retrieve:
Return the details about the given Event id.

list:
List all Event objects.

GET /api/v1/events/?format=api&offset=160&ordering=event__label_link
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

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            "description": "<p>Le stress et l’anxiété font aujourd’hui partie intégrante du quotidien, d’autant plus dans un cadre professionnel. Pression de performance, surcharge d’informations, incertitudes et distractions digitales, nous affectent toutes et tous. Lorsqu’ils deviennent chroniques, ces états impactent la santé mentale, le sommeil, la concentration, la motivation, les relations sociales et la qualité du travail.<br>\r\n<br>\r\nComprendre ces mécanismes, apprendre à les réguler, et surtout identifier ses propres déclencheurs et ressources devient alors essentiel pour évoluer dans un cadre professionnel et promouvoir un travail stable et une qualité de vie plus saine.<br>\r\n<br>\r\nCette formation vise à renforcer votre résilience, vous permettre d’identifier vos déclencheurs personnels, et d’activer des ressources internes et externes pour retrouver calme, clarté mentale et stabilité au quotidien.</p>",
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            "description": "<p>European Framework Programs for Research and Innovation.<br>\r\n<br>\r\nIs your laboratory involved in one or several European projects, and is one of your responsibilities to ensure their effective administrative, financial, and human‑resources management? If so, it is important to take the time to become familiar with the structure of these projects and with the specific management rules that apply to them.<br>\r\n<br>\r\nThis training course will guide you through the contractual documents and their relevant content for project management. Administrative, financial, and HR management rules will be presented and discussed using practical case studies.<br>\r\nThe training will also help participants become familiar with the European portal and the SEFRI reporting platform.<br>\r\n<br>\r\nIt is recommended to attend this training as early as possible, ideally at the start of the project.</p>",
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            "id": 71000,
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            "description": "<p>Programmes-cadres européens de la recherche et de l’innovation.<br>\r\n<br>\r\nVotre laboratoire participe à un ou plusieurs projets européens et une de vos missions est d’en assurer une gestion efficace au niveaux administratif, financier et celui des ressources humaines ? Pour cela, il est important de prendre le temps de vous familiariser avec la structure de ces projets et avec certaines règles de gestion qui leurs sont spécifiques.<br>\r\n<br>\r\nCette formation vous propose de prendre connaissance des documents contractuels et de leur contenu qui est utile pour votre gestion. Les règles de gestion administrative, financière et RH seront présentées et discutées en se basant sur des cas pratiques.<br>\r\nLa formation permettra aussi aux participants de se familiariser avec le portail européen et la plateforme de reporting du SEFRI.<br>\r\n<br>\r\nIl est recommandé de suivre cette formation le plus tôt possible, idéalement vers le commencement du projet.</p>",
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            "description": "<p>Programmes-cadres européens de la recherche et de l’innovation.<br>\r\n<br>\r\nVotre laboratoire participe à un ou plusieurs projets européens et une de vos missions est d’en assurer une gestion efficace au niveaux administratif, financier et celui des ressources humaines ? Pour cela, il est important de prendre le temps de vous familiariser avec la structure de ces projets et avec certaines règles de gestion qui leurs sont spécifiques.<br>\r\n<br>\r\nCette formation vous propose de prendre connaissance des documents contractuels et de leur contenu qui est utile pour votre gestion. Les règles de gestion administrative, financière et RH seront présentées et discutées en se basant sur des cas pratiques.<br>\r\nLa formation permettra aussi aux participants de se familiariser avec le portail européen et la plateforme de reporting du SEFRI.<br>\r\n<br>\r\nIl est recommandé de suivre cette formation le plus tôt possible, idéalement vers le commencement du projet.</p>",
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            "id": 71411,
            "title": "Life Science Seminar: Hitoshi Kurumizaka",
