retrieve:
Return the details about the given Event id.

list:
List all Event objects.

GET /api/v1/events/?format=api&offset=80&ordering=-start_date
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

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            "title": "PChem Seminar - Camila Bacellar",
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            "start_date": "2026-12-10",
            "end_date": "2026-12-10",
            "start_time": "17:00:00",
            "end_time": "19:00:00",
            "description": "<p>Title TBA</p>",
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            "creation_date": "2026-10-01T19:35:51",
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            "speaker": "Camila Bacellar (PSI, SwissFEL) ",
            "organizer": "Christoph Bostedt",
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            "id": 72308,
            "title": "BMI Distinguished Seminar // Attila Losonczy",
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            "start_date": "2026-12-09",
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            "start_time": "12:15:00",
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            "description": "<p>TBD</p>",
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            "speaker": "Attila Losonczy, Columbia, US",
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            "id": 73113,
            "title": "Workshop for Postdocs on the Creative Scientific Process",
            "slug": "workshop-for-postdocs-on-the-creative-scientific-2",
            "event_url": "https://memento.epfl.ch/event/workshop-for-postdocs-on-the-creative-scientific-2",
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            "start_date": "2026-12-09",
            "end_date": "2026-12-09",
            "start_time": null,
            "end_time": null,
            "description": "<p>Where do new scientific ideas come from? And can we create the conditions that make it easier to look at our research from a different perspective?<br>\r\n<br>\r\nScience progress moves between two complementary modes: <em>Day Science</em>, the rigorous testing of ideas, and <em>Night Science</em>, the creative process where those ideas first emerge. Indeed, what we call the scientific method tells us what to do once we have a hypothesis – but where do these hypotheses come from in the first place? François Jacob famously called this part the realm of ‘<em>Night Science’</em>.<br>\r\n<br>\r\nDrawing on the <a href=\"https://night-science.org/home/learn/\">Night Science training framework</a> developed by Profs Itai Yanai and Martin Lercher, this workshop offers postdoctoral researchers a first introduction to approaches that can help foster more exploratory and creative scientific thinking. A central element of the workshop is the “Science Buddy” approach. Through one-to-one interactions with other researchers, participants will explore how conversation and the perspective of someone outside their field can help them step outside of familiar patterns of thinking.<br>\r\n<br>\r\n<strong>This interactive workshop is designed specifically to:</strong>\r\n</p><ul>\r\n\t<li>Explore the distinction between analytical and creative modes of scientific thinking</li>\r\n\t<li>Experience Night Science exercises with a Science Buddy to look at research questions or challenges from different perspectives</li>\r\n\t<li>Expand thinking beyond conventional frameworks</li>\r\n\t<li>Step into the creative side of the scientific process</li>\r\n</ul>\r\n<strong><em>When and Where</em></strong><strong>:</strong> <strong>December 9<sup>th</sup> 2026, 08:30-14:00</strong><strong>.</strong> On-site only, room <a href=\"https://plan.epfl.ch/?dim_floor=0&amp;lang=en&amp;dim_lang=en&amp;tree_groups=centres_nevralgiques_grp%2Cmobilite_acces_grp%2Crestauration_et_commerces_grp%2Censeignement%2Cservices_campus_grp%2Cequipements_grp&amp;tree_group_layers_centres_nevralgiques_grp=&amp;tree_group_layers_mobilite_acces_grp=metro&amp;tree_group_layers_restauration_et_commerces_grp=&amp;tree_group_layers_enseignement=guichet_etudiants&amp;tree_group_layers_services_campus_grp=information_epfl&amp;tree_group_layers_equipements_grp=&amp;baselayer_ref=grp_backgrounds&amp;map_x=2533099&amp;map_y=1152409&amp;map_zoom=14\">MED0 1618</a> (Lausanne campus). A light breakfast and lunch are provided.<br>\r\n<br>\r\n<strong><em>Programme:</em></strong><br>\r\n<strong>08:30-08:45</strong>Breakfast + Welcome coffee <br>\r\n<strong>08:45-10:15</strong>Session 1: Night science, openness, improvisation, takes two to think + Exercise<br>\r\n<strong>10:15-10:30</strong>Coffee break<br>\r\n<strong>10:30-12:00</strong>Session 2: Import/export, 2 languages + Exercise<br>\r\n<strong>12:00-12:30</strong>Lunch<br>\r\n<strong>12:30-13:30</strong>Session 3: Hypothesis is a liability, what’s the question + Exercise<br>\r\n<strong>13:30-14:00</strong>Wrap-up Discussion <br>\r\n<br>\r\n<strong><em>Registration</em></strong><strong>:</strong> Participation limited to <strong>30 attendees</strong>, on a first-come first-served basis. Register <a href=\"https://forms.cloud.microsoft/e/HLink3N15f\">here</a> early to secure your spot. A waiting list will be organised but registration will close once this is filled. Attendance will be confirmed by email by the 2<sup>nd</sup> December at the latest.<br>\r\n<br>\r\nThis course is provided by a certified Night Science trainer from the <a href=\"https://www.epfl.ch/research/services/units/research-office/\">EPFL Research Office</a>. <br>\r\n<br>\r\nAny questions? Contact us at <a href=\"mailto:[email protected]\">[email protected]</a>.",
