Lachaud lab
@LabLachaud
I am deputy director at cancer research Center of Marseille, and group leader involved in DNA repair, genome instability and blood disorder
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BIG ANNOUNCEMENT📣: I haven’t been this excited to be part of something new in 15 years… Thrilled to reveal the passion project I’ve been working on for the past year and a half!🙀🥳 It started from my frustration with the depressing effect that the current publishing system has…
NANEMIAR team participate on The European Researchers' Night (September 26,2025 Murcia, Spain) #FFIS #IMIB #MurciaSalud #ArrixacaAreaI #CNRS #MERCURNA #ResearchersNight #Murcia #ScientificResearch #CongenitalAnemias #Hematology #Health #MedicalInnovation #Research
We are delighted to announce that the NANEMIAR project has been chosen as ambassador for the TIMERUN event, marking the launch of a major solidarity campaign. You can support us by sponsoring us for every kilometre we run, or come and challenge us.
We share a new NANEMIAR story from Lucas Huijs, Scientist at Mercurna (Netherlands) nanemiar.eu/nanemiar/detal…
JOB ALERT 🚨 We are hiring TWO principal investigators in cell, molecular, systems, or chemical biology in Toronto, Canada. We provide a generous startup, fully funded salary and academic appointment at U of Toronto. nature.com/naturecareers/… Please repost!
Advanced research and exploration of CRISPR technology in the field of directed evolution sciencedirect.com/science/articl…
NANEMIAR has its Third Consortium Meeting and General Assembly in the Netherlands This ambitious project is funded by the Horizon Europe program and involves key partners from Spain (FFIS-IMIB), France (CNRS), and the Netherlands (MERCURNA).
I'm super excited to announce that registrations are now open for the 19th Australian Cell Cycle, DNA Repair and Telomere Workshop. Awesome international speaker line-up, with plenty of locals being invited! Book now to secure your earlybird rate. australiancellcycle.org
Today is #InternationalThalassemiaDay. We raise awareness and support those living with this congenital blood disorder. We stand with initiatives like the 🇪🇺 #NANEMIAR project, driving research into congenital anemias. #FFIS #IMIB #MurciaSalud #Mercurna
📢 For all DNA fiber enthusiasts! 🟥🟩 We are thrilled to announce the release of our long-awaited AI-based workflow for the automated and quantitative analysis of DNA fibers. It's an exciting step forward—check it out on bioRxiv! lnkd.in/dQWUPtsP
New preprint online..
RNA polymerase II processing facilitates DNA repair and prevents DNA damage-induced neuronal and developmental failure biorxiv.org/content/10.110… #biorxiv_molbio
Philippe Baptiste, ministre en charge de l'ESR, était en déplacement à Marseille jeudi 13 mars pour échanger notamment sur les avancées en cancérologie et visiter les plateformes de pointe du @crcm_marseille @CNRS @CNRSbiologie @Insermpacacorse @paoli_calmettes
Dernière ligne droite avant de connaître les gagnants 🤞 linkedin.com/posts/departem…
🎤✨ Karaoké au Blackstone – Mercredi Soirée Moustache 🎶 Chantez vos tubes préférés 🎩 Sortez vos plus belles moustaches, qu'elles soient naturelles ou factices, tout est permis ! Venez nombreux chanter, rire, et montrer votre soutien à une noble cause !
Online Now: Profound synthetic lethality between SMARCAL1 and FANCM dlvr.it/TG2RpJ
Yesterday, Drs. Ana Belén Pérez Oliva and Vanesa Roldán Schilling participated in the Lyceum roundtable to discuss congenital anemias, 'the great unknowns' in the field of rare diseases. This was a key event to raise awareness and promote research in this much-needed area.
Fue todo un placer poder presentar parte de nuestra labor. Gracias a @AMIFP1 por darme esta oportunidad. @IMIB_RMurcia @FFIS_CARM @FundacionSeneca
👏 Nuestra compañera IMIB/FFIS, la doctora Núñez Sánchez, participó ayer en las jornadas 'Envejecimiento y Discapacidad' organizadas por la Fundación Amifp en San Javier. Durante su intervención, habló sobre envejecimiento y salud metabólica. #LaInvestigaciónEstáEnTi
On October 30th, there will be an informative talk to give a voice to rare diseases, specifically, congenital anemias. The talk will take place at the Casino de Murcia, at 7 pm. We look forward to seeing you.
Orphanet es un recurso único que reúne y mejora el conocimiento sobre las enfermedades raras para progresar en el diagnóstico, atención y tratamiento. 🙌🏻 Trabaja con la comunidad de enfermedades raras para ofrecer información actualizada de calidad y de mejorar sus servicios.
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