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            "description": "<strong>Title:</strong> <br>\r\nStructural molecular biology for the nucleosome as a regulator on genomic DNA<br>\r\n<br>\r\n<strong>Abstract:</strong><br>\r\nIn eukaryotic cells, genomic DNA is highly compacted into chromatin through its association with histone proteins. The fundamental unit of chromatin, the nucleosome, consists of ~147 base pairs of DNA wrapped around a histone octamer composed of H2A, H2B, H3, and H4. These nucleosomes are connected by linker DNA, forming a “beads-on-a-string” structure that enables efficient packaging of the genome.<br>\r\nBeyond structural compaction, nucleosomes play a central role in regulating genome function. They can restrict access to DNA and act as barriers to essential processes such as transcription, replication, and repair. At the same time, nucleosomes serve as key epigenetic platforms, where histone modifications and histone variants modulate chromatin structure and dynamics to control gene activity.<br>\r\nTo better understand these regulatory mechanisms, we employ biochemical and structural approaches to investigate nucleosome structure and dynamics. Our studies aim to elucidate how structural transitions of nucleosomes influence DNA accessibility and ultimately govern genomic regulation. I will present our recent structural and biochemical insights and discuss their implications for understanding nucleosome-mediated genome regulation.<br>\r\n<br>\r\n<strong>Bio:</strong><br>\r\nHitoshi Kurumizaka is a Professor at the Institute for Quantitative Biosciences, The University of Tokyo, Japan. After receiving his Ph.D. degree in 1995, he started his postdoctoral training at NIH in the USA, in the laboratory of Molecular Embryology (Alan Wolffe Lab), where he began chromatin research. In 1997, he joined RIKEN as a Research Scientist. He subsequently moved to Waseda University, where he served as Associate Professor and later as Professor of Molecular and Structural Biology. Since 2018, he has been Professor at the Institute for Quantitative Biosciences, The University of Tokyo. His research focuses on the structural basis of chromatin and epigenetic regulation in eukaryotic genomes. In 2020, he established an in-house cryogenic electron microscopy (cryo-EM) platform to advance high-resolution structural studies of chromatin and genome-associated protein complexes. Professor Kurumizaka has made significant contributions to the field of chromatin biology through structural and mechanistic studies of nucleosomes and genome-associated protein complexes. His work has been published in leading international journals and has substantially advanced our understanding of chromatin architecture and epigenetic regulation.<br>\r\n ",
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            "description": "<p>This presentation treats space and mobility as inseparable, where space is produced through movement, coordination, and pause, while mobility is always spatially formatted by routes, nodes, and boundaries. Their intersection is therefore not an overlap but a relational field in which placement and movement continuously reify one another. This perspective invites complex mixed methods approaches based on methodological mapping across different forms of evidence, which can show how movements cluster or stretch, while narrative interviews, participatory mapping, and field observation can uncover how actors interpret routes, obstacles, and anchors in everyday life. The aim is not merely conventional triangulation, but conceptual integration: Using different methods to move between patterns in systems and interpretation of experience. Mixed methods research can theorize space-mobility while also exploring how they are experienced, governed, and contested.<br>\r\n <br>\r\nManfred Max Bergman is Chair of Social Research and Methodology at the University of Basel and Director of the Social Transitions Research Group. He works on methodological innovations to the study of sustainability transitions, inequality, health, corporate responsibility, and social change, with particular expertise in mixed methods research and case study design. He has contributed to scholarship on mobility, inequality, and public space through international comparative and interdisciplinary projects, and previously served as Editor in Chief of the Journal of Mixed Methods Research. His current international engagements include service on the Swiss National Science Foundation’s Indo-Swiss Joint Scientific Board, collaboration with ICSSR in India on an innovative research methods training programme, and a visiting professorship at NUS in Singapore focused on implementation science and transdisciplinary research.</p>",
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        {
            "id": 70824,
            "title": "MoRAT: Mathematics of Randomized linear Algebra Techniques - Summer School 2026",
