon carcinoma ». Dans Molecular Pathology, Colorectal Carcinoma, and Prostate Carcinoma, 255–65. Elsevier, 2002. http://dx.doi.org/10.1016/s1874-5784(02)80031-9.
Texte intégralZielinska, Aleksandra, Magorzata Latocha, Magdalena Jurzak et Dariusz Kusmierz. « Expression of Matrix Metalloproteinases and Theirs Tissue Inhibitors in Fibroblast Cultures and Colo-829 and SH-4 Melanoma Cultures After Photodynamic Therapy ». Dans Recent Advances in the Biology, Therapy and Management of Melanoma. InTech, 2013. http://dx.doi.org/10.5772/54935.
Texte intégralActes de conférences sur le sujet "Colon fibroblasts"
FARINON, MIRIAN, PATRÍCIA GNIESLAW OLIVEIRA, MONICA GUMA et RICARDO MACHADO XAVIER. « THE ROLE OF GASTRIN-RELEASING PEPTIDE IN MYOFIBROBLAST ACTIVATION OF COLON FIBROBLASTS ». Dans 36º Congresso Brasileiro de Reumatologia. São Paulo : Editora Blucher, 2019. http://dx.doi.org/10.5151/sbr2019-593.
Texte intégralFénié, Nicolas, Claudine Bertrand, Aurélien Lacombe, Serge Roche, Corinne Bousquet, Valérie Gouazé-Andersson, Christine Toulas, Elizabeth Moyal et Audrey Ferrand. « Abstract B16 : Progastrin activates colon fibroblasts and participates to the dialogue between tumor epithelial cells and stromal fibroblasts in colorectal cancer ». Dans Abstracts : AACR Special Conference on Cellular Heterogeneity in the Tumor Microenvironment ; February 26 — March 1, 2014 ; San Diego, CA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.chtme14-b16.
Texte intégralCheng, KL, CC Chen et KC Yang. « PO-299 Aberrant TXNDC5 expression in colon stromal fibroblasts promotes colorectal cancer carcinogenesis ». Dans Abstracts of the 25th Biennial Congress of the European Association for Cancer Research, Amsterdam, The Netherlands, 30 June – 3 July 2018. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/esmoopen-2018-eacr25.812.
Texte intégralModis, Katalin, Manjit Maskey, Paul Johnson, Csaba Szabo, Mark R. Hellmich et Celia Chao. « Abstract 2980 : Cystathionine-beta-synthase (CBS)-derived hydrogen sulfide (H2S) supports proliferation, migration and bioenergetics in colon cancer-associated fibroblasts (CAFs) ». Dans Proceedings : AACR Annual Meeting 2017 ; April 1-5, 2017 ; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-2980.
Texte intégralKitagawa, H., N. Yamamoto, G. Kosaki et H. Yamazaki. « AN IMPORTANT ROLE OF CARBOHYDRATE MOIETIES ON CANCER CELL MEMBRANE GLYCOPROTEINS IN CANCER CELL-INDUCED PLATELET AGGREGATION ». Dans XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644667.
Texte intégralIrene, Gomez, Martin Paloma, Herrera Mercedes, Martinez Esther, Herrera Alberto, garcia Vanesa, Silva javier et al. « Abstract 1298:TWIST1is expressed by cells with fibroblastic phenotype in colon carcinoma ». Dans 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.am2012-1298.
Texte intégralJumanov, I. I., R. A. Safarov et O. I. Djumanov. « Error Control of Identification and Filtering of Micro-Object Images ». Dans III All-Russian Scientific Conference with International Participation "Science, technology, society : Environmental engineering for sustainable development of territories". Krasnoyarsk Science and Technology City Hall, 2022. http://dx.doi.org/10.47813/nto.3.2022.6.109-124.
Texte intégralMcCorry, Amy M., Niamh A. Leonard, Rene Jackstadt, Dustin J. Flanagan, Owen J. Sansom, Tim Maughan, Simon Leedham et al. « Abstract 3867 : STAT1-related antigen processing and presentation dictates prognosis in the fibroblast-rich subtype of stage II/III colon cancer ». Dans Proceedings : AACR Annual Meeting 2020 ; April 27-28, 2020 and June 22-24, 2020 ; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-3867.
Texte intégralWoo, Jong Kyu, Ju-Hee Kang, Keumju Shin, Seong-Won Song, Jung Ju Kim, Sang-Jin Lee et Seung Hyun Oh. « Abstract A15 : Humanized anti-hepatocyte growth factor (HGF) antibody, suppresses innate irinotecan resistance induced by fibroblast-derived HGF in colon cancer cells ». Dans Abstracts : AACR Special Conference : Tumor Immunology and Immunotherapy : A New Chapter ; December 1-4, 2014 ; Orlando, FL. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/2326-6074.tumimm14-a15.
Texte intégralSuetsugu, Atsushi, Masashi Momiyama, Yosuke Osawa, Hisataka Moriwaki, Michael Bouvet, Shigetoyo Saji et Robert M. Hoffman. « Abstract 2688 : Color-coded imaging of the pre-metastatic niche in the lung and liver indicates the involvement of cancer-associated fibroblasts ». Dans 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.am2012-2688.
Texte intégralRapports d'organisations sur le sujet "Colon fibroblasts"
Sadot, Einat, Christopher Staiger et Zvi Kam Weizmann. functional genomic screen for new plant cytoskeletal proteins and the determination of their role in actin mediated functions and guard cells regulation. United States Department of Agriculture, janvier 2003. http://dx.doi.org/10.32747/2003.7587725.bard.
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