Fundación MEDINA, the Drugs for Neglected Diseases initiative (DNDi) and Institut Pasteur Korea have been awarded a grant of EUR 995,000 from “la Caixa” Health Research 2020 program to identify n...
Read moreÓscar Fernández-Capetillo, jefe del Grupo de Inestabilidad Genómica, recibe 300.000 euros para estudiar el potencial de la proteína SETD8 como diana en cáncer. SETD8 se ha relacionado con e...
Read moreWith the German CRO joining the European group, Kymos will strengthen its activity in the biologics and advanced therapies market and broaden its services portfolio while offering three local sites in...
Read moreLa detección temprana de COVID-19 se lleva a cabo en estos momentos principalmente mediante PCR, la prueba que ofrece mayor alto nivel de especificidad y sensibilidad, pero que requiere de equipos co...
Read moreEl grupo de investigación del CiQUS de la Universidade de Santiago de Compostela (USC) dirigido por el Prof. José Luis Mascareñas consigue un nuevo impulso en el campo de la catálisis artificial e...
Read moreResearchers at IRB Barcelona’s Cellular Plasticity and Disease Laboratory propose a more efficient way to limit cell plasticity without causing cell damage. The new method sheds light on processe...
Read moreCientíficos del Centro de Investigación del Cáncer descubren que el gen HSF2BP es responsable de una forma de insuficiencia ovárica
Read moreLa herramienta de edición genética CRISPR-Cas empleada por investigadores de la Universidad Pablo de Olavide actúa como unas ‘tijeras’ moleculares para cortar y pegar trozos de material genéti...
Read moreAs gene therapies move towards commercialization, a robust, scalable and affordable manufacturing process is critical to ensure these novel therapies reach the patient and that a pipeline of clinical ...
Read moreResearchers at the Institute for Bioengineering of Catalonia (IBEC) and the Catalan Institute of Nanoscience and Nanotechnology (ICN2) have developed a new type of encapsulated enzyme nanomotors.
Read moreDuring meiosis, recombination ensures allelic exchanges through crossovers (COs) between the homologous chromosomes. Advances in our understanding of the rules of COs have come from studies of mutatio...
Read moreDown’s syndrome is one of the most common causes of learning disabilities. Caused by the presence of all or part of a third copy of chromosome 21, it is a genetic disorder with no known cure or trea...
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