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            "description": "<p>This summer school, organized by seven PhD students from EPFL and ETH Zurich, brings together leading researchers and postgraduate students. Participants will learn modern mathematical and probabilistic methods for linear algebra through lectures by experts in randomized numerical linear algebra. The program also includes networking opportunities with fellow participants, lecturers, and industry representatives.<br>\r\n<br>\r\nThe summer school takes place in a modern hotel in the middle of the historic lakeside town of Murten/Morat. Accommodation, food, and all other costs during the summer school will be covered. All participants are charged a small registration fee.<br>\r\n<br>\r\n<a href=\"http://morat2026.epfl.ch/registration\">Registrations</a> can be made until February 15 and are primarily open to doctoral students from the ETH domain, with limited exceptions for international and master’s students. It is possible to obtain 2 ECTS credits for attending MoRAT.</p>",
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        {
            "id": 70952,
            "title": "Multi-scale and multi-purpose simulations of DNA: the importance of data",
            "slug": "multi-scale-and-multi-purpose-simulations-of-dna-t",
            "event_url": "https://memento.epfl.ch/event/multi-scale-and-multi-purpose-simulations-of-dna-t",
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            "description": "<p>You can apply to participate and find all the relevant information (speakers, abstracts, program,...) on the event website: <a href=\"https://www.cecam.org/workshop-details/multi-scale-and-multi-purpose-simulations-of-dna-the-importance-of-data-1484\">https://www.cecam.org/workshop-details/multi-scale-and-multi-purpose-simulations-of-dna-the-importance-of-data-1484</a>.<br>\r\n<br>\r\nRegistration is required to attend the full event, take part in the social activities and present a poster at the poster session (if any).  However, the EPFL community is welcome to attend specific lectures without registration if the topic is of interest to their research. Do not hesitate to contact the <a href=\"mailto:[email protected]\">CECAM Event Manager</a> if you have any question.<br>\r\n<br>\r\n<strong>Description</strong><br>\r\n<br>\r\nDNA is a dramatic example of a multiscale system, where Å-scale details impact the global properties of a meter-long fiber and where femtosecond processes can impact on the entire genome years later. This implies that any theoretical study on DNA should take into consideration the vast variety of space and time scales, making it necessary the adoption of multi-physics approaches, covering the entire range of theoretical methods from quantum chemistry to rough mesoscopic models. Within this scenario the importance of data to bias simulations and as a reference to calibrate low resolution methods (Dans et al. 2017; Neguembor et al. 2022; Schultz et al. 2025).<br>\r\nLarge efforts have been made to develop accurate low level DFT and semiempirical methods that can be data-providers for a new generation of force-field, as well as integrated in QM/MM packages for an efficient representation of DNA reactivity (Aranda et al. 2019). Atomistic force-field have gained accuracy, showing good ability to reproduce unusual forms of DNA and long segments of DNA in the context of chromatin (Collepardo-Guevara et al. 2015; Genna et al. 2025) and providing very useful data for the calibration of lower level coarse-grained or mesoscopic methods(De Pablo 2011; Farré-Gil et al. 2024) ,which have gained sequence specificity, scalability and computational efficiency, allowing to simulate kilo-to-megabase fragments of DNA. Very remarkable efforts have been made to move up these methods to represent chromatin, which requires the introduction of biases derived from experimental data (MNAseq, chromosome conformation capture, and even static or dynamic pictures obtained by ultra-resolution microscopy, and others (Buitrago et al. 2019; Neguembor et al. 2022; Li and Schlick 2024)). This has opened the possibility to recover dynamic “base-pair” resolution pictures of chromatin and study aspects from local and global chromatin rearrangements to inter-play between effector proteins and nucleosomes, the impact of lesions in chromatin structure, and even the role of phase separation in defining local chromatin arrangements (Joseph et al. 2021; Liu et al. 2025; Park et al. 2025).<br>\r\nAs the target systems move from the small atomistic detail to the entire chromatin fiber, the community is broken into different sub-communities. This generates a risk of disconnection, which would lead to a waste of effort reformulating solutions to already solved problems, or ignoring the characteristic that a method should have to maintain coherence with more accurate models, or to scale to represent systems of real biological interest. This will be the main objective of this meeting, which will join a variety of sub-communities with a common interest: the DNA.