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            "id": 72480,
            "title": "A unified theory of order flow, market impact, and volatility",
            "slug": "a-unified-theory-of-order-flow-market-impact-and-v",
            "event_url": "https://memento.epfl.ch/event/a-unified-theory-of-order-flow-market-impact-and-v",
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            "start_date": "2026-12-08",
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            "description": "<p>We propose a microstructural model for the order flow in financial markets that distinguishes between core orders and reaction flow, both modelled as Hawkes processes. This model has a natural scaling limit that reconciles a number of salient empirical properties: persistent signed order flow, rough trading volume and volatility, and power-law market impact. In our framework, all these quantities are pinned down by a single statistic H, which measures the persistence of the core flow. Specifically, the signed flow converges to the sum of a fractional process with Hurst index H and a martingale, while the limiting traded volume is a rough process with Hurst index H - 1/2. No-arbitrage constraints imply that volatility is rough, with Hurst parameter 2H - 3/2, and that the price impact of trades follows a power law with exponent 2 - 2H. The analysis of signed order flow data yields an estimate H around 3/4. This is not only consistent with the square-root law of market impact, but also turns out to match estimates for the roughness of traded volumes and volatilities remarkably well.<br>\r\n<br>\r\nJoint work with Youssef Ouazzani Chahdi, Mathieu Rosenbaum and Gregoire Szymanski.<br>\r\n </p>",
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        {
            "id": 72898,
            "title": "From Nitrogen Fixation to Carbon Valorization: Engineering Nitrogenases for New Chemistry - CH-636",
            "slug": "from-nitrogen-fixation-to-carbon-valorization-engi",
            "event_url": "https://memento.epfl.ch/event/from-nitrogen-fixation-to-carbon-valorization-engi",
            "visual_url": "https://memento.epfl.ch/image/34103/200x112.jpg",
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            "lang": "en",
            "start_date": "2026-12-08",
            "end_date": "2026-12-08",
            "start_time": "16:15:00",
            "end_time": "17:15:00",
            "description": "<strong>Speaker: </strong>Prof. Dr. Johannes Rebelein (University Düsseldorf &amp; Forschungszentrum Jülich)<br>\r\n<br>\r\n<strong>Abstract: </strong>Nitrogenases are the only known enzymes that catalyze the reduction of molecular nitrogen (N<sub>2</sub>) to ammonia (NH<sub>3</sub>), and with this driving the global nitrogen cycle. Besides the conversion of N<sub>2</sub>, we showed that nitrogenases convert carbon dioxide (CO<sub>2</sub>) to carbon monoxide, formate and hydrocarbons (1-3), suggesting new pathways for CO<sub>2 </sub>activation and the formation of value-added products.<br>\r\nThe mechanistic basis and structural determinants for these activities, substrate specificity and product profiles remain poorly understood. We demonstrated that the iron (Fe)-nitrogenase reduces CO₂ nearly threefold more efficiently than the canonical molybdenum (Mo) nitrogenase (2). This catalytic preference is conserved <em>in vivo</em>, where <em>Rhodobacter capsulatus</em> strains expressing the Fe-nitrogenase physiologically convert CO₂ to formate and methane. Leveraging high-resolution cryo-EM (3-5), we map structural features governing substrate channeling and catalysis of nitrogenase(-like) enzymes, to obtain a better understanding of the structure-function relationship (Figure 1, 3-6). Why do the different nitrogenase isoforms, the molybdenum (Mo), the vanadium (V) and the iron (Fe) nitrogenase have different activities and specificities for the reduction of N<sub>2</sub>, CO and CO<sub>2</sub>? Even more surprising is that the nitrogenase-like methylthio-alkane reductase cleaves carbon-sulfur bonds<sub> </sub><em>in vivo </em>and is unable to activate N<sub>2</sub> although it harbors a nitrogenase P- and L-cluster (5). <br>\r\nGuided by these insights, we engineered nitrogenase variants that shift the product profile toward hydrocarbons and significantly enhance CO₂ reduction selectivity in the presence of N₂ (3). These findings redefine nitrogenase substrate promiscuity, provide a mechanistic blueprint for engineering CO₂-reducing biocatalysts, and establish Fe-nitrogenase as a promising platform for sustainable carbon valorization.