Littérature scientifique sur le sujet « Syndecan interaction »
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Articles de revues sur le sujet "Syndecan interaction"
Hudák, Anett, Annamária Letoha, László Szilák et Tamás Letoha. « Contribution of Syndecans to the Cellular Entry of SARS-CoV-2 ». International Journal of Molecular Sciences 22, no 10 (19 mai 2021) : 5336. http://dx.doi.org/10.3390/ijms22105336.
Texte intégralHudák, Anett, Katalin Jósvay, Ildikó Domonkos, Annamária Letoha, László Szilák et Tamás Letoha. « The Interplay of Apoes with Syndecans in Influencing Key Cellular Events of Amyloid Pathology ». International Journal of Molecular Sciences 22, no 13 (30 juin 2021) : 7070. http://dx.doi.org/10.3390/ijms22137070.
Texte intégralPalomino, Rafael, Hsiau-Wei Lee et Glenn L. Millhauser. « The agouti-related peptide binds heparan sulfate through segments critical for its orexigenic effects ». Journal of Biological Chemistry 292, no 18 (6 mars 2017) : 7651–61. http://dx.doi.org/10.1074/jbc.m116.772822.
Texte intégralBaston-Buest, Dunja Maria, Olga Altergot-Ahmad, Sarah Jean Pour, Jan-Steffen Krüssel, Udo Rudolf Markert, Tanja Natascha Fehm et Alexandra Petra Bielfeld. « Syndecan-1 Acts as an Important Regulator of CXCL1 Expression and Cellular Interaction of Human Endometrial Stromal and Trophoblast Cells ». Mediators of Inflammation 2017 (2017) : 1–14. http://dx.doi.org/10.1155/2017/8379256.
Texte intégralVainio, S., M. Jalkanen et I. Thesleff. « Syndecan and tenascin expression is induced by epithelial-mesenchymal interactions in embryonic tooth mesenchyme. » Journal of Cell Biology 108, no 5 (1 mai 1989) : 1945–53. http://dx.doi.org/10.1083/jcb.108.5.1945.
Texte intégralMiettinen, H. M., et M. Jalkanen. « The cytoplasmic domain of syndecan-1 is not required for association with Triton X-100-insoluble material ». Journal of Cell Science 107, no 6 (1 juin 1994) : 1571–81. http://dx.doi.org/10.1242/jcs.107.6.1571.
Texte intégralEthell, Iryna M., Kazuki Hagihara, Yoshiaki Miura, Fumitoshi Irie et Yu Yamaguchi. « Synbindin, a Novel Syndecan-2–Binding Protein in Neuronal Dendritic Spines ». Journal of Cell Biology 151, no 1 (2 octobre 2000) : 53–68. http://dx.doi.org/10.1083/jcb.151.1.53.
Texte intégralSanderson, R. D., T. B. Sneed, L. A. Young, G. L. Sullivan et A. D. Lander. « Adhesion of B lymphoid (MPC-11) cells to type I collagen is mediated by integral membrane proteoglycan, syndecan. » Journal of Immunology 148, no 12 (15 juin 1992) : 3902–11. http://dx.doi.org/10.4049/jimmunol.148.12.3902.
Texte intégralCarulli, Sonia, Konrad Beck, Guila Dayan, Sophie Boulesteix, Hugues Lortat-Jacob et Patricia Rousselle. « Cell Surface Proteoglycans Syndecan-1 and -4 Bind Overlapping but Distinct Sites in Laminin α3 LG45 Protein Domain ». Journal of Biological Chemistry 287, no 15 (20 février 2012) : 12204–16. http://dx.doi.org/10.1074/jbc.m111.300061.
Texte intégralMunesue, Seiichi, Yasuo Yoshitomi, Yuri Kusano, Yoshie Koyama, Akiko Nishiyama, Hayao Nakanishi, Kaoru Miyazaki et al. « A Novel Function of Syndecan-2, Suppression of Matrix Metalloproteinase-2 Activation, Which Causes Suppression of Metastasis ». Journal of Biological Chemistry 282, no 38 (10 juillet 2007) : 28164–74. http://dx.doi.org/10.1074/jbc.m609812200.
Texte intégralThèses sur le sujet "Syndecan interaction"
Garcia, Manon. « Développement de nouveaux agents anticancéreux inhibiteurs de la syntenin ». Electronic Thesis or Diss., Aix-Marseille, 2021. http://theses.univ-amu.fr.lama.univ-amu.fr/210312_GARCIA_59el396udxeux306vl471dzd_TH.pdf.