<br>\r\n<br>\r\n<strong>References</strong><br>\r\n<br>\r\n<a href=\"https://doi.org/10.1038/s41929-019-0290-y\" target=\"_blank\">[1] J. Aranda, M. Terrazas, H. Gómez, N. Villegas, M. Orozco, Nat. Catal., <strong>2</strong>, 544-552 (2019)</a><br>\r\n<a href=\"https://doi.org/10.1093/nar/gkz759\" target=\"_blank\">[2] D. Buitrago, L. Codó, R. Illa, P. de Jorge, F. Battistini, O. Flores, G. Bayarri, R. Royo, M. Del Pino, S. Heath, A. Hospital, J. Gelpí, I. Heath, M. Orozco, Nucleic Acids Research, <strong>47</strong>, 9511-9523 (2019)</a><br>\r\n<a href=\"https://doi.org/10.1021/jacs.5b04086\" target=\"_blank\">[3] R. Collepardo-Guevara, G. Portella, M. Vendruscolo, D. Frenkel, T. Schlick, M. Orozco, J. Am. Chem. Soc., <strong>137</strong>, 10205-10215 (2015)</a><br>\r\n<a href=\"https://doi.org/10.1093/nar/gkw1355\" target=\"_blank\">[4] P. Dans, I. Ivani, A. Hospital, G. Portella, C. González, M. Orozco, Nucleic. Acids. Res., gkw1355 (2017)</a><br>\r\n<a href=\"https://doi.org/10.1146/annurev-physchem-032210-103458\" target=\"_blank\">[5] J. de Pablo, Annu. Rev. Phys. Chem., <strong>62</strong>, 555-574 (2011)</a><br>\r\n<a href=\"https://doi.org/10.1093/nar/gkae444\" target=\"_blank\">[6] D. Farré-Gil, J. Arcon, C. Laughton, M. Orozco, Nucleic Acids Research, <strong>52</strong>, 6791-6801 (2024)</a><br>\r\n<a href=\"https://doi.org/10.1093/nar/gkaf170\" target=\"_blank\">[7] V. Genna, G. Portella, A. Sala, M. Terrazas, I. Serrano-Chacón, J. González, N. Villegas, L. Mateo, C. Castellazzi, M. Labrador, A. Aviño, A. Hospital, A. Gandioso, P. Aloy, I. Brun-Heath, C. Gonzalez, R. Eritja, M. Orozco, Nucleic Acids Research, <strong>53</strong>, (2025)</a><br>\r\n<a href=\"https://doi.org/10.1038/s43588-021-00155-3\" target=\"_blank\">[8] J. Joseph, A. Reinhardt, A. Aguirre, P. Chew, K. Russell, J. Espinosa, A. Garaizar, R. Collepardo-Guevara, Nat. Comput. Sci., <strong>1</strong>, 732-743 (2021)</a><br>\r\n<a href=\"https://doi.org/10.1093/nar/gkad1121\" target=\"_blank\">[9] Z. Li, T. Schlick, Nucleic Acids Research, <strong>52</strong>, 583-599 (2023)</a><br>\r\n<a href=\"https://doi.org/10.1021/acs.biochem.4c00737\" target=\"_blank\">[10] S. Liu, C. Wang, B. Zhang, Biochemistry, <strong>64</strong>, 1750-1761 (2025)</a><br>\r\n<a href=\"https://doi.org/10.1038/s41594-022-00839-y\" target=\"_blank\">[11] M. Neguembor, J. Arcon, D. Buitrago, R. Lema, J. Walther, X. Garate, L. Martin, P. Romero, J. AlHaj Abed, M. Gut, J. Blanc, M. Lakadamyali, C. Wu, I. Brun Heath, M. Orozco, P. Dans, M. Cosma, Nat. Struct. Mol. Biol., <strong>29</strong>, 1011-1023 (2022)</a><br>\r\n<a href=\"https://doi.org/10.1038/s41586-025-08971-7\" target=\"_blank\">[12] S. Park, R. Merino-Urteaga, V. Karwacki-Neisius, G. Carrizo, A. Athreya, A. Marin-Gonzalez, N. Benning, J. Park, M. Mitchener, N. Bhanu, B. Garcia, B. Zhang, T. Muir, E. Pearce, T. Ha, Nature, (2025)</a><br>\r\n<a href=\"https://doi.org/10.1002/wcms.70024\" target=\"_blank\">[13] E. Schultz, J. Kaplan, Y. Wu, S. Kyhl, R. Willett, J. de Pablo, WIREs. Comput. Mol. Sci., <strong>15</strong>, (2025)</a></p>",
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            "contact": "<a href=\"mailto:[email protected]\"><strong>Cornelia Bujenita</strong></a>, CECAM Events and Operations Manager",
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        },
        {
            "id": 71324,
            "title": "EPFL Xplore - unveiling 2026",
            "slug": "epfl-xplore-unveiling-2026",
            "event_url": "https://memento.epfl.ch/event/epfl-xplore-unveiling-2026",
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            "end_date": "2026-05-06",
            "start_time": "18:00:00",
            "end_time": "23:00:00",
            "description": "<p>Come discover the new rover prototype of the EPFL Xplore team at SPOT </p>",
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        {
            "id": 71498,
            "title": "From Helical Motifs to Oral Drugs: Design Principles for Bioavailable Macrocyclic Peptides",
            "slug": "from-helical-motifs-to-oral-drugs-design-principle",
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            "start_date": "2026-04-20",
            "end_date": "2026-04-20",
            "start_time": "14:15:00",
            "end_time": "15:15:00",
            "description": "<p>In this seminar, I will discuss our efforts to design conformationally constrained helical macrocyclic peptides and outline the principles that enable effective targeting of protein–protein interactions beyond classical stapled peptides. In the second part, I will show how a subtle isosteric backbone modification—thioamidation—can be used to impart oral bioavailability to bioactive macrocyclic peptides. I will further illustrate how conformational restriction enhances membrane permeability and highlight the critical role of metabolic stability in achieving oral bioavailability.</p>",
            "image_description": "Prof. Jayanta Chatterjee",
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            "speaker": "Prof. Jayanta Chatterjee, Indian Institute of Science, Bangalore, India",
            "organizer": "C. Heinis",
            "contact": "C. Heinis",
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