Bioengineer. Group leader at the IFYBINE, CONICET-Universidad de Buenos Aires. @ifibyne #betacell #pancreas #development #regeneration Opinions are my own.

Ciudad Autónoma de Buenos Aire
Joined August 2020
Santiago Rodríguez Seguí retweeted
El Premio Nobel que revolucionó la medicina y eligió no patentar su descubrimiento 👨‍⚕️🇦🇷 El 8 de Octubre de 1927 nació César Milstein, Licenciado y Doctor de Química en @Exactas_UBA.
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Fabuloso video de la UBA en defensa de la ciencia argentina.
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LAUNCHING ⛓️‍💥 The Palantir Pledge Palantir is plotting a coup against our democracies. Together with @BDSmovement, @ituc, @DiEM_25 and many more, the @ProgIntl is organising our representatives to stop them — before it is too late. Join us: buff.ly/YNLuJKC
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[Writing this in a personal capacity, not on behalf of my employer (Anthropic).] Jacob’s thread is very worth reading. Here’s my birds-eye view of the situation with risks from AI: 1. AI developers believe their technology could cause human extinction (or similarly bad outcomes). This could happen in the next few years. In general, the more senior the employee, the more concerned they are. 2. Why do AI developers continue despite the risk? Due to a mixture of commercial incentives and a belief that they are in a race with other, less responsible AI developers that will abuse the technology or develop it less safely. 3. Unlike traditional software, we can’t “program” AIs to behave how we’d like. AIs frequently severely misbehave. For instance, AIs from multiple developers recently hacked their way out of secure evaluation environments and into real-world companies, even though no one asked them to do this. 4. We have methods that can nudge AIs towards better behavior, but nothing that can robustly align them. Insofar as there is a plan, it’s to make sure that AIs are good enough at alignment training that they can align their successors better than we can align current AIs. 5. Many AI developer staff desperately want to slow down to figure out how to build AI more safely. That was the intent of this open letter (which I signed): pacingthefrontier.com/ I work on safety research at Anthropic because I hope my work will reduce the chance of these extinction-level bad outcomes.
I resigned from Anthropic today. I spent the last three years doing pretraining research at both OpenAI and Anthropic. Neither company is acting responsibly. They are racing straight to self-improving superintelligence and gambling with our lives. More thoughts below.
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Santiago Rodríguez Seguí retweeted
I resigned from Anthropic today. I spent the last three years doing pretraining research at both OpenAI and Anthropic. Neither company is acting responsibly. They are racing straight to self-improving superintelligence and gambling with our lives. More thoughts below.
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Santiago Rodríguez Seguí retweeted
"La forma de tratar a la gente que trabaja en Ciencia es una vergüenza" Adrián Paenza advirtió que los trabajadores del área de Ciencia y Tecnología están "en una situación de precariedad" y afirmó: "Esto se puede revertir, no nos vamos a entregar".
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Santiago Rodríguez Seguí retweeted
🇦🇷 La ciencia argentina se puso la camiseta. Salimos a la calle para defender la ciencia que construimos a diario, orque cuando se trata de construir el futuro de nuestro país, somos parte del mismo equipo. #MePongoLaCamiseta
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Santiago Rodríguez Seguí retweeted
Salimos desde distintos puntos de Buenos Aires para encontrarnos en el Obelisco a defender nuestros colores, nuestra ciencia y nuestra soberanía. #CienciaArgentina #MePongoLaCamiseta
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Santiago Rodríguez Seguí retweeted
Más de 6400 investigadores/as, que fueron formados durante décadas, han perdido su empleo desde diciembre de 2023. 🇦🇷Hoy a las 16 h nos vemos en el Obelisco.🔬
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#Cientificidio Durísima declaración del Consejo Interuniversitario Nacional 👇
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Santiago Rodríguez Seguí retweeted
