An innovative model for studying key cells in heart development and repair

by Universitat de Barcelona

A recent study led by the University of Barcelona presents an innovative in vitro model that enables the precise analysis of the activation mechanisms, cellular identity and functional properties of c...

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Microbes show almost universal potential for biodegrading plastics

by Universitat Autònoma de Barcelona (UAB)

Researchers have identified more than 600,000 microbial proteins capable of breaking down natural and synthetic plastics, revealing a far broader biodegradation potential across microbes than previous...

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Metabolomics and lipidomics in drug discovery and development: analytical approaches for biomarker discovery and preclinical research

by AMSbiopharma

The search for safer, more effective medicines increasingly depends on understanding how biological systems respond to disease, genetic variation, and therapeutic interventions at the molecular level....

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Integrated DNA Technologies Expands Coralville Manufacturing Footprint to Support Growing Global Demand for MRD Solutions

by Integrated DNA Technologies

IDT has expanded its Coralville manufacturing footprint, boosting synthesis capacity by threefold, to meet the rapidly growing demand for MRD and NGS-based oncology research workflows

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Un gen determina si las células de cáncer de mama forman metástasis o permanecen ‘dormidas’

by CSIC - Centro Superior de Investigaciones Científicas

Un estudio del Instituto de Neurociencias (CSIC-UMH) identifica el gen Prrx1 como regulador del potencial metastásico en el cáncer de mama

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Un mecanismo genético permite a las neuronas cambiar su identidad según el entorno

by CSIC - Centro Superior de Investigaciones Científicas

Un estudio del Instituto de Biomedicina de Valencia (CSIC) muestra que un pequeño cambio en los genes permite a las neuronas adquirir nuevas funciones y alterar su comportamiento

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A study expands the genetic basis of an encephalopathy associated with epilepsy and autism

by Universitat de Barcelona

A multicentre study describes the wide variability in clinical symptoms among patients and reveals that the severity of the disease does not depend exclusively on the SYNGAP1 gene, but on other geneti...

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Las mutaciones de novo explican casos graves de deficiencia de antitrombina sin antecedentes familiares

by Universidad de Murcia

Demuestran el papel relevante de las mutaciones de novo en la deficiencia de antitrombina, una enfermedad genética rara causada por alteraciones en el gen SERPINC1 que incrementa significativamente e...

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Mutations in the 'translators' of the human cell alter the reading of the genetic code in cancer and ageing

by IRB Barcelona - Instituto de Investigación Biomédica

A study by IRB Barcelona reveals that transfer RNA (tRNA) genes accumulate mutations at a frequency up to nine times higher than average

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Identificada una respuesta protectora de la pared vascular en el aneurisma de aorta abdominal

by CIBER - ISCIII

El estudio identifica un nuevo mecanismo protector implicado en el desarrollo del aneurisma de aorta abdominal (AAA), una enfermedad cardiovascular grave para la que actualmente no existen tratamiento...

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El Centro de Investigación del Cáncer reivindica el Día del ADN para explicar qué dice realmente la ciencia sobre genética, cáncer y epigenética

by Centro de Investigación del Cáncer

En el marco del Día del ADN, el Centro de Investigación del Cáncer de Salamanca ha reivindicado la necesidad de reforzar la cultura científica de la ciudadanía con información rigurosa sobre gen...

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