Texte intégralThe thesis describes the identification and optimization of selective inhibitors targeting the syntenin/syndecan complex, using a “Fragment-based drug design” (FBDD) strategy, which could pave the way for new anticancer therapies. The syntenin/syndecan interaction plays a major role in the recycling of endosomes to the plasma membrane, as well as in the biogenesis and release of exosomes derived from tumor cells. Therefore, we performed an FBDD program targeting selectively the syntenin/syndecan interaction. To do this, two different fragment library screenings were performed, one experimental the other virtual, and two fragments hits were identified that specifically inhibit the interaction of the syntenin/syndecan complex. The resolution of 3D crystallographic structures of the complexes between these two fragments and syntenin allowed their optimization by a structure-based drug design approach based on information about their binding site and the mode. SAR studies and fragment growing optimization steps, based on molecular docking studies, were carried out. My work consisted in synthesizing chemical libraries of targeted analogues resulting from molecular docking and demonstrating strong interactions with syntenin. Among all the synthesized analogues, we identified the most promising inhibitors which exhibit sub-micromolar IC50 and which affect the release pathway of exosomes derived from tumor cells, dependent on syntenin/syndecan activity
Kaksonen, Marko. « Syndecan-3 in neural plasticity : from cell surface interactions to cytoskeletal regulation ». Helsinki : University of Helsinki, 2002. http://ethesis.helsinki.fi/julkaisut/mat/bioti/vk/kaksonen/.
Texte intégralMolteni, Alexandra. « Interactions entre proteoglycannes sulfates et facteur de croissance fibroblastique-2 dans la chondro-osteogenese du condyle mandibulaire et l'osteogenese de la calotte cranienne de rat ». Paris 5, 1998. http://www.theses.fr/1998PA05M106.
Texte intégralHuang, Jin-Wen, et 黃勁文. « The functional role of syndecan-2 in the molecular interaction with RACK1 in cells ». Thesis, 2006. http://ndltd.ncl.edu.tw/handle/37579606587413121193.
Texte intégral國立臺灣大學
動物學研究研究所
94
In this study, RACK1 (Receptor for Activated C Kinase 1) was found to be reactive with syndecan-2 in vitro and in vivo. Through affinity column chromatography and immunoprecipitation analysis as well as immunocytochemical colocalization studies, the reaction between RACK1 and syndecan-2 was evidenced in BALB/3T3 cells. Recombinant syndecan-2 and PEP Syn-2-cyto were applied to demonstrate that tyrosine 180 of syndecan-2 is a targeted site for Src tyrosine kinase and the reaction with RACK1 is enhanced after this tyrosine phosphorylation. In parallel, when granulocyte-macrophage colony-stimulating factor (GM-CSF) was applied to activate cellular tyrosine kinase of HeLa cells, a significant positive interaction was revealed between syndecan-2 and RACK1 with time and dose-dependence. HeLa cells were further subject to transfections with wild type and mutant syndecan-2 vectors(Syn-2-Y180F、Syn-2-Y192F、Syn-2-Y180/192F) to show that the reaction of syndecan-2 with RACK1 was suppressed when tyrosine 180 phosphorylation site was absent. To elucidate the physiological significance of this selective reaction between syndecan-2 and RACK1, studies with adhesion, migration, and poliferation were focused. HeLa cells transfected with Syn-2-Y180F mutant vectors exhibited less motile and adhesion ability. Furthermore, the morphology of Syn-2-Y180F transfants became round and refractile. These results imply that tyrosine 180 of syndecan-2 may involve in the cytoskeleton organization, focal contacts formation, and tyrosine kinase regulation through selective reaction with RACK1.
McFall, Aidan J. « Molecular interactions of the extracellular protein domain of syndecan-4 ». 1998. http://catalog.hathitrust.org/api/volumes/oclc/40737394.html.
Texte intégralTypescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 168-185).
Dews, Ian Charles. « Characterization of transmembrane domain interactions by the syndecan family of integral membrane proteins ». Thesis, 2008. http://hdl.handle.net/1911/22270.
Texte intégralLivres sur le sujet "Syndecan interaction"
Grootjans, Jan Johann. Cytoplasmic interactions of the syndecans. Leuven : Leuven University Press, 2000.
Trouver le texte intégralActes de conférences sur le sujet "Syndecan interaction"
Risquez, Cristobal F., Avignat Patel, Juan C. Osorio, Isis E. Fernandez, Andrew Goodwin, Ying Shi, Xiaomeng Tang, Danielle Morse, Ivan O. Rosas et Yuanyuan Shi. « Syndecan-2 And CCL2 Interactions Promote Alveolar Macrophage Recruitment During Acute Lung Injury ». Dans American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a3700.
Texte intégralShi, Yuanyuan, Isis Fernandez, Guoying Yu, Jiaofei Cao, Zhihua Chen, Zhijian Gao, Gustavo Pacheco-Rodriguez, Stefan W. Ryter, Danielle Morse et Ivan O. Rosas. « Syndecan-2 Dependent Scavenging Of TGF-²1 Via Caveolin-1 And TGF-²RI Interactions In Human Monocytes ». Dans American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a3524.
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