<br>\r\n \r\n<figure class=\"image\"><img alt=\"\" height=\"306\" src=\"//memento.epfl.ch/public/upload/fckeditorimage/84/f4/7c1b42ba.jpg\" width=\"600\">\r\n<figcaption>© 2026 EPFL</figcaption>\r\n</figure>\r\n<br>\r\n<strong>Figure 1.</strong> A schematic overview of FeMoco maturase, Mo-nitrogenase and methylthio-alkane reductase with their contained metalloclusters responsible for electron transfer and catalysis. The catalyzed main reactions are shown below.<br>\r\n<br>\r\n<strong>References :</strong>\r\n\r\n<ol>\r\n\t<li>N. N. Oehlmann, J. G. Rebelein, <em>ChemBioChem</em> 23, e202100453 (2022).</li>\r\n\t<li>N. N. Oehlmann et al., <em>Sci. Adv.</em> 10, eado7729 (2024).</li>\r\n\t<li>N. N. Oehlmann et al., <em>bioRxiv</em>. doi:10.64898/2026.07.08.737278 (2026).</li>\r\n\t<li>F. V. Schmidt et al., <em>Nat. Struct. Mol. Biol</em>. 31, 150-158 (2024).</li>\r\n\t<li>Lago-Maciel et al., <em>Nat. Catal. </em>8, 1086-1099 (2025).</li>\r\n\t<li>Lago-Maciel et al., <em>Trends Biochem</em>. Sci. 51, 187-202 (2026).</li>\r\n</ol>\r\n<br>\r\n<strong>Biography: </strong>Prof. Dr. Johannes Rebelein is Professor of Sustainable Biotechnology at Heinrich Heine University Düsseldorf and Director of the Institute for Molecular Enzyme Technology (IMET) at Forschungszentrum Jülich. His research focuses on metalloenzyme biochemistry and catalysis, particularly nitrogenase and nitrogenase-like enzymes. Combining biochemical, structural, synthetic microbiology and enzyme-engineering approaches, his group investigates how complex metallocofactors convert small molecules, including nitrogen and carbon dioxide, and how these principles can be harnessed to develop sustainable biotechnological solutions for greenhouse-gas valorization and artificial metalloenzyme design.<br>\r\nBefore his appointment in Düsseldorf/Jülich, Rebelein led an Emmy Noether Research Group at the Max Planck Institute for Terrestrial Microbiology in Marburg and was a Junior Group Leader at the LOEWE Center for Synthetic Microbiology at Philipps-University Marburg. He completed postdoctoral training with Prof. Thomas Ward at the University of Basel and earned his Ph.D. in Biological Sciences at the University of California, Irvine, under Prof. Markus W. Ribbe. He holds B.Sc. and M.Sc. degrees in Biotechnology, with honors, from TU Braunschweig. Prof. Rebelein’s contributions to the field have been recognized with several prestigious honors, including the European Molecular Biology Organization (EMBO) Young Investigator Award and the VAAM (Association for General and Applied Microbiology) Research Award.<br>\r\n ",
            "image_description": "",
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            "speaker": "Prof. Johannes Rebelein (University Düsseldorf &amp; Forschungszentrum Jülich)",
            "organizer": "Prof. Markus Jeschek",
            "contact": "<a href=\"https://search.epfl.ch/?filter=people&amp;q=jeschek\">Prof. Markus Jeschek</a>",
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        {
            "id": 73023,
            "title": "Vision and Cognition Seminar // Gregory Francis: Many studies of attention are massively underpowered, and what we can do about it",
            "slug": "vision-and-cognition-seminar-gregory-francis-many",
            "event_url": "https://memento.epfl.ch/event/vision-and-cognition-seminar-gregory-francis-many",
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            "start_date": "2026-12-08",
            "end_date": "2026-12-08",
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            "end_time": "15:00:00",
            "description": "",
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            "creation_date": "2026-10-30T23:33:57",
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            "canceled": "False",
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            "speaker": "<strong>Gregory Francis, </strong>Derpartment of Psychology, University of Southern Denmark, Denmark",
            "organizer": "BMI LPSY  Host: Michale Herzog  ",
            "contact": "[email protected]",
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            "title": "EPFL BioEngineering Talks",
