MitoMetLab
@mitometlab
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Inherited Metabolic Diseases and Muscular Diseases Research Group at Institut d'Investigacions Biomèdiques August Pi i Sunyer and Hospital Clínic of Barcelona
IDIBAPS, Barcelona
Joined April 2023
Today it's #RareDiseaseDay2024 and we want to help rising awareness about Rare Diseases (RD) and research by sharing our contributions to the #RareDiseasesResearch. Do you want to learn more?.A thread 🪡🧵. @idibaps @hospitalclinic @ciberer @NoInvisibles @rarediseaseday
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RT @idibaps: En el Dia de la Fenilcetonúria, una malaltia metabòlica causada per la falta d'un enzim necessari per a la síntesi de l'aminoà….
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Blazing-fast image creation – using just your voice. Try Grok Imagine.
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RT @msahsorin: When we stop viewing biology as static and start seeing it as a dynamic energy landscape, new patterns & opportunties for in….
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RT @AEPMI: Avances en el estudio del Síndrome de Kearns-Sayre febrero 2025, con Gloria Garrabou, Mariona Guitart y Laura Valls https://t.co….
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RT @idibaps: 📻No et perdis el programa Diga-li Ciència @radio4_rne en què Glòria Garrabou parla de tècniques multiòmiques i de recerca en m….
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Glòria Garrabou. Investigadora biomèdica (IDIBAPS). Tècniques multiòmiques per conèixer les malalties
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Encara no heu escoltat el programa d'ahir de Diga-li ciència? Doncs et deixem aquí avall l'enllaç, que hem parlat d'òmiques i d'investigació en malalties minoritàries. @rtve @RTVECatalunya @idibaps @hospitalclinic @UniBarcelona
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RT @idibaps: 📻En el #DiaMundialMalaltiesMinoritaries no us perdeu l'entrevista a Glòria Garrabou de l'IDIBAPS en el capítol dedicat a "La C….
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RT @idibaps: El grup ➡️Malalties metabòliques hereditàries i malalties musculars⬅️ ha identificat nous gens i mecanismes moleculars associa….
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🧬📡 Hoy es el Día de las Enfermedades Raras y estamos en Burgos con el @CentroCREER donde Glòria, Mariona y Frede nos hablarán sobre los retos que supone estudiar EERR y la importancia de impulsar a los jóvenes investigadores. Link en vivo:
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🧬📄🤩 We recently published our latest IBM model using induced Pluripotent Stem Cells (iPSC). By reprogramming IBM patients fibroblasts we were able to differentiate these iPSC into myotubes, that have been validated as they reproduce some hallmarks of the disease.
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🤩🤩🤩 This Thursday!!!.
🗓️ Save the date! Feb 20th, our KSS researchers will be giving a webinar about our latest works. Join us in this link below!. @idibaps @hospitalclinic @AEPMI @CIBERER @UniBarcelona
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RT @GDunnArt: Check out that neuron layering in the cerebral cortex! Neurons are arranged into distinct processing layers in order to most….
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RT @Share4Rare_es: 🎙 #LaCienciadeloSingular ⚡ Volvemos con un grupo de #enfermedadesraras que se originan por un fallo en el funcionamiento….
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RT @Share4Rare_es: @IRSJD_info @CIBERER @CibererBiobank @CIBER_ISCIII @AEPMI @hospitalclinic 🗣️ Hablamos con Mar O’Callaghan @SJDbarcelona_….
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🔊 We hope all assistents enjoyed and learnt from all the speakers but specially from our IP Glòria who gave a great talk about the PKU Marató TV3 results! 🧪🔬 @hospitalclinic @idibaps @UniBarcelona @CIBERER @la_marato
On Saturday Feb 8th we will be talking about the transition of pediatric patients into the adult hospital (HSJdD - HCB) and the research on PKU derived from the Marato de TV3 grant.
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🗓️ Save the date! Feb 20th, our KSS researchers will be giving a webinar about our latest works. Join us in this link below!. @idibaps @hospitalclinic @AEPMI @CIBERER @UniBarcelona
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🐦🦋 Hey! Do you want to keep track of our lab news? Follow us also in @\or in the link below 👇.
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On Saturday Feb 8th we will be talking about the transition of pediatric patients into the adult hospital (HSJdD - HCB) and the research on PKU derived from the Marato de TV3 grant.
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