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Artykuły w czasopismach na temat "Syntenin/syndecan interaction"
Zimmermann, Pascale, Zhe Zhang, Gisèle Degeest, Eva Mortier, Iris Leenaerts, Christien Coomans, Joachim Schulz, Francisca N’Kuli, Pierre J. Courtoy i Guido David. "Syndecan Recyling Is Controlled by Syntenin-PIP2 Interaction and Arf6". Developmental Cell 9, nr 3 (wrzesień 2005): 377–88. http://dx.doi.org/10.1016/j.devcel.2005.07.011.
Pełny tekst źródłaZimmermann, Pascale, Zhe Zhang, Gisèle Degeest, Eva Mortier, Iris Leenaerts, Christien Coomans, Joachim Schulz, Francisca N’Kuli, Pierre J. Courtoy i Guido David. "Syndecan Recycling Is Controlled by Syntenin-PIP2 Interaction and Arf6". Developmental Cell 9, nr 5 (listopad 2005): 721. http://dx.doi.org/10.1016/j.devcel.2005.10.011.
Pełny tekst źródłaBASS, Mark D., i Martin J. HUMPHRIES. "Cytoplasmic interactions of syndecan-4 orchestrate adhesion receptor and growth factor receptor signalling". Biochemical Journal 368, nr 1 (15.11.2002): 1–15. http://dx.doi.org/10.1042/bj20021228.
Pełny tekst źródłaLee, Hawon, Yeonhee Kim, Youngsil Choi, Sojoong Choi, Eunkyung Hong i Eok-Soo Oh. "Syndecan-2 cytoplasmic domain regulates colon cancer cell migration via interaction with syntenin-1". Biochemical and Biophysical Research Communications 409, nr 1 (maj 2011): 148–53. http://dx.doi.org/10.1016/j.bbrc.2011.04.135.
Pełny tekst źródłaImjeti, Naga Sailaja, Kerstin Menck, Antonio Luis Egea-Jimenez, Celine Lecointre, Frederique Lembo, Habib Bouguenina, Ali Badache i in. "Syntenin mediates SRC function in exosomal cell-to-cell communication". Proceedings of the National Academy of Sciences 114, nr 47 (6.11.2017): 12495–500. http://dx.doi.org/10.1073/pnas.1713433114.
Pełny tekst źródłaPradhan, Anjan K., Jinkal Modi, Santanu Maji, Amit Kumar, Praveen Bhoopathi, Padmanabhan Mannangatti, Chunqing Guo i in. "Abstract 3394: Simultaneous targeting of the PDZ1 and PDZ2 domains of MDA-9 inhibits melanoma metastasis". Cancer Research 83, nr 7_Supplement (4.04.2023): 3394. http://dx.doi.org/10.1158/1538-7445.am2023-3394.
Pełny tekst źródłaZhao, Tian, Xiaolan Yang, Guangfei Duan, Jialin Chen, Kefeng He, Yong‐Xiang Chen i Shi‐Zhong Luo. "Phosphorylation‐regulated phase separation of syndecan‐4 and syntenin promotes the biogenesis of exosomes". Cell Proliferation, 11.04.2024. http://dx.doi.org/10.1111/cpr.13645.
Pełny tekst źródłaPradhan, Anjan K., Jinkal Modi, Santanu Maji, Amit Kumar, Praveen Bhoopathi, Padmanabhan Mannangatti, Chunqing Guo i in. "Dual Targeting of the PDZ1 and PDZ2 Domains of MDA-9/Syntenin Inhibits Melanoma Metastasis". Molecular Cancer Therapeutics, 18.09.2023, OF1—OF13. http://dx.doi.org/10.1158/1535-7163.mct-22-0653.
Pełny tekst źródłaHoffer, Laurent, Manon Garcia, Raphael Leblanc, Mikael Feracci, Stéphane Betzi, Khaoula Ben Yaala, Avais M. Daulat i in. "Discovery of a PDZ Domain Inhibitor Targeting the Syndecan/Syntenin Protein–Protein Interaction: A Semi-Automated “Hit Identification-to-Optimization” Approach". Journal of Medicinal Chemistry, 20.03.2023. http://dx.doi.org/10.1021/acs.jmedchem.2c01569.
Pełny tekst źródłaLiu, Jing, Weiwei Bai, Tianxing Zhou, Yongjie Xie, Bo Yang, Jingyan Sun, Yifei Wang i in. "SDCBP promotes pancreatic cancer progression by preventing YAP1 from β-TrCP-mediated proteasomal degradation". Gut, 24.02.2023, gutjnl—2022–327492. http://dx.doi.org/10.1136/gutjnl-2022-327492.
Pełny tekst źródłaRozprawy doktorskie na temat "Syntenin/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.
Pełny tekst źródłaThe 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