Un estudio propone un novedoso enfoque para frenar la degeneración neuromuscular en pacientes con Esclerosis Lateral Amiotrófica (ELA). Esta patología provoca la pérdida de neuronas motoras y la p...
Read moreUn estudio liderado por el CSIC descubre un mecanismo por el cual la ruta de señalización del ácido retinoico, resultante del metabolismo de la vitamina A, afecta la formación de los vertebrados ...
Read moreThe multi-faceted consortium proposes an innovative approach to overcome these limitations and to construct a pathway for developing improved vectors for clinical gene transfer. By synergising French,...
Read moreEl análisis exhaustivo de un caso permite observar cómo evolucionan paralelamente la genética del tumor y el sistema inmunitario de la paciente. La investigación resalta la necesidad de implementa...
Read moreEl análisis de las células provenientes de varios pacientes con mutaciones en ATAD3 reveló que las mitocondrias y su ADN presentan algunas alteraciones estructurales y que el colesterol celular est...
Read moreRIN4, a protein of the RIN4-like/NOI family, is a central immune signal in the interactions of plants and pathogens. In this study, we demonstrate the participation of NOI10 and NOI11 in the RIN4-medi...
Read moreResearchers at the Centre for Genomic Regulation (CRG) reveal that the Snhg11 gene is critical for the function and formation of neurons in the hippocampus. Experiments with mice and human tissues rev...
Read moreA partir de las evidencias científicas disponibles hasta el momento, la Sociedad Americana de Oncología Clínica ha actualizado sus recomendaciones consenso sobre el análisis de mutaciones germinal...
Read moreOne of them is related to heart disease, according to the CARGENCORS study. The work has allowed finding a significant association of new genetic variants previously related to heart disease, thrombos...
Read moreIt is the result of a study led by the IISPV, the Hospital Institut Pere Mata and CIBERSAM, which has made it possible to identify genetic variants involved in the cognitive impairment experienced by ...
Read moreApproximately 80% of RRDs are genetic in origin, while the remaining 20% are the result of infectious, immunological, degenerative or proliferative diseases. The most important problem faced by patien...
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