Cell atlases are becoming coordinate systems for biology. Excited to share our latest preprint from the Human Cell Atlas Pancreas Bionetwork. 🎉🧬 We set out to build a healthy reference framework that allows us to interpret pancreatic disease, compare experimental models, and benchmark regenerative approaches within a common coordinate system. This work brings together more than 2 million pancreatic transcriptomes analyzed within a single framework, including: 🔹 815,126 healthy single cell and single nucleus transcriptomes 🔹 109 healthy donors 🔹 12 independent studies 🔹 94 harmonized cell types and transcriptional states And extending this healthy reference to: 🔹 1,018,479 transcriptomes from 261 donors spanning diabetes, pancreatic cancer, and stem cell derived islets 🔹 193,435 mouse endocrine cells for quantitative benchmarking of disease models Some highlights: 🧩 A unified healthy reference that captures cellular diversity across donors, technologies, and biological variation. 🔬 Identification and multimodal support for a putative rare polyhormonal endocrine state, providing a candidate population for future investigation. 📍 Diabetes associated endocrine cells are best understood as remodeling within healthy cellular state space rather than as entirely new cell identities. 🎯 Distinct injury associated and malignancy associated epithelial ecosystem regions emerge when pancreatic cancer is viewed relative to the healthy reference. 🧪 Quantitative benchmarking of mouse diabetes models and stem cell derived islets against adult human pancreatic reference states. More broadly, I believe this illustrates where the field is heading. Reference atlases are evolving from static cell catalogs into analytical frameworks. They provide a common coordinate system for interpreting disease biology, comparing experimental models, and ultimately accelerating translation into medicine. Congratulations to Shrey Parikh, Daniel Strobl, Malte Luecken, Diego Balboa, the Human Cell Atlas Pancreas Bionetwork, and all collaborators on this outstanding team effort. It has been a privilege to be part of this journey. Preprint: biorxiv.org/content/10.64898… #HumanCellAtlas #SingleCell #Diabetes
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Santiago Rodríguez Seguí retweeted
⚠️La Corte Suprema de Justicia de la Nación declaró inadmisible el recurso del Gobierno Nacional y dejó firme la medida cautelar que obliga al Estado a aplicar la Ley de Financiamiento Universitario. ¿Qué significa esto para nuestras universidades? 🧵
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Now online! Long-term reversal of Duchenne muscular dystrophy via circular arRNA-guided exon skipping in monkeys and humans dlvr.it/TT0Jdr
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🚨Pre-print alert!🚨 (1/7) Happy to share our latest work on glucocorticoid receptor (GR) biology, led by Cecilia De Rossi from @VLeviLab and @PresmanLab biorxiv.org/content/10.64898…
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Santiago Rodríguez Seguí retweeted
Only a few spots left for the #EISG2026 meeting in Barcelona (June 17–19) at the @the_prbb auditorium! Outstanding lineup of speakers 👇 tacticsmd.net/congreso/islet… Sponsors: @Mercodia @BreakthroughT1D @BiorepDevTeam @VectorBuilder @HaploXGlobal and PeptiGrowth.
Excited to announce #EISG2026 in Barcelona (June 17–19) at PRBB Auditorium! ⏰ Early-bird registration open until April 14 tacticsmd.net/congreso/islet… 🎤 Short talks will be selected from submitted abstracts ✨ Amazing lineup of speakers Please share & encourage trainees to apply!
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Santiago Rodríguez Seguí retweeted
Con el gran @l_masu Luciano Masullo estamos buscando un candidato/a a beca doctoral para un proyecto que nos ilusiona mucho fusionando la microscopia de súper resolución y la inmunoterapia
Junto a @gabyrabi buscamos candidato/a doctoral (Física, Ing. Electrónica o afín) para trabajar en microscopía de súper resolución, con foco en óptica avanzada, single-molecule imaging, DNA nanotech y glico-inmunología. Beca CONICET 2026. ¡Se agradece difusión!
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Santiago Rodríguez Seguí retweeted
¿POR QUÉ MARCHAMOS MAÑANA? Marchamos para exigir al Gobierno Nacional que cumpla la Ley de Financiamiento Universitario y de Recomposición Salarial, que fue sancionada y ratificada por el Congreso de la Nación.
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Santiago Rodríguez Seguí retweeted
🇦🇷 MARCHA FEDERAL Por el cumplimiento de la Ley de Financiamiento Universitario 📅 Martes 12 de mayo de 2026 📍 Plaza de Mayo CABA #UniversidadPúblicaSiempre
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