retrieve:
Return the details about the given Event id.

list:
List all Event objects.

GET /api/v1/events/?format=api&offset=220&ordering=event__url_online_room
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

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            "id": 71338,
            "title": "Probing Ultrafast Electron Motion with Attosecond X-ray Free Electron Lasers",
            "slug": "probing-ultrafast-electron-motion-with-attosecond",
            "event_url": "https://memento.epfl.ch/event/probing-ultrafast-electron-motion-with-attosecond",
            "visual_url": "https://memento.epfl.ch/image/32692/200x112.jpg",
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            "start_date": "2026-04-23",
            "end_date": "2026-04-23",
            "start_time": "17:15:00",
            "end_time": "18:30:00",
            "description": "<p>The ultrafast motion of electrons is a frontier problem for photochemical processes, as electron motion is a key ingredient of all chemical reactions. Electronic rearrangement is also the means by which light energy is harnessed in photochemistry. The timescale for coherent electron dynamics is set by the energetic splitting of the electronic states, which in small molecular systems, is on the scale of an electron volt (eV). This sets the natural timescale for electronic motion to be few-to-sub femtosecond (fs).<br>\r\n<br>\r\nTo approach these extreme timescales, we can use short pulses of light to excite small quantum systems. For instance, the impulsive interactions between a light field and a quantum system can induce time-dependent oscillations in the charge density. Such electronic wavepacket motion (in the absence of nuclear motion) has come to be referred to as charge migration [1]. While the initial charge dynamics following impulsive excitation (or ionization) begins as purely electronic motion, this wavepacket will couple to other degrees of freedom in the system (i.e. nuclear motion or chemical dynamics) and lead to localization of the charge.  The transfer of electronic charge across molecular bonds is fundamental to an understanding of charge transfer phenomena.<br>\r\n<br>\r\nThe study of these fundamental phenomena requires state-of-the-art light sources, such as the Linac Coherent Light Source (LCLS), an X-ray free electron laser (XFEL) facility which produces high-brightness, ultrashort pulses, with wavelength continuously tunable across the x-ray regime. Schemes to provide isolated, sub-femtosecond pulses from an FEL are being explored at facilities world-wide, and recently we have demonstrated such pulses at the LCLS [2]; opening the door for time-resolved measurements of ultrafast electron dynamics on their natural timescale. In my talk, I will highlight our recent developments in probing electronic motion in small molecular systems. We have employed sub-femtosecond pulses from the XFEL to study ultrafast charge dynamics in both core-excited [3,4,5] and low-lying cationic systems [6]. We are also developing nonlinear x-ray spectroscopies [7,8] to initiate and control electron dynamics. The control of coherent electron motion represents a significant step towards achieving charge-directed reactivity [9], a grand challenge for the field of attosecond science.<br>\r\n<br>\r\n[1] Cederbaum and Zobeley 1999 Chemical Physics Letters 307 205–210<br>\r\n[2] Duris and Li et al. 2020 Nature Photonics 14 30-36<br>\r\n[3] Li and Driver et al. 2022 Science 375 285-290<br>\r\n[4] Driver et al. 2024 Nature 632 762-767 (2024)<br>\r\n[5] Wang and Driver et al. Phys. Rev. X 15 011008 (2005)<br>\r\n[6] Driver et al. ArXiv:2411.01700<br>\r\n[7] O’Neal et al. 2020 Phys. Rev. Lett. 125 073203<br>\r\n[8] Biggs et al. 2023 Proc. Nat. Acad. Sci. 110 15597-15601<br>\r\n[9] F. Remacle, R. D. Levine, and M. A. Ratner 1998 Chem. Phys. Lett. 285, 25<br>\r\n </p>",
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            "speaker": "James Cryan, Stanford Univ. / SLAC",
            "organizer": "Christoph Bostedt",
            "contact": "Christoph Bostedt",
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            "id": 70833,
            "title": "EESS seminar talk on \"Biogeochemical Controls on Arsenic Methylation and Demethylation in Rice Paddy Soils\"",
            "slug": "eess-seminar-talk-on-biogeochemical-controls-on--2",
            "event_url": "https://memento.epfl.ch/event/eess-seminar-talk-on-biogeochemical-controls-on--2",
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            "start_date": "2026-04-28",
            "end_date": "2026-04-28",