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            "description": "<p>Weekly BioEngineering Talks (Lunch Provided)<br>\r\n<br>\r\n<strong>INVITED SPEAKER:</strong><br>\r\n<br>\r\n<strong>Intracellular architecture and mechanics: new rheostats of metastasis</strong><br>\r\n<a href=\"https://www.goetzlab.fr/\"><strong>Dr. Jacky Goetz</strong></a>, INSERM / University of Strasbourg<br>\r\nHost: <a href=\"https://people.epfl.ch/li.tang?lang=en\">Prof. Li Tang</a><br>\r\n<br>\r\n<u><strong>Abstract:</strong></u><br>\r\nEmerging evidence suggests that the function and position of organelles, together with their mechanical adaptation of cells, are pivotal for tumor metastasis. Lysosomes integrate metabolic sensing with gene regulation and protease secretion, while circulating tumor cells (CTCs) must adjust their mechanics to overcome constraints during hematogenous spread. Yet, how spatial distribution of organelles and how cell-intrinsic mechanics control metastasis remains elusive. Here, we analyze lysosome subcellular distribution in patient-derived melanoma cells and biopsies and show that lysosome spreading scales with melanoma aggressiveness, while in parallel assessing how CTC deformability affects dissemination and identifying mechanical phenotypes that favor metastatic extravasation. Using chemo-genetic control of lysosome positioning, intravital microscopy with CTC-mimicking beads, mechanical tuning in tumor lines and profiling of patient-derived cells, we demonstrate that perinuclear lysosome clustering impairs secretion, matrix degradation and invasion, and that the mechanical properties of circulating objects dictate their ability to enter constraining vessels. We identify cellular viscosity as a rheostat of CTC circulation, arrest and extravasation, and show that impairing lysosome spreading significantly reduces invasive outgrowth in mouse and zebrafish models, with traits that favor extravasation and outgrowth being partially distinct. Altogether, these findings establish lysosome positioning and CTC viscosity as key rheostats of metastatic progression and suggest their potential utility for diagnosis and therapeutic targeting of metastatic cancers. Whether they are interconnected determinants and how they control immune surveillance will be our next goals<br>\r\n<br>\r\n<u><strong>Bio:</strong></u><br>\r\nJacky graduated in Pharmacology and Cell Biology from University of Strasbourg (France) in the laboratory of K.TAKEDA. He then moved to the laboratory of I.R. NABI in Montreal (University of Montreal, Canada), and later in Vancouver (University of British Columbia, Canada), where he obtained his Ph.D. in 2007. He performed two postdoctoral stays, one at the CNIC in Madrid (Spain) in the laboratory of M.A. DEL POZO, and one in the lab of J.VERMOT at the IGBMC in Strasbourg (France). Fascinated by tumor metastasis, its mechanical aspects and the use of state-of-the-art microscopy approaches in several animal models, he created the TUMOR BIOMECHANICS LAB in 2013. Quickly joined by a team of experts in imaging, mechanobiology, extracellular vesicles, he built a task force aiming at further dissecting the mechanisms and mechanics of tumor dissemination. The team made several exciting discoveries around tumor metastasis that were acknowledged by several prizes (SBCF, Ruban Rose, French Academy of Sciences, Fondation de France, EuroLife). When he is not in the lab, Jacky is either running, swimming or biking and loves competing during half IronMan triathlons (70.3). You can also find him traveling with his family, during sabbaticals (Australia, South Africa), always thinking about the next trip. Fascinated by Japan but also by Alsace, where he grew up, he could « kill » for sushi and loves the alsatian architecture<br>\r\n<br>\r\n<strong>STUDENT SPEAKER:<br>\r\n<br>\r\nStructural Analysis of Intravenous Immunoglobulin (IVIG) Interactions with Enteroviral Surfaces Using Cryo-EM Based Polyclonal Epitope Mapping</strong><br>\r\n<strong><a href=\"https://people.epfl.ch/yash.garodia?lang=en\">Yash Garodia</a>, </strong><a href=\"https://www.epfl.ch/labs/antanasijevic-lab/\">Antanasijevic Lab</a><br>\r\n<br>\r\n<br>\r\n------------------------------------------------------------------------------<br>\r\n<br>\r\n<strong>BioEngineering Talks mandatory EDBB Seminar Attendance (1st-Year PhD Students)</strong>\r\n</p><ul>\r\n\t<li> Attendance sheet to print <a class=\"text-link\" href=\"https://docs.google.com/document/d/1kusGxCFPAvWaRD8eUGEBkSVzD1ppMf1g/edit\" target=\"_blank\">HERE </a></li>\r\n</ul>\r\n<strong>The BioEngineering Student Seminar Series</strong> is an official course for which students can register and earn credits.\r\n\r\n<ul>\r\n\t<li>Register <a class=\"text-link\" href=\"https://edu.epfl.ch/studyplan/fr/ecole_doctorale/biotechnologie-et-genie-biologique/coursebook/bioengineering-student-seminar-series-BIOENG-613\" target=\"_blank\">HERE</a></li>\r\n\t<li>Attendance sheet to print <a class=\"text-link\" href=\"https://docs.google.com/document/d/1ZGrPnt8LlLuWOApzx32s6L5UPPH8Hyoo/edit\" target=\"_blank\">HERE</a></li>\r\n</ul>\r\n<strong>General information:</strong><br>\r\nIn-person attendance is preferred to support your fellow students. 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