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            "description": "<strong>Abstract:</strong>\r\n<div class=\"page\">\r\n<div class=\"layoutArea\">\r\n<div class=\"column\">Arsenic methylation and demethylation reactions influence arsenic speciation and fate in rice paddy soils, and understanding the balance between methylation and demethylation is important for assessing risks of arsenic toxicity in rice. Rice paddy soils are rich in organic carbon, and the conventional understanding has been that organic carbon enhances microbial arsenic methylation by fueling microbial activity.  This presentation will describe a series of recent investigations — spanning pure culture to greenhouse-scale experiments — that challenge this conceptual model.  First, the presentation will describe the role of carbon catabolite repression (CCR) in regulating cellular uptake and subsequent enzymatic methylation of arsenite.  A combination of biosensor, gene expression, and arsenic speciation analyses demonstrate that sugars lead to CCR and a decrease in arsenic methylation, while low molecular weight organic acids do not impact arsenite uptake.  The presentation will then examine couplings between methanogenesis and arsenic demethylation, wherein a greater abundance of methylotrophic carbon substrates (methanol, methylamines) promote arsenic demethylation by methanogens and limit the accumulation of methylated arsenic compounds.  A genome-resolved metatranscriptomic analysis of anaerobic soil slurry experiments resolved links between methylotrophic substrate utilization and arsenic demethylation, while greenhouse experiments showed that higher levels of methanogenesis in soils were associated with lower concentrations of methylated arsenic in rice grains. Taken together, these results provide a more nuanced understanding of how utilization of distinct carbon substrates impacts arsenic methylation-demethylation dynamics, and provides mechanistic insights into how paddy soil management practices influence arsenic speciation in rice.</div>\r\n</div>\r\n</div>\r\n<br>\r\n<br>\r\n<br>\r\n<strong>Biography:</strong>\r\n\r\n<div class=\"page\">\r\n<div class=\"layoutArea\">\r\n<div class=\"column\">Dr. Matthew Reid is an associate professor in the School of Civil and Environmental Engineering at Cornell University and directs the Biogeochemistry and Ecosystem Engineering Research Group. His research program focuses on biogeochemical element cycling in natural and nature-based systems with applications to water quality.  Research in the Reid Group spans physical scales and integrates mechanistic and molecular-level investigation with field-scale observation to build quantitative models for contaminant dynamics in complex biogeochemical systems. Dr. Reid's research has been recognized with early career awards from NSF and DOE. Dr. Reid was a postdoctoral scientist in the Environmental Microbiology Laboratory at EPFL, and completed his Ph.D. in Civil and Environmental Engineering at Princeton University.</div>\r\n</div>\r\n</div>",
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            "place_and_room": "GC B1 10",
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            "speaker": "Prof. <a href=\"https://www.engineering.cornell.edu/people/matthew-charles-reid/\">Matthew Reid</a>, Cornell University ",
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            "contact": "Prof. Rizlan Latmani, <a href=\"https://www.epfl.ch/labs/eml/\">EML</a>",
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            "keywords": "Arsenic, Methylation, Demethylation, Rice paddy soil, Carbon catabolite repression, Methanogenesis",
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            "id": 70992,
            "title": "La « locomotive à fumée ». Histoire de la pollution de l'air par le chemin de fer au temps de la vapeur (France, Grande-Bretagne, années 1820-1960)",
            "slug": "la-locomotive-a-fumee-histoire-de-la-pollution-d-2",
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            "start_date": "2026-05-07",
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            "end_time": null,
            "description": "<p>Thesis Directors: Prof. J. Baudry, Dr F. Jarrige<br>\r\nArchitecture and Sciences of the City doctoral program<br>\r\nThesis Nr. 11656<br>\r\n<br>\r\nTo take part in the public defense, please contact directly the speaker</p>",
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            "creation_date": "2026-01-29T09:46:54",
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            "speaker": "<a href=\"http://[email protected]\"><strong>Arthur Grégoire Jacques EMILE</strong></a>",
            "organizer": "",
            "contact": "<a href=\"http://[email protected]\"><strong>Arthur Grégoire Jacques EMILE</strong></a>",
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            "id": 70719,
            "title": "Training \"Up to Speed with Zotero\"",
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            "start_time": "09:30:00",
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            "description": "<div class=\"all_text\"><strong>This workshop is for people who want to start using Zotero, an open source software which enables you to collect, organize and share bibliographic references. From a thesis to an academic paper, Zotero can spare you a huge amount of time.</strong><br>\r\n<br>\r\nAt the end of this workshop, which will be <strong>held on Zoom only</strong>, you will be able to:\r\n<ul>\r\n\t<li>Collect bibliographic references from different sources.</li>\r\n\t<li>Organize your references in a neat manner.</li>\r\n\t<li>Get to know what a reference style is and how to switch it easily.</li>\r\n\t<li>Create a bibliography with a few clicks.</li>\r\n</ul>\r\n<a href=\"https://bookwhen.com/epfl_library/e/ev-sal5m-20260512093000\">Registration</a><br>\r\n<br>\r\nMore information about <a href=\"https://www.epfl.ch/campus/library/training/\">EPFL Library Teaching offer</a></div>",
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            "id": 71088,
            "title": "Seminar by Raju Venugopalan, Brookhaven National Laboratory",
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            "start_date": "2026-05-11",
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            "link_label": "",
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            "canceled": "False",
            "cancel_reason": "",
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            "id": 70040,
            "title": "“The end of KRAS cancers?”",
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            "start_date": "2026-05-07",
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            "description": "<strong>A Lola and John Grace Distinguished Lecture in Cancer Research</strong>\r\n<div class=\"elementor-element elementor-element-98cefd8 elementor-widget elementor-widget-heading\">\r\n<div class=\"elementor-widget-container\"><br>\r\nFrank McCormick, PhD, is a Professor at the UCSF Helen Diller Family Comprehensive Cancer Center and holds the David A. Wood Chair of Tumor Biology and Cancer Research. Prior to joining the UCSF faculty, Dr. McCormick pursued cancer-related work with several Bay Area biotechnology firms and held positions with Cetus Corporation (Director of Molecular Biology, 1981-1990; Vice President of Research, 1990-1991) and Chiron Corporation, where he was Vice President of Research. In 1992 he founded Onyx Pharmaceuticals, a company dedicated to developing new cancer therapies, and served as its Chief Scientific Officer until 1996. At Onyx Pharmaceuticals, he initiated drug discovery efforts that led to the approval of Sorafenib in 2005 for treatment of renal cell cancer, and for liver cancer in 2007, and the approval of ONYX-015 in 2006 in China for treatment of nasopharyngeal cancer. In addition, Dr. McCormick’s group led to the identification of the CDK4 kinase inhibitor, Palbociclib, approved for treating advanced breast cancer. Dr. McCormick's current research interests center on ways of targeting Ras proteins and their regulators, including the NF1 protein neurofibromin.<br>\r\n<br>\r\nDr. McCormick was Director of the Helen Diller Family Comprehensive Cancer Center from 1997 to 2014 and he served as President, 2012-2013, for the American Association for Cancer Research. Since 2013, Dr. McCormick has led the National Cancer Institute’s Ras Initiative at the Frederick National Laboratories for Cancer Research overseeing the national effort to develop therapies against Ras-driven cancers. Dr. McCormick was recently awarded (September 2025) the Inaugural Stephenson Global Prize Award in recognition of his research and discoveries that have transformed the field of RAS-driven cancers. <br>\r\n<br>\r\nDr. McCormick is the author of over 430 scientific publications and holds more than 20 issued patents and is a Fellow of the Royal Society and a member of the National Academy of Sciences.<br>\r\n </div>\r\n</div>\r\n\r\n<div class=\"elementor-element elementor-element-e552a16 elementor-widget elementor-widget-text-editor\">\r\n<div class=\"elementor-widget-container\"> </div>\r\n</div>",
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        {
            "id": 70782,
            "title": "“Mechanisms driving the rapid evolution of genomes”",
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            "start_date": "2026-06-04",
            "end_date": "2026-06-04",
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            "description": "<strong>A Lola and John Grace Distinguished Lecture in Cancer Research</strong>\r\n<div class=\"elementor-element elementor-element-98cefd8 elementor-widget elementor-widget-heading\">\r\n<div class=\"elementor-widget-container\">\r\n<div class=\"is-active tabs-panel\">\r\n<div class=\"bundle--tabs paragraph paragraph--type--tabs paragraph--view-mode--default\">\r\n<div class=\"row\">\r\n<div class=\"columns small-12\">\r\n<div class=\"body field__item\">David Pellman, M.D. is the Margaret M. Dyson Professor of Pediatric Oncology at the Dana-Farber Cancer Institute, a Professor of Cell Biology at Harvard Medical School, an Investigator of the Howard Hughes Medical Institute, and the Associate Director for Basic Science at the Dana-Farber/Harvard Cancer Center.  He received his undergraduate and medical degrees from the University of Chicago.  During medical school, he did research at the Rockefeller University.  His postdoctoral fellowship was at the Whitehead Institute/Massachusetts Institute of Technology.<br>\r\n<br>\r\nThe Pellman Lab works on the mechanism of cell division and how certain cell division errors drive rapid genome evolution.  His research has contributed to the understanding of cell division, the origin of cell division errors in cancer, how cell division errors drive genetic instability and the mechanisms driving rapid evolution of cancer genomes. Our contributions include (1) the co-discovery of formin-dependent actin nucleation and a mechanism for spindle positioning during asymmetric cell division, (2) discoveries establishing that whole genome duplication can drive tumorigenesis, alter cell physiology, and accelerate evolutionary adaptation, and (3) the discovery of a mechanism explaining chromothripsis, a mutational process that generates rapid karyotype evolution in cancer and congenital disease.</div>\r\n</div>\r\n</div>\r\n</div>\r\n</div>\r\n</div>\r\n</div>\r\n\r\n<div class=\"elementor-element elementor-element-e552a16 elementor-widget elementor-widget-text-editor\">\r\n<div class=\"elementor-widget-container\"> </div>\r\n</div>",
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            "organizer": "Prof. Pierre Gönczy",
            "contact": "Lisa Smith, ISREC Administrative Assistant",
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        {
            "id": 70990,
            "title": "\"Mapping the Human Body One Cell at a Time.\"",
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            "start_date": "2026-04-30",
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            "description": "<strong>A Lola and John Grace Distinguished Lecture in Cancer Research</strong>\r\n<div class=\"elementor-element elementor-element-98cefd8 elementor-widget elementor-widget-heading\">\r\n<div class=\"elementor-widget-container\"><br>\r\nSarah Teichmann completed her PhD at the MRC Laboratory of Molecular Biology in Cambridge, UK, and was a Beit Memorial Fellow at University College London. She established her research group at the MRC Laboratory of Molecular Biology in 2001, where her main discoveries included the finding that protein assembly pathways are stereotypical and conserved. In 2013, she transitioned to the Wellcome Genome Campus, where she became the first and, to date, the only faculty member appointed across both the EMBL-European Bioinformatics Institute and the Wellcome Sanger Institute. In 2016, she was appointed as the Head of the Cellular Genetics programme at the Wellcome Sanger Institute and co-founded the Human Cell Atlas initiative. From April 2024, she was appointed chair in Stem Cell Medicine at the University of Cambridge, within the Department of Medicine and the Cambridge Stem Cell Institute. Additionally, Sarah dedicates part of her time to GlaxoSmithKline and to EnsoCell Therapeutics, the startup company she co-founded. The Teichmann lab focuses on developing and applying cell atlas technologies to understand human tissue architecture, particularly examining how cellular diversity is generated in the immune system and during development.</div>\r\n</div>\r\n\r\n<div class=\"elementor-element elementor-element-e552a16 elementor-widget elementor-widget-text-editor\">\r\n<div class=\"elementor-widget-container\"> </div>\r\n</div>",
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            "speaker": "<strong>Sarah Teichmann FMedSci FRS</strong> (Group Leader), Cambridge Stem Cell Institute &amp; Department of Medicine, Jeffrey Cheah Biomedical Centre, University of Cambridge",
            "organizer": "Prof. Charlotte Bunne",
            "contact": "Lisa Smith, ISREC Administrative Assistant",
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        {
            "id": 70903,
            "title": "lunch&LEARN:  Learning with AI: Designing AI Tutors that foster learning in robotics and CS courses",
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            "start_date": "2026-06-09",
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            "start_time": "12:15:00",
            "end_time": "13:00:00",
            "description": "<strong>// NEW DATE // This event has been rescheduled from 17 March to 9 June 2026!</strong><br>\r\n<br>\r\nHow can AI tutors be designed to support learning rather than shortcutting it?<br>\r\n<br>\r\nIn this presentation, Jérôme Brender (EPFL) will examine how undergraduate students learn with AI tutors in robotics and computer science courses.<br>\r\n<br>\r\nAcross multiple design iterations, he investigated how features such as course-grounded retrieval (RAG), Socratic questioning, and real-time prompt feedback, and debate chatbot, shape students’ engagement, prompting behavior, and learning outcomes.<br>\r\n<br>\r\nHis work focuses on how AI tutors can help students better understand course concepts and become more reflective and effective users of AI tools. The findings provide insights into designing AI tutors that foster critical thinking and support sustainable learning practices.",
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            "creation_date": "2026-01-21T13